Drug General Information
Drug ID
D0SV6C
Former ID
DNC010199
Drug Name
PRONTOCIL
Drug Type
Small molecular drug
Indication Discovery agent Investigative [529030]
Structure
Download
2D MOL

3D MOL

Formula
C18H16N4O10S3
Canonical SMILES
CC(=O)NC1=C(C=C2C=C(C(=NNC3=CC=C(C=C3)S(=O)(=O)N)C(=O)C<br />2=C1)S(=O)(=O)O)S(=O)(=O)O
InChI
1S/C18H16N4O10S3/c1-9(23)20-14-8-13-10(6-15(14)34(27,28)29)7-16(35(30,31)32)17(18(13)24)22-21-11-2-4-12(5-3-11)33(19,25)26/h2-8,21H,1H3,(H,20,23)(H2,19,25,26)(H,27,28,29)(H,30,31,32)/b22-17+
InChIKey
RFBIZWALEVAHDX-OQKWZONESA-N
PubChem Compound ID
Target and Pathway
Target(s) Carbonic anhydrase Target Info Inhibitor [529030]
Carbonic anhydrase II Target Info Inhibitor [530292]
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 529030Bioorg Med Chem. 2007 Dec 1;15(23):7229-36. Epub 2007 Aug 25.Carbonic anhydrase inhibitors: cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides.
Ref 529030Bioorg Med Chem. 2007 Dec 1;15(23):7229-36. Epub 2007 Aug 25.Carbonic anhydrase inhibitors: cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides.
Ref 530292Bioorg Med Chem Lett. 2009 Sep 1;19(17):4929-32. Epub 2009 Jul 22.Carbonic anhydrase inhibitors. Inhibition of the Rv1284 and Rv3273 beta-carbonic anhydrases from Mycobacterium tuberculosis with diazenylbenzenesulfonamides.

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