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首页> 外文期刊>Carbohydrate research >Concepts for improved regioselective placement of O-sulfo, N-sulfo, N-acetyl, and N-carboxymethyl groups in chitosan derivatives
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Concepts for improved regioselective placement of O-sulfo, N-sulfo, N-acetyl, and N-carboxymethyl groups in chitosan derivatives

机译:改善壳聚糖衍生物中O-磺基,N-磺基,N-乙酰基和N-羧甲基基团的区域选择性位置的概念

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摘要

In the present paper a new strategy has been studied to introduce solely or in combination N -sulfo, O-sulfo, N -acetyl, and N -carboxymethyl groups into chitosan with highest possible regioselectivity and completeness and defined distribution along the polymer chain. The aim was to generate compounds having lowest toxicity for determining the pharmacological structure- function relationships among different backbone structures and differ- ently arranged functional groups compared to those of heparin and heparan sulfate. The water-soluble starting material, chitosan, with a degree of acetylation (DA) of 0.14 and a molecular weight of 29 kD, allows one to apply most of the known reactions of chitosan as well as some reactions of hepari~ chemistry successfully and with improved regioselectivity and completeness. On the other hand, a number of these reactions were not successful by application to water-soluble high-molecular-weight chitosan (DA 0.45 and 150 kD). The starting material showed statistical N-acetyl (N-Ac) distribution along the polymer chain according to the rules of Bernoulli, with highest abundance of the GlcNAc-GlcNAc diad along with a lower abundance of triads, tetrads, and pentads. The space between the N -Ac groups was filled up in homogeneous reactions by N -sulfo and/or N -carboxymethyl groups, which also resulted in a Bernoulli statistical distribution. The N-substitution reaction showed highest regioselectivity and completeness with up to three combined different functional groups. The regioselectivity of the 3-0-sulfo groups was improved by regioselective 6-desulfation of nearly completely sulfated 3,6-di-O-sulfochitosan. By means of desul- fation reactions, all of the possible intermediate sulfated products are possible. 6-0-Sulfo groups can also be introduced with highest regioselectivity and completeness, and a number of partially 6-desulfated products are possible.
机译:在本文中,已经研究了一种新的策略,以将N-磺基,O-磺基,N-乙酰基和N-羧甲基基团单独或组合引入壳聚糖中,具有最高的区域选择性和完整性,并沿着聚合物链具有确定的分布。目的是产生毒性最低的化合物,以测定与肝素和硫酸乙酰肝素相比,在不同主链结构和不同排列的官能团之间的药理结构-功能关系。水溶性原料壳聚糖的乙酰化度(DA)为0.14,分子量为29 kD,使人们能够成功地应用大多数已知的壳聚糖反应以及某些肝化学反应,并且改善区域选择性和完整性。另一方面,通过将其应用于水溶性高分子量壳聚糖(DA 0.45和150 kD),这些反应中的许多反应均不成功。根据伯努利规则,起始原料沿聚合物链显示统计的N-乙酰基(N-Ac)分布,其中GlcNAc-GlcNAc二单元组的丰度最高,而三元组,四元组和五元组的丰度较低。 N-Ac基团之间的空间在N-磺基和/或N-羧甲基基团的均相反应中被填充,这也导致了伯努利统计分布。 N-取代反应具有最高的区域选择性和完全性,最多具有三个结合的不同官能团。 3-0-磺基的区域选择性通过几乎完全硫酸化的3,6-二-O-磺基壳聚糖的区域选择性6-脱硫而提高。通过脱硫反应,所有可能的中间体硫酸化产物都是可能的。也可以以最高的区域选择性和完整性引入6-0-磺基,并且许多部分6-脱硫的产物是可能的。

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