ID: ALA242365

Max Phase: Preclinical

Molecular Formula: C28H31NO5

Molecular Weight: 461.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(CCc1ccccc1)C(=O)Cc1ccc(OCCCOc2ccc(CC(=O)O)cc2)cc1

Standard InChI:  InChI=1S/C28H31NO5/c1-29(17-16-22-6-3-2-4-7-22)27(30)20-23-8-12-25(13-9-23)33-18-5-19-34-26-14-10-24(11-15-26)21-28(31)32/h2-4,6-15H,5,16-21H2,1H3,(H,31,32)

Standard InChI Key:  BVLDGYFEULVSKK-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: 461.56Molecular Weight (Monoisotopic): 461.2202AlogP: 4.41#Rotatable Bonds: 13
Polar Surface Area: 76.07Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.07CX Basic pKa: CX LogP: 4.45CX LogD: 1.33
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.38Np Likeness Score: -0.60

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