摘要:
To provide a novel pesticide, especially a fungicide and a nematocide. An oxime-substituted amide compound represented by the formula (I) or its salt, and a pesticide containing it: wherein G 1 is a structure represented by G 1 -1 or the like, G 2 is a structure represented by G 2 -2 or the like: W is an oxygen atom or the like, X 1 is a halogen atom, methyl, trifluoromethyl or the like, each of X 2 , X 3 , X 4 and X 5 is independently a hydrogen atom, a halogen atom or the like, each of Y 1 and Y 3 is independently a halogen atom, cyano, methyl, trifluoromethyl, C 2 -C 6 alkynyl or the like, each of Y 2 and Y 4 is independently a hydrogen atom, a halogen atom or the like, R 1 is C 1 -C 6 alkyl, C 1 -C 4 haloalkyl, (C 1 -C 4 )alkyl substituted with R 18 , C 3 -C 6 cycloalkyl, C 3 -C 6 alkenyl or the like, each of R 2 and R 3 is independently a hydrogen atom, methyl or the like, R 4 is a hydrogen atom or the like, R 18 is C 3 -C 6 cycloalkyl, phenyl, phenyl substituted with (Z)m or the like, Z is a halogen atom or the like, and m is an integer of 1, 2 or 3.
摘要:
The present invention provides compounds of Formula (I) for the treatment of parasitic diseases including malaria, as well as neurodegenerative diseases. Formula (I) wherein R3, R4, X and Y have the meaning given in claim 1.
摘要:
The invention concerns a composition made from at least one sulphated polysaccharide, in particular from an algae, and combined with at least one food ingredient. This composition can be used, in particular, in the field of food or in the treatment or prevention of an infection caused by microsporidia in humans or animals. It has useful properties as an antiparasitic agent in humans or animals; for the treatment or prevention of an infection caused by at least one microsporidia in humans or animals; in particular for the treatment or prevention of an infection caused in bees by the microsporidia Nosema , preferably Nosema ceranae or Nosema apis , or indeed for stimulating the immune defences of bees.
摘要:
A composition for exterminating an animal parasite, the composition including, as an active ingredient, at least one of 3-aminoxalylaminobenzamide derivatives represented by the following Formula (1):
(R 1 and R 2 represent a halogen atom, a C1-C5 haloalkyl group, a C1-C5 alkyl group, or the like. R 3 and R 4 represent a C1-C8 alkyl group, a C1-C8 haloalkyl group, or the like. R 5 represents a C1-C5 haloalkyl group. R 6 and R 7 represent a hydrogen atom, a C1-C5 alkyl group, or the like. Y represents a halogen atom or the like. Z represents a halogen atom or the like. n represents 0-4, and m represents 0-2.)
摘要:
The invention provides novel indazole-substituted diaminopyrimidines of formula I, to methods of preparing such compounds, to pharmaceutical compositions containing such compounds,and to methods for using such compounds in treatment of diseases including cancer; wherein R 1 -R 8 are as defined in the specification.
摘要:
The invention relates to novel pyrimidinone-based heterocyclic compounds which are parasite growth inhibitors, having the general formula (I) in which Y is a morpholine chosen from three bridged morpholines, L is a bond or a linker, n=0 or 1 and R2 is a methyl group when n=0 and a hydrogen atom when n=1. Process for the preparation thereof and therapeutic use thereof.