CAS: 15474-96-1; (2-Chloroacetyl)Glycylglycine

该化合物是属于氨基酸衍生物类的合成化合物,其特征是:存在一个附属于甘基甘基糖脊柱的氯乙基基化合物组,由两种甘基糖单位组成,该基柱由一种浸泡物联结联系在一起.该化合物通常具有诸如极地溶剂中因其氨基和碳酸酯功能组而溶解性等特性,并且由于其结构上与天然丙酰胺相似,可能会显示生物活动.N-Chlolooacetylglycylcyclycine可用于各种化学应用,包括作为石化合成的试剂和与蛋白改变有关的研究.其再活性受到氯基酸盐混合物的干扰,可参与核糖替代反应.在处理这一化合物时,应采取安全防范措施,因为它可能会造成氯基衍生物的危害,包括潜在的毒性和再活性.总体,N-Chlologyalyal化学作为重要的化学剂.

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合成工艺路线路线简述

    📜甘氨酸酐置于sodium Hydroxide体系中,化学反应生成氯乙酰基甘氨酰甘氨酸
    参考文献:Fischer,E.,Chemische Berichte,1906,Vol. 39,P. 2931
    标题:Fischer,E.,Chemische Berichte,1906,Vol. 39,P. 2931

    海关参考信息

    专利信息


    专利号:US-4786684-A
    优先权日:1986-08-21
    标题 :Benzylthioether-linked solid support-bound thiol compounds and method for peptide synthesis
    发明人:GLASS JOHN D
    权利人:SINAI SCHOOL MEDICINE
    摘要:A method for the synthesis of sulfydryl-containing peptides which comprises forming a benzylthioether-linked solid support-bound thiol compound having at least one functional group for generating at least one peptide bond, sequentially coupling at least one protected amino acid or peptide to the compound until a peptide having desired amino acid sequence is obtained, and cleaving the benzylthioether linkage to release the peptide from the support with concomitant regenertion of the sulfydryl group in the peptides. The invention also encompasses compounds having the general formula wherein X is H, NH2, or acyl-NHY, said acyl being an amino acid or a peptide; Y is H, COOH, CONHNH2, the ester COOR1 in which R1 is selected from the group consisting of methyl, ethyl, phenyl, ortho-nitrophenyl and para-nitrophenyl, the amide CONH2, or the amide CONHR2 in which R2 is an amino acid or peptide; and providing that X and Y cannot both be H.

    专利号:US-5066716-A
    优先权日:1988-12-13
    标题:Synthesis of chloroacetyl and bromoacetyl modified peptides for the preparation of synthetic peptide polymers, conjugated peptides, and cyclic peptides
    发明人:ROBEY FRANK A; FIELDS RAYMOND L; LINDNER WOLFGANG
    权利人:US HEALTH
    摘要:A method to incorporate bromoacetyl and chloroacetyl moieties on amino groups of synthetic peptides using a standard program with an automated peptide synthesizer has been developed. The bromoacetyl and chloroacetyl-derivatized peptides react well with sulfhydryl-containing proteins and with peptides containing cysteine residues. Autopolymerization or cyclization occurs by reaction of the free sulfhydryl of cysteine in a peptide with the bromoacetyl group (or chloroacetyl group) and reactions can generally be controlled by controlling the concentrations of starting peptide in neutral pH buffers. Analytical methods for evaluating the polymers or cyclized peptides include gel filtration chromatography, reverse phase HPLC, SDS-PAGE and amino acid analysis where the degree of reaction can be evaluated by quantifying the amount of S-carboxymethylcysteine formed after HCl hydrolysis. N-bromoacetyl-derivatized peptides are useful as reagents for potential peptide immunogens, vaccines and therapeutics, and for substances such as peptides linked to polymers, plastics, enamels, and ceramics.

    专利号:TW-205552-B
    优先权日:1992-09-19
    标题:Novel synthesis of radiopharmaceuticals for renal function imaging

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/978-3-642-99499-9_24
    摘要:Fischer E, Otto E. Synthese von Derivaten einiger Dipeptide. 1906. In: Untersuchungen über Aminosäuren, Polypeptide und Proteïne (1899–1906). : Springer Berlin Heidelberg; 1906.
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