N-formyl-D,L-norvaline | 112624-75-6

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: N-formyl-D,L-norvaline
• 英文别名: N-Formyl-DL-norvalin；N-Formyl-norvalin；2-Formamidopentanoic acid
• CAS: 112624-75-6
• 化学式: C₆H₁₁NO₃
• 分子量: 145.158
• InChiKey: SPPVMYHDPUFDCA-UHFFFAOYSA-N

物化性质

• 沸点：
  366.5±25.0 °C(Predicted)
• 密度：
  1.127±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  10
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  66.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-formyl-D,L-norvaline 在 水 、 cobalt(II) chloride 作用下， 反应 0.8h， 生成 L-正缬氨酸
  参考文献：
  名称：

  酰胺水解酶工艺：扩大使用 lN-氨基甲酰酶/N-琥珀酰氨基酸消旋酶串联生产不同的光学纯 l-氨基酸

  摘要：

  摘要 已经开发了包含来自嗜热土芽孢杆菌 CECT4264 (GkNSAAR) 的 N-琥珀酰氨基酸消旋酶和来自嗜热脂肪地芽孢杆菌 CECT43 (BsLcar) 的对映特异性 1-N-氨基甲酰化酶的双酶系统。这种生物催化剂已经能够通过动态动力学拆分从 N-乙酰-、N-甲酰基-和 N-氨基甲酰基-氨基酸的外消旋混合物开始生产光学纯的天然和非天然 l-氨基酸。N-甲酰基-氨基酸的转化率最快，其次是N-氨基甲酰基-和N-乙酰-氨基酸，并且GkNSAAR由于其较低的比活性被证明是该系统的限制步骤。金属离子钴对于生物催化剂的活性是必不可少的，当 Co 2+ 直接添加到反应混合物中时，系统的活性最佳。对于 N-甲酰基-和 N-氨基甲酰基-氨基酸底物，生物催化剂的最佳 pH 值证明为 8.0，而 N-甲酰基-氨基酸的最佳温度范围为 45-55 °C，而对于 N-甲酰基-氨基酸，最佳温度范围为 55-70

  DOI：

  10.1016/j.procbio.2014.04.013
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 马钱子碱 作用下， 生成 N-formyl-D,L-norvaline
  参考文献：
  名称：

  Abderhalden; Kuerten, Fermentforschung, vol. 4, p. 329

  摘要：

  DOI：

文献信息

• Remote Binding Energy in Antibody Catalysis:  Studies of a Catalytically Unoptimized Specificity Pocket
  作者：Herschel Wade、Thomas S. Scanlan

  DOI：10.1021/ja983017e

  日期：1999.2.1

  Binding interactions remote from the hydrolytic reaction center have been probed with substrate and phosphonate transition state analogues to understand how these types of interactions are used to promote catalysis in the 17E8 system, We find that the hapten-generated recogniton pocket in 17E8 has properties that are analogous to those of specificity pockets in enzymes, pie have also found that there are specific requirements to form catalytically productive interactions between the side chain and the recognition pocket including conformation, size, and geometry. An additional requirement includes Favorable simultaneous interactions between the side chain and binding packet along with favorable interactions with the oxyanion hole. The 17E8 side chain recognition pocket seems to be less catalytically efficient than analogous pockets in enzymatic systems. The apparent binding energy gained from the methylene-packet interactions in the 17E8 system is significantly smaller than those observed in natural enzymes. Furthermore, 17E8 does not use specific interactions in the recognition pocket to significantly affect catalytic turnover (k(cat)) which is thought to be a trait of an unoptimized catalyst. Analysis of the crystal structure of the 17E8,hapten complex has allowed for the identification of differences between the active sites of 17E8; and several proteases, The identified differences give insight to the sources of the inefficient use of binding energy.
• Abderhalden; Schweitzer, Fermentforschung, 1931, vol. 12, p. 241
  作者：Abderhalden、Schweitzer

  DOI：——

  日期：——
• Abderhalden; Kuerten, Fermentforschung, vol. 4, p. 330
  作者：Abderhalden、Kuerten

  DOI：——

  日期：——
• MAGNUS, PHILIP;SLATER, MARTIN, TETRAHEDRON LETT., 28,(1987) N 25, 2829-2832
  作者：MAGNUS, PHILIP、SLATER, MARTIN

  DOI：——

  日期：——
• SELF-ASSEMBLED MICRO-AND NANOSTRUCTURES
  申请人：NORTHWESTERN UNIVERSITY

  公开号：US20160115196A1

  公开（公告）日：2016-04-28

  The present invention discloses self-assembled bioadhesive anti-microbial, anti-fouling and/or anti-oxidant micro- and nano-structures comprising a plurality of amino acids or peptides, wherein each amino acid is an aromatic amino acid comprising a catecholic moiety, and/or each peptide comprises at least one aromatic amino acid comprising a catecholic moiety. Further disclosed are methods and kits for preparing these micro- and nano-structures. Further disclosed are uses of these micro- and nano-structures in pharmaceutical, cosmetic and medical devices applications.