Drug Information
Drug General Information | Top | |||
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Drug ID |
D0Y1UL
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Former ID |
DNC010328
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Drug Name |
(E)-3-(4-hydroxybenzylidene)indolin-2-one
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Synonyms |
CHEMBL103307; (E)-3-(4-hydroxybenzylidene)indolin-2-one; 3-(4-Hydroxybenzylidenyl)indolin-2-one; SCHEMBL16442341; BDBM50131995; ZINC12568108; AKOS001309473; 3-(4-hydroxybenzylidene)indolin-2-one; NCGC00343741-01; ACM293302144; AB00756566-01
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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 |
C15H11NO2
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Canonical SMILES |
C1=CC=C2C(=C1)C(=CC3=CC=C(C=C3)O)C(=O)N2
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InChI |
1S/C15H11NO2/c17-11-7-5-10(6-8-11)9-13-12-3-1-2-4-14(12)16-15(13)18/h1-9,17H,(H,16,18)/b13-9+
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InChIKey |
PLAOAGFXNCEZMZ-UKTHLTGXSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Proto-oncogene c-Ret (RET) | Target Info | Inhibitor | [1] |
KEGG Pathway | Endocytosis | |||
Pathways in cancer | ||||
Thyroid cancer | ||||
Central carbon metabolism in cancer | ||||
Pathway Interaction Database | Signaling events regulated by Ret tyrosine kinase | |||
Posttranslational regulation of adherens junction stability and dissassembly | ||||
WikiPathways | SIDS Susceptibility Pathways | |||
Dopaminergic Neurogenesis |
References | Top | |||
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REF 1 | Synthesis, structure-activity relationship and crystallographic studies of 3-substituted indolin-2-one RET inhibitors. Bioorg Med Chem. 2010 Feb 15;18(4):1482-96. |
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