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.
| 製品名 | CAS # | カタログ # | 数量 | 価格 | 引用文献 | レーティング |
|---|---|---|---|---|---|---|
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
特定のチロシンキナーゼを阻害し、細胞シグナル伝達と増殖に影響を及ぼす。 | ||||||
Erlotinib Hydrochloride | 183319-69-9 | sc-202154 sc-202154A | 10 mg 25 mg | $74.00 $119.00 | 33 | |
上皮成長因子受容体(EGFR)キナーゼを阻害し、シグナル伝達経路に影響を及ぼす。 | ||||||
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 | |
生化学研究に用いられるセリンプロテアーゼ阻害剤。 | ||||||
Okadaic Acid | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $285.00 $520.00 $1300.00 | 78 | |
プロテイン・ホスファターゼ1および2Aを強力に阻害する。 | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $58.00 $170.00 | 15 | |
L型カルシウムチャネルを阻害し、カルシウム依存性のシグナル伝達に影響を及ぼす。 | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
オートファジーとリソソーム分解を阻害し、SERTM1に関連するタンパク質のターンオーバーに影響を及ぼす可能性がある。 | ||||||
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 | |
HDAC阻害剤で、遺伝子発現に影響を与え、SERTM1に影響を与える可能性がある。 | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
がん治療に用いられるHDAC阻害剤は、SERTM1に関連する経路に影響を与える可能性がある。 | ||||||