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
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)
Approval Year
PubMed
Title | Date | PubMed |
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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 |
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Antidiabetic sulphonylureas activate mitochondrial permeability transition in rat skeletal muscle. | 2005 Jul |
Patents
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Classification Tree | Code System | Code | ||
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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
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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
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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
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Code System | Code | Type | Description | ||
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C72801
Created by
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25046-79-1
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246-579-5
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100000084205
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DB01289
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32778
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2923
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H7SC0I332I
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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
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PRIMARY | Merck Index | ||
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DTXSID9023097
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1305
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admin on Fri Dec 15 15:29:35 UTC 2023 , Edited by admin on Fri Dec 15 15:29:35 UTC 2023
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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
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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
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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
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PRIMARY |
ACTIVE MOIETY