ID: ALA5093550

Max Phase: Preclinical

Molecular Formula: C25H25FN8O

Molecular Weight: 472.53

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1nc2ccc(-c3nc(Nc4ccc(C(=O)N5CCN(C)CC5)cn4)ncc3F)cc2nc1C

Standard InChI:  InChI=1S/C25H25FN8O/c1-15-16(2)30-21-12-17(4-6-20(21)29-15)23-19(26)14-28-25(32-23)31-22-7-5-18(13-27-22)24(35)34-10-8-33(3)9-11-34/h4-7,12-14H,8-11H2,1-3H3,(H,27,28,31,32)

Standard InChI Key:  JKMZYDDGZWQHSL-UHFFFAOYSA-N

Associated Targets(Human)

Cyclin-dependent kinase 6 1724 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serine/threonine-protein kinase PIM1 9629 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

K562 73714 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: 472.53Molecular Weight (Monoisotopic): 472.2135AlogP: 3.37#Rotatable Bonds: 4
Polar Surface Area: 100.03Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.62CX Basic pKa: 6.78CX LogP: 2.45CX LogD: 2.36
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.48Np Likeness Score: -1.56

References

1. Yuan K, Ji M, Xie S, Qiu Z, Chen W, Min W, Xia F, Zheng M, Wang X, Li J, Hou Y, Kuang W, Wang L, Gu W, Li Z, Yang P..  (2022)  Discovery of Dual CDK6/PIM1 Inhibitors with a Novel Structure, High Potency, and Favorable Druggability for the Treatment of Acute Myeloid Leukemia.,  65  (1.0): [PMID:34958208] [10.1021/acs.jmedchem.1c02019]

Source