CAS: 16063-79-9; 2-Amino-4,4,4-Trifluoro-3-Methylbutanoic Acid

该化合物是谷类的氟化氨酸衍生物,其特点是有三种氟原子,附于valine结构的阿尔法碳;这一改变显著改变了其化学特性,包括水分疏松性增加和生物活动的潜在变化;氟的存在可以增强分子的稳定性,影响其与生物系统的相互作用,使其对制药研究和开发感兴趣;该化合物通常是在室温下的一种白色晶状固体,在极地溶剂中可溶解;其独特的结构使其能够作为各种和蛋白综合体的一个构件,特别是在涉及氟化化合物的研究中.此外,4,4-4-三氟-二氟-valine可能呈现出与非氟对应体相比不同的代谢途径,这对于了解其在生物化学过程中的作用至关重要.应当参考安全数据以便处理,因为氟化合物可以具有特定的毒性特征.

结构式图片

相似化合物

409333-57-9 107739-65-1 409333-54-6

上下游产品

2-Azido-4,4,4-trifluoro-3-methyl-butyric acid ethyl ester N-acetyl-4,4,4-trifluorovaline 2-Acetylamino-2-(1-benzenesulfonylmethyl-2,2,2-trifluoro-ethyl)-malonic acid diethyl ester (-)-3-trifluoromethylbutanoic acid

合成工艺路线路线简述

  • 合成目标产物 4,4,4-Trifluoro-Dl-Valine 主要起始原料 Valine, N-Acetyl-4,4,4-Trifluoro-
  • (文献来源)合成步骤主要原料 Valine, N-Acetyl-4,4,4-Trifluoro-
📜N-Acetyl-4,4,4-Trifluorovaline置于盐酸体系中,化学反应 20.0H,以78%的收率获得4,4,4-三氟-Dl-缬氨酸
参考文献:New And Effective Routes To Fluoro Analogs Of Aliphatic And Aromatic Amino Acids
标题:New And Effective Routes To Fluoro Analogs Of Aliphatic And Aromatic Amino Acids
摘要:
Doi:10.1021/jo00280A014

海关参考信息

专利信息


专利号:US-9206222-B2
优先权日:2009-06-29
标题:Solid phase peptide synthesis of peptide alcohols
发明人:CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN
权利人:CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN; CENTRE NAT RECH SCIENT
摘要:The present invention relates to the synthesis of depsipeptides on solid phase support. Said depsipeptides are then implicated in a solution phase O—N acyl shift enabling to obtain the corresponding peptide alcohols.

专利号:US-2022243244-A1
优先权日:2019-10-10
标 题 :Compositions and methods for in vivo synthesis of unnatural polypeptides
发明人:ROMESBERG FLOYD E; FISCHER EMIL C; HASHIMOTO KOJI; FELDMAN AARON W; DIEN VIVIAN T; ZHANG YORKE
权利人:SCRIPPS RESEARCH INST
摘要:Disclosed herein are compositions, methods, and kits for a cell incorporating unnatural amino acids into an unnatural polypeptide. Also disclosed herein are compositions, methods, and kits for increasing activity and yield of the unnatural polypeptide synthesized by the cell.

专利号:US-7371867-B2
优先权日:2001-02-27
标题 :Non-racemic trifluoroleucine, and methods of making and using
发明人:FICHERA ALFIO; BILGICER ZIHNI; KUMAR KRISHNA; XING XUECHAO
权利人:TUFTS COLLEGE
摘要:One aspect of the invention relates to hexafluoroleucine and congeners thereof, and methods of making the compounds. Another aspect of the invention relates to the synthesis of protein cores comprising hexafluoroleucine and congeners thereof. Certain peptides comprising hexafluoroleucine and congeners thereof have been characterized using comparative biophysical studies. In general, the fluorinated peptides show higher thermal stability and enhanced resistance to chemical denaturation. Further, mixed hydrocarbon-fluorocarbon cores self-sort into homogeneous bundles, suggesting new avenues for the design and manipulation of protein-protein interfaces.

专利号:US-2023037284-A9
优先权日:2018-11-30
标题:Combination therapy of peptidomimetic macrocycles
发明人:GUERLAVAIS VINCENT; ANNIS DAVID ALLEN
权利人:AILERON THERAPEUTICS INC
摘要:The present disclosure describes the synthesis of peptidomimetic macrocycles and methods of using peptidomimetic macrocycles to treat a condition. The present disclosure also describes methods of using peptidomimetic macrocycles in combination with at least one additional pharmaceutically-active agent for the treatment of a condition, for example, cancer.

专利号:US-2025084410-A1
优先权日:2015-01-12
标 题:Incorporation of unnatural nucleotides and methods thereof
发明人:PTACIN JEROD; MALYSHEV DENIS A; CAFFARO CAROLINA E
权利人:SYNTHORX INC
摘要:Disclosed herein are methods, compositions and kits for the synthesis of proteins which comprises unnatural amino acids that utilize a mutant tRNA.

专利号:US-8546533-B2
优先权日:2008-08-29
标 题:Pipecolic linker and its use for chemistry on solid support
发明人:MARTINEZ JEAN; ZAJDEL PAWEL; PAWLOWSKI MACIEJ; SUBRA GILLES
权利人:MARTINEZ JEAN; ZAJDEL PAWEL; PAWLOWSKI MACIEJ; SUBRA GILLES; CENTRE NAT RECH SCIENT; UNIV MONTPELLIER 1; UNIV JAGELLONE; UNIV MONTPELLIER II
摘要:The present invention relates to a pipecolic linker and its use as a solid-phase linker in organic synthesis. Said pipecolic solid-phase linker may be used for coupling functional groups chosen between primary amines, secondary amines, aromatic amines, alcohols, phenols and thiols. In particular, said pipecolic solid-phase linker may be used for peptide or pseudopeptide synthesis, such as the reverse N to C peptide synthesis or the retro-inverso peptide synthesis, or for the synthesis of small organic molecules.

供应商参考报价(招募中)

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

合成参考文献


摘要:H. M. Walborsky and J. H. Lang. J. Am. Chem. Soc. 78, 4314 (1956).
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知