ID: ALA5208060

Max Phase: Preclinical

Molecular Formula: C17H11NO3

Molecular Weight: 277.28

Associated Items:

Representations

Canonical SMILES:  COc1ccc2cc(C(=O)c3ccc(C#N)cc3)oc2c1

Standard InChI:  InChI=1S/C17H11NO3/c1-20-14-7-6-13-8-16(21-15(13)9-14)17(19)12-4-2-11(10-18)3-5-12/h2-9H,1H3

Standard InChI Key:  RPRSCHYTOJQFOV-UHFFFAOYSA-N

Associated Targets(non-human)

Glycogen synthase kinase 3 64 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 277.28Molecular Weight (Monoisotopic): 277.0739AlogP: 3.54#Rotatable Bonds: 3
Polar Surface Area: 63.23Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.21CX LogD: 3.21
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.69Np Likeness Score: -0.81

References

1. Galal KA, Truong A, Kwarcinski F, de Silva C, Avalani K, Havener TM, Chirgwin ME, Merten E, Ong HW, Willis C, Abdelwaly A, Helal MA, Derbyshire ER, Zutshi R, Drewry DH..  (2022)  Identification of Novel 2,4,5-Trisubstituted Pyrimidines as Potent Dual Inhibitors of Plasmodial PfGSK3/PfPK6 with Activity against Blood Stage Parasites In Vitro.,  65  (19.0): [PMID:36166733] [10.1021/acs.jmedchem.2c00996]

Source