Cytochrome c Inhibitors encompass a diverse range of compounds that specifically target and interfere with the normal function of cytochrome c, a crucial protein involved in various cellular processes. Cytochrome c is an essential component of the mitochondrial electron transport chain, facilitating the transfer of electrons between Complexes III and IV during oxidative phosphorylation. This process is vital for the generation of adenosine triphosphate (ATP), the main energy currency of the cell. Cytochrome c inhibitors disrupt this electron transfer by impeding the interaction between cytochrome c and other components of the electron transport chain.
These inhibitors often work through distinct mechanisms that perturb cytochrome c's role in electron transport or apoptosis. Some compounds, like azide and sodium cyanide, target cytochrome c oxidase (Complex IV) directly, binding to the enzyme's heme groups and obstructing electron flow, thus hampering ATP synthesis. Others, such as rotenone and antimycin A, interfere with upstream complexes (Complex I and Complex III) of the electron transport chain, indirectly influencing cytochrome c's involvement in the process. Moreover, certain inhibitors, including hydrogen sulfide and gossypol, may modulate cytochrome c's engagement in apoptosis signaling pathways, impacting cellular survival and programmed cell death. The structural diversity of cytochrome c inhibitors spans a wide spectrum, with various chemical entities exhibiting distinct binding affinities and modes of interaction with cytochrome c or associated components. Researchers have harnessed the elucidation of these compounds' mechanisms to gain insights into the fundamental roles of cytochrome c in cellular processes, thereby contributing to our understanding of mitochondrial function and apoptotic pathways. By targeting cytochrome c, these inhibitors offer valuable tools for studying cellular biology and unraveling the intricacies of mitochondrial electron transport and apoptosis regulation.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Sodium azide | 26628-22-8 | sc-208393 sc-208393B sc-208393C sc-208393D sc-208393A | 25 g 250 g 1 kg 2.5 kg 100 g | $42.00 $152.00 $385.00 $845.00 $88.00 | 8 | |
Azide interferes with electron transport in the mitochondrial respiratory chain by inhibiting cytochrome c oxidase (Complex IV), disrupting the final step of aerobic respiration. | ||||||
Rotenone | 83-79-4 | sc-203242 sc-203242A | 1 g 5 g | $89.00 $254.00 | 41 | |
Rotenone inhibits Complex I of the mitochondrial electron transport chain, indirectly affecting cytochrome c by blocking the transfer of electrons from NADH to ubiquinone. | ||||||
Antimycin A | 1397-94-0 | sc-202467 sc-202467A sc-202467B sc-202467C | 5 mg 10 mg 1 g 3 g | $54.00 $62.00 $1642.00 $4600.00 | 51 | |
Antimycin A inhibits Complex III of the electron transport chain, leading to a decrease in electron flow to cytochrome c and disrupting oxidative phosphorylation. | ||||||
Myxothiazol | 76706-55-3 | sc-507550 | 1 mg | $145.00 | ||
Myxothiazol, similar to antimycin A, inhibits Complex III and subsequently hampers the transfer of electrons to cytochrome c, impacting mitochondrial respiration. | ||||||
Ferrostatin 1 | 347174-05-4 | sc-498126 sc-498126A | 10 mg 50 mg | $162.00 $442.00 | 15 | |
Ferrostatin-1 prevents lipid peroxidation and ferroptosis by indirectly influencing mitochondrial membrane permeabilization and the release of cytochrome c. | ||||||
Gossypol | 303-45-7 | sc-200501 sc-200501A | 25 mg 100 mg | $114.00 $225.00 | 12 | |
Gossypol interferes with anti-apoptotic Bcl-2 family proteins, affecting their interactions with cytochrome c and influencing mitochondrial-mediated apoptosis pathways. | ||||||
Cisplatin | 15663-27-1 | sc-200896 sc-200896A | 100 mg 500 mg | $76.00 $216.00 | 101 | |
Cisplatin can impact cytochrome c release during apoptosis by affecting the cellular response to DNA damage and indirectly influencing mitochondrial membrane permeability. |