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Cat. No. | Product Name | Target | Signaling Pathways |
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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。 | |||
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.. | |||
T13230 |
TXNIP-IN-1
|
Others | Others |
TXNIP-IN-1 是硫氧还蛋白-硫氧还蛋白相互作用蛋白复合物抑制剂。它在 TXNIP-TRX 复合物相关代谢紊乱的糖尿病、心血管疾病或炎症疾病方面有研究的价值。 | |||
T5481 |
TRi-1
|
Others | Others |
TRi-1 是不可逆的胞质硫氧还蛋白还原酶1 的特异性抑制剂(IC50:12 nM)。它有抗肿瘤作用,且线粒体毒性很小。 | |||
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。 | |||
T9118 |
KEA1-97
|
Apoptosis; Others; Caspase | Apoptosis; Others; Proteases/Proteasome |
KEA1-97 是一种选择性硫氧还蛋白-半胱天冬酶 3相互作用干扰剂,IC50为10 μM。它在不影响硫氧还蛋白活性的情况下, 破坏硫氧还蛋白与 caspase 3 的相互作用,激活半胱天冬酶,诱导细胞凋亡。 | |||
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. | |||
T4414 |
Eprenetapopt
APR-246,PRIMA-1Met |
Apoptosis; Others; Ferroptosis; p53; Autophagy | Apoptosis; Autophagy; Others |
Eprenetapopt (PRIMA-1Met) 是一种在 TP53突变细胞中恢复野生型 p53功能的小分子,可引发肿瘤细胞凋亡,还抑制硒蛋白硫氧还蛋白还原酶 1。 | |||
T60446 |
LCS3
|
Apoptosis; Glutathione reductase | Apoptosis; oxidation-reduction |
LCS3是一种可逆和非竞争性的谷胱甘肽二硫化物还原酶(GSR)和硫氧还蛋白还原酶1(TXNRD1)的协同抑制剂,IC50分别为3.3μM 和3.8μM。LCS3具有抗肿瘤活性,可诱导细胞凋亡,可用于研究肺腺癌(LUAD)。 | |||
T2283 |
PX-12
2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12 |
Thioredoxin | Metabolism |
PX-12 (PX12) 是一种可逆的硫氧还蛋白-1(Trx-1)抑制剂,能够抑制 MCF-7 细胞(IC50:1.9 μM)和HT-29 细胞(IC50:2.9 μM)的生长。 | |||
T23166 |
PMX 464
|
Others | Others |
inhibitor of the thioredoxin-thioredoxin reductase (Trx-TrxR) system | |||
T70131 |
TPP2a bromide
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TPP2a is a mitochondrial thioredoxin reductase (TrxR) inhibitor. | |||
T24593 |
PAO-PDT
PAO PDT |
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PAO-PDT is a highly selective thioredoxin reductase inhibitor. | |||
T33413 |
Mito-TRFS
MitoTRFS |
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Mito-TRFS is the first off-on probe for imaging the mitochondrial thioredoxin reductase (TrxR2) in live cells. | |||
T29018 |
TrxR inhibitor D9
D9,TrxR-IN-D9 |
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TrxR-IN-D9 is a novel inhibitor of thioredoxin reductase (TrxR). | |||
T28906 |
T6603185
T-6603185,T 6603185 |
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T6603185 is a novel inhibitor of peroxiredoxin (Prx) and thioredoxin (Trx) systems. | |||
T34922 |
TRFS-red
TRFSred |
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TRFS-red is the first red emission off-on probe for thioredoxin reductase. | |||
T39048 |
Sel-green
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Sel-green is a selective selenol fluorescent probe used for quantifying the selenocysteine (Sec) content in the selenoenzyme thioredoxin reductase, as well as imaging endogenous Sec in live HepG2 cells. | |||
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). | |||
T11130 | DVD-445 | Others | Others |
Dvd-445 has good anti-cancer effect.Dvd-445 is an effective peptide covalent thioredoxin reductase 1 (TrxR1) inhibitor with IC50 value of 0.60 mol/L M. | |||
T39915 |
Trx-red
Trx-red,NBL-SS perchlorate |
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Trx-red (NBL-SS perchlorate) is a red-emitting fluorescent probe derived from the nile blue fluorophore. It is specifically designed for imaging thioredoxin (Trx) in live cells and in vivo, with excitation and emission wavelengths of 615 nm and 661 nm, respectively. | |||
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。 | |||
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。 | |||
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。 | |||
T36399 |
PAO-Nap
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PAO-Nap is a chemically modified version of PAO, in which a naphthalimide fluorophore is attached to the compound using a linker called aminocaproic acid. This modified compound, PAO-Nap, exhibits a selective targeting of thioredoxin reductase, leading to the induction of apoptosis in HL-60 cells through oxidative stress mechanisms[1]. | |||
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]. | |||
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。 | |||
T62294 |
SRI-37330 hydrochloride
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SRI-37330 hydrochloride 是一种口服具有活力的硫氧还蛋白相互作用蛋白(TXNIP)抑制剂。SRI-37330 hydrochloride 对胰高血糖素分泌和功能具有抑制作用,可以降低肝脏葡萄糖的产生,逆转肝脏脂肪变性。SRI-37330 hydrochloride 能够用于研究 2 型糖尿病。 | |||
T73512 | ZC0109 | ||
ZC0109 是 IDO1和硫氧还蛋白还原酶 1 (TrxR1) 的双抑制剂,IC50分别为 50 nM 和 3.0 μM。ZC0109 诱导活性氧 (ROS) 积累,使细胞周期阻滞于 G1/S 期,导致癌细胞凋亡 (apoptosis)。 | |||
T78158 |
MitoCur-1
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Others | Others |
MitoCur-1为一种姜黄素类似物,作为线粒体抗氧化硫氧还蛋白还原酶2(TrxR2)抑制剂,展现亲电性与线粒体靶向特性。该化合物能特异性诱导活性氧(ROS)生成,表现出抗肿瘤活性。 | |||
T35811 |
CAY10410
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CAY10410 is an analog of prostaglandin D2/prostaglandin J2 (PGD2/PGJ2) with structural modifications intended to give it PPARγ ligand activity and resistance to metabolism. 15-deoxy-δ12,14-PGJ2 has been shown to be a potent ligand for PPARγ. Metabolism of the cyclopentenone prostaglandins PGA2, PGJ2, and δ12-PGJ2 occurs via glutathione addition across the α,β unsaturated enone. CAY10410 was designed as an analog of the PPARγ-binding prostaglandins which could not undergo this conjugation reactio... | |||
T83871 |
Ferroptocide
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Ferroptocide是一种抑制剂,可抑制硫氧还蛋白(Trx)活性,并且是pleuromutilin的衍生物。在20 µM的浓度下,Ferroptocide能够抑制ES-2卵巢癌细胞中的Trx活性,并对ES-2细胞具有细胞毒性(IC50 = 1.6 µM)。5 µM的Ferroptocide能够诱导ES-2细胞发生铁死亡,这一效应可以通过铁螯合剂去铁胺(DFO)、抗氧化剂Trolox或铁死亡抑制剂ferrostatin-1来阻断。在使用免疫完整但非免疫缺陷小鼠的4T1小鼠乳腺癌模型中,每周两次以50 mg/kg剂量给药时,Ferroptocide能够减少肿瘤体积。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T5372 |
L-SelenoMethionine
L-(+)-Selenomethionine,L-硒代蛋氨酸 |
Apoptosis; Amino Acids and Derivatives; Endogenous Metabolite | Apoptosis; Metabolism |
L-SelenoMethionine (L-(+)-Selenomethionine) 是 Selenomethionine 的 L-异构体,是硒的主要天然食物形式。它是一种癌症化学预防剂,可以增加谷胱甘肽过氧化物酶的表达,还可以通过饮食补充降低癌症的发生率并诱导癌细胞凋亡。 |