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Cat. No. | Product Name | Target | Signaling Pathways |
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T17316 |
α-Lipoic acid-NHS
DL-α-Lipoic acid-NHS |
Others | Others |
α-Lipoic acid-NHS is an alkyl/ether-based PROTAC linker utilized in the synthesis of PROTACs [1]. | |||
T26599 |
Alpha-Lipoic Acid Choline Ester
EV-06,EV 06,alphaLACE,alpha-LACE,EV06,alpha LACE |
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Alpha-Lipoic Acid Choline Ester is used potentially to treat presbyopia. | |||
T6157 |
Devimistat
CPI-613,辛酸,CPI613,CPI 613,6,8-Bis(benzylthio)octanoic acid |
Apoptosis; Dehydrogenase; Mitochondrial Metabolism | Apoptosis; Metabolism |
Devimistat (6,8-Bis(benzylthio)octanoic acid) 是一种线粒体代谢抑制剂,还是一种lipoic acid 拮抗剂,能阻断线粒体能量代谢,诱导多种癌细胞凋亡。 | |||
T35628 |
AN-7
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α-Lipoic acid is a cyclic disulfide antioxidant that interconverts with its reduced dithiol form. It is an essential cofactor for decarboxylation reactions of the citric acid cycle and acts as a general antioxidant. AN-7 is a more lipophilic analog of α-lipoic acid with enhanced potency and 1.5-fold increased maximal capacity to stimulate glucose transport into myocytes. This identifies the analogs of lipoic acid as potential new treatments for diabetes. | |||
T37827 |
CAY10506
CAY10506 |
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Anti-diabetic drugs of the thiazolidinedione (TZD) structural class as well as α-lipoic acid activate peroxisome proliferator-activated receptor γ (PPARγ), a nuclear transcription factor that controls glucose metabolism and lipid homeostasis. CAY10506 is a hybrid lipoic acid-TZD derivative that transactivates human PPARγ with an EC50 value of 10 μM. | |||
T21234 |
(R)-Dihydrolipoic acid
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(R)-Dihydrolipoic acid is a R-isomer of Dihydrolipoic acid. It is optically active, but only the R-enantiomer is biochemically significant. The lipoic acid/dihydrolipoic acid pair participate in a variety of biochemical transformations. | |||
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。 | |||
T74496 |
LA-Bac8c
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LA-Bac8c为经硫辛酸修饰的抗菌肽,展现出增强的抗菌效能。针对金黄色葡萄球菌、MRSA、表皮葡萄球菌、大肠杆菌及铜绿假单胞菌的MIC值分别为1、4、8、8和8μg/mL,显示其对上述菌株具有强效的抑制作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T2930 |
α-Lipoic Acid
Lipoic acid,Alphalipoic acid,硫辛酸 |
NF-κB; HIV Protease; Mitochondrial Metabolism; Endogenous Metabolite | Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
α-Lipoic Acid (Alphalipoic acid) 抑制 NF-κB 依赖性 HIV-1 LTR 活化。 α-硫辛酸诱导内质网 (ER) 应激介导的肝癌细胞凋亡。α-硫辛酸是一种抗氧化剂,是线粒体酶复合物的重要辅助因子。 | |||
T0200 |
α-Lipoic Acid
Thioctic acid,DL-α-Lipoic acid,(±)-α-Lipoic acid,α-硫辛酸,硫辛酸 |
Apoptosis; NF-κB; HIV Protease; Mitochondrial Metabolism; Endogenous Metabolite | Apoptosis; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
α-Lipoic Acid (DL-α-Lipoic acid) 是线粒体酶复合物的重要辅助因子,是一种抗氧化剂,可抑制NF-κB 依赖性的HIV-1LTR 活化。它还可诱导内质网应激介导的肝癌细胞凋亡。 | |||
T22235 |
Lipoic acid
R-(+)-硫辛酸,硫辛酸,R-(+)-Thioctic acid,(R)-(+)-1,2-Dithiolane-3-pentanoic acid,(R)-(+)-α-Lipoic acid |
Reactive Oxygen Species; Mitochondrial Metabolism; Endogenous Metabolite | Immunology/Inflammation; Metabolism; NF-κB |
Lipoic acid (R-(+)-Thioctic acid) ((R)-(+)-α-Lipoic acid) 是一种抗氧化剂,是线粒体酶复合物的重要辅助因子。与外消旋 Lipoic acid 相比,Lipoic acid ((R)-(+)-α-Lipoic acid)更有效。 | |||
T72429 |
α-Lipoic Acid sodium
Thioctic acid sodium,DL-α-Lipoic acid sodium,Thioctic acid sodium ; (±)-α-Lipoic acid sodium ; DL-α-Lipoic acid sodium,(±)-α-Lipoic acid sodium |
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α-Lipoic Acid (Thioctic acid) sodium 是一种抗氧化剂,是线粒体酶复合物的重要辅助因子。α-Lipoic Acid sodium 可抑制NF-κB 依赖性的HIV-1LTR 活化。α-Lipoic Acid sodium 诱导内质网应激 (ERS) 介导的肝癌细胞凋亡 (apoptosis)。α-Lipoic Acid sodium 可与CPUL1 合成自组装的纳米聚合体 CPUL1-LA NA,其抗肿瘤效果优于 CPUL1。 |