In one embodiment, the present application relates to methods and materials for weed control of a field of a crop plant using a cellulose biosynthesis inhibitor selected from the group consisting of ES20 and ES20-1 to ES20-9 of FIG. 1A. In another embodiment, the present disclosure relates to a method for treatment or prevention of an infection through inhibition of biofilm formation of microorganisms comprising the step of applying a therapeutic effective amount of a cellulose biosynthesis inhibitor selected from the group consisting of ES20 and ES20-1?ES20-9 of FIG. 1A, or a salt thereof, in combination with one or more other commonly used antibiotics. A composition matter comprising said compounds and methods of use are within the scope of the present invention.

In one embodiment, the present application relates to methods and materials for weed control of a field of a crop plant using a cellulose biosynthesis inhibitor selected from the group consisting of ES20 and ES20-1 to ES20-9 of FIG. 1A. In another embodiment, the present disclosure relates to a method for treatment or prevention of an infection through inhibition of biofilm formation of microorganisms comprising the step of applying a therapeutic effective amount of a cellulose biosynthesis inhibitor selected from the group consisting of ES20 and ES20-1?ES20-9 of FIG. 1A, or a salt thereof, in combination with one or more other commonly used antibiotics. A composition matter comprising said compounds and methods of use are within the scope of the present invention.

In one embodiment, the present application relates to methods and materials for weed control of a field of a crop plant using a cellulose biosynthesis inhibitor selected from the group consisting of ES20 and ES20-1 to ES20-9 of FIG. 1A. In another embodiment, the present disclosure relates to a method for treatment or prevention of an infection through inhibition of biofilm formation of microorganisms comprising the step of applying a therapeutic effective amount of a cellulose biosynthesis inhibitor selected from the group consisting of ES20 and ES20-1?ES20-9 of FIG. 1A, or a salt thereof, in combination with one or more other commonly used antibiotics. A composition matter comprising said compounds and methods of use are within the scope of the present invention.

The invention relates to herbicidal active compound combinations comprising, carbamoyltriazolinones, and herbicidally active compounds, which combinations are suitable for controlling weeds.

The invention relates to herbicidal active compound combinations comprising, carbamoyltriazolinones, and herbicidally active compounds, which combinations are suitable for controlling weeds.

The present disclosure relates to antimicrobial, antiviral or biocide coatings, coated objects and coating methods including a first component and a second component where the first component can provide persistent antimicrobial, antiviral or biocide kill (e.g. physically ruptures the cell membrane of the microorganism to kill upon contact).

The present disclosure relates to antimicrobial, antiviral or biocide coatings, coated objects and coating methods including a first component and a second component where the first component can provide persistent antimicrobial, antiviral or biocide kill (e.g. physically ruptures the cell membrane of the microorganism to kill upon contact).

The present invention relates to novel herbicidally active substituted 1-pyridyl-5-azinylpyrazolyl-3-oxyalkyl acids, 1-pyridyl-5-azinylpyrazolyl-3-sulfanylalkyl acids, 1-pyridyl-5-azinylpyrazolyl-3-sulfinylalkyl acids and 1-pyridyl-5-azinylpyrazolyl-3-sulfonylalkyl acids, and to the derivatives thereof according to the general formula (I) or agrochemically acceptable salts thereof. The present invention further relates to processes for preparing these compounds and to the use thereof for controlling broad-leaved weeds and weed grasses.

The present invention relates to novel herbicidally active substituted 1-pyridyl-5-azinylpyrazolyl-3-oxyalkyl acids, 1-pyridyl-5-azinylpyrazolyl-3-sulfanylalkyl acids, 1-pyridyl-5-azinylpyrazolyl-3-sulfinylalkyl acids and 1-pyridyl-5-azinylpyrazolyl-3-sulfonylalkyl acids, and to the derivatives thereof according to the general formula (I) or agrochemically acceptable salts thereof. The present invention further relates to processes for preparing these compounds and to the use thereof for controlling broad-leaved weeds and weed grasses.

Embodiments provide a pest control agent that is excellent in safety, controlling effect, residual activity, and so on. According to an embodiment, there is provided a pyrazole derivative represented by general formula [I], or an agriculturally acceptable salt thereof, and a pest control agent containing the same as an active ingredient: ##STR00001## wherein, p represents an integer of 0 or 1, R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 represent a hydrogen atom, halogen atom, C.sub.1-C.sub.6 alkyl group, or the like, A represents an oxygen atom or sulfur atom, Q represents a halogen atom, C.sub.6-C.sub.10 aryl group that is unsubstituted or substituted with (R.sup.8).sub.m, or the like, and R.sup.6 and R.sup.7 represent a hydrogen atom, C.sub.1-C.sub.6 alkyl group, or the like.