ID: ALA1956046

Max Phase: Preclinical

Molecular Formula: C32H31N3O5S

Molecular Weight: 569.68

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc2cc(CCC(=O)CC(Nc3ccc(S(=O)(=O)Nc4cc(C)on4)cc3)c3ccccc3)ccc2c1

Standard InChI:  InChI=1S/C32H31N3O5S/c1-22-18-32(34-40-22)35-41(37,38)30-16-12-27(13-17-30)33-31(24-6-4-3-5-7-24)21-28(36)14-9-23-8-10-26-20-29(39-2)15-11-25(26)19-23/h3-8,10-13,15-20,31,33H,9,14,21H2,1-2H3,(H,34,35)

Standard InChI Key:  XYHVTKRWUAZCBU-UHFFFAOYSA-N

Associated Targets(Human)

Peroxisome proliferator-activated receptor 137 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: 569.68Molecular Weight (Monoisotopic): 569.1984AlogP: 6.69#Rotatable Bonds: 12
Polar Surface Area: 110.53Molecular Species: ACIDHBA: 7HBD: 2
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 6.15CX Basic pKa: 1.70CX LogP: 6.03CX LogD: 5.24
Aromatic Rings: 5Heavy Atoms: 41QED Weighted: 0.17Np Likeness Score: -0.95

References

1. Wang H, Yan JF, Song XL, Fan L, Xu J, Zhou GM, Jiang L, Yang DC..  (2012)  Synthesis and antidiabetic performance of β-amino ketone containing nabumetone moiety.,  20  (6): [PMID:22364952] [10.1016/j.bmc.2012.01.028]

Source