The present invention relates to monoterpenoid and phenylpropanoid containing derivative compounds, methods of making the compounds, compositions comprising the compounds, and methods of repelling pests using the compounds and/or compositions.

The present invention relates to a composition comprising at least a sesterterpene for use as medicament like antibiotic or antifungal. Furthermore, the present invention relates to the use of at least a sesterterpene for increasing, assisting and/or enhancing the bacteriostatic and/or bactericidal activity of an antibiotic or the fungicidal activity of an antifungal compound.

The present invention relates to a composition comprising at least a sesterterpene for use as medicament like antibiotic or antifungal. Furthermore, the present invention relates to the use of at least a sesterterpene for increasing, assisting and/or enhancing the bacteriostatic and/or bactericidal activity of an antibiotic or the fungicidal activity of an antifungal compound.

Antimicrobial compositions comprising a terpenoid in combination with an antimicrobial agent are provided. In addition, uses of such compositions in various applications involving preventing, combating or treating microbial infections, or preventing microbial growth or establishment are provided.

Antimicrobial compositions comprising a terpenoid in combination with an antimicrobial agent are provided. In addition, uses of such compositions in various applications involving preventing, combating or treating microbial infections, or preventing microbial growth or establishment are provided.

Foamable formulations of agriculturally active ingredients are provided, as well as methods for using them. The formulations allow improved delivery active ingredients by the ability to deliver high amounts of active ingredient with a low volume of formulation used.

Foamable formulations of agriculturally active ingredients are provided, as well as methods for using them. The formulations allow improved delivery active ingredients by the ability to deliver high amounts of active ingredient with a low volume of formulation used.

The application relates to a process for producing fibrous material with antimicrobial properties, wherein in the first step coniferous resin acid composition is emulsified into aqueous solution with emulsifier and wetting agent, and in the second step thus formed emulsion is transferred into fibrous material by impregnation. Further, the application relates to an aqueous antimicrobial composition for use as a water-soluble concentrate in the treatment of fibrous materials, and to a fibrous material with antimicrobial properties, and to its use in e.g. fabrics, fur, leather, clothes, canvas, tissues, plastics, webs, accessories, packaging materials, wallpapers, food-related products, household products, footwear, construction materials, insulating materials and medical products.

The application relates to a process for producing fibrous material with antimicrobial properties, wherein in the first step coniferous resin acid composition is emulsified into aqueous solution with emulsifier and wetting agent, and in the second step thus formed emulsion is transferred into fibrous material by impregnation. Further, the application relates to an aqueous antimicrobial composition for use as a water-soluble concentrate in the treatment of fibrous materials, and to a fibrous material with antimicrobial properties, and to its use in e.g. fabrics, fur, leather, clothes, canvas, tissues, plastics, webs, accessories, packaging materials, wallpapers, food-related products, household products, footwear, construction materials, insulating materials and medical products.

Compositions and methods for using cyclopropanated structural analogs of fatty acid biofilm dispersal agents are characterized by superior biofilm dispersion. When used in combination with antimicrobials, these analogs decrease the minimum inhibitory concentration of antimicrobial agents required for eradication of the biofilm and/or treatment of infection. Methods for using these analogs include direct application to a surface, blending with lipid based carriers, or covalent anchoring the molecule to a surface. Typically, the cyclopropanated structural analog has the structure according to formula (I): ##STR00001## wherein R.sub.1 is a C.sub.1-C.sub.24 linear or branched alkyl group; or an acid halide or acid anhydride thereof.