ID: ALA2229331

Max Phase: Preclinical

Molecular Formula: C14H12ClN7O4

Molecular Weight: 377.75

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N/C(=N\[N+](=O)[O-])N(Cc1ccc(Cl)nc1)/N=C/c1ccccc1[N+](=O)[O-]

Standard InChI:  InChI=1S/C14H12ClN7O4/c15-13-6-5-10(7-17-13)9-20(14(16)19-22(25)26)18-8-11-3-1-2-4-12(11)21(23)24/h1-8H,9H2,(H2,16,19)/b18-8+

Standard InChI Key:  BXILQSBJZBIXIQ-QGMBQPNBSA-N

Associated Targets(non-human)

Brevicoryne brassicae 33 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Myzus persicae 1112 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: 377.75Molecular Weight (Monoisotopic): 377.0639AlogP: 1.99#Rotatable Bonds: 6
Polar Surface Area: 153.15Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.73CX Basic pKa: 0.27CX LogP: 2.13CX LogD: 2.13
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.27Np Likeness Score: -1.30

References

1. Su W, Zhou Y, Ma Y, Wang L, Zhang Z, Rui C, Duan H, Qin Z..  (2012)  N'-Nitro-2-hydrocarbylidenehydrazinecarboximidamides: design, synthesis, crystal structure, insecticidal activity, and structure-activity relationships.,  60  (20): [PMID:22546079] [10.1021/jf300616x]

Source