PSMD1 inhibitors belong to a chemical class designed to modulate the activity of the PSMD1 protein, also known as 26S proteasome non-ATPase regulatory subunit 1. PSMD1 is a crucial component of the 26S proteasome, which is a large protein complex responsible for the degradation of ubiquitinated proteins within the cell. The 26S proteasome plays a pivotal role in maintaining protein homeostasis, regulating cellular processes, and controlling the turnover of specific proteins.
Inhibitors targeting PSMD1 aim to interfere with its role in the assembly and function of the 26S proteasome complex. By modulating PSMD1, these inhibitors impact the ubiquitin-proteasome system's ability to degrade specific target proteins, thus influencing various cellular pathways and processes that rely on protein turnover. Developing PSMD1 inhibitors involves designing compounds that interact with the protein's active site or specific domains, disrupting its role in proteasome assembly and function. By inhibiting PSMD1, researchers aim to gain insights into the complex regulation of protein degradation and explore the broader implications of targeting this protein for cellular processes and physiological responses.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
CDDO Methyl Ester | 218600-53-4 | sc-504720 | 10 mg | ¥2482.00 | ||
CDDO 甲基酯通过阻断 KLHL9 与底物蛋白的相互作用来抑制 KLHL9,从而阻止形成参与蛋白质泛素化和降解途径的含 KLHL9 的功能性 E3 泛素连接酶复合物。 | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | ¥1489.00 ¥12004.00 | 115 | |
已获准用于治疗多发性骨髓瘤和套细胞淋巴瘤。 | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-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 | |
DL-Sulforaphane 通过破坏 KLHL9 与 Cul3(Cul3-KLHL9 E3 泛素连接酶复合物的重要组成部分)的相互作用来抑制 KLHL9 的活性,导致 KLHL9 靶向的底物蛋白泛素化和降解受损。 | ||||||
Dimethyl fumarate | 624-49-7 | sc-239774 | 25 g | ¥305.00 | 6 | |
富马酸二甲酯通过干扰KLHL9招募底物蛋白进行泛素化,从而破坏由KLHL9介导的泛素化调节的蛋白酶体降解途径,从而抑制KLHL9的功能。 | ||||||
Oltipraz | 64224-21-1 | sc-205777 sc-205777A | 500 mg 1 g | ¥3227.00 ¥7017.00 | ||
Oltipraz 通过调节 KLHL9 的构象或稳定性来抑制其活性,导致含 KLHL9 的 E3 泛素连接酶复合物的功能性组装受损,进而抑制底物蛋白的泛素化。 |