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Cat. No.	Product Name	Target	Signaling Pathways
T19780	2,2′-Dipyridyl disulfide 2,2'-Dipyridyl disulfide,OPSS,2,2'-二硫二吡啶,Aldrithiol 2,Orthopyridyl disulfide	Others	Others
	2,2′-Dipyridyl disulfide (Aldrithiol 2) 是肽化学中的常用试剂，是测定巯基的有用试剂，常用于氧化还原缩合以形成肽键或用于偶联反应以形成二硫键连接的异二聚体。
T25372	EMD57033 EMD-57033,(+)-EMD 57033,EMD 57033	Calcium Channel; Carbonic Anhydrase	Membrane transporter/Ion channel; Metabolism
	EMD57033是一种心脏肌钙蛋白C（cTnC）激活剂，是一种显性的Ca2+增敏剂。EMD57033通过与心脏/慢速骨骼肌钙蛋白C 异构体结合从而发挥促进心脏收缩的功能。
T78870	TWIK-1/TREK-1-IN-3	Potassium Channel	Membrane transporter/Ion channel
	TWIK-1/TREK-1-IN-3 是一种具有选择性和有效性的钾通道 TREK-1 抑制剂，对含有双孔域钾(K2p)通道的TREK-1同二聚体和TWIK-1/TREK-1异二聚体有抑制作用。TWIK-1/TREK-1-IN-3 具有抗抑郁活性，可用于研究抑郁症。
T32107	HX-603 HX 603
	HX-603 is a selectivity agonist of RXR that inhibits the activation of RAR-RXR heterodimers as well as RXR homodimers.
T78868	TWIK-1/TREK-1-IN-1	Potassium Channel	Membrane transporter/Ion channel
	TWIK-1/TREK-1-IN-1 (compound 2a) 是一种针对 TWIK 相关钾通道 (Potassium Channel) TREK-1 的抑制剂，有效抑制 TREK-1 的双孔域钾 (K2p) 通道，阻止其二聚化形成 TREK-1 同二聚体和 TWIK-1/TREK-1 异二聚体。作为抗抑郁治疗的潜在靶点，TWIK-1/TREK-1-IN-3 对 TREK-1 同二聚体和 TWIK-1/TREK-1 异二聚体表现出相当的选择性，IC50s 分别是 9.36 μM 和 14.6 μM，显示出抗抑郁样活性。
T61401	3-(3-Phenoxybenzyl)amino-β-carboline
	3-(3-Phenoxybenzyl)amino-β-carboline is a highly effective tubulin inhibitor, selectively degrading αβ-tubulin heterodimers. It induces cell cycle arrest and apoptosis in the G2/M phase. Additionally, 3-(3-Phenoxybenzyl)amino-β-carboline displays notable anticancer activity [1].
T38460	SN52
	SN52 is a powerful, competitive, and cell-permeable inhibitor of NF-κB2. It is a variant of the SN50 peptide. SN52 effectively prevents the nuclear translocation of p52-RelB heterodimers, exhibiting a robust radiosensitization effect on prostate cancer cells. This compound holds significant potential for cancer research purposes.
T15748	LG100754 UVI 2112	PPAR	DNA Damage/DNA Repair; Metabolism
	LG100754 (UVI 2112)是一种通过RXR 发挥作用的胰岛素增敏剂。LG100754是RXR 二聚体调节剂。LG100754是RXR:RXR 同二聚体拮抗剂，以及RXR:PPARα和RXR:PPPARγ异二聚体的激动剂。