ID: ALA12083

Max Phase: Preclinical

Molecular Formula: C9H8ClF3O4S3

Molecular Weight: 368.81

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CSC(S(=O)(=O)c1ccc(Cl)cc1)S(=O)(=O)C(F)(F)F

Standard InChI:  InChI=1S/C9H8ClF3O4S3/c1-18-8(20(16,17)9(11,12)13)19(14,15)7-4-2-6(10)3-5-7/h2-5,8H,1H3

Standard InChI Key:  CCFVWIDQXCAODS-UHFFFAOYSA-N

Associated Targets(non-human)

Stomoxys calcitrans 84 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: 368.81Molecular Weight (Monoisotopic): 367.9225AlogP: 2.69#Rotatable Bonds: 4
Polar Surface Area: 68.28Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.71CX LogD: 4.71
Aromatic Rings: 1Heavy Atoms: 20QED Weighted: 0.82Np Likeness Score: -1.13

References

1. Wickiser DI, Wilson SA, Snyder DE, Dahnke KR, Smith CK, McDermott PJ..  (1998)  Synthesis and endectocidal activity of novel 1-(arylsulfonyl)-1-[(trifluoromethyl)sulfonyl]methane derivatives.,  41  (7): [PMID:9544209] [10.1021/jm970678y]

Source