par 1 inhibitor Search Results


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Axon Medchem LLC par1 inhibitors vorapaxar (sch530348)
Par1 Inhibitors Vorapaxar (Sch530348), supplied by Axon Medchem LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Eisai Inc par1 antagonists
Par1 Antagonists, supplied by Eisai Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Merck & Co mark/par1 inhibitor
Primary neurons at 15 DIV were pre-treated (30 min) with various kinases inhibitors including, Compound C (Comp C, 10 μM), <t>MARK/Par1</t> (20 μM), roscovitine (Rosco, 10 μM), PD98059 (PD98, 10 μM), H-89 (20 μM), Rapamycin (Rapa, 10 nM) and LY294002 (LY29, 20 μM) prior to AICAR treatment (1 mM, 2 h). Cell lysates were analyzed by WB for ACC, p-Ser 79 ACC (pACC), phosphorylated tau at epitopes Ser 262/356 and Thr 231 , total tau and actin ( a ). Quantification of phosphorylated tau at epitopes Ser 262/356 ( b ), and Thr 231 ( c ) expressed in ratio of Ctrl. Results represent mean ± SD, n = 4. a.u, arbitrary units. ***p < 0.001 compared to AICAR, One way ANOVA with Bonferroni’s post hoc test.
Mark/Par1 Inhibitor, supplied by Merck & Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Merck & Co vorapaxar (zontivity
Primary neurons at 15 DIV were pre-treated (30 min) with various kinases inhibitors including, Compound C (Comp C, 10 μM), <t>MARK/Par1</t> (20 μM), roscovitine (Rosco, 10 μM), PD98059 (PD98, 10 μM), H-89 (20 μM), Rapamycin (Rapa, 10 nM) and LY294002 (LY29, 20 μM) prior to AICAR treatment (1 mM, 2 h). Cell lysates were analyzed by WB for ACC, p-Ser 79 ACC (pACC), phosphorylated tau at epitopes Ser 262/356 and Thr 231 , total tau and actin ( a ). Quantification of phosphorylated tau at epitopes Ser 262/356 ( b ), and Thr 231 ( c ) expressed in ratio of Ctrl. Results represent mean ± SD, n = 4. a.u, arbitrary units. ***p < 0.001 compared to AICAR, One way ANOVA with Bonferroni’s post hoc test.
Vorapaxar (Zontivity, supplied by Merck & Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/vorapaxar (zontivity/product/Merck & Co
Average 90 stars, based on 1 article reviews
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Sankyo Co inhibitor of par-1 receptor r-99224/cs 747
Primary neurons at 15 DIV were pre-treated (30 min) with various kinases inhibitors including, Compound C (Comp C, 10 μM), <t>MARK/Par1</t> (20 μM), roscovitine (Rosco, 10 μM), PD98059 (PD98, 10 μM), H-89 (20 μM), Rapamycin (Rapa, 10 nM) and LY294002 (LY29, 20 μM) prior to AICAR treatment (1 mM, 2 h). Cell lysates were analyzed by WB for ACC, p-Ser 79 ACC (pACC), phosphorylated tau at epitopes Ser 262/356 and Thr 231 , total tau and actin ( a ). Quantification of phosphorylated tau at epitopes Ser 262/356 ( b ), and Thr 231 ( c ) expressed in ratio of Ctrl. Results represent mean ± SD, n = 4. a.u, arbitrary units. ***p < 0.001 compared to AICAR, One way ANOVA with Bonferroni’s post hoc test.
Inhibitor Of Par 1 Receptor R 99224/Cs 747, supplied by Sankyo Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Primary neurons at 15 DIV were pre-treated (30 min) with various kinases inhibitors including, Compound C (Comp C, 10 μM), MARK/Par1 (20 μM), roscovitine (Rosco, 10 μM), PD98059 (PD98, 10 μM), H-89 (20 μM), Rapamycin (Rapa, 10 nM) and LY294002 (LY29, 20 μM) prior to AICAR treatment (1 mM, 2 h). Cell lysates were analyzed by WB for ACC, p-Ser 79 ACC (pACC), phosphorylated tau at epitopes Ser 262/356 and Thr 231 , total tau and actin ( a ). Quantification of phosphorylated tau at epitopes Ser 262/356 ( b ), and Thr 231 ( c ) expressed in ratio of Ctrl. Results represent mean ± SD, n = 4. a.u, arbitrary units. ***p < 0.001 compared to AICAR, One way ANOVA with Bonferroni’s post hoc test.

Journal: Scientific Reports

Article Title: AMP-activated protein kinase modulates tau phosphorylation and tau pathology in vivo

doi: 10.1038/srep26758

Figure Lengend Snippet: Primary neurons at 15 DIV were pre-treated (30 min) with various kinases inhibitors including, Compound C (Comp C, 10 μM), MARK/Par1 (20 μM), roscovitine (Rosco, 10 μM), PD98059 (PD98, 10 μM), H-89 (20 μM), Rapamycin (Rapa, 10 nM) and LY294002 (LY29, 20 μM) prior to AICAR treatment (1 mM, 2 h). Cell lysates were analyzed by WB for ACC, p-Ser 79 ACC (pACC), phosphorylated tau at epitopes Ser 262/356 and Thr 231 , total tau and actin ( a ). Quantification of phosphorylated tau at epitopes Ser 262/356 ( b ), and Thr 231 ( c ) expressed in ratio of Ctrl. Results represent mean ± SD, n = 4. a.u, arbitrary units. ***p < 0.001 compared to AICAR, One way ANOVA with Bonferroni’s post hoc test.

Article Snippet: AICAR, metformin, PD98059, H-89, LY294002 were purchased from Tocris; roscovitin and MARK/Par1 inhibitor from Merck; Compound C was from Santa-Cruz Biotechnology and rapamycin was from Cell Signaling Technology.

Techniques: