ID: ALA5206250

Max Phase: Preclinical

Molecular Formula: C28H29N5O2

Molecular Weight: 467.57

Associated Items:

Representations

Canonical SMILES:  O=C(c1ccc(Nc2nccc(-c3cc4ccccc4o3)n2)cc1)N1CCC(N2CCCC2)CC1

Standard InChI:  InChI=1S/C28H29N5O2/c34-27(33-17-12-23(13-18-33)32-15-3-4-16-32)20-7-9-22(10-8-20)30-28-29-14-11-24(31-28)26-19-21-5-1-2-6-25(21)35-26/h1-2,5-11,14,19,23H,3-4,12-13,15-18H2,(H,29,30,31)

Standard InChI Key:  NOFKWJNMOAZTGW-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: 467.57Molecular Weight (Monoisotopic): 467.2321AlogP: 5.33#Rotatable Bonds: 5
Polar Surface Area: 74.50Molecular Species: BASEHBA: 6HBD: 1
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.31CX Basic pKa: 9.76CX LogP: 4.01CX LogD: 1.68
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.43Np Likeness Score: -1.20

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