ID: ALA2392666

Max Phase: Preclinical

Molecular Formula: C19H20F3N3O4

Molecular Weight: 411.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CO/C=C(/C(=O)OC)c1ccccc1COc1cc(C(F)(F)F)nc(N(C)C)n1

Standard InChI:  InChI=1S/C19H20F3N3O4/c1-25(2)18-23-15(19(20,21)22)9-16(24-18)29-10-12-7-5-6-8-13(12)14(11-27-3)17(26)28-4/h5-9,11H,10H2,1-4H3/b14-11+

Standard InChI Key:  FUDUCLWLRHMZIT-SDNWHVSQSA-N

Associated Targets(Human)

HL-60 67320 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Tetranychus cinnabarinus 1124 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: 411.38Molecular Weight (Monoisotopic): 411.1406AlogP: 3.30#Rotatable Bonds: 7
Polar Surface Area: 73.78Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.93CX LogP: 4.39CX LogD: 4.39
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.39Np Likeness Score: -0.63

References

1. Chai BS, Liu CL, Li HC, He XM, Luo YM, Huang G, Zhang H, Chang JB..  (2010)  Design, synthesis and acaricidal activity of novel strobilurin derivatives containing pyrimidine moieties.,  66  (11): [PMID:20681007] [10.1002/ps.1997]
2. Chai B, Wang S, Yu W, Li H, Song C, Xu Y, Liu C, Chang J..  (2013)  Synthesis of novel strobilurin-pyrimidine derivatives and their antiproliferative activity against human cancer cell lines.,  23  (12): [PMID:23664877] [10.1016/j.bmcl.2013.04.045]

Source