Aralkyl and aralkenyl glycosides as inhibitors of antigen-specific
T-cell proliferation
    7.
    发明授权
    Aralkyl and aralkenyl glycosides as inhibitors of antigen-specific T-cell proliferation 失效
    芳烷基和芳烯基糖苷作为抗原特异性T细胞增殖的抑制剂

    公开(公告)号:US4554349A

    公开(公告)日:1985-11-19

    申请号:US540594

    申请日:1983-10-11

    IPC分类号: C07H15/18 C07H5/06

    CPC分类号: C07H15/18

    摘要: The invention disclosed herein relates to novel 1-deoxyglycosides, preferably 1-deoxy-D-mannopyranosides and 1-deoxy-L-rhamnopyranosides, having in the 1-position of the pyranose ring an aralkylthio/aralkenylthio, aralkyloxy/aralkenyloxy or aralkanoylamino/aralkenoylamino substituent; and to novel processes for preparing these 1-substituted-1-deoxyglycosides starting with the corresponding tetra-O-acetylglycopyranosyl bromide or amine. The 6-hydroxy group of 1-substituted-1 deoxyglycopyranosides can also be replaced by other functional groups. These aralkylthio/aralkenylthio, aralkyloxy/aralkenyloxy and aralkanoylamino/aralkenoylamino 1-deoxyglycosides are potent inhibitors of antigen-specific T-cell proliferation and are also useful as inhibitors of delayed-type hypersensitivity reactions.

    摘要翻译: 本文公开的本发明涉及新的1-脱氧糖苷,优选1-脱氧-D-甘露吡喃糖苷和1-脱氧-L-鼠李糖吡喃糖苷,其在吡喃糖环的1-位具有芳烷硫基/芳烯基硫基,芳烷氧基/芳烯基氧基或芳烷酰氨基/芳烯基酰氨基 取代基; 以及由相应的四-O-乙酰基吡喃葡糖基溴或胺开始制备这些1-取代-1-脱氧糖苷的新方法。 1-取代-1脱氧吡喃糖苷的6-羟基也可以被其它官能团取代。 这些芳烷硫基/芳烯基硫基,芳烷氧基/芳烯基氧基和芳烷酰氨基/芳烯酰氨基-1-脱氧糖苷是抗原特异性T细胞增殖的有效抑制剂,也可用作延迟型超敏反应的抑制剂。

    1-Substituted glycopyranosides
    8.
    发明授权
    1-Substituted glycopyranosides 失效
    1-取代的吡喃糖苷

    公开(公告)号:US4228274A

    公开(公告)日:1980-10-14

    申请号:US922897

    申请日:1978-07-10

    CPC分类号: C07H13/04 C07H15/04 C07H15/14

    摘要: The invention disclosed herein relates to novel 1-deoxy-glycopyranosides, preferably 1-deoxy-D-mannopyranosides, having in the 1-position of the pyranoside ring an .omega.-aminoalkylthio, .omega.-aminoalkyloxy or .omega.-aminoalkanoylamino substituent; and to novel processes for preparing these 1-substituted-1-deoxy-glycopyranosides starting with the corresponding tetra-O-acetyl-glycopyranosyl bromide or amine. These .omega.-amino(alkylthio, alkyloxy or alkanoylamino)-1-deoxy-glycopyranosides, and in particular 1-[(6'-aminohexyl)thio or oxy]-1-deoxy-D-mannopyranosides, possess insulin-like activity.

    摘要翻译: 本文公开的本发明涉及在吡喃糖苷环的1位具有ω-氨基烷硫基,ω-氨基烷氧基或ω-氨基烷酰基氨基取代基的1-脱氧-D-甘露吡喃糖苷类的新型1-脱氧-D-吡喃甘露糖苷, 以及由相应的四-O-乙酰基 - 吡喃葡糖基溴或胺开始制备这些1-取代-1-脱氧 - 糖吡喃糖苷的新方法。 这些ω-氨基(烷硫基,烷氧基或烷酰氨基)-1-脱氧 - 糖吡喃糖苷,特别是1 - [(6'-氨基己基)硫代或氧基] -1-脱氧-D-甘露吡喃糖苷类,具有胰岛素样活性。