| Weight | 254.476 g/mol |
|---|---|
| Formula | C8H4Cl3O3- |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
2,4,5-trichlorophenoxyacetate
Score:
#1 in i
,
#653 in Chemistry
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- Orientationally-selected two-dimensional ESEEM spectroscopy of the Rieske-type iron-sulfur cluster in 2,4,5-trichlorophenoxyacetate monooxygenase from Burkholderia cepacia AC1100 (Journal of the American Chemical Society, 1996)
- Differential activation and inhibition of different forms of rat liver glutathione S-transferase by the herbicides 2,4-dichlorophenoxyacetate (2,4-D) and 2,4,5-trichlorophenoxyacetate (2,4,5-T) (Toxicology and Applied Pharmacology, 1984)
- Purification and properties of component B of 2,4,5-trichlorophenoxyacetate oxygenase from Pseudomonas cepacia AC1100 (Applied and Environmental Microbiology, 1995)
- Interaction of 2,4-dichlorophenoxyacetate (2,4-D) and 2,4,5-trichlorophenoxyacetate (2,4,5-t) with the acyl-CoA: Amino acid N-acyltransferase enzymes of bovine liver mitochondria (Biochemical Pharmacology, 1986)
- Transport of 2,4,5-trichlorophenoxyacetate in the isolated, perfused rat kidney. (Journal of Pharmacology and Experimental Therapeutics, 1979)
- Studies on the mechanism of renal transport depression caused by pretreatment with 2,4,5trichlorophenoxyacetate (Journal of Toxicology and Environmental Health, 1976)
-
SMILESC1=C(C(=CC(=C1Cl)Cl)Cl)OCC(=O)[O-]
-
InChIKeySMYMJHWAQXWPDB-UHFFFAOYSA-M
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