3-(4-fluorophenyl)-2,2-dimethyl-N-(3-(6-methyl-2-oxopyridin-1(2H)-yl)propyl)cyclopropanecarboxamide

ID: ALA4228872

Chembl Id: CHEMBL4228872

PubChem CID: 145986795

Max Phase: Preclinical

Molecular Formula: C21H25FN2O2

Molecular Weight: 356.44

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cccc(=O)n1CCCNC(=O)C1C(c2ccc(F)cc2)C1(C)C

Standard InChI:  InChI=1S/C21H25FN2O2/c1-14-6-4-7-17(25)24(14)13-5-12-23-20(26)19-18(21(19,2)3)15-8-10-16(22)11-9-15/h4,6-11,18-19H,5,12-13H2,1-3H3,(H,23,26)

Standard InChI Key:  BPIYVMAAHNWDHX-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4228872

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Associated Targets(Human)

SUP-B15 (167 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
REH (364 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: 356.44Molecular Weight (Monoisotopic): 356.1900AlogP: 3.24#Rotatable Bonds: 6
Polar Surface Area: 51.10Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.45CX LogD: 2.45
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.81Np Likeness Score: -0.96

References

1. Nair RR, Geldenhuys WJ, Piktel D, Sadana P, Gibson LF..  (2018)  Novel compounds that target lipoprotein lipase and mediate growth arrest in acute lymphoblastic leukemia.,  28  (10): [PMID:29650292] [10.1016/j.bmcl.2018.03.061]

Source