Drug Information
Drug General Information | |||||
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Drug ID |
D00YNA
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Former ID |
DNC009344
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Drug Name |
3,3-(1,3-Thiazole-2,5-diyl)diphenol
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Drug Type |
Small molecular drug
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Indication | Discovery agent | Investigative | [529748] | ||
Structure |
Download2D MOL |
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Formula |
C15H11NO2S
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Canonical SMILES |
C1=CC(=CC(=C1)O)C2=CN=C(S2)C3=CC(=CC=C3)O
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InChI |
1S/C15H11NO2S/c17-12-5-1-3-10(7-12)14-9-16-15(19-14)11-4-2-6-13(18)8-11/h1-9,17-18H
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InChIKey |
OYFRXCWZMBHNHW-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Estradiol 17 beta-dehydrogenase 1 | Target Info | Inhibitor | [529748] | |
Cytochrome P450 3A4 | Target Info | Inhibitor | [529748] | ||
KEGG Pathway | Steroid hormone biosynthesis | ||||
Metabolic pathways | |||||
Ovarian steroidogenesishsa00140:Steroid hormone biosynthesis | |||||
Linoleic acid metabolism | |||||
Retinol metabolism | |||||
Metabolism of xenobiotics by cytochrome P450 | |||||
Drug metabolism - cytochrome P450 | |||||
Drug metabolism - other enzymes | |||||
Bile secretion | |||||
Chemical carcinogenesis | |||||
NetPath Pathway | FSH Signaling Pathway | ||||
PANTHER Pathway | Androgen/estrogene/progesterone biosynthesis | ||||
WikiPathways | Steroid Biosynthesis | ||||
Metabolism of steroid hormones and vitamin D | |||||
Prostate CancerWP702:Metapathway biotransformation | |||||
Aflatoxin B1 metabolism | |||||
Estrogen metabolism | |||||
Benzo(a)pyrene metabolism | |||||
Tamoxifen metabolism | |||||
Tryptophan metabolism | |||||
Oxidation by Cytochrome P450 | |||||
Nuclear Receptors in Lipid Metabolism and Toxicity | |||||
Nuclear Receptors Meta-Pathway | |||||
Farnesoid X Receptor Pathway | |||||
Vitamin D Receptor Pathway | |||||
Felbamate Metabolism | |||||
Lidocaine metabolism | |||||
Nifedipine Activity | |||||
Colchicine Metabolic Pathway | |||||
Irinotecan Pathway | |||||
Drug Induction of Bile Acid Pathway | |||||
Fatty Acid Omega Oxidation | |||||
Codeine and Morphine Metabolism | |||||
References | |||||
Ref 529748 | J Med Chem. 2008 Nov 13;51(21):6725-39. Epub 2008 Oct 15.Design, synthesis, biological evaluation and pharmacokinetics of bis(hydroxyphenyl) substituted azoles, thiophenes, benzenes, and aza-benzenes as potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1). | ||||
Ref 529748 | J Med Chem. 2008 Nov 13;51(21):6725-39. Epub 2008 Oct 15.Design, synthesis, biological evaluation and pharmacokinetics of bis(hydroxyphenyl) substituted azoles, thiophenes, benzenes, and aza-benzenes as potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1). |
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