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part1 of Alkaloids report, History up to Quinolines Alkaloids

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  2. 2. OBJECTIVES To know what are the characteristics of alkaloids To know the different sources of alkaloids To determine the importance of alkaloids and to identify their applications in pharmacy To know the different test in determining the presence of alkaloids
  3. 3. WHAT ARE ALKALOIDS? These are commonly applied to basic nitrogenous compounds of plant origin that are physiologically active. Organic nitrogenous compounds with a limited distribution in native nature.
  5. 5. CHARACTERISTICS: They are bitter in taste. Derived from amino acids Alkaloids form double salts with compounds of mercury, gold, platinum and other heavy metals. These salts are obtained as precipitate which are microcrystallographic.
  6. 6.  Most but not all alkaloids possess basic properties owing to the presence of amino nitrogen. Structurally complex end products of energy- requiring reaction sequences.
  7. 7.  Alkaloids usually contain one nitrogen atom but some may contain 5 nitrogen atoms such as ergotamine. The nitrogen may exist as a primary amine (RNH2), secondary amine (R2NH), tertiary amine (RN), or as quaternary.
  8. 8. PROPERTIES OF ALKALOIDS Insoluble or sparingly soluble in water, but the salts formed on reaction with acids are usually freely soluble. Most are crystalline solids although a few are amorphous.
  9. 9.  Free alkaloids are usually soluble in ether, chloroform, or other relatively non- polar immiscible solvents. Some alkaloids are liquid because of lacking of oxygen in their molecules. (e.g coniine, nicotine, spartenine)
  10. 10.  The degree of basicity varies greatly, depending on the structure of the molecule and the presence and location of other functional groups. Have high melting points
  11. 11. SOURCES AND OCCURRENCE OF ALKALOIDS Alkaloids can occur in plant kingdoms; among the angiosperms, the Leguminosae, Papaveraceae, Ranunculaceae, Rubiaceae, Solanaceae, and Berberidaceae are outstanding alkaloid-yielding plants.
  12. 12.  The Labiatae and Rosaceae are almost free of alkaloids; the gymnosperms only rarely contain them (Taxaceae). Specific alkaloids are confined to specific plant families such as hyoscyamine in Solanaceae, colchicine in Liliaceae
  13. 13.  Although it has been claimed that the monocotyledons do not generally produce alkaloids, investigations indicate that the Amaryllidaceae and Liliaceae are two of the most promising families (of a list 11) in which to search for alkaloid- yielding plants.
  14. 14.  Occur in fungi (e.g ergot from Claviceps purpurea) Occur in various parts of the plant; in seeds (physostigma, areca), underground stems (sanguinaria), roots (belladonna root), rhizomes and roots (ipecac, hydrastis), barks (cinchona).
  15. 15. USES OF ALKALOIDS IN PLANTS: Poisonous agents which protect plants against insects and herbivores End products of detoxification reactions representing a metabolic locking-up of compounds otherwise harmful to the plants.
  16. 16.  For regulatory growth factors Reserve substance capable of supplying nitrogen or other elements necessary to the plant’s economy
  17. 17. PHARMACOLOGIC ACTION OF ALKALOIDS:  Analgesic (morphine, codeine)  Narcotics (strychnine, brucine which are central stimulant)  Mydriatics (atropine)  Miotics (physostigmine, pilocarpine)  Ephedrine (rises in blood pressure)  Reserpine (produce fall in excessive hypertension)
  19. 19.  The biosynthesis of many alkaloidal structures can be rationalized through simple chemical reactions that involve amino acids. The amino acids that are most often serve as alkaloidal precursors are: phenylalanine, tyrosine, tryptophan, histidine, a nthranilic acid, lysine and ornithine.
  20. 20.  Some of the general reactions that are of particular importance include: decarboxylation (removal of carboxyl group or carbon dioxide) and transamination (transfer of an amino group from one molecule to another without the formation of ammonia) of the amino acids to yield a corresponding amine or aldehyde. These can react to form a Schiff base which, in turn can react with carbanion in a Mannich-type condensation.
  21. 21. TEST FOR ALKALOIDSWagner’s Test(+) Reddish brown precipitateReagent used: Wagner’s Reagent [Solution of iodine in potassium iodide]Mayer’s Test(+) Cream color precipitatesReagent used: Mayer’s Reagent [Potassium mercuric iodide solution]
  22. 22. Dragendorff’s test(+) Orange precipitateReagent used: Dragendorff’s reagent [Potassium bismuth iodide solution]Hagers test(+) Yellow color precipitateReagent used: Hagers reagent [saturated solution of Picric acid]
  23. 23. Tannic acid test(+)buff color precipitateReagent used: 10% Tannic acid solutionValser’s Test(+) white precipitateReagent used: Valser’s reagent (Mercuric Iodide TS
  24. 24. NAMING FOR ALKALOIDS From the generic name or the genus of the plant yielding them (e.g hydrastine, atropine) The specific name or species of the plant yielding alkaloids ( e.g cocaine, belladonnine) Common name of the drug yielding them (e.g ergotamine)
  25. 25.  From their physiologic activity (e.g emetine, morphine) From the discoverer (e.g pelletierine)~ All names of alkaloids should end in “-ine”.~ A prefix or suffix is added to the name of a principal alkaloid from the same source. (quinine, quinidine, hydroquinine)
  26. 26. CLASSIFICATION OF ALKALOIDS  Pyridine- Piperidine Combined  Tropane  Quinoline  Isoquinoline  Indole  Imidazole  Steroid  Alkaloidal amine  Purine
  27. 27. PYRIDINE- PIPERIDINE COMBINED Also referred to as Pyrrolizidine alkaloids Upon reduction, the tertiary base, pyridine, is converted into the secondary base, piperidine.
  28. 28. 3 Subgroups Derivatives of piperidine Derivatives of nicotinic acid Derivatives of both pyridine and pyrrolidine
  29. 29. Important alkaloidal drugs and alkaloids that are classified in this group are: Areca Arecoline Hydrobromide Lobelia Lobeline Nicotine
  30. 30. NICOTINE A primarily product of root metabolism, but the formation of small amounts, as well as subsequent reactions such as demethylation of nicotine, can occur in leaves of plants.
  31. 31.  It is a pyridine alkaloid obtained from the dried leaves of the tobacco plant Nicotiana tabacum Linné (Fam. Solanaceae) Nicotiana – was named after Jean Nicot who introduced tobacco in Europe
  32. 32.  Tabacum – refers to the Indian name for the pipe or tube used in smoking it It is colorless to pale yellow, very hygroscopic, oily, volatile liquid with unpleasant, pungent odor and a sharp, burning, persistent taste.
  33. 33. USES: It is bound to an ion exchange resin in a chewing gum base as a temporary aid to the cigarette smoker seeking to give up smoking. Chronic use of nicotine may result in psychological and physical dependence.
  34. 34. ARECA Areca nut or Betel Nut A dried, ripe seed of Areca catechu (Fam. Palmae) Areca- a Spanish and Portuguese term for betel nut
  35. 35.  Catechu- East Indian name for an astringent extract or juice Areca mixed with lime, the leaves of Piper bette Linné and occasionally gambir is known as “PUNSUPARI”. This mixture is used as a stimulant masticatory. Consists of 0.45% alkaloids, 15% tannins, lipids, volatile oils and gum.
  36. 36. Uses: Pharmaceutic purposes Anthelmintic or vermicide in veterinary practice Taenifuge
  37. 37. Constituents: These are reduced pyridine derivatives. Arecoline (arecaidine methyl ester) <most abundant and physiologically active> Arecaidine (N-methyl guvacine) Guvacine (Tetrahydronicotinic acid) Guvacoline (Guvacine methyl ester)
  38. 38. LOBELIA Indian tobacco Consists of dried leaves and tops of Lobelia inflata Linné (Fam. Lobeliaceae) Lobelia – named in honour of a Flemish botanist Matthias de L’ Obel
  39. 39.  Inflata – refers to a hollow and distended fruit Substitute for tobaccoUses:• Similar but weaker pharmacological effects in nicotine on the peripheral circulation, neuromuscular junctions, and CNS.• Anti-smoking preparations
  40. 40.  Lobeline sulfate incorporated in tablets or lozenges are smoking deterrents. Lobeline had placebo effect on decreasing the physical craving for cigarettes. Traditionally used by the Native Americans for asthma Chronic bronchitis Injection of lobeline hydrochloride is used in the resuscitation of newborn infants
  41. 41. Constituents: Contains 14 alkaloids which LOBELINE is the major and most important. It has a pungent, volatile oil, resin, lipids, and gum.  Lobeline, (-) – lobeline or alpha lobeline  This occurs as colorless crystals which are slightly soluble in water but readily soluble in hot alcohol.
  42. 42. TROPANE ALKALOIDS A dicyclic compound formed by the condensation of a pyrrolidine precursor (ornithine) with three acetate- derived carbon atoms. Both pyrrolidine and piperidine ring system can be discerned in the molecule. The 3-hydroxy derivative of tropane is known as tropine. Its esterification with (-)- tropic acid yields hyoscamine (tropine, tropate), which may be racemized to form atropine.
  43. 43. Important alkaloidal drugs and alkaloids that are classified in this group are: Belladonna leaf Hyoscyamus Stramonium Atropine Hyoscyamine Scopolamine Coca Cocaine
  44. 44. BELLADONNA Belladonna leaf, Belladonna herb or deadly nightshade leaf Consists of dried leaf and flowering or fruiting top of Atropa belladonna Linné or of its variety acuminata Royle ex Lindley (Fam. Solanaceae)
  45. 45.  Atropa – is from Atropos meaning inflexible Belladonna – from Italian word “bella” meaning beautiful and “donna” meaning ladyUses: It acts as an antimuscarinic agent which accounts for its use as a spasmolytic drug. Treating diarrhea, diverticulitis , pancreatitis
  46. 46.  Used as a adjunctive therapy in the treatment of peptic ulcer; functional digestive disorders It possesses anticholinergic properties and is used to control excess motor activity of the GI tract and spasm of the urinary tract. It is commonly administered in the tincture (3mg alkaloids/ 100ml) or the extract (1.25 g alkaloids/100g)
  47. 47. Constituents: (-)- hyoscyamine remainder atropine Apoatropine Belladonnine Cuscohygrine Scopolamine
  48. 48. SOLANACEOUS ALKALOIDSThe principal alkaloids of this group are: (-) hyoscyamine atropine [(±) – hyoscyamine] scopolamine (also known as hyoscine)
  49. 49. These are tropine derivatives and esters and may be prepared synthetically but are usually obtained by extraction from plants of the Solanaceae such as: Atropa belladonna Datura stramonium Hyoscyamus niger Hyoscyamus muticus (also known as Henbane) Dubosia plants
  50. 50. Atropine An antidote in case of poisoning caused by cholinesterase inhibitors. It is a CNS stimulant.
  51. 51. Scopolamine It has a depressant activity on the CNS. It is used to treat motion sickness. It is employed for preanesthetic sedation and for obstetric amnesia in conjunction with analgesics and to calm delirium.
  52. 52. Toxicity symptoms occur in using atropine, scopolamine and belladonna tincture include: Skin rash Skin flushing Mouth dryness Difficulty in urination Eye pain Blurred vision Light sensitivity
  53. 53. Hyoscyamine a tropine ester of (-)-tropic acidHyoscyamine sulfate extremely poisonous It occurs as white, odourless crystals or as crystalline powder. It is a deliquescent and is affected of light.
  54. 54.  It is an anticholinergic and used as an aid in the control of gastric secretion, visual spasm, hypermotility in spastic colitis, pylorospasm and abdominal cramps. In Parkinsonism, it is used to reduce rigidity and tremors and to control associated sialorrhea and hyperhidrosis.
  55. 55. Atropine sulfate It occurs as colorless crystals or as a white, crystalline powder. It is extremely poisonous. It effloresces in dry air and is slowly affected by light. It is an anticholinergic, used in surgery as an antisialogogue.
  56. 56. Scopolamine or hyoscine An alkaloid abundant in Datura fastuosa var. alba and in D. Metel. It is an ester that, upon hydrolysis, yields tropic acid and scopoline. It occurs as an almost colorless, syrupy liquid from its chloroformic solution and colorless crystals from its ether solution. LEVOROTATORY
  57. 57. Scopolamine hydrobromide or hyoscine hydrobromide It occurs as colorless or white crystals or as a white, granular powder that is odourless and slightly efflorescent in dry air. It is extremely poisonous. It is classified as anticholinergic. It is employed for preanesthetic sedation and for obstetric amnesia in conjunction with analgesics and to calm delirium. It is administered SC or IM in
  58. 58. Hyoscyamus Also known as Henbane dried leaf with or without the stem and flowering or fruiting crop of Hyoscyamus niger Linné (Fam. Solanaceae) It contains not less than 0.04% alkaloids of hyoscyamus.
  59. 59.  Hyoscyamus (a Greek and Latin name formed from two Greek words, meaning hog and bean. The plant is poisonous to swine. The alkaloids, hyoscyamine and scopolamine, 0.05% to 0.15% of which three fourths is hyoscyamine are the active ingredients.
  60. 60. HYOSCYAMUS
  61. 61. STRAMONIUM Also known as Jimson weed, Jamestown weed dried leaf with or without the stem and flowering or fruiting crop of Datura stramonium Linné (Fam. Solanaceae)
  62. 62.  It yields not less than 0.25% of alkaloids. Datura (from Sanskrit dhatura, and from Arabic tatura or tatula, the native name) Stramonium (from the French word stramoine meaning stinkweed) It was used as a “pot herb” It can serves as atropine
  63. 63. STRAMONIUM SEED from D. stramonium The seed contains 0.4% of alkaloids, principally hyoscyamine with a small portion of scopolamine and traces of atropine.
  64. 64.  It is generally regarded as a noxious weed and has frequently caused poisoning in children when seeds were ingested.The chief toxic symptoms are those of atropine: Dilated pupils Impaired visions Dryness of the skin Secretions Extreme thirst Hallucination Loss of consciousness
  65. 65. COCAINE Coca leaves or Coca Dried leaves of Erythroxylum coca Lamarck which is commercially known as “Huanuco coca” or of E. truxillense Rusby “Truxillo coca” (Fam. Erythroxylaceae)
  66. 66.  Erythroxylum (is from the two Greek words meaning red and wood) Coca ( is the Spanish name for the tree) Truxillense (from Truxillo a coastal city in Peru)Contains three basic types of alkaloids: Derivatives of ecgonine Derivatives of tropine Derivatives of hygrine
  67. 67. Huanuco coca Contains 0.5 to 1% of ester alkaloids, derivatives of tropine and ecgonine Cuscohygrine is the principal nonester alkaloid in the leaf.
  68. 68. Truxillo coca Has lower content of ester alkaloids but higher percentage of cocaine (75%) The shrub was known as “The Divine Plant of the Incas”
  69. 69. Cocaine hydrochloride Colorless crystals or as a white, crystalline powder. Ingredient in Brompton’s cocktail Use to control severe pain CNS stimulant Administered IV or SC while cocaine free- based is smoked
  70. 70. Crack extremely addictive smokable forms of cocaine processed from cocaine hydrochloride Its name refers to the sound made when rocks of cocaine are smoked.
  71. 71. QUINOLINE ALKALOIDS These are alkaloids which contain quinoline as their nucleus including those obtained from cinchona (quinine, quinidine, cinchonine, and cinchonidine) Cinchona and its alkaloids are the only members of this group that are therapeutically important at present. Cinchonine, is isomeric with cinchonidine which is the parent alkaloid of the quinine series. Quinine and its isomer, quinidine, represent 6- methoxycinchonine.
  73. 73.  Cinchona bark or Peruvian bark dried bark of the stem or of the root of Cinchona succirubra Pavon et Klotzch or its hybrids, known in commerce as red cinchona or of C. ledgeriana (Howard) Moens et Trimen, C. calisaya Weddell, or hybrids of these with other species of Cinchona, known in commerce as calisaya bark or yellow cinchona (Fam. Rubiaceae)
  74. 74.  Cinchona (named in honor of the Countess of Chinchon, wife of viceroy of Peru) Succirubra (Latin word meaning red juice) Calisaya (a tree) Ledgeriana ( named in honor of Charles Ledger)
  75. 75.  Cinchona toxicity results in temporary loss of hearing and in impaired sight. Ringing in the ears is one of the symptoms of toxicity. When these symptoms are produced as the result of continuous use of cinchona or of quinine. The condition has been called cinchoism. Cinchona was formerly given in doses of 1g.
  76. 76. CUPREA BARK obtained from Remijia purdieana Triana and R. Pedunculata Fluckiger (Fam.Rubiaceae) it has a copper red color hard , compact, and heavy it contains numerous transversely elongated stone cells and 2-6 % of alkaloids of which 1/3 maybe quinine it’s a commercial source of quinidine.
  77. 77. CINCHONA ALKALOIDSQuinidine It’s a stereoisomer of quinine and is present in cinchona barks to the extent of 0.25- 1.25%. It depresses myocardial excitability, conduction velocity and to a lesser extent, contractility.
  78. 78.  Use to treat various cardiac arrhythmias such as mature atrial , AV junctional, and ventricular contractions : atrial flutter and atrial fibrilations. When administered orally, the peak serum levels are slightly lower with the gluconate and poylgalacturonate salt than with sulfate salt .
  79. 79.  The usual real dose available is 10 to 20 mg/kg/day in 4 to 6 divided doses in order to obtain the average therapeutic serum levels of 3 to 6mcg/ml. A toxic reaction occurs at levels above 8mcg/ml. The patient should be instructed to notify the physician if skin rash,fever,unusual bleeding/bruising,ringing in the ears,or visual disturbance occurs.
  80. 80. Quinidine sulfate sulfate of an alkaloid obtain from cinchona from Remijia pedunculata or prepared from quinine. It occurs as fine needle like white crystals that frequently cohere in masses. It is odorless , has a bitter taste and darkens when exposed to light. It is readily soluble in water, alcohol, methanol and chloroform.
  81. 81. Quinidine gluconate It occurs as a white powder odorless and has a bitter taste available in sustained release tablet.
  82. 82. Quinidine polygalacturonate It affords control and more uniforms absorptions through the intestinal mucosa than does quinidine sulfate. In addition it produces a lower incidence of GI irritation
  83. 83. Quinine Diastereoisomer of quinidine It occurs as white, odourless, bulky crystals or as a crystalline powder. It darkens when exposed to light and effloresces in dry air. It is freely soluble in alcohol, ether and chloroform but slightly soluble in water.
  84. 84. Quinine Sulfate a sulfate of an alkaloid obtained from the bark of Cinchona species. A white, odourless, bitter, fine, needlelike crystals that are usually lusterless. It becomes brownish when exposed to light. It is not readily soluble in water, alcohol, chloroform or ether.
  85. 85. Uses Antimalarial For treating of chloroquinine resistant falciparum malaria combination with pyrimethamine and sulfadoxine or tetracycline or clindamycin. It has a skeletal muscle relaxant effect. It is widely used for the prevention and treatment of nocturnal recumbency leg cramps.