Anti-cancer activity of carbamate derivatives of melampomagnolide B

被引:30
|
作者
Janganati, Venumadhav [1 ]
Penthala, Narsimha Reddy [1 ]
Madadi, Nikhil Reddy [1 ]
Chen, Zheng [1 ]
Crooks, Peter A. [1 ]
机构
[1] Univ Arkansas Med Sci, Dept Pharmaceut Sci, Coll Pharm, Little Rock, AR 72205 USA
关键词
Parthenolide; Melampomagnolide B; Anti-cancer activity; Carbamates; Heterocyclic amines; NF-KAPPA-B; SESQUITERPENE LACTONE PARTHENOLIDE; MYELOGENOUS LEUKEMIA STEM; ACUTE MYELOID-LEUKEMIA; IN-VITRO; PROGENITOR CELLS; APOPTOSIS; ACTIVATION; DISCOVERY; CARCINOMA;
D O I
10.1016/j.bmcl.2014.05.059
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Melampomagnolide B (MMB) is a natural sesquiterpene structurally related to parthenolide (PTL). We have shown that MMB exhibits anti-leukemic properties similar to PTL. Unlike PTL, the presence of a primary hydroxyl group in the MMB molecule allows the opportunity for examining the biological activity of a variety of conjugated analogs of MMB. We have now synthesized a series of carbamate analogs of MMB and evaluated these derivatives for anti-cancer activity against a panel of sixty human cancer cell lines. Analogs 6a and 6e exhibited promising anti-leukemic activity against human leukemia cell line CCRF-CEM with GI(50) values of 680 and 620 nM, respectively. Analog 6a also showed GI(50) values of 1.98 and 1.38 mu M respectively, against RPMI-8226 and SR leukemia cell lines and GI(50) values of 460 and 570 nM against MDA-MB-435 melanoma and MDA-MB-468 breast cancer cell lines, respectively. Analog 6e had GI(50) values of 650 and 900 nM against HOP-92 non-small cell lung and RXF 393 renal cancer cell lines. (C) 2014 Published by Elsevier Ltd.
引用
收藏
页码:3499 / 3502
页数:4
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