CAS: 1999-45-7; Dl-Alanyl-Dl-Phenylalanine

该化合物是一种由氨基酸丙胺和苯丙烯组成的二酸二甲酸酯,其特征是其结构,包括一种将氨基亚麻ine的碳酸酯组与氨基苯丙氨组连接起来的碳酸酯联结,该化合物表面上一般为白对白,在水中可溶解,适合各种生物化学应用.Alanylbonaline对生物化学和药理学领域很感兴趣,因为它在蛋白合成中具有潜在作用,并且是更为复杂的和蛋白质的建筑块.它还可能展示具体的生物活动,例如影响代谢途径或作为...

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上下游产品

Cbz-HN-Ala-Phe2-[2-(2-Cyano-ethylamino)-propionylamino]-3-phenyl-propionic acid 1-(2'-cyanoethyl)-2-benzyl-6-methyl-2,5(4H)-piperazinedione N-Pyruvylphenylalanine

合成工艺路线路线简述

  • 合成目标产物 Dl-Alanyl-Dl-Phenylalanine 主要起始原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
  • (文献来源)合成步骤主要原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
📜在 水,Lithium Hydroxide体系中,用 四氢呋喃 用作溶剂,化学反应 3.0H,以92%的收率获得dl-丙氨酰基-Dl-苯基丙氨酸
参考文献:三(4-甲酰基苯基)膦酸酯衍生物的合成作为肽合成的可回收三等价载体.
标题:三(4-甲酰基苯基)膦酸酯衍生物的合成作为肽合成的可回收三等价载体.
摘要:为了寻求有机磷化合物的新应用,本文成功合成了设计的三(4-甲酰基苯基)膦酸酯(tfp)衍生物,这些衍生物可用作液相肽中氨基酸或更绿色的三当量支持物的c端保护基合成(lpps).通过tfp衍生物的辅助沉淀作用,可在不进行色谱纯化的情况下,通过快速沉淀和便捷过滤分离并收集肽合成过程中的肽中间体.此外,从目标肽上剪下后,Tfp衍生物载体可以直接循环再利用,而无需进一步再生.
Doi:10.1021/acs.Joc.9B03023

海关参考信息

专利信息


专利号:US-5714127-A
优先权日:1992-10-08
标题 :System for multiple simultaneous synthesis
发明人:DEWITT SHEILA H H; KIELY JOHN S; PAVIA MICHAEL R; SCHROEDER MEL C; STANKOVIC CHARLES J
权利人:WARNER LAMBERT CO
摘要:A system for the multiple, simultaneous synthesis of compounds preferably uses a reaction apparatus comprising a reservoir rack having a plurality of reaction wells, a plurality of reaction tubes, usually gas dispersion tubes, having filters on their lower ends, a holder block, having a plurality of apertures, and a manifold, which has ports to allow introduction/maintenance of a controlled environment. The manifold top wall has a plurality of apertures in axial alignment with the reaction tubes and a gasket which allows penetration by a needle in order to dispense and aspirate materials from the reaction tubes. Sealing members, such as gaskets, are placed between the holder block, manifold and reservoir rack and the components are releasably fastened together. A robotic sample processor is used to automate the synthesis process using the reaction apparatus.

专利号:US-5702672-A
优先权日:1992-10-08
标 题 :Apparatus and method for multiple simultaneous synthesis
发明人:DEWITT SHEILA H H; KELL MICHAEL; PAVIA MICHAEL R; KIELY JOHN S; SCHROEDER MEL C; STANKOVIC CHARLES J; WARE STEVEN
权利人:WARNER LAMBERT CO
摘要:An apparatus for multiple, simultaneous synthesis of compounds which consists of: a reservoir block having a plurality of wells; a plurality of reaction tubes, usually gas dispersion tubes, having filters on their lower ends; a holder block, having a plurality of apertures; and a manifold, which may have ports to allow introduction/maintenance of a controlled environment. The manifold top wall has apertures and a detachable plate with identical apertures. The apparatus is constructed from materials which will accommodate heating, cooling, agitation, or corrosive reagents. Gaskets are placed between the components. Rods or clamps are provided for fastening the components together. Apparatus operation involves placing the filters on the lower ends of the reaction tubes in the reservoir block wells, and the upper ends passing through the holder block apertures and into the manifold.

专利号:US-5766556-A
优先权日:1992-10-08
标题:Apparatus and method for multiple simultaneous synthesis
发明人:DEWITT SHEILA HELEN HOBBS; KIELY JOHN STEVEN; PAVIA MICHAEL RAYMOND; SCHROEDER MEL CONRAD; STANKOVIC CHARLES JOHN
权利人:WARNER LAMBERT CO
摘要:An apparatus and method which provides a suitable location for multiple, simultaneous synthesis of compounds. The apparatus consists of: a reservoir block having a plurality of wells; a plurality of reaction tubes, usually gas dispersion tubes, having filters on their lower ends; a holder block, having a plurality of apertures; and a manifold, which may have ports to allow introduction/maintenance of a controlled environment. The manifold top wall has apertures and a detachable plate with identical apertures. The apparatus is constructed from materials which will accommodate heating, cooling, agitation, or corrosive reagents. Gaskets are placed between the components. Rods or clamps are provided for fastening the components together. Apparatus operation involves placing the filters on the lower ends of the reaction tubes in the reservoir block wells, and the upper ends passing through the holder block apertures and into the manifold. The apparatus provides in excess of 1 mg of each product with structural knowledge and control over each compound. The apparatus can be adapted to manual, semiautomatic or fully automatic performance. Using the apparatus a series of building blocks are covalently attached to a solid support. These building blocks are then modified by covalently adding additional different building blocks or chemically modifying some existing functionality until the penultimate structure is achieved. This is then cleaved from the solid support by another chemical reaction into the solution within the well yielding an array of newly synthesized individual compounds, which after postreaction modification, if necessary, are suitable for testing for activity.

专利号:US-5567391-A
优先权日:1992-10-08
标题 :Apparatus for multiple simultaneous synthesis
发明人:DEWITT SHEILA H H; KIELY JOHN S; PAVIA MICHAEL R; SCHROEDER MEL C; STANKOVIC CHARLES J
权利人:WARNER LAMBERT CO
摘要:An apparatus and method which provides a suitable location for multiple, simultaneous synthesis of compounds. The apparatus consists of: a reservoir block having a plurality of wells; a plurality of reaction tubes, usually gas dispersion tubes, having filters on their lower ends; a holder block, having a plurality of apertures; and a manifold, which may have ports to allow introduction/maintenance of a controlled environment. The manifold top wall has apertures and a detachable plate with identical apertures. The apparatus is constructed from materials which will accommodate heating, cooling, agitation, or corrosive reagents. Gaskets are placed between the components. Rods or clamps are provided for fastening the components together. Apparatus operation involves placing the filters on the lower ends of the reaction tubes in the reservoir block wells, and the upper ends passing through the holder block apertures and into the manifold. The apparatus provides in excess of 1 mg of each product with structural knowledge and control over each compound. The apparatus can be adapted to manual, semiautomatic or fully automatic performance. Using the apparatus a series of building blocks are covalently attached to a solid support. These building blocks are then modified by covalently adding additional different building blocks or chemically modifying some existing functionality until the penultimate structure is achieved. This is then cleaved from the solid support by another chemical reaction into the solution within the well yielding an array of newly synthesized individual compounds, which after postreaction modification, if necessary, are suitable for testing for activity.

专利号:WO-9630393-A1
优先权日:1995-03-27
标 题:A method for the synthesis of mixtures of compounds
发明人:BECKER KATHERINE; DEWITT SHEILA HOBBS
权利人:WARNER LAMBERT CO
摘要:Described is a method of synthesizing a plurality of compounds in a plurality of wells comprising the steps of: (a) providing a plurality of test wells in a plurality of arrays of the wells; (b) reacting in at least a one step reaction a first reagent with a plurality of reagents called building blocks in the test well to obtain a unique product designed to be the same in each array; and (c) continuing to react reagents such that there are multiple reagents resulting in mixtures of multiple different products in each well.

专利号:US-9751911-B2
优先权日:2012-11-27
标 题:Solomonamide analogue compounds, pharmaceuticals containing solomonamide analogue compounds, and processes for the preparation thereof
发明人:REDDY DUMBALA SRINIVASA; KOMIRISHETTY KASHINATH; NATARAJAN VASUDEVAN
权利人:COUNCIL SCIENT IND RES
摘要:Solomanamide analogs of Formula-I having anti-inflammatory activity, and viable synthetic routes for the preparation of such analogs, including the synthesis of macrocyclic core of Salomanamide analogs. The Solomanamide analogs of Formula-I or their pharmaceutical salt may be provided in a pharmaceutical composition and administered in an effective amount for the treatment of inflammation and/or pain.

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主要参考文献

[参考文献]: Esteban E Baquero, Et Al. Single-Conformation Ultraviolet And Infrared Spectroscopy Of Model Synthetic Foldamers: Beta-Peptides Ac-Beta3-Hphe-Beta3-Hala-Nhme And Ac-Beta3-Hala-Beta3-Hphe-Nhme. J Am Chem Soc. 2008 Apr 9;130(14):4795-807.
[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]: J Li, Et Al. Estimation Of The Ph-Independent Binding Constants Of Alanylphenylalanine And Leucylphenylalanine Stereoisomers With Beta-Cyclodextrin In The Presence Of Urea. Electrophoresis. 1999 Jan;20(1):171-9.
[参考文献]: Nick C Polfer, Et Al. Alkali Metal Complexes Of The Dipeptides Pheala And Alaphe: Irmpd Spectroscopy. Chemphyschem. 2008 Mar 14;9(4):579-89.
[参考文献]: Qiqin Wang, Et Al. Separation Of N-Derivatized Di- And Tri-Peptide Stereoisomers By Micro-Liquid Chromatography Using A Quinidine-Based Monolithic Column - Analysis Of L-Carnosine In Dietary Supplements. J Chromatogr A. 2016 Jan 8:1428:176-84.

合成参考文献


参考文献:10.1007/bf00128958
摘要:Uhm JH, Dooley NP, Villemure JG, Yong VW. Glioma invasion in vitro: regulation by matrix metalloprotease-2 and protein kinase C. Clin Exp Metastasis. 1996 Oct;14(5):421–33. doi: 10.1007/bf00128958.
参考文献:10.1007/s00018-004-3449-9
摘要:Tamura K, Alexander RW. Peptide synthesis through evolution. Cellular and Molecular Life Sciences (CMLS). 2004 May 01;61(11):1317–30. doi: 10.1007/s00018-004-3449-9.
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