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

ID: ALA523808

Chembl Id: CHEMBL523808

PubChem CID: 44565146

Max Phase: Preclinical

Molecular Formula: C25H25FN4

Molecular Weight: 400.50

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CN1CCN(Cc2ccc3c(-c4ccncc4)c(-c4ccc(F)cc4)[nH]c3c2)CC1

Standard InChI:  InChI=1S/C25H25FN4/c1-29-12-14-30(15-13-29)17-18-2-7-22-23(16-18)28-25(20-3-5-21(26)6-4-20)24(22)19-8-10-27-11-9-19/h2-11,16,28H,12-15,17H2,1H3

Standard InChI Key:  ZSDRWLQDGWEYAF-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

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: 400.50Molecular Weight (Monoisotopic): 400.2063AlogP: 4.78#Rotatable Bonds: 4
Polar Surface Area: 35.16Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 8.11CX LogP: 4.00CX LogD: 3.21
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.54Np Likeness Score: -1.04

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