N'-benzoyl-N-tert-butyl-2-(trifluoromethyl)benzohydrazide

ID: ALA2286420

Chembl Id: CHEMBL2286420

Cas Number: 112426-67-2

PubChem CID: 15452034

Max Phase: Preclinical

Molecular Formula: C19H19F3N2O2

Molecular Weight: 364.37

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)(C)N(NC(=O)c1ccccc1)C(=O)c1ccccc1C(F)(F)F

Standard InChI:  InChI=1S/C19H19F3N2O2/c1-18(2,3)24(23-16(25)13-9-5-4-6-10-13)17(26)14-11-7-8-12-15(14)19(20,21)22/h4-12H,1-3H3,(H,23,25)

Standard InChI Key:  BHSQODKUEYDLIS-UHFFFAOYSA-N

Associated Targets(non-human)

Ecdysone receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EcR Ecdysone receptor (281 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EcR 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

Calculated Properties

Molecular Weight: 364.37Molecular Weight (Monoisotopic): 364.1399AlogP: 4.29#Rotatable Bonds: 2
Polar Surface Area: 49.41Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 9.92CX Basic pKa: CX LogP: 4.24CX LogD: 4.24
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.81Np Likeness Score: -0.90

References

1. Soin T, De Geyter E, Mosallanejad H, Iga M, Martín D, Ozaki S, Kitsuda S, Harada T, Miyagawa H, Stefanou D, Kotzia G, Efrose R, Labropoulou V, Geelen D, Iatrou K, Nakagawa Y, Janssen CR, Smagghe G, Swevers L..  (2010)  Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.,  66  (5): [PMID:20069627] [10.1002/ps.1903]
2. 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