N-(4-Methoxybenzyloxycarbonyl)-O-benzyl-L-serine | 4218-63-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(4-Methoxybenzyloxycarbonyl)-O-benzyl-L-serine
• 英文别名: Z(OMe)-Ser(Bzl)-OH；Z(OCH3)-Ser(CH2-Ph)；Nalpha-p-Methoxybenzyloxycarbonyl-O-benzyl-L-serine；(2S)-2-[(4-methoxyphenyl)methoxycarbonylamino]-3-phenylmethoxypropanoic acid
• CAS: 4218-63-7
• 化学式: C₁₉H₂₁NO₆
• 分子量: 359.379
• InChiKey: YVPIYHXGRNXEPU-KRWDZBQOSA-N

物化性质

• 熔点：
  72-73 °C
• 沸点：
  567.8±50.0 °C(Predicted)
• 密度：
  1.253±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  26
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  94.1
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  N-(4-Methoxybenzyloxycarbonyl)-O-benzyl-L-serine 在 茴香硫醚 、 (2,4,6-trimethylphenoxy)trimethylsilane 作用下， 以 三氟乙酸 为溶剂， 反应 1.0h， 以93.5%的产率得到L-丝氨酸
  参考文献：
  名称：

  蛋白质化学合成的新策略

  摘要：

  对于蛋白质的化学合成，描述了通过组合硬酸，三甲基甲硅烷基三氟甲磺酸盐和软亲核试剂例如硫代苯甲醚进行的有效脱保护程序。对于二硫键的形成，提出了两种新的方法。一种通过三氟乙酸al（III）氧化而另一种通过酸催化反应进行，涉及S取代的半胱氨酸亚砜。

  DOI：

  10.1016/s0040-4020(01)86118-4
• 作为产物：
  描述：

  2-(4-methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile 在 sodium hydride 、 三乙胺 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 11.0h， 生成 N-(4-Methoxybenzyloxycarbonyl)-O-benzyl-L-serine
  参考文献：
  名称：

  A New Synthesis ofO-Benzyl-L-serine

  摘要：

  使用 4-甲氧基苄氧羰基进行 N 保护，从丝氨酸制备 O-苄基-L-丝氨酸的高效三步法，总产率达 85%。

  DOI：

  10.1055/s-1989-27138

文献信息

• Amino Acids and Peptides. XX. Preparation of .BETA.-Cyclododecyl Aspartate and Its Application to Synthesis of Fibronectin- and Laminin-Related Peptides.
  作者：Koichi KAWASAKI、Tomohiro MURAKAMI、Kazuyoshi KOSHINO、Machiko NAMIKAWA、Mitsuko MAEDA、Takao HAMA、Tadanori MAYUMI

  DOI：10.1248/cpb.42.792

  日期：——

  beta-Cyclododecyl aspartate was prepared and its application to peptide synthesis was examined. Derivatives of beta-cyclododecyl aspartate are more likely to crystallize and should be useful for peptide synthesis. The cyclododecyl ester was much stable to bases than the benzyl ester and rather more stable than the cyclohexyl ester. It was removable by HF treatment and trifluoromethanesulfonic acid treatment

  制备了β-环十二烷基天冬氨酸盐，并研究了其在肽合成中的应用。β-环十二烷基天冬氨酸的衍生物更容易结晶，应该对肽合成有用。环十二烷基酯对碱的稳定性比苄基酯高，但比环己基酯更稳定。可通过HF处理和三氟甲磺酸处理将其除去。β-环十二烷基天冬氨酸盐通过固相和液相方法用于合成层粘连蛋白和纤连蛋白相关肽。
• Synthesis of canine motilin, a gastric motor activity-stimulating polypeptide, and its N1-substituted analogs.
  作者：KOUKI KITAGAWA、KUNIO YONETO、SHINYA KIYAMA、KENSHI ANDO、TATSUHIKO KAWAMOTO、TADASHI AKITA、ATSUKO INOUE、TOMIO SEGAWA

  DOI：10.1248/cpb.33.3307

  日期：——

  The docosapeptide corresponding to the entire amino acid sequence of canine motilin, a newly characterized gastric motor activity-stimulating polypeptide, was synthesized by the conventional solution method. All protecting groups employed were removed by 1 M trifluoromethanesulfonic acid-thioanisole-trifluoroacetic acid and the deprotected peptide was purified by gel-filtration on Sephadex G-25, followed by partition chromatography and reverse phase high performance liquid chromatography. When contractile activity on rabbit duodenal muscle was examined, synthetic canine motilin was as active as synthetic porcine motilin. The relative potencies of Lys1 and Ser1 derivatives prepared in the same manner as canine motilin were ca. 1/1000 and 1/250, respectively.

  合成了与犬动脉肽（犬motilin）完整氨基酸序列对应的多肽，这是一种新特征的刺激胃肠运动活性的多肽，使用传统的溶液法合成。所有使用的保护基团均通过1 M三氟甲烷磺酸-硫醚-三氟乙酸去除，去保护的多肽通过Sephadex G-25的凝胶过滤进行纯化，随后进行分配色谱和反相高效液相色谱。在对兔十二指肠肌肉的收缩活性进行检验时，合成的犬动脉肽活性与合成的猪动脉肽相当。以与犬动脉肽相同的方法制备的赖氨酸1和丝氨酸1衍生物的相对效能分别约为1/1000和1/250。
• Studies on peptides. CXXVII. Synthesis of a tripentacontapeptide with epidermal growth factor activity.
  作者：KENICHI AKAJI、NOBUTAKA FUJII、HARUAKI YAJIMA、KYOZO HAYASHI、KAZUHIKO MIZUTA、MITSURU AONO、MOTOYUKI MORIGA

  DOI：10.1248/cpb.33.184

  日期：——

  The tripentacontapeptide corresponding to the entire linear sequence of epidermal growth factor was synthesized by assembling 15 peptide fragments and one His residue (position 22), followed by deprotection with trifluoromethanesulfonic acid-thioanisole in trifluoroacetic acid. The deprotected peptide was subjected to air-oxidation. After purification by ion-exchange chromatography on diethyl aminoethyl cellulose followed by high performance liquid chromatography, a peptide with powerful anti-gastric activity was obtained.

  通过组装15个肽片段和一个组氨酸残基（位置22），合成了对应于表皮生长因子整个线性序列的三十五肽。随后，通过三氟甲磺酸-噻吩在三氟乙酸中进行脱保护。脱保护的肽进行空气氧化。经过二乙氨基乙基纤维素上的离子交换色谱法纯化，接着用高效液谱法，获得了一种具有强大抗胃活性的肽。
• Studies on peptides. CLII. Hard acid deprotecting procedure for peptide synthesis.
  作者：NOBUTAKA FUJII、AKIRA OTAKA、OSAMU IKEMURA、MIKA HATANO、AKIRA OKAMACHI、SUSUMU FUNAKOSHI、MITSUYA SAKURAI、TAKAYUKI SHIOIRI、HARUAKI YAJIMA

  DOI：10.1248/cpb.35.3447

  日期：——

  The use of trimethylsilyl trifluoromethanesulfonate as a peptide deprotecting reagent was examined, together with the role of soft bases employed. A new deprotecting procedure based on the hard acid principle is presented.

  考察了使用三甲基硅烷三氟甲磺酸酯作为肽脱保护试剂的效果，并探讨了软碱的作用。基于硬酸原理，提出了一种新的脱保护程序。
• Studies on peptides. CXXXIII. Synthesis and biological activity of galanin, a novel porcine intestinal polypeptide.
  作者：HARUAKI YAJIMA、SHIROH FUTAKI、NOBUTAKA FUJII、KENICHI AKAJI、SUSUMU FUNAKOSHI、MITSUYA SAKURAI、SHINICHI KATAKURA、KAZUTOMO INOUE、RYO HOSOTANI、TAKAYOSHI TOBE、TOMIO SEGAWA、ATSUKO INOUE、KAZUHIKO TAKEMOTO、VIKTOR MUTT

  DOI：10.1248/cpb.34.528

  日期：——

  A new porcine gastrointestinal 29-residue peptide, galanin, was synthesized in a satisfactory yield by assembling seven peptide fragments followed by deprotection with 1 M trifluoromethane-sulfonic acid-thioanisole in trifluoroacetic acid. Nin-Mesitylenesulfonyltryptophan was employed to suppress indole alkylation during Na-deprotection. β-Cycloheptylaspartate was employed to suppress base-catalyzed succinimide formation. The synthetic peptide exhibited a powerful contractile activity on rat ileum, but not on guinea pig ileum and caused sustained hyperglycemia in dogs.

  一种新的猪胃肠道29残基肽——加拉宁，通过组合七个肽片段合成，并在三氟醋酸中使用1 M三氟甲烷磺酸-硫代苯醚进行去保护，获得了令人满意的产率。在钠去保护过程中，采用了九甲苯磺酰色氨酸以抑制吲哚烷基化。使用β-环庚基天冬氨酸来抑制碱催化的琥珀酰亚胺形成。合成的肽在大鼠回肠上表现出强有力的收缩活性，但在豚鼠回肠上没有影响，并且在狗身上引起持续性高血糖。