Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D09ZUN
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| Former ID |
DNC009128
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| Drug Name |
2,6-di-tert-butyl-4-methoxyphenol
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| Synonyms |
2,6-DI-TERT-BUTYL-4-METHOXYPHENOL; 489-01-0; 3,5-Di-tert-butyl-4-hydroxyanisole; Topanol 354; Phenol, 2,6-bis(1,1-dimethylethyl)-4-methoxy-; 3,5-di-t-Butyl-4-hydroxyanisole; UNII-616072TMXY; CCRIS 5219; 2,6-Bis(1,1-dimethylethyl)-4-methoxyphenol; EINECS 207-693-0; NSC 14451; Phenol, 2,6-di-tert-butyl-4-methoxy-; CHEMBL98253; 2,6-di-t-butyl-4-methoxyphenol; SLUKQUGVTITNSY-UHFFFAOYSA-N; 2,6-ditert-butyl-4-methoxyphenol; 616072TMXY; 2,6-bis(tert-butyl)-4-methoxyphenol; 2,6-Di-tert-butyl-4-methoxyphenol, 97%; DTBHA; ACMC-1ALDH
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C15H24O2
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| Canonical SMILES |
CC(C)(C)C1=CC(=CC(=C1O)C(C)(C)C)OC
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| InChI |
1S/C15H24O2/c1-14(2,3)11-8-10(17-7)9-12(13(11)16)15(4,5)6/h8-9,16H,1-7H3
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| InChIKey |
SLUKQUGVTITNSY-UHFFFAOYSA-N
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| CAS Number |
CAS 489-01-0
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|
| REF 1 | Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols. Bioorg Med Chem. 2009 Apr 15;17(8):3207-11. | |||
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