5-(4-chlorophenyl)-N-(3-(piperidin-1-ylsulfonyl)phenyl)-1H-pyrazole-4-carboxamide

ID: ALA5266739

Chembl Id: CHEMBL5266739

Max Phase: Preclinical

Molecular Formula: C21H21ClN4O3S

Molecular Weight: 444.94

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1cccc(S(=O)(=O)N2CCCCC2)c1)c1cn[nH]c1-c1ccc(Cl)cc1

Standard InChI:  InChI=1S/C21H21ClN4O3S/c22-16-9-7-15(8-10-16)20-19(14-23-25-20)21(27)24-17-5-4-6-18(13-17)30(28,29)26-11-2-1-3-12-26/h4-10,13-14H,1-3,11-12H2,(H,23,25)(H,24,27)

Standard InChI Key:  LIKPCUYPZUOYKD-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5266739

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Associated Targets(Human)

KIF18A Tchem Kinesin-like protein KIF18A (889 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KIF11 Tchem Kinesin-like protein 1 (1720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CENPE Tchem Centromere-associated protein E (102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-157 (173 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

Calculated Properties

Molecular Weight: 444.94Molecular Weight (Monoisotopic): 444.1023AlogP: 4.16#Rotatable Bonds: 5
Polar Surface Area: 95.16Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.60CX Basic pKa: 1.68CX LogP: 3.44CX LogD: 3.42
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.62Np Likeness Score: -2.20

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