ID: ALA4636410

Max Phase: Preclinical

Molecular Formula: C18H14N4O

Molecular Weight: 302.34

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(-c2ncnc(Nc3cccc(C#N)c3)c2O)cc1

Standard InChI:  InChI=1S/C18H14N4O/c1-12-5-7-14(8-6-12)16-17(23)18(21-11-20-16)22-15-4-2-3-13(9-15)10-19/h2-9,11,23H,1H3,(H,20,21,22)

Standard InChI Key:  QRNSWXQJLICAKS-UHFFFAOYSA-N

Associated Targets(Human)

Coagulation factor IX 922 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Coagulation factor X 9693 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

Properties

Molecular Weight: 302.34Molecular Weight (Monoisotopic): 302.1168AlogP: 3.77#Rotatable Bonds: 3
Polar Surface Area: 81.83Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.59CX Basic pKa: 4.62CX LogP: 4.18CX LogD: 3.97
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.77Np Likeness Score: -1.39

References

1. Jayne CL, Andreani T, Chan TY, Chelliah MV, Clasby MC, Dwyer M, Eagen KA, Fried S, Greenlee WJ, Guo Z, Hawes B, Hruza A, Ingram R, Keertikar KM, Neelamkavil S, Reichert P, Xia Y, Chackalamannil S..  (2020)  Discovery of hydroxy pyrimidine Factor IXa inhibitors.,  30  (15): [PMID:32527459] [10.1016/j.bmcl.2020.127279]

Source