CAS: 2899-36-7; Ethyl L-Methionate Hydrochloride

该化合物是氨基酸L-甲基硫化物的衍生物,通常用于peptide合成和生化化学研究;乙基酯的修改提高了其在有机溶剂中的溶性,便于其在固相或溶相合成过程中将其纳入peptide链;盐盐的形态提高了稳定性和处理能力;该化合物是制药和生物技术应用中的多用途构件,特别是用于引入具有受控再活性的甲基磷残留物;其高纯度和连续性能使其适合敏感的合成工艺;该产品的特点主要是NMR和HPLC,以确保质量,满足研究和工业应用的需求.

结构式图片

相似化合物

6297-53-6 2899-37-8 348-67-4

上下游产品

CAS号64-17-5 乙醇 | CAS号63-68-3 L-蛋氨酸 | CAS号2899-37-8 L-(-)-蛋氨醇 | CAS号117196-96-0 ethyl (2S)-2-[[...

合成工艺路线路线简述

    乙醇,L-蛋氨酸置于氯化亚砜体系中,化学反应 25.0H,反应生成L-蛋氨酸乙酯盐酸盐
    参考文献:用于水杨酸转化为离子液体的生物相容性氨基酸酯的表征和细胞毒性评估
    标题:用于水杨酸转化为离子液体的生物相容性氨基酸酯的表征和细胞毒性评估
    摘要:图形化的抽象图.没有可用的字幕.&na; 活性药物成分(api)转化为离子液体(ils)后,其技术实用性将大大提高.与固体或结晶药物相比,Api‐il具有更好的溶解性,热稳定性和局部给药功效.但是,Api-Ils的毒理学问题是其在药物输送中的主要挑战.为了解决这个问题,合成了11种氨基酸酯(aae)并作为水溶性低的药物水杨酸(sal)形成sal-Il的生物相容性抗衡阳离子进行了研究.使用1 H和13 C NMR,Ftir,元素分析和热重分析对aae进行表征.使用哺乳动物细胞系(l929和hela)研究了aae阳离子,Sal-Ils和游离sal的细胞毒性.随着阳离子侧基中包含长烷基链,硫和芳香环,Aae阳离子的毒性大大提高.选择丙氨酸,天冬氨酸和脯氨酸乙酯作为低细胞毒性aae.与sal结合到阳离子中的aae相比,Sal‐ils的细胞毒性急剧增加,与游离sal相当.有趣的是,Sal-Il的水混
    Doi:10.1016/j.Ijpharm.2018.05.021

    海关参考信息

    专利信息


    专利号:US-9556301-B1
    优先权日:2015-12-02
    标题:Cyclopolymer containing residues of methionine and synthesis and uses thereof
    发明人:JAFAR MAZUMDER MOHAMMAD ABU; AL-MUALLEM HASAN ALI; ALI SHAIKH ASROF; Estaitie Mohamad Khalid
    权利人:UNIV KING FAHD PET & MINERALS; King Fahd Universoty of Petroleum and Minerals
    摘要:Cyclopolymers and N,N-diallyl methionine-based monomers or salts, solvates, tautomers or stereoisomers as corrosion inhibitors. A process for producing the cyclopolymers by Butler cyclopolymerization of the monomers in the presence of sulfur dioxide. In addition, a method for determining a percent inhibition efficiency of metal corrosion for the cyclopolymers and monomers as well as applications and methods for the cyclopolymers as coatings, compositions, and formulations for preventing metal corrosion.

    专利号:EP-0946499-B1
    优先权日:1996-11-22
    标 题 :N-(aryl/heteroaryl/alkylacetyl) amino acid amides, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:WU JING; TUNG JAY S; NISSEN JEFFREY S; MABRY THOMAS E; LATIMER LEE H; EID CLARK NORMAN; AUDIA JAMES E
    权利人:ELAN PHARM INC; LILLY CO ELI
    摘要:Disclosed are compounds which inhibit beta -amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits beta -amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions. Said compounds are represented by formula (I), wherein R<1> is selected from the group consisting of: a) alkyl, alkenyl, alkaryl, alkcycloalkyl, aryl, cycloalkyl, cycloalkenyl, heteroaryl and heterocyclic; b) a substituted phenyl group of formula (II), wherein R is alkylene of from 1 to 8 carbon atoms, m is an integer equal to 0 or 1, and c) 1- or 2-naphthyl substituted at the 5, 6, 7 and/or 8 positions, R<2> is selected from the group consisting of hydrogen, alkyl of from 1 to 4 carbon atoms, alkylalkoxy of from 1 to 4 carbon atoms, alkylthioalkoxy of from 1 to 4 carbon atoms; and R<3> and R<3'> are independently selected from the group consisting of: (a) hydrogen, (b) alkyl, (c) -(R<7>)n(W)p, wherein R<7> is an alkylene group, W is selected from the group consisting of (i) formula (A); (ii) heteroaryl; and (iii) N-heterocyclic, and n is an integer equal to 0 or 1, and p is an integer equal to 1 to 3; (d) -CH( phi )CH2C(O)O-Q where Q is selected from the group consisting of alkyl, aryl, heteroaryl and heterocyclic; X' is hydrogen, hydroxy or fluoro; X'' is hydrogen, hydroxy or fluoro, or X' and X'' together form an oxo group, Z is selected from the group consisting of a bond covalently linking R<1> to -CX'X''-, oxygen and sulfur.

    专利号:US-6849650-B2
    优先权日:1998-02-27
    标 题:Heterocyclic compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:THORSETT EUGENE D; PORTER WARREN J; NISSEN JEFFREY S; LATIMER LEE H; AUDIA JAMES E; DROSTE JAMES
    权利人:ATHENA NEUROSCIENCES INC; LILLY CO ELI
    摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

    专利号:EP-0951464-B1
    优先权日:1996-11-22
    标题:N-(aryl/heteroarylacetyl) amino acid esters, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:WU JING; THORSETT EUGENE D; NISSEN JEFFREY S; MABRY THOMAS E; LATIMER LEE H; JOHN VARGHESE; FANG LAWRENCE Y; AUDIA JAMES E
    权利人:ELAN PHARM INC; LILLY CO ELI
    摘要:Disclosed are compounds which inhibit beta -amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits beta -amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

    专利号:EP-0951466-B1
    优先权日:1996-12-23
    标题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:WU JING; TUNG JAY S; THORSETT EUGENE D; PLEISS MICHAEL A; NISSEN JEFFREY S; NEITZ JEFFREY; LATIMER LEE H; JOHN VARGHESE; FREEDMAN STEPHEN; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; DROSTE JAMES J; HENRY STEVEN S; MCDANIEL STACEY L; SCOTT WILLIAM L; STUCKY RUSSELL D
    权利人:ELAN PHARM INC; LILLY CO ELI
    摘要:Disclosed are compounds for Formula (I) wherein the substituents are as defined in the claims which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

    专利号:US-6262302-B1
    优先权日:1996-11-22
    标题:N-(aryl/heteroaryl/alkylacetyl) amino acid amides, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:WU JING; TUNG JAY S; NISSEN JEFFREY S; MABRY THOMAS E; LATIMER LEE H; EID CLARK N; AUDIA JAMES E
    权利人:ELAN PHARM INC; LILLY CO ELI
    摘要:Disclosed are compounds which inhibit beta-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed pharmaceutical compositions comprising a compound which inhibits beta-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.
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    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.
    [参考文献]: Griet Van Zeebroeck, Et Al. Transport And Signaling Via The Amino Acid Binding Site Of The Yeast Gap1 Amino Acid Transceptor. Nat Chem Biol. 2009 Jan;5(1):45-52.
    [参考文献]: K Eszter Borbas, Et Al. Design And Synthesis Of Mono- And Multimeric Targeted Radiopharmaceuticals Based On Novel Cyclen Ligands Coupled To Anti-Muc1 Aptamers For The Diagnostic Imaging And Targeted Radiotherapy Of Cancer. Bioconjug Chem. 2007 Jul-Aug;18(4):1205-12.

    合成参考文献


    参考文献:10.1038/nchembio.132
    摘要:Van Zeebroeck G, Bonini BM, Versele M, Thevelein JM. Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor. Nat Chem Biol. 2009 Jan;5(1):45–52. doi: 10.1038/nchembio.132.
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