Date published: 2025-9-11

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creatine kinase-B Inhibitors

Creatine kinase-B inhibitors, as categorized here, are a diverse group of chemicals that influence the activity of CK-B indirectly by affecting various cellular processes or pathways related to energy metabolism. These chemicals do not inhibit CK-B directly but modulate its activity through alterations in cellular energy states, redox balance, or by interacting with key functional groups within the enzyme. The primary method by which these chemicals can influence CK-B involves the alteration of cellular energy metabolism. Compounds such as Malonate, Sodium Fluoride, Beta-GPA, Metformin, Dichloroacetate, Sodium Azide, Rotenone, and Oligomycin affect different aspects of energy production and utilization within the cell. By altering pathways such as glycolysis, the Krebs cycle, or oxidative phosphorylation, these compounds can impact the availability of ATP and creatine, which are substrates or products of CK-B. For instance, Malonate inhibits succinate dehydrogenase, leading to changes in the Krebs cycle, which can indirectly affect CK-B activity by altering the cellular energy state.In addition to these, other compounds listed such as 2,4-Dinitrofluorobenzene, Iodoacetamide, Nitrate, and Allopurinol, interact with or influence specific biochemical groups or pathways that can impact CK-B function. For example, 2,4-Dinitrofluorobenzene and Iodoacetamide can modify cysteine residues, which are crucial for CK-B's enzymatic activity. Alterations in the redox state by compounds like Nitrate can also affect CK-B indirectly, as redox changes can influence various metabolic enzymes and pathways. In summary, CK-B inhibitors, as classified here, are compounds that impact the activity of CK-B through indirect mechanisms by modulating cellular energy states, redox balance, or directly interacting with functional groups on the enzyme. Their influence on CK-B is rooted in their ability to alter the cellular environment, particularly in terms of energy availability and metabolism, thereby affecting the functional context in which CK-B operates within the cell. These inhibitors showcase the complex interplay between cellular metabolism and the functional modulation of key metabolic enzymes like CK-B.

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