| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA11972
Max Phase: Preclinical
Molecular Formula: C10H10ClF3O4S2
Molecular Weight: 350.77
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCC(S(=O)(=O)c1ccc(Cl)cc1)S(=O)(=O)C(F)(F)F
Standard InChI: InChI=1S/C10H10ClF3O4S2/c1-2-9(20(17,18)10(12,13)14)19(15,16)8-5-3-7(11)4-6-8/h3-6,9H,2H2,1H3
Standard InChI Key: VFOAYTNJTDQUAC-UHFFFAOYSA-N
Associated Targets(non-human)
Stomoxys calcitrans 84 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 350.77 | Molecular Weight (Monoisotopic): 349.9661 | AlogP: 2.78 | #Rotatable Bonds: 4 |
| Polar Surface Area: 68.28 | Molecular Species: | HBA: 4 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 3.71 | CX LogD: 3.71 |
| Aromatic Rings: 1 | Heavy Atoms: 20 | QED Weighted: 0.84 | Np Likeness Score: -1.05 |
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
Source(1):