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AMIDES OF MONO AND BICARBOXYLIC ACIDS WITH AMINO ACIDS OR GLYCOSAMINES, SELECTIVELY ACTIVE ON THE CANNABINOID PERIPHERAL RECEPTOR

机译:单价和双羧酸与氨基酸或糖胺的酰胺,对大麻素外围受体具有选择性活性

摘要

The vast number of theoretically conceivable compounds resulting from the combination of all claimed substituents in formula (I) precludes a comprehensive search. For economical reasons the search has been limited to the following compounds: R1 is a hydrocarbon radical unsubstituted or substituted by only one OH-group and having a linear chain of at least 8 carbons atoms(A); the NR2R3 group is either a linear alpha-, beta-, or gamma-, amino acid (e.g. amino acids like proline are not included), or a glycosamine residue. Despite the above limitation the search revealed too many relevant compounds. Therefore the search was further limited to compounds with NR2R3 = Glycine, beta-Alamine, gamma-amino-butyric acid, Serine- or Cysteine derivatives, or glycosamine of the following structures: (a), (b), (c). Still too many pertinent compounds where retrieved which can not all be cited in the search report. The documents cited are only an arbitrary selection and the search report has to be regarded as incomplete.
机译:由式(I)中所有要求保护的取代基的组合产生的大量理论上可能的化合物排除了全面的研究范围。出于经济原因,该搜索仅限于以下化合物:R1是未取代或仅被一个OH-取代且具有至少8个碳原子的线性链的烃基(A); NR2R3基团是线性α-,β-或γ-氨基酸(例如不包括脯氨酸之类的氨基酸)或糖胺残基。尽管存在上述限制,但搜索仍发现了太多相关化合物。因此,搜索进一步限于具有以下结构的NR2R3 =甘氨酸,β-丙胺,γ-氨基丁酸,丝氨酸或半胱氨酸衍生物或糖胺的化合物:(a),(b),(c)。检索到的相关化合物仍然太多,无法在搜索报告中全部引用。所引用的文件只是随意选择的,并且搜索报告必须被视为不完整。

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