L3900
月桂酸 N-羟基琥珀酰亚胺酯
≥98% (TLC)
别名:
琥珀酰亚胺基月桂酸酯
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关于此项目
经验公式（希尔记法）:
C16H27NO4
化学文摘社编号:
分子量:
297.39
MDL编号:
UNSPSC代码:
12352211
PubChem化学物质编号:
NACRES:
NA.25
方案
≥98% (TLC)
脂质类型
saturated FAs
储存温度
−20°C
SMILES字符串
CCCCCCCCCCCC(=O)ON1C(=O)CCC1=O
InChI
1S/C16H27NO4/c1-2-3-4-5-6-7-8-9-10-11-16(20)21-17-14(18)12-13-15(17)19/h2-13H2,1H3
InChI key
LRKGVVJOUNKTGG-UHFFFAOYSA-N
生化/生理作用
月桂酸 N-羟基琥珀酰亚胺酯可用于N-酰基氨基酸的合成和多肽的脂化或使用 N-羟基琥珀酰亚胺酯缀合化学的其他应用。
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Y Lapidot et al.
Journal of lipid research, 8(2), 142-145 (1967-03-01)
Several crystalline N-hydroxysuccinimide esters of short- and long-chain fatty acids have been synthesized. These compounds react with free amino acids to form preferentially N-acylamino acids. The reaction of the N-hydroxysuccinimide esters with hydroxylamine and the behavior of the N-acylamino acids
H M Ekrami et al.
FEBS letters, 371(3), 283-286 (1995-09-11)
A novel method allowing the conjugation of a fatty acid to a peptide or protein in aqueous buffer is described in this paper. L-Cysteinyl 2-pyridyl disulfide (CPD) (III), which was obtained by reacting L-cysteine (I) with 2,2-dithiopyridine (II), was reacted
Lipidization of human interferon-α: a new approach toward improving the delivery of protein drugs.
Yuan L, Wang J, Shen WC.
J. Controlled Release, 129, 11-17 (2008)
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