ID: ALA242369

Max Phase: Preclinical

Molecular Formula: C28H30ClNO5

Molecular Weight: 496.00

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(CCc1ccccc1)C(=O)Cc1ccc(OCCCOc2ccc(CC(=O)O)cc2Cl)cc1

Standard InChI:  InChI=1S/C28H30ClNO5/c1-30(15-14-21-6-3-2-4-7-21)27(31)19-22-8-11-24(12-9-22)34-16-5-17-35-26-13-10-23(18-25(26)29)20-28(32)33/h2-4,6-13,18H,5,14-17,19-20H2,1H3,(H,32,33)

Standard InChI Key:  YANSZGDFOATIKO-UHFFFAOYSA-N

Associated Targets(Human)

Leukotriene B4 receptor 773 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Rattus norvegicus 775804 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 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: 496.00Molecular Weight (Monoisotopic): 495.1813AlogP: 5.06#Rotatable Bonds: 13
Polar Surface Area: 76.07Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 3.69CX Basic pKa: CX LogP: 5.05CX LogD: 1.74
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.34Np Likeness Score: -0.84

References

1. Junek R, Brůnová B, Kverka M, Panajotová V, Jandera A, Kuchar M..  (2007)  Antileukotrienic N-arylethyl-2-arylacetamides in the treatment of ulcerative colitis.,  42  (8): [PMID:17448575] [10.1016/j.ejmech.2007.01.014]

Source