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Details

Stereochemistry ABSOLUTE
Molecular Formula C46H58N4O9.H2O4S
Molecular Weight 909.053
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VINBLASTINE SULFATE

SMILES

OS(O)(=O)=O.[H][C@@]12N3CC[C@@]14C5=CC(=C(OC)C=C5N(C)[C@@]4([H])[C@](O)([C@H](OC(C)=O)[C@]2(CC)C=CC3)C(=O)OC)[C@]6(C[C@H]7CN(C[C@](O)(CC)C7)CCC8=C6NC9=C8C=CC=C9)C(=O)OC

InChI

InChIKey=KDQAABAKXDWYSZ-PNYVAJAMSA-N
InChI=1S/C46H58N4O9.H2O4S/c1-8-42(54)23-28-24-45(40(52)57-6,36-30(15-19-49(25-28)26-42)29-13-10-11-14-33(29)47-36)32-21-31-34(22-35(32)56-5)48(4)38-44(31)17-20-50-18-12-16-43(9-2,37(44)50)39(59-27(3)51)46(38,55)41(53)58-7;1-5(2,3)4/h10-14,16,21-22,28,37-39,47,54-55H,8-9,15,17-20,23-26H2,1-7H3;(H2,1,2,3,4)/t28-,37-,38+,39+,42-,43+,44+,45-,46-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C46H58N4O9
Molecular Weight 810.9741
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:50 UTC 2023
Edited
by admin
on Fri Dec 15 14:59:50 UTC 2023
Record UNII
N00W22YO2B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VINBLASTINE SULFATE
EP   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
USAN  
Official Name English
NSC-49842
Code English
VINBLASTINE SULFATE [USP-RS]
Common Name English
29060LE
Code English
VINBLASTINE SULFATE [MART.]
Common Name English
ALKABAN-AQ
Common Name English
VLB MONOSULFATE
Common Name English
VINBLASTINE SULFATE [IARC]
Common Name English
29060-LE
Code English
VINBLASTINE SULPHATE
Common Name English
VINBLASTINE SULFATE [USP MONOGRAPH]
Common Name English
VINCALEUKOBLASTINE, SULFATE (1:1) (SALT)
Common Name English
VINBLASTINE SULFATE [WHO-IP]
Common Name English
VINBLASTINE SULFATE [ORANGE BOOK]
Common Name English
Vinblastine sulfate [WHO-DD]
Common Name English
VINBLASTINE SULFATE [MI]
Common Name English
VELBAN
Brand Name English
VINBLASTINI SULFAS [WHO-IP LATIN]
Common Name English
VINCALEUKOBLASTINE SULFATE
Common Name English
VINBLASTINE SULFATE [EP MONOGRAPH]
Common Name English
VINBLASTINE SULFATE [USAN]
Common Name English
VINBLASTINE SULFATE [JAN]
Common Name English
VINBLASTINE SULFATE [VANDF]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C67422
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
FDA ORPHAN DRUG 867921
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
NCI_THESAURUS C932
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
Code System Code Type Description
WHO INTERNATIONAL PHARMACOPEIA
VINBLASTINE SULFATE
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY Description: A white to slightly yellow, amorphous or crystalline powder. Solubility: Freely soluble in water; very slightly soluble in ethanol (~750 g/l) TS; practically insoluble in ether R. Category: Cytotoxic drug. Storage: Vinblastine sulfate should be kept in a tightly closed container, protected from light, and stored at a temperature between 2 and 8 ?C. Additional information: CAUTION: Vinblastine sulfate must be handled with care, avoiding contact with the skin and inhalation of airborne particles. It is very hygroscopic and unstable. Before the bottle is opened, it should be allowed to come to room temperature in a desiccator. Requirement: Vinblastine sulfate contains not less than 96.0% and not more than the equivalent of 101.0% of C46H58N4O9,H2SO4, calculated with reference to the dried substance.
NCI_THESAURUS
C931
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
RS_ITEM_NUM
1713004
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
SMS_ID
100000087899
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
FDA UNII
N00W22YO2B
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
RXCUI
11199
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY RxNorm
MERCK INDEX
m11449
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID601017133
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
NSC
49842
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
EVMPD
SUB05098MIG
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
DAILYMED
N00W22YO2B
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
ECHA (EC/EINECS)
205-606-0
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
DRUG BANK
DBSALT000644
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
CAS
143-67-9
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
CHEBI
9984
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
PUBCHEM
5388983
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL159
Created by admin on Fri Dec 15 14:59:50 UTC 2023 , Edited by admin on Fri Dec 15 14:59:50 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY