| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2289572
Max Phase: Preclinical
Molecular Formula: C8H15NOS2
Molecular Weight: 205.35
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(=O)C1SCC(N(C)C)CS1
Standard InChI: InChI=1S/C8H15NOS2/c1-6(10)8-11-4-7(5-12-8)9(2)3/h7-8H,4-5H2,1-3H3
Standard InChI Key: WQSPDHYMUSNPFK-UHFFFAOYSA-N
Associated Targets(non-human)
Henosepilachna vigintioctopunctata 143 Activities
Tetranychus urticae 2600 Activities
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Chilo suppressalis 440 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 205.35 | Molecular Weight (Monoisotopic): 205.0595 | AlogP: 1.31 | #Rotatable Bonds: 2 |
| Polar Surface Area: 20.31 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 13.13 | CX Basic pKa: 7.99 | CX LogP: 1.25 | CX LogD: 0.56 |
| Aromatic Rings: 0 | Heavy Atoms: 12 | QED Weighted: 0.68 | Np Likeness Score: -0.04 |
References
| 1. MITSUDERA H, KONISHI K. (1991) Synthesis and Insecticidal Activity of 1, 3-Dithianes, 16 (3): [10.1584/jpestics.16.387] |
Source
Source(1):