| Weight | 396.381 g/mol |
|---|---|
| Formula | C16H17F5N2O2S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
Thiazopyr (117718-60-2)
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- Thiazopyr and thyroid disruption: case study within the context of the 2006 IPCS Human Relevance Framework for analysis of a cancer mode of action. (Critical Reviews in Toxicology, 2006)
- Mechanism of thiazopyr-induced effects on thyroid hormone homeostasis in male Sprague-Dawley rats. (Toxicology and Applied Pharmacology, 1997)
- Engineering plant resistance to thiazopyr herbicide via expression of a novel esterase deactivation enzyme (Pesticide Biochemistry and Physiology, 1997)
- Enhancement of thiazopyr bioefficacy by inhibitors of monooxygenases (Pesticide Science, 1995)
- Inhibition of thiazopyr metabolism in plant seedlings by inhibitors of monooxygenases (Pesticide Science, 1995)
- In Vitro Transformation of Thiazopyr by Rat Liver Enzymes: Sulfur and Carbon Oxidations by Microsomes (Pesticide Biochemistry and Physiology, 1994)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)CC1=C(C(=NC(=C1C(=O)OC)C(F)F)C(F)(F)F)C2=NCCS2
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InChIKeyYIJZJEYQBAAWRJ-UHFFFAOYSA-N
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