ID: ALA5282084

Max Phase: Preclinical

Molecular Formula: C22H25F2N3O3S

Molecular Weight: 449.52

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1cccc(S(=O)(=O)C2CCCC2)c1)c1cccnc1N1CCC(F)(F)CC1

Standard InChI:  InChI=1S/C22H25F2N3O3S/c23-22(24)10-13-27(14-11-22)20-19(9-4-12-25-20)21(28)26-16-5-3-8-18(15-16)31(29,30)17-6-1-2-7-17/h3-5,8-9,12,15,17H,1-2,6-7,10-11,13-14H2,(H,26,28)

Standard InChI Key:  XIDRBRUIPMEOSE-UHFFFAOYSA-N

Associated Targets(Human)

Kinesin-like protein KIF18A 889 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

OVCAR-3 48710 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: 449.52Molecular Weight (Monoisotopic): 449.1585AlogP: 4.29#Rotatable Bonds: 5
Polar Surface Area: 79.37Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.03CX LogP: 4.12CX LogD: 4.12
Aromatic Rings: 2Heavy Atoms: 31QED Weighted: 0.74Np Likeness Score: -1.69

References

1. Tamayo NA, Bourbeau MP, Allen JR, Ashton KS, Chen JJ, Kaller MR, Nguyen TT, Nishimura N, Pettus LH, Walton M, Belmontes B, Moriguchi J, Chen K, McCarter JD, Hanestad K, Chung G, Ninniri MSS, Sun J, Poppe L, Spahr C, Hui J, Jia L, Wu T, Dahal UP, Edson KZ, Payton M..  (2022)  Targeting the Mitotic Kinesin KIF18A in Chromosomally Unstable Cancers: Hit Optimization Toward an In Vivo Chemical Probe.,  65  (6.0): [PMID:35286090] [10.1021/acs.jmedchem.1c02030]

Source