ID: ALA2229372

Max Phase: Preclinical

Molecular Formula: C23H27N3O5

Molecular Weight: 425.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1c(C(=O)NN(C(=O)c2ccc([N+](=O)[O-])cc2)C(C)(C)C)ccc2c1CC(C)(C)O2

Standard InChI:  InChI=1S/C23H27N3O5/c1-14-17(11-12-19-18(14)13-23(5,6)31-19)20(27)24-25(22(2,3)4)21(28)15-7-9-16(10-8-15)26(29)30/h7-12H,13H2,1-6H3,(H,24,27)

Standard InChI Key:  UBVKDPDUIBSXTA-UHFFFAOYSA-N

Associated Targets(non-human)

Culicidae 80 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mythimna separata 3306 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: 425.49Molecular Weight (Monoisotopic): 425.1951AlogP: 4.20#Rotatable Bonds: 3
Polar Surface Area: 101.78Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.34CX Basic pKa: CX LogP: 4.40CX LogD: 4.40
Aromatic Rings: 2Heavy Atoms: 31QED Weighted: 0.59Np Likeness Score: -0.53

References

1. Huang Z, Cui Q, Xiong L, Wang Z, Wang K, Zhao Q, Bi F, Wang Q..  (2009)  Synthesis and insecticidal activities and SAR studies of novel benzoheterocyclic diacylhydrazine derivatives.,  57  (6): [PMID:19222202] [10.1021/jf8036193]

Source