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Cat. No. | Product Name | Target | Signaling Pathways |
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T9766 |
GW590735
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PPAR | DNA Damage/DNA Repair; Metabolism |
GW590735 是一种有效的选择性 PPARα 激动剂,对 PPARα 的 EC50 为 4 nM,比 PPARδ 和 PPARγ 的选择性至少高 500 倍。 GW590735 可用于血脂异常研究。 | |||
T1319 |
Sodium diatrizoate
Diatrizoic acid sodium salt,Sodium amidotrizoate,Hypaque sodium,泛影酸钠,Diatrizoate sodium,amidotrizoate sodium,Triombrin |
Apoptosis; Others | Apoptosis; Others |
Sodium diatrizoate (Hypaque sodium) 是一种碘化不透射线 X 射线造影剂,在血管造影、尿路造影和放射造影中用作诊断辅助工具。它可通过钙失调诱导线粒体更新和氧化应激,激活细胞凋亡。 | |||
T73912 |
Maysin
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Maysin 是一种具有神经保护作用的 C-糖基黄酮,可以从玉米须中分离得到。Maysin 对 Syn 淀粉样蛋白聚集体-低聚物和原纤维引起的损伤具有保护作用。Maysin 可防止氧化应激和细胞内钙稳态失衡,激活自噬降解过程。Maysin 可用于帕金森病(PD) 的研究。 | |||
T70365 |
JTP-4819
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JTP-4819 is a potent and selective prolyl endopeptidase (PEP) inhibitor with potential for treating Alzheimer's disease. At nanomolar concentration, JTP-4819 inhibited the degradation of substance P, arginine-vasopressin, and thyrotropin-releasing hormone by PEP in supernatants of the rat cerebral cortex and hippocampus. Repeated administration of JTP-4819 reversed the aging-induced decrease in brain substance P-like and thyrotropin-releasing hormone-like immunoreactivity, suggesting that this d... | |||
T127402 |
Coenzyme Q0
CoQ0 |
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Coenzyme Q0 (CoQ0),一种从Antrodia cinnamomea提取的口服醌类化合物,具备促进细胞凋亡(apoptosis)与自噬(autophagy)的作用。该化合物通过抑制HER-2/AKT/mTOR信号通路,增强凋亡和自噬机制;同时,调控NFκB/AP-1活化,提升Nrf2稳定性,从而缓解炎症及氧化还原失衡。此外,Coenzyme Q0还表现出抗血管生成特性,通过下降MMP-9/NF-κB并提升HO-1信号路径发挥作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T0846 |
L-Carnitine
L(-)-Carnitine,Levocarnitine,左旋肉碱 |
Endogenous Metabolite; Fatty Acid Synthase | Metabolism |
L-Carnitine (L(-)-Carnitine) 是一种人内源性分子,在人体内以蛋氨酸和赖氨酸为底物进行生物合成,并参与脂肪酸代谢。L-Carnitine 将长链脂肪酰辅酶A 转运到线粒体。L-Carnitine 能够改善许多先天性代谢错误的代谢失衡。 | |||
T3S1319 |
(+)-Magnoflorine
Escholin,Magnoflorine,Thalictrin,Escholine,木兰花碱 |
Others; Antifungal | Microbiology/Virology; Others |
(+)-Magnoflorine (Thalictrin) 是从 Acoruscalamus 中分到的一种阿朴啡生物碱,可以减少 C. albicans 生物膜的形成,具有抗真菌、抗氧化、抗糖尿病、镇静和抗焦虑的作用。 | |||
T36563 |
(E)-Guggulsterone
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Bile acids are essential for solubilization and transport of dietary lipids, are the major products of cholesterol catabolism, and are physiological ligands for farnesoid X receptor (FXR), a nuclear receptor that regulates genes involved in lipid metabolism.1They are also inherently cytotoxic, as physiological imbalance contributes to increased oxidative stress.2,3Bile acid-controlled signaling pathways are promising novel targets to treat such metabolic diseases as obesity, type II diabetes, hy... |