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Alkaloids
Submitted By:
Ananya Azad Hrisha- 1558
Alkaloids
Alkaloids are basic (alkali-like), nitrogen-containing organic constituents found in some plants. They give
positive responses with Dragendorff, Mayer, Hager and Wagner reagents .Alkaloids are organic bases.
Many alkaloids are poisonous, others are addictive (e.g. cocaine), and some are used clinically (e.g.
morphine). More than 10 000 alkaloids are now known, the first discovered being narcotine, isolated from
opium by Derosne in 1803. (Plant Alkaloids, Jack G Woolley) 1
Alkaloids are normally classified according to the heterocyclic ring system they possess, but some authors
prefer a classification based on their biosynthetic origins from amino acids, e.g. phenylalanine, tyrosine or
tryptophan. (Justin et al.)2
Many individual names are formed by adding the suffix "-ine" to the species or
generic alkaloids. For example, atropine is isolated from the plant Atropa belladonna, strychnine is obtained
from the seed of Strychnine tree.4
Alkaloids are important chemical compounds that serve as a rich reservoir
for drug discovery. Several alkaloids isolated from natural herbs exhibit antiproliferation and antimetastasis
effects on various types of cancers both in vitro and in vivo. Alkaloids, such as camptothecin and
vinblastine, have already been successfully developed into anticancer drugs. (Jin-Jian Lu et al., 2012)3
.
Classification of Alkaloids
 Currently, alkaloids are classified according to both chemical structure and origin. In Table 1 an
alkaloid classification is presented. (Emin Cadar et al., 2015)5
Table-1: Alkaloid classification according to structure of derivatives
Group Representatives
Tropane derivatives Atropine, cocaine, ecgonine, scopolamine
Isoquinoline derivatives Opium alkaloids, morphine, codeine, thebaine,
papaverine, narcotine, sanguinarine, narceine,
hydrastiane, berberine
Quinoline derivatives Quinine, quinidine, dihydroquinone,
dihyrdoqunidine, strychnine, brucine, veratrine,
cevadine
Pyridine derivatives Piperine, coniine, trigonelline, arecaidine,
guvacine, pilocarpine, cytosine, nicotine,
sparteine, pelletierine
Pyrolidine derivatives Hygrine, cuschygrine, nicotine
Terpeness From aconite: aconitine
Sterols: solanine, samandarine
Betaine derivatives (with quaternary azoth) Muscarine, choline, neurine
Phenethylamine derivatives Mescalime, ephedrine
Indole derivatives Tryptamie derivatives: dimethyltryptamine
(DMT), NMT, psilocybin, serotonin, melatonin
Ergolines: alkaloids originating from ergot:
ergine, ergotamine, lyseric acid, and so on.;
derivatives of lysergic acid (LSD)
Beta-carbolines: harmine, yohimbine, reserpină,
emetine
Purine derivatives Xanthine derivatives: caffeine, theobromine,
theophylline
 Alkaloids are often divided into the following major groups: (Anonymous)
1. "True alkaloids”: which contain nitrogen in the heterocycle and originate from amino acids. Their
characteristic examples are atropine, nicotine and morphine. This group also includes some alkaloids which
beside nitrogen heterocycle contain terpene (e.g. evonine) or peptide fragments (e.g. ergotamine). This
group also includes piperidine alkaloids coniine and coniceine although they do not originate from amino
acids.
2. "Protoalkaloids”: which contain nitrogen and also originate from amino acids. Examples include
mescaline, adrenaline and ephedrine.
3. Polyamine alkaloids: derivatives of putrescine, spermidine and spermine.
4. Peptide and cyclopeptide alkaloids.
5. Pseudalkaloids: alkaloid-like compounds which do not originate from amino acids. This group includes,
terpene-like and steroid-like alkaloids, as well as purine-like alkaloids such as caffeine, theobromine and
theophylline. Some authors classify as pseudoalkaloids such compounds such as ephedrine and cathinone.
Those originate from the amino acid phenylalanine, but acquire their nitrogen atom not from the amino acid
but through transamination.
Table-2: Brief description on Alkaloids
Alkaloid Name Source
(Genus/Family)
Source
Type &
Inhabitant
Therapeutic Uses
Qunine Cinchona bark,
extract
Family: Rubeceae1
Genus: Cinchona
 Cinchona
calisaya Wedd.
(1848)
 Cinchona
officinalis L.
(1753)
 Cinchona
pubescens Vahl
(1790)
Tree,
medicinal
plant.
They are native
to the
tropical Andea
n forests of
western South
America.
(Motley and
Cheryl, 2010)
6.
 Antimalarial1
, anti-
pyretic, and slight
analgesic.5
 Can be used in
persistent febrile
states, migraine.5
Qunidine Antiarrhythmic (heart)
Vinblastine Periwinkle plant
Catharanthus roseus
and other vinca
plants.
Subshrub
 Component of a
number
of chemotherapy
regimens
 also used to treat
histiocytosis.7
Vinca
Alkal
oids
Vincristine
Genus: Catharanthus
Family: Apocynaceae
Endemic to
Madagascar
 Delivered
via intravenous infusi
on for use in various
types
of chemotherapy
regimens
 Occasionally used as
an immunosuppressa
nt, for example, in
treating thrombotic
thrombocytopenic
purpura(TTP) or
chronic idiopathic
thrombocytopenic
purpura (ITP).8
Vindesine  Is an anti-
mitotic vinca
alkaloid used
in chemotherapy.
 Used to treat many
different types of
cancer, including
leukaemia, lymphom
a, melanoma, breast
cancer, and lung
cancer.
Vinorelbine  Chemotherapy
medication used to
treat a number of
types of cancers like
breast cancer, non-
small cell lung
cancer.
 Also active
in rhabdomyosarcom
a.9
Codeine Obtained from poppy
plant Papaver
somniferum
Genus: Papaver
Family: Papaveraceae
Annual herb.
Native range
is probably the
eastern
Mediterranean
.
.
 Used as a central
analgesic, sedative,
hypontic,
antinonciceptive,
antiperistaltic.10
 Suppress both
artificially induced
and disease-related
cough.11
 Widely used as anti-
tussivedrug.12
Morphine Primary source of
morphine is isolation
Annual herb.  Used to treat acute
and chronic pain.5
Vin
ca
Alk
aloi
ds
from poppy straw of
the opium poppy.13
Genus: Papaver
Family: Papaveraceae
Native range
is probably the
eastern
Mediterranean
.
.
 Immediate-release
morphine is
beneficial in reducing
the symptom
of shortness of
breath due to
both cancer and
noncancer causes.14,15
 Sustained-release
morphine
significantly reduces
breathlessness safely,
with its benefits
maintained over
time.16,17
Papaverine Papaverine is
extracted from the
milky juice of raw
poppy capsules
(opium).5
Genus: Papaver
Family: Papaveraceae
Annual herb.
Native range
is probably the
eastern
Mediterranean
.
 An
opiumalkaloidantispa
smodic drug, used
primarily in the
treatment of visceral
spasm, vasospasm
(especially those
involving the heart
and the brain), and
occasionally in the
treatment of erectile
dysfunction.
 Effect is exerted
directly on smooth
muscles.5
Strychnine
The strychnine
tree (Strychnos nux-
vomica L.), also
known as nux
vomica, poison
nut, semen
strychnos and quaker
buttons.
Genus: Strychnos
Family: Loganiaceae
A deciduous tr
opicaltree nati
ve to India,
and southeast
Asia.
 Very toxic.
 Convulsant.2
 Effective in digestive
problems, different
types of pains etc.
Atropine  Datura
stramonium L.
(syn. D. inermis).
 Datura anoxia
 Atropa
belladonna
 Herbaceo
us,
leafy annu
als and
short-
lived pere
nnial.
 Atropine is used as
an antidote in
muscarine
intoxications.5
 In ophthalmology, it
is used for pupil
dilation (mydriasis)
 Mandragora
officinarum
Genus: Datura
Family: Solanaceae
 Believed
to have
originated
in Mexico,
but has
now
become
naturalize
d in many
other
regions.
in ocular
examinations.5
 Competitive
antagonist of
muscarinic
acetylcholine
receptors.2
 Anti-cholinergic,
anti-myopia effects.2
Berberine Berberis species,
Hydrastis,
Canadensis,
Xanthorhiza
simplicissima,
Phellodendron
amurense, Coptis
chinensis, Tinospora
cordifolia, Argemone
mexicana and
Eschscholzia
californica
Many
plants/trees of
various places.
 Anti inflammatory,
anti bacterial/viral,
recently experiments
showed anti diabetic
and beneficial effects
on cardiovascular
system and anti
cancer and others
disorders such as
intestinal2
Cytisine (baptitoxine,
sophorine)
Labum and Cytisus of
Family: Fabaceae
Shrub
Native to
western and
central
Europe.
 Acetylcholine
agonist, smoking
cessation drug.
Nicotine Nicotiana
tobacum
Genus: Nicotiana
Family: Solanaceae
Forb/herb
Originated in
the tropical
Americas
(South
America,
Mexico, and
the West
Indies)
 Stimulant,
antiherbivore,
insectide, anti-
inflammatory.2
Caffeine Found in coffee, tea,
cola nuts, mate,
guarana, and cocoa.
 Stimulant of the
CNS, increase of
pulse and arterial
blood pressure,
bronchial dilator,
stimulant of intestinal
peristalsis.
Reference:
1. Plant Alkaloids Jack G Woolley, De Montfort University, Leicester, UK
2. Plant Secondary Metabolites: Biosynthesis, Classification, Function and Pharmacological
Properties Justin N. Kabera1
, Edmond Semana1
, Ally R. Mussa1
and Xin He1, 2
1) Department of Pharmacology, School of Chinese Materia Medica, Tianjin University of
Traditional Chinese Medicine, Tianjin 300193, China
2) Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China
3. Review Article: Alkaloids Isolated from Natural Herbs as the Anticancer Agents, Jin-Jian Lu, Jiao
Lin Bao, Xiu-Ping Chen, Min Huang, and Yi-Tao Wang, State Key Laboratory of Quality Research
in Chinese Medicine (University of Macau) and Institute of Chinese Medical Sciences, University
of Macau, Avenue Padre Toma’s Pereira, Taipa 999078, Macao, China, Received 11 May 2012;
Revised 17 July 2012; Accepted 30 July 2012, Academic Editor: Alvin J. Beitz, Copyright © 2012
Jin-Jian Lu et al.
4. Chemical Encyclopedia: http://www.xumuk.ru/encyklopedia/119.html
Emetine
Ipecac
Cephalelisipecacuan
ha A. Rich. (Rio
Ipecac)
and
C. acuminata H. Karst
(Cartagena ipecac).
Family: Rubiaceae
Shrubby plant.
Grows in
Brazilian
rainforests and
other locations
in Central and
South
America.
 Ipecac is used in the
treatment of
poisoning by
induction of emesis
and production of
expectoration.
 Ipecac syrup
(Clinical
applications)-Ipecac
syrup is used to
induce vomiting,
after the ingestion of
toxic compounds or
after a drugs
overdose.18
Cephaeline
SORBICILLACTONE-A Salt-water culture of
a Penicillium
chrysogenum
strain isolated from a
specimen of the
Mediterranean
sponge
Irciniafasciculata.19,20
Mediterranean
.
 Active against
leukemia cells
without showing
notable
cytotoxicity.21
 Has anti-tumour,
antiviral and
neuroprotective
properties.22,23,24
5. The Impact of Alkaloids Structures from Natural Compounds on Public Health, Emin Cadar (Umf
Carol Davila Bucharest, Faculty of Pharmacy), Str. Traian Vuia (Nr. 6, Sector 2, Bucharest,
Romania); Aneta Tomescu (Corresponding Author, Tomescu.Aneta@Gmail.com, Ovidius
University of Constanta, Faculty Of medicine, Campus Corp B, University Alley Nr. 1, Constanta,
Romania); Cristina-Luiza Erimia (Ovidius University of Constanta, Faculty of Pharmacy, Campus
Corp B, University Alley Nr. 1, Constanta, Romania); Alef Mustafa (Ovidius University of
Constanta, Faculty of Pharmacy, Campus Corp B, University Alley Nr. 1, Constanta, Romania);
Rodica Sîrbu (Ovidius University of Constanta, Faculty of Pharmacy, Campus Corp B, University
Alley Nr. 1, Constanta, Romania); ISSN 2411-9563 (Print); ISSN 2312-8429 (Online); European
Journal of Social Sciences Education and Research; Sep – Dec 2015 Vol 5, Nr. 1.
6. Motley, Cheryl. "Cinchona and its product--Quinine". Ethnobotanical leaflets. Southern Illinois
University Herbarium. Retrieved 11 June 2010.
7. Vinblastine Sulfate. The American Society of Health-System Pharmacists. Retrieved Jan 2, 2015
8. Brayfield, A, ed. (13 December 2013). "Vincristine". Martindale: The Complete Drug Reference.
Pharmaceutical Press. Retrieved 15 April 2014.
9. Casanova, M; Ferrari, A; Spreafico, F; Terenziani, M; Massimino, M; Luksch, R; Cefalo, G;
Polastri, D; et al. (2002). "Vinorelbine in previously treated advanced childhood sarcomas:
Evidence of activity in rhabdomyosarcoma". Cancer. 94 (12): 3263–
8.doi:10.1002/cncr.10600. PMID 12115359.
10. Recent updates on codeine by Monika Bhandari, Anil Bhandari, and Aakanksha Bhandari, Pharm
Methods. 2011 Jan-Mar; 2(1): 3–8, doi: 10.4103/2229-4708.81082, PMCID: PMC3658028
11. Matthys H, Bleicher B, Bleicher U(1983) Dextromethorphan and codeine: objective assessment of
antitussive activity in patients with chronic cough. J Int Med Res. 11:92–100.
12. Dayer P, Desmeules J, Leemann T, Striberni R. Bioactivation of the narcotic drug codeine in human
liver is mediated by the polymorphic monooxygenase catalyzing debrisoquine 4-hydroxylation
(cytochrome P-450 dbl/bufI). BiochemBiophys Res Commun 1988; 152: 411–416.
13. Narcotic Drugs Estimated World Requirements for 2008, Statistics for 2006. New York: United
Nations Pubns. 2008. p. 77. ISBN 9789210481199.
14. Schrijvers D, van Fraeyenhove F (2010). "Emergencies in palliative care". Cancer J. 16(5): 514–
20. doi:10.1097/PPO.0b013e3181f28a8d. PMID 20890149.
15. Naqvi F, Cervo F, Fields S (August 2009). "Evidence-based review of interventions to improve
palliation of pain, dyspnea, depression". Geriatrics. 64 (8): 8–10, 12–4. PMID 20722311.
16. Mahler DA, Selecky PA, Harrod CG, Benditt JO, Carrieri-Kohlman V, Curtis JR, Manning HL,
Mularski RA, Varkey B, Campbell M, Carter ER, Chiong JR, Ely EW, Hansen-Flaschen J,
O'Donnell DE, Waller A (March 2010). "American College of Chest Physicians consensus
statement on the management of dyspnea in patients with advanced lung or heart
disease". Chest. 137 (3): 674–91. doi:10.1378/chest.09-1543. PMID 20202949.
17. Mattick RP; Digiusto E; Doran C; O’Brien S; Kimber J; Henderson N; Breen B; Shearer J;
Gates J; Shakeshaft A; NEPOD Trial Investigators (2004). National Evaluation of
Pharmacotherapies for Opioid Dependence (NEPOD): Report of Results and
Recommendation (PDF). Monograph Series No. 52. Australian Government. ISBN 0-642-82459-
2.
18. Alexander J. German, Jill E. Maddison, Grant Guilford, in Small Animal Clinical Pharmacology
(Second Edition), 2008.
19. Bringmann G, Lang G, Mühlbacher J, Schaumann K, Steffens S, Rytik PG, Hentschel U,
Morschhäuser J, Brun R. In: Sponges (Porifera) Müller WEG, editor. Vol. 1. Springer; Berlin:
2003. pp. 231–253.
20. Bringmann G, Lang G, Gulder TAM, Hideyuki H, Mühlbacher J, Maksimenka K, Steffens S,
Schaumann K, Stöhr R, Wiese J, Imhoff JF, Perovi-Ottstadt S, Boreiko O, Müller WEG. The first
sorbicillinoid alkaloids, the antileukemicsorbicillactones A and B, from a sponge derived
Penicilliumchrysogenum strain. Tetrahedron. 2005;61:7252–7265.
21. Large-Scale Biotechnological Production of the Antileukemic Marine Natural Product
Sorbicillactone A, Gerhard Bringmann,1,* Tobias A. M. Gulder,1 Gerhard Lang,1,2
Stefanie Schmitt,1 Rüdiger Stöhr,2 Jutta Wiese,2 Kerstin Nagel,2 and Johannes F.
Imhoff2,*Mar Drugs. 2007 Jun; 5(2): 23–30.Published online 2007 Jun 25. PMCID:
PMC2365691.
22. Bringmann G, Lang G, Gulder TAM, Hideyuki H, Mühlbacher J, Maksimenka K, Steffens
S, Schaumann K, Stöhr R, Wiese J, Imhoff JF, Perovi-Ottstadt S, Boreiko O, Müller WEG.
The first sorbicillinoid alkaloids, the antileukemicsorbicillactones A and B, from a sponge
derived Penicilliumchrysogenum strain. Tetrahedron. 2005;61:7252–7265.
23. Bringmann G, Lang G, Mühlbacher J, Schaumann K, Steffens S, Müller WEG.
Sorbicillactone A derivatives for the treatment of tumor and viral diseases. International
Patent Application. WO 2004/026854. 1.4.2004.
24. SORBICILLACTONE-A DERIVATIVES FOR THE TREATMENT OF TUMOUR AND VIRAL
DISEASES, No.: WO/2004/026854, International Application No.: PCT/EP2003/007805,
Publication Date: 01.04.2004, International Filing Date: 17.07.2003, Chapter 2, Demand Filed:

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Alkaloids

  • 2. Alkaloids Alkaloids are basic (alkali-like), nitrogen-containing organic constituents found in some plants. They give positive responses with Dragendorff, Mayer, Hager and Wagner reagents .Alkaloids are organic bases. Many alkaloids are poisonous, others are addictive (e.g. cocaine), and some are used clinically (e.g. morphine). More than 10 000 alkaloids are now known, the first discovered being narcotine, isolated from opium by Derosne in 1803. (Plant Alkaloids, Jack G Woolley) 1 Alkaloids are normally classified according to the heterocyclic ring system they possess, but some authors prefer a classification based on their biosynthetic origins from amino acids, e.g. phenylalanine, tyrosine or tryptophan. (Justin et al.)2 Many individual names are formed by adding the suffix "-ine" to the species or generic alkaloids. For example, atropine is isolated from the plant Atropa belladonna, strychnine is obtained from the seed of Strychnine tree.4 Alkaloids are important chemical compounds that serve as a rich reservoir for drug discovery. Several alkaloids isolated from natural herbs exhibit antiproliferation and antimetastasis effects on various types of cancers both in vitro and in vivo. Alkaloids, such as camptothecin and vinblastine, have already been successfully developed into anticancer drugs. (Jin-Jian Lu et al., 2012)3 . Classification of Alkaloids  Currently, alkaloids are classified according to both chemical structure and origin. In Table 1 an alkaloid classification is presented. (Emin Cadar et al., 2015)5 Table-1: Alkaloid classification according to structure of derivatives Group Representatives Tropane derivatives Atropine, cocaine, ecgonine, scopolamine Isoquinoline derivatives Opium alkaloids, morphine, codeine, thebaine, papaverine, narcotine, sanguinarine, narceine, hydrastiane, berberine Quinoline derivatives Quinine, quinidine, dihydroquinone, dihyrdoqunidine, strychnine, brucine, veratrine, cevadine Pyridine derivatives Piperine, coniine, trigonelline, arecaidine, guvacine, pilocarpine, cytosine, nicotine, sparteine, pelletierine Pyrolidine derivatives Hygrine, cuschygrine, nicotine Terpeness From aconite: aconitine Sterols: solanine, samandarine Betaine derivatives (with quaternary azoth) Muscarine, choline, neurine
  • 3. Phenethylamine derivatives Mescalime, ephedrine Indole derivatives Tryptamie derivatives: dimethyltryptamine (DMT), NMT, psilocybin, serotonin, melatonin Ergolines: alkaloids originating from ergot: ergine, ergotamine, lyseric acid, and so on.; derivatives of lysergic acid (LSD) Beta-carbolines: harmine, yohimbine, reserpină, emetine Purine derivatives Xanthine derivatives: caffeine, theobromine, theophylline  Alkaloids are often divided into the following major groups: (Anonymous) 1. "True alkaloids”: which contain nitrogen in the heterocycle and originate from amino acids. Their characteristic examples are atropine, nicotine and morphine. This group also includes some alkaloids which beside nitrogen heterocycle contain terpene (e.g. evonine) or peptide fragments (e.g. ergotamine). This group also includes piperidine alkaloids coniine and coniceine although they do not originate from amino acids. 2. "Protoalkaloids”: which contain nitrogen and also originate from amino acids. Examples include mescaline, adrenaline and ephedrine. 3. Polyamine alkaloids: derivatives of putrescine, spermidine and spermine. 4. Peptide and cyclopeptide alkaloids. 5. Pseudalkaloids: alkaloid-like compounds which do not originate from amino acids. This group includes, terpene-like and steroid-like alkaloids, as well as purine-like alkaloids such as caffeine, theobromine and theophylline. Some authors classify as pseudoalkaloids such compounds such as ephedrine and cathinone. Those originate from the amino acid phenylalanine, but acquire their nitrogen atom not from the amino acid but through transamination.
  • 4. Table-2: Brief description on Alkaloids Alkaloid Name Source (Genus/Family) Source Type & Inhabitant Therapeutic Uses Qunine Cinchona bark, extract Family: Rubeceae1 Genus: Cinchona  Cinchona calisaya Wedd. (1848)  Cinchona officinalis L. (1753)  Cinchona pubescens Vahl (1790) Tree, medicinal plant. They are native to the tropical Andea n forests of western South America. (Motley and Cheryl, 2010) 6.  Antimalarial1 , anti- pyretic, and slight analgesic.5  Can be used in persistent febrile states, migraine.5 Qunidine Antiarrhythmic (heart) Vinblastine Periwinkle plant Catharanthus roseus and other vinca plants. Subshrub  Component of a number of chemotherapy regimens  also used to treat histiocytosis.7 Vinca Alkal oids
  • 5. Vincristine Genus: Catharanthus Family: Apocynaceae Endemic to Madagascar  Delivered via intravenous infusi on for use in various types of chemotherapy regimens  Occasionally used as an immunosuppressa nt, for example, in treating thrombotic thrombocytopenic purpura(TTP) or chronic idiopathic thrombocytopenic purpura (ITP).8 Vindesine  Is an anti- mitotic vinca alkaloid used in chemotherapy.  Used to treat many different types of cancer, including leukaemia, lymphom a, melanoma, breast cancer, and lung cancer. Vinorelbine  Chemotherapy medication used to treat a number of types of cancers like breast cancer, non- small cell lung cancer.  Also active in rhabdomyosarcom a.9 Codeine Obtained from poppy plant Papaver somniferum Genus: Papaver Family: Papaveraceae Annual herb. Native range is probably the eastern Mediterranean . .  Used as a central analgesic, sedative, hypontic, antinonciceptive, antiperistaltic.10  Suppress both artificially induced and disease-related cough.11  Widely used as anti- tussivedrug.12 Morphine Primary source of morphine is isolation Annual herb.  Used to treat acute and chronic pain.5 Vin ca Alk aloi ds
  • 6. from poppy straw of the opium poppy.13 Genus: Papaver Family: Papaveraceae Native range is probably the eastern Mediterranean . .  Immediate-release morphine is beneficial in reducing the symptom of shortness of breath due to both cancer and noncancer causes.14,15  Sustained-release morphine significantly reduces breathlessness safely, with its benefits maintained over time.16,17 Papaverine Papaverine is extracted from the milky juice of raw poppy capsules (opium).5 Genus: Papaver Family: Papaveraceae Annual herb. Native range is probably the eastern Mediterranean .  An opiumalkaloidantispa smodic drug, used primarily in the treatment of visceral spasm, vasospasm (especially those involving the heart and the brain), and occasionally in the treatment of erectile dysfunction.  Effect is exerted directly on smooth muscles.5 Strychnine The strychnine tree (Strychnos nux- vomica L.), also known as nux vomica, poison nut, semen strychnos and quaker buttons. Genus: Strychnos Family: Loganiaceae A deciduous tr opicaltree nati ve to India, and southeast Asia.  Very toxic.  Convulsant.2  Effective in digestive problems, different types of pains etc. Atropine  Datura stramonium L. (syn. D. inermis).  Datura anoxia  Atropa belladonna  Herbaceo us, leafy annu als and short- lived pere nnial.  Atropine is used as an antidote in muscarine intoxications.5  In ophthalmology, it is used for pupil dilation (mydriasis)
  • 7.  Mandragora officinarum Genus: Datura Family: Solanaceae  Believed to have originated in Mexico, but has now become naturalize d in many other regions. in ocular examinations.5  Competitive antagonist of muscarinic acetylcholine receptors.2  Anti-cholinergic, anti-myopia effects.2 Berberine Berberis species, Hydrastis, Canadensis, Xanthorhiza simplicissima, Phellodendron amurense, Coptis chinensis, Tinospora cordifolia, Argemone mexicana and Eschscholzia californica Many plants/trees of various places.  Anti inflammatory, anti bacterial/viral, recently experiments showed anti diabetic and beneficial effects on cardiovascular system and anti cancer and others disorders such as intestinal2 Cytisine (baptitoxine, sophorine) Labum and Cytisus of Family: Fabaceae Shrub Native to western and central Europe.  Acetylcholine agonist, smoking cessation drug. Nicotine Nicotiana tobacum Genus: Nicotiana Family: Solanaceae Forb/herb Originated in the tropical Americas (South America, Mexico, and the West Indies)  Stimulant, antiherbivore, insectide, anti- inflammatory.2 Caffeine Found in coffee, tea, cola nuts, mate, guarana, and cocoa.  Stimulant of the CNS, increase of pulse and arterial blood pressure, bronchial dilator, stimulant of intestinal peristalsis.
  • 8. Reference: 1. Plant Alkaloids Jack G Woolley, De Montfort University, Leicester, UK 2. Plant Secondary Metabolites: Biosynthesis, Classification, Function and Pharmacological Properties Justin N. Kabera1 , Edmond Semana1 , Ally R. Mussa1 and Xin He1, 2 1) Department of Pharmacology, School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China 2) Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin 300193, China 3. Review Article: Alkaloids Isolated from Natural Herbs as the Anticancer Agents, Jin-Jian Lu, Jiao Lin Bao, Xiu-Ping Chen, Min Huang, and Yi-Tao Wang, State Key Laboratory of Quality Research in Chinese Medicine (University of Macau) and Institute of Chinese Medical Sciences, University of Macau, Avenue Padre Toma’s Pereira, Taipa 999078, Macao, China, Received 11 May 2012; Revised 17 July 2012; Accepted 30 July 2012, Academic Editor: Alvin J. Beitz, Copyright © 2012 Jin-Jian Lu et al. 4. Chemical Encyclopedia: http://www.xumuk.ru/encyklopedia/119.html Emetine Ipecac Cephalelisipecacuan ha A. Rich. (Rio Ipecac) and C. acuminata H. Karst (Cartagena ipecac). Family: Rubiaceae Shrubby plant. Grows in Brazilian rainforests and other locations in Central and South America.  Ipecac is used in the treatment of poisoning by induction of emesis and production of expectoration.  Ipecac syrup (Clinical applications)-Ipecac syrup is used to induce vomiting, after the ingestion of toxic compounds or after a drugs overdose.18 Cephaeline SORBICILLACTONE-A Salt-water culture of a Penicillium chrysogenum strain isolated from a specimen of the Mediterranean sponge Irciniafasciculata.19,20 Mediterranean .  Active against leukemia cells without showing notable cytotoxicity.21  Has anti-tumour, antiviral and neuroprotective properties.22,23,24
  • 9. 5. The Impact of Alkaloids Structures from Natural Compounds on Public Health, Emin Cadar (Umf Carol Davila Bucharest, Faculty of Pharmacy), Str. Traian Vuia (Nr. 6, Sector 2, Bucharest, Romania); Aneta Tomescu (Corresponding Author, Tomescu.Aneta@Gmail.com, Ovidius University of Constanta, Faculty Of medicine, Campus Corp B, University Alley Nr. 1, Constanta, Romania); Cristina-Luiza Erimia (Ovidius University of Constanta, Faculty of Pharmacy, Campus Corp B, University Alley Nr. 1, Constanta, Romania); Alef Mustafa (Ovidius University of Constanta, Faculty of Pharmacy, Campus Corp B, University Alley Nr. 1, Constanta, Romania); Rodica Sîrbu (Ovidius University of Constanta, Faculty of Pharmacy, Campus Corp B, University Alley Nr. 1, Constanta, Romania); ISSN 2411-9563 (Print); ISSN 2312-8429 (Online); European Journal of Social Sciences Education and Research; Sep – Dec 2015 Vol 5, Nr. 1. 6. Motley, Cheryl. "Cinchona and its product--Quinine". Ethnobotanical leaflets. Southern Illinois University Herbarium. Retrieved 11 June 2010. 7. Vinblastine Sulfate. The American Society of Health-System Pharmacists. Retrieved Jan 2, 2015 8. Brayfield, A, ed. (13 December 2013). "Vincristine". Martindale: The Complete Drug Reference. Pharmaceutical Press. Retrieved 15 April 2014. 9. Casanova, M; Ferrari, A; Spreafico, F; Terenziani, M; Massimino, M; Luksch, R; Cefalo, G; Polastri, D; et al. (2002). "Vinorelbine in previously treated advanced childhood sarcomas: Evidence of activity in rhabdomyosarcoma". Cancer. 94 (12): 3263– 8.doi:10.1002/cncr.10600. PMID 12115359. 10. Recent updates on codeine by Monika Bhandari, Anil Bhandari, and Aakanksha Bhandari, Pharm Methods. 2011 Jan-Mar; 2(1): 3–8, doi: 10.4103/2229-4708.81082, PMCID: PMC3658028 11. Matthys H, Bleicher B, Bleicher U(1983) Dextromethorphan and codeine: objective assessment of antitussive activity in patients with chronic cough. J Int Med Res. 11:92–100. 12. Dayer P, Desmeules J, Leemann T, Striberni R. Bioactivation of the narcotic drug codeine in human liver is mediated by the polymorphic monooxygenase catalyzing debrisoquine 4-hydroxylation (cytochrome P-450 dbl/bufI). BiochemBiophys Res Commun 1988; 152: 411–416. 13. Narcotic Drugs Estimated World Requirements for 2008, Statistics for 2006. New York: United Nations Pubns. 2008. p. 77. ISBN 9789210481199. 14. Schrijvers D, van Fraeyenhove F (2010). "Emergencies in palliative care". Cancer J. 16(5): 514– 20. doi:10.1097/PPO.0b013e3181f28a8d. PMID 20890149. 15. Naqvi F, Cervo F, Fields S (August 2009). "Evidence-based review of interventions to improve palliation of pain, dyspnea, depression". Geriatrics. 64 (8): 8–10, 12–4. PMID 20722311.
  • 10. 16. Mahler DA, Selecky PA, Harrod CG, Benditt JO, Carrieri-Kohlman V, Curtis JR, Manning HL, Mularski RA, Varkey B, Campbell M, Carter ER, Chiong JR, Ely EW, Hansen-Flaschen J, O'Donnell DE, Waller A (March 2010). "American College of Chest Physicians consensus statement on the management of dyspnea in patients with advanced lung or heart disease". Chest. 137 (3): 674–91. doi:10.1378/chest.09-1543. PMID 20202949. 17. Mattick RP; Digiusto E; Doran C; O’Brien S; Kimber J; Henderson N; Breen B; Shearer J; Gates J; Shakeshaft A; NEPOD Trial Investigators (2004). National Evaluation of Pharmacotherapies for Opioid Dependence (NEPOD): Report of Results and Recommendation (PDF). Monograph Series No. 52. Australian Government. ISBN 0-642-82459- 2. 18. Alexander J. German, Jill E. Maddison, Grant Guilford, in Small Animal Clinical Pharmacology (Second Edition), 2008. 19. Bringmann G, Lang G, Mühlbacher J, Schaumann K, Steffens S, Rytik PG, Hentschel U, Morschhäuser J, Brun R. In: Sponges (Porifera) Müller WEG, editor. Vol. 1. Springer; Berlin: 2003. pp. 231–253. 20. Bringmann G, Lang G, Gulder TAM, Hideyuki H, Mühlbacher J, Maksimenka K, Steffens S, Schaumann K, Stöhr R, Wiese J, Imhoff JF, Perovi-Ottstadt S, Boreiko O, Müller WEG. The first sorbicillinoid alkaloids, the antileukemicsorbicillactones A and B, from a sponge derived Penicilliumchrysogenum strain. Tetrahedron. 2005;61:7252–7265. 21. Large-Scale Biotechnological Production of the Antileukemic Marine Natural Product Sorbicillactone A, Gerhard Bringmann,1,* Tobias A. M. Gulder,1 Gerhard Lang,1,2 Stefanie Schmitt,1 Rüdiger Stöhr,2 Jutta Wiese,2 Kerstin Nagel,2 and Johannes F. Imhoff2,*Mar Drugs. 2007 Jun; 5(2): 23–30.Published online 2007 Jun 25. PMCID: PMC2365691. 22. Bringmann G, Lang G, Gulder TAM, Hideyuki H, Mühlbacher J, Maksimenka K, Steffens S, Schaumann K, Stöhr R, Wiese J, Imhoff JF, Perovi-Ottstadt S, Boreiko O, Müller WEG. The first sorbicillinoid alkaloids, the antileukemicsorbicillactones A and B, from a sponge derived Penicilliumchrysogenum strain. Tetrahedron. 2005;61:7252–7265. 23. Bringmann G, Lang G, Mühlbacher J, Schaumann K, Steffens S, Müller WEG. Sorbicillactone A derivatives for the treatment of tumor and viral diseases. International Patent Application. WO 2004/026854. 1.4.2004. 24. SORBICILLACTONE-A DERIVATIVES FOR THE TREATMENT OF TUMOUR AND VIRAL DISEASES, No.: WO/2004/026854, International Application No.: PCT/EP2003/007805, Publication Date: 01.04.2004, International Filing Date: 17.07.2003, Chapter 2, Demand Filed: