Method for producing 2-substituted-thiazolidine-4-carboxylic acids
    4.
    发明公开
    Method for producing 2-substituted-thiazolidine-4-carboxylic acids 失效
    生产2-取代的噻唑烷-4-羧酸的方法

    公开(公告)号:EP0101052A3

    公开(公告)日:1984-12-27

    申请号:EP83107857

    申请日:1983-08-09

    IPC分类号: C12P17/14 C07D277/06

    CPC分类号: C07D277/06 C12P17/14

    摘要: A 2-substituted-thiazolldine-4-carboxylic acid is produced in a high yield by holding 2-amino-2-thiazoline-4-carboxylic acid and a carbonyl compound of the formula:
    wherein R, and R 2 are identical or different and each represents a hydrogen atom, a formyl group, a carboxyl group, a substituted or unsubstituted saturated or unsaturated alkyl group, or a substituted or unsubstituted aryl group, in aqueous solution in the presence of an effective amount of an enzyme of a microorganism, said enzyme being capable of converting 2-amino-thiazoline-4-carboxylic acid to L-cysteine, and said microorganism being capable of growing in a medium containing 2-amino-thiazoline-4-carboxylic acid as a nitrogen source and producing said enzyme.

    Method for producing 2-substituted-thiazolidine-4-carboxylic acids
    6.
    发明公开
    Method for producing 2-substituted-thiazolidine-4-carboxylic acids 失效
    Verfahren zur Herstellung von 2-substitutionierter噻唑烷-4-碳。

    公开(公告)号:EP0101052A2

    公开(公告)日:1984-02-22

    申请号:EP83107857.1

    申请日:1983-08-09

    IPC分类号: C12P17/14 C07D277/06

    CPC分类号: C07D277/06 C12P17/14

    摘要: A 2-substituted-thiazolldine-4-carboxylic acid is produced in a high yield by holding 2-amino-2-thiazoline-4-carboxylic acid and a carbonyl compound of the formula:
    wherein R, and R 2 are identical or different and each represents a hydrogen atom, a formyl group, a carboxyl group, a substituted or unsubstituted saturated or unsaturated alkyl group, or a substituted or unsubstituted aryl group,
    in aqueous solution in the presence of an effective amount of an enzyme of a microorganism, said enzyme being capable of converting 2-amino-thiazoline-4-carboxylic acid to L-cysteine, and said microorganism being capable of growing in a medium containing 2-amino-thiazoline-4-carboxylic acid as a nitrogen source and producing said enzyme.

    摘要翻译: 通过保持2-氨基-2-噻唑啉-4-羧酸和下式的羰基化合物,其中R 1和R 2相同,以高产率制备2-取代的噻唑烷-4-羧酸 或不同的,并且各自表示氢原子,甲酰基,羧基,取代或未取代的饱和或不饱和烷基或取代或未取代的芳基,在有效量的 微生物,所述酶能够将2-氨基 - 噻唑啉-4-羧酸转化为L-半胱氨酸,并且所述微生物能够在含有2-氨基 - 噻唑啉-4-羧酸的培养基中生长,作为氮源,并产生 说酶。

    Use of ethylamine derivatives as antihypertensive agents
    8.
    发明公开
    Use of ethylamine derivatives as antihypertensive agents 失效
    Verwendung vonÄthylamin-Derivaten als antihypertensive Wirkstoffe。

    公开(公告)号:EP0294183A1

    公开(公告)日:1988-12-07

    申请号:EP88305012.2

    申请日:1988-06-01

    摘要: Novel ethylamine derivatives of the formula (I) and salts thereof are useful as antihypertensive agents.
    wherein A is a linking group wherein the linkage is formed by a carbon or nitrogen atom; B is an aryl-containing group; C is hydrogen or optionally substituted alkyl, aralkyl or aryl, or C may be bonded to A to form an optionally substituted alkylene bridge; Q is an aryl- or heterocyclic aryl-containing group; X is a linking group wherein the linkage is formed by optionally substituted alkylene having from 2 to 20 carbon atoms and/or one or more hetero atoms selected from nitrogen and sulfur.

    摘要翻译: 新的式(I)乙胺衍生物及其盐可用作抗高血压药。 其中A是连接基,其中连接是由碳或氮原子形成的; B是含芳基的基团; C是氢或任选取代的烷基,芳烷基或芳基,或C可以与A键合以形成任选取代的亚烷基桥; Q是含芳基或杂环芳基的基团; X是连接基团,其中连接是由具有2至20个碳原子的任选取代的亚烷基和/或一个或多个选自氮和硫的杂原子形成的。