Conopharyngine
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Conopharyngine is the major
alkaloid Alkaloids are a class of basic, naturally occurring organic compounds that contain at least one nitrogen atom. This group also includes some related compounds with neutral and even weakly acidic properties. Some synthetic compounds of similar ...
present in the leaves and stem-bark of ''
Tabernaemontana pachysiphon ''Tabernaemontana pachysiphon'' grows as a shrub or small tree up to tall, with a trunk diameter of up to . Its fragrant flowers feature white to pale yellow corolla lobes. The fruit is green, almost spherical, up to in diameter. Its habitat is ...
'' and '' Conopharyngia durissima''. It is closely related
voacangine Voacangine (12-methoxyibogamine-18-carboxylic acid methyl ester) is an alkaloid found predominantly in the root bark of the '' Voacanga africana'' tree, as well as in other plants such as ''Tabernanthe iboga'', '' Tabernaemontana africana'', ''Tra ...
and
coronaridine Coronaridine, also known as 18-carbomethoxyibogamine, is an alkaloid found in ''Tabernanthe iboga'' and related species, including ''Tabernaemontana divaricata'' for which (under the now obsolete synonym ''Ervatamia coronaria'') it was named. Li ...
. Conopharyngine pseudoindoxyl, a derivative of it, is also found in the same plant ''Tabernaemontana pachysiphon''.


Pharmacology

It possess central nervous system stimulant activity and produces bradycardia and
hypotension Hypotension is low blood pressure. Blood pressure is the force of blood pushing against the walls of the arteries as the heart pumps out blood. Blood pressure is indicated by two numbers, the systolic blood pressure (the top number) and the dia ...
in cats. It has weak acetylcholinesterase inhibitory activity and significantly increases hexobarbitone induced sleeping time.


Toxicity

It has low intravenous toxicity in mice (LD50 = 143 mg/kg).


See also

* Ibogaline


References

Alkaloids found in Iboga Methoxy compounds Heterocyclic compounds with 5 rings Methyl esters Nitrogen heterocycles Tryptamine alkaloids {{Alkaloid-stub