TMC-86A, B and TMC-96, new proteasome inhibitors from Streptomyces sp TC 1084 and Saccharothrix sp TC 1094 II. Physico-chemical properties and structure determination

Koguchi Y.; Suzuki S.; Nishio M.; Takahashi K.; Ohnuki T. Komatsubara S.; Kohno J.

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TMC-86A, B and TMC-96, new proteasome inhibitors from Streptomyces sp TC 1084 and Saccharothrix sp TC 1094 II. Physico-chemical properties and structure determination

机译：TMC-86A，B和TMC-96，来自链霉菌属TC 1084和糖酵母属TC 1094 II的新型蛋白酶体抑制剂。理化性质和结构测定

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来源
《The Journal of Antibiotics: An International Journal》 |2000年第1期|共3页
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Koguchi Y.; Suzuki S.; Nishio M.; Takahashi K.; Ohnuki T. Komatsubara S.; Kohno J.;
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正文语种 eng
中图分类药学;药品;
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1. TMC-86A, B and TMC-96, new proteasome inhibitors from Streptomyces sp TC 1084 and Saccharothrix sp TC 1094 II. Physico-chemical properties and structure determination [J] . Koguchi Y., Suzuki S., Nishio M., The Journal of Antibiotics: An International Journal . 2000,第1期

机译：TMC-86A，B和TMC-96，来自链霉菌属TC 1084和糖酵母属TC 1094 II的新型蛋白酶体抑制剂。理化性质和结构测定
2. A-94964, novel inhibitor of bacterial translocase I, produced by Streptomyces sp. SANK 60404. II. Physico-chemical properties and structure elucidation. [J] . Fujita Y, Murakami R, Muramatsu Y, The Journal of Antibiotics: An International Journal . 2008,第9期

机译：A-94964，一种由细菌链霉菌属产生的新型细菌转座酶I抑制剂。 SANK 60404。理化性质和结构阐明。
3. A-94964, novel inhibitor of bacterial translocase I, produced by Streptomyces sp. SANK 60404. II. Physico-chemical properties and structure elucidation. [J] . Fujita Y, Murakami R, Muramatsu Y, The Journal of Antibiotics: An International Journal . 2008,第9期

机译：A-94964，由Streptomyces SP产生的细菌易位酶I的新型抑制剂。 SANK 60404.II。物理化学性质和结构阐明。
4. The Effect of (Non)-covalent Interactions of Small Inhibitors on the Structure of Agrobacterium sp. strain ATCC 21400 (Abg) β-glucosidase [C] . Negar Rajabi, Donald J. Douglas American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics . 2012

机译：小抑制剂对SP杆菌结构结构的（非） - 共价相互作用的影响。菌株ATCC 21400（ABG）β-葡糖苷酶
5. The Design and Synthesis of Novel Proteasome Inhibitors: Studies on the Synthesis of Nagelamide M and Analogs, the Synthesis of Rapamycin Based Proteasome Inhibitors, and the Synthesis of TCH Based Molecular Probes for Binding Site Determination. [D] . Giletto, Matthew Basil. 2017

机译：新型蛋白酶体抑制剂的设计与合成：Nagelamide M和类似物的合成，雷帕霉素基蛋白酶体抑制剂的合成以及TCH基分子探针的结合位点测定的研究。
6. Prediction and Fourier-transform infrared-spectroscopy estimation of the secondary structure of a recombinant beta-glucosidase from Streptomyces sp. (ATCC 11238). [O] . J A Perez-Pons, E Padros, E Querol 1995

机译：链霉菌重组β-葡萄糖苷酶二级结构的预测和傅里叶变换红外光谱估计。（ATCC 11238）。
7. TMC-86A, B and TMC-96, New Proteasome Inhibitors from Streptomyces sp. TC 1084 and Saccharothrix sp. TC 1094. II. Physico-chemical Properties and Structure Determination. [O] . YUTAKA KOGUCHI, JUN KOHNO, SFFLN-ICHI SUZUKI, 2000

机译：TMC-86A，B和TMC-96，来自Streptomyces SP的新蛋白酶体抑制剂。 TC 1084和Saccharothrix sp。 TC 1094.II。物理化学性质和结构测定。

TMC-86A, B and TMC-96, new proteasome inhibitors from Streptomyces sp TC 1084 and Saccharothrix sp TC 1094 II. Physico-chemical properties and structure determination

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