Gm8994 inhibitors are a class of chemical compounds specifically designed to inhibit the activity of the Gm8994 protein, a protein whose biological function is not yet fully characterized but is believed to be involved in critical cellular processes, possibly including signal transduction, regulatory functions, or protein-protein interactions. The inhibitors targeting Gm8994 work by binding to specific regions of the protein, such as the active site or other key functional domains, thereby preventing the protein from carrying out its normal biological activities. This inhibition can be achieved through various mechanisms, including competitive inhibition, where the inhibitor directly competes with the natural substrate for binding to the active site, or through allosteric inhibition, where the inhibitor binds to a site other than the active site and induces conformational changes that reduce the protein's activity.
The development of Gm8994 inhibitors involves a deep understanding of the protein's structure and the molecular interactions that are essential for its function. Researchers typically employ high-throughput screening methods to identify initial lead compounds that exhibit potential inhibitory effects against Gm8994. These lead compounds are then optimized through structure-activity relationship (SAR) studies to enhance their potency, selectivity, and overall stability. The chemical structures of Gm8994 inhibitors are diverse, often featuring functional groups that enable strong and specific interactions with the protein. These interactions may include hydrogen bonds, hydrophobic contacts, and van der Waals forces, which help to stabilize the inhibitor within the protein's binding pocket. Advanced structural biology techniques such as X-ray crystallography and nuclear magnetic resonance (NMR) spectroscopy are frequently used to visualize these interactions at an atomic level, providing detailed insights that guide the design and refinement of these inhibitors. Achieving high selectivity is a key objective in the development of Gm8994 inhibitors, ensuring that these compounds specifically target Gm8994 without affecting other proteins that may have similar structures or functions. This selectivity is crucial for enabling precise modulation of Gm8994's activity, allowing researchers to explore its role in cellular processes and its broader implications in the context of cellular biology.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
A flavonoid with antioxidant properties, Quercetin can modulate kinase activity, potentially influencing protein function. | ||||||
Temozolomide | 85622-93-1 | sc-203292 sc-203292A | 25 mg 100 mg | $91.00 $255.00 | 32 | |
Alkylates/methylates DNA, Temozolomide can affect DNA repair mechanisms, impacting protein interactions. | ||||||
Cisplatin | 15663-27-1 | sc-200896 sc-200896A | 100 mg 500 mg | $138.00 $380.00 | 101 | |
Forms DNA adducts, Cisplatin can disrupt DNA replication and transcription, affecting protein synthesis. | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $37.00 $152.00 | 11 | |
Inhibits thymidylate synthase, 5-Fluorouracil can disrupt DNA synthesis, influencing protein function. | ||||||
Bleomycin | 11056-06-7 | sc-507293 | 5 mg | $275.00 | 5 | |
Causes DNA strand breaks, Bleomycin can affect DNA replication and repair, impacting protein synthesis. | ||||||
Doxorubicin | 23214-92-8 | sc-280681 sc-280681A | 1 mg 5 mg | $176.00 $426.00 | 43 | |
Interferes with DNA and RNA synthesis, Doxorubicin can disrupt protein expression pathways. | ||||||
Taxol | 33069-62-4 | sc-201439D sc-201439 sc-201439A sc-201439E sc-201439B sc-201439C | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $41.00 $74.00 $221.00 $247.00 $738.00 $1220.00 | 39 | |
Stabilizes microtubules, Paclitaxel can disrupt cell division, affecting protein distribution and function. | ||||||
Vinblastine | 865-21-4 | sc-491749 sc-491749A sc-491749B sc-491749C sc-491749D | 10 mg 50 mg 100 mg 500 mg 1 g | $102.00 $235.00 $459.00 $1749.00 $2958.00 | 4 | |
Inhibits microtubule formation, Vinblastine can disrupt cell division and protein function. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $94.00 $213.00 | 33 | |
Inhibits dihydrofolate reductase, Methotrexate can affect nucleotide synthesis and protein function. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $51.00 $231.00 $523.00 | 63 | |
Inhibits DNA topoisomerase II, Etoposide can disrupt DNA replication and transcription, affecting protein synthesis. | ||||||