clodinafop and propargyl-alcohol

clodinafop has been researched along with propargyl-alcohol* in 2 studies

Other Studies

2 other study(ies) available for clodinafop and propargyl-alcohol

Article	Year
Phototransformation of clodinafop-propargyl. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 2005, Volume: 40, Issue:4 Photodegradation of the herbicide clodinafop-propargyl was investigated on glass surface under sunlight and UV light. Four photoproducts were identified by NMR, IR, and MS. Major photolysis products were 2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoic acid and prop-2-ynyl-2-[(5-chloro-3-hydroxy-2-pyridyloxy) phenoxy] propanoate, while minor were ethyl 2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoate and 1-hydroxypropanyl-2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoate. Rate of photodegradation followed first-order kinetics with significant correlation coefficient. The major photoproducts were observed in maximum quantity on the 7th and 10th day and further degraded within 15-20 days. Topics: Alkynes; Environmental Pollution; Herbicides; Kinetics; Photochemistry; Photolysis; Propanols; Propionates; Pyridines; Sunlight; Time Factors; Ultraviolet Rays	2005
Clotrimazole, ketoconazole, and clodinafop-propargyl as potent growth inhibitors of equine Babesia parasites during in vitro culture. The Journal of parasitology, 2003, Volume: 89, Issue:3 The antifungal agents clotrimazole (CLT) and ketoconazole (KC) and the herbicide clodinafop-propargyl (CP) inhibit growth of Plasmodium sp., Toxoplasma sp., and Trypanosoma sp. In the present study, we evaluated these drugs against the in vitro growth of the equine protozoan parasites Babesia equi and B. caballi. Clotrimazole (IC50: 2 and 17 microM), KC (IC50: 6 and 22 microM), and CP (IC50: 450 and 354 microM) were effective growth inhibitors. Interestingly, intraerythrocytic KC-treated Babesia sp. were observed to be in immediate contact with the plasma fraction of the blood in electron microscopy. These results demonstrate the babesiacidial activities of these compounds and suggest their chemotherapeutic potential for the treatment of equine babesioses. Topics: Alkynes; Animals; Antifungal Agents; Babesia; Babesiosis; Clotrimazole; Equidae; Growth Inhibitors; Herbicides; Horse Diseases; Horses; Ketoconazole; Microscopy, Electron; Propanols; Propionates; Pyridines	2003

Article

Year

Phototransformation of clodinafop-propargyl.

Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 2005, Volume: 40, Issue:4

Photodegradation of the herbicide clodinafop-propargyl was investigated on glass surface under sunlight and UV light. Four photoproducts were identified by NMR, IR, and MS. Major photolysis products were 2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoic acid and prop-2-ynyl-2-[(5-chloro-3-hydroxy-2-pyridyloxy) phenoxy] propanoate, while minor were ethyl 2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoate and 1-hydroxypropanyl-2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoate. Rate of photodegradation followed first-order kinetics with significant correlation coefficient. The major photoproducts were observed in maximum quantity on the 7th and 10th day and further degraded within 15-20 days.

Topics: Alkynes; Environmental Pollution; Herbicides; Kinetics; Photochemistry; Photolysis; Propanols; Propionates; Pyridines; Sunlight; Time Factors; Ultraviolet Rays

2005

Clotrimazole, ketoconazole, and clodinafop-propargyl as potent growth inhibitors of equine Babesia parasites during in vitro culture.

The Journal of parasitology, 2003, Volume: 89, Issue:3

The antifungal agents clotrimazole (CLT) and ketoconazole (KC) and the herbicide clodinafop-propargyl (CP) inhibit growth of Plasmodium sp., Toxoplasma sp., and Trypanosoma sp. In the present study, we evaluated these drugs against the in vitro growth of the equine protozoan parasites Babesia equi and B. caballi. Clotrimazole (IC50: 2 and 17 microM), KC (IC50: 6 and 22 microM), and CP (IC50: 450 and 354 microM) were effective growth inhibitors. Interestingly, intraerythrocytic KC-treated Babesia sp. were observed to be in immediate contact with the plasma fraction of the blood in electron microscopy. These results demonstrate the babesiacidial activities of these compounds and suggest their chemotherapeutic potential for the treatment of equine babesioses.

Topics: Alkynes; Animals; Antifungal Agents; Babesia; Babesiosis; Clotrimazole; Equidae; Growth Inhibitors; Herbicides; Horse Diseases; Horses; Ketoconazole; Microscopy, Electron; Propanols; Propionates; Pyridines

2003