SERTM1 inhibitors are a class of chemical compounds designed to specifically inhibit the SERTM1 protein, a lesser-known member of a larger family of proteins involved in cellular processes such as signaling, transport, and regulation of various biological functions. SERTM1 is thought to play a role in membrane transport or signaling pathways within cells, although its exact functions are not fully elucidated. By inhibiting SERTM1, these compounds can interfere with its role in cellular processes, potentially disrupting pathways where SERTM1 is involved. This can affect cellular communication, signal transduction, or other transport-related mechanisms where the protein plays a regulatory or supporting role.
The development of SERTM1 inhibitors involves structural studies of the protein to identify key binding sites or domains that are critical for its function. These inhibitors are often designed to bind specifically to these active or regulatory regions, blocking SERTM1's interaction with its substrates or other cellular components. The goal is to achieve high specificity in inhibiting SERTM1 while avoiding cross-reactivity with other related proteins that may share structural similarities. This requires a detailed understanding of the molecular architecture of SERTM1, often obtained through techniques like molecular modeling, crystallography, or computational docking studies. By inhibiting SERTM1, these compounds provide valuable tools for studying the protein's role in cellular transport and signaling pathways, helping to clarify its broader significance in maintaining cellular homeostasis and regulation of intracellular processes. The development of SERTM1 inhibitors contributes to the larger field of research focused on understanding membrane proteins and their roles in coordinating complex cellular activities.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
抑制特定的酪氨酸激酶,影响细胞信号传导和生长。 | ||||||
Erlotinib Hydrochloride | 183319-69-9 | sc-202154 sc-202154A | 10 mg 25 mg | $74.00 $119.00 | 33 | |
抑制表皮生长因子受体(EGFR)激酶,影响信号传导途径。 | ||||||
AEBSF hydrochloride | 30827-99-7 | sc-202041 sc-202041A sc-202041B sc-202041C sc-202041D sc-202041E | 50 mg 100 mg 5 g 10 g 25 g 100 g | $50.00 $120.00 $420.00 $834.00 $1836.00 $4896.00 | 33 | |
一种丝氨酸蛋白酶抑制剂,用于生化研究。 | ||||||
Okadaic Acid | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $285.00 $520.00 $1300.00 | 78 | |
蛋白磷酸酶 1 和 2A 的强效抑制剂。 | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $58.00 $170.00 | 15 | |
抑制 L 型钙通道,影响钙依赖性信号传导。 | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
抑制自噬和溶酶体降解,可能影响与 SERTM1 有关的蛋白质周转。 | ||||||
Trichostatin A | 58880-19-6 | sc-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 | |
一种 HDAC 抑制剂,可影响基因表达,从而可能影响 SERTM1。 | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
用于癌症治疗的 HDAC 抑制剂可能会影响与 SERTM1 有关的通路。 |