Drug Information
Drug General Information | Top | |||
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Drug ID |
D00QDE
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Former ID |
DNC007968
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Drug Name |
7-bromo-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 |
C16H10BrNO3
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Canonical SMILES |
C1C2=C(C3=C(C=CC(=C3)O)N=C2C4=C(O1)C=C(C=C4)O)Br
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InChI |
1S/C16H10BrNO3/c17-15-11-5-8(19)2-4-13(11)18-16-10-3-1-9(20)6-14(10)21-7-12(15)16/h1-6,19-20H,7H2
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InChIKey |
UHDQHUPIXKORDL-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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