Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA12083
Max Phase: Preclinical
Molecular Formula: C9H8ClF3O4S3
Molecular Weight: 368.81
Molecule Type: Small molecule
Associated Items:
ID: ALA12083
Max Phase: Preclinical
Molecular Formula: C9H8ClF3O4S3
Molecular Weight: 368.81
Molecule Type: Small molecule
Associated Items:
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
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 368.81 | Molecular Weight (Monoisotopic): 367.9225 | AlogP: 2.69 | #Rotatable Bonds: 4 |
Polar Surface Area: 68.28 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 4.71 | CX LogD: 4.71 |
Aromatic Rings: 1 | Heavy Atoms: 20 | QED Weighted: 0.82 | Np Likeness Score: -1.13 |
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] |
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