Biochem J : 15— FEBS Lett : — Other methods Protein concentrations were determined by the method of Bradford [ 45 ] using BSA as a standard. The entrapment of inhibitory MgADP at catalytic sites terminates catalysis. Support Center Support Center. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. Biophys J 98 : — Tyler N. Mitochondrial respiratory activity was quantified by spectrophotometry as described previously [ 7 ] and cellular survival expressed as a percentage relative to the corrected control values.
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ε Subunit of Bacillus subtilis F1ATPase Relieves MgADP Inhibition
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Nat Rev Mol Cell Biol 2 : — Nat Struct Mol Biol 18 : — The spectroscopic and spectrometric data of 2 were nearly identical to those of 1. Anticancer potential of silymarin: From bench to bed side.
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The following day, stock solutions of pure compounds were prepared in DMSO. Davis-Searles PR, Nakanishi Y, Kim NC, Graf TN, Oberlies NH, Wani MC, Wall.
Figure S2: Enlargement of the part of Figure 4. Compounds 1 and 2 were isolated from a pool of these fractions.
Experiments using B.
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Cancer Lett. Figure 3. Acknowledgments We thank Professor F.
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In contrast, its ability to attenuate MgADP inhibition may be its primary role in the regulatory system.
The entrapment of inhibitory MgADP at catalytic sites terminates catalysis. Figure S2 Enlargement of the part of Figure 4.
Isosilibinin inhibits advanced human prostate cancer growth in athymic nude mice: comparison with silymarin and silibinin.
The ATP concentrations are indicated in the figure.
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|Mitochondrial respiratory activity was quantified by spectrophotometry as described previously [ 7 ] and cellular survival expressed as a percentage relative to the corrected control values.
Cancer Lett. In the process of isolating gram quantities of isosilybin B 6which retained the longest on RP-HPLC of the seven major flavonolignan diastereoisomers [ 1 ], numerous fractions were obtained that contained minor compounds that eluted after 6. IC 50 values of compounds against three human prostate cancer cell lines. This article has been cited by other articles in PMC.