Drug Information
Drug General Information | Top | |||
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Drug ID |
D0S6GK
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Former ID |
DNC003360
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Drug Name |
3,5-Difluorobenzenesulfonamide
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Synonyms |
3,5-DIFLUOROBENZENESULFONAMIDE; 140480-89-3; 3,5-Difluorobenzenesulphonamide; Benzenesulfonamide, 3,5-difluoro-; 3,5-difluorobenzene-1-sulfonamide; Buttpark 27\07-04; FBU; PubChem11783; ACMC-20ai3d; AC1L9JFC; KSC493S5P; SCHEMBL602631; CHEBI:42566; CTK3J3957; DTXSID20332219; MKQPOVUFDWKPNO-UHFFFAOYSA-N; MolPort-000-150-739; ZINC2576766; JRD-1790; MFCD02091379; BBL100443; 6828AA; STL554237; ANW-74375; SBB091558; 3,5-Difluorobenzenesulfonamide, 97%; AKOS000148222; DB02087; VZ25762; TRA0083487; PS-8315; MCULE-4003409613; RTR-005258; CJ-10108
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C6H5F2NO2S
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Canonical SMILES |
C1=C(C=C(C=C1F)S(=O)(=O)N)F
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InChI |
1S/C6H5F2NO2S/c7-4-1-5(8)3-6(2-4)12(9,10)11/h1-3H,(H2,9,10,11)
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InChIKey |
MKQPOVUFDWKPNO-UHFFFAOYSA-N
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CAS Number |
CAS 140480-89-3
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PubChem Compound ID | ||||
PubChem Substance ID |
822665, 3215901, 6563736, 7887434, 10299863, 12107785, 24879622, 26697242, 29202650, 36888742, 46506239, 50312136, 87628557, 90342652, 104636156, 104696645, 117651878, 118509304, 125340759, 126643963, 126681916, 135591229, 136911676, 136987643, 137184181, 143460404, 143515394, 152244672, 160841873, 160965305, 162303126, 162762275, 163406914, 163784280, 163809890, 164799741, 165374865, 184554924, 202541381, 204403709, 206247233, 223495462, 223551723, 223658876, 224568647, 226905154, 241034647, 246946646, 249806533, 251888527
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ChEBI ID |
CHEBI:42566
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Target and Pathway | Top | |||
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Target(s) | Carbonic anhydrase II (CA-II) | Target Info | Inhibitor | [1] |
KEGG Pathway | Nitrogen metabolism | |||
Proximal tubule bicarbonate reclamation | ||||
Collecting duct acid secretion | ||||
Gastric acid secretion | ||||
Pancreatic secretion | ||||
Bile secretion | ||||
NetPath Pathway | IL4 Signaling Pathway | |||
EGFR1 Signaling Pathway | ||||
Reactome | Erythrocytes take up carbon dioxide and release oxygen | |||
Erythrocytes take up oxygen and release carbon dioxide | ||||
Reversible hydration of carbon dioxide | ||||
WikiPathways | Reversible Hydration of Carbon Dioxide | |||
Uptake of Carbon Dioxide and Release of Oxygen by Erythrocytes | ||||
Uptake of Oxygen and Release of Carbon Dioxide by Erythrocytes |
References | Top | |||
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REF 1 | How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6. |
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