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Details

Stereochemistry ACHIRAL
Molecular Formula C14H21N3O2S.C4H6O4
Molecular Weight 413.488
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SUMATRIPTAN SUCCINATE

SMILES

OC(=O)CCC(O)=O.CNS(=O)(=O)CC1=CC=C2NC=C(CCN(C)C)C2=C1

InChI

InChIKey=PORMUFZNYQJOEI-UHFFFAOYSA-N
InChI=1S/C14H21N3O2S.C4H6O4/c1-15-20(18,19)10-11-4-5-14-13(8-11)12(9-16-14)6-7-17(2)3;5-3(6)1-2-4(7)8/h4-5,8-9,15-16H,6-7,10H2,1-3H3;1-2H2,(H,5,6)(H,7,8)

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
SUMATRIPTAN SUCCINATE
EP   JAN   MART.   MI   ORANGE BOOK   USAN   USP-RS   VANDF   WHO-DD  
USAN  
Official Name English
TREXIMET COMPONENT SUMATRIPTAN SUCCINATE
Common Name English
SUMATRIPTAN SUCCINATE [USP-RS]
Common Name English
ZEMBRACE SYMTOUCH
Brand Name English
Sumatriptan succinate [WHO-DD]
Common Name English
SUMATRIPTAN SUCCINATE [MART.]
Common Name English
SUMATRIPTAN SUCCINATE [USAN]
Common Name English
ONZETRA XSAIL
Brand Name English
SUMATRIPTAN SUCCINATE [USP MONOGRAPH]
Common Name English
TREXIMET
Common Name English
SUMATRIPTAN SUCCINATE [EP MONOGRAPH]
Common Name English
SUMATRIPTAN SUCCINATE [JAN]
Common Name English
SUMATRIPTAN SUCCINATE [VANDF]
Common Name English
SUMATRIPTAN SUCCINATE [ORANGE BOOK]
Common Name English
SUMATRIPTAN GALPHARM
Brand Name English
NSC-760362
Code English
1H-INDOLE-5-METHANESULFONAMIDE, 3-(2-(DIMETHYLAMINO)ETHYL)-N-METHYL-, BUTANEDIOATE (1:1)
Systematic Name English
GR-43175C
Code English
SUMATRIPTAN SUCCINATE [MI]
Common Name English
SUMATRIPTAN SUCCINATE COMPONENT OF TREXIMET
Common Name English
GR 43175C
Code English
SUMATRIPTAN (AS SUCCINATE)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47794
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
EMA ASSESSMENT REPORTS SUMATRIPTAN GALPHARM (REFUSED: MIGRAINE DISORDERS)
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
Code System Code Type Description
DRUG BANK
DBSALT001003
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
RXCUI
67158
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY RxNorm
PUBCHEM
59772
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
EPA CompTox
DTXSID60145966
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
EVMPD
SUB15437MIG
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
SMS_ID
100000077527
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
RS_ITEM_NUM
1642201
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
USAN
AA-44
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
FDA UNII
J8BDZ68989
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
DAILYMED
J8BDZ68989
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
NCI_THESAURUS
C29470
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
CAS
103628-48-4
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
MERCK INDEX
m10396
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY Merck Index
CHEBI
64359
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
NSC
760362
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
ChEMBL
CHEMBL128
Created by admin on Fri Dec 15 15:12:39 UTC 2023 , Edited by admin on Fri Dec 15 15:12:39 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of SUMATRIPTAN
PARENT (SALT/SOLVATE)
Structure of SUCCINIC ACID
NIH
NCATS
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