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N-lactulosylisoleucine | 247564-39-2

中文名称
——
中文别名
——
英文名称
N-lactulosylisoleucine
英文别名
——
N-lactulosylisoleucine化学式
CAS
247564-39-2
化学式
C18H33NO12
mdl
——
分子量
455.46
InChiKey
IHVAGOPYIMZXCW-MXGXWOTQSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -4.46
  • 重原子数:
    31.0
  • 可旋转键数:
    13.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    226.47
  • 氢给体数:
    9.0
  • 氢受体数:
    12.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    L-异亮氨酸β-乳糖甲醇二甲基亚砜 为溶剂, 反应 8.0h, 生成 N-lactulosylisoleucine
    参考文献:
    名称:
    Studies on N-Terminal Glycation of Peptides in Hypoallergenic Infant Formulas:  Quantification of α-N-(2-Furoylmethyl) Amino Acids
    摘要:
    To obtain information about the extent of the early Maillard reaction between the N-termini of peptides and lactose, alpha-N-(2-furoylmethyl) amino acids (FMAAs) were quantified together with is an element of-N-(2-furoylmethyl) lysine (furosine) in acid hydrolyzates of hypoallergenic infant formulas, conventional infant formulas, and human milk samples using RP-HPLC with UV-detection. FMAAs are formed during acid hydrolysis of peptide-bound N-terminal Amadori products (APs), and furosine is formed from the Amadori products of peptide-bound lysine. Unambiguous identification was achieved by means of LC/MS and UV-spectroscopy using independently prepared reference material. The extent of acid-induced conversion of APs to FMAAs was studied by RP-HPLC with chemiluminescent nitrogen detection (CLND). Depending on the corresponding alpha-N-lactulosyl amino acid, between 6.0% and 18.1% of FMAAs were formed during hydrolysis for 23 h at 110 degrees C in 8 N HCl. From is an element of-N-lactulosyllysine, 50% furosine is formed under these conditions. Whereas furosine was detectable in all assayed samples, five different FMAAs, alpha-FM-Lys, alpha-FM-Ala, alpha-FM-Val, alpha-FM-Ile, and alpha-FM-Leu, were exclusively detected in acid hydrolyzates of hypoallergenic infant formulas in amounts ranging from 35 to 396 mu mol/100 g protein. Taking the conversion factors into account, modification of N-terminal amino acids in peptides by reducing carbohydrates was between 0.3% and 8.4%. This has to be considered within the discussion concerning the nutritional quality of peptide- containing foods.
    DOI:
    10.1021/jf061821b
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