Drug Information
Drug General Information | |||||
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Drug ID |
D0V4PL
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Former ID |
DNC008335
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Drug Name |
3-(3,3-dimethyl-2-oxoindolin-5-yl)benzonitrile
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Drug Type |
Small molecular drug
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Indication | Discovery agent | Investigative | [1] | ||
Structure |
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Download2D MOL |
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Formula |
C17H14N2O
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Canonical SMILES |
CC1(C2=C(C=CC(=C2)C3=CC=CC(=C3)C#N)NC1=O)C
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InChI |
1S/C17H14N2O/c1-17(2)14-9-13(6-7-15(14)19-16(17)20)12-5-3-4-11(8-12)10-18/h3-9H,1-2H3,(H,19,20)
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InChIKey |
WZZPSUKZMZKXTQ-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Progesterone receptor | Target Info | Inhibitor | [1] | |
KEGG Pathway | Oocyte meiosis | ||||
Progesterone-mediated oocyte maturation | |||||
Pathway Interaction Database | Cellular roles of Anthrax toxin | ||||
Reactome | Nuclear signaling by ERBB4 | ||||
Nuclear Receptor transcription pathway | |||||
WikiPathways | Ovarian Infertility Genes | ||||
Signaling by ERBB4 | |||||
Nuclear Receptors | |||||
References | |||||
REF 1 | J Med Chem. 2008 Mar 27;51(6):1861-73. Epub 2008 Mar 5.Design, synthesis, and SAR of new pyrrole-oxindole progesterone receptor modulators leading to 5-(7-fluoro-3,3-dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-1-methyl-1H-pyrrole-2-carbonitrile (WAY-255348). | ||||
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