Type and position of linkage govern the cytotoxicity of oleanolic acid rhodamine B hybrids

被引:10
作者
Heise, Niels [1 ]
Hoenke, Sophie [1 ]
Simon, Vivienne [1 ]
Deigner, Hans-Peter [2 ]
Al-Harrasi, Ahmed [3 ]
Csuk, Rene [1 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Organ Chem, Kurt Mothes Str 2, D-06120 Halle, Saale, Germany
[2] Furtwangen Univ, Med & Life Sci Fac, Jakob Kienzle Str 17, D-78054 Villingen Schwenning, Germany
[3] Univ Nizwa, Chair Omans Med Plants & Marine Nat Prod, POB 33, Birkat Al Manz 616, Nizwa, Oman
关键词
Oleanolic acid; Rhodamine B; Hybrids; Cytotoxicity; TRITERPENE CARBOXYLIC-ACID; INHIBITORY-ACTIVITY; BETULINIC ACID; ANTITUMOR; DERIVATIVES; NITRODERIVATIVES;
D O I
10.1016/j.steroids.2021.108876
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oleanolic acid/rhodamine B hybrids exhibit different cytotoxicity depending on the way these two structural elements are linked. While a hybrid holding a piperazinyl spacer at C-28 proved to be cytotoxic in the nano-molar concentration range, hybrids with a direct linkage of the Rho B residue to C-3 of the triterpenoid skeleton are cytotoxic only in the low micro-molar concentration range without any selectivity. This once again underlines the importance of selecting the right spacer and the most appropriate position on the skeleton of the triterpene to achieve the most cytotoxic hybrids possible.
引用
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页数:7
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