Laursen Jane B, Petersen Lars, Jensen Knud J, Nielsen John
Department of Chemistry, The Royal Veterinary and Agricultural University DK-1871 Frederiksberg C, Denmark.
Org Biomol Chem. 2003 Sep 21;1(18):3147-53. doi: 10.1039/b306789k.
Inspired by the occurrence and function of phenazines in natural products, new glycosylated analogs were designed and synthesized. DISAL (methyl 3,5-dinitrosalicylate) glycosyl donors were used in an efficient and easily-handled glycosylation protocol compatible with combinatorial chemistry. Benzoylated D-glucose, D-galactose and L-quinovose DISAL glycosyl donors were synthesized in high yields and used under mild conditions to glycosylate methyl saphenate and 2-hydroxyphenazine. The glycosides were screened for biological activity and one compound showed inhibitory activity towards topoisomerase II.
受天然产物中吩嗪的出现和功能启发,设计并合成了新的糖基化类似物。3,5-二硝基水杨酸甲酯(DISAL)糖基供体用于一种与组合化学兼容的高效且易于操作的糖基化方案。高产率合成了苯甲酰化的D-葡萄糖、D-半乳糖和L-鸡纳糖DISAL糖基供体,并在温和条件下用于使马钱子酸甲酯和2-羟基吩嗪糖基化。对这些糖苷进行了生物活性筛选,其中一种化合物表现出对拓扑异构酶II的抑制活性。