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3-脱氧-D-甘露-2-辛酮糖酸(Kdo)的C-(β-D-糖基)类似物的合成作为CMP-Kdo合成酶的潜在抑制剂

Synthesis of C-(beta-D-glycosyl) analogues of 3-deoxy-D-manno-2-octulosonic acid (Kdo) as potential inhibitors of CMP-Kdo synthetase.

作者信息

Wåglund T, Luthman K, Orbe M, Claesson A

机构信息

Department of Organic Pharmaceutical Chemistry, University of Uppsala, Sweden.

出版信息

Carbohydr Res. 1990 Oct 10;206(2):269-76. doi: 10.1016/0008-6215(90)80066-c.

DOI:10.1016/0008-6215(90)80066-c
PMID:1963573
Abstract

Eight C-(beta-D-glycosyl) analogues (14-21) of Kdo (3-deoxy-D-manno-2-octulosonic acid) were obtained from isopropylidene-protected ester precursors and tested in vitro for their inhibitory activity on CMP-Kdo synthetase. None had more than minor inhibitory activity.

摘要

从异亚丙基保护的酯前体中获得了8种Kdo(3-脱氧-D-甘露-2-辛酮糖酸)的C-(β-D-糖基)类似物(14-21),并在体外测试了它们对CMP-Kdo合成酶的抑制活性。没有一种具有超过轻微的抑制活性。

相似文献

1
Synthesis of C-(beta-D-glycosyl) analogues of 3-deoxy-D-manno-2-octulosonic acid (Kdo) as potential inhibitors of CMP-Kdo synthetase.3-脱氧-D-甘露-2-辛酮糖酸(Kdo)的C-(β-D-糖基)类似物的合成作为CMP-Kdo合成酶的潜在抑制剂
Carbohydr Res. 1990 Oct 10;206(2):269-76. doi: 10.1016/0008-6215(90)80066-c.
2
Synthesis of analogues of 3-deoxy-D-manno-octulosonic acid (KDO) as potential inhibitors of CMP-KDO synthetase.3-脱氧-D-甘露糖辛酮酸(KDO)类似物的合成作为CMP-KDO合成酶的潜在抑制剂
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Synthesis of a simplified transition-state analogue in an attempt to obtain an inhibitor of CMP-KDO synthetase.
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Synthesis of some C-8-modified 3-deoxy-beta-D-manno-2-octulosonic acid analogs as inhibitors of CMP-Kdo synthetase.
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Efficient Large Scale Syntheses of 3-Deoxy-D-manno-2-octulosonic acid (Kdo) and Its Derivatives.高效大规模合成 3-脱氧-D-甘露-2-辛酮酸(Kdo)及其衍生物。
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Stereoselective synthesis of the alpha-allyl C-glycoside of 3-deoxy-D-manno-2-octulosonic acid (KDO) by use of radical chemistry.利用自由基化学方法立体选择性合成3-脱氧-D-甘露-2-辛酮糖酸(KDO)的α-烯丙基碳苷。
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