Drug General Information |
Drug ID |
D05WQF
|
Former ID |
DNC011169
|
Drug Name |
2-Hydroxycinnamic acid
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Formula |
C9H8O3
|
Canonical SMILES |
C1=CC=C(C(=C1)C=CC(=O)O)O
|
InChI |
1S/C9H8O3/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-6,10H,(H,11,12)
|
InChIKey |
PMOWTIHVNWZYFI-UHFFFAOYSA-N
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CAS Number |
CAS 614-60-8
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PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Carbonic anhydrase II |
Target Info |
Inhibitor |
[1]
|
Carbonic anhydrase I |
Target Info |
Inhibitor |
[1]
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KEGG Pathway
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Nitrogen metabolism
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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
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NetPath Pathway
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IL4 Signaling Pathway
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EGFR1 Signaling Pathway
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Pathway Interaction Database
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C-MYB transcription factor network
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PathWhiz Pathway
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Gastric Acid Production
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Reactome
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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
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References |
REF 1 | Bioorg Med Chem Lett. 2010 Sep 1;20(17):5050-3. Epub 2010 Jul 13.Carbonic anhydrase inhibitors. Antioxidant polyphenols effectively inhibit mammalian isoforms I-XV. |