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MedChemExpress psb 603
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
Psb 603, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Tocris psb603
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
Psb603, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Tocris psb 603
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
Psb 603, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Tocris a2br antagonist 8
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
A2br Antagonist 8, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TargetMol psb-603
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
Psb 603, supplied by TargetMol, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TargetMol psb 603
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
Psb 603, supplied by TargetMol, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
Tocris chlorophenzyl piperazide 1 sulfonyl phenyl 1 propylxanthine
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
Chlorophenzyl Piperazide 1 Sulfonyl Phenyl 1 Propylxanthine, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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psb  (Tocris)
94
Tocris psb
Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C <t>),</t> <t>PSB-603</t> for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.
Psb, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C ), PSB-603 for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.

Journal: Scientific Reports

Article Title: Synergistic effects of HDAC inhibitor tucidinostat and ENT inhibitor dipyridamole in T-cell malignancies

doi: 10.1038/s41598-026-43642-1

Figure Lengend Snippet: Synergistic effect of dipyridamole and tucidinostat involves adenosine receptor activation. ( A ) MT-1 cells were treated with adenosine (250 µM), tucidinostat (Tuc; 360 nM), or their combination for 72 h. Cell viability was measured using the CCK-8 assay. Data are shown as means ± SD. *** p < 0.001, **** p < 0.0001. The synergy score was calculated using the SynergyFinder R package. (B-E) MT-1 cells were pretreated for 2 h with the indicated concentrations of selective adenosine receptor antagonists: DPCPX for A1 ( B ), ZM241385 for A2a ( C ), PSB-603 for A2b ( D ), or MRS1523 for A3 ( E ), followed by treatment with dipyridamole (Dip; 16 µM), tucidinostat (Tuc; 360 nM), or their combination for 48 h. Cell viability was assessed by CCK-8 assay. Data are presented as means ± SD. * p < 0.05, *** p < 0.001. Experiments were independently performed three times, and representative results are shown.

Article Snippet: DPCPX was purchased from Abcam, MRS1523 from Cayman Chemical Co. Ltd., and PSB-603 from MedChem Express.

Techniques: Activation Assay, CCK-8 Assay