ID: ALA5286737

Max Phase: Preclinical

Molecular Formula: C24H21F3N6O2

Molecular Weight: 482.47

Associated Items:

Representations

Canonical SMILES:  CC1CN(c2ccncc2NC(=O)c2ccnn3cc(-c4ccc(C(F)(F)F)cc4)nc23)CCO1

Standard InChI:  InChI=1S/C24H21F3N6O2/c1-15-13-32(10-11-35-15)21-7-8-28-12-19(21)31-23(34)18-6-9-29-33-14-20(30-22(18)33)16-2-4-17(5-3-16)24(25,26)27/h2-9,12,14-15H,10-11,13H2,1H3,(H,31,34)

Standard InChI Key:  WWEHEGICBBJKLI-UHFFFAOYSA-N

Associated Targets(Human)

GSK3A Tclin Glycogen synthase kinase-3 alpha (3764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAPT Tclin Microtubule-associated protein tau (95507 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: 482.47Molecular Weight (Monoisotopic): 482.1678AlogP: 4.29#Rotatable Bonds: 4
Polar Surface Area: 84.65Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.98CX LogP: 3.74CX LogD: 3.21
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.47Np Likeness Score: -1.92

References

1. Hartz RA, Ahuja VT, Sivaprakasam P, Xiao H, Krause CM, Clarke WJ, Kish K, Lewis H, Szapiel N, Ravirala R, Mutalik S, Nakmode D, Shah D, Burton CR, Macor JE, Dubowchik GM..  (2023)  Design, Structure-Activity Relationships, and In Vivo Evaluation of Potent and Brain-Penetrant Imidazo[1,2-b]pyridazines as Glycogen Synthase Kinase-3β (GSK-3β) Inhibitors.,  66  (6): [PMID:36950863] [10.1021/acs.jmedchem.3c00133]

Source