ID: ALA2228756

Max Phase: Preclinical

Molecular Formula: C19H12F3NO4

Molecular Weight: 375.30

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(NC(=O)c1c(F)cccc1F)OCc1ccc(-c2ccc(F)cc2)o1

Standard InChI:  InChI=1S/C19H12F3NO4/c20-12-6-4-11(5-7-12)16-9-8-13(27-16)10-26-19(25)23-18(24)17-14(21)2-1-3-15(17)22/h1-9H,10H2,(H,23,24,25)

Standard InChI Key:  GMTNBFMRMGBCCN-UHFFFAOYSA-N

Associated Targets(non-human)

Thanatephorus cucumeris 609 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium oxysporum 3998 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Corynespora cassiicola 104 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Botrytis cinerea 4183 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plutella xylostella 1838 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Culex pipiens pallens 759 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: 375.30Molecular Weight (Monoisotopic): 375.0718AlogP: 4.43#Rotatable Bonds: 4
Polar Surface Area: 68.54Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.30CX Basic pKa: CX LogP: 4.21CX LogD: 2.50
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.73Np Likeness Score: -1.27

References

1. Li Y, Li BJ, Ling Y, Miao HJ, Shi YX, Yang XL..  (2010)  Synthesis and fungicidal activity of aryl carbamic acid-5-aryl-2-furanmethyl ester.,  58  (5): [PMID:20151651] [10.1021/jf9043277]

Source