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| Catalog | name | Description | price |
|---|---|---|---|
| R-C-3059 | HUN86320 CAS:882286-32-0 | TSPC is an inhibitor for GA perception by in vitro and in planta evaluations. | price> |
| R-R-4729 | Mono-2-O-(p-toluenesulfonyl)-y-cyclodextrin CAS No.97227-32-2 | Mono-2-O-(p-toluenesulfonyl)-γ-cyclodextrin/Mono-2-O-(p-toluenesulfonyl)-gamma-cyclodextrin/CAS No.97227-32-2 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | price> |
| R-C-3060 | BRD3731 cas:2056262-07-6 | BRD3731 is a selective GSK3β inhibitor, with IC50s of 15 nM and 215 nM for GSK3β and GSK3α, respectively. BRD3731 inhibits the phosphorylation of CRMP2 in SH-SY5Y cells. BRD3731 decreases β-catenin S33/37/T41 phosphorylation and induces β-catenin S675 phosphorylation in HL-60 cells. BRD3731 impairs colony formation in TF-1 and increases colony forming ability in the MV4-11 cell line. | price> |
| R-R-4730 | Mono-6-O-(p-toluenesulfonyl)-a-cyclodextrin CAS No.97227-32-2 | Mono-6-O-(p-toluenesulfonyl)-α-cyclodextrin/Mono-6-O-(p-toluenesulfonyl)-alpha-cyclodextrin/CAS No.97227-32-2 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | price> |
| R-C-3061 | BRD3308 CAS:1550053-02-5 | BRD3308 is a highly selective HDAC3 inhibitor with an IC50 of 54 nM. | price> |
| R-R-4731 | Mono-6-O-mesitylenesulfonyl-y-cyclodextrin CAS No.174010-62-9 | Mono-6-O-mesitylenesulfonyl-γ-cyclodextrin/CAS No.174010-62-9 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | price> |
| R-C-3062 | BRD0705 CAS:2056261-41-5 | BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. | price> |
| R-R-4732 | Mono-6-O-(p-toluenesulfonyl)-y-cyclodextrin CAS No.97227-33-3 | Mono-6-O-(p-toluenesulfonyl)-γ-cyclodextrin is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | price> |
| R-C-3063 | SB415286 CAS: 264218-23-7 | SB415286 is a potent GSK3α inhibitor with IC50/Ki of 78 nM/31 nM with equally effective inhibition of GSK-3β. SB415286 causes MM cell growth arrest and apoptosis. | price> |
| R-R-4733 | Hexakis (2,3,6-tri-O-methyl)-a-cyclodextrin CAS No.68715-56-0 | Hexakis (2,3,6-tri-O-methyl)-α-cyclodextrin/Hexakis (2,3,6-tri-O-methyl)-alpha-cyclodextrin/CAS No.68715-56-0 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | price> |
| R-C-3064 | LY2090314 CAS:603288-22-8 | LY2090314 is a potent GSK-3 inhibitor for GSK-3α/β with IC50 of 1.5 nM/0.9 nM; may improve the efficacy of platinum-based chemotherapy regimens. LY2090314 is highly selective towards GSK3 as demonstrated by its fold selectivity relative to a large panel of kinases. | price> |
| R-R-4734 | Heptakis(2,3,6-tri-O-ethyl)-b-cyclodextrin CAS No.111689-01-1 | Heptakis(2,3,6-tri-O-ethyl)-β-cyclodextrin/CAS No.111689-01-1 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | price> |
| R-C-3065 | BX517 CAS:850717-64-5 | BX517 is a potent and selective inhibitor of PDK1 that binds to the ATP binding pocket of the protein (IC50 = 6 nM). | price> |
| R-R-4735 | Heptakis-(2,6-di-O-ethyl)-b-cyclodextrin CAS No.111689-03-3 | Heptakis-(2,6-di-O-ethyl)-β-cyclodextrin/DE-beta-Cyd/CAS No.111689-03-3 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | price> |
| R-C-3066 | GSK2334470 CAS:1227911-45-6 | GSK2334470 is a novel PDK1 inhibitor with IC50 of ~10 nM in a cell-free assay, with no activity at other close related AGC-kinases.Only for scientific research, not for human body. | price> |
| R-R-4736 | Maltooctaose CAS No.66567-45-1 | Maltooctaose/CAS No.66567-45-1, a specific-length maltooligosaccharide, can be produced by PFTA (Pyrococcus furiosus). | price> |
| R-C-3067 | SL-0101-1 cas:77307-50-7 | SL 0101-1 is a selective p90 ribosomal S6 kinase (RSK) inhibitor for RSK2 with an IC50 of 89 nM. The IC50 of kaempferol, the flavonoid constituent of SL 0101-1, is 15 μM for RSK. The rhamnose moiety of SL 0101-1 increases the affinity for RSK by >150-fold. Only for scientific research, not for human body. | price> |
| R-R-4737 | HBV-IN-4 CAS No.2305897-84-9 | HBV-IN-4/CAS No.2305897-84-9, a phthalazinone derivative, is a potent and orally active HBV DNA replication inhibitor with an IC50 of 14 nM. HBV-IN-4 induces the formation of genome-free capsids and has potent anti-HBV potencies. | price> |
| R-C-3068 | BI-D1870 CAS:501437-28-1 | BI-D1870 is a potent and specific inhibitor of the p90 ribosomal S6 kinase (RSK) isoforms in vitro and in vivo, which inhibits RSK1, RSK2, RSK3 and RSK4 in vitro with an IC50 of 10–30 nM.Only for scientific research, not for human body. | price> |
| R-R-4738 | Sodium Camptothecin CAS No.25387-67-1 | Sodium Camptothecin/CAS No.25387-67-1 is a plant alkaloid, with antitumor activity. Sodium Camptothecin is a reversible inhibitor of RNA synthesis. Sodium Camptothecin is an effective inhibitor of adenovirus replication. Sodium Camptothecin inhibits DNA synthesis and causes breaks in intracellular preformed viral DNA. | price> |

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