ID: ALA2286741

Max Phase: Preclinical

Molecular Formula: C20H24N2O2

Molecular Weight: 324.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCc1ccccc1C(=O)N(NC(=O)c1ccccc1)C(C)(C)C

Standard InChI:  InChI=1S/C20H24N2O2/c1-5-15-11-9-10-14-17(15)19(24)22(20(2,3)4)21-18(23)16-12-7-6-8-13-16/h6-14H,5H2,1-4H3,(H,21,23)

Standard InChI Key:  ZTRFLUQOXMKABJ-UHFFFAOYSA-N

Associated Targets(non-human)

Ecdysone receptor 281 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ecdysone receptor 183 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: 324.42Molecular Weight (Monoisotopic): 324.1838AlogP: 3.83#Rotatable Bonds: 3
Polar Surface Area: 49.41Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.92CX Basic pKa: CX LogP: 4.32CX LogD: 4.32
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.87Np Likeness Score: -0.68

References

1. Soin T, Swevers L, Kotzia G, Iatrou K, Janssen CR, Rougé P, Harada T, Nakagawa Y, Smagghe G..  (2010)  Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.,  66  (11): [PMID:20672340] [10.1002/ps.1998]

Source