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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.
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页码:1069 / 1073
页数:5
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