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2-(4-fluorophenyl)-6-(1-methylpiperidin-4-yl)-3-(pyridin-4-yl)-1H-indole ID: ALA489128
Chembl Id: CHEMBL489128
PubChem CID: 44565047
Max Phase: Preclinical
Molecular Formula: C25H24FN3
Molecular Weight: 385.49
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CN1CCC(c2ccc3c(-c4ccncc4)c(-c4ccc(F)cc4)[nH]c3c2)CC1
Standard InChI: InChI=1S/C25H24FN3/c1-29-14-10-17(11-15-29)20-4-7-22-23(16-20)28-25(19-2-5-21(26)6-3-19)24(22)18-8-12-27-13-9-18/h2-9,12-13,16-17,28H,10-11,14-15H2,1H3
Standard InChI Key: WRBWQEVWLVOZMN-UHFFFAOYSA-N
Associated Targets(non-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: 385.49Molecular Weight (Monoisotopic): 385.1954AlogP: 5.85#Rotatable Bonds: 3Polar Surface Area: 31.92Molecular Species: BASEHBA: 2HBD: 1#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 9.17CX LogP: 4.70CX LogD: 2.93Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.48Np Likeness Score: -0.56
References 1. Scribner A, Moore JA, Ouvry G, Fisher M, Wyvratt M, Leavitt P, Liberator P, Gurnett A, Brown C, Mathew J, Thompson D, Schmatz D, Biftu T.. (2009) Synthesis and biological activity of anticoccidial agents: 2,3-diarylindoles., 19 (5): [PMID:19195883 ] [10.1016/j.bmcl.2009.01.001 ]