U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C51H69N5O9
Molecular Weight 896.1217
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VINLEUCINOL

SMILES

[H][C@@]12N3CC[C@@]14C5=C(C=C(OC)C(=C5)[C@]6(C[C@@]7([H])CN(C[C@](O)(CC)C7)CCC8=C6NC9=C8C=CC=C9)C(=O)OC)N(C)[C@@]4([H])[C@](O)([C@H](O)[C@]2(CC)C=CC3)C(=O)N[C@@H]([C@@H](C)CC)C(=O)OCC

InChI

InChIKey=QSTPFUDHVVIGCL-MIESHYDTSA-N
InChI=1S/C51H69N5O9/c1-9-30(5)39(41(57)65-12-4)53-45(59)51(62)43-49(20-23-56-21-15-19-48(11-3,42(49)56)44(51)58)34-24-35(38(63-7)25-37(34)54(43)6)50(46(60)64-8)27-31-26-47(61,10-2)29-55(28-31)22-18-33-32-16-13-14-17-36(32)52-40(33)50/h13-17,19,24-25,30-31,39,42-44,52,58,61-62H,9-12,18,20-23,26-29H2,1-8H3,(H,53,59)/t30-,31-,39-,42-,43+,44+,47-,48+,49+,50-,51-/m0/s1

HIDE SMILES / InChI
Vinleucinol (also known as vinblastine-isoleucinate or V-LEU) was developed as a vinca alkaloid derivative. This compound exhibited superior antitumor activity in malignant melanoma, small cell lung carcinoma, and breast cancer lines. Experiments on animals have shown that metabolite of vinleucinol was mainly responsible for the antitumor.

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative antitumour activity of vinblastine-isoleucinate and related vinca alkaloids in human tumour xenografts.
1992
Name Type Language
VINLEUCINOL
INN  
INN  
Official Name English
(23(1S,2S))-4-DEACETYL-3-((1-CARBOXY-2-METHYLBUTYL)CARBAMOYL)-3-DE(METHOXYCARBONYL)VINCALEUKOBLASTINE, ETHYL ESTER
Common Name English
VINBLASTINE ISOLEUCINATE
Common Name English
N-(O4-DEACETYL-23-VINBLASTINOYL) ETHYL L-ISOLEUCINATE
Common Name English
vinleucinol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C932
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
Code System Code Type Description
INN
6673
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
ChEMBL
CHEMBL2103976
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
EVMPD
SUB00067MIG
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
FDA UNII
MUJ5BW9BWR
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
CAS
81571-28-0
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
PUBCHEM
10033679
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
SMS_ID
100000079113
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
MESH
C080984
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY
NCI_THESAURUS
C95239
Created by admin on Fri Dec 15 15:53:37 GMT 2023 , Edited by admin on Fri Dec 15 15:53:37 GMT 2023
PRIMARY