CAS: 28798-28-9; H-Cys(Acm)-Oh Hcl

该化合物是一种合成氨酸衍生物,具有硫醇组的特点,具有细胞性特征,有助于其反应和潜在的生物活动;该化合物通常以白色为白,与白外晶状粉状成白,在水中可溶解,适合各种生化应用;乙胺甲基组作为盐盐,常常用于研究环境,特别是涉及蛋白合成,酶活动和红氧化反应的研究,因为其有能力参与硫醇-二硫化物交换反应;此外,乙酰胺组的存在可能会影响其与其他生物分子的相互作用,并可能影响其在细胞过程中的作用;安全数据表明,与许多含有硫化物的化合物一样,应小心处理,避免皮肤和呼吸刺激;

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19746-37-3 86060-81-3 168300-88-7

上下游产品

CAS号19746-37-3 S-乙酰胺基甲基-N-叔丁氧羰... | CAS号56-89-3 L-胱氨酸

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    专利信息


    专利号:US-4038306-A
    优先权日:1967-08-07
    标题 :N-t-butoxycarbonyl-s-lower alkanoylamidomethyl-cysteine and p-nitrophenyl esters
    发明人:MILKOWSKI JOHN D; VEBER DANIEL F; HIRSCHMANN RALPH F
    权利人:MERCK & CO INC
    摘要:Novel protecting groups for peptides containing a cysteine residue. Process for the synthesis of peptides containing a cysteine residue wherein the mercapto function of the cysteine residue is protected by an acetamidomethyl radical or other labile blocking group. Novel intermediates useful in peptide synthesis.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Luckose F, Et Al. Effects Of Amino Acid Derivatives On Physical, Mental, And Physiological Activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-807.
    [参考文献]: D F Veber, Et Al. Acetamidomethyl. A Novel Thiol Protecting Group For Cysteine. J Am Chem Soc. 1972 Jul 26;94(15):5456-61.
    [参考文献]: E V Kudriavtseva, Et Al. [参考文献]: Bioorg Khim. 1996 May;22(5):370-5.
    [参考文献]: H Lamthanh, Et Al. Side Reaction During The Deprotection Of (S-Acetamidomethyl)Cysteine In A Peptide With A High Serine And Threonine Content. Int J Pept Protein Res. 1993 Jan;41(1):85-95.
    [参考文献]: H Lamthanh, Et Al. Side Reaction Of S-To-N Acetamidomethyl Shift During Disulfide Bond Formation By Iodine Oxidation Of S-Acetamidomethyl-Cysteine In A Glutamine-Containing Peptide. Pept Res. 1995 Nov-Dec;8(6):316-20.

    合成参考文献


    参考文献:10.1007/0-306-46862-x_114
    摘要:Chen L, Skinner SR, Gordon TD, Taylor JE, Barany G, Morgan BA. Isolation, characterization, and synthesis of a trisulfide related to the somatostatin analog lanreotide. 2002. In: Peptides Frontiers of Peptide Science. : Kluwer Academic Publishers; 2002.
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