Drug Information

Drug General Information
Drug ID
D06OVA
Former ID
DNC012907
Drug Name
1-pentenyl-4-(aminosulfonyl)benzoate
Drug Type
Small molecular drug
Indication Discovery agent Investigative [527786]
Formula
C12H15NO4S
Canonical SMILES
C=CCCCOC(=O)C1=CC=C(C=C1)S(=O)(=O)N
InChI
1S/C12H15NO4S/c1-2-3-4-9-17-12(14)10-5-7-11(8-6-10)18(13,15)16/h2,5-8H,1,3-4,9H2,(H2,13,15,16)
InChIKey
IEMQKTRDDVFPKZ-UHFFFAOYSA-N
PubChem Compound ID
11630396
Target and Pathway
Target(s) Carbonic anhydrase II Target Info Inhibitor [527786]
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
Ref 527786Bioorg Med Chem Lett. 2005 Dec 15;15(24):5429-33. Epub 2005 Oct 6.Synthesis and structure-activity relationships of novel benzene sulfonamides with potent binding affinity for bovine carbonic anhydrase II.
Ref 527786Bioorg Med Chem Lett. 2005 Dec 15;15(24):5429-33. Epub 2005 Oct 6.Synthesis and structure-activity relationships of novel benzene sulfonamides with potent binding affinity for bovine carbonic anhydrase II.

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