TTC22 inhibitors, within the realm of chemical compounds, belong to a specific class of molecules designed to target and modulate the activity of the TTC22 protein. TTC22, short for Tetratricopeptide Repeat Domain 22, is a protein encoded by the TTC22 gene, and it plays a crucial role in various cellular processes. Inhibitors of TTC22 are chemical compounds meticulously crafted to interfere with the protein's normal function or expression, thereby exerting a regulatory influence on cellular activities that rely on TTC22. These inhibitors are characterized by their ability to interact with TTC22 either directly or indirectly, resulting in altered cellular responses and pathways.
The design and development of TTC22 inhibitors typically involve extensive research into the structural and functional aspects of TTC22. Scientists aim to identify specific binding sites on the protein where inhibitors can interact effectively. The inhibitors may function by binding to these sites and disrupting TTC22's interactions with other proteins or molecules, ultimately affecting downstream signaling pathways. Additionally, TTC22 inhibitors may be designed to modulate the expression of TTC22 at the genetic level, controlling its synthesis within the cell. These inhibitors hold promise for unraveling the intricate mechanisms underlying various cellular processes that involve TTC22, offering invaluable insights into fundamental biology and paving the way for future applications in research and beyond.
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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 inhibits RNA synthesis, thereby preventing the transcription of genes into mRNA. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
α-Amanitin inhibits RNA polymerase II, which is responsible for mRNA synthesis. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide inhibits the elongation step in protein synthesis by blocking the translocation step. | ||||||
Mycophenolic acid | 24280-93-1 | sc-200110 sc-200110A | 100 mg 500 mg | $68.00 $261.00 | 8 | |
Mycophenolic acid inhibits inosine monophosphate dehydrogenase, affecting purine synthesis and thereby RNA and DNA synthesis. | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $36.00 $149.00 | 11 | |
5-Fluorouracil is an analogue of uracil and inhibits thymidylate synthase, affecting DNA synthesis. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
Camptothecin inhibits DNA topoisomerase I, preventing DNA unwinding and replication. | ||||||
Doxorubicin | 23214-92-8 | sc-280681 sc-280681A | 1 mg 5 mg | $173.00 $418.00 | 43 | |
Doxorubicin intercalates into DNA, disrupting its structure and inhibiting RNA and DNA synthesis. | ||||||
Emetine | 483-18-1 | sc-470668 sc-470668A sc-470668B sc-470668C | 1 mg 10 mg 50 mg 100 mg | $352.00 $566.00 $1331.00 $2453.00 | ||
Emetine inhibits protein synthesis by blocking the movement of the ribosome along mRNA. | ||||||
Puromycin dihydrochloride | 58-58-2 | sc-108071 sc-108071B sc-108071C sc-108071A | 25 mg 250 mg 1 g 50 mg | $40.00 $210.00 $816.00 $65.00 | 394 | |
Puromycin causes premature chain termination during translation by acting as an analog of the aminoacyl-tRNA. | ||||||
Chloramphenicol | 56-75-7 | sc-3594 | 25 g | $53.00 | 10 | |
Chloramphenicol inhibits protein synthesis in bacteria by binding to the 50S ribosomal subunit. | ||||||