摘要:
A flat wiping cloth for arrangement on a wiping cloth holder includes an elongated base body and an active ingredient that inhibits or suppresses the growth of bacteria or viruses. The active ingredient is allocated to the base body. The base body has at least one of fibers, yarns or fringe, which have free ends that can be oriented to face a surface to be cleaned during use. The active ingredient is distributed within a material of which the fibers, yarns or fringe is made, or is distributed in a component of the base body.
摘要:
The invention relates to a flat wiping cloth (3) to be arranged on a wiping cloth holder (1), comprising an elongate basic body (4), wherein an active substance that inhibits or suppresses the growth of bacteria and/or viruses is associated with the basic body (4), wherein fibres (5), yarns (6) or fringes (7) are associated with the basic body (4) and wherein the active substance is distributed within the material from which the fibres (5), yarns (6) or fringes (7) are produced and/or in a component of the basic body (4). The aim of the invention is to configure and modify a flat wiping cloth of the aforementioned type in such a way that the antimicrobially effective active substance remains in the flat wiping cloth as long as possible, wherein the flat wiping cloth picks up dirt particularly quickly from moist surfaces. To achieve said aim, the invention is characterised in that the fibres (5), yarns (6) or fringes (7) have a free end that can be turned towards the area to be cleaned.
摘要:
The present invention relates to 5,6-bisaryl-2-pyridinecarboxamides, to their preparation and to their therapeutic use as urotensin II receptor antagonists.
摘要:
The present invention relates to derivatives of 5,6-bisaryl-2-pyridine-carboxamide, their preparation and their application in therapeutics as antagonists of urotensin II receptors.
摘要:
The present invention relates to derivatives of 5,6-bisaryl-2-pyridine-carboxamide, their preparation and their application in therapeutics as antagonists of urotensin II receptors.
摘要:
The present invention relates to compounds of the formula I, wherein R1; R2; R3; R4; R5, R13, R16, X and M have the meanings indicated in the claims. The compounds of formula I are valuable pharmacologically active compounds. They exhibit a strong anti-thrombotic effect and are suitable, for example, for the therapy and prophylaxis of cardio-vascular disorders like thromboembolic diseases or restenoses. They are reversible inhibitors of the blood clotting enzymes factor Xa (FXa) and thrombin and can in general be applied in conditions in which an undesired activity of factor Xa and/or thrombin are present or for the cure or prevention of which an inhibition of factor Xa and thrombin are intended. The invention furthermore relates to processes for the preparation of compounds of the formula I, their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical preparations comprising them.
摘要:
The present invention is directed to compounds of the general formula: as well as pharmaceutical compositions thereof. The invention is also directed to their therapeutic use as urotensin II receptor antagonists, e.g., in the treatment of cardiac, coronary, and central nervous system disorders. In particular embodiments, the invention relates to 5,6-bisaryl-2-pyridinecarboxamides, to their preparation and to their therapeutic use as urotensin II receptor antagonists.