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  2. Pyrinuron - Wikipedia

    en.wikipedia.org/wiki/Pyrinuron

    Pyrinuron (Pyriminil, Vacor) is a chemical compound formerly used as a rodenticide. [1] Commercial distribution was voluntarily suspended in 1979 and it is not approved by the Environmental Protection Agency for use in the United States. [2]

  3. Vector control - Wikipedia

    en.wikipedia.org/wiki/Vector_control

    Insecticides, larvicides, rodenticides, Lethal ovitraps and repellents can be used to control vectors. For example, larvicides can be used in mosquito breeding zones; insecticides can be applied to house walls or bed nets, and use of personal repellents can reduce incidence of insect bites and thus infection.

  4. Category:Rodenticides - Wikipedia

    en.wikipedia.org/wiki/Category:Rodenticides

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  5. Diphenadione - Wikipedia

    en.wikipedia.org/wiki/Diphenadione

    Diphenadione is a vitamin K antagonist that has anticoagulant effects and is used as a rodenticide against rats, mice, voles, ground squirrels and other rodents. The chemical compound is an anti-coagulant with active half-life longer than warfarin and other synthetic 1,3-indandione anticoagulants.

  6. Difethialone - Wikipedia

    en.wikipedia.org/wiki/Difethialone

    Difethialone is an anticoagulant used as a rodenticide. [1] It is considered a second generation agent. [2] In May 2008, the EPA added restrictions on the sale of difethialone in consumer-use rodenticide products and also for exterior use by commercial applicators. [3] [4]

  7. Chlorophacinone - Wikipedia

    en.wikipedia.org/wiki/Chlorophacinone

    The KH 2 is converted to vitamin K 2,3 epoxide (KO) during the carboxylation reaction. The KH 2 cofactor is created within the vitamin K redox cycle. Chlorophacinone interferes with the vitamin K redox cycle by inhibiting vitamin K epoxide reductase (VKOR), an integral membrane protein present in the endoplasmic reticulum (ER).

  8. Difenacoum - Wikipedia

    en.wikipedia.org/wiki/Difenacoum

    Because other species of mammals and birds may prey upon affected rodents, or directly ingest rodenticide bait, there is a risk of primary, secondary or tertiary exposure; examples are described in a 2012 publication on veterinary toxicology. [3]

  9. Flocoumafen - Wikipedia

    en.wikipedia.org/wiki/Flocoumafen

    Flocoumafen is a fluorinated, second-generation anticoagulant of the 4-hydroxycoumarin vitamin K antagonist type. [1] It is a second generation (i.e., high potency) chemical in this class, used commercially as a rodenticide.