CAS: 39608-31-6; N-((Benzyloxy)Carbonyl)-N-Methylglycine

该化合物是属于氨基酸和衍生物类的有机化合物,具有甘油主干,经甲基组和苯甲基苯氧基碳基组的出现而改变,具有独特的特性,包括其在极地溶剂中的潜在溶解性,因为氨基和碳基的功能组的存在而使其具有潜在的溶解性.苯丙基碳基辛酸会加强其亲脂性,从而影响其生物活动和相互作用.该化合物可能表现出氨基酸的典型特性,例如参与丙酸联结和作为蛋白质合成的建筑块.此外,可以探讨其衍生物的制药用途,特别是在药物设计和合成方面,因为其具有粘积天然氨基酸的能力,同时提供更强的稳定性或生物活性.

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相似化合物

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合成工艺路线路线简述

    📜Ethyl 2-(((Benzyloxy)Carbonyl)(Methyl)Amino)Acetate置于水,Lithium Hydroxide,盐酸体系中,用 四氢呋喃,甲醇,水 作为反应溶剂,化学反应 3.0H,反应生成 苄氧羰酰基肌氨酸
    参考文献: Cyclohexyl-Azetidinyl Antagonists Of Ccr2[fr] Antagonistes Du Ccr2 à Base De Cyclohexyl-Azétidinyle
    标题: Cyclohexyl-Azetidinyl Antagonists Of Ccr2[fr] Antagonistes Du Ccr2 à Base De Cyclohexyl-Azétidinyle
    摘要:本发明包括公式(I)的化合物.其中:R1,R2,R4,J,Q和a如说明书所述定义.本发明还包括预防,治疗或改善综合征,障碍或疾病的方法,其中所述综合征,障碍或疾病为2型糖尿病,肥胖和哮喘.本发明还包括通过管理治疗有效量的至少一种公式(I)化合物来抑制哺乳动物中的ccr2活性的方法.

    海关参考信息

    专利信息


    专利号:US-2025091989-A1
    优先权日:2023-09-19
    标 题 :Small molecule protein synthesis modulators
    发明人:GYGI DAVID; BAHMANYAR SOGOLE SAMI; HAMANN LAWRENCE
    权利人:INTERDICT BIO INC
    摘要:The present disclosure provides compounds of the formulae herein (e.g., Formula (I)), and pharmaceutically acceptable salts thereof, which are useful for modulating protein synthesis (e.g., modulating synthesis of BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D). The present disclosure also provides pharmaceutical compositions and kits comprising the compounds, or pharmaceutically acceptable salts thereof, and methods of treating or preventing diseases or disorders (e.g., diseases or disorders associated with BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D) by administering to a subject in need thereof the compounds, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions thereof.

    专利号:US-5021550-A
    优先权日:1986-10-07
    标 题 :Method for preventing deletion sequences in solid phase synthesis
    发明人:ZEIGER ALLEN R
    权利人:UNIV JEFFERSON
    摘要:Improved methods for solid-state synthesis of polymers, especially polypeptides and polynucleotides, are provided. In accordance with a preferred embodiment, selectively activatable and reactive bonding moieties are covalently bonded to solid supports for polynucleotide and polypeptide syntheses. Products of failed reactions and some side products are caused to react with the selectively activatable and reactive bonding moiety to cause divalent bonding of unwanted products to the solid support. Upon cleavage of the initial situs of covalent bonding to the solid support, desired products are free to be collected while unwanted products remain covalently bonded to the support. Ease of purification of such polymers is a principal object of the present invention. The methods of the invention are amenable to automation and digital control and novel solid supports, activatable, reactive bonding moieties and other compositions are presented. The expression of polynucleotides prepared in accordance with preferred embodiments produces novel polypeptides.

    专利号:US-RE29669-E
    优先权日:1973-04-23
    标 题:Production of 4-hydroxy-1,2-benzothiazine-3-carboxamides
    摘要:A process for the synthesis of N-aryl-3,4-dihydro-2-alkyl-4-oxo-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxides by treatment of N-aryl-N'-alkyl-N'-(2'-alkoxycarbonylbenzenesulfonyl)glycineamides, useful intermediates for said process, with an alkali or alkaline earth metal hydride in a reaction-inert solvent at 50°-150° C., said products being antiinflammatory agents.

    专利号:US-4250086-A
    优先权日:1979-11-19
    标 题:Method and composition for preparation of H-SAR-LYS-SAR-GLN-NH2
    发明人:HEAVNER GEORGE
    权利人:ORTHO PHARMA CORP
    摘要:A method for solution synthesis of H-SAR-LYS-SAR-GLN-NH2 in good yield and compositions useful therein are disclosed.

    专利号:US-9035061-B2
    优先权日:2010-07-13
    标题:Process for preparing a biphenyl-2-ylcarbamic acid
    发明人:COLSON PIERRE-JEAN
    权利人:COLSON PIERRE-JEAN; THERAVANCE BIOPHARMA R & D IP LLC
    摘要:The invention provides a process of preparing an intermediate useful in the synthesis of biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-carbamoylpiperidin-1-ylmethyl)benzoyl]methylamino}ethyl)piperidin-4-yl ester, and a process of preparing a crystalline freebase of the ester.

    专利号:US-4369137-A
    优先权日:1980-06-17
    标 题 :N-Protected pentapeptides useful as intermediates in the preparation of thymopoietin pentapeptide
    发明人:HEAVNER GEORGE
    权利人:ORTHO PHARMA CORP
    摘要:The present invention relates to methods for preparing useful peptides, more particularly to solution synthesis methods for preparing H-ARG-X-Z-Y-TYR-R, intermediates in the preparation of this peptide and to compositions of this peptide useful in thymic function.

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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

    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):1793-1144.

    合成参考文献


    摘要:Yamashita, M., Science of Synthesis, (2007) 30, 664.
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