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.
関連項目
Items 1 to 10 of 11 total
画面:
| 製品名 | CAS # | カタログ # | 数量 | 価格 | 引用文献 | レーティング |
|---|---|---|---|---|---|---|
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 | |
クルクミンは、TRIM42の発現に関与する転写因子をダウンレギュレートする可能性がある。 | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
レスベラトロールはNF-kBシグナル伝達を阻害する可能性があり、TRIM42の発現を低下させる可能性がある。 | ||||||
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 | |
スルフォラファンはNrf2活性を調節し、TRIM42の発現に負の影響を与えるかもしれない。 | ||||||
(−)-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は遺伝子のプロモーター活性を減弱させ、おそらくTRIM42の発現を低下させる可能性がある。 | ||||||
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 | |
ケルセチンはPI3K/ACT経路を阻害し、TRIM42の発現を減少させる可能性がある。 | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002はPI3K阻害剤であり、TRIM42のような遺伝子の転写活性を低下させる可能性がある。 | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
シロリムスはmTORを阻害するので、間接的にTRIM42タンパク質のレベルを低下させる可能性がある。 | ||||||
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はグルコーストランスポーターを阻害し、ストレス応答としてTRIM42の発現をダウンレギュレートする可能性がある。 | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059は、MEKを阻害することによって、TRIM42のようなMAPK経路によって制御されるタンパク質の発現を低下させることができる。 | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125はJNKを阻害し、その転写因子に影響を与えることによってTRIM42の発現を低下させるのかもしれない。 | ||||||