Synthesis and Cytotoxicity of Semisynthetic Withalongolide A Analogues

被引:16
作者
Motiwala, Hashim F. [1 ]
Bazzill, Joseph [2 ]
Samadi, Abbas [3 ]
Zhang, Huaping [4 ]
Timmermann, Barbara N. [4 ]
Cohen, Mark S. [2 ]
Aube, Jeffrey [1 ]
机构
[1] Univ Kansas, Dept Med Chem, Del Shankel Struct Biol Ctr, Lawrence, KS 66047 USA
[2] Univ Michigan Hosp & Hlth Syst, Dept Surg, Div Endocrine Surg, Ann Arbor, MI 48109 USA
[3] Univ Kansas, Med Ctr, Sch Med, Dept Pharmacol, Kansas City, KS 66160 USA
[4] Univ Kansas, Sch Pharm, Dept Med Chem, Lawrence, KS 66045 USA
关键词
Withalongolide A; withaferin A; triacetate; jaborosalactone; macrocycle; DRO81-1; WITHANIA-SOMNIFERA; WITHANOLIDES; WITHAFERIN; ACID;
D O I
10.1021/ml400267q
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The natural product withaferin A exhibits potent antitumor activity and other diverse pharmacological activities. The recently discovered withalongolide A, a C-19 hydroxylated congener of withaferin A, was recently reported to possess cytotoxic activity against head and neck squamous cell carcinomas. Semisynthetic acetylated analogues of withalongolide A were shown to be considerably more cytotoxic than the parent compound. To further explore the structure activity relationships, 20 new semisynthetic analogues of withalongolide A were synthesized and evaluated for cytotoxic activity against four different cancer cell lines. A number of derivatives were found to be more potent than the parent compound and withaferin A.
引用
收藏
页码:1069 / 1073
页数:5
相关论文
共 33 条
[11]  
ISHIGURO M, 1974, TETRAHEDRON LETT, P1421
[12]   REDUCTIVE ELIMINATION OF VICINAL OXYGEN FUNCTIONS WITH PALLADIUM(0) - APPLICATIONS IN THE WITHANOLIDE SERIES [J].
KEINAN, E ;
SAHAI, M ;
KIRSON, I .
JOURNAL OF ORGANIC CHEMISTRY, 1983, 48 (15) :2550-2555
[13]  
Khan ZA, 2010, J MED PLANTS RES, V4, P490
[14]   A convenient protocol for the α-iodination of α,β-unsaturated carbonyl compounds with I2 in an aqueous medium [J].
Krafft, ME ;
Cran, JW .
SYNLETT, 2005, (08) :1263-1266
[15]   New cytotoxic withanolides from Physalis peruviana [J].
Lan, Yu-Hsuan ;
Chang, Fang-Rong ;
Pan, Mei-Jung ;
Wu, Chin-Chung ;
Wu, Shu-Jing ;
Chen, Su-Li ;
Wang, Shyh-Shyan ;
Wu, Ming-Jung ;
Wu, Yang-Chang .
FOOD CHEMISTRY, 2009, 116 (02) :462-469
[16]   Barrier protective effects of withaferin A in HMGB1-induced inflammatory responses in both cellular and animal models [J].
Lee, Wonhwa ;
Kim, Tae Hoon ;
Ku, Sae-Kwang ;
Min, Kyoung-jin ;
Lee, Hyun-Shik ;
Kwon, Taeg Kyu ;
Bae, Jong-Sup .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2012, 262 (01) :91-98
[17]   Withanolides from Withania aristata and their cytotoxic activity [J].
LLanos, Gabriel G. ;
Araujo, Liliana M. ;
Jimenez, Ignacio A. ;
Moujir, Laila M. ;
Vazquez, Jesus T. ;
Bazzocchi, Isabel L. .
STEROIDS, 2010, 75 (12) :974-981
[18]   Antiproliferative Activity of Withanolides against Human Breast Cancer Cell Lines [J].
Machin, Ruben P. ;
Veleiro, Adriana S. ;
Nicotra, Viviana E. ;
Oberti, Juan C. ;
Padron, Jose M. .
JOURNAL OF NATURAL PRODUCTS, 2010, 73 (05) :966-968
[19]   Biaryl-Bridged Macrocyclic Peptides: Conformational Constraint via Carbogenic Fusion of Natural Amino Acid Side Chains [J].
Meyer, Falco-Magnus ;
Collins, James C. ;
Borin, Brendan ;
Bradow, James ;
Liras, Spiros ;
Limberakis, Chris ;
Mathiowetz, Alan M. ;
Philippe, Laurence ;
Price, David ;
Song, Kun ;
James, Keith .
JOURNAL OF ORGANIC CHEMISTRY, 2012, 77 (07) :3099-3114
[20]   New 19-hydroxywithanolides from Jaborosa leucotricha [J].
Misico, RI ;
Oberti, JC ;
Veleiro, AS ;
Burton, G .
JOURNAL OF NATURAL PRODUCTS, 1996, 59 (01) :66-68