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Synthesis and biological evaluation of novel exo-methylene cyclopentanone tetracyclic diterpenoids as antitumor agents

โœ Scribed by Jing Li; Dayong Zhang; Xiaoming Wu


Book ID
104005128
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
451 KB
Volume
21
Category
Article
ISSN
0960-894X

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โœฆ Synopsis


The structure of exo-methylene cyclopentanone, which exists in nature tetracyclic diterpenoids products, has been proved to be an innate group for the treatment of cancer and inflammation. In this letter, four different scaffolds of tetracyclic diterpenoids including the structure exo-methylene cyclopentanone were synthesized from steviol and isosteviol and evaluated in vitro for their antitumor activity against three human cancer lines. Compounds 1a, 1b, 2b and 3b showed significant cytotoxicity, particularly, tetracyclic diterpenoids 2b, 3b were identified as the most potent and selective anticancer agents superior to adriamycin with IC(50) values of 0.9 ฮผM and 1.5 ฮผM, against Hep-G2 and MDA-MB-231 cell lines, respectively.


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โœ A. Srinivas; A. Nagaraj; Ch. Sanjeeva Reddy ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› Journal of Heterocyclic Chemistry ๐ŸŒ English โš– 299 KB ๐Ÿ‘ 1 views

## Abstract magnified image In a one pot procedure, a series of novel methyleneโ€bisโ€thiazolidinone derivatives **5** and **6** was prepared by condensation of 5โ€(3โ€formylโ€4โ€methoxybenzyl)โ€2โ€methoxybenzaldehyde **3** with mercapto acids and primary aromatic amines **4** in presence of ZnCl~2~ under