50 results about "Parasite Control" patented technology

The present invention provides for, inter alia, novel topical formulations comprising at least one 1-N-arypyrazole derivative and amitraz and to methods for treating, controlling, or preventing parasite infestations on mammals or birds The inventive formulations include spot-on, pour-on or spray formulations and may include a further ectoparasiticide, such as an IGR compound, an avermectin or milbemycin derivative, or a pyrethroid insecticides, and anthelmintics, such as benzimidazoles and imidazothiazoles. The inventive formulation provides a larger duration of parasite control at a faster rate of control. The inventive formula remains effective up to three months from the first application. Moreover, the inventive formulations prevent tick attachment to the animal, thereby providing protection against tick borne diseases. The ectoparasites which may be controlled, treated or prevented by the present invention includes ticks, fleas, mites, mange, lice, mosquitoes, flies and cattle grubs.

The present invention provides for, inter alia, novel topical formulations comprising at least one 1-N-arypyrazole derivative and amitraz and to methods for treating, controlling, or preventing parasite infestations on mammals or birds The inventive formulations include spot-on, pour-on or spray formulations and may include a further ectoparasiticide, such as an IGR compound, an avermectin or milbemycin derivative, or a pyrethroid insecticides, and anthelmintics, such as benzimidazoles and imidazothiazoles. The inventive formulation provides a larger duration of parasite control at a faster rate of control. The inventive formula remains effective up to three months from the first application. Moreover, the inventive formulations prevent tick attachment to the animal, thereby providing protection against tick borne diseases. The ectoparasites which may be controlled, treated or prevented by the present invention includes ticks, fleas, mites, mange, lice, mosquitoes, flies and cattle grubs.

Provided are an endoparasite control agent comprising a carboxamide derivative represented by the general formula (I):ora salt thereof as an active ingredient, and a method for controlling endoparasites, comprising orally or parenterally administering the endoparasite control agent.

An object of the present invention is to provide a novel endoparasite control agent as a parasiticide, an antiprotozoal or the like. Provided is an endoparasite control agent comprising a carboxamide derivative represented by the general formula (I):(wherein Het represents a 5- or 6-membered heterocyclic group), ora salt thereof as an active ingredient.

Provided are an endoparasite control agent comprising a carboxamide derivative represented by the general formula (I):ora salt thereof as an active ingredient, and a method for controlling endoparasites, comprising orally or parenterally administering the endoparasite control agent.

This invention relates to a method of controlling or preventing infestations of ectoparasites, preferably hematophageous ectoparasites, on an animal by administering to the animal a composition comprising an parasiticidally effective amount of a compound of Formula 1, or an N-oxide, or a pharmaceutically or veterinarily acceptable salt thereof,whereinR1 is Me, Cl, Br or F;R2 is F, Cl, Br, C1-C4 haloalkyl or C1-C4 haloalkoxy;R3 is F, Cl or Br;R4 is H; C1-C4 alkyl, C3-C4 alkenyl, C3-C4 alkynyl, C3-C5 cycloalkyl, or C4-C6 cycloalkylalkyl, each optionally substituted with one substituent selected from the group consisting of halogen, CN, SMe, S(O)Me, S(O)2Me, and OMe;R5 is H or Me;R6 is H, F or Cl; andR7 is H, F or Cl.

A parasite control agent or parasiticide that has an exceptional effect for controlling or exterminating parasites, especially endoparasites, and that can be safely used contains as an active ingredient at least one selected from compounds represented by formula (I) or salts thereof. (In formula (I), Cy represents a heteroaryl group or the like; X represents a halogeno group or the like; n is any integer of 0-5; when n is 2 or higher, the X may be the same as or different from each other; R1 represents an optionally substituted C1-6 alkyl group or the like; A represents a nitrogen atom or the like; R2, R3, and R4 each independently represent a hydrogen atom, optionally substituted C1-6 alkyl group, or the like; and R5 represents an optionally substituted C6-10 aryl group, optionally substituted heteroaryl group, or the like.)

Methods and formulations for treating animal ectoparasites, effective against parasites such as fleas and ticks are provided. The methods comprise topically co-administering a non-mobile insect growth regulator and a mobile insect growth regulator to the animal. Parasiticidal formulations for treating animal ectoparasites are also provided, which can be safe to use and avoid the many common deleterious side effects of conventional topical formulations. The topical formulations comprise a combination of two insect growth regulators, a non-mobile insect growth regulator and a mobile insect growth regulator. The topical formulation can be packaged with the two insect growth regulators together or packaged to prevent mixing of the two insect growth regulators prior to administering the topical insecticide formulation to the animal.

The present invention provides an animal ectoparasite-controlling agent containing as an active ingredient a hydrazide compound represented by the formula (1)wherein R3 represents a fluorine atom, a chlorine atom, a bromine atom, a methyl group, an ethyl group or a hydrogen atom, R5 and R6 are the same or different each other and each represents a methyl group or a hydrogen atom, R4 represents a C3-C6 cycloalkyl group, which shows excellent controlling effects on animal ectoparasites.

The invention discloses an isophthalamide compound and application thereof. The structure of the compound is shown as a general formula I, wherein the definition of each substituent group in the formula is shown in the specification; the specification also discloses the uses of the compound as insecticides and animal parasite control agents.

Disclosed is a method for controlling fish parasites, which comprises continuously administering a folic acid synthesis inhibitor and / or a folic acid activation inhibitor to a fish at a dose of 1 to 50 mg / kg fish body weight per day for one to two weeks. Preferably, a combination of a folic acid synthesis inhibitor and a folic acid activation inhibitor is used. As the folic acid synthesis inhibitor, a sulfa drug is preferred. As the folic acid activation inhibitor, a dihydrofolate reductase inhibitor, a folic acid antagonist, or the like can be used. The parasite control agent can control fish parasites through oral administration. The parasite control agent is particularly effective on ciliate fish parasites.

An object of the present invention is to provide a novel endoparasite control agent as a parasiticide, an antiprotozoal or the like. Provided is an endoparasite control agent comprising a carboxamide derivative represented by the general formula (I):or a salt thereof as an active ingredient.

An animal ectoparasite-controlling agent comprising a benzylamide compound represented by the formula (1): wherein R3 represents a hydrogen atom; a halogen atom; a cyano group; a C1-C6 alkyl group; a C1-C6 haloalkyl group; a C1-C6 alkoxy group or a C1-C6 haloalkoxy group; and R4 represents a C1-C6 alkyl group substituted with one or more C1-C6 alkoxy group(s); a C1-C6 alkyl group substituted with one or more cyano group(s); a C1-C6 alkyl group; a C1-C6 haloalkyl group or a C3-C6 cycloalkyl group, as an active ingredient and an inert carrier, has an excellent controlling effect on animal ectoparasites.

An objective of the present invention is to provide an ectoparasite control agent for homothermic animals, which has high control effect and is safe. The compounds according to the present invention are compounds represented by formula (I) and salts thereof: wherein R1 represents optionally substituted alkyl; optionally substituted alkenyl; optionally substituted alkynyl; OR5 wherein R5 represents optionally substituted alkyl, optionally substituted alkenyl, or optionally substituted alkynyl; or SR5 wherein R5 is as defined above, R2 represents optionally substituted alkyl, any one of R3 and R4 represents hydrogen and the other represents fluorine, chlorine, bromine, or CF3, and X represents fluorine or chlorine.

Disclosed is a composition for use in controlling ectoparasites, comprising as an active ingredient at least one of compounds represented by formula (I) or (III) or salts thereof. The present invention provides a composition for use in controlling ectoparasites that has excellent ectoparasite control effect and is highly safe.

The invention discloses an isoxazoline compound and application thereof. The structure of the isoxazoline compound is shown as a general formula I, wherein the definitions of the substituent groups inthe formula are shown in the specification. Also disclosed in the specification is the use of the compound shown as the general formula I as an insecticide, an acaricide and an animal parasite control agent.

The present invention is intended to provide a novel parasiticide, antiprotozoal or other endoparasite control agents which are effective for controlling animal endoparasites that have been impossible to control by conventional ones. Provided is an endoparasite control agent comprising, as an active ingredient, a carboxamide derivative represented by the general formula (I):or a salt thereof.

The invention discloses a bisamide compound and application thereof. The structure of the compound is shown as a general formula I, wherein definitions of substituent groups in the formula are shown in the specification; the specification also discloses the uses of the compound as insecticides and animal parasite control agents.

The present invention is intended to provide a novel parasiticide, antiprotozoal or other endoparasite control agents which are effective for controlling animal endoparasites that have been impossible to control by conventional ones. Provided is an endoparasite control agent comprising, as an active ingredient, a heterocyclic carboxamide derivative represented by the general formula (I):or a salt thereof.

The invention discloses a sniffing medicine for treating tuberculosis and a preparation method thereof. The sniffing medicine for treating tuberculosis disclosed by the invention comprises the following bulk pharmaceutical components in parts by weight: 1-2 parts of lead sulfate, 20-40 parts of calomel, 20-40 parts of vermilion, 40-80 parts of croton seeds and 300-600 parts of red jujubes. The preparation method of the sniffing medicine for treating tuberculosis disclosed by the invention comprises the following steps: removing pits of the red jujubes, and then sequentially placing the croton seeds, the lead sulfate, the calomel and vermilion in parts by weight in the red jujubes; then, wrapping the red jujubes three layers by using cabbage leaves, and roasting the obtained product 15-30 minutes by using charcoal fire; and finally, removing the cabbage leaves, and grinding the red jujubes into paste. The effect of the sniffing medicine on treating diseases such as tuberculosis and the like is obvious. The sniffing medicine is taken orally, and does not hurt the stomach, intestines, the liver and the kidney; and the sniffing medicine treats liver complaints, and the sniffing medicine directly reaches the lungs and enters the blood circulation so as to achieve effects of toxic substance counteracting, sterilization and parasite control.

The present invention provides an animal ectoparasite-controlling agent containing as an active ingredient a hydrazide compound represented by the formula (1)wherein R3 represents a fluorine atom, a chlorine atom, a bromine atom, a methyl group, an ethyl group or a hydrogen atom, R5 and R6 are the same or different each other and each represents a methyl group or a hydrogen atom, R4 represents a C1-C6 alkyl group, which shows excellent controlling effects on animal ectoparasites.

There is described an herbal hematophagous parasite control composition which comprises Picraena excelsa (Quassia), Foeniculum vulgare (fennel) and Azadirachta indica folium (Neem) provided that the composition is substantially free Juglans nigra folia (black walnut) and / or Allium sativim (garlic). There are also described a method of controlling hematophagous parasites.

The invention discloses an eco-organic and efficient fish-turtle polyculture method. The method includes the steps of building of a standard culture pond, artificial breeding of earthworm bait, pond disinfection, fry putting, young turtle putting, feeding management, water quality control and disease and parasite control. According to the method, biomass feed is used for breeding earthworms, the earthworms are used as bait for feeding fishes and turtles, the use of chemical substances causing pollution is eradicated, and thus the fishes and turtles produced through the method are green organicfood and can enrich the food structure of people and increase the dietary nutrition of people; organic food is provided for the society, and the economic income of farmers is increased.

The invention discloses a preparation process of a slow-release gastric floating tablet for the prevention and treatment of endoparasites in ruminants, and relates to the technical field of gastric floating preparations, comprising the following steps: (1) preparation of a composite carrier, (2) modification of the composite carrier , (3) Preparation of gastric floating tablets. The slow-release gastric floating tablet prepared by the invention is suitable for the prevention and control of endoparasites in ruminants, is non-toxic and harmless, and has no potential safety hazard; it is in a floating state after entering the gastric juice of ruminants, and the contained endoparasite control agent is slowly released, Effectively prolong the residence time of the endoparasite control agent in the stomach, thereby prolonging the release time of the drug effect molecule, improving the bioavailability of the drug effect molecule, thereby ensuring the control effect on the endoparasites of ruminants and reducing the number of drugs.

The present invention provides an animal ectoparasite-controlling agent containing as an active ingredient a hydrazide compound represented by the formula (1)wherein R3 represents a fluorine atom, a chlorine atom, a bromine atom, a methyl group, an ethyl group or a hydrogen atom, R5 and R6 are the same or different each other and each represents a methyl group or a hydrogen atom, R4 represents a C1-C6 alkyl group substituted by a C1-C6 alkoxy group, which shows excellent controlling effects on animal ectoparasites.

The present invention provides an animal ectoparasite-controlling agent containing as an active ingredient a hydrazide compound represented by the formula (1) wherein R 3 represents a fluorine atom, a chlorine atom, a bromine atom, a methyl group, an ethyl group or a hydrogen atom, R 5 and R 6 are the same or different each other and each represents a methyl group or a hydrogen atom, R 4 represents a C1-C6 alkyl group, which shows excellent controlling effects on animal ectoparasites.

The present invention provides an animal ectoparasite-controlling agent containing as an active ingredient a hydrazide compound represented by the formula (1)wherein R3 represents a fluorine atom, a chlorine atom, a bromine atom, a methyl group, an ethyl group or a hydrogen atom, R5 and R6 are the same or different each other and each represents a methyl group or a hydrogen atom, R4 represents a C1-C6 haloalkyl group, which shows excellent controlling effects on animal ectoparasites.