Tom23 inhibitors are a class of chemical compounds specifically designed to target and inhibit the Tom23 protein, a key component of the mitochondrial translocase complex involved in transporting proteins into the mitochondria. These inhibitors function by binding to critical regions of the Tom23 protein, most commonly the active or binding sites, where they disrupt the protein's normal interaction with its substrates. By occupying these sites, Tom23 inhibitors effectively block the passage of proteins through the mitochondrial membrane, altering the normal biological processes associated with Tom23's function. In addition to direct active-site binding, some Tom23 inhibitors may act allosterically by attaching to sites distant from the active region. This allosteric binding induces conformational changes that weaken or inhibit the protein's overall activity. The stability of the inhibitor-protein complex is often maintained through a range of non-covalent interactions, including hydrogen bonds, van der Waals forces, hydrophobic interactions, and ionic interactions.
Structurally, Tom23 inhibitors exhibit considerable diversity, allowing them to interact effectively with various regions of the protein. These inhibitors often feature key structural motifs such as aromatic rings, heterocyclic backbones, and functional groups like hydroxyl, carboxyl, or amine groups. These functional groups enable the formation of hydrogen bonds and other critical interactions with amino acid residues in the Tom23 protein's binding or allosteric sites. Aromatic rings and non-polar regions in the inhibitors can also enhance hydrophobic interactions with non-polar regions of the protein, increasing the stability of the inhibitor-protein complex. The physicochemical properties of Tom23 inhibitors, such as molecular weight, solubility, lipophilicity, and polarity, are carefully optimized to ensure that the inhibitors bind effectively and remain stable in different biological environments. By balancing hydrophilic and hydrophobic regions, Tom23 inhibitors are designed to interact with both polar and non-polar areas of the protein, ensuring strong and selective inhibition while maintaining structural integrity under a variety of conditions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
Actinomycin D binds to DNA and obstructs the elongation phase of RNA synthesis by RNA polymerase, which could downregulate TOMM23 transcription and consequently reduce Tom23 protein levels. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide disrupts protein synthesis by inhibiting the translocation step on the ribosome, which would decrease the production of Tom23 as part of a generalized suppression of protein translation. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
By inhibiting the mTOR pathway, rapamycin may downregulate protein synthesis, leading to a decrease in Tom23 synthesis as part of its action to reduce overall protein translation rates. | ||||||
Doxorubicin | 23214-92-8 | sc-280681 sc-280681A | 1 mg 5 mg | $173.00 $418.00 | 43 | |
Doxorubicin intercalates into DNA and can interfere with the function of topoisomerase II, potentially leading to reduced expression of Tom23 by hindering proper transcription of the TOMM23 gene. | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $36.00 $149.00 | 11 | |
Fluorouracil impedes thymidylate synthase, leading to a nucleotide imbalance that can cause a decrease in TOMM23 mRNA synthesis, thereby reducing the level of Tom23 protein. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A inhibits histone deacetylases, leading to hyperacetylation of histones, which could downregulate TOMM23 transcription and lower Tom23 protein expression. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine disrupts lysosomal acidification and can alter the cellular environment, potentially leading to a decrease in TOMM23 gene expression and subsequent lower levels of Tom23 protein. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid acts as a ligand for nuclear receptors, altering the transcription of genes; it may downregulate the expression of the TOMM23 gene, resulting in decreased synthesis of Tom23. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
Mithramycin A binds to DNA and can selectively inhibit transcription of certain genes; it may decrease TOMM23 transcription, leading to reduced synthesis of Tom23. | ||||||
Spliceostatin A | 391611-36-2 | sc-507481 | 1 mg | $1800.00 | ||
Spliceostatin A interferes with spliceosome assembly and function, potentially leading to defective splicing of TOMM23 pre-mRNA and a subsequent decrease in mature Tom23 protein. | ||||||