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Cytisin

Baptisia australis, B. tinctoria R. Br. and other species. Cytisine. A... [Pg.116]

C. stenopetalus belong to group (c) and contain up to 0-4 per cent, of alkaloids mainly cytisine and methylcytisine with traces of anagyrine in some specimens of the second species. C. monspes-sulanus also belongs to group (c) and contains 0-9 per cent, of alkaloids chiefly methylcytisine with some cytisine and a new alkaloid monspessulanine (p. 146), probably of the lupanine group. (1946). [Pg.117]

Genista celnensis. Seeds contain cytisine plants contain retamine,... [Pg.117]

From cytisine COOH. CHMe. CHj. CHMe. COOH... [Pg.142]

Constitution. On electrolytic reduction cytisine yields tetrahydrode-oxycytisine, C44H20N2, an alkaline oil, b.p. 270°, yielding a crystalline hydrochloride, B. HCl, m.p. 282°, [aju — 10-25°. With phosphorus and hydriodic acid cytisine furnishes ammonia and cytisoline, C41H44ON,... [Pg.142]

In 1931 Ing pointed out that formula (II) and (III) do not contain methyl or potential methyl groups in j ositions 6 and 8 which they occupy in cytisoline. Further, a partially reduced quinoline ought to oxidise easily to a benzenecarboxylic acid and so far the only simple oxidation, products recorded from cytisine were ammonia, oxalic acid and isovaleric acid. Distillation of cytisine with zinc dust or soda-lime yields pyrrole and pyridine, but no quinoline. On these grounds Ing suggested that cytisine should be formulated without a quinoline nucleus, and that the reactions which indicate the presence of an aromatic nucleus in the alkaloid can be accounted for by an a-pyridone ring. This a-pyridone nucleus can... [Pg.143]

Cytisine. This base belongs to the same pharmacological group as nicotine.It is a powerful poison causing nausea, convulsions and death by failure of respiration. The nicotine-like action is shared by A -methyl-cytisine but the latter, according to Scott and Chen, who have made a detailed study of its action, is weaker and has about one-fortieth the toxicity of nicotine. [Pg.153]

Vlex euTopaeus, 118, 140 Ulexine (cytisine), 140, 142 Umbellatine, 329, 340, 345 Ungernia sewertzooii imgemine, 406 Upas tree, 554... [Pg.803]

Lupanine, Sparteine, Anagyrine, Cytisine, Matrine and Associated Bases. . . . . . . -. ... [Pg.809]


See other pages where Cytisin is mentioned: [Pg.275]    [Pg.183]    [Pg.526]    [Pg.33]    [Pg.49]    [Pg.116]    [Pg.116]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.140]    [Pg.141]    [Pg.141]    [Pg.141]    [Pg.141]    [Pg.142]    [Pg.143]    [Pg.143]    [Pg.143]    [Pg.144]    [Pg.145]    [Pg.145]    [Pg.145]    [Pg.145]    [Pg.149]    [Pg.150]    [Pg.150]    [Pg.151]    [Pg.372]    [Pg.789]    [Pg.801]    [Pg.278]    [Pg.854]    [Pg.854]   
See also in sourсe #XX -- [ Pg.188 ]

See also in sourсe #XX -- [ Pg.188 ]

See also in sourсe #XX -- [ Pg.188 ]




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Alkaloids cytisine

Cytisine

Cytisine

Cytisine Group

Cytisine agonist

Cytisine effects

Cytisine methylation

Cytisine neuronal nicotinic receptor

Cytisine pharmacological action

Cytisine structure

Laburnum [Cytisine

Lupin alkaloids cytisine

Methyl cytisine

The lupinine, lupanine, sparteine and cytisine synthesis pathway

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