β-defensin 14 inhibitors are a class of chemical compounds designed to specifically target and inhibit the activity of β-defensin 14, a member of the defensin family of small, cysteine-rich antimicrobial peptides. β-defensin 14 plays an essential role in the innate immune system, contributing to the defense against pathogens such as bacteria, fungi, and viruses by disrupting their cell membranes. This peptide is known for its ability to bind to microbial cell surfaces, leading to membrane destabilization and the destruction of pathogens. Inhibitors of β-defensin 14 aim to block its antimicrobial activity, potentially affecting the peptide's ability to bind to microbial membranes or interact with specific components of the immune response.
The development of β-defensin 14 inhibitors involves a detailed understanding of the peptide's structure, particularly its β-sheet-rich conformation stabilized by disulfide bridges, which is essential for its function in binding to microbial surfaces. These inhibitors are designed to interact with key regions of the peptide, such as its positively charged surface or hydrophobic regions, which are critical for membrane binding and antimicrobial activity. Structural biology techniques, including molecular modeling and X-ray crystallography, are commonly employed to identify these critical regions and to design inhibitors that specifically bind to them, preventing β-defensin 14 from carrying out its membrane-disrupting functions. Achieving high specificity is crucial in this process, as β-defensin 14 shares structural and functional similarities with other members of the defensin family. These inhibitors are valuable tools for studying the detailed mechanisms of host-microbe interactions, shedding light on the complex dynamics of innate immune responses and the role of defensins in protecting against microbial invaders.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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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 | ¥1681.00 ¥5303.00 ¥6995.00 ¥13527.00 ¥23579.00 | 33 | |
Trichostatin A 可抑制组蛋白去乙酰化酶,从而可能通过改变染色质结构减少 RIM-BP3B 的表达。 | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | ¥3159.00 | 4 | |
这种DNA甲基转移酶抑制剂可通过影响基因甲基化模式来降低RIM-BP3B的表达。 | ||||||
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 | ¥824.00 ¥2685.00 ¥8089.00 ¥28453.00 ¥241660.00 | 53 | |
放线菌素 D 可与 DNA 结合,阻止 RNA 聚合酶的作用,从而可能减少 RIM-BP3B mRNA 的合成。 | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | ¥2933.00 ¥11609.00 | 26 | |
α-鹅膏蕈素会抑制 RNA 聚合酶 II,从而导致 RIM-BP3B 的转录物减少。 | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | ¥699.00 ¥1749.00 ¥3610.00 | 233 | |
西罗莫司抑制 mTOR,可能会通过影响蛋白质合成途径来下调 RIM-BP3B 的表达。 | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | ¥451.00 ¥925.00 ¥2888.00 | 127 | |
环己亚胺能抑制真核生物蛋白质的合成,从而可能减少 RIM-BP3B 的生成。 | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | ¥767.00 | 2 | |
氯喹可碱化溶酶体,可能会干扰 RIM-BP3B mRNA 的降解途径。 | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | ¥1365.00 ¥4423.00 | 148 | |
LY294002 是一种 PI3K 抑制剂,可通过影响下游信号导致 RIM-BP3B 的表达减少。 | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | ¥609.00 | 6 | |
Mithramycin A 与 DNA 结合,可能会通过抑制 RNA 合成来减少 RIM-BP3B 的表达。 | ||||||
2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | ¥733.00 ¥2369.00 | 26 | |
它能抑制糖酵解,从而减少 RIM-BP3B 表达和其他细胞过程所需的能量。 |