Drug Information
Drug General Information | Top | |||
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Drug ID |
D07XJC
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Former ID |
DNC007965
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Drug Name |
7-ethyl-6H-chromeno[4,3-b]quinoline-3,9-diol
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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 |
C18H15NO3
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Canonical SMILES |
CCC1=C2COC3=C(C2=NC4=C1C=C(C=C4)O)C=CC(=C3)O
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InChI |
1S/C18H15NO3/c1-2-12-14-7-10(20)4-6-16(14)19-18-13-5-3-11(21)8-17(13)22-9-15(12)18/h3-8,20-21H,2,9H2,1H3
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InChIKey |
OGDCTCUVBBYZTK-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Estrogen-related receptor-alpha (ESRRA) | Target Info | Inhibitor | [1] |
Reactome | PPARA activates gene expression | |||
Transcriptional activation of mitochondrial biogenesis | ||||
Nuclear Receptor transcription pathway | ||||
WikiPathways | Mitochondrial Gene Expression | |||
Regulation of Lipid Metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha) | ||||
Nuclear Receptors |
References | Top | |||
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REF 1 | ERbeta ligands. Part 6: 6H-Chromeno[4,3-b]quinolines as a new series of estrogen receptor beta-selective ligands. Bioorg Med Chem Lett. 2007 Jul 15;17(14):4053-6. |
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