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7-Hydroxy-2-oxo-2H-chromene-3-carboxylic Acid [3-(4-Hydroxyphenyl)propyl]amide ID: ALA4081954
Chembl Id: CHEMBL4081954
PubChem CID: 137646927
Max Phase: Preclinical
Molecular Formula: C19H17NO5
Molecular Weight: 339.35
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=C(NCCCc1ccc(O)cc1)c1cc2ccc(O)cc2oc1=O
Standard InChI: InChI=1S/C19H17NO5/c21-14-6-3-12(4-7-14)2-1-9-20-18(23)16-10-13-5-8-15(22)11-17(13)25-19(16)24/h3-8,10-11,21-22H,1-2,9H2,(H,20,23)
Standard InChI Key: IRTLXYIOFBGNOF-UHFFFAOYSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 339.35Molecular Weight (Monoisotopic): 339.1107AlogP: 2.57#Rotatable Bonds: 5Polar Surface Area: 99.77Molecular Species: NEUTRALHBA: 5HBD: 3#RO5 Violations: ┄HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): ┄CX Acidic pKa: 7.69CX Basic pKa: ┄CX LogP: 2.64CX LogD: 2.46Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.49Np Likeness Score: -0.19
References 1. Endo S, Xia S, Suyama M, Morikawa Y, Oguri H, Hu D, Ao Y, Takahara S, Horino Y, Hayakawa Y, Watanabe Y, Gouda H, Hara A, Kuwata K, Toyooka N, Matsunaga T, Ikari A.. (2017) Synthesis of Potent and Selective Inhibitors of Aldo-Keto Reductase 1B10 and Their Efficacy against Proliferation, Metastasis, and Cisplatin Resistance of Lung Cancer Cells., 60 (20): [PMID:28976752 ] [10.1021/acs.jmedchem.7b00830 ]