ID: ALA4068934

Max Phase: Preclinical

Molecular Formula: C24H23N3O3

Molecular Weight: 401.47

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1c(-c2ccc(CN3CCOCC3)cc2)cc2onc(-c3ccccc3)c2c1=O

Standard InChI:  InChI=1S/C24H23N3O3/c1-26-20(18-9-7-17(8-10-18)16-27-11-13-29-14-12-27)15-21-22(24(26)28)23(25-30-21)19-5-3-2-4-6-19/h2-10,15H,11-14,16H2,1H3

Standard InChI Key:  TYFDJJNBSDHYLQ-UHFFFAOYSA-N

Associated Targets(Human)

dCTP pyrophosphatase 1 562 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

Properties

Molecular Weight: 401.47Molecular Weight (Monoisotopic): 401.1739AlogP: 3.69#Rotatable Bonds: 4
Polar Surface Area: 60.50Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.89CX LogP: 2.89CX LogD: 2.77
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.52Np Likeness Score: -1.16

References

1. Llona-Minguez S, Häggblad M, Martens U, Johansson L, Sigmundsson K, Lundbäck T, Loseva O, Jemth AS, Lundgren B, Jensen AJ, Scobie M, Helleday T..  (2017)  Diverse heterocyclic scaffolds as dCTP pyrophosphatase 1 inhibitors. Part 2: Pyridone- and pyrimidinone-derived systems.,  27  (15): [PMID:28655422] [10.1016/j.bmcl.2017.06.039]

Source