Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T35329L |
EAD1 TFA(1644388-26-0 Free base)
EAD1 HCL(1644388-26-0 Free base) |
Apoptosis; Autophagy | Apoptosis; Autophagy |
EAD1 HCL 是一种有效的自噬 (autophagy) 抑制剂,在肺癌和胰腺癌细胞中具有抗增殖活性。EAD1 HCL 还诱导凋亡 (apoptosis)。 | |||
T41180 |
JQAD1
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
JQAD1是一种有效的、选择性的组蛋白乙酰转移酶 EP300降解剂(PROTAC;DC50≤31.6nM);其包含 EP300抑制剂A485,通过连接体连接至脑啡肽E3连接酶配体。JQAD1以蛋白酶体依赖的方式导致神经母细胞瘤细胞系中EP300的降解。JQAD1抑制H3K27ac 和EP300的表达水平并诱导细胞凋亡。JQAD1抑制Kelly 细胞异种移植的NSG 小鼠的肿瘤生长。CRC 和MYCN 基因表达水平在JQAD1治疗的肿瘤中下调。JQAD1在诱导EP300降解的浓度下对共活化剂CBP 没有显著影响。 | |||
T78915 |
AD186
|
Sigma receptor | GPCR/G Protein |
AD186, 作为一种选择性S1R激动剂,具有高效率,其Ki值对 S1R 为2.7 nM,对 S2R 为27 nM。同时,AD186 能够完全抵消BD-1063对痛觉异常的抑制作用。 | |||
T39531 |
RAD16-I hydrochloride
RAD16-I hydrochloride |
||
RAD16-I hydrochloride is a self-assembling peptide with nanofibrous morphology that provides an optimal microenvironment for the proliferation and differentiation of human mesenchymal stem cells (hMSC) into chondrocytes. This peptide, known as RAD16-I, has been extensively studied and serves as a model to assess the amyloid-like staining properties of self-assembling peptide nanofibers (SAPNFs). | |||
T83753 |
RAD17-derived Peptide TFA
|
||
RAD17衍生肽是一种针对共济失调-毛细血管扩张及RAD3相关蛋白/激酶(ATR)的肽类底物。它已被用于识别ATR的抑制剂。 | |||
T35329 |
EAD1
|
Autophagy | Autophagy |
EAD1是一种有效的自噬(autophagy)抑制剂,在 BxPC3细胞中 IC50为5.8 μM。它在肺癌和胰腺癌细胞中具有抗增殖活性。 | |||
T81885 |
Mad1 (6-21) (TFA)
|
||
Mad1 (6-21) TFA,作为Mad1蛋白的6-21片段,与哺乳动物Sin3A PAH2结合,其Kd约为29 nM。 | |||
T41012 |
Mad1 (6-21)
Mad1 (6-21) |
||
Mad1 (6-21) is a peptide fragment derived from the Mad1 protein, specifically encompassing residues 6 to 21. This fragment exhibits binding affinity towards the mammalian Sin3A PAH2 domain, with a Kd value of approximately 29 nM. |