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| Product | Description | |
|---|---|---|
| Ruboxistaurin HCl | Ruboxistaurin, also called as LY 333531, initially developed for the treatment of diabetic retinopathy, inhibits isolated enzymes PKCβI and PKCβII with a half-maximal inhibitory constant of 4.5 and 5.9 nM, respectively. The half-life of ruboxistaurin, which can be orally administered, is approximately 9h and that of its metabolite 16h, therefore allowing once-daily dosing. Based on data from clinicalTrials.gov, Children's Hospital Medical Center, Cincinnati plan a phase I/II trial of the effect of ruboxistaurin for its safety, tolerability, and effectiveness in treating adult patients with heart failure on June 9, 2016. Uses: Enzyme inhibitors. Group: Pharmaceutical. CAS No. 169939-93-9. Pack Sizes: 10 mg. Product ID: B0084-263880. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| Ruboxistaurin Impurities | Ruboxistaurin Impurities are essential reference materials utilized in the quality control and analysis of Ruboxistaurin. This compound primarily targets diabetic retinopathy and macular edema. Accurate identification and quantification of these impurities ensure the safety and efficacy of the therapeutic application of Ruboxistaurin. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
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