ID: ALA2386121

Max Phase: Preclinical

Molecular Formula: C26H23NO3

Molecular Weight: 397.47

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)/C(=C1\C(=O)N(Cc2cccc(C(=O)O)c2)c2ccccc21)c1ccccc1

Standard InChI:  InChI=1S/C26H23NO3/c1-17(2)23(19-10-4-3-5-11-19)24-21-13-6-7-14-22(21)27(25(24)28)16-18-9-8-12-20(15-18)26(29)30/h3-15,17H,16H2,1-2H3,(H,29,30)/b24-23+

Standard InChI Key:  OXQOQYXJZXMGOQ-WCWDXBQESA-N

Associated Targets(Human)

AMPK alpha2/beta1/gamma1 210 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: 397.47Molecular Weight (Monoisotopic): 397.1678AlogP: 5.50#Rotatable Bonds: 5
Polar Surface Area: 57.61Molecular Species: ACIDHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.03CX Basic pKa: CX LogP: 5.54CX LogD: 2.40
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.58Np Likeness Score: -0.59

References

1. Yu LF, Li YY, Su MB, Zhang M, Zhang W, Zhang LN, Pang T, Zhang RT, Liu B, Li JY, Li J, Nan FJ..  (2013)  Development of Novel Alkene Oxindole Derivatives As Orally Efficacious AMP-Activated Protein Kinase Activators.,  (5): [PMID:24900695] [10.1021/ml400028q]

Source