CAS: 42294-52-0; S-(4-Methylbenzyl)-L-Cysteine

该化合物是一种氨基酸衍生物,其特点是存在一个带有4-甲基苯基的细胞脊柱,并附于氨基氮原子的四甲基苯基组,该化合物具有氨基氨基基酸组和一个蛋白酸组,典型的氨基酸组,允许其参与各种生物化学反应.西steine结构中的硫磺原子的存在有助于其独特的特性,包括形成解硫化物联结的能力,这对蛋白质结构和稳定性至关重要.N-(4-甲基苯基)-L-cysteine可能由于硫醇组而表现出抗氧化性,使其对生物化学和药物研究感兴趣.该化合物在水和有机溶剂中的溶解性可因pH和其他功能组的存在而不同.

结构式图片

上下游产品

CAS号52-90-4 L-半胱氨酸 | CAS号104-82-5 对甲基氯苄 | CAS号52-89-1 L-半胱氨酸盐酸盐(无水物) | CAS号589-18-4 4-甲基苄醇 | CAS号104-81-4 4-甲基溴苄 | CAS号198991-77-4 (4R)-2-(4-methy... | CAS号61925-77-7 N-叔丁氧羰基-S-(4-甲基... | CAS号56-89-3 L-胱氨酸 | CAS号136050-67-4 Fm°C-S-(4-甲基苄基)...

合成工艺路线路线简述

    📜(2Rs,4R)-2-(4-Methylphenyl)-1,3-Thiazolidine-4-Carboxylic Acid置于三乙基硅烷,三氟乙酸体系中,用 二氯甲烷 作为反应溶剂,化学反应 16.0H,反应生成 L-半胱氨酸
    参考文献:引入巯基苄基保护基的两种新方法
    标题:引入巯基苄基保护基的两种新方法
    摘要:描述了两种新的硫醇苄基化方法:A)用对位取代的苄基阳离子直接进行s-烷基化;b)2-氨基硫醇的还原性s-烷基化.两种方法均提供了以高收率引入苄基型保护基的有效途径.
    DOI:10.1016/0040-4039(94)88305-X

    海关参考信息

    专利信息


    专利号:US-2025289851-A1
    优先权日:2022-04-22
    标 题:Cyclic peptides for delivering therapeutics
    发明人:DOUGHERTY PATRICK; TOTARO KYLE A; DOMBROSKI AMANDA; GIESLER RILEY; ZHOU MING; STREETER MATTHEW; GOFFIN ALEC; QIAN ZIQING
    权利人:ENTRADA THERAPEUTICS INC
    摘要:The present disclosure relates to the synthesis of cyclic peptides that are able to effectively deliver cargo, e.g., a therapeutic moiety (TM), inside a cell to treat a variety of conditions and diseases.

    专利号:US-4960881-A
    优先权日:1984-02-16
    标 题 :α-chlorinated carbonates, their method of manufacture and application in the protection of the amine functions of amino acids
    发明人:BARCELO GERARD; SENET JEAN-PIERRE; SENNYEY GERARD
    权利人:POUDRES & EXPLOSIFS STE NALE
    摘要:The invention relates to carbonates of formula: ##STR1## in which X is a fluorine, chlorine or bromine atom and R 1 is different from the ##STR2## group and represents: a substituted or non-substituted, saturated or unsaturated, aliphatic, araliphatic, primary, secondary, tertiary or cycloaliphatic radical. These α-chlorinated carbonates are prepared by the action of a compound of formula R 1 OH on a chloroformate of formula: ##STR3## in a solvent medium in the presence of an acid scavenger which is added after the two preceding compounds. They are used to block the amine function of amino acids. The α-chlorinated carbonate and amino acid are reacted in a solvent medium at a temperature of -5° to 100° C. in the presence of an acid scavenger. Blocked amines are very useful in peptide synthesis.

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    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:Lubell, W. D.; Blankenship, J. W.; Fridkin, G.; Kaul, R., Science of Synthesis, (2005) 21, 741.
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