ID: ALA2227695

Max Phase: Preclinical

Molecular Formula: C22H24N4O7

Molecular Weight: 456.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1c(C(=O)NN(C(=O)c2cc([N+](=O)[O-])cc([N+](=O)[O-])c2)C(C)(C)C)ccc2c1CC(C)O2

Standard InChI:  InChI=1S/C22H24N4O7/c1-12-8-18-13(2)17(6-7-19(18)33-12)20(27)23-24(22(3,4)5)21(28)14-9-15(25(29)30)11-16(10-14)26(31)32/h6-7,9-12H,8H2,1-5H3,(H,23,27)

Standard InChI Key:  JCPSVNBTGSVKFN-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: 456.46Molecular Weight (Monoisotopic): 456.1645AlogP: 3.72#Rotatable Bonds: 4
Polar Surface Area: 144.92Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 11HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.34CX Basic pKa: CX LogP: 4.06CX LogD: 4.06
Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.54Np Likeness Score: -0.48

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