Abstract:
The present invention provides a method for producing ?-3 polyunsaturated fatty acids by culturing specific myxobacterial stains and myxobacterial strains suitable for said method.
Abstract:
The use of a compound of formula (I) or a salt thereof, where the symbols have the meanings given in the description, for the control of phytopathogenic mircroorganisms of harmful animals.
Abstract:
The invention relates to the use of, and methods of use employing, certain glycolipid compounds as defined in detail below and having preservative or antimicrobial properties, novel compounds of the glycolipid class, and related invention embodiments. The compounds have the formula (I) wherein m is (3) to (5), n is (2) to (5), o is (0) or (1) and p is (3) to (17), with the proviso that the sum m + n + o + p is not less than (14); and R is a carbohydrate moiety bound via one of its carbon atoms to the binding oxygen, and/or a physiologically, especially pharmaceutically or nutraceutically or cosmetically, acceptable salt thereof, or an ester thereof, as such or in the form of a composition, where the compound may be present in open chain form and/or in the form of a lactone.
Abstract translation:本发明涉及使用以下详细定义的具有防腐或抗微生物性质的某些糖脂化合物的使用和使用方法,糖脂类的新型化合物和相关的发明实施方案。 化合物具有式(I)其中m为(3)至(5),n为(2)至(5),o为(0)或(1),p为(3)至(17) 条件是总和m + n + o + p不小于(14); 并且R是通过其碳原子之一与结合氧结合的碳水化合物部分,和/或其生理学上,特别是其药学上或药学上可接受的盐或其酯,或者以组合物的形式, 其中化合物可以以开链形式和/或以内酯的形式存在。
Abstract:
The present invention relates to an isolated polynucelotide encoding a polypeptide with protoilludene synthase activity and comprising a sequence selected from the group consisting of a) SEQ ID Nos. 1 or 14 of the attached sequence listing; b) a nucleic acid sequence complementary to SEQ ID Nos. 1 or 14; c) nucleic acid sequences which hybridize under stringent conditions to the nucleic acid sequences defined in a) and b) or their complementary strands, as well as to the polypeptide encoded by the isolated polynucleotide, as well as their uses for the production of melleolides.
Abstract translation:本发明涉及一种编码具有原始烯醇合酶活性的多肽的分离的聚赖苷,并且包含选自所附序列表中的a)SEQ ID NO:1或14的序列; b)与SEQ ID NO:1或14互补的核酸序列; c)在严格条件下与a)和b)或其互补链中所定义的核酸序列以及由分离的多核苷酸编码的多肽以及它们用于生产melleolides的用途杂交的核酸序列。
Abstract:
The invention relates to the use, or methods (especially with regard to animals, especially human, that are in need of such treatment) comprising the use, respectively, of an extract and/or especially one or more natural spiro triterpenoids and derivatives thereof, especially from the blazeispirol family, obtainable from Agaricus species, alone or as supplement, as active ingredient in the prophylactic and/or therapeutic treatment of a disease, disorder or condition that responds to the modulation of Liver X receptor, either in humans or in other mammals, and/or to the use of said extract and/or natural compound(s) or mixtures for the treatment of said disease, disorder or condition, as well as corresponding methods of treatment, or their use in the manufacture of a pharmaceutical or nutraceutical formulation for said treatment. The invention relates also to said extract and/or compound(s) for use in the treatment or in the preparation of a medicament (including a nutraceutical) for the prophylactic and/or therapeutic treatment of said disorder, disorder or condition, as well as their preparation. It also relates to pharmaceutical or nutraceutical formulations comprising said extract and/or natural compound(s) which are useful in said prophylactic and/or therapeutic treatment. They can also be used for non-therapeutic, e.g. cosmetic, purposes only.
Abstract:
This invention relates to a new biological active compound as shown in formula (I) and its biological active derivates; whereas derivates are produced by the reaction of formula (I) with nucleophiles.
Abstract:
The present invention provides a method for producing ω-3 polyunsaturated fatty acids by culturing specific myxobacterial stains and myxobacterial strains suitable for said method.
Abstract:
The present invention relates to substituted heterocycles, processes for their preparation, and their use in medicaments, especially for the treatment of inflammatory disease, i.e. asthma, or cancer.
Abstract:
The present invention relates to substituted heterocycles, processes for their preparation, and their use in medicaments, especially for the treatment of inflammatory disease, i.e. asthma, or cancer.
Abstract:
Die vorliegende Erfindung betrifft Zwischenverbindungen zur Herstellung von Spinosynen, verschiedene Verfahren zu deren Herstellung, sowie die Verwendung dieser Zwischenverbindungen zur Herstellung von Spinosyn-Derivaten.