ID: ALA2228782

Max Phase: Preclinical

Molecular Formula: C21H17ClF3NO7

Molecular Weight: 487.81

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)/C(C)=C(\C)OC(=O)c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-]

Standard InChI:  InChI=1S/C21H17ClF3NO7/c1-4-31-19(27)11(2)12(3)32-20(28)15-10-14(6-7-17(15)26(29)30)33-18-8-5-13(9-16(18)22)21(23,24)25/h5-10H,4H2,1-3H3/b12-11+

Standard InChI Key:  SKWMRSGABDORKM-VAWYXSNFSA-N

Associated Targets(non-human)

Abutilon theophrasti 831 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Digitaria sanguinalis 1594 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Echinochloa crus-galli 3685 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: 487.81Molecular Weight (Monoisotopic): 487.0646AlogP: 6.07#Rotatable Bonds: 7
Polar Surface Area: 104.97Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 6.03CX LogD: 6.03
Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.15Np Likeness Score: -0.94

References

1. Yu H, Yang H, Cui D, Lv L, Li B..  (2011)  Synthesis and herbicidal activity of diphenyl ether derivatives containing unsaturated carboxylates.,  59  (21): [PMID:21958315] [10.1021/jf2039444]

Source