ID: ALA5270227

Max Phase: Preclinical

Molecular Formula: C28H24N6O2

Molecular Weight: 476.54

Associated Items:

Representations

Canonical SMILES:  N[C@H](Cc1ccccc1)C(=O)Nc1cncc(-c2ccc3[nH]nc(NC(=O)c4ccccc4)c3c2)c1

Standard InChI:  InChI=1S/C28H24N6O2/c29-24(13-18-7-3-1-4-8-18)28(36)31-22-14-21(16-30-17-22)20-11-12-25-23(15-20)26(34-33-25)32-27(35)19-9-5-2-6-10-19/h1-12,14-17,24H,13,29H2,(H,31,36)(H2,32,33,34,35)/t24-/m1/s1

Standard InChI Key:  FOBQDUDIHLWHMU-XMMPIXPASA-N

Associated Targets(Human)

Cyclin-dependent kinase 7 1512 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cyclin-dependent kinase 2 9050 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: 476.54Molecular Weight (Monoisotopic): 476.1961AlogP: 4.39#Rotatable Bonds: 7
Polar Surface Area: 125.79Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.99CX Basic pKa: 8.00CX LogP: 3.95CX LogD: 3.26
Aromatic Rings: 5Heavy Atoms: 36QED Weighted: 0.28Np Likeness Score: -0.99

References

1. Yang B, Zhang H, Li N, Gao L, Jiang H, Kan W, Yuan H, Li J, Zhao D, Xiong B, Zhou Y, Guo D, Liu T..  (2022)  Discovery of Novel N-(5-(Pyridin-3-yl)-1H-indazol-3-yl)benzamide Derivatives as Potent Cyclin-Dependent Kinase 7 Inhibitors for the Treatment of Autosomal Dominant Polycystic Kidney Disease.,  65  (23.0): [PMID:36384292] [10.1021/acs.jmedchem.2c01334]

Source