A01N57/32

Pyrabactin analogues to modulate plant development

The present invention relates to compounds which can be used to control plant development. Indeed, the present invention discloses a new class of pyrabactin analogues which have a physiological effect onfor exampleseed germination, and/or stomatal closure, and/or have developmental effects on root and shoot development and organogenesis. Hence, the latter compounds can be used to control plant development such asfor exampleincreasing the tolerance of plants to drought stress or to control physiological phenomena such as pre-harvest sprouting, tolerance to pathogens etc.

Active ingredient combinations comprising pyridylethylbenzamides and other active ingredients

The present invention relates to novel active ingredient combinations which consist of fluopyram and other known active ingredients and are very well suited for the control of animal pests, such as insects and/or unwanted acarids and/or nematodes, in foliar and soil application and/or in the treatment of seeds, and are also suitable for increasing yields.

Active ingredient combinations comprising pyridylethylbenzamides and other active ingredients

The present invention relates to novel active ingredient combinations which consist of fluopyram and other known active ingredients and are very well suited for the control of animal pests, such as insects and/or unwanted acarids and/or nematodes, in foliar and soil application and/or in the treatment of seeds, and are also suitable for increasing yields.

Active ingredient combinations comprising pyridylethylbenzamides and other active ingredients

The present invention relates to novel active ingredient combinations which consist of fluopyram and other known active ingredients and are very well suited for the control of animal pests, such as insects and/or unwanted acarids and/or nematodes, in foliar and soil application and/or in the treatment of seeds, and are also suitable for increasing yields.

Salts, prodrugs and polymorphs of fab I inhibitors

In part, the present invention is directed to antibacterial compounds and salts thereof.

Salts, prodrugs and polymorphs of fab I inhibitors

In part, the present invention is directed to antibacterial compounds and salts thereof.

N-[1-((6-CHLOROPYRIDIN-3-YL)METHYL)PYRIDIN-2(1H)-YLIDENE]-2,2,2- TRIFLUOROACETAMIDE FOR CONTROL OF AGRICULTURAL/HORTICULTURAL PESTS

A compound of formula (Ie):

##STR00001##

wherein Ar, R.sub.1, R.sub.4e and Y are as defined herein and a method of controlling pests using the compound.

N-[1-((6-CHLOROPYRIDIN-3-YL)METHYL)PYRIDIN-2(1H)-YLIDENE]-2,2,2- TRIFLUOROACETAMIDE FOR CONTROL OF AGRICULTURAL/HORTICULTURAL PESTS

A compound of formula (Ie):

##STR00001##

wherein Ar, R.sub.1, R.sub.4e and Y are as defined herein and a method of controlling pests using the compound.

PESTICIDAL COMPOSITIONS

A method of controlling pest with a pesticidal composition comprising synergistically effective amounts of at least one anthranilamide compound represented by the formula (I) or its salt and other pesticide:

##STR00001##

wherein each of R.sup.1a and R.sup.1b which are independent of each other, is halogen; each of R.sup.2 and R.sup.3 is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy or cyano; A is alkyl substituted by Y; Y is C.sub.3-4 cycloalkyl which may be substituted by at least one substituent selected from the group consisting of halogen, alkyl and haloalkyl; n is 0 or 1; and q is an integer of from 0 to 4; provided that R.sup.1a and R.sup.1b are not simultaneously chlorine nor bromine.

PESTICIDAL COMPOSITIONS

A method of controlling pest with a pesticidal composition comprising synergistically effective amounts of at least one anthranilamide compound represented by the formula (I) or its salt and other pesticide:

##STR00001##

wherein each of R.sup.1a and R.sup.1b which are independent of each other, is halogen; each of R.sup.2 and R.sup.3 is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy or cyano; A is alkyl substituted by Y; Y is C.sub.3-4 cycloalkyl which may be substituted by at least one substituent selected from the group consisting of halogen, alkyl and haloalkyl; n is 0 or 1; and q is an integer of from 0 to 4; provided that R.sup.1a and R.sup.1b are not simultaneously chlorine nor bromine.