CAS: 1466-83-7; N-Benzoyl-L-Leucine

该化合物是一种氨基酸衍生物,其特征是附于氨基酸的苯并基组,该化合物一般是白色的到白的晶状粉,可溶于乙醇和丙酮等有机溶剂,但在水中溶解性有限,经常用于生化研究和药物应用,因为它在Peptide合成中起着建筑构件的作用,在不对称合成中具有作为手性辅助剂的潜力.苯并呋喃组的存在可加强其亲性,因为它会影响其生物活动和其他分子的相互作用.此外,苯并硫-L-leucine由于其具有风气性质,可能会显示特定的光学活动,因此在涉及立体化学学的研究中具有相关性.应当参考安全数据,以便处理和使用,如同任何化学物质一样,确保采取适当的预防措施.

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相似化合物

17966-67-5 38449-08-0 2241925-37-9

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合成工艺路线路线简述

    📜Dl-亮氨酸置于sodium Hydroxide,葡萄糖,Corn Steep Liquor,Fungus Beauveria Bassiana Atcc 7159体系中,用 乙醇,水 用作溶剂,化学反应 74.0H,反应生成N-苯甲酰-L-亮氨酸
    参考文献:Beauveria Bassiana Atcc 7159 Containsan L-Specific A-Amino Acid Benzamidase
    标题:Beauveria Bassiana Atcc 7159 Containsan L-Specific A-Amino Acid Benzamidase
    摘要:Biotransformation Of A Series Of Racemic N-Benzoyl Alpha-Amino Acids By The Fungus Beauveria Bassiana Atcc 7159 Results In Isolation Of The Corresponding D-Amino Acid Benzamides In High Enantiomeric Purity And Yield.
    Doi:10.1007/s007060070095

    海关参考信息

    专利信息


    专利号:US-5202235-A
    优先权日:1986-08-18
    标题 :Enzymatic method for the synthesis and separation of peptides
    发明人:IACOBUCCI GUILLERMO A
    权利人:COCA COLA CO
    摘要:The present invention provides a method for the enzymatic synthesis of peptides accomplished by shifting the chemical equilibrium that exists in a reaction mixture between charged or ionized reacting amino acids and uncharged or non-ionized peptide product in the presence of a proteolytic enzyme such as thermolysin. The equilibrium is shifted by diffusion of the uncharged peptide product across an ion-rejection membrane which removes the uncharged peptide from the reaction mixture and preferably the diffused uncharged peptide is quickly converted to a charged species that cannot back-diffuse into the reaction mixture so that the uncharged peptide is effectively 'pulled' across the membrane.

    专利号:US-5350681-A
    优先权日:1986-08-18
    标题 :Enzymatic membrane method for the synthesis and separation of peptides
    发明人:IACOBUCCI GUILLERMO A; BROSE DANIEL J; RAY RODERICK J; VAN EIKEREN PAUL
    权利人:COCA COLA CO
    摘要:The present invention discloses a method for the enzymatic synthesis of a peptide. A protected peptide having a C-terminal carboxylate group or a protected, N-acyl amino acid having an alpha carboxylate group is reacted with a protected peptide having an N-terminal ammonium group or a protected amino acid having an alpha ammonium group in the presence of a condensation enzyme under conditions in which the carboxylate group and the ammonium group condense to form a protected, uncharged, peptide product. This peptide product is transported across a water-immiscible hydrophobic phase into an aqueous product phase and prevented from back diffusing across the water-immiscible hydrophobic phase. The peptide product can be converted, chemically or enzymatically, to a charged species that cannot back diffuse across the water-immiscible phase into the aqueous reaction phase. The water-immiscible hydrophobic phase is an ion rejection membrane separating the aqueous reaction phase from the product phase creating oil/water interfaces with each of the aqueous phases.

    专利号:US-5002871-A
    优先权日:1986-08-18
    标 题:Enzymatic membrane method for the synthesis and separation of peptides
    发明人:IACOBUCCI GUILLERMO A
    权利人:COCA COLA CO
    摘要:The present invention provides a membrane method for the enzymatic synthesis of peptides accomplished by shifting the chemical equilibrium that exists in a reaction mixture between charged or ionized reacting amino acids and uncharged or non-ionized peptide product in the presence of a proteolytic enzyme such as thermolysin. The equilibrium is shifted by diffusion of the unchanged peptide product across an ion-rejection membrane which removes the uncharged peptide from the reaction mixture and preferably the diffused uncharged peptide is quickly converted to a charged species that cannot back-diffuse into the reaction mixture so that the uncharged peptide is effectively 'pulled' across the membrane. An enzymatic conversion of the uncharged species utilizing an esterase having proteolytic activity such as aminoacylase I is disclosed. Copermeating reactants can be separated from the product mixture and returned to the reaction mixture. Also, the ion-rejection membrane can be utilized to resolve enantiomers of racemic carboxylic acids including D,L-amino acids.

    专利号:US-10676423-B2
    优先权日:2017-02-21
    标题 :Structure and synthesis of highly fluorinated amino acid derivatives
    发明人:WEAVER JIMMIE DEAN; TEEGARDIN KIP ALLEN; ARORA AMANDEEP
    权利人:UNIV OKLAHOMA STATE
    摘要:Methods of synthesizing polyfluorinated amino acid derivatives are disclosed, along with polyfluorinated amino acid derivatives produced from said methods, as well as compositions containing same. The synthesis methods utilize an oxazolone and a perfluoroarene to produce the polyfluorinated amino acid derivatives.

    专利号:US-8124794-B2
    优先权日:2002-04-17
    标题:Method for the asymmetric synthesis of beta-lactone compounds
    发明人:SMITH JEFFREY W; AXELROD FUMIKO; KRIDEL STEVEN J; ROMO DANIEL; PUROHIT VIKRAM; MA GIL
    权利人:SMITH JEFFREY W; AXELROD FUMIKO; KRIDEL STEVEN J; ROMO DANIEL; PUROHIT VIKRAM; MA GIL; SANFORD BURNHAM MED RES INST
    摘要:The present invention features methods of treating a cancer in a subject by administering an effective amount of a beta-lactone to the subject. The invention also features methods of inhibiting angiogenesis in a subject by administering an effective amount of an inhibitor of fatty acid synthase to the subject. These methods can be used to treat a variety of cancers and other diseases and conditions. The invention also features methods of identifying beta-lactones and other compounds that can be used in the methods of the invention for the treatment of tumors, inhibition of angiogenesis, and the treatment of diseases and conditions that involve pathological angiogenesis. The invention also features methods of synthesizing beta-lactones and features novel beta-lactone compounds.

    专利号:US-5336601-A
    优先权日:1986-08-18
    标 题:Enzymatic membrane method for the snythesis and separation of peptides
    发明人:IACOBUCCI GUILLERMO A
    权利人:COCA COLA CO
    摘要:The present invention discloses a method for the enzymatic synthesis of a peptide. A protected peptide having a C-terminal carboxylate group or a protected, N-acyl amino acid having an alpha carboxylate group is reacted with a protected peptide having an N-terminal ammonium group or a protected amino acid having an alpha ammonium group in the presence of a condensation enzyme under conditions in which the carboxylate group and the ammonium group condense to form a protected, uncharged, peptide product. This peptide product is transported across a water-immiscible hydrophobic phase into an aqueous product phase. This peptide product is removed from the aqueous product phase to prevent back diffusion across the water-immiscible hydrophobic phase. Reverse osmosis and other separation techniques may be utilized to remove the peptide product. The water-immiscible hydrophobic phase is an ion rejection membrane separating the aqueous reaction phase from the product phase creating oil/water interfaces with each of the aqueous phases.

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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.
    [参考文献]: Miguel A. Bailén, Et Al. 2-Mercaptopyridone 1-Oxide-Based Uronium Salts: New Peptide Coupling Reagents(1)(,)(2). J Org Chem. 1999 Nov 26;64(24):8936-8939.

    合成参考文献


    摘要:Lubell, W. D.; Blankenship, J. W.; Fridkin, G.; Kaul, R., Science of Synthesis, (2005) 21, 748.
    摘要:Zhdankin, V. V., Science of Synthesis, (2007) 31, 170.
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