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

Details

Stereochemistry ACHIRAL
Molecular Formula C20H27N5O5S
Molecular Weight 449.524
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLISOXEPIDE

SMILES

CC1=CC(=NO1)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NN3CCCCCC3

InChI

InChIKey=ZKUDBRCEOBOWLF-UHFFFAOYSA-N
InChI=1S/C20H27N5O5S/c1-15-14-18(23-30-15)19(26)21-11-10-16-6-8-17(9-7-16)31(28,29)24-20(27)22-25-12-4-2-3-5-13-25/h6-9,14H,2-5,10-13H2,1H3,(H,21,26)(H2,22,24,27)

HIDE SMILES / InChI
Glisoxepide (BS 4231) is a sulfonylurea compound with glucose-lowering activity. Glisoxepide is a specific inhibitor of the L- aspartate/L-glutamate antiport system. Glisoxepide also inhibits transport of bile acids into hepatocytes

Approval Year

PubMed

PubMed

TitleDatePubMed
Screening, library-assisted identification and validated quantification of oral antidiabetics of the sulfonylurea-type in plasma by atmospheric pressure chemical ionization liquid chromatography-mass spectrometry.
2002 Jun 15
Antidiabetic sulphonylureas activate mitochondrial permeability transition in rat skeletal muscle.
2005 Jul
Patents

Patents

Name Type Language
GLISOXEPIDE
INN   MART.   WHO-DD  
INN  
Official Name English
BAY-B-4231
Code English
1-(HEXAHYDRO-1H-AZEPIN-1-YL)-3-((P-(2-(5-METHYL-3-ISOXAZOLECARBOXAMIDO)ETHYL)PHENYL)SULFONYL)UREA
Common Name English
RP-22410
Code English
FBB-4231
Code English
FBB 4231
Code English
GLISOXEPIDE [MART.]
Common Name English
GLISOXEPID [MI]
Common Name English
RP 22410
Code English
glisoxepide [INN]
Common Name English
BAY B 4231
Code English
Glisoxepide [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QA10BB11
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
NCI_THESAURUS C97936
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
WHO-ATC A10BB11
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C72801
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
CAS
25046-79-1
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
ECHA (EC/EINECS)
246-579-5
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
SMS_ID
100000084205
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
DRUG BANK
DB01289
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
PUBCHEM
32778
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
INN
2923
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
FDA UNII
H7SC0I332I
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
MERCK INDEX
m5749
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID9023097
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
DRUG CENTRAL
1305
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
WIKIPEDIA
GLISOXEPIDE
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106618
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY
EVMPD
SUB07933MIG
Created by admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
PRIMARY