Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA2228782
Max Phase: Preclinical
Molecular Formula: C21H17ClF3NO7
Molecular Weight: 487.81
Molecule Type: Small molecule
Associated Items:
ID: ALA2228782
Max Phase: Preclinical
Molecular Formula: C21H17ClF3NO7
Molecular Weight: 487.81
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCOC(=O)/C(C)=C(\C)OC(=O)c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-]
Standard InChI: InChI=1S/C21H17ClF3NO7/c1-4-31-19(27)11(2)12(3)32-20(28)15-10-14(6-7-17(15)26(29)30)33-18-8-5-13(9-16(18)22)21(23,24)25/h5-10H,4H2,1-3H3/b12-11+
Standard InChI Key: SKWMRSGABDORKM-VAWYXSNFSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
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 |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 487.81 | Molecular Weight (Monoisotopic): 487.0646 | AlogP: 6.07 | #Rotatable Bonds: 7 |
Polar Surface Area: 104.97 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 8 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 6.03 | CX LogD: 6.03 |
Aromatic Rings: 2 | Heavy Atoms: 33 | QED Weighted: 0.15 | Np Likeness Score: -0.94 |
1. Yu H, Yang H, Cui D, Lv L, Li B.. (2011) Synthesis and herbicidal activity of diphenyl ether derivatives containing unsaturated carboxylates., 59 (21): [PMID:21958315] [10.1021/jf2039444] |
Source(1):