CAS: 535-32-0; (R)-2-Amino-4-(Ethylthio)Butanoic Acid

该化合物是一种氨酸衍生物,其特点是含有硫磺的结构,是一种非蛋白性氨基酸,在翻译过程中没有将其纳入蛋白质中.D-Ethionine以其在各种生化过程中的作用而著称,特别是在含有硫化合物的化合物的新陈代谢过程中的作用著称.它具有氨基酸的典型特性,例如形成Zwitters的能力,这种分子既含有积极又含有消极的电荷.该化合物经常被研究其对生物系统的潜在影响,包括它对肝功能的影响及其在解毒途径中的作用.D-Ethionine在某些情况下也因其作为肝毒剂的潜力而得到承认,因此在毒理学和药理学中引起兴趣.它在水和其他溶剂中的溶解性可以变化,影响其在研究和工业中的应用.

结构式图片

相似化合物

67-21-0 13073-35-3 1396988-59-2

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号13073-47-7 S-benzyl-D-homo... | CAS号36506-17-9 4-ethylsulfanyl...

合成工艺路线路线简述

    📜S-Benzyl-D-Homocysteine置于氨,Sodium体系中,化学反应生成 D-乙硫氨基酪酸
    参考文献:Stekol; Weiss,Journal Of Biological Chemistry,1949,Vol. 179,P. 1050
    标题:Stekol; Weiss,Journal Of Biological Chemistry,1949,Vol. 179,P. 1050

    海关参考信息

    专利信息


    专利号:US-9803180-B2
    优先权日:2013-11-06
    标 题 :S-adenosylmethionine (SAM) synthase variants for the synthesis of artificial cofactors
    发明人:DIPPE MARTIN; BRANDT WOLFGANG; WESSJOHANN LUDGER A; ROST HANNES; PORZEL ANDREA
    权利人:LEIBNIZ-INSTITUT FUR PFLANZENBIOCHEMIE STIFTUNG DES OFFENTLICHEN RECHTS; Leibniz-Institut für Pflanzenbiochemie Stiftung des öffentlichen Rechts
    摘要:The present invention relates to isolated polypeptides that are derived from wildtype Bacillus subtilis S-Adenosylmethionine (SAM) synthase or from a biologically active fragment thereof, wherein said isolated polypeptides comprise an amino acid sequence that, in relation to the amino acid sequence of said wildtype Bacillus subtilis SAM synthase or of the biologically active fragment thereof, comprises at least one amino acid substitution, selected from the group consisting of amino acid substitutions at positions I317 and I105. The present invention further relates to respective isolated nucleic acids, vectors, host cells, uses and methods for the production of SAM derivatives.

    专利号:US-5892038-A
    优先权日:1997-12-08
    标 题 :Hydroxy-amino acid amides
    发明人:DOLLE III ROLAND ELLWOOD; PATEL HITESH K
    权利人:PHARMACOPEIA INC
    摘要:Compounds of Formula I I are disclosed as inhibitors of plasmepsin and cathepsin D. The compounds are therefore useful to treat diseases such as malaria. In preferred compounds of formula I, Y is the residue of an N-acylated amino acid, a substituted 4-aminoproline or a substituted piperazinealkanoic acid. Intermediates in the solid phase synthesis of compounds of formula I, in which the compounds are attached to a solid support, are also disclosed.

    专利号:US-2017240870-A9
    优先权日:2013-11-06
    标 题:S-adenosylmethionine (sam) synthase variants for the synthesis of artificial cofactors

    专利号:EP-3066197-B1
    优先权日:2013-11-06
    标题:S-adenosylmethionine (sam) synthase variants for the synthesis of artificial cofactors

    专利号:EP-3066197-A1
    优先权日:2013-11-06
    标题:S-adenosylmethionine (sam) synthase variants for the synthesis of artificial cofactors

    专利号:US-5872262-A
    优先权日:1996-11-05
    标 题:Hydroxy-amino acid amides
    发明人:DOLLE ROLAND ELLWOOD III; JOHNSON THEODORE O JR; TAO SHIWEI
    权利人:PHARMACOPEIA INC
    摘要:Compounds of Formula I I are disclosed as inhibitors of plasmepsin and cathepsin D. The compounds are therefore useful to treat diseases such as malaria. In preferred compounds of formula I, Y is the residue of an N-acylated amino acid, a substituted 4-aminoproline or a substituted piperazinealkanoic acid. Intermediates in the solid phase synthesis of compounds of formula I, in which the compounds are attached to a solid support, are also disclosed.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 590
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知