ID: ALA259484

Max Phase: Preclinical

Molecular Formula: C25H23ClN4O3

Molecular Weight: 462.94

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(=O)c1c(-c2ccccc2)c2cc(Cl)ccc2c(=O)n1Cc1cn(C(=O)NC)c(C)n1

Standard InChI:  InChI=1S/C25H23ClN4O3/c1-4-21(31)23-22(16-8-6-5-7-9-16)20-12-17(26)10-11-19(20)24(32)30(23)14-18-13-29(15(2)28-18)25(33)27-3/h5-13H,4,14H2,1-3H3,(H,27,33)

Standard InChI Key:  QRQZGNPFYXQURD-UHFFFAOYSA-N

Associated Targets(Human)

c-Jun N-terminal kinase 1 5038 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mitogen-activated protein kinase 8 32 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 462.94Molecular Weight (Monoisotopic): 462.1459AlogP: 4.66#Rotatable Bonds: 5
Polar Surface Area: 85.99Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.49CX LogP: 3.26CX LogD: 3.26
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.44Np Likeness Score: -0.91

References

1. Asano Y, Kitamura S, Ohra T, Itoh F, Kajino M, Tamura T, Kaneko M, Ikeda S, Igata H, Kawamoto T, Sogabe S, Matsumoto S, Tanaka T, Yamaguchi M, Kimura H, Fukumoto S..  (2008)  Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (2).,  16  (8): [PMID:18313930] [10.1016/j.bmc.2008.02.028]

Source