It is an object of the present invention to synthesize a carba cyclic phosphatidic acid derivative having a novel structure by substituting O at position sn-2 of the glycerol skeleton with CH
2
, and study the action of the obtained derivative to suppress cancer cell invasion. The present invention provides a compound represented by the following formula (I):
wherein R represents a linear or branched alkyl group containing 1 to 30 carbon atoms, a linear or branched alkenyl group containing 2 to 30 carbon atoms, or a linear or branched alkynyl group containing 2 to 30 carbon atoms, wherein these groups may comprise a cycloalkane ring or aromatic ring; and M represents a hydrogen atom or counter cation.
本发明的目的是通过将
甘油骨架上sn-2位置的O替换为
CH2来合成具有新结构的碳环
磷脂酸衍
生物,并研究所得衍
生物抑制癌细胞侵袭的作用。本发明提供了以下式子(I)所表示的化合物:
其中,R代表1到30个碳原子的线性或支链烷基、2到30个碳原子的线性或支链烯基,或2到30个碳原子的线性或支链炔基,这些基团可能包括环烷基或芳香环;M代表氢原子或计数阳离子。