IDS Activators can be defined as a class of compounds that enhance the activity of the enzyme Iduronate 2-sulfatase (IDS). The chemicals in this class engage in a diverse set of interactions and mechanisms to influence IDS activity, often by modulating pathways and processes related to IDS function. The IDS enzyme plays a crucial role in the degradation of glycosaminoglycans (GAGs) within the lysosome. Therefore, compounds that influence GAG metabolism, lysosomal function, or related cellular processes may serve as indirect activators of IDS. For instance, Mannose-6-phosphate, N-acetyl-D-glucosamine, Glucosamine, and Chondroitin sulfate are all involved in GAG metabolism and could indirectly affect IDS activity by modulating the levels of its substrate. Ascorbic acid also influences GAG metabolism and could potentially affect IDS activity in the same manner.
Moreover, other activators like Manganese(II) chloride, Trehalose, Resveratrol, Quercetin, Tauroursodeoxycholic acid, Pyridoxal phosphate, and N-acetyl cysteine have diverse actions that can enhance cellular metabolism, lysosomal function, and stress responses. These compounds can indirectly influence IDS activity by creating an environment conducive to its function.
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