Drug Information
Drug General Information | Top | |||
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Drug ID |
D0A2PD
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Former ID |
DNC003377
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Drug Name |
3-Mercuri-4-Aminobenzenesulfonamide
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Synonyms |
3-Mercuri-4-Aminobenzenesulfonamide; (2-amino-5-sulfamoylphenyl)mercury; AC1L4WFQ; SCHEMBL678556; CTK7D7985; CHEBI:49484; [2-amino-5-(sulfamoyl)phenyl]mercury; DB04203
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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 |
C6H7HgN2O2S
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Canonical SMILES |
C1=CC(=C(C=C1S(=O)(=O)N)[Hg])N
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InChI |
1S/C6H7N2O2S.Hg/c7-5-1-3-6(4-2-5)11(8,9)10;/h1,3-4H,7H2,(H2,8,9,10);
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InChIKey |
KGGLGSZFQPTPPT-UHFFFAOYSA-N
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PubChem Compound ID | ||||
PubChem Substance ID | ||||
ChEBI ID |
CHEBI:49484
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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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