Date published: 2025-9-10

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ZFP873 抑制因子

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

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产品名称CAS #产品编号数量价格应用排名

Curcumin

458-37-7sc-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
(1)

姜黄素可能会下调参与 TRIM42 表达的转录因子。

Resveratrol

501-36-0sc-200808
sc-200808A
sc-200808B
100 mg
500 mg
5 g
$60.00
$185.00
$365.00
64
(2)

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

4478-93-7sc-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
(1)

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

989-51-5sc-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
(1)

EGCG可以减弱基因启动子的活性,从而可能降低TRIM42的表达。

Quercetin

117-39-5sc-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
(2)

槲皮素可能会抑制 PI3K/AKT 通路,从而导致 TRIM42 的表达减少。

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

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

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

西罗莫司可抑制 mTOR,从而间接降低 TRIM42 蛋白的水平。

Wiskostatin

253449-04-6sc-204399
sc-204399A
sc-204399B
sc-204399C
1 mg
5 mg
25 mg
50 mg
$48.00
$122.00
$432.00
$812.00
4
(1)

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

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$39.00
$90.00
212
(2)

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

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$65.00
$267.00
257
(3)

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。