CAS: 2743-40-0; H-Leu-Oet.Hcl

该化合物是基本氨基酸L-L-Leucine的衍生物,在蛋白合成和代谢过程中起着关键作用,该化合物的特点是乙酯形态,与免费氨基酸相比,提高了溶性和生物利用率.作为盐酸盐,通常比较稳定,更容易在各种配方中处理.该物质似乎是白到白的晶状粉,在水中可以溶解,适合药物和营养补充品的各种应用.L-L-Lucine因其在肌肉修复和生长中的作用而闻名,其酯状可能被用于旨在加强肌肉恢复和性能的配方.此外,重要的是,必须谨慎地处理该化合物,如同所有化学品一样,遵循适当的安全准则以避免任何潜在危害.总的说,L-Lucine, 乙酯,盐酸因其在研究和商业应用中的功能特性而具有价值.

结构式图片

相似化合物

17016-87-4 2743-60-4 73913-65-2

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号64-17-5 乙醇 | CAS号61-90-5 L-亮氨酸 | CAS号37787-76-1 (L)-N-B°C leuci... | CAS号7533-40-6 L-亮氨醇 | CAS号3253-28-9 Leucine,N-[N-(b... | CAS号1421-69-8 Z-Gly-Leu-OH | CAS号73401-65-7 B°C-亮氨酰-亮氨酸 | CAS号78603-97-1 (S)-(-)-2-氨-4-甲... | CAS号62246-49-5 ethyl 2-isothio... | CAS号64505-10-8 2-异氰酰-4-甲基戊酸乙酯

合成工艺路线路线简述

    L-亮氨酸置于氯化亚砜体系中,用 乙醇 用作溶剂,化学反应生成L-亮氨酸乙酯盐酸盐
    参考文献:N-Heterocyclic Alcohol Renin Inhibitors
    标题:N-Heterocyclic Alcohol Renin Inhibitors
    摘要:公式为##str1##的化合物被披露,其中r.Sub.1是n-杂环基团.这些化合物通过抑制肾素干预将血管紧张素转化为血管紧张素ii,因此可用作降压药物.

    海关参考信息

    专利信息


    专利号:WO-9305065-A1
    优先权日:1991-08-30
    标 题:Preparation of peptides by a solid-phase synthesis and intermediates therefor
    发明人:SHARMA RAM PRAKASH
    权利人:PORTON DEV LTD
    摘要:The invention relates to the preparation of polypeptides by solid phase synthesis by attachment of carboxy-protected amino acids to the carboxyl end of a peptide chain bound at its N-terminal to a solid support. The carboxy-protection is by a tertiary alkoxy silyl group. Novel tertiary alkoxy silyl amino acid esters are disclosed which may be used as intermediates.

    专利号:US-2012282652-A1
    优先权日:2011-02-28
    标题 :Preparation of peptide mixtures by protease catalysis designed to provide useful biological and physical properties
    发明人:GROSS RICHARD A; VISWANATHAN KODANDARAMAN; QIN XU
    权利人:GROSS RICHARD A; VISWANATHAN KODANDARAMAN; QIN XU; POLITECHNIC INST UNIV NEW YORK
    摘要:A process for preparing unique peptide mixtures with a broad range of uses using combinations of natural and non-natural amino acid alkyl ester monomers and specific combinations of these monomers as dimers, trimers and higher oligomers selected from the large group of structural motifs that lead to useful physical and/or biological properties and that have been or may be identified from solid state peptide synthesis, isolation of peptides from natural sources, and production of peptides by recombinant DNA methods, or identification of peptides by recombinant methods such as phage display, the method of peptide synthesis comprising a) admixing one or more natural and non-natural amino acid alkyl ester monomer, dimer, trimer and higher oligomers with one or more proteases in a reaction medium; b) heating the mixture to between about 5° C. to about 90° C. for between 5 minutes and 24 hours; and c) recovering the formed oligopeptide.

    专利号:US-2006252134-A1
    优先权日:1999-10-29
    标 题 :Enantioselective oligomerization of alpha-hydroxy carboxylic acids and alpha-amino acids
    发明人:LORBERT STEVE; SCHASTEEN CHARLES S; URAIZEE FAROOQ; KAPILA SHUBHENDER
    权利人:NOVUS INT INC
    摘要:An enzymatic synthesis and composition of oligomers and co-oligomers comprised of α-hydroxy carboxylic acids and α-amino acids or peptides is disclosed. In a preferred embodiment, a α-hydroxy carboxylic acid with a specific chiral configuration is linked by an amide linkage to a α-amino acid specific with a specific chiral configuration or linked by an amide linkage to a peptide made up of α-amino acid monomers having identical chiral configurations. Proteolytic enzymes catalyze oligomerization of the α-hydroxy carboxylic acid and α-amino acid. The degree and distribution of oligomerization varies upon the type and concentrations of different reaction mixtures utilized and upon the length of allowed reaction time. The resultant oligomers may be provided to animals such as ruminants as bioavailable amino acid supplements that are resistant to degradation in the rumen and other animals such as swine, poultry and aquatic animals.

    专利号:US-6939693-B2
    优先权日:1999-10-29
    标 题 :Enantioselective oligomerization of α-hydroxy carboxylic acids and α-amino acids
    发明人:LORBERT STEPHEN J; SCHASTEEN CHARLES S; NAM PAUL K S; FORCINITI DANIEL; RAJESH MATHUR P; KAPILA SHUBHENDER
    权利人:NOVUS INT INC
    摘要:An enzymatic synthesis and composition of oligomers and co-oligomers comprised of α-hydroxy carboxylic acids and α-amino acids or peptides is disclosed. In a preferred embodiment, a α-hydroxy carboxylic acid with a specific chiral configuration is linked by an amide linkage to a α-amino acid specific with a specific chiral configuration or linked by an amide linkage to a peptide made up of α-amino acid monomers having identical chiral configurations. Proteolytic enzymes catalyze oligomerization of the α-hydroxy carboxylic acid and α-amino acid. The degree and distribution of oligomerization varies upon the type and concentrations of different reaction mixtures utilized and upon the length of allowed reaction time. The resultant oligomers may be provided to animals such as ruminants as bioavailable amino acid supplements that are resistant to degradation in the rumen and other animals such as swine, poultry and aquatic animals.

    专利号:US-6605590-B1
    优先权日:1999-10-29
    标题 :Oligomers and oligomeric segments of alpha-hydroxy carboxylic acids and alpha-amino acids
    发明人:LORBERT STEPHEN J; SCHASTEEN CHARLES S; NAM PAUL K S; FORCINITI DANIEL; RAJESH MATHUR P; KAPILA SHUBHENDER
    权利人:NOVUS INT INC
    摘要:An enzymatic synthesis and composition of alpha-hydroxy carboxylic acid and alpha-amino acid or peptide co-oligomers is disclosed wherein a residue of the alpha-hydroxy carboxylic acid is linked to a residue of the alpha-amino acid or peptide by an amide linkage. Proteolytic enzyme papain catalyzes co-oligomerization of the alpha-hydroxy carboxylic acid and alpha-amino acid. The degree and distribution of oligomerization varies upon the type and concentrations of different reaction mixtures utilized and upon the length of allowed reaction time. The resultant oligomers may be provided to ruminants as bioavailable amino acid supplements that are resistant to degradation in the rumen.

    专利号:US-8461289-B2
    优先权日:2006-10-17
    标 题:Bioresorbable polymers synthesized from monomer analogs of natural metabolites
    发明人:KOHN JOACHIM B; BOLIKAL DURGADAS
    权利人:KOHN JOACHIM B; BOLIKAL DURGADAS; UNIV RUTGERS
    摘要:New bioresorbable polymers are synthesized from monomer analogs of natural metabolites In particular, polymers are polymerized from analogs of amino acids that contribute advantageous synthesis, processing and material properties to the polymers prepared therefrom, including particularly advantageous degradation profiles.
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    主要参考文献


    1: Vujić JM, Cvijović M, Kaluderović GN, Milovanović M, Zmejkovski BB, Volarević V, Arsenijević N, Sabo TJ, Trifunović SR. Palladium(II) complexes with R(2)edda derived ligands. Part IV. O,O'-dialkyl esters of (S,S)-ethylenediamine-N,N'-di-2-(4-methyl)-pentanoic acid dihydrochloride and their palladium(II) complexes: synthesis, characterization and in vitro antitumoral activity against chronic lymphocytic leukemia (CLL) cells. Eur J Med Chem. 2010 Sep;45(9):3601-6. doi: 10.1016/j.ejmech.2010.05.005. Epub 2010 May 12. doi: 10.1016/j.foodchem.2013.07.099. Epub 2013 Jul 27.

    合成参考文献


    摘要:Uozumi, Y., Science of Synthesis: Water in Organic Synthesis, (2012) 1, 515.
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