2-(4-fluorophenyl)-6-(piperidin-4-yl)-3-(pyridin-4-yl)-1H-indole

ID: ALA521910

Chembl Id: CHEMBL521910

PubChem CID: 44565046

Max Phase: Preclinical

Molecular Formula: C24H22FN3

Molecular Weight: 371.46

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Fc1ccc(-c2[nH]c3cc(C4CCNCC4)ccc3c2-c2ccncc2)cc1

Standard InChI:  InChI=1S/C24H22FN3/c25-20-4-1-18(2-5-20)24-23(17-9-13-27-14-10-17)21-6-3-19(15-22(21)28-24)16-7-11-26-12-8-16/h1-6,9-10,13-16,26,28H,7-8,11-12H2

Standard InChI Key:  AIXLZYVZYBHMSA-UHFFFAOYSA-N

Associated Targets(non-human)

PKG cGMP-dependent protein kinase (275 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Eimeria tenella (990 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Eimeria acervulina (464 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Eimeria mitis (216 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Eimeria maxima (199 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: 371.46Molecular Weight (Monoisotopic): 371.1798AlogP: 5.50#Rotatable Bonds: 3
Polar Surface Area: 40.71Molecular Species: BASEHBA: 2HBD: 2
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 10.05CX LogP: 4.32CX LogD: 1.76
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.50Np Likeness Score: -0.34

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]

Source