Date published: 2025-11-7

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ZFP873 Inhibidores

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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Nombre del productoNÚMERO DE CAS #Número de catálogoCantidadPrecioMENCIONESClasificación

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
¥406.00
¥767.00
¥1207.00
¥2414.00
¥2640.00
¥9725.00
¥22203.00
47
(1)

La curcumina puede regular a la baja los factores de transcripción que intervienen en la expresión de TRIM42.

Resveratrol

501-36-0sc-200808
sc-200808A
sc-200808B
100 mg
500 mg
5 g
¥677.00
¥2087.00
¥4118.00
64
(2)

El resveratrol inhibe potencialmente la señalización NF-kB, lo que podría disminuir la expresión de TRIM42.

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
¥1692.00
¥3227.00
¥5404.00
¥14655.00
¥93629.00
¥10323.00
22
(1)

El sulforafano podría modular la actividad de Nrf2, influyendo negativamente en la expresión de TRIM42.

(−)-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
¥474.00
¥812.00
¥1399.00
¥2685.00
¥5867.00
¥13922.00
11
(1)

El EGCG podría atenuar la actividad promotora de los genes, reduciendo posiblemente la expresión de TRIM42.

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
¥124.00
¥192.00
¥1218.00
¥2764.00
¥10357.00
¥553.00
33
(2)

La quercetina puede inhibir la vía PI3K/AKT, lo que podría conducir a una disminución de la expresión de TRIM42.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
¥1365.00
¥4423.00
148
(1)

LY294002 es un inhibidor de PI3K que puede provocar una reducción de la actividad transcripcional de genes como TRIM42.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
¥699.00
¥1749.00
¥3610.00
233
(4)

Sirolimus inhibe mTOR, lo que podría disminuir indirectamente los niveles de la proteína TRIM42.

Wiskostatin

253449-04-6sc-204399
sc-204399A
sc-204399B
sc-204399C
1 mg
5 mg
25 mg
50 mg
¥542.00
¥1376.00
¥4874.00
¥9161.00
4
(1)

WZB117 puede inhibir los transportadores de glucosa, regulando potencialmente a la baja la expresión de TRIM42 como respuesta al estrés.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
¥440.00
¥1015.00
212
(2)

El PD98059, al inhibir MEK, podría reducir la expresión de proteínas reguladas por la vía MAPK, como TRIM42.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
¥301.00
¥1128.00
257
(3)

SP600125 inhibe JNK, lo que podría conducir a una disminución de la expresión de TRIM42 al afectar a sus factores de transcripción.