| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2269805
Max Phase: Preclinical
Molecular Formula: C16H17F3N2O2S
Molecular Weight: 358.39
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCOC(=O)/N=c1/sc(C(C)C)cn1-c1cccc(C(F)(F)F)c1
Standard InChI: InChI=1S/C16H17F3N2O2S/c1-4-23-15(22)20-14-21(9-13(24-14)10(2)3)12-7-5-6-11(8-12)16(17,18)19/h5-10H,4H2,1-3H3/b20-14+
Standard InChI Key: YXDGOPGSJTUDFS-XSFVSMFZSA-N
Associated Targets(non-human)
Ipomoea nil 52 Activities
Abutilon theophrasti 831 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Echinochloa frumentacea 115 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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 358.39 | Molecular Weight (Monoisotopic): 358.0963 | AlogP: 4.74 | #Rotatable Bonds: 3 |
| Polar Surface Area: 43.59 | Molecular Species: NEUTRAL | 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: 4.97 | CX LogD: 4.97 |
| Aromatic Rings: 2 | Heavy Atoms: 24 | QED Weighted: 0.80 | Np Likeness Score: -1.60 |
References
| 1. Sanemitsu Y, Kawamura S, Satoh J, Katayama T, Hashimoto S. (2006) Synthesis and herbicidal activity of 2-acylimino-3-phenyl-1,3-thiazolines—A new family of bleaching herbicides—, 31 (3): [10.1584/jpestics.31.305] |
Source
Source(1):