This work involved preparation of cyclic compounds are containing of more than one hetero atoms in their structures like (N)-nitrogen atom. A seven-member ring compounds were prepared by condensation of N,N-di methyl amino benzaldehyde with aromatic amines to give compounds [N2-N17], these compounds were found to react with maleic anhydride to give 7-memberd ring [N18-N32]. All these compounds [N2- N32] were prepared by pericyclic reactions.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
This Journal publishes original research work that contributes significantly to further the scientific knowledge in pharmacy.
An efficient synthesis, characterization and antibacterial activity of novel ...iosrjce
IOSR Journal of Applied Chemistry (IOSR-JAC) is a double blind peer reviewed International Journal that provides rapid publication (within a month) of articles in all areas of applied chemistry and its applications. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Chemical Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
Synthesis and Characterization of Schiff Base from Aromatic Amine and Aromati...ijtsrd
The synthesis of Schiff base From Aromatic Amine And Aromatic P Nitro benzaldehyde was performed by a novel method of stirring followed by the addition of p nitro benzaldehydeandm nitro aniline 0.02M . Characterization of the synthesized compounds, determination of purity and identity of the compounds using following spectroscopic and chromatographic techniques Solubility, Thin Layer Chromatographic studies, Ultra Violet studied rotational and vibrational studies FT IR studies. The compounds were investigated for their Antimicrobial activity by cup plate method. Compound1 nitro 4 1 imino,4 nitrophenyl benzene was found to be the most active according to pharmacological evaluation exhibited antimicrobial. Ms. Chetana D. Patil | Mr. Digamber N. Bhosale | Ms. Smita P. Bedis "Synthesis and Characterization of Schiff Base from Aromatic Amine and Aromatic P-Nitro Benzaldehyde" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-5 , August 2019, URL: https://www.ijtsrd.com/papers/ijtsrd26401.pdfPaper URL: https://www.ijtsrd.com/pharmacy/medicinal-chemistry/26401/synthesis-and-characterization-of-schiff-base-from-aromatic-amine-and-aromatic-p-nitro-benzaldehyde/ms-chetana-d-patil
Mixed Ligand, Palladium(II) and Platinum(II) Complexes of Tertiary Diphosphin...Karwan Omer
Palladium(II) and platinum(II) complexes containing the mixed ligands tertiary
diphosphinesdppm. dppp and dppf with Thioester ligand S-1H benzo[d] imidazole-2-yl benzothioate
(HSBIBT) have been prepared by the reaction of PdCl2 and PtCl2 with one equiv of tertiary
diphosphines ligands to form [Pd(k2-dppf)Cl2], [Pd(k2-dppp)Cl2] and [Pt(k2-dppmCl)Cl2] complexes
and then add the ligand HSBIBT to these complexes to form mixed ligand complexes. The prepared
complexes have been characterized by single-crystal X-ray diffraction, elemental analysis, magnetic
susceptibility, molar conductance, IR spectral data and UV-Visible. The results suggested that the
ligand HSBIBT bonded to the metal through N atom and square planner geometries were assigned
for the complexes.
Syntheses and Characterizations of Some New N-alkyl, Isoxazole and Dioxazole ...IJAEMSJORNAL
N-alkyl and cycloadducts derivatives of 5-Chloroisatin were synthesized in good to excellent yields. The method evidences a selective N-alkylation when using 1,2-bis (2-chloroethoxy) ethane as efficient spacer at room temperature on the 5-Chloroisatin moiety. A general method for the 1,3-dipolar cycloaddition of 4-Chlorobenzaldoxime to alkynes provides a useful alternative route to get newisoxazole et dioxazole derivatives.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
This Journal publishes original research work that contributes significantly to further the scientific knowledge in pharmacy.
An efficient synthesis, characterization and antibacterial activity of novel ...iosrjce
IOSR Journal of Applied Chemistry (IOSR-JAC) is a double blind peer reviewed International Journal that provides rapid publication (within a month) of articles in all areas of applied chemistry and its applications. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Chemical Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
Synthesis and Characterization of Schiff Base from Aromatic Amine and Aromati...ijtsrd
The synthesis of Schiff base From Aromatic Amine And Aromatic P Nitro benzaldehyde was performed by a novel method of stirring followed by the addition of p nitro benzaldehydeandm nitro aniline 0.02M . Characterization of the synthesized compounds, determination of purity and identity of the compounds using following spectroscopic and chromatographic techniques Solubility, Thin Layer Chromatographic studies, Ultra Violet studied rotational and vibrational studies FT IR studies. The compounds were investigated for their Antimicrobial activity by cup plate method. Compound1 nitro 4 1 imino,4 nitrophenyl benzene was found to be the most active according to pharmacological evaluation exhibited antimicrobial. Ms. Chetana D. Patil | Mr. Digamber N. Bhosale | Ms. Smita P. Bedis "Synthesis and Characterization of Schiff Base from Aromatic Amine and Aromatic P-Nitro Benzaldehyde" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-5 , August 2019, URL: https://www.ijtsrd.com/papers/ijtsrd26401.pdfPaper URL: https://www.ijtsrd.com/pharmacy/medicinal-chemistry/26401/synthesis-and-characterization-of-schiff-base-from-aromatic-amine-and-aromatic-p-nitro-benzaldehyde/ms-chetana-d-patil
Mixed Ligand, Palladium(II) and Platinum(II) Complexes of Tertiary Diphosphin...Karwan Omer
Palladium(II) and platinum(II) complexes containing the mixed ligands tertiary
diphosphinesdppm. dppp and dppf with Thioester ligand S-1H benzo[d] imidazole-2-yl benzothioate
(HSBIBT) have been prepared by the reaction of PdCl2 and PtCl2 with one equiv of tertiary
diphosphines ligands to form [Pd(k2-dppf)Cl2], [Pd(k2-dppp)Cl2] and [Pt(k2-dppmCl)Cl2] complexes
and then add the ligand HSBIBT to these complexes to form mixed ligand complexes. The prepared
complexes have been characterized by single-crystal X-ray diffraction, elemental analysis, magnetic
susceptibility, molar conductance, IR spectral data and UV-Visible. The results suggested that the
ligand HSBIBT bonded to the metal through N atom and square planner geometries were assigned
for the complexes.
Syntheses and Characterizations of Some New N-alkyl, Isoxazole and Dioxazole ...IJAEMSJORNAL
N-alkyl and cycloadducts derivatives of 5-Chloroisatin were synthesized in good to excellent yields. The method evidences a selective N-alkylation when using 1,2-bis (2-chloroethoxy) ethane as efficient spacer at room temperature on the 5-Chloroisatin moiety. A general method for the 1,3-dipolar cycloaddition of 4-Chlorobenzaldoxime to alkynes provides a useful alternative route to get newisoxazole et dioxazole derivatives.
Mechanistic Aspects of Oxidation of P-Bromoacetophen one by Hexacyanoferrate ...IJERA Editor
The kinetics of oxidation of p-bromoacetophenone by hexacyanoferrate (III) has been studied in alkaline
medium. The order of reaction with respect of both acetophenone and hexacynoferrate (III) has been found to be
unity. The rate of reaction increases with increase in the concentration of sodium hydroxide.On addition of
neutral KCl, reaction rate increases. The effects of solvent and temperature have been also studied. The product
p-bromophenyl glyoxal have been characterized by IR studies.
Synthesis, Spectroscopic study & Biological Activity Of Some Organotin(Iv) De...IOSR Journals
Some di-and triorganotin(IV) derivatives of (2E)-N-methyl-(2
oxo1,2diphenylethylidne)hydrazinecarbothioamide synthesised by the reactions of the corresponding di and
triorganotin(IV) chlorides with the sodium salt of (2E)-N-methyl-(2-
oxo1,2diphenylethylidne)hydrazinecarbothioamide in different molar ratios. These derivatives have been
characterized by elemental analyses ,molecular weights, conductivity measurements and spectral(IR, 1H, 13C
and 119 Sn NMR) studies.
Synthesis of substituted 1, 2, 4-triazole derivatives by Microwave irradiationIOSR Journals
Various substituted Triazole-Thiol containing different functional group have been synthesized by microwave method. The title product 1-[(3H-indol-2-ylamino) methyl]-4-phenyl-4, 5-dihydro-1H-1, 2, 4-triazole-3-thiol is synthesized by using amino benzothiazole. The final structures have been established on the basis of their chemical analysis and spectral data. All micro-wave synthesized compounds results into good yield as compared to conventional method of which fluoro substituted compound shows maximum yield.
Synthesis, Characterization and Study of Antioxidant Activities of Some New P...IJRES Journal
A series of substituted pyrazoline derivatives 5(a-c) have been synthesized by the reaction of substituted chalcones 4(a-c) with isatinhydrazide. The starting materials, chalcones were prepared by clasien schimidt condensation of appropriate 1-hydroxy-2-acetonaphthone with substituted aldehydes in the presence of sodium hydroxide and in poly ethylene glycol (PEG-400). The structures of the synthesized compounds were confirmed by IR, 1HNMR & Mass spectral data. The synthesized compounds were screened for Antioxidant Activity by DPPH method.
Synthesis, characterization, in vitro cytotoxic and antioxidant activities of...ijperSS
ABSTRACT
A series of novel (Z)-3-(2-(4-(2-oxo-2H-chromen-3-yl) thiazol-2-yl-)hydrazono)indolin-2-one (8a-8d, 9) were synthesized with various substituted indole derivatives. Structures of the newly synthesized compounds were elucidated by FT-IR, 1H-NMR, 13C-NMR and API-ES Mass spectral data. The in vitro cytotoxic activities of the complexes measurement against the human cancer T-lymphocyte cell lines. In vitro evaluation of these title complexes revealed cytotoxicity from 6.8-18µg/mL against CEM, 9.2-21µg/mL against L1210, 10-19µg/mL against Molt4/C8, 8-12µg/mL against HL60 and 8-16µg/mL against BEL7402. Coumarin derivatives 8c and 8d showed that quite significant anticancer activities. The antioxidant activity of the synthesized compounds was evaluated by DPPH scavenging method. Compounds 8c, 8d and 9 showed significant antioxidant activity compared with that of standard drug, ascorbic acid.
Key words: Coumarin, DPPH, Cytotoxic activity.
A green and efficient friendly process for synthesis of drug against dormant ...Premier Publishers
The objective of this study is the synthesis of (2E,6E)-2,6-bis(4-nitrobenzylidene)cyclohexanone by the cross-aldol condensation between 4-nitrobenzaldehyde and cyclopentanone catalyzed by modified fluorapatite in aqueous media and the reaction conditions were optimized by the response surface methodology. This process is an important protocol for the synthesis of drug against dormant version of the Mycobacterium tuberculosis H37Ra. The work-up procedure is simplified by simple filtration with high yield and by-products of usual undesirable reaction are not observed.
A series of novel 5-[2-(4-fluorobenzyl)-6-aryl-imidazo[2,1-b][1,3,4]thiadiazol-5-ylmethylene] thiazolidine-2,4-dione derivatives (4a-d) were synthesized. These final compounds (4a-d) were synthesized by Knoevenagel condensation of 2-(4-fluorobenzyl)-6-arylimidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehydes (3a-d) with thiazolidine-2,4-dione. All the newly synthesized compounds were screened for their invivo hypoglycemic and hypolipidemic activity in male Wister rats. The Structures of all the newly synthesized compounds were established by analytical and spectral data.
Bio-active phytoconstituents from non-polar extracts of Diospyros lotus stems...Jing Zang
The objective of this study is to isolate phytoconstituents from Diospyros lotus stems extracts and to evaluate antifungal, lectin and trypsin inhibitory activities of the extracts. The stems were extracted with petroleum ether, diethyl ether and chloroform, respectively, three compounds were isolated and identified as β-sitosterol, stigmasterol and protocatechic acid from both petroleum ether and ether extracts. Chloroform extract was subjected to silica gel column chromatography using CHCl3 as eluent and an increasing amount of EtOAc and MeOH gradually resulted in the isolation and identification of kaempferol 8-O-methylether, apigenin, kaempferol, kaempferol 3-O-α-rhamnoside and luteolin 7-O-β-glucoside. The petroleum ether, diethyl ether and chloroform extracts of Diospyros lotus were tested at the concentration of 0.1 mg/ml for their effect against the fungus Mycosphaerella arachidicola and for their lectin and trypsin inhibitory activities. The results showed that the extracts exhibited significant antifungal activity but had no hemagglutinating and trypsin inhibitory activities.
FACTORS ASSOCIATED WITH UNNECESSARY DRUG THERAPY AND INAPPROPRIATE DOSAGE IN ...Jing Zang
To assess factors associated with unnecessary drug therapy and inappropriate dosage in hospitalized patients. A hospital based cross-sectional study design was employed. The study was conducted in Jimma University Specialized Hospital, Jimma, which is 345 Km from South west of Addis Ababa. All patients who were admitted to medical ward from February 5 – March 21, 2011 were included in the study. Data on socio-demographic variables, past medical history, past medication history, current diagnosis, current medications, vital signs and relevant laboratory data were collected by using bed side patient interview guided semi-structured questionnaire and data abstraction formats for card review. The data were analysed by using SPSS version 16 for windows. Descriptive statistics, cross-tabs, chi-square and logistic regression were done. Out of 257 study participants 140(54.5%) had unnecessary drug therapy or inappropriate dosage. The only independent factors which predicted the unnecessary drug therapy in study population was polypharmacy while not considering organ function test, polypharmacy and clinically significant potential drug-drug interaction were independent factors associated with inappropriate dosage . The prevalence of unnecessary drug therapy or inappropriate dosage is significantly high.
Mechanistic Aspects of Oxidation of P-Bromoacetophen one by Hexacyanoferrate ...IJERA Editor
The kinetics of oxidation of p-bromoacetophenone by hexacyanoferrate (III) has been studied in alkaline
medium. The order of reaction with respect of both acetophenone and hexacynoferrate (III) has been found to be
unity. The rate of reaction increases with increase in the concentration of sodium hydroxide.On addition of
neutral KCl, reaction rate increases. The effects of solvent and temperature have been also studied. The product
p-bromophenyl glyoxal have been characterized by IR studies.
Synthesis, Spectroscopic study & Biological Activity Of Some Organotin(Iv) De...IOSR Journals
Some di-and triorganotin(IV) derivatives of (2E)-N-methyl-(2
oxo1,2diphenylethylidne)hydrazinecarbothioamide synthesised by the reactions of the corresponding di and
triorganotin(IV) chlorides with the sodium salt of (2E)-N-methyl-(2-
oxo1,2diphenylethylidne)hydrazinecarbothioamide in different molar ratios. These derivatives have been
characterized by elemental analyses ,molecular weights, conductivity measurements and spectral(IR, 1H, 13C
and 119 Sn NMR) studies.
Synthesis of substituted 1, 2, 4-triazole derivatives by Microwave irradiationIOSR Journals
Various substituted Triazole-Thiol containing different functional group have been synthesized by microwave method. The title product 1-[(3H-indol-2-ylamino) methyl]-4-phenyl-4, 5-dihydro-1H-1, 2, 4-triazole-3-thiol is synthesized by using amino benzothiazole. The final structures have been established on the basis of their chemical analysis and spectral data. All micro-wave synthesized compounds results into good yield as compared to conventional method of which fluoro substituted compound shows maximum yield.
Synthesis, Characterization and Study of Antioxidant Activities of Some New P...IJRES Journal
A series of substituted pyrazoline derivatives 5(a-c) have been synthesized by the reaction of substituted chalcones 4(a-c) with isatinhydrazide. The starting materials, chalcones were prepared by clasien schimidt condensation of appropriate 1-hydroxy-2-acetonaphthone with substituted aldehydes in the presence of sodium hydroxide and in poly ethylene glycol (PEG-400). The structures of the synthesized compounds were confirmed by IR, 1HNMR & Mass spectral data. The synthesized compounds were screened for Antioxidant Activity by DPPH method.
Synthesis, characterization, in vitro cytotoxic and antioxidant activities of...ijperSS
ABSTRACT
A series of novel (Z)-3-(2-(4-(2-oxo-2H-chromen-3-yl) thiazol-2-yl-)hydrazono)indolin-2-one (8a-8d, 9) were synthesized with various substituted indole derivatives. Structures of the newly synthesized compounds were elucidated by FT-IR, 1H-NMR, 13C-NMR and API-ES Mass spectral data. The in vitro cytotoxic activities of the complexes measurement against the human cancer T-lymphocyte cell lines. In vitro evaluation of these title complexes revealed cytotoxicity from 6.8-18µg/mL against CEM, 9.2-21µg/mL against L1210, 10-19µg/mL against Molt4/C8, 8-12µg/mL against HL60 and 8-16µg/mL against BEL7402. Coumarin derivatives 8c and 8d showed that quite significant anticancer activities. The antioxidant activity of the synthesized compounds was evaluated by DPPH scavenging method. Compounds 8c, 8d and 9 showed significant antioxidant activity compared with that of standard drug, ascorbic acid.
Key words: Coumarin, DPPH, Cytotoxic activity.
A green and efficient friendly process for synthesis of drug against dormant ...Premier Publishers
The objective of this study is the synthesis of (2E,6E)-2,6-bis(4-nitrobenzylidene)cyclohexanone by the cross-aldol condensation between 4-nitrobenzaldehyde and cyclopentanone catalyzed by modified fluorapatite in aqueous media and the reaction conditions were optimized by the response surface methodology. This process is an important protocol for the synthesis of drug against dormant version of the Mycobacterium tuberculosis H37Ra. The work-up procedure is simplified by simple filtration with high yield and by-products of usual undesirable reaction are not observed.
A series of novel 5-[2-(4-fluorobenzyl)-6-aryl-imidazo[2,1-b][1,3,4]thiadiazol-5-ylmethylene] thiazolidine-2,4-dione derivatives (4a-d) were synthesized. These final compounds (4a-d) were synthesized by Knoevenagel condensation of 2-(4-fluorobenzyl)-6-arylimidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehydes (3a-d) with thiazolidine-2,4-dione. All the newly synthesized compounds were screened for their invivo hypoglycemic and hypolipidemic activity in male Wister rats. The Structures of all the newly synthesized compounds were established by analytical and spectral data.
Bio-active phytoconstituents from non-polar extracts of Diospyros lotus stems...Jing Zang
The objective of this study is to isolate phytoconstituents from Diospyros lotus stems extracts and to evaluate antifungal, lectin and trypsin inhibitory activities of the extracts. The stems were extracted with petroleum ether, diethyl ether and chloroform, respectively, three compounds were isolated and identified as β-sitosterol, stigmasterol and protocatechic acid from both petroleum ether and ether extracts. Chloroform extract was subjected to silica gel column chromatography using CHCl3 as eluent and an increasing amount of EtOAc and MeOH gradually resulted in the isolation and identification of kaempferol 8-O-methylether, apigenin, kaempferol, kaempferol 3-O-α-rhamnoside and luteolin 7-O-β-glucoside. The petroleum ether, diethyl ether and chloroform extracts of Diospyros lotus were tested at the concentration of 0.1 mg/ml for their effect against the fungus Mycosphaerella arachidicola and for their lectin and trypsin inhibitory activities. The results showed that the extracts exhibited significant antifungal activity but had no hemagglutinating and trypsin inhibitory activities.
FACTORS ASSOCIATED WITH UNNECESSARY DRUG THERAPY AND INAPPROPRIATE DOSAGE IN ...Jing Zang
To assess factors associated with unnecessary drug therapy and inappropriate dosage in hospitalized patients. A hospital based cross-sectional study design was employed. The study was conducted in Jimma University Specialized Hospital, Jimma, which is 345 Km from South west of Addis Ababa. All patients who were admitted to medical ward from February 5 – March 21, 2011 were included in the study. Data on socio-demographic variables, past medical history, past medication history, current diagnosis, current medications, vital signs and relevant laboratory data were collected by using bed side patient interview guided semi-structured questionnaire and data abstraction formats for card review. The data were analysed by using SPSS version 16 for windows. Descriptive statistics, cross-tabs, chi-square and logistic regression were done. Out of 257 study participants 140(54.5%) had unnecessary drug therapy or inappropriate dosage. The only independent factors which predicted the unnecessary drug therapy in study population was polypharmacy while not considering organ function test, polypharmacy and clinically significant potential drug-drug interaction were independent factors associated with inappropriate dosage . The prevalence of unnecessary drug therapy or inappropriate dosage is significantly high.
Acute toxicity and anti-ulcerogenic activity of an aqueous extract from the s...Jing Zang
Terminalia superba is a plant used in traditional medicine to treat many illnesses particularly gastro-intestinal disorders. This study was aimed to evaluate the acute toxicity and gastric anti-ulcer activity of an aqueous extract of Terminalia superba (AETs). The LD50 was determined by the graphic method of Miller and Tainter (1944) and the calculation method of Dragsted and Lang (1957) in mice. The preventive anti-ulcerogenic action of the extract was assessed using four models of gastric ulcer induction namely HCl/Ethanol solution, indomethacin solution, pylorus ligation and cold restraint stress in rats. The LD50 obtained by the oral administration of AETs was 12.2 ± 0.21 g/kg b.w. and 12.33 ± 0.87 g/kg b.w. by the graphic method and the calculation method respectively. The administration of AETs intraperitoneally gave 1.97 ± 0.29 g/kg b.w. (graphic method) and 1.93 ± 0.21 g/kg b.w. (calculation method) as LD50s. The preventive gastric anti-ulcer study revealed that for doses ranging from 125 to 500 mg/kg body weight, EATs significantly (P<0.05)>< 0.05) increased mucus production and reduced gastric acid secretion. Phytochemical screening of the aqueous extract of the stem bark of Terminalia superba showed the presence of polyphenols, tannins, flavonoids, quinones, coumarines, saponins, reduced sugar, sterols and polyterpenes. These results suggested that the preventive anti-ulcer activity of AETs may be due to a cytoprotective effect. The LD50s found indicated that the extract was not toxic and that the phytochemical coumpounds present in EATs could be responsible for its effects. In conclusion, the preventive gastric anti-ulcer and the non toxic effects of the aqueous extract of Terminalia superba could justify the use of this plant in traditional medicine to treat abdominal disorder and pains.
SIMULTANEOUS QUANTIFICATION OF TELMISARTAN AND METOPROLOL SUCCINATE IN TABLET...Jing Zang
An accurate and precise liquid chromatographic method was developed for the simultaneous estimation of telmisartan and metoprolol succinate in tablets. The chromatographic analysis was performed on Nucleosil C18 Column (250*4.6mm 5µ particle size) with mobile phase consisting of acetonitrile and potassium di-hydrogen orthophosphate buffer (pH- 2.8) in the ratio 60:40v/v, at a flow rate of 0.8ml/min and eluents monitored at 220nm. The retention time for telmisartan was found to be 3.392 and for metoprolol succinate it was found to be 5.221 minutes. The proposed method is simple, accurate and precise and could be successfully employed in routine quality control for the simultaneous estimation of telmisartan and metoprolol succinate in tablets.
Involvement of pH and Internal Surface of Cans on the Budesonide Solution Sta...Jing Zang
The purpose of stability testing is to provide evidence on how the quality of a drug substance or drug product varies with the time under the influence of a variety of environmental factors such as temperature, humidity, pH and light, and to establish a retest period for the drug substance or a shelf life for the drug product and recommended storage conditions. Due to high lipophilicity of budesonide, it is not possible to prepare simple solution having the desired concentration of this drug without using co-solvent. Aim of this study was to compare the stability of budesonide at different canisters (standard aluminium, anodized aluminium direct surface modification (DSM) and fluorocarbon polymer (FCP) and pH values. Two type of formulation without and with acid were prepared to evaluate the effect of pH on stability of budesonide solution in anodized aluminium, DSM and FCP cans. After addition of strong acid, under accelerated stability conditions, only a slight decrease in the assay is observed after six months. In this study the best results have been obtained with anodized aluminium cans and solution with a pH of 3.5.
The aim of the present work is to carry out acute toxicity study for root bark powder of Argemone mexicana. It is one of the potent liver tonics used for liver disorders. The exposure of this powder in the form of aqueous slurry on Swiss mice was carried out and the exposure route was oral single administration with water. The observations of changes in body weight, food and water intake as well as cage side observations were reported. The observations prove that the plant material is found to be nontoxic.
INNOVATIVE MEDICINES, TECHNOLOGIES AND APPROACHES FOR IMPROVING PATIENTS' HE...Jing Zang
Despite remarkable scientific and technological achievements during the 20th century, the 21st century has already witnessed additional new and profound changes in all areas of medical science and research, including innovations and discoveries in biology, cellular biology, genomics and proteomics, pharmaceuticals, medical devices, and information technology. This review is an up-date on some of the existing therapies, drug delivery technologies, and approaches that aimed to improve patients’ health care and quality of their life.
INFLUENCE OF AYURVEDIC ANTIDIABETIC AGENT ON THE PHARMACODYNAMICS OF GLIMEPIRIDEJing Zang
The present study is planned to explore the influence of ayurvedic antidibetic drug Madhumehari on the pharmacodynamics of glimepiride. Wistar albino rats of either sex were induced diabetes with alloxan and were used. The study was done in two phases, acute phase and chronic phase. In acute phase the diabetic rats were divided into six groups each consisting of 6. The diabetic control (Group-I) was treated with 0.5%W/V CMC suspension orally. To the diabetic group II, III and IV glimepiride 4mg/kg body wt, madhumehari 100mg/kg body wt. and madhumehari 200mg/kg body wt. were administered orally respectively. Groups V and VI were given orally the combination of glimepiride 4mg/kg body wt + madhumehari 100mg/kg body wt and glimepiride 4mg/kg body wt + madhumehari 200mg/kg body wt. In chronic study the protocol was similar to that of acute study but treatment was given for 7 days. Blood samples were collected from retro orbital plexus at predetermined time intervals for serum glucose level estimation after the oral dosing of glimepiride. The combination of glimepiride + madhumehari has shown antidiabetic activity at 3rd hour. Glimepiride when administered along with madhumehari 100 & 200mg orally the fall in serum glucose level was found to be more significant when compared with the per se treatment of glimepiride, madhumehari 100 & 200mg in both acute and chronic studies. From the above study it may be concluded that there is additive type of Pharmacodynamic interaction is possible between glimepiride and madhumehari.
TRIAZOLOTHIADIAZOLES AS ANTIMICROBIAL AGENT: A SHORT RIVIEWJing Zang
Triazolothiadiazole is a fused heterocyclic contained triazole and thiadizole nucleus and exhibited immense pharmacological activities. The triazolothiadiazole nucleus is present in compounds are evaluating for new products that possess some remarkable pharmacological activities. triazolothiadiazole constitute an important class of biologically active drug molecules which has attracted attention of medicinal chemists due to their wide range of pharmacological properties. These compounds are being synthesized as drugs by many researchers in order to combat diseases with minimal toxicity and maximal effects. These predictions has provided therapeutic pathway to develop new effective biologically active triazolothiadiazole.
Targeted Intermediates of Eudesmic Acid: Synthesis and X-ray Investigationsijtsrd
it was carried out synthesis of esters and their dinitro derivatives of 3,4,5-trimethoxybenzoic (eudesmic) acid. Esterification of eudesmic acid carried out n absolute methanol or ethanol and corresponding methyl and ethyl 3,4,5-trimethoxybenzoates (2, 3) have been synthesized in good yields. It was revealed that nitration of these esters gives only dinitro products. The structure of the synthesized compounds of the methyl and ethyl 2,6-dinitro-3,4,5-trimethoxybenzoates (4, 5) was determined by X-ray diffraction analysis (XRD). In the asymmetric part of the crystal structures of 4, 5 one and two molecules are observed, respectively. In crystalline structures a flat nitro groups and carboxylic groups do not participate in the conjugation with aromatic rings. In the crystal structure of 4, an intermolecular C8-H...O9 hydrogen bond is observed, these H bonds link the molecules along the [010] axis. In the crystal structure of 5, intermolecular C9B-H...O4A and C10B-H...O8A hydrogen bonds form chains along the [011] axis. The formed chains are cross linked by the intermolecular C9B-H...O5A hydrogen bonds. Olimova M.I. | Okmanov R. Ya. | Elmuradov B. Zh."Targeted Intermediates of Eudesmic Acid: Synthesis and X-ray Investigations" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-1 | Issue-6 , October 2017, URL: http://www.ijtsrd.com/papers/ijtsrd2417.pdf http://www.ijtsrd.com/chemistry/other/2417/targeted-intermediates-of-eudesmic-acid--synthesis-and-x-ray-investigations/olimova-mi
Synthesis and Anti-Inflammatory activity of Sulpha/substituted 1,2-Diazolesinventionjournals
A Novel compound namely N1 (3 Nicotinoyl) 3,5 dimethyl-4-(N-4-sulfamoyl-azo)-1,2-diazoles has been synthesized by two step processes. Synthesis of N1 -4-sulfamoylphenylhydrazono-3,5-dimethyl propane-1,3-dione and sulfonamide, which interacting with 3-Nicotinoyl hydrazine to form final compound. The newly synthesized compound N1 -(3-Nicotinoyl)-3,5-dimethyl 4-(N1 -4-sulfamoyl phenyl azo) 1,2-diazoles was screened for antiinflammatory activity
Synthesis and Anti-Inflammatory activity of Sulpha/substituted 1,2-Diazolesinventionjournals
A Novel compound namely N1 (3 Nicotinoyl) 3,5 dimethyl-4-(N-4-sulfamoyl-azo)-1,2-diazoles has been synthesized by two step processes. Synthesis of N1 -4-sulfamoylphenylhydrazono-3,5-dimethyl propane-1,3-dione and sulfonamide, which interacting with 3-Nicotinoyl hydrazine to form final compound. The newly synthesized compound N1 -(3-Nicotinoyl)-3,5-dimethyl 4-(N1 -4-sulfamoyl phenyl azo) 1,2-diazoles was screened for antiinflammatory activity
SiO2@FeSO4 nano composite: A recoverable nano-catalyst for eco-friendly synth...Iranian Chemical Society
Various aldoximes and ketoximes synthesis of corresponding aldehydes and ketones in the presence of SiO2@FeSO4 nano composite as recoverable nano catalyst and NH2OH·HCl. The SiO2@FeSO4 nano composite system was carried out between 10 to 15 min in oil bath (70-80 °C) under solvent-free condition in excellent yields in addition this protocol can be used for industrial scales. This method offers some advantages in term of clean reaction conditions, easy work-up procedure, short reaction time, applied to convert α-diketones to α-diketoximes (as longer than other carbonyl compounds), α,β-unsaturated aldehydes and ketones to corresponding oximes and suppression of any side product. So we think that NH2OH•HCl/SiO2@FeSO4 nano composite system could be considered a new and useful addition to the present methodologies in this area. Structure of products and nano composite elucidation was carried out by 1H NMR, 13C NMR, FT-IR, scanning electron microscopy (SEM).
Visible Spectrophotometric Determination of Gemigliptin Using Charge Transfer...Ratnakaram Venkata Nadh
A visible spectrophotometric method was developed and validated for the determination of gemigliptin present in bulk drug and tablet formulation. It involves an indirect method of charge transfer complex formation in presence of NBS, metol and suphanilic acid. Gemigliptin was subjected to oxidation with excess amount of oxidant (NBS) and the unconsumed NBS oxidizes metol to give p-N-methylbenzoquinone monoamine (PNMM) which in turn forms a charge transfer complex with sulphanilic acid. Then validated the above developed method as per the current ICH guidelines. An excellent correlation coefficient (> 0.999) was found for the obtained regression equation
(y = –0.0302x + 0.928) in the range of 2.0–30.0 μg mL-1. The method was found to be simple and rapid because it does not involve any solvent extraction. The recovery levels of the drug were in the range 99.92 – 100.08.
Visible Spectrophotometric Determination of Gemigliptin Using Charge Transfer...Ratnakaram Venkata Nadh
A visible spectrophotometric method was developed and validated for the determination of gemigliptin present in bulk drug and tablet formulation. It involves an indirect method of charge transfer complex formation in presence of NBS, metol and suphanilic acid. Gemigliptin was subjected to oxidation with excess amount of oxidant (NBS) and the unconsumed NBS oxidizes metol to give p-N-methylbenzoquinone monoamine (PNMM) which in turn forms a charge transfer complex with sulphanilic acid. Then validated the above developed method as per the current ICH guidelines. An excellent correlation coefficient (> 0.999) was found for the obtained regression equation
(y = –0.0302x + 0.928) in the range of 2.0–30.0 μg mL-1. The method was found to be simple and rapid because it does not involve any solvent extraction. The recovery levels of the drug were in the range 99.92 – 100.08.
Molecular docking studies of abelmoschus esculentus for anti diabetics and a...Jing Zang
Okra (Abelmoschus esculentus (L) Moench) or bhendi also known as ladies finger is an important vegetable crop in India, and African regions. Abelmoscus esculentus having the medicinal property of anti inflammatory , anti diabetics, anti oxidant activities . In this studies we are going to analysis the anti diabetics and anti inflammatory property of Abelmoscus esculentus by using molecular docking studies. Diabetics is a major cause of death and the number of new cases, as well as the number of individuals living with Diabetics, is expanding continuously. Now a days It is one of the most common diseases in the worldwide .Foot ulceration remains a major health problem for diabetic patients and has a major impact on the cost of diabetes treatment. One major complication of diabetes is foot ulceration, which occurs in as many as 15–25% of type 1 and type 2 diabetic patients over their lifetimes. The phytochemicals of Abelmoscus esculentus are analysed and optimized with the Arguslab to investigate the interactions between the target compounds and the amino acid residues of the Mafa and Mmp9. All the compound have shown binding pose between from – 3.25 to -7.95 and -7.95 into -11.40 out of ten compound . [E,E] Farenesal with Mafa protein and gossypol with Mmp9 protein show best ligand energy -10.55 and -8.88 Kcal/mol with 1 and 1 hydrogen bond of distance is 3.0 and 2.3 respectively .
Molecular docking studies of gloriosa superba for anti cancer and anti tuberc...Jing Zang
Gloriosa superba is a medicinal plant generally found in western parts of Tamilnadu and kerala in India. Gloriosa superba having the medicinal property of anticancer, antibacterial, antifungal, anti Tuberculosis and mutagenic activities. In this studies we are going to analysis the anti cancer and anti tuberculosis property of Gloriosa superba by using molecular docking studies. Cancer is a major cause of death and the number of new cases, as well as the number of individuals living with cancer, is expanding continuously. Cervical cancer is one of the most common cancers among women worldwide . Tuberculosis is a common and often deadly infectious disease caused by mycobacteria , usually Mycobacterium tuberculosis in humans. Tuberculosis usually attacks the lungs but can also affect other parts of the body. The phytochemicals of Gloriosa superba are analysed and optimized with the Arguslab to investigate the interactions between the target compounds and the amino acid residues of the E7 and DAHP. All the compound have shown binding pose between from – 3.25 to -7.95 and -7.95 into -11.40 out of ten compound .Chrysophanic acid with E7 protein and Colchicine with DAHP protein show best ligand energy -9.52049 and -7.47679Kcal/mol with 1 and 3 hydrogen bond of distance is 2.3 and 2.2,2.9 and 3.2 respectively .
A systemic review on antibiotic use evaluation in paediatricsJing Zang
Drug utilization is the marketing, distribution, prescription, and use of drug in a society, with special emphasis on the resulting medical, social and economic consequences. Antibiotics are valuable discoveries of modern medicine and their definitive and or appropriate use has led to a decline in the morbidity and mortality associated with various infectious diseaseswhile inappropriate use of antibiotics can increase morbidity, mortality, patient cost and bacterial antibiotic resistance.Antimicrobial agents are among the most commonly prescribed drug in Paediatrics. Because of an overall rise in health care costs, lack of uniformity in drug prescribing and the emergence of antibiotic resistance, monitoring and control of antibiotic use are of growing concern and strict antibiotic policies should be warranted. The caution use for antimicrobial agents is very important as their unavailability or resistance can be life threatening. Irrational drug use is a common practice in developing countries. In India, clinician often prescribe three or four drugs to treat the most trivial conditions for the sake of satisfying the patients need to receive drugs or the drug sellers need for profit. Thus drug use evaluation studies are required for all drugs in general and particularly for antibiotics.
A review on medicinal properties of Camel milkJing Zang
Many research findings proved that Camel milk is closer to human milk than any other milk. It is often easily digested by lactose-intolerant individuals. It is rich in healthy vitamins and minerals, especially B vitamins, vitamin C and iron. The lactoferrin in camel milk has antibacterial, antiviral and anti-tumor properties. It contains disease-fighting immunoglobulins which are small in size, allowing penetration of antigens and boosting the effectiveness of the immune system. It is a rich source of insulin and also it containing approximately 52 units of insulin in each liter of camel milk, making it a great treatment option for Type 1 or Type 2 diabetics as well as Gestational Diabetes. This review focused on the medicinal properties of camel milk which will be more useful to generate value added products formation from camel milk.
Formulation and Evaluation of Solid dispersion for Dissolution Enhancement of...Jing Zang
Nifedipine, a calcium channel blocker antihypertensive drug, is a poorly water soluble drug and belongs to BCS class II. The objective of the research work was to formulate and optimize solid dispersions (SDs) of a poorly water soluble drug, nifedipine, with sodium starch glycollate, croscarmellose sodium, eudragit E-100. Solid dispersions were prepared by solvent evaporation techniques in different weight ratios of polymers. The results indicated that homogeneous or heterogeneous conditions during the preparation methods employed governed the internal structures of the polymer matrices while retaining the drug in an amorphous form. The physical mixtures and solid dispersions were subjected to drug content and dissolution test. The best formulation, nifedipine with croscarmellose sodium in 1:7 ratio, among all was further adsorbed on neusilin US2 to form ternary mixture. The increased dissolution was achieved by more than 70percent and 30percent comparatively to the nifedipine API and marketed product respectively. The tablet dosage form prepared from ternary mixture was stable at stressed conditions 40±2°C and 75±5% RH. The release kinetics of drug from formulation and marketed product follows peppas model. The similar factor f2 was within limit for the product at stressed conditions with the product at room temperature at the same time.
Glucose lowering potential of hydromethanolic extract of RauwolfiaJing Zang
The objective of the present study was to evaluate the phytochemistry, acute toxicity and glucose lowering potential of hydromethanolic roots extract (HMREt) of Rauwolfia serpentina. The qualitative analysis of HMREt showed the presence of many important phyto-constituents except anthraquinones, carbohydrates and saponins whereas quantitatively it found rich in total phenols. In acute toxicity study, orally administrated HMREt from 5-250 mg/ kg was observed safe and non-sedative while its doses from 500-2500 mg/kg were found sedative and induced mortalities (17-100%) within 4 hours of administration. The median lethal dose (LD50) of same extract was calculated as 1412.54 mg / kg (log LD50 = 3.15 mg/ kg) from log doses verses probit graph. The HMREt in doses of 50, 100 and 150 mg/kg induced significant percent decrease in blood glucose level at 30, 60 and 120 minutes in normo-hyperglycemic test mice as compared to control and negative control groups (p<0.05). The results concluded that HMREt has glucose lowering potential either by developing glucose tolerance or by pancreatic action in normo-hyperglycemic mice.
Nutritive and Anti-nutritive composition of Wild grown Canavalia gladiata seedsJing Zang
The wild Canavalia gladiata seeds were widely distributed in Nupeland, North Central Nigeria. It was obtained and processed by decoating, sun drying and grinding into powder. Using petroleum ether (40-60oC), the fats was extracted, the protein content, ash content, crude fibre, moisture, carbohydrate with respective values of 3.60±0.14, 11.1±0.83, 4.25±0.11, 3.39±0.27, 5.85±0.47 and 72.3±0.08 % as well as the mineral contents were determined using standard methods. The mineral composition determined from the C. gladiata seeds shows higher values of potassium, zinc, iron and calcium 25.15±0.03, 25.89±0.27, 18.3±0.14 and 17.25±0.49 mg/100 g respectively. This seed analyzed contains low yield of anti-nutritional contents which suggested that, it could be safe for human consumption since it fell below the lethal dose limit. The sample contains reasonable amount of essential and non-essential amino acids with yield varying between 48 and 52%. The presence of unsaturated and saturated fatty acids in the C. gladiata was 96 and 4% respectively. The higher percentage of unsaturated fatty acid present makes this seed desirable for consumption by the person with heart diseases. In addition, from the data obtained this oil becomes attractive options for commercial purposes since it is suitable for the manufacture of soaps, lubricating oil, candles as well as pharmaceutical industries.
Pharmacovigilance in South Africa: Undocumented undergraduate training and pr...Jing Zang
Pharmacovigilance is a clinical discipline that is gaining more and more attention worldwide and in Africa. The rolling out of large scale programs on HIV/AIDS, tuberculosis and malaria has heightened the need to step up efforts to have pharmacovigilance concepts to be operationalized in clinical practice. A quick search in PubMed and Google Scholar and a review of available literature was conducted in order to establish whether medical, nursing and pharmacy undergraduate students are taught pharmacovigilance concepts and skills for effective practice. It seems that there is a paucity of data on the undergraduate training in pharmacovigilance in South Africa. It may be that there might be inadequate training on pharmacovigilance during undergraduate training of medical, nursing and pharmacy students in South Africa. More studies are needed to document the views and experiences of South African students and healthcare professionals on training and practice of pharmacovigilance.
Black Seed (Nigella sativa) Possess Bioactive Compounds Act as Anti-Helicobac...Jing Zang
ABSTRACT
Gastrointestinal associated problems are physiological processes effects almost every individual at some stage of their life. Among the various plants studied previously Nigella sativa possess numerous therapeutic properties including its anti-ulcer potential. This seed carries significant anti-ulcer properties arbitrated by antimicrobial activities specifically against gastric damage induced by Helicobacter pylori. Evidence is available supporting the utilization of NS and its bioactive components in a daily diet for health improvement. This review is envisioned to emphasis on the curative role of NS and to provide an evidence for being a functional food to protect from a range of malaises. An attempt is also made to emphasize aspects that need further investigations for it to be use in clinics in future.
In vitro enzyme inhibition studies on new sulfonamide derivatives of 4-tosyl ...Jing Zang
Sulfonamides are considered to be pharmaceutically important class of compounds. In the present work, N-(2,4-dimethylphenyl)-4-toluenesulfonamide (3) was synthesized by the reaction of 2,4-dimethylaniline (1) and 4-tosyl chloride (2; 4-methylbenzenesulfonyl chloride) using 10% aqueous Na2CO3 solution as reaction medium. At the second step, the synthesized molecule 3 was made to react with different alkyl/aralkyl halides (4a-o) to yield the target compounds, 5a-o, using N,N-dimethylformamide (DMF) as reaction medium and lithium hydride as an activator. The synthesis of all the compounds was verified by spectral techniques using IR, 1H-NMR and EIMS; and further examined for their anti-enzymatic activities. The synthesized compound 5f represented a suitable inhibitory potential against α-glucosidase and lipoxygenase enzymes.
In vitro sun screening activity of Sri Lankan orthodox black tea (Camellia Si...Jing Zang
Currently, there is demand for the development of herbal sunscreen formulations to suppress harmful effects of UV rays. In this regard, this study, was conducted to investigate the sun screen potential of Sri Lankan Orthodox black tea (made from buds and top most leaves of Camellia sinensis L plant) using three grades (Dust No:1, Broken Orange Pekoe and Orange Pekoe) using UV spectroscopic technique and Mansur equation. Sun Protection Factor (SPF) value was determined using 20% aqueous extracts (Black tea brews). The results revealed that all three tea samples had markedly high absorbance values (1.4 to 4.2) at 290-320 nm range and SPF values above 15 which are considered as the threshold value for good sunscreen. The SPF value of Dust No:1, B.O.P.F and O.P were respectively 36, 23 and 22. This is a novel finding for Sri Lankan black tea. It is concluded that Sri Lankan black tea, especially, Dust No: 1 can function as an efficient sunscreen agent and has great promise to be developed as cheap, safe and effective topical botanical sunscreen acting via multiple mechanisms (considering its other reported bioactivities).
HPTLC determination of carotenoid profile in the leaf and bark samples of lor...Jing Zang
Influence of host plants on the carotenoid profile of Loranthus longiflorus leaf and bark samples collected from Casuarina equisetifolia and Ficus religiosa host trees were determined by HPTLC method. The methanol extract of L. longiflorus leaf samples obtained from C. equisetifolia host trees showed 9 compounds while it was 8 compounds in the leaf samples collected from F. religiosa host tree. Among the compounds, 5 and 3 compound in each sample, respectively, was identified as carotinoids while the others were unknown. Four compounds from each leaf samples collected from C. equisetifolia (peak no. 4- 6 & 8) and F. religiosa (peak no. 1-3 & 6) host trees showed similar Rf values (0.15, 0.19, 0.23 & 0.53, respectively). Similarly, the methanol extract of L. longiflorus bark sample collected from C. equisetifolia and F. religiosa host trees contained 8 compounds each. Of these compounds only 3 from each sample was identified as carotenoids whereas others were unknown and none of these compounds showed any similar Rf values. One compound from leaf and park samples of L. longiflorus collected from C. equisetifolia (peak no. 6 & 4) and F. religiosa (peak no. 4 & 3) showed similar Rf values (0.23 & 0.26), respectively.
Antinociceptive and Diuretic Activities of Tagetes erecta LinnJing Zang
In the present investigation, the possible antinociceptive and diuretic activities of methanolic extract of Tagetes erecta has been tested in animal models. The methanol extract of both aerial part and root of the plant exhibited significant antinociceptive activity at higher dose (400 mg/kg body weight) in Swiss albino mice. The root extract was found to reduce the writhing more effectively than that of aerial part which is comparable to that produced by aminopyrine, used as standard drug. In addition, crude whole plant extract was also showed efficient diuresis at higher dose 400 mg/kg tested. Diuretic activity was proved by the electrolyte loss ratio (Na+/K+ excretion ratio) and we used furosemide as the reference.
PREVAILENCE OF MIGRIANE IN A LOW INCOME COMMUNITY OF KARACHIJing Zang
Migraine is the most common problem affecting large population, with prevalence frequency 10-12 %. This study was conducted to evaluate the prevalence of migraine in a low income community in Karachi from June-Oct, 2013. Three hundred and seven participants were involved in this study. For this purpose cross-sectional community based questionnaire was designed in accordance with the diagnostic criteria given by International Headache Society. Data collection was carried out by personal visit to patients and through clinics. It was observed that females (65.5%) are more affected from migraine then male. 32.9% housewives reported that they are suffering from migraine. This medical problem is common among youngsters (38.1%) than old citizens. Employees working in different organizations (39.7%), were found to be mostly affected from migraine then self employed persons. Majority of the migraine patients (41%) reported that they are suffering from common symptoms including: photophobia, phonophobia, nausea, vomiting etc. Dietary habits of individuals were found to be closely associated with migraine such as use of caffeine, chocolate are prominent; and their use is common among 75% patients cumulatively. It was evaluated that certain disease conditions i.e. stress (33.6%), depression (22.1%) and anxiety (18.9%) are more common among sufferers of migraine.
The French Revolution, which began in 1789, was a period of radical social and political upheaval in France. It marked the decline of absolute monarchies, the rise of secular and democratic republics, and the eventual rise of Napoleon Bonaparte. This revolutionary period is crucial in understanding the transition from feudalism to modernity in Europe.
For more information, visit-www.vavaclasses.com
Macroeconomics- Movie Location
This will be used as part of your Personal Professional Portfolio once graded.
Objective:
Prepare a presentation or a paper using research, basic comparative analysis, data organization and application of economic information. You will make an informed assessment of an economic climate outside of the United States to accomplish an entertainment industry objective.
Biological screening of herbal drugs: Introduction and Need for
Phyto-Pharmacological Screening, New Strategies for evaluating
Natural Products, In vitro evaluation techniques for Antioxidants, Antimicrobial and Anticancer drugs. In vivo evaluation techniques
for Anti-inflammatory, Antiulcer, Anticancer, Wound healing, Antidiabetic, Hepatoprotective, Cardio protective, Diuretics and
Antifertility, Toxicity studies as per OECD guidelines
2024.06.01 Introducing a competency framework for languag learning materials ...Sandy Millin
http://sandymillin.wordpress.com/iateflwebinar2024
Published classroom materials form the basis of syllabuses, drive teacher professional development, and have a potentially huge influence on learners, teachers and education systems. All teachers also create their own materials, whether a few sentences on a blackboard, a highly-structured fully-realised online course, or anything in between. Despite this, the knowledge and skills needed to create effective language learning materials are rarely part of teacher training, and are mostly learnt by trial and error.
Knowledge and skills frameworks, generally called competency frameworks, for ELT teachers, trainers and managers have existed for a few years now. However, until I created one for my MA dissertation, there wasn’t one drawing together what we need to know and do to be able to effectively produce language learning materials.
This webinar will introduce you to my framework, highlighting the key competencies I identified from my research. It will also show how anybody involved in language teaching (any language, not just English!), teacher training, managing schools or developing language learning materials can benefit from using the framework.
Francesca Gottschalk - How can education support child empowerment.pptxEduSkills OECD
Francesca Gottschalk from the OECD’s Centre for Educational Research and Innovation presents at the Ask an Expert Webinar: How can education support child empowerment?
Instructions for Submissions thorugh G- Classroom.pptxJheel Barad
This presentation provides a briefing on how to upload submissions and documents in Google Classroom. It was prepared as part of an orientation for new Sainik School in-service teacher trainees. As a training officer, my goal is to ensure that you are comfortable and proficient with this essential tool for managing assignments and fostering student engagement.
How to Make a Field invisible in Odoo 17Celine George
It is possible to hide or invisible some fields in odoo. Commonly using “invisible” attribute in the field definition to invisible the fields. This slide will show how to make a field invisible in odoo 17.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
June 3, 2024 Anti-Semitism Letter Sent to MIT President Kornbluth and MIT Cor...Levi Shapiro
Letter from the Congress of the United States regarding Anti-Semitism sent June 3rd to MIT President Sally Kornbluth, MIT Corp Chair, Mark Gorenberg
Dear Dr. Kornbluth and Mr. Gorenberg,
The US House of Representatives is deeply concerned by ongoing and pervasive acts of antisemitic
harassment and intimidation at the Massachusetts Institute of Technology (MIT). Failing to act decisively to ensure a safe learning environment for all students would be a grave dereliction of your responsibilities as President of MIT and Chair of the MIT Corporation.
This Congress will not stand idly by and allow an environment hostile to Jewish students to persist. The House believes that your institution is in violation of Title VI of the Civil Rights Act, and the inability or
unwillingness to rectify this violation through action requires accountability.
Postsecondary education is a unique opportunity for students to learn and have their ideas and beliefs challenged. However, universities receiving hundreds of millions of federal funds annually have denied
students that opportunity and have been hijacked to become venues for the promotion of terrorism, antisemitic harassment and intimidation, unlawful encampments, and in some cases, assaults and riots.
The House of Representatives will not countenance the use of federal funds to indoctrinate students into hateful, antisemitic, anti-American supporters of terrorism. Investigations into campus antisemitism by the Committee on Education and the Workforce and the Committee on Ways and Means have been expanded into a Congress-wide probe across all relevant jurisdictions to address this national crisis. The undersigned Committees will conduct oversight into the use of federal funds at MIT and its learning environment under authorities granted to each Committee.
• The Committee on Education and the Workforce has been investigating your institution since December 7, 2023. The Committee has broad jurisdiction over postsecondary education, including its compliance with Title VI of the Civil Rights Act, campus safety concerns over disruptions to the learning environment, and the awarding of federal student aid under the Higher Education Act.
• The Committee on Oversight and Accountability is investigating the sources of funding and other support flowing to groups espousing pro-Hamas propaganda and engaged in antisemitic harassment and intimidation of students. The Committee on Oversight and Accountability is the principal oversight committee of the US House of Representatives and has broad authority to investigate “any matter” at “any time” under House Rule X.
• The Committee on Ways and Means has been investigating several universities since November 15, 2023, when the Committee held a hearing entitled From Ivory Towers to Dark Corners: Investigating the Nexus Between Antisemitism, Tax-Exempt Universities, and Terror Financing. The Committee followed the hearing with letters to those institutions on January 10, 202
2. Nagham et al., World J Pharm Sci 2013; 1(4): 163-167
some drops of acetic acid was refluxed for (3 hrs) .
The reaction mixture was then allowed to cool to
room temperature and solid product was filtered
and recrystallized from ethanol to give colored
crystals from compounds [N2-N17]
FT.IR spectra: FT.IR-showed appearance band at
(1620-1640)cm- due to imine(20,21) group (C=N) of
compounds [N2- N33],while this band is disappear
and two bands are appear at (1700,1670) cm-1 due
to(11,12) (lactone/lactam) group of oxazepine
compounds [N18-N33], this evidence to formation of
compounds [N2- N33] . Other data of functional
groups shown in the following, Table (1) .
Synthesis of 2-(p-N.N-dimethyl amino benzyl)-3aryl-2,3-dihydro
[1,3]-oxazepine-4-7diones.(Oxazepine derivatives) [N18-N33] .
General procedure (11,12,18): A mixture of equimolar
amounts (0.02 mole) of schiff's bases [N2-N17] and
maleic anhydride in dry benzene was refluxed for
(4-5 hrs) , the solvent was removed and the
resulting
colored
crystalline
solid
was
recrystallized from dry 1,4-dioxane to give the title
products of compounds [N18-N33].
UV-spectra & (C. H. N)-Analysis: UV spectra,
most of compounds have electron transition (n-π)
due to(6,22) the hetro atoms (O,N) in these
compounds beside of transition (π-π) of conjugated
system. the UV-spectra of compounds how Uv-Vis
spectrum Table (3) of compounds [N18-N33] ,
showed the absorbance bands data were appeared
at (λmax = 315 - 400 nm) (6,11), these compounds
have chromophore group with oxochromic group
due to hyperchromic effect such as conjugated
system and carbonyl group in oxazepine compound
with (-OH) group as oxochromic group of
compound [N18] , (iodine) in compound [N19] , (NH-CO-) group in compound [N20,N32], (C=N) ,
(C-S) in compound [N22 , N23, N25] , (-N=C-N=)
group in compounds [N24 ,N32 , N33 ] , (-NO2) group
in compound [N21] , (COOH) groups in compounds
[N26-N29] , for this reason , the bands shift to the
maximum wave length data for compounds [N18N33] are listed in Table (3) .
RESULTS AND DISCUSSION
The reaction of any anhydride with anil compounds
are classified as a[5+2=7] ,5-atom component plus
2-atom component leading to 7-memberd ring, the
pericyclic reactions in this work involves synthesis
of compounds by condensation with aromatic
amines to give Schiff's base [[N2-N17]] according to
well-known procedure(6,11,18)). Compounds [N2-N17]
react with maleic anhydride to produce 7-memberd
hetero cyclic compounds [N18-N33] of oxazepine.
Synthesized compounds [N2- N33] have been
characterized
by their melting point
and
spectroscopic methods (UV-Visble , FT.IR ,
H.NMR spectrum , and (C. H. N)-analysis) .
ACKNOWLEDGEMENT
H.NMR-spectrum: H.NMR-spectrum of compound
[N2- N33] shown: singlet signal at δ 9.92-9.97 for
one proton of anil
group(7,11) (-CH=N) in
compound [N2-N17] ,singlet signal at δ 10.2 that
could be attributed to the proton(11,18) of oxazepine
(O-CH-N) group in compound [N18-N33] ,and other
peaks .
I would like to express my thanks to Mr. Audai .S
in center Lab-Institute of Earth and Environmental
science-Al-Bayt University H.J.K in Jordan for
providing C.H.N element analytical, H.NMRspectrum.
[N18-N33]
164
4. Nagham et al., World J Pharm Sci 2013; 1(4): 163-167
Figure (3)-H-NMR spectrum of compound [N22
Figure (4)-H-NMR spectrum of compound
REFERENCES
1.
2.
3.
4.
5.
6.
7.
8.
9.
Francis.A and Richard.J .,(1983)..,"chemistry of imino bases and reactions " , Adv org chem ,p.A 2 nd
ed ,plenum press .New York ,p.243.
Abid., O.H., (2001)., "synthesis of cyclic compounds from Schiff base" ,National j Chem., (3), 480492 ,
Jarrahpour.A ,Motamedifar.M and Paskhir.k., ,(2004). ," preparation of schiff base derivatives" ,
Molecule, 9, (875),1420
Nagham.M., (2005).,"synthesis and characterization of macro cycle of schiff bases " .,Al-Mustan J
Sci., 16(3), 17-29,
Baluja.A ,Solanki and Kachhadia.N.) ., (2006), " preparation of heterocyclic from anhydrids" ,
J.Ir.Chem. Soc., 3 (4),313.
Nagham.M. ., (2006).," synthesis and identification of macro cycles as a ligands with some ions " ,J
Babylon., 11 (3), 537-542 ,
Davar.B , Sabounchi. S and Rayati . S. ; (2000)., "synthesis of schiff bases from amino acids ",. MetOrg. Chem., 30(8),1535
Abdul-Z ; (2000), "schiff base as a ligands with ions II2b" , J.Chin. Chem. Soc ., 48,153-158
Sanjayf.T and Obaki.J , ,(2007)., "Identification & biological activity of derivitives of imines
compounds " , , J .Chem., 15 (1) 48-54.
166
5. Nagham et al., World J Pharm Sci 2013; 1(4): 163-167
10. Nair.R,Shah.A and Baluja.S; (2007) , " study effect of cyclization of Nicompounds on fungi"
,.J.Serb.Chem.Soc.,71 (7), 733,
11. Nagham.M. , (2010)., " synthesis and characterization of derivatives of amide "., J Babylon., 3 (18),
925-942,
12. Tawfiq, M.T. , (2004). ,"synthesis and characterization of 1 ,3-oxazepine - 3,7-dione " ,ph. D. Thesis,
University of Baghdad . ,College of Iben alhaitham.
13. Leovac.V; (2005)., "preparation of cyclic compounds from schiff bases through condensation reaction
" ,Serb .Chem .Soc.70 (3), 393-399..
14. Huda.H ; (2005). ,"sysesnthesis of new hetro cyclic compounds from schiff ba " , M. Sc. Thesis,
University of Al-Mustansiriyah .,College of science.
15. Filinonov.V and.Trmosh C ; (1986)., "characterization of some new heterocyclic compunds as a
ligands " ,J . Org . Chem. Of USSR ,22, (4),.2214-2219.
16. Hassan, H.A. , (2005). , "synthesis and investigation of new derivatives of aldamine compounds " , M.
Sc. Thesis, University of Al-Mustansiriyah .,College of science
17. Hassan, Y.K. , (2003)., M.Sc., " preparation of series of imines compounds through cyclization" ,
Thesis, University of Al-Mustansiriya . College of science
18. Hassein F.A. and Abid, O.H. (2001)., " synthesis and identification of seven memberd ring of
oxazepine" , Iraqi Journal of Chemistry, 27, (3),. 493-504.
19. Salih, N. , (2002) , " synthesis and characterization of derivatives of schiff bases with ascorbic acide"
,.M. Sc. Thesis, University of Kufa . College of education.
20. Muthukumar. C ,Sabastyan. A ,Ramesh.M ., (2012 )., " identification of N,N-di amine compounds",
Int. J. ChemTech.Res ,4,(4),1322-1328.
21. Xia . J and Wang .G ., (2005) ., " preparation of derivative of hydrazine in fused ring" J .Synthesis
.,4(8), 2379 – 2383.
22. Lee . K and Kong .K ., (2002) ,"synthesis of cyclic of hetero atom" ,Bull . Korean . Chem. Soc ., 4,
(23) , 1505 – 1506.
167
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