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Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
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货期:1-2天
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MedChemExpress LLC
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1845.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥800.0 |
| 规格: | 5 mg | 产品价格: | ¥2000.0 |
| 规格: | 10 mg | 产品价格: | ¥3500.0 |
| 规格: | 25 mg | 产品价格: | ¥6000.0 |
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Roflumilast N-oxide
CAS No. : 292135-78-5
MCE 国际站:Roflumilast N-oxide
产品活性:Roflumilast N-oxide 是一个 PDE 4 型抑制剂。
研究领域:Metabolic Enzyme/Protease
作用靶点:Phosphodiesterase (PDE)
In Vitro: Roflumilast N-oxide at 2 nM partly mitigates the cigarette smoke extract (CSE)-induced epithelial to mesenchymal transition (EMT) in WD-HBEC in vitro. Roflumilast N-oxide (2 nM) reverses the compromised expression of E-cadherin transcripts following CSE by 45%. The expression of collagen type I is abrogated by Roflumilast N-oxide (2 nM). The epithelial cell phenotype appears protected when cells are co-incubated with Roflumilast N-oxide (2 nM). Pre-incubation with Roflumilast N-oxide (2 nM) also partly attenuates the nuclear translocation of β-catenin.
In Vivo: Single treatment of db/db mice with 10 mg/kg Roflumilast N-oxide enhances plasma glucagon-like peptide-1 (GLP-1) 4-fold. Chronic treatment of db/db mice with Roflumilast N-oxide at 3 mg/kg shows prevention of disease progression. Roflumilast-N-oxide abolishes the increase in blood glucose, reduces the increment in HbA1c by 50% and doubles fasted serum insulin compare with vehicle, concomitants with preservation of pancreatic islet morphology. Furthermore, Roflumilast-N-oxide amplifies forskolin-induced insulin release in primary islets. Roflumilast-N-oxide also shows stronger glucose-lowering effects than its parent compound.
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文献和实验高脂饮食的危害又添实锤!用这种方式悄悄影响你的心脏,一种肠炎
导读高脂肪饮食通常与心血管疾病有关,部分原因是高脂肪饮食中富含胆碱,而胆碱会被肠道微生物转化为三甲胺(Trimethylamine, TMA)。TMA 在肠道中被吸收后转运到肝脏中,进而被氧化为 TMAO(Trimethylamine N-oxide),TMAO 则是一种促进动脉粥样硬化的代谢产物。不过,TMAO 生成途径中仍然存在一个关键但尚未探索的难题:高脂肪饮食下宿主生理和微生物群落之间的相互作用是如何影响 TMAO 产生的?专性厌氧梭菌科(厚壁菌门)和兼性厌氧肠杆菌科(变形菌门)中普遍
with 5-diethoxylphosphoryl-5-methyl-1-pyrroline N -oxide (DEPMPO), indicating that FMN/FMN-binding domain (complex I), ubiquinone (complex I and III), FAD/FAD-binding domain (complex II), and cytochrome b (complex III) control the mediation of O2 •– production
Crystallization of Kinesin Family Motor Proteins
Kar3+N11 (WT)PDB: 1F9TP21a=43.6 Åb=78.8 Åc=47.2 Åß=105.0°1.5 ÅMolecular replacement Kar3 N650KPDB: 1F9UP21a=43.6 Åb=78.0 Åc=47.3 Åß=105.1°1.7 ÅMolecular replacement Kar3 R598APDB: 1F9VP21a=43.9 Åb=77.4 Åc=47.7 Åß=105.9°1.3 ÅMolecular replacement Kar3 E
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