Drug General Information
Drug ID	D0D1HC
Former ID	DNC010930
Drug Name	5-oxo-1-tosyl-2,5-dihydro-1Hpyrrol-2-yl acetate
Drug Type	Small molecular drug
Indication	Discovery agent		Investigative	[530979]
Structure		Download 2D MOL 3D MOL
Formula	C13H13NO5S
Canonical SMILES	CC1=CC=C(C=C1)S(=O)(=O)N2C(C=CC2=O)OC(=O)C
InChI	1S/C13H13NO5S/c1-9-3-5-11(6-4-9)20(17,18)14-12(16)7-8-13(14)19-10(2)15/h3-8,13H,1-2H3
InChIKey	JVIFWMPUUHEQPE-UHFFFAOYSA-N
PubChem Compound ID	46871782
Target and Pathway
Target(s)	Carbonic anhydrase I	Target Info	Inhibitor	[530979]
KEGG Pathway	Nitrogen metabolism
Pathway Interaction Database	C-MYB transcription factor network
PathWhiz Pathway	Gastric Acid Production
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 530979	Bioorg Med Chem. 2010 Jun 15;18(12):4468-74. Epub 2010 May 28.A novel and one-pot synthesis of new 1-tosyl pyrrol-2-one derivatives and analysis of carbonic anhydrase inhibitory potencies.
Ref 530979	Bioorg Med Chem. 2010 Jun 15;18(12):4468-74. Epub 2010 May 28.A novel and one-pot synthesis of new 1-tosyl pyrrol-2-one derivatives and analysis of carbonic anhydrase inhibitory potencies.

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