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                同义名:
                    
                        
                            
                                Phellodendrine (chloride)
                            
                        
                    
                
                
                
                    
                     
                
            
Phellodendrine chloride是从黄柏树皮中分离纯化的天然产物,具有抗肾炎作用,可能通过抑制小管中的巨噬细胞和细胞毒性 T 淋巴细胞的增殖或迁移起作用。还通过调节 AKT/NF-κB 通路抑制 AAPH 引起的氧化应激。
 
                                 
                                
                            

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| 产品名称 | Akt ↓ ↑ | Akt1 ↓ ↑ | Akt2 ↓ ↑ | Akt3 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Honokiol | ✔ | MEK | 98% | ||||||||||||||||
| PF-04691502 | ++++ P-Akt (S473), IC50: 3.8 nM P-Akt (T308), IC50: 7.5 nM | 98+% | |||||||||||||||||
| PHT-427 | + Akt, Ki: 2.7 μM | 99%+ | |||||||||||||||||
| Deguelin | ✔ | PI3K | 99%+ | ||||||||||||||||
| TIC10 isomer | ✔ | ERK | 98+% | ||||||||||||||||
| Perifosine | + Akt, IC50: 4.7 μM | 98% | |||||||||||||||||
| Miltefosine | ✔ | PI3K,PKC | 98% | ||||||||||||||||
| Triciribine | + Akt, IC50: 130 nM | 99%+ | |||||||||||||||||
| Uprosertib | + Akt1, IC50: 180 nM | + Akt2, IC50: 328 nM | ++ Akt3, IC50: 38 nM | 99%+ | |||||||||||||||
| Afuresertib | ++++ Akt1, Ki: 0.08 nM | ++++ Akt2, Ki: 2 nM | ++++ Akt3, Ki: 2.6 nM | 99%+ | |||||||||||||||
| Miransertib | ++++ Akt1, IC50: 5 nM | ++++ Akt2, IC50: 4.5 nM | ++ Akt3, IC50: 16 nM | 98+% | |||||||||||||||
| GSK-690693 | ++++ Akt1, IC50: 2 nM | +++ Akt2, IC50: 13 nM | +++ Akt3, IC50: 9 nM | 99%+ | |||||||||||||||
| AT7867 | ++ Akt1, IC50: 32 nM | ++ Akt2, IC50: 17 nM | ++ Akt3, IC50: 47 nM | PKA | 99%+ | ||||||||||||||
| AKT inhibitor VIII | ++ Akt1, IC50: 58 nM | + Akt2, IC50: 210 nM | + Akt3, IC50: 2119 nM | 97% | |||||||||||||||
| MK-2206 2HCl | +++ Akt1, IC50: 8 nM | +++ Akt2, IC50: 12 nM | + Akt3, IC50: 65 nM | 99%+ | |||||||||||||||
| Ipatasertib | ++++ Akt1, IC50: 5 nM | ++ Akt2, IC50: 18 nM | +++ Akt3, IC50: 8 nM | 99%+ | |||||||||||||||
| AT13148 | ++ Akt1, IC50: 38 nM | + Akt2, IC50: 402 nM | ++ Akt3, IC50: 50 nM | PKA | 95% | ||||||||||||||
| Capivasertib | ++++ Akt1, IC50: 3 nM | +++ Akt2, IC50: 8 nM | +++ Akt3, IC50: 8 nM | 99%+ | |||||||||||||||
| A-674563 HCl | +++ Akt1, Ki: 11 nM | PKA | 99% | ||||||||||||||||
| CCT128930 | +++ Akt2, IC50: 6 nM | PKA | 95% | ||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | Phellodendrine HCl, an isoquinoline alkaloid, is one of important characteristic ingredients in the Phellodendri chinensis cortex. Phellodendrine inhibited AChE activity in a dose-dependent manner with IC50 of 36.51 μM[2]. Phellodendrine, but not berberine, exhibited antioxidant activity by increasing radical scavenging activity. Phellodendrine may promote autophagy by regulating the AMPK-mTOR signalling pathway, thereby reducing intestinal injury due to UC(ulcerative colitis)[3]. And PHE (Phellodendrine) exerted the protective activity against AAPH-induced oxidative stress through down-regulating AKT phosphorylation and NF-kB3 expression, which associate with modulation of IKK phosphorylation in zebrafish embryos[4]. | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.65mL 0.53mL 0.26mL | 13.23mL 2.65mL 1.32mL | 26.46mL 5.29mL 2.65mL | |
| CAS号 | 104112-82-5 | 
| 分子式 | C20H24ClNO4 | 
| 分子量 | 377.86 | 
| SMILES Code | C[N@+]1(CC2=C(C=C(O)C(OC)=C2)C3)[C@]3([H])C4=C(C=C(OC)C(O)=C4)CC1.[Cl-] | 
| MDL No. | MFCD01732398 | 
| 别名 | Phellodendrine (chloride) | 
| 运输 | 蓝冰 | 
| InChI Key | DGLDSNPMIYUWGN-OOJQBDKLSA-N | 
| Pubchem ID | 59818 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C | 
| 溶解方案 | DMSO: 50 mg/mL(132.32 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
 
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