Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2287913
Max Phase: Preclinical
Molecular Formula: C12H17F3N2O3
Molecular Weight: 294.27
Molecule Type: Small molecule
Associated Items:
ID: ALA2287913
Max Phase: Preclinical
Molecular Formula: C12H17F3N2O3
Molecular Weight: 294.27
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCN(C)C(=O)COc1onc(C(F)(F)F)c1C
Standard InChI: InChI=1S/C12H17F3N2O3/c1-4-5-6-17(3)9(18)7-19-11-8(2)10(16-20-11)12(13,14)15/h4-7H2,1-3H3
Standard InChI Key: YSYKTWOAYUMPDT-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: 294.27 | Molecular Weight (Monoisotopic): 294.1191 | AlogP: 2.64 | #Rotatable Bonds: 6 |
Polar Surface Area: 55.57 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.49 | CX LogD: 2.49 |
Aromatic Rings: 1 | Heavy Atoms: 20 | QED Weighted: 0.81 | Np Likeness Score: -1.55 |
1. KAI H, HORITA Y, MIKI N, IDE K, TAKASE A. (1998) Synthesis and Herbicidal Activities of 2-(5-Isoxazolyloxy)-acetamide Derivatives, 23 (3): [10.1584/jpestics.23.255] |
Source(1):