ID: ALA4648776

Max Phase: Preclinical

Molecular Formula: C18H14N4O2

Molecular Weight: 318.34

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(-c2ncnc(Nc3ccc4ncoc4c3)c2O)cc1

Standard InChI:  InChI=1S/C18H14N4O2/c1-11-2-4-12(5-3-11)16-17(23)18(20-9-19-16)22-13-6-7-14-15(8-13)24-10-21-14/h2-10,23H,1H3,(H,19,20,22)

Standard InChI Key:  ZTMRGLGHRWHSBX-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: 318.34Molecular Weight (Monoisotopic): 318.1117AlogP: 4.04#Rotatable Bonds: 3
Polar Surface Area: 84.07Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.44CX Basic pKa: 4.62CX LogP: 3.67CX LogD: 3.64
Aromatic Rings: 4Heavy Atoms: 24QED Weighted: 0.59Np Likeness Score: -0.84

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