公开(公告)号：EP0532026A3

公开(公告)日：1993-10-06

申请号：EP92115574.3

申请日：1992-09-11

申请人： DAINIPPON INK AND CHEMICALS, INC.

发明人： Tadao, Shoji ,  Takahashi, Nahoko ,  Ikushima, Naoya ,  Uryu, Toshiyuki ,  Yoshida, Takashi ,  Yamamoto, Naoki ,  Nakashima, Hideki ,  Katsuraya, Kaname ,  Adachi, Koichiro ,  Kataoka, Fusayo

IPC分类号： C07H15/203 ,  A61K31/70 ,  C08B37/00 ,  A61K31/72

CPC分类号： C07H15/203 ,  C08B37/006

摘要： A oligosaccharide aromatic glycoside sulfate or a physiologically acceptable salt of the same which is formed from same or different monosaccharides bonded by glycoside bonds, wherein the hydrogen atom in the hydroxyl group at the position-1 carbon atom at the terminal of the oligosaccharide is substituted with a group represented by Formula (I):
        - Y - (O) n - R   (I)
(in the formula, R represents an alkyl group having 1-18 carbon atoms, n is 0 or 1, O represents an oxygen atom, and Y represents an allylene group) and at least 10% of the remaining hydroxyl groups of the sugar subunits have been subjected to sulfated esterification; an anti-viral agent containing this oligosaccharide aromatic glycoside sulfate or physiologically acceptable salt of the same as an active component; and a oligosaccharide aromatic glycoside which functions as a production intermediate are disclosed. The anti-viral agent exhibits low toxicity and superior anti-viral activity, and is especially effective against viruses which are known to cause AIDS.

公开(公告)号：EP0532026A2

公开(公告)日：1993-03-17

申请号：EP92115574.3

申请日：1992-09-11

申请人： DAINIPPON INK AND CHEMICALS, INC.

发明人： Tadao, Shoji ,  Takahashi, Nahoko ,  Ikushima, Naoya ,  Uryu, Toshiyuki ,  Yoshida, Takashi ,  Yamamoto, Naoki ,  Nakashima, Hideki ,  Katsuraya, Kaname ,  Adachi, Koichiro ,  Kataoka, Fusayo

IPC分类号： C07H15/203 ,  A61K31/70 ,  C08B37/00 ,  A61K31/72

CPC分类号： C07H15/203 ,  C08B37/006

摘要： A oligosaccharide aromatic glycoside sulfate or a physiologically acceptable salt of the same which is formed from same or different monosaccharides bonded by glycoside bonds, wherein the hydrogen atom in the hydroxyl group at the position-1 carbon atom at the terminal of the oligosaccharide is substituted with a group represented by Formula (I):



        - Y - (O) n - R   (I)



(in the formula, R represents an alkyl group having 1-18 carbon atoms, n is 0 or 1, O represents an oxygen atom, and Y represents an allylene group) and at least 10% of the remaining hydroxyl groups of the sugar subunits have been subjected to sulfated esterification; an anti-viral agent containing this oligosaccharide aromatic glycoside sulfate or physiologically acceptable salt of the same as an active component; and a oligosaccharide aromatic glycoside which functions as a production intermediate are disclosed. The anti-viral agent exhibits low toxicity and superior anti-viral activity, and is especially effective against viruses which are known to cause AIDS.

摘要翻译： 由通过糖苷键键合的相同或不同的单糖形成的寡糖芳香糖苷硫酸盐或其生理学上可接受的盐，其中寡糖末端的位置-1个碳原子上的羟基中的氢原子被 式（I）表示的基团：-Y - （O）n -R（I>（式中，R表示碳原子数1〜18的烷基，n表示0或1，O表示氧原子， Y表示烯丙基），并且将糖亚基的剩余羟基中的至少10％进行硫酸酯化反应，含有该寡糖芳香族糖苷硫酸盐的抗病毒剂或与活性成分相同的生理学上可接受的盐 ;和作为生产中间体发挥作用的寡糖芳香糖苷，抗病毒剂具有低毒性和优良的抗病毒活性，特别有效对抗 已知导致艾滋病的病毒。