7-Fluoro-3-(pyridin-4-ylmethyl)-4H-chromen-4-one

ID: ALA3793091

Chembl Id: CHEMBL3793091

PubChem CID: 127028499

Max Phase: Preclinical

Molecular Formula: C15H10FNO2

Molecular Weight: 255.25

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=c1c(Cc2ccncc2)coc2cc(F)ccc12

Standard InChI:  InChI=1S/C15H10FNO2/c16-12-1-2-13-14(8-12)19-9-11(15(13)18)7-10-3-5-17-6-4-10/h1-6,8-9H,7H2

Standard InChI Key:  OCBNOJQCXPPEOP-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3793091

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Associated Targets(Human)

CYP11B2 Tchem Cytochrome P450 11B2 (2325 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP11B1 Tclin Cytochrome P450 11B1 (1750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP19A1 Tclin Cytochrome P450 19A1 (6099 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP17A1 Tclin Cytochrome P450 17A1 (3627 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 255.25Molecular Weight (Monoisotopic): 255.0696AlogP: 2.92#Rotatable Bonds: 2
Polar Surface Area: 43.10Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.04CX LogP: 2.57CX LogD: 2.57
Aromatic Rings: 3Heavy Atoms: 19QED Weighted: 0.71Np Likeness Score: -0.35

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]

Source