Jutamas Apisornopas, Patamawadee Silalai, Teerapich Kasemsuk, Anan Athipornchai, Uthaiwan Sirion, Kanoknetr Suksen, Pawinee Piyachaturawat, Apichart Suksamrarn, Rungnapha Saeeng
文献索引:10.1016/j.bmcl.2018.03.068
全文:HTML全文
New iridoid glycoside derivatives from durantoside I, the latter from the dried flowers and leaves of Citharexylum spinosum, were synthesized by variously modifying a sugar moiety by silylation or acetylation and/or removal of cinnamate group at C-7 position and subsequent screening for comparative cytotoxicity against several cancer cell lines. Addition of alkylsilane to durantoside I and removal of cinnamate group were most effective in improving cytotoxicity.
|
Design, synthesis, evaluation, and molecular docking of urso...
2018-04-11 [10.1016/j.bmcl.2018.04.021] |
|
Covalent inhibitors of nicotinamide N-methyltransferase (NNM...
2018-04-10 [10.1016/j.bmcl.2018.04.017] |
|
Valproic Acid Induces Three Novel Cytotoxic Secondary Metabo...
2018-04-10 [10.1016/j.bmcl.2018.04.018] |
|
Agonists of the γ-Aminobutyric Acid Type B (GABAB) Receptor ...
2018-04-07 [10.1016/j.bmcl.2018.04.003] |
|
Synthesis of 3-(3-hydroxyphenyl)pyrrolidine dopamine D3 rece...
2018-04-04 [10.1016/j.bmcl.2018.03.084] |
首页 |
期刊大全 |
MSDS查询 |
化工产品分类 |
生物活性化合物 |
关于我们 |
免责声明:知识产权问题请联系 service1@chemsrc.com
Copyright © 2026 ChemSrc All Rights Reserved