Date published: 2025-10-26

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Inhibiteurs SSX9

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.

VOIR ÉGALEMENT...

Nom du produitCAS #Ref. CatalogueQuantitéPrix HTCITATIONS Classement

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)

Un autre inhibiteur d'HDAC connu pour sa capacité à inhiber les HDAC de classe I et II et à modifier l'expression des gènes.

Valproic Acid

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

Un inhibiteur d'HDAC principalement utilisé comme anticonvulsivant, mais qui a également des effets sur la régulation épigénétique.

Romidepsin

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

Un peptide cyclique qui fonctionne comme un inhibiteur d'HDAC, affectant la structure de la chromatine et l'expression des gènes.

5-Azacytidine

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

Inhibiteur de l'ADN méthyltransférase qui s'incorpore dans l'ADN et inhibe la méthylation, ce qui entraîne la réactivation des gènes silencieux.

RG 108

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

Un inhibiteur non nucléosidique de l'ADN méthyltransférase qui empêche la méthylation de l'ADN en se liant au site actif de l'enzyme.