Drug General Information
Drug ID	D09SFY
Former ID	DNC010024
Drug Name	2-(4-hydroxybenzylideneamino)ethanesulfonamide
Drug Type	Small molecular drug
Indication	Discovery agent		Investigative	[530416]
Structure		Download 2D MOL 3D MOL
Formula	C9H12N2O3S
Canonical SMILES	C1=CC(=O)C=CC1=CNCCS(=O)(=O)N
InChI	1S/C9H12N2O3S/c10-15(13,14)6-5-11-7-8-1-3-9(12)4-2-8/h1-4,7,11H,5-6H2,(H2,10,13,14)
InChIKey	BXISHYAYPPUYAY-UHFFFAOYSA-N
PubChem Compound ID	45483188
Target and Pathway
Target(s)	Carbonic anhydrase II	Target Info	Inhibitor	[530416]
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 530416	Bioorg Med Chem Lett. 2009 Nov 1;19(21):6014-7. Epub 2009 Sep 17.Carbonic anhydrase II-induced selection of inhibitors from a dynamic combinatorial library of Schiff's bases.
Ref 530416	Bioorg Med Chem Lett. 2009 Nov 1;19(21):6014-7. Epub 2009 Sep 17.Carbonic anhydrase II-induced selection of inhibitors from a dynamic combinatorial library of Schiff's bases.

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