Phenylpyrazole_insecticides Knowpia

Phenylpyrazole insecticides are a class of chemically-related broad-spectrum insecticides. The chemical structures of these insecticides are characterized by a central pyrazole ring with a phenyl group attached to one of the nitrogen atoms of the pyrazole.

Chemical structure of fipronil, a common phenylpyrazole insecticide

History edit

Phenylpyrazole insecticides were developed in response to increasing pesticide resistance to other chemicals. Now, along with neonicotinoids, they are some of the most widely-used pesticides.^[1]

Mode of Action edit

Phenylpyrazole insecticides function by blocking glutamate-activated chloride channels in insects. Mammals do not have this type of chloride channel, making them much less susceptible to its effects. However, they do have the capacity to disrupt epithelial cells in the human intestine and adversely impact human health.^[1]

Examples edit

Examples include:

acetoprole
ethiprole
fipronil
flufiprole
pyraclofos
pyrafluprole
pyriprole
pyrolan
vaniliprole

References edit

^ ^a ^b Vidau, C.; Brunet, J. L.; Badiou, A.; Belzunces, L. P. (2009). "Phenylpyrazole insecticides induce cytotoxicity by altering mechanisms involved in cellular energy supply in the human epithelial cell model Caco-2". Toxicology in Vitro. 23 (4): 589–597. doi:10.1016/j.tiv.2009.01.017.

External links edit

Media related to phenylpyrazole insecticides at Wikimedia Commons

[Vidau_2009-1] Vidau, C.; Brunet, J. L.; Badiou, A.; Belzunces, L. P. (2009). "Phenylpyrazole insecticides induce cytotoxicity by altering mechanisms involved in cellular energy supply in the human epithelial cell model Caco-2". Toxicology in Vitro. 23 (4): 589–597. doi:10.1016/j.tiv.2009.01.017.

[1]

Summary

History edit

Mode of Action edit

Examples edit

References edit

External links edit