Histatin 1 inhibitors constitute a distinctive class of chemical compounds designed to selectively target and inhibit the activity of Histatin 1, a naturally occurring peptide in human saliva. Histatin 1, part of the histatin family of peptides, is characterized by its unique sequence of amino acids, which endows it with specific functional properties. These peptides are known for their role in the maintenance of oral health, primarily attributed to their ability to interact with various components in the oral cavity. The structure of Histatin 1 is relatively small and compact, yet it exhibits a complex conformation that allows it to bind to different molecular targets. This binding ability is key to its functional role in the oral environment. The molecular mechanism of Histatin 1 involves interactions at the molecular level with various components found in the oral cavity. Understanding these interactions is crucial for the development of inhibitors that can specifically target and modulate the function of Histatin 1.
The development of Histatin 1 inhibitors is a sophisticated process that requires an in-depth understanding of the peptide's structure and function at a molecular level. These inhibitors are usually small molecules or modified peptides designed to bind to Histatin 1, thereby inhibiting its natural interactions and functions. The design of these inhibitors involves detailed studies of the peptide's structure, often employing advanced techniques such as nuclear magnetic resonance (NMR) spectroscopy or X-ray crystallography. These techniques provide insights into the three-dimensional conformation of Histatin 1 and its interaction sites, which are critical for designing effective inhibitors. Additionally, computational methods play a significant role in the development process. Techniques like molecular docking and virtual screening are used to predict how inhibitors might interact with Histatin 1, guiding the synthesis of compounds with optimal binding properties. The process of developing these inhibitors is iterative, involving continuous testing and refinement of compounds to achieve the desired level of specificity and efficacy. The field of Histatin 1 inhibitors is an area of active research, advancing with ongoing scientific discoveries and technological developments, contributing to a deeper understanding of peptide interactions and functions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 | |
An HDAC inhibitor that causes changes in chromatin structure, potentially downregulating a variety of genes. | ||||||
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, generally suppressing gene 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, impacting mRNA synthesis and thus potentially protein expression. | ||||||
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 and could decrease gene transcription broadly. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
Inhibits topoisomerase I, leading to DNA damage and potentially affecting transcription. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Cyclin-dependent kinase inhibitor that may result in downregulation of genes by affecting the cell cycle. | ||||||
Rocaglamide | 84573-16-0 | sc-203241 sc-203241A sc-203241B sc-203241C sc-203241D | 100 µg 1 mg 5 mg 10 mg 25 mg | $270.00 $465.00 $1607.00 $2448.00 $5239.00 | 4 | |
A natural product that can inhibit translation and potentially impact protein expression globally. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Inhibits eukaryotic protein synthesis by interfering with the translocation step in protein synthesis. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $65.00 $99.00 $140.00 | 85 | |
Alkylates DNA and can lead to a decrease in DNA synthesis and potentially gene expression. | ||||||
Puromycin | 53-79-2 | sc-205821 sc-205821A | 10 mg 25 mg | $163.00 $316.00 | 436 | |
Causes premature chain termination during protein synthesis, affecting overall protein expression. | ||||||