Date published: 2025-9-9

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SSX9 Inibidores

SSX9 inhibitors represent a class of chemical compounds that specifically target and inhibit the activity of the SSX9 protein. SSX9, part of the Synovial Sarcoma X breakpoint protein family, is a transcriptional regulator involved in various cellular processes. These inhibitors function by binding to specific active sites or regulatory domains of the SSX9 protein, thereby hindering its ability to interact with other molecular targets or participate in the transcriptional machinery. This inhibition can result in the modulation of gene expression patterns, which can have far-reaching effects on cellular functions such as differentiation, proliferation, and apoptosis. The design and synthesis of SSX9 inhibitors involve a thorough understanding of the protein's structure, including its active sites, binding pockets, and interaction surfaces. Techniques such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and computational modeling are often employed to elucidate these structural details and guide the development of potent and selective inhibitors.

The chemical architecture of SSX9 inhibitors can vary widely, incorporating diverse functional groups and scaffolds to achieve optimal binding affinity and specificity. Common structural features include heterocyclic cores, aromatic rings, and hydrophobic moieties that enhance interactions with the SSX9 protein. Additionally, these inhibitors may be designed to possess favorable physicochemical properties, such as solubility and stability, to facilitate their experimental use. Advanced synthetic techniques, including combinatorial chemistry and high-throughput screening, are often utilized to generate and evaluate large libraries of potential inhibitors. Once promising candidates are identified, further refinement through medicinal chemistry approaches, such as structure-activity relationship (SAR) studies, can optimize their inhibitory efficacy. Overall, the development of SSX9 inhibitors involves a multidisciplinary approach, integrating structural biology, synthetic chemistry, and molecular biology to achieve precise modulation of the SSX9 protein's activity.

VEJA TAMBÉM

Nome do ProdutoCAS #Numero de CatalogoQuantidadePrecoUso e aplicacaoNOTAS

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$149.00
$470.00
$620.00
$1199.00
$2090.00
33
(3)

Outro inibidor da HDAC conhecido pela sua capacidade de inibir as HDAC de classe I e II e de alterar a expressão genética.

Valproic Acid

99-66-1sc-213144
10 g
$85.00
9
(1)

Um inibidor da HDAC que é utilizado principalmente como anticonvulsivo, mas que também tem efeitos na regulação epigenética.

Romidepsin

128517-07-7sc-364603
sc-364603A
1 mg
5 mg
$214.00
$622.00
1
(1)

Um péptido cíclico que funciona como inibidor da HDAC, afectando a estrutura da cromatina e a expressão genética.

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

Um inibidor da DNA metiltransferase que se incorpora no DNA e inibe a metilação, levando à reativação de genes silenciados.

RG 108

48208-26-0sc-204235
sc-204235A
10 mg
50 mg
$128.00
$505.00
2
(1)

Um inibidor não nucleósido da DNA metiltransferase que impede a metilação do DNA ligando-se ao local ativo da enzima.