Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)-alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131.
Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)-alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131.
复制标题
[L-Arg-L/D-3-(2-萘基)-丙氨酸]-型(E)-烯烃二肽电子等排体的立体选择性合成及其在CXCR4拮抗剂FC131的伪肽类似物的合成和生物学评价中的应用。
DOI:
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发表时间:
2005
期刊:
影响因子:
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通讯作者:
H.Tamamura
中科院分区:
文献类型:
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作者:
Xu G;Kanezaki R;Toki T;Watanabe S;Takahashi Y;Terui K;Kitabayashi I;Ito E.;Tanioka T. et al.;A.Niida;H.Tamamura