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Details

Stereochemistry ACHIRAL
Molecular Formula C24H34N4O5S
Molecular Weight 490.616
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLIMEPIRIDE

SMILES

CCC1=C(C)CN(C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)N[C@H]3CC[C@H](C)CC3)C1=O

InChI

InChIKey=WIGIZIANZCJQQY-RUCARUNLSA-N
InChI=1S/C24H34N4O5S/c1-4-21-17(3)15-28(22(21)29)24(31)25-14-13-18-7-11-20(12-8-18)34(32,33)27-23(30)26-19-9-5-16(2)6-10-19/h7-8,11-12,16,19H,4-6,9-10,13-15H2,1-3H3,(H,25,31)(H2,26,27,30)/t16-,19-

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
GLIMEPIRIDE
EMA EPAR   EP   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
Glimepiride [WHO-DD]
Common Name English
GLIMEPIRIDE [ORANGE BOOK]
Common Name English
AMARYL
Brand Name English
GLIMEPIRIDE [USP-RS]
Common Name English
GLIMEPIRIDE [MI]
Common Name English
GLIMEPIRIDE [EP MONOGRAPH]
Common Name English
GLIMEPIRIDE [USP IMPURITY]
Common Name English
HOE 490
Code English
NSC-759809
Code English
DUETACT COMPONENT GLIMEPIRIDE
Common Name English
GLIMEPIRIDE [USP MONOGRAPH]
Common Name English
GLIMEPIRIDE [MART.]
Common Name English
glimepiride [INN]
Common Name English
GLIMEPIRIDE [VANDF]
Common Name English
1H-PYRROLE-1-CARBOXAMIDE, 3-ETHYL-2,5-DIHYDRO-4-METHYL-N-(2-(4-(((((4-METHYLCYCLOHEXYL)AMINO)CARBONYL)AMINO)SULFONYL)PHENYL)ETHYL)-2-OXO-, TRANS-
Common Name English
GLIMEPIRIDE [USAN]
Common Name English
GLIMEPIRIDE [JAN]
Common Name English
GLIMEPIRIDE COMPONENT OF DUETACT
Common Name English
GLIMEPIRIDE [EMA EPAR]
Common Name English
1-((P-(2-(3-ETHYL-4-METHYL-2-OXO-3-PYRROLINE-1-CARBOXAMIDO)ETHYL)PHENYL)SULFONYL)-3-(TRANS-4-METHYLCYCLOHEXYL)UREA
Common Name English
Classification Tree Code System Code
NDF-RT N0000008054
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
LIVERTOX 459
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
NDF-RT N0000008054
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
WHO-VATC QA10BD06
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
NDF-RT N0000008054
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
WHO-VATC QA10BB12
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
NCI_THESAURUS C97936
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
WHO-ATC A10BB12
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
WHO-ATC A10BD06
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
WHO-ATC A10BD04
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
NDF-RT N0000175608
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
WHO-VATC QA10BD04
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL1481
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
NCI_THESAURUS
C29073
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
RXCUI
25789
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
GLIMEPIRIDE
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
RS_ITEM_NUM
1292303
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
MERCK INDEX
m5745
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY Merck Index
CAS
93479-97-1
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
LACTMED
Glimepiride
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
FDA UNII
6KY687524K
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
CHEBI
5383
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
SMS_ID
100000085456
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
EVMPD
SUB07925MIG
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
INN
5718
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
DRUG BANK
DB00222
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
NSC
759809
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
IUPHAR
6820
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
DAILYMED
6KY687524K
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
MESH
C057619
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID5040675
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
USAN
EE-37
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
DRUG CENTRAL
1300
Created by admin on Fri Dec 15 15:51:28 UTC 2023 , Edited by admin on Fri Dec 15 15:51:28 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of GLIMEPIRIDE
METABOLITE LESS ACTIVE (PARENT)
Structure of HYDROXYGLIMEPIRIDE, TRANS-
NIH
NCATS
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