Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7814 |
Alloxan monohydrate
|
Proteasome | Proteases/Proteasome; Ubiquitination |
Alloxan Monohydrate 是一种能够引起糖尿病的致糖尿病药物。它作为蛋白酶体抑制剂,破坏胰腺中能够分泌胰岛素的B 细胞,导致实验动物患糖尿病。 | |||
T2154 |
MG-132
Z-LLL-al,Z-Leu-Leu-Leu-CHO |
Apoptosis; Proteasome; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome; Ubiquitination |
MG-132 (Z-Leu-Leu-Leu-al) 是一种 26S 蛋白酶体抑制剂 (IC50=100 nM),具有细胞渗透性、可逆性。MG-132 可作为自噬激活剂,可诱导凋亡。 | |||
T78353 |
alpha-2,6-Sialyltransferase (Pd26ST)
|
||
alpha-2,6-Sialyltransferase (Pd26ST) 能够催化末端和内部半乳糖及N-乙酰半乳糖胺的唾液酸化,形成末端α2,6-唾液酸苷。 | |||
T9090 |
MUN57694
|
Proteasome | Proteases/Proteasome; Ubiquitination |
MUN57694 是 26S 蛋白酶体的抑制剂。 | |||
T1932 |
B-AP15
NSC 687852 |
Apoptosis; DUB | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination |
B-AP15 (NSC-687852) 是 26S 蛋白酶体的去泛素化酶 Usp14 和 UCHL5 的选择性抑制剂。 它阻断 26S 蛋白酶体的去泛素化活性。 | |||
T36902 |
RA375
RA375 |
Proteasome | Proteases/Proteasome; Ubiquitination |
RA375 是一种 RPN13(26S 蛋白酶体调节亚基)抑制剂。 RA375 激活 UPR 信号、ROS 产生和细胞凋亡。 RA375 对癌症细胞的活性比 RA190 高 10 倍,这反映了它的硝基环取代基和氯乙酰胺弹头的添加。 | |||
T60487 |
DDO-7263
|
Nrf2 | Immunology/Inflammation |
DDO-7263 是一种 1,2,4-Oxadiazole 衍生物, 通过与 Rpn6 结合上调 Nrf2,从而阻断 26S 蛋白酶体的组装和随后Nrf2 的泛素化降解。DDO-7263 是一种有效的Nrf2激活剂,能够激活 Nrf2-ARE 信号通路并发挥抗炎活性。 | |||
T21617 |
MG-115
Z-LL-Nva-CHO |
Proteasome | Proteases/Proteasome; Ubiquitination |
MG-115 (Z-LL-Nva-CHO) 是一种有效且可逆的蛋白酶体抑制剂,对20S 和26S 蛋白酶体的 Ki 值分别为 21 nM 和 35 nM。MG-115 特异性抑制蛋白酶体的胰凝乳蛋白酶样活性,诱导 p53 依赖性细胞凋亡。 | |||
T77796 |
DL-Borneol
(endo)-Borneol,Borneol,(±)-Borneol |
GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
DL-Borneol ((endo)-Borneol) 是一种从中药中提取的小分子,是一种可口服的生物佐剂,可以改善药物向大脑的输送,常用作治疗心脑血管疾病的中药的辅助成分。 | |||
T37011 |
Boc-LRR-AMC
|
||
Boc-LRR-AMC is a fluorogenic substrate for the trypsin-like activity of the 26S proteasome or 20S proteolytic core. Upon enzymatic cleavage by the 26S proteasome or 20S proteolytic core, amino-4-methylcoumarin (AMC) is released and its fluorescence can be used to quantify 26S proteasome or 20S proteolytic core trypsin-like activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively. | |||
T76038 |
Ac-Nle-Pro-Nle-Asp-AMC
|
||
Ac-Nle-Pro-Nle-Asp-AMC 是26S 蛋白酶体(26Sproteasome)的特异性底物,适用于分析26S 蛋白酶体中caspase样活性。 | |||
T77939 |
WBC100
14-D-Valine-TPL |
c-Myc | Cell Cycle/Checkpoint |
WBC100(14-D-Valine-TPL),一款高效、选择性和具口服活性的c-Myc小分子降解剂,通过针对泛素E3连结酶CHIP介导的26S蛋白酶体途径实现其作用。主要应用于c-Myc过表达肿瘤的研究领域。 | |||
T37417 |
Z-LLE-AMC
|
||
Z-LLE-AMC is a fluorogenic substrate for the caspase-like post-glutamate peptide hydrolase of the 26S proteasome or 20S proteolytic core. Caspase-like activity can be quantified by fluorescent detection of free AMC (also known as 7-amino-4-methylcoumarin), which is excited at 340-360 nm and emits at 440-460 nm. Z-LLE-AMC is typically used in cell lysates after experimental treatment. | |||
T37418 |
Z-LLL-AMC
|
||
Z-LLL-AMC is a fluorogenic substrate for the chymotrypsin-like activity of the 26S proteasome or 20S proteolytic core. Chymotrypsin-like activity can be quantified by fluorescent detection of free AMC (also known as 7-amino-4-methylcoumarin), which is excited at 340-360 nm and emits at 440-460 nm. Z-LLL-AMC is typically used in cell lysates after experimental treatment. | |||
T62080 |
GSK3494245
|
||
GSK3494245 (DDD01305143) 是一种有效的、选择性的、口服具有活力的、可在夹在 β4 和 β5 亚基之间的位点结合寄生虫蛋白酶体 (proteasome) 的糜蛋白酶样活性抑制剂,能够作用于 WTL.donovani 蛋白酶体,其 IC50 值为 0.16μM。GSK3494245 表现出良好的生物安全特性。GSK3494245 对人蛋白酶体的糜蛋白酶样活性具有适当的抑制作用 (IC50: 26S=13 μM;富集的 THP-1 提取物 IC50=40 μM)。 |