Catharanthine

Catharanthine

Names
Other names Methyl(5|A)-3,4-didehydroibogamine-18-carboxylate
Identifiers
CAS Number	2468-21-5 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:3469
ChemSpider	4572197
ECHA InfoCard	100.017.806
PubChem CID	5458190
UNII	WT0YJV846J Y
CompTox Dashboard (EPA)	DTXSID80947621
InChI InChI=1S/C21H24N2O2/c1-3-14-10-13-11-21(20(24)25-2)18-16(8-9-23(12-13)19(14)21)15-6-4-5-7-17(15)22-18/h4-7,10,13,19,22H,3,8-9,11-12H2,1-2H3/t13-,19+,21-/m0/s1 Key: CMKFQVZJOWHHDV-NQZBTDCJSA-N InChI=1/C21H24N2O2/c1-3-14-10-13-11-21(20(24)25-2)18-16(8-9-23(12-13)19(14)21)15-6-4-5-7-17(15)22-18/h4-7,10,13,19,22H,3,8-9,11-12H2,1-2H3/t13-,19+,21-/m0/s1 Key: CMKFQVZJOWHHDV-NQZBTDCJBW
SMILES CCC1=C[C@H]2C[C@]3([C@@H]1N(C2)CCc4c3[nH]c5c4cccc5)C(=O)OC
Properties
Chemical formula	C21H24N2O2
Molar mass	336.435 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Catharanthine is a terpene indole alkaloid produced by the medicinal plant Catharanthus roseus and Tabernaemontana_divaricata. Catharanthine is derived from strictosidine, but the exact mechanism by which this happens is currently unknown. Catharanthine is one of the two precursors that form vinblastine, the other being vindoline.

Uses

Modern Medicine

It showed anti-tumorogenic effect as well as inhibited cAMP phosphodiesterase activity It increased the intracellular level of cAMP in neurons and thus may lead to improved neuronal activity

External links

• Catharanthine dilates small mesenteric arteries and decreases heart rate and cardiac contractility by inhibition of voltage-operated calcium channels on vascular smooth muscle cells and cardiomyocytes