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Chemical modification of reveromycin A and its biological activities.

作者信息

Shimizu Takeshi, Usui Takeo, Machida Kiyotaka, Furuya Kouichi, Osada Hiroyuki, Nakata Tadashi

机构信息

Synthetic Organic Chemistry Laboratory, RIKEN (The Institute of Physical and Chemical Research), Wako, Saitama, Japan.

出版信息

Bioorg Med Chem Lett. 2002 Dec 2;12(23):3363-6. doi: 10.1016/s0960-894x(02)00782-5.

DOI:10.1016/s0960-894x(02)00782-5
PMID:12419362
Abstract

Various derivatives of reveromycin A, a novel inhibitor of eukaryotic cell growth, were prepared and their inhibitory effects on both isoleucyl-tRNA synthetase activity and in vitro protein synthesis, and activities on the morphological reversion of src(ts)-NRK cells were assayed. The C5 hydroxyl group and C24 carboxyl group are particularly important for these activities.

摘要

相似文献

1
Chemical modification of reveromycin A and its biological activities.
Bioorg Med Chem Lett. 2002 Dec 2;12(23):3363-6. doi: 10.1016/s0960-894x(02)00782-5.
2
Synthesis and biological activities of reveromycin A and spirofungin A derivatives.瑞弗霉素A和螺旋真菌素A衍生物的合成及生物活性
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3
Structure-function analyses of cytochrome P450revI involved in reveromycin A biosynthesis and evaluation of the biological activity of its substrate, reveromycin T.参与瑞弗霉素A生物合成的细胞色素P450revI的结构-功能分析及其底物瑞弗霉素T的生物活性评估。
J Biol Chem. 2014 Nov 21;289(47):32446-58. doi: 10.1074/jbc.M114.598391. Epub 2014 Sep 25.
4
Reveromycin A, a new antibiotic which inhibits the mitogenic activity of epidermal growth factor.瑞弗霉素A,一种抑制表皮生长因子促有丝分裂活性的新型抗生素。
J Antibiot (Tokyo). 1991 Feb;44(2):259-61. doi: 10.7164/antibiotics.44.259.
5
Reveromycins, new inhibitors of eukaryotic cell growth. II. Biological activities.瑞威霉素,新型真核细胞生长抑制剂。II. 生物活性。
J Antibiot (Tokyo). 1992 Sep;45(9):1414-9. doi: 10.7164/antibiotics.45.1414.
6
Chemical and biological studies of reveromycin A.瑞弗霉素A的化学与生物学研究
J Antibiot (Tokyo). 2016 Oct;69(10):723-730. doi: 10.1038/ja.2016.57. Epub 2016 Jun 8.
7
Identification of Saccharomyces cerevisiae isoleucyl-tRNA synthetase as a target of the G1-specific inhibitor Reveromycin A.
J Biol Chem. 2002 Aug 9;277(32):28810-4. doi: 10.1074/jbc.M203827200. Epub 2002 Jun 5.
8
Reveromycins, new inhibitors of eukaryotic cell growth. I. Producing organism, fermentation, isolation and physico-chemical properties.
J Antibiot (Tokyo). 1992 Sep;45(9):1409-13. doi: 10.7164/antibiotics.45.1409.
9
Enantioselective synthesis of the [6,6] spiroketal core of reveromycin A.瑞弗霉素A的[6,6]螺环缩酮核心的对映选择性合成。
Org Lett. 2000 Jan 27;2(2):207-10. doi: 10.1021/ol991290v.
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Design and synthesis of spiro[indole-thiazolidine]spiro[indole-pyrans] as antimicrobial agents.设计和合成螺[吲哚-噻唑烷]螺[吲哚-吡喃]作为抗菌剂。
Bioorg Med Chem Lett. 2011 Sep 15;21(18):5465-9. doi: 10.1016/j.bmcl.2011.06.121. Epub 2011 Jul 2.

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Biosynthesis of reveromycin derivatives by altering the regioselectivity of cytochrome P450revI.通过改变细胞色素P450revI的区域选择性来生物合成瑞弗霉素衍生物。
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Studies on Streptomyces sp. SN-593: reveromycin biosynthesis, β-carboline biomediator activating LuxR family regulator, and construction of terpenoid biosynthetic platform.链霉菌 SN-593 的研究:雷沃霉素生物合成、β-咔啉生物调节剂激活 LuxR 家族调控因子,以及萜类生物合成平台的构建。
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Inhibitory mechanism of reveromycin A at the tRNA binding site of a class I synthetase.
reveromycin A 在 I 类合成酶的 tRNA 结合位点的抑制机制。
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Chemical and biological studies of reveromycin A.瑞弗霉素A的化学与生物学研究
J Antibiot (Tokyo). 2016 Oct;69(10):723-730. doi: 10.1038/ja.2016.57. Epub 2016 Jun 8.
6
Structure-function analyses of cytochrome P450revI involved in reveromycin A biosynthesis and evaluation of the biological activity of its substrate, reveromycin T.参与瑞弗霉素A生物合成的细胞色素P450revI的结构-功能分析及其底物瑞弗霉素T的生物活性评估。
J Biol Chem. 2014 Nov 21;289(47):32446-58. doi: 10.1074/jbc.M114.598391. Epub 2014 Sep 25.
7
Asymmetric synthesis of naturally occurring spiroketals.天然存在的螺环缩酮的不对称合成。
Molecules. 2008 Aug 28;13(8):1942-2038. doi: 10.3390/molecules13081942.