PHG 322 PHARMACOGONSY II LECTURE 3 PRESENTED BY ASSISTANT PROF. DR. EBTESAM ALSHEDDI بسم الله الرحمن الرحيم.

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Presentation transcript:

PHG 322 PHARMACOGONSY II LECTURE 3 PRESENTED BY ASSISTANT PROF. DR. EBTESAM ALSHEDDI بسم الله الرحمن الرحيم

III. Alkaloids of the Isoquinoline group Ipeca Opium Curare

Raw opium Raw opium: is the air dried latex obtained by the incisions from the unripe capsules of Papaver somniferum (Papaveraceae).latexPapaveraceae Opium is the source of many alkaloids, including morphine, thebaine, codeine, papaverine, and noscapine. morphinethebainecodeinepapaverine noscapine Morphine is the predominant one.

CALIFORNIA POPPIES Papaver spp Do not contain morphine or codeine, but like all poppies have papaverine (the “poppy alkaloid”).

OPIUM POPPY Papaver somniferum

Opium alkaloids occur naturally combined with specific acid (meconic acid). Occurs only in opium Specific test: Meconic acid + FeCl3 gives purplish red colour Not destroyed by dilute HCl (c.f. from ferric acetate and formate) Unaffected by addition of HgCl2 (c.f. from thiocyanate)

CLASSIFICATION Natural opiates: are alkaloids contained in the latex of opium as morphine, codeine, and thebaine. Semi-synthetic opioids: created from the natural opiates, such as heroin, oxycodone, and hydrocodone are derived from morphine, codeine, and thebaine.heroin oxycodonehydrocodone Fully synthetic opioids: such as pethidine, methadone, tramadol. Endogenous opioid peptides, produced naturally in the body, such as endorphins, enkephalins, dynorphins, and endomorphins. 

Opium alkaloids are subclassified into 3 groups: Benzylisoquinoline alk. Phenylethylamine alk. Phenanthrene alk. 8

 BENZYLISOQUINOLINE: Papaverine Properties: It is a weak base and is optically inactive. Tests for identification  Warren's test (specific for papaverine): Papaverine + crushed crystal of KMnO 4 + Marqui's reagent  green color  blue. Uses: Papaverine possesses smooth muscle relaxant activity. It is used as antispasmodic for GIT spasms, clots and in bronchial asthma in a dose up to 600 mg of papaverine HCl daily.

Phenylalkylamines: Narceine Properties: It is a tertiary Alkaloids. Narceine is an amphoteric alkaloid since it contain a carboxylic group.

 PHENANTHEREN GROUP: Morphine: Properties: Morphine is levorotatory, insoluble in water, sparingly soluble in ethanol (1:250) and chloroform (1:1500), practically insoluble in ether and benzene. It contains 2 OH groups, one is a phenolic at C-3 (gives a soluble phenate with alkali) and the other is a 2ry alcoholic at C-6.

 TESTS FOR IDENTIFICATION: Tests due to phenolic properties: 1- Morphine gives a blue color with FeCl Nitrous acid test: solution of morphine in dilute HCl + NaN0 2 + NaOH  red color. 3- Morphine + dil H 2 SO 4 + HI→ I 2 give violet colour when dissolve in CHCl 3 Tests with alkaloidal color reagents: 1- Liebermann' s reagent  black color. 2- Mandalin's reagent  bluish-gray color. 3- Marquis' reagent  violet color. 4- HNO 3 → red colour convert to yellow on heating.

 USES: Morphine act as a narcotic analgesic (reduce pain & induce sleep) in a dose of 5-20 mg of morphine hydrochloride, sulfate or tartrate, administered orally or parentrally, every 4 hours. Used before and after surgical operations and to terminally ill cancer patients. Suppress peristaltic movement so stops diarrhea. Adverse Effects: Two major problems are associated to morphine use: Addiction and Tolerance.

Morphine

Codeine: Properties:  It is soluble in H 2 O, boiling H 2 O, ethanol, CHCl 3 and ether, (c.f. morphine).  Codeine is non Phenolic. Test:  Codeine + concentrated H 2 SO 4 + FeCl 3, warm in water bath  bluish violet color + HNO 3  Red color. Uses: It has less narcotic analgesic than morphine. It is mainly used as antitussive.

Codeine

Thebaine Thebaine (paramorphine) is an opiate alkaloid. A minor constituent of opium, thebaine is chemically similar to both morphine and codeine, but produces stimulatory, with strychnine-like convulsions, rather than depressant effects. Thebaine is not used therapeutically, but is converted industrially into a variety of compounds including oxycodone, oxymorphone, nalbuphine, naloxone, naltrexone, buprenorphine and etorphine.

SEMI-SYNTHETIC DERIVATIVES OF MORPHINE: Heroin It is the diacetyl derivative of morphine. It has no any medical applications but it is one of the most dangerous abused substance. Morphine is easily acetylated to diacetylmorphine using acetic anhydride. morphine Heroin is more potent than morphine (it takes less for the same effect), lasts longer, and is more addicting.

Apomorphine Obtained by heating morphine with coc. HCl in sealed vials. During this reaction rearrangement and elimination of water takes place. Apomorphine is used in the treatment of Parkinson’s disease and erectile dysfunction. + HCl, Δ morphine

Ether bridge opening (ring E): Resulted in group of compounds called morphinans. Synthetic morphinans are racemic compounds. Only the levo isomers have analgesic activity. Levorphanol is 8 times as active as morphine. The dextro isomers as dextromethorphane lack the CNS and analgesic effects, however, they are used as cough suppressants.

The C-6 Hydroxyl group and ring c modifications: Removal or derivitization of the alcoholic hydroxyl group at C-6 increase lipophilicity and consequently the analgesic activity. Reduction of the 7,8 double bond, oxidation of C-6 hydroxyl and addition of OH group at C-14 all increase the activity.

The C-3 Hydroxyl group: Etherification of this phenolic OH decrease the analgesic activity and the compounds are used mainly as antitussive e.g. Codeine and Pholcodine.

Similar synthetic manipulations make hydrocodone more potent than codeine Hydrocodone or dihydrocodeinone (marketed as Vicodin, Anexsia, Dicodid, Hycodan, Hycomine, Lorcet, Lortab (or Loritab), Norco, Novahistex, Hydroco, Tussionex, Vicoprofen, Xodol) is a semi- synthetic opioid derived from two of the naturally occurring opiates, codeine and thebaine. Hydrocodone is an orally active narcotic analgesic and antitussive. Sales and production of this drug have increased significantly in recent years, as have diversion and illicit use. Hydrocodone is commonly available in tablet, capsule and syrup form.Vicodinopioidopiates codeinethebainenarcoticanalgesicantitussivedrug

Oxycodone

Oxycodone is a potent and potentially addictive opioid analgesic medication synthesized from thebaine. Its name is derived from codeine - the chemical structures are very similar. opioidanalgesicmedication thebainecodeine It is effective orally and is marketed in combination with aspirin (Percodan, Endodan, Roxiprin) or paracetamol/acetaminophen (Percocet, Endocet, Roxicet, Tylox) for the relief of pain. More recently, ibuprofen has been added to oxycodone (Combunox).aspirinparacetamolacetaminophenpainibuprofen

N atom substitution: Methyl group in nitrogen resulted in compounds with analgesic effects. Ethyl morphine is also analgesic. Compounds with 3- 5 carbons alkyl group on nitrogen are antagonists. More than 5 carbons the compounds again are analgesic.

3- CURARE ALKALOIDS Occurrence: Curare or South American arrow poison is the dried crude extract, obtained mainly from Chondrodendron tomentosum (Menispermaceae) and certain Strychnos species, (Loganiaceae). Curare contains several alkaloids (4-7%), the most important is d-tubocurarine.

Properties: d-tubocurarine (4ary alkaloid) is freely soluble in H 2 O. It is a phenolic dextrorotatory alkaloid. It is a bis-benzyltetrahydroisoquinoline alkaloid. Tests:  Saturated aqueous solution + FeCl 3  faint green color  green color.  Solution of the alkaloidal HC1 + Na 2 CO 3  yellow brown precipitate. Uses:  Tubocurarine chloride is mainly used by i.m. or i.v. routes as skeletal muscle relaxant.  It is used to control and reduce convulsions of strychnine poisoning and of tetanus.  It is used as a diagnostic aid in myasthenia gravis.