ID: ALA5198285

Max Phase: Preclinical

Molecular Formula: C23H22N4O

Molecular Weight: 370.46

Associated Items:

Representations

Canonical SMILES:  Cc1cccc(NC(=O)NCCc2cccc(-c3cnc4[nH]ccc4c3)c2)c1

Standard InChI:  InChI=1S/C23H22N4O/c1-16-4-2-7-21(12-16)27-23(28)25-10-8-17-5-3-6-18(13-17)20-14-19-9-11-24-22(19)26-15-20/h2-7,9,11-15H,8,10H2,1H3,(H,24,26)(H2,25,27,28)

Standard InChI Key:  NYTRCRVOIPGPHC-UHFFFAOYSA-N

Associated Targets(Human)

Cell division protein kinase 8 1536 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: 370.46Molecular Weight (Monoisotopic): 370.1794AlogP: 4.90#Rotatable Bonds: 5
Polar Surface Area: 69.81Molecular Species: NEUTRALHBA: 2HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.59CX Basic pKa: 3.13CX LogP: 4.52CX LogD: 4.52
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.47Np Likeness Score: -1.33

References

1. Zhang XX, Xiao Y, Yan YY, Wang YM, Jiang H, Wu L, Shi JB, Liu XH..  (2022)  Discovery of the Novel 1H-Pyrrolo[2,3-b]pyridine Derivative as a Potent Type II CDK8 Inhibitor against Colorectal Cancer.,  65  (18.0): [PMID:36068975] [10.1021/acs.jmedchem.2c00820]

Source