ID: ALA5175800

Max Phase: Preclinical

Molecular Formula: C22H23Cl2N5OS

Molecular Weight: 476.43

Associated Items:

Representations

Canonical SMILES:  CN1CCN(Cc2ccc(Nc3nc(N)c(C(=O)c4c(Cl)cccc4Cl)s3)cc2)CC1

Standard InChI:  InChI=1S/C22H23Cl2N5OS/c1-28-9-11-29(12-10-28)13-14-5-7-15(8-6-14)26-22-27-21(25)20(31-22)19(30)18-16(23)3-2-4-17(18)24/h2-8H,9-13,25H2,1H3,(H,26,27)

Standard InChI Key:  RAFISFVOOKCYLW-UHFFFAOYSA-N

Associated Targets(Human)

CDK11A Tchem PITSLRE serine/threonine-protein kinase CDC2L2 (327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK4 Tclin Cyclin-dependent kinase 4/cyclin D1 (2340 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCND1 Tchem CDK6/cyclin D1 (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCNT1 Tchem CDK9/cyclin T1 (2643 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: 476.43Molecular Weight (Monoisotopic): 475.1000AlogP: 4.75#Rotatable Bonds: 6
Polar Surface Area: 74.49Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.48CX Basic pKa: 8.05CX LogP: 5.76CX LogD: 5.02
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.50Np Likeness Score: -1.57

References

1. Li Z, Ishida R, Liu Y, Wang J, Li Y, Gao Y, Jiang J, Che J, Sheltzer JM, Robers MB, Zhang T, Westover KD, Nabet B, Gray NS..  (2022)  Synthesis and Structure-Activity relationships of cyclin-dependent kinase 11 inhibitors based on a diaminothiazole scaffold.,  238  [PMID:35597007] [10.1016/j.ejmech.2022.114433]

Source