5-hydroxy-N-isopentyl-2-(1-methylpiperidin-2-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide

ID: ALA3617289

Chembl Id: CHEMBL3617289

PubChem CID: 137100192

Max Phase: Preclinical

Molecular Formula: C16H26N4O3

Molecular Weight: 322.41

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)CCNC(=O)c1nc(C2CCCCN2C)[nH]c(=O)c1O

Standard InChI:  InChI=1S/C16H26N4O3/c1-10(2)7-8-17-15(22)12-13(21)16(23)19-14(18-12)11-6-4-5-9-20(11)3/h10-11,21H,4-9H2,1-3H3,(H,17,22)(H,18,19,23)

Standard InChI Key:  MGMPIAQXIRSXOC-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3617289

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Associated Targets(Human)

ERCC1 Tbio DNA excision repair protein ERCC-1/DNA repair endonuclease XPF (129 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FEN1 Tchem Flap endonuclease 1 (12055 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: 322.41Molecular Weight (Monoisotopic): 322.2005AlogP: 1.41#Rotatable Bonds: 5
Polar Surface Area: 98.32Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 7.51CX Basic pKa: 6.30CX LogP: 0.60CX LogD: 0.53
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.76Np Likeness Score: -0.48

References

1. Chapman TM, Wallace C, Gillen KJ, Bakrania P, Khurana P, Coombs PJ, Fox S, Bureau EA, Brownlees J, Melton DW, Saxty B..  (2015)  N-Hydroxyimides and hydroxypyrimidinones as inhibitors of the DNA repair complex ERCC1-XPF.,  25  (19): [PMID:26321360] [10.1016/j.bmcl.2015.08.024]

Source