N-((2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)methyl)-3-phenylbutanamide

ID: ALA4447265

Chembl Id: CHEMBL4447265

PubChem CID: 155518930

Max Phase: Preclinical

Molecular Formula: C18H19N3O2

Molecular Weight: 309.37

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(CC(=O)NCc1ccc2[nH]c(=O)[nH]c2c1)c1ccccc1

Standard InChI:  InChI=1S/C18H19N3O2/c1-12(14-5-3-2-4-6-14)9-17(22)19-11-13-7-8-15-16(10-13)21-18(23)20-15/h2-8,10,12H,9,11H2,1H3,(H,19,22)(H2,20,21,23)

Standard InChI Key:  RZOGGCPIZGOCNR-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4447265

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Associated Targets(Human)

AGPS Tbio Alkyldihydroxyacetonephosphate synthase, peroxisomal (31 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 309.37Molecular Weight (Monoisotopic): 309.1477AlogP: 2.67#Rotatable Bonds: 5
Polar Surface Area: 77.75Molecular Species: NEUTRALHBA: 2HBD: 3
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 12.70CX Basic pKa: CX LogP: 2.66CX LogD: 2.66
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.68Np Likeness Score: -1.06

References

1. Stazi G, Battistelli C, Piano V, Mazzone R, Marrocco B, Marchese S, Louie SM, Zwergel C, Antonini L, Patsilinakos A, Ragno R, Viviano M, Sbardella G, Ciogli A, Fabrizi G, Cirilli R, Strippoli R, Marchetti A, Tripodi M, Nomura DK, Mattevi A, Mai A, Valente S..  (2019)  Development of alkyl glycerone phosphate synthase inhibitors: Structure-activity relationship and effects on ether lipids and epithelial-mesenchymal transition in cancer cells.,  163  [PMID:30576903] [10.1016/j.ejmech.2018.11.050]

Source