New Mandelalides Expand a Macrolide Series of Mitochondrial Inhibitors.
New Mandelalides Expand a Macrolide Series of Mitochondrial Inhibitors.
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新的曼德拉内酯扩展了大环内酯系列线粒体抑制剂。
DOI:
10.1021/acs.jmedchem.7b00990
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发表时间:
2017
影响因子:
7.3
通讯作者:
McPhail,KerryL
中科院分区:
文献类型:
--
作者:
Nazari,Mohamad;Serrill,JeffreyD;Wan,Xuemei;Nguyen,MinhH;Anklin,Clemens;Gallegos,DavidA;Smith3rd,AmosB;Ishmael,JaneE;McPhail,KerryL
Mandelalides A–D (1–4) are macrocyclic polyketides known to have an unusual bioactivity profile influenced by compound glycosylation and growth phase of cultured cells. The isolation and characterization of additional natural congeners, mandelalides E–L (5–12), and the supply of synthetic compounds1and12, as well asseco-mandelalide A methyl ester (13), have now facilitated mechanism of action and structure–activity relationship studies. Glycosylated mandelalides are effective inhibitors of aerobic respiration in living cells. Macrolides1and2inhibit mitochondrial function similar to oligomycin A and apoptolidin A, selective inhibitors of the mammalian ATP synthase (complex V).1inhibits ATP synthase activity from isolated mitochondria and triggers caspase-dependent apoptosis in HeLa cells, which are more sensitive to inhibition by1in the presence of the glycolysis inhibitor 2-deoxyglucose. Thus, mandelalide cytotoxicity depends on basal metabolic phenotype; cells with an oxidative phenotype are most likely to be inhibited by the mandelalides.
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影响因子:
7.7
作者:
Young JD
通讯作者:
Young JD
影响因子:
4.3
作者:
Bruetsch, Tobias Michael;Bucher, Pascal;Altmann, Karl-Heinz
通讯作者:
Altmann, Karl-Heinz
DOI:
--
发表时间:
2000
期刊:
The Journal of pharmacology and experimental therapeutics.
影响因子:
--
作者:
Kuh,HJ;Jang,SH;Wientjes,MG;Au,JL
通讯作者:
Au,JL
影响因子:
16.6
作者:
DeGuire, Sean M.;Earl, David C.;Du, Yu;Crews, Brenda A.;Jacobs, Aaron T.;Ustione, Alessandro;Daniel, Cristina;Chong, Katherine M.;Marnett, Lawrence J.;Piston, David W.;Bachmann, Brian O.;Sulikowski, Gary A.
通讯作者:
Sulikowski, Gary A.
DOI:
10.1073/pnas.0400051101
发表时间:
2004-04-20
影响因子:
11.1
作者:
Jensen, R;Glazer, PM
通讯作者:
Glazer, PM