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

Details

Stereochemistry ABSOLUTE
Molecular Formula 2C14H18N6O.H2O4S
Molecular Weight 670.743
Optical Activity ( - )
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ABACAVIR SULFATE

SMILES

OS(O)(=O)=O.NC1=NC2=C(N=CN2[C@@H]3C[C@H](CO)C=C3)C(NC4CC4)=N1.NC5=NC6=C(N=CN6[C@@H]7C[C@H](CO)C=C7)C(NC8CC8)=N5

InChI

InChIKey=WMHSRBZIJNQHKT-FFKFEZPRSA-N
InChI=1S/2C14H18N6O.H2O4S/c2*15-14-18-12(17-9-2-3-9)11-13(19-14)20(7-16-11)10-4-1-8(5-10)6-21;1-5(2,3)4/h2*1,4,7-10,21H,2-3,5-6H2,(H3,15,17,18,19);(H2,1,2,3,4)/t2*8-,10+;/m11./s1

HIDE SMILES / InChI

Approval Year

Name Type Language
ABACAVIR SULFATE
HSDB   JAN   MART.   MI   ORANGE BOOK   USAN   USP-RS   VANDF   WHO-DD   WHO-IP  
USAN  
Official Name English
ZIAGEN
Brand Name English
1592U89 SULFATE
Code English
(1S,4R)-4-(2-AMINO-6-(CYCLOPROPYLAMINO)-9H-PURIN-9-YL)-2-CYCLOPENTENE-1-METHANOL SULPHATE (SALT) (2:1)
Common Name English
ABACAVIR (AS SULFATE) [EMA EPAR]
Common Name English
ABACAVIR SULFATE [ORANGE BOOK]
Common Name English
Abacavir sulfate [WHO-DD]
Common Name English
ABACAVIR SULFATE [EP MONOGRAPH]
Common Name English
ABACAVIR SULFATE [MART.]
Common Name English
ABAMUNE
Common Name English
EPZICOM COMPONENT ABACAVIR SULFATE
Common Name English
(1S,4R)-4-(2-AMINO-6-(CYCLOPROPYLAMINO)-9H-PURIN-9-YL)-2-CYCLOPENTENE-1-METHANOL SULFATE (SALT) (2:1)
Common Name English
ABACAVIR SULFATE [USP-RS]
Common Name English
ABACAVIR SULFATE COMPONENT OF EPZICOM
Common Name English
ABACAVIR SULFATE [USP MONOGRAPH]
Common Name English
ABACAVIR SULFATE [VANDF]
Common Name English
NSC-760063
Code English
2-CYCLOPENTENE-1-METHANOL, 4-(2-AMINO-6-(CYCLOPROPYLAMINO)-9H-PURIN-9-YL)-, (1S,4R)-, SULFATE (2:1)
Systematic Name English
ABACAVIR SULFATE COMPONENT OF TRIZIVIR
Brand Name English
ABACAVIR SULFATE [WHO-IP]
Common Name English
ABACAVIR SULFATE COMPONENT OF TRIUMEQ
Brand Name English
DRG-0257
Code English
KIVEXA COMPONENT ABACAVIR SULFATE
Common Name English
TRIUMEQ COMPONENT ABACAVIR SULFATE
Brand Name English
ABACAVIR SULPHATE
Common Name English
TRIZIVIR COMPONENT ABACAVIR SULFATE
Brand Name English
ABACAVIRI SULFAS [WHO-IP LATIN]
Common Name English
ABACAVIR HEMISULFATE
Common Name English
ABACAVIR SULFATE [MI]
Common Name English
ABACAVIR (AS SULFATE)
EMA EPAR  
Common Name English
ABACAVIR SULFATE [JAN]
Common Name English
ABACAVIR SULPHATE COMPONENT OF TRIZIVIR
Common Name English
ABACAVIR SULFATE [HSDB]
Common Name English
ABACAVIR SULFATE [USAN]
Common Name English
Classification Tree Code System Code
EMA ASSESSMENT REPORTS TRIZIVIR (AUTHORIZED: HIV INFECTIONS)
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
EMA ASSESSMENT REPORTS TRIUMEQ (AUTHORIZED: HIV INFECTIONS)
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
EMA ASSESSMENT REPORTS ZIAGEN (AUTHORIZED: HIV INFECTIONS)
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
EMA ASSESSMENT REPORTS KIVEXA (AUTHORIZED: HIV INFECTIONS)
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
NCI_THESAURUS C97452
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C28804
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
PUBCHEM
441384
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
DRUG BANK
DBSALT000871
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
ChEMBL
CHEMBL1380
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
FDA UNII
J220T4J9Q2
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
HSDB
7154
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
RXCUI
221052
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY RxNorm
MERCK INDEX
m1271
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY Merck Index
USAN
JJ-59
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
DAILYMED
J220T4J9Q2
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
EVMPD
SUB00231MIG
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
RS_ITEM_NUM
1000408
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
EPA CompTox
DTXSID40894147
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
CHEBI
2361
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
NSC
760063
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
SMS_ID
100000090705
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
ABACAVIR SULFATE
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY Description: White to almost white powder. Solubility: Soluble in water. Category: Antiretroviral (Nucleoside Reverse Transcriptase Inhibitor). Storage: Abacavir sulfate should be kept in a well-closed container. Definition: Abacavir sulfate contains not less than 99.0% and not more than 101.0% of (C14H18N6O)2,H2SO4 calculated with reference to the anhydrous substance. Manufacture: The production method is validated to demonstrate that the substance, if tested, would comply with a limit of not more than 0.5% for (1R, 4S)-abacavir enantiomer using a suitable chiral chromatographic method.
CAS
188062-50-2
Created by admin on Fri Dec 15 15:47:38 UTC 2023 , Edited by admin on Fri Dec 15 15:47:38 UTC 2023
PRIMARY