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18469-1A cell-permeable inhibitor of cathepsin B and L in vivo and in whole cells used to study the role of cathepsin B in neurodegeneration, cancer cell metastasis, necrosis, and rheumatoid arthritis.
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18469-5A cell-permeable inhibitor of cathepsin B and L in vivo and in whole cells used to study the role of cathepsin B in neurodegeneration, cancer cell metastasis, necrosis, and rheumatoid arthritis.
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18469-500A cell-permeable inhibitor of cathepsin B and L in vivo and in whole cells used to study the role of cathepsin B in neurodegeneration, cancer cell metastasis, necrosis, and rheumatoid arthritis.
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C3352-5 mg
Thomas Scientific
Ca2+-sensing receptor agonist used to treat secondary hyperparathyroidism with chronic kidney disease. It decreases parathyroid hormone secretion and prevents the development of renal fibrosis. (C08-0488-458)
Price: $122.30List Price: $135.89Cinacalcet is an agonist at Ca2+-sensing receptors that is clinically used to treat secondary hyperparathyroidism with chronic kidney disease. Cinacalcet also displays anti-fibrotic activity. -
C3352-25 mg
Thomas Scientific
Ca2+-sensing receptor agonist used to treat secondary hyperparathyroidism with chronic kidney disease. It decreases parathyroid hormone secretion and prevents the development of renal fibrosis. (C08-0489-064)
Price: $306.50List Price: $340.56Cinacalcet is an agonist at Ca2+-sensing receptors that is clinically used to treat secondary hyperparathyroidism with chronic kidney disease. Cinacalcet also displays anti-fibrotic activity. -
C3352-100 mg
Thomas Scientific
Ca2+-sensing receptor agonist used to treat secondary hyperparathyroidism with chronic kidney disease. It decreases parathyroid hormone secretion and prevents the development of renal fibrosis. (C08-0489-535)
Price: $657.20List Price: $730.22Cinacalcet is an agonist at Ca2+-sensing receptors that is clinically used to treat secondary hyperparathyroidism with chronic kidney disease. Cinacalcet also displays anti-fibrotic activity. -
C0016-1 mgCaerulomycin A is a bipyridyl antifungal antibiotic. Caerulomycin A is toxic to Entamoeba in animal models of infection. Additionally, caerulomycin may exhibit anticancer and immunosuppressive activities. Grade: &ge96%
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13999-10A natural diterpene which elevates serum cholesterol and triglycerides in humans, an effect which does not seem to occur in monkeys, hamsters, rats or gerbils increase total cholesterol and triglycerides in ApoE3Leiden mice, an effect which is
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13999-5A natural diterpene which elevates serum cholesterol and triglycerides in humans, an effect which does not seem to occur in monkeys, hamsters, rats or gerbils increase total cholesterol and triglycerides in ApoE3Leiden mice, an effect which is
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13999-50A natural diterpene which elevates serum cholesterol and triglycerides in humans, an effect which does not seem to occur in monkeys, hamsters, rats or gerbils increase total cholesterol and triglycerides in ApoE3Leiden mice, an effect which is
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17873-100An ester of a naturally occurring phenolic compound that demonstrates antihyperglycemic and antidiabetic activity as well as induces anti-inflammatory and antinociceptive effects.
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17873-250An ester of a naturally occurring phenolic compound that demonstrates antihyperglycemic and antidiabetic activity as well as induces anti-inflammatory and antinociceptive effects.