ZFP873 inhibitors are a class of chemical compounds specifically designed to target and inhibit the function of Zinc Finger Protein 873 (ZFP873), a transcription factor known for its role in regulating gene expression. ZFP873 belongs to the large family of zinc finger proteins, which are characterized by the presence of zinc finger motifs that allow them to bind to specific DNA sequences. These proteins play critical roles in the regulation of gene transcription by either activating or repressing the expression of target genes. ZFP873 is thought to influence key biological processes by controlling the transcription of genes involved in cell differentiation, development, and various metabolic pathways. Inhibitors of ZFP873 work by disrupting its ability to bind to DNA, effectively blocking its regulatory activity and altering the transcriptional landscape in the cell.
Chemically, ZFP873 inhibitors are often designed to interact with the zinc finger domains of the protein, which are responsible for recognizing and binding specific DNA sequences. These inhibitors may function by competitively blocking the DNA-binding sites or by inducing conformational changes that prevent ZFP873 from adopting the correct structure needed for gene regulation. The development of these inhibitors requires a detailed understanding of the three-dimensional structure of ZFP873, particularly its zinc finger motifs and their interaction with DNA. Specificity is crucial in the design process to ensure that the inhibitors selectively target ZFP873 without affecting other zinc finger proteins that perform different regulatory functions. Researchers studying ZFP873 inhibitors aim to gain deeper insights into the role of this transcription factor in cellular processes and how its inhibition affects gene expression networks, contributing to our broader understanding of transcriptional regulation and protein-DNA interactions in various biological contexts.
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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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Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
姜黄素可能会下调参与 TRIM42 表达的转录因子。 | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
白藜芦醇可能会抑制 NF-kB 信号传导,从而降低 TRIM42 的表达。 | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | $150.00 $286.00 $479.00 $1299.00 $8299.00 $915.00 | 22 | |
红豆杉可能会调节 Nrf2 的活性,从而对 TRIM42 的表达产生负面影响。 | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
EGCG可以减弱基因启动子的活性,从而可能降低TRIM42的表达。 | ||||||
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 $108.00 $245.00 $918.00 $49.00 | 33 | |
槲皮素可能会抑制 PI3K/AKT 通路,从而导致 TRIM42 的表达减少。 | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 是一种 PI3K 抑制因子,可能会导致 TRIM42 等基因的转录活性降低。 | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
西罗莫司可抑制 mTOR,从而间接降低 TRIM42 蛋白的水平。 | ||||||
Wiskostatin | 253449-04-6 | sc-204399 sc-204399A sc-204399B sc-204399C | 1 mg 5 mg 25 mg 50 mg | $48.00 $122.00 $432.00 $812.00 | 4 | |
WZB117 可能会抑制葡萄糖转运体,作为一种应激反应,可能会下调 TRIM42 的表达。 | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 通过抑制 MEK,可以减少受 MAPK 通路调控的蛋白质(如 TRIM42)的表达。 | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $65.00 $267.00 | 257 | |
SP600125 可抑制 JNK,这可能会通过影响其转录因子而导致 TRIM42 的表达减少。 |