<p>Comparison of the inhibitory activities of PBZ on HDACs 5, 6. and 9 with those for TSA and SAHA.</p
We have screened our compound collection in an established cell based assay that mea-sures the derep...
<p>Fadu, Cal-27 and Hep-2 cells were exposed to different concentrations ofDHA, AZD1480 and AG490 or...
<p>Correlation between activity inhibition and IF studies of compounds (1), (2), (3) and (4) on hTS....
<p>Dose response curves of <b>9a-9d</b> comparative inhibition of HDAC6 vs. HDAC1 activity using pur...
<p>(A) % inhibition of human recombinant Class I enzymes HDAC1 (red), HDAC2 (green), HDAC3 (black) a...
<p>Panobinostat, trichostatin A, and SAHA are pan-isoform inhibitors. Entinostat is a class I select...
<p>(A) Screening of cell free supernatants (CFS) from 79 bacterial strains for total HDAC inhibition...
Butyric acid and trichostatin A (TSA) are anti-cancer compounds that cause the upregulation of genes...
<p>(A) Inhibition of HDACs activity in HeLa nuclear extracts. Data were expressed as the mean of at ...
<p>(A) Nuclear extracts from NIH3T3 cells, treated with the inhibitor PJ34 (5 μM) for 1 h, and assay...
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...
<p>Hela nuclear extract was used as a source of class I and II HDAC activity (<b>Panel A</b>) where ...
The CDNB activities were measured with concentrations of the substrates GSH and CDNB at 1 mM, while ...
Screening of Anti-KSHV+ lymphoma activities of newly synthesized HDACs/BRD4 dual inhibitors.</p
Butyric acid and trichostatin A (TSA) are anti-cancer compounds that cause the upregulation of genes...
We have screened our compound collection in an established cell based assay that mea-sures the derep...
<p>Fadu, Cal-27 and Hep-2 cells were exposed to different concentrations ofDHA, AZD1480 and AG490 or...
<p>Correlation between activity inhibition and IF studies of compounds (1), (2), (3) and (4) on hTS....
<p>Dose response curves of <b>9a-9d</b> comparative inhibition of HDAC6 vs. HDAC1 activity using pur...
<p>(A) % inhibition of human recombinant Class I enzymes HDAC1 (red), HDAC2 (green), HDAC3 (black) a...
<p>Panobinostat, trichostatin A, and SAHA are pan-isoform inhibitors. Entinostat is a class I select...
<p>(A) Screening of cell free supernatants (CFS) from 79 bacterial strains for total HDAC inhibition...
Butyric acid and trichostatin A (TSA) are anti-cancer compounds that cause the upregulation of genes...
<p>(A) Inhibition of HDACs activity in HeLa nuclear extracts. Data were expressed as the mean of at ...
<p>(A) Nuclear extracts from NIH3T3 cells, treated with the inhibitor PJ34 (5 μM) for 1 h, and assay...
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...
<p>Hela nuclear extract was used as a source of class I and II HDAC activity (<b>Panel A</b>) where ...
The CDNB activities were measured with concentrations of the substrates GSH and CDNB at 1 mM, while ...
Screening of Anti-KSHV+ lymphoma activities of newly synthesized HDACs/BRD4 dual inhibitors.</p
Butyric acid and trichostatin A (TSA) are anti-cancer compounds that cause the upregulation of genes...
We have screened our compound collection in an established cell based assay that mea-sures the derep...
<p>Fadu, Cal-27 and Hep-2 cells were exposed to different concentrations ofDHA, AZD1480 and AG490 or...
<p>Correlation between activity inhibition and IF studies of compounds (1), (2), (3) and (4) on hTS....
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