Date published: 2025-9-11

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pelota Ativadores

If such a class were to be recognized, it would imply a group of chemical compounds specifically designed to modulate the activity of the biological entity termed 'pelota'. Assuming 'pelota' refers to a protein or biochemical pathway, activators of this class would interact with the 'pelota' entity to enhance its biological function. This could be through direct binding to the protein, which may stabilize it in an active conformation, or by facilitating its interaction with other proteins or substrates. The nature of these activators would be determined by the structural requirements of the 'pelota' binding sites, leading to a diverse array of molecular structures, possibly encompassing small organic compounds, peptides, or other biologically active molecules, each with specific affinities and selectivities towards their target.

The identification and development of 'pelota Activators' would involve a combination of computational chemistry and experimental biology. Initially, a detailed understanding of the 'pelota' structure and function would be required, which could be gleaned from X-ray crystallography, NMR spectroscopy, or cryo-electron microscopy data. With this information, virtual screening processes could be employed to identify potential activator compounds, which would then be synthesized and assessed for their ability to enhance 'pelota' activity. Biochemical assays would be crucial for this assessment, testing the effects of these compounds on the activity of 'pelota' in vitro. Such assays would likely include activity measurements in the presence of substrate molecules or binding studies to determine the affinity and kinetics of interaction between the 'pelota' protein and the activators. The results of these experiments would inform further optimization of the compounds, potentially leading to the development of a diverse chemical class of 'pelota Activators'. However, it is important to note that this concept is speculative and is not based on current scientific consensus or literature.

VEJA TAMBÉM

Nome do ProdutoCAS #Numero de CatalogoQuantidadePrecoUso e aplicacaoNOTAS

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$40.00
$82.00
$256.00
127
(5)

Inibe a síntese proteica eucariótica, o que pode levar a uma resposta ao stress que regula positivamente os factores de reciclagem dos ribossomas, como o PELO.

Puromycin dihydrochloride

58-58-2sc-108071
sc-108071B
sc-108071C
sc-108071A
25 mg
250 mg
1 g
50 mg
$40.00
$210.00
$816.00
$65.00
394
(15)

Provoca a terminação prematura da cadeia durante a síntese proteica, aumentando potencialmente a necessidade de mecanismos de reciclagem dos ribossomas.

Anisomycin

22862-76-6sc-3524
sc-3524A
5 mg
50 mg
$97.00
$254.00
36
(2)

Inibe a síntese proteica ao bloquear a formação de ligações peptídicas, desencadeando potencialmente uma resposta celular para aumentar o PELO.

Chloramphenicol

56-75-7sc-3594
25 g
$53.00
10
(1)

Liga-se aos ribossomas bacterianos e inibe a síntese proteica, o que pode aumentar a expressão de proteínas associadas aos ribossomas em resposta.

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$73.00
$238.00
$717.00
$2522.00
$21420.00
53
(3)

Intercala-se no ADN e impede a síntese de ARN, o que pode afetar indiretamente as vias de síntese proteica, influenciando a expressão de PELO.

Emetine

483-18-1sc-470668
sc-470668A
sc-470668B
sc-470668C
1 mg
10 mg
50 mg
100 mg
$352.00
$566.00
$1331.00
$2453.00
(0)

Inibe a síntese proteica através do bloqueio da translocação, levando potencialmente a um aumento da expressão da proteína de reciclagem do ribossoma.

Tetracycline

60-54-8sc-205858
sc-205858A
sc-205858B
sc-205858C
sc-205858D
10 g
25 g
100 g
500 g
1 kg
$62.00
$92.00
$265.00
$409.00
$622.00
6
(1)

Inibe a síntese proteica nas bactérias e pode causar indiretamente uma regulação positiva dos factores de recuperação dos ribossomas em resposta ao stress.

α-Amanitin

23109-05-9sc-202440
sc-202440A
1 mg
5 mg
$260.00
$1029.00
26
(2)

Inibe a RNA polimerase II e afecta a síntese de mRNA, o que pode levar indiretamente a alterações nos níveis da proteína de reciclagem dos ribossomas.