VINCANTRIL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C14H13ClN2O
Molecular Weight	260.719
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of VINCANTRIL

Structure Search

SMILES

ClC1=CC=C2N3C4=C(CCNC4CCC3=O)C2=C1

InChI

InChIKey=KJRKCWPQTXNNOM-UHFFFAOYSA-N

InChI=1S/C14H13ClN2O/c15-8-1-3-12-10(7-8)9-5-6-16-11-2-4-13(18)17(12)14(9)11/h1,3,7,11,16H,2,4-6H2

HIDE SMILES / InChI

Molecular Formula	C14H13ClN2O
Molecular Weight	260.719
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: https://apps.who.int/iris/bitstream/handle/10665/275695/WHO-EMP-RHT-TSN-2018.1-eng.pdf?sequence=1&isAllowed=y | https://books.google.ru/books?id=0vXTBwAAQBAJ&pg=PA1278&lpg=PA1278&dq=VINCANTRIL retrieved from The Dictionary of Drugs: Chemical Data. Chemical Data, Structures and Bibliographies. Editors: Elks, J., p. 1278.

Vincantril is a vinca alkaloid. It is antianoxia agent.

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:02:15 GMT 2025` Edited by `admin` on `Mon Mar 31 19:02:15 GMT 2025`
Record UNII	S0KXB0NKWN
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

vincantril [INN]

Preferred Name

English

VINCANTRIL

Official Name

English

Classification Tree Code System Code

NCI_THESAURUS

C29707

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

Code System Code Type Description

PUBCHEM

68854

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

NCI_THESAURUS

C77081

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

EVMPD

SUB00056MIG

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

EPA CompTox

DTXSID20867132

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

FDA UNII

S0KXB0NKWN

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

INN

5554

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

SMS_ID

100000079107

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

ChEMBL

CHEMBL2105586

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

CAS

65285-58-7

Created by admin on Mon Mar 31 19:02:15 GMT 2025 , Edited by admin on Mon Mar 31 19:02:15 GMT 2025

PRIMARY

Related Record Type Details


					XW6SRW982X

VINCANTRIL, (R)-

ENANTIOMER -> RACEMATE


					579T4WI8SW

VINCANTRIL, (S)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					S0KXB0NKWN

ACTIVE MOIETY