Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0SF3B
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| Former ID |
DNC006487
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| Drug Name |
2-butylamido-5-sulfonamidoindane
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| Synonyms |
CHEMBL208531; 2-butylamido-5-sulfonamidoindane; Indanesulfonamide Derivative 12f; N-(5-sulfamoyl-2,3-dihydro-1H-inden-2-yl)pentanamide
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C14H20N2O3S
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| Canonical SMILES |
CCCCC(=O)NC1CC2=C(C1)C=C(C=C2)S(=O)(=O)N
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| InChI |
1S/C14H20N2O3S/c1-2-3-4-14(17)16-12-7-10-5-6-13(20(15,18)19)9-11(10)8-12/h5-6,9,12H,2-4,7-8H2,1H3,(H,16,17)(H2,15,18,19)
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| InChIKey |
VPKYLHQTQYEJLJ-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Indanesulfonamides as carbonic anhydrase inhibitors. Toward structure-based design of selective inhibitors of the tumor-associated isozyme CA IX. J Med Chem. 2006 May 4;49(9):2743-9. | |||
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