首页> 外国专利> Sesquiterpenes, their preparation and their use as inhibitors acting on gamma-aminobutyric acid-benzodiazepine receptors (Sesquiterpenes, their preparations and their use as inhibitors acting on the GABA-benzodiazepine receptor)

Sesquiterpenes, their preparation and their use as inhibitors acting on gamma-aminobutyric acid-benzodiazepine receptors (Sesquiterpenes, their preparations and their use as inhibitors acting on the GABA-benzodiazepine receptor)

机译:倍半萜烯,它们的制备及其作为对γ-氨基丁酸-苯并二氮杂receptor受体起作用的抑制剂的用途(倍半萜烯,它们的制备及其作为对GABA-苯并二氮杂receptor受体起作用的抑制剂的用途)

摘要

The sesquiterpenes and pharmaceutically or veterinarily acceptable salts thereof of the following general formula (I) obtainable from the strain Acremonium atrictum XO6 / 15/458 can be obtained from the GABA-benzodiazepine C1 - ion transport receptor Is a binding inhibitor of betodiazepine to complexes.;In this formula, And Are each a single bond, or one is a single bond and the other is a double bond; A, , And RTI ID = 0.0 A / RTI ; / RTI Y is a double bond, or when A is a ring (a) as defined above, Y is a double bond, or an epoxy bond .;These compounds can be prepared by (i) fermenting a strain X06 / 15/458 (IMI 354451) or its mutant producing sesquiterpene in a source of carbon, nitrogen and inorganic salts, (ii) isolating sesquiterpene from the fermentation medium (Iii) optionally, converting the sesquiterpene into a pharmaceutically or veterinarily acceptable salt thereof.
机译:可以从Acremonium atrictum XO6 / 15/458菌株获得的下列通式(I)的倍半萜类及其药学或兽医学上可接受的盐可以从GABA-苯并二氮杂卓C1 -离子转运受体获得在该公式中,和是每个单键,或一个为单键,另一个为双键。其中,Y是双键,或者当A是如上定义的环(a)时,Y是双键或环氧键。 ;这些化合物可以通过(i)在碳,氮和无机盐的来源中发酵X06 / 15/458菌株(IMI 354451)或产生其倍半萜的突变体来制备,(ii)从发酵培养基(Iii)中分离倍半萜任选地,将倍半萜转化为其药学上或兽医学上可接受的盐。

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