Drug General Information |
Drug ID |
D01GNQ
|
Former ID |
DNC005115
|
Drug Name |
Phenoxyarsonous acid
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Formula |
C6H7AsO3
|
Canonical SMILES |
C1=CC=C(C=C1)O[As](O)O
|
InChI |
1S/C6H7AsO3/c8-7(9)10-6-4-2-1-3-5-6/h1-5,8-9H
|
InChIKey |
NOJGJOHOYAWLBB-UHFFFAOYSA-N
|
PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Carbonic anhydrase II |
Target Info |
Inhibitor |
[1]
|
Carbonic anhydrase I |
Target Info |
Inhibitor |
[1]
|
KEGG Pathway
|
Nitrogen metabolism
|
Proximal tubule bicarbonate reclamation
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Collecting duct acid secretion
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Gastric acid secretion
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Pancreatic secretion
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Bile secretionhsa00910:Nitrogen metabolism
|
NetPath Pathway
|
IL4 Signaling Pathway
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EGFR1 Signaling Pathway
|
Pathway Interaction Database
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C-MYB transcription factor network
|
PathWhiz Pathway
|
Gastric Acid Production
|
Reactome
|
Erythrocytes take up carbon dioxide and release oxygen
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Erythrocytes take up oxygen and release carbon dioxide
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Reversible hydration of carbon dioxideR-HSA-1237044:Erythrocytes take up carbon dioxide and release oxygen
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Reversible hydration of carbon dioxide
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WikiPathways
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Reversible Hydration of Carbon Dioxide
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Uptake of Carbon Dioxide and Release of Oxygen by Erythrocytes
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Uptake of Oxygen and Release of Carbon Dioxide by ErythrocytesWP2770:Reversible Hydration of Carbon Dioxide
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Uptake of Oxygen and Release of Carbon Dioxide by Erythrocytes
|
References |
REF 1 | Bioorg Med Chem Lett. 2004 Nov 1;14(21):5435-9.Carbonic anhydrase inhibitors. Inhibition of the newly isolated murine isozyme XIII with anions. |