发明名称 SPHINGOSINE ANALOGUES
摘要 <p>The present invention aims to provide a novel sphingosine analogue, which is useful as an intermediate for syntheses of novel lipid derivatives such as sphingolipid derivatives and the like that can regulate the effects of sphingolipid. The present invention relates to a sphingosine analogue represented by the general formula (I) described below. <CHEM> In the formula, as for Q<1>, Q<2> and Q<3>, Q<1> and Q<2>, which are the same or different each other, are hydrogen, alkyl groups having 1-4 of carbon atoms, acyl groups having 2-5 of carbon atoms, or protecting groups of the amino group, and Q<3> is a hydrogen or a protecting group of the hydroxyl group; or Q<2> and Q<3> make up an isopropylidene group and Q<1> is a hydrogen or a protecting group of the amino group. Q<4> and Q<5>, which are the same or different each other, are hydroxyl groups, acyl groups having 2-5 of carbon atoms, -O-Q<6>, or hydrogen; or Q<4> and Q<5> make up a covalent bond. Q<6> is a protecting group of the hydroxyl group. X<1> is -COOH, -CONH2, -CO-Q<7>, -CH2OH, or -CH2O-Q<8>. Q<7> is a protecting group of the carboxyl group, and Q<8> is a protecting group of the hydroxyl group.</p>
申请公布号 EP1002790(A1) 申请公布日期 2000.05.24
申请号 EP19980907195 申请日期 1998.03.12
申请人 TAKARA SHUZO CO, LTD. 发明人 TAKESAKO, KAZUTOH;KUROME, TORU;AWAZU, NAOYUKI;KATO, IKUNOSHIN
分类号 C07C215/10;C07C215/24;C07C229/22;C07C229/30;C07C237/08;C07C237/22;C07C251/08;C07C271/22;C07D263/06;C07D307/33;(IPC1-7):C07C215/10 主分类号 C07C215/10
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