ID: ALA4565235

Max Phase: Preclinical

Molecular Formula: C25H25ClN2O4

Molecular Weight: 452.94

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cc(N(CC2CC2)c2ccc(Cl)c3ccccc23)cnc1C(=O)CCCC(=O)O

Standard InChI:  InChI=1S/C25H25ClN2O4/c1-32-23-13-17(14-27-25(23)22(29)7-4-8-24(30)31)28(15-16-9-10-16)21-12-11-20(26)18-5-2-3-6-19(18)21/h2-3,5-6,11-14,16H,4,7-10,15H2,1H3,(H,30,31)

Standard InChI Key:  APQRJPZYCYILCT-UHFFFAOYSA-N

Associated Targets(Human)

Leukotriene C4 synthase 198 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 452.94Molecular Weight (Monoisotopic): 452.1503AlogP: 5.88#Rotatable Bonds: 10
Polar Surface Area: 79.73Molecular Species: ACIDHBA: 5HBD: 1
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 3.69CX Basic pKa: 2.56CX LogP: 4.53CX LogD: 1.49
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.39Np Likeness Score: -0.73

References

1. Munck Af Rosenschöld M, Johannesson P, Nikitidis A, Tyrchan C, Chang HF, Rönn R, Chapman D, Ullah V, Nikitidis G, Glader P, Käck H, Bonn B, Wågberg F, Björkstrand E, Andersson U, Swedin L, Rohman M, Andreasson T, Bergström EL, Jiang F, Zhou XH, Lundqvist AJ, Malmberg A, Ek M, Gordon E, Pettersen A, Ripa L, Davis AM..  (2019)  Discovery of the Oral Leukotriene C4 Synthase Inhibitor (1S,2S)-2-({5-[(5-Chloro-2,4-difluorophenyl)(2-fluoro-2-methylpropyl)amino]-3-methoxypyrazin-2-yl}carbonyl)cyclopropanecarboxylic Acid (AZD9898) as a New Treatment for Asthma.,  62  (17): [PMID:31415176] [10.1021/acs.jmedchem.9b00555]

Source