The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
7-Fluoro-2-pyridin-4-ylmethylchromen-4-one ID: ALA3794417
Chembl Id: CHEMBL3794417
PubChem CID: 127028817
Max Phase: Preclinical
Molecular Formula: C15H10FNO2
Molecular Weight: 255.25
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=c1cc(Cc2ccncc2)oc2cc(F)ccc12
Standard InChI: InChI=1S/C15H10FNO2/c16-11-1-2-13-14(18)9-12(19-15(13)8-11)7-10-3-5-17-6-4-10/h1-6,8-9H,7H2
Standard InChI Key: BAYJSUFIUXAGBB-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: 255.25Molecular Weight (Monoisotopic): 255.0696AlogP: 2.92#Rotatable Bonds: 2Polar Surface Area: 43.10Molecular Species: NEUTRALHBA: 3HBD: 0#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: 5.04CX LogP: 2.45CX LogD: 2.45Aromatic Rings: 3Heavy Atoms: 19QED Weighted: 0.71Np Likeness Score: -0.22
References 1. Gobbi S, Hu Q, Zimmer C, Engel M, Belluti F, Rampa A, Hartmann RW, Bisi A.. (2016) Exploiting the Chromone Scaffold for the Development of Inhibitors of Corticosteroid Biosynthesis., 59 (6): [PMID:26938274 ] [10.1021/acs.jmedchem.5b01609 ]