Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T29018 |
TrxR inhibitor D9
D9,TrxR-IN-D9 |
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TrxR-IN-D9 is a novel inhibitor of thioredoxin reductase (TrxR). | |||
T29017 |
TrxR1-IN-B19
TrxR1INB19,Go Y015,TrxR1 IN B19,Go-Y015 |
Others | Others |
TrxR1-IN-B19 (TrxR1 IN B19) 是一种 TrxR1 抑制剂,通过靶向 TrxR1 和 ROS 介导的 ER 应激激活,通过小分子选择性杀死胃癌细胞。 | |||
T60453 |
TrxR-IN-3
|
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TrxR-IN-3 (Compound 2c) 是TrxR 的有效抑制剂。TrxR-IN-3 对五种人类癌细胞系表现出强大的抗增殖活性,特别是对乳腺肿瘤细胞。TrxR-IN-3 增加 ROS 水平并通过调节乳腺癌细胞中细胞凋亡相关蛋白的表达导致明显的细胞凋亡。TrxR-IN-3 还通过促进 LC3-II 和 Beclin-1 的表达并减少 LC3-I 和 p62 蛋白的表达,来触发自噬体和自溶酶体的形成。 | |||
T62021 | TrxR-IN-2 | ||
TrxR-IN-2 是潜在的硫氧还蛋白还原酶(TrxR)抑制剂。TrxR-IN-2在治疗耐药性肝细胞癌中有研究价值。 | |||
T61647 | TrxR-IN-5 | ||
TrxR-IN-5 (compound 4f) is an efficacious inhibitor of TrxR (thioredoxin reductase) with an IC50 of 0.16 μM. By elevating the levels of reactive oxygen species (ROS), TrxR-IN-5 fosters robust antiproliferative impacts. Additionally, TrxR-IN-5 demonstrates pronounced effects against cancer proliferation and metastasis [1]. | |||
T73254 | TrxR-IN-4 | ||
TrxR-IN-4 (Compound 1b) 是一种针对 TrxR 的有效抑制剂,能够通过激活 ERS 诱导 HepG2 细胞的凋亡。此外,TrxR-IN-4 通过下调 TrxR 表达量和降低炎症水平,有效改善了 CCl4 诱导的肝损伤。 | |||
T20168 |
Aurothiomalate sodium
金硫丁二钠,Myocrisin,Myocrisine,Miochrysin,Sodium aurothiomalate,Myochrysine,gold sodium thiomalate |
Others; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Others |
Aurothiomalate sodium (Miochrysin) 是一种选择性的致癌 PKCι信号传导抑制剂,可抑制肿瘤细胞增殖。它是一种硫氧还蛋白还原酶 (TrxR) 抑制剂,也是一种抗风湿剂。 | |||
T78781 |
TrxR1-IN-1
|
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TrxR1-IN-1 (Compound 5j) 是一种具有针对性的TrxR1抑制剂,显示出IC50值为8.8 μM的抑制效能。该化合物在治疗癌症方面表现出潜在效果,其对多种癌细胞系的IC50值分别为:MCF-7细胞系1.5 μM、HeLa细胞系1.7 μM、BGC-823细胞系2.4 μM、SW-480细胞系2.8 μM和 A549细胞系2.1 μM。此外,TrxR1-IN-1还表现出了抗氧化特性,能有效清除DPPH自由基。 | |||
T77762 |
ROS-generating agent 1
|
Apoptosis; Ferroptosis; ROS Kinase | Apoptosis; Tyrosine Kinase/Adaptors |
ROS-generating agent 1 具有抗癌活性,通过共价修饰 TrxR 的 Sec-498 残基以生成 ROS。ROS-generating agent 1 降低细胞内 TrxR 蛋白水平,促进 NCI-H460 细胞中 ROS 依赖的性细胞凋亡 (apoptosis) 和铁死亡 (ferroptosis)。 | |||
T39664 |
Ethaselen
BBSKE |
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Ethaselen (BBSKE), a selective thioredoxin reductase (TrxR) inhibitor, is orally active with IC50s of 0.5 and 0.35 μM for wild-type human TrxR1 and rat TrxR1, respectively. Ethaselen specifically binds to the unique selenocysteine-cysteine redox pair located in the C-terminal active site of mammalian TrxR1. As an organoselenium compound, it demonstrates potent antitumor activity against non-small cell lung cancer (NSCLC) by targeting TrxR. | |||
TP1604L |
Thioredoxin reductase peptide acetate
Thioredoxin reductase peptide acetate(950890-23-0 free base) |
Others | Others |
Thioredoxin reductase peptide acetate(950890-23-0 free base) 对应于硫氧还蛋白还原酶 (TrxR) 中的 53–67 位残基,用于硫氧还蛋白还原酶研究。哺乳动物硫氧还蛋白还原酶 (TR) 催化硫氧还蛋白 (Trx) 的氧化还原活性二硫键的还原,并且在结构和谷胱甘肽还原酶的作用机制,除了 C 末端的 16 个氨基酸延伸部分含有一个罕见的连位硒硫键。 | |||
T1303 |
Auranofin
醋硫葡金,SKF-39162 |
Others; SARS-CoV; Antibacterial | Microbiology/Virology; Others |
Auranofin (SKF-39162) 是硫氧还蛋白还原酶抑制剂,IC50为0.2 μM。它也是一种抗风湿剂,用于治疗类风湿性关节炎,改善关节炎症状。 | |||
T70131 |
TPP2a bromide
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TPP2a is a mitochondrial thioredoxin reductase (TrxR) inhibitor. | |||
T40946 |
Seph-PAO
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Seph-PAO, a modified form of polyalphaolefin (PAO) compound, is created by coupling a sepharose fluorophore. Its primary application lies in the detection of thioredoxin reductase (TrxR). | |||
T23166 |
PMX 464
|
Others | Others |
inhibitor of the thioredoxin-thioredoxin reductase (Trx-TrxR) system | |||
T79198 | S-Gem | Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
S-Gem为TrxR依赖性前药,是Gemcitabine的衍生物,能够被TrxR选择性激活。与Gemcitabine相比,S-Gem展现出较低的细胞毒性。 | |||
T75351 | TP-TRFS | ||
TP-TRFS 是高度选择性的一个硫氧还蛋白还原酶 (TrxR) 双光子荧光探针。 | |||
TP1604 |
Thioredoxin reductase peptide
|
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Thioredoxin reductase peptide corresponds to residues 53–67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.Mammalian thioredoxin reductase (TR) catalyzes the reduction of the redox-active disulfide bond of thioredoxin (Trx) and is | |||
TP1375 |
Thioredoxin reductase peptide TFA
|
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Thioredoxin reductase peptide TFA corresponds to residues 53-67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.. | |||
T73825 | TRFS-green | ||
TRFS-green 是用于检测活细胞中、硫氧还蛋白还原酶 (TrxR)、且具有高度选择性的、off−on 荧光探针。TRFS-green 的 λmax 是 377 nm。 | |||
T60618 |
ZC0101
|
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ZC0101 是一种有效的、具有口服活性的 IDO1和 TrxR 双重抑制剂,IC50值分别为 0.084 μM 和 7.98 μM。ZC0101 可诱导癌细胞的凋亡和活性氧的积累。 | |||
T73547 | CPUL1 | ||
CPUL1 是一种TrxR 抑制剂,对 A549 细胞显示出增殖抑制和抗转移活性。CPUL1 通过抑制TrxR1酶活性来诱导 ROS 介导的ERK/JNK 信号传导从而影响上皮-间质转化 (EMT)。CPUL1 与α-Lipoic Acid 或Dithiodipropionic acid 联合使用效果更好。 |