H2-M2 inhibitors constitute a specific class of chemical compounds designed to modulate the activity of the H2-M2 protein. H2-M2, also known as histocompatibility 2, M region locus 2, is a protein component of the major histocompatibility complex (MHC) in mice. The MHC system plays a critical role in the immune response by presenting antigenic peptides to T cells, allowing the immune system to recognize and mount responses against foreign pathogens. H2-M2, similar to other MHC molecules, is involved in the complex process of antigen presentation, a fundamental mechanism that enables the body to initiate immune responses against infections. The development of H2-M2 inhibitors is primarily driven by the objective of selectively interacting with the H2-M2 protein, potentially influencing its antigen-presenting activity and impacting immune recognition processes.
Typically, H2-M2 inhibitors consist of small molecules or chemical compounds specifically engineered to bind to H2-M2, targeting either its active site or allosteric sites. This interaction can lead to the modulation of H2-M2's behavior, potentially affecting its ability to present antigenic peptides to T cells and, consequently, influencing the immune response against foreign antigens. Researchers are primarily dedicated to unraveling the molecular mechanisms and functions of H2-M2 within the MHC system and how inhibiting its activity with these compounds may provide insights into the complex immune recognition processes. The development of H2-M2 inhibitors represents an active and evolving area of research within the fields of immunology and molecular pharmacology, contributing to a deeper understanding of the immune system's functioning and its role in detecting and responding to foreign antigens.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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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 | |
Interacts with DNA and inhibits RNA polymerase action, thereby preventing transcription. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
A potent inhibitor of RNA polymerase II and, to a lesser extent, RNA polymerase III. | ||||||
Rifampicin | 13292-46-1 | sc-200910 sc-200910A sc-200910B sc-200910C | 1 g 5 g 100 g 250 g | $95.00 $322.00 $663.00 $1438.00 | 6 | |
Binds to the beta subunit of RNA polymerase, inhibiting RNA synthesis. | ||||||
Cordycepin | 73-03-0 | sc-203902 | 10 mg | $99.00 | 5 | |
A nucleoside analog that can terminate RNA chain elongation. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
A diterpene triepoxide that can inhibit the transcription of various genes. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
A cyclin-dependent kinase inhibitor that can affect transcription regulation. | ||||||
DRB | 53-85-0 | sc-200581 sc-200581A sc-200581B sc-200581C | 10 mg 50 mg 100 mg 250 mg | $42.00 $185.00 $310.00 $650.00 | 6 | |
Inhibits RNA polymerase II transcription elongation. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
Stabilizes the DNA-topoisomerase I complex, inhibiting the relegation step of the DNA cleavage-relegation reaction during transcription. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $65.00 $99.00 $140.00 | 85 | |
Crosslinks DNA, which can inhibit DNA replication and RNA transcription. | ||||||
Betulinic Acid | 472-15-1 | sc-200132 sc-200132A | 25 mg 100 mg | $115.00 $337.00 | 3 | |
Modulates various signaling pathways, potentially affecting transcription. |