2,5-二氧代吡咯烷-1-基十二酸酯
2,5-二氧代吡咯烷-1-基十二酸酯结构式
|
常用名 | 2,5-二氧代吡咯烷-1-基十二酸酯 | 英文名 | lauric acid n-hydroxy-succinimide ester |
|---|---|---|---|---|
| CAS号 | 14565-47-0 | 分子量 | 297.39000 | |
| 密度 | 1.07g/cm3 | 沸点 | 392.3ºC at 760mmHg | |
| 分子式 | C16H27NO4 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 191.1ºC |
|
Water-soluble fatty acid derivatives as acylating agents for reversible lipidization of polypeptides.
FEBS Lett. 371 , 283-286, (1995) 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 ... |
|
|
Use of esters of N-hydroxysuccinimide in the synthesis of N-acylamino acids.
J. Lipid Res. 8 , 142-145, (1967) 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 hydroxylamin... |
|
|
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)
|