CATHARANTHINE HYDROCHLORIDE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H24N2O2.ClH
Molecular Weight	372.888
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CATHARANTHINE HYDROCHLORIDE

Structure Search

SMILES

Cl.CCC1=C[C@@H]2C[N@]3CCC4=C(NC5=C4C=CC=C5)[C@@](C2)([C@@H]13)C(=O)OC

InChI

InChIKey=AVBOKMGDTOZFMW-GYMDHWDQSA-N

InChI=1S/C21H24N2O2.ClH/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;1H/t13-,19+,21-;/m0./s1

HIDE SMILES / InChI

Molecular Formula	C21H24N2O2
Molecular Weight	336.4275
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23532933
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/13641069 | https://www.ncbi.nlm.nih.gov/pubmed/23532933

Catharanthine is a terpene indole alkaloid produced by the medicinal plant Catharanthus roseus. 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.

Originator

Approval Year

Targets

Primary Target	Pharmacology	Potency
Transient receptor potential cation channel subfamily M member 8 18 Target ID: CHEMBL3108632 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25052206	Antagonist 2849	0.9 µM [IC50]
Transient receptor potential cation channel subfamily A member 1 38 Target ID: CHEMBL6007 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25052206	Partial Agonist 297	9000.0 nM [EC50]
Vanilloid receptor 53 Target ID: CHEMBL4794 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25052206	Partial Agonist 297	20.0 µM [EC50]
Voltage-gated L-type calcium channel 95 Target ID: CHEMBL2095177 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23532933	Inhibitor 8504	220.0 µM [IC50]

Conditions

Condition	Modality	Targets	Highest Phase	Product
Unknown 2596

PubMed

Title	Date	PubMed
A note on the alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.). II. Catharanthine, lochnericine, vindolinine, and vindoline.	1959-04	13641069

Patents

Sample Use Guides

In Vivo Use Guide

Intravenous administration of catharanthine (0.5–20 mg/kg) to anesthetized rats induced rapid, dose-dependent decreases in blood pressure, heart rate, left ventricular blood pressure, cardiac contractility, and the slope of the end-systolic pressure-volume relationship curve.

Route of Administration: Intravenous

In Vitro Use Guide

Catharanthine evoked concentrationdependent decreases in endothelium-independent tonic responses of aortic rings to phenylephrine (PE) and KCl (IC50 = 5 28 uM for PE and IC50 =5 34 mM for KCl) and of thirdorder branches of the small mesenteric artery (IC50 = 3 mM for PE and IC50 = 6 mM for KCl)

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:52:45 GMT 2025` Edited by `admin` on `Mon Mar 31 22:52:45 GMT 2025`
Record UNII	V75368O53K
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

(+)-CATHARANTHINE HYDROCHLORIDE

Preferred Name

English

CATHARANTHINE HYDROCHLORIDE

Common Name

English

METHYL (2.ALPHA.,5.BETA.,6.ALPHA.)-3,4-DIDEHYDROIBOGAMINE-18.BETA.- CARBOXYLATE MONOHYDROCHLORIDE

Common Name

English

IBOGAMINE-18-CARBOXYLIC ACID, 3,4-DIDEHYDRO-, METHYL ESTER, MONOHYDROCHLORIDE, (2.ALPHA.,5.BETA.,6.ALPHA.,18.BETA.)-

Systematic Name

English

Code System Code Type Description

PUBCHEM

5458189