货号:A758766
同义名:
栗精胺
/ 6,7-Diepicastanospermine; NSC 625381
Castanospermine是一种天然生物碱,能够抑制 α/β-葡萄糖苷酶,具有抗炎、抗病毒和抗前列腺癌转移作用。
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快速发货 顺丰冷链运输,1-2 天到达
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描述 | Castanospermine inhibits all forms of α- and β-glucosidases, especially glucosidase l (required for glucoprotein processing by transfer of mannose and glucose from asparagine-linked lipids). |
Concentration | Treated Time | Description | References | |
HepG2 cells | 0.5 mM | Prolonged the association of transferrin with chaperones (calnexin and calreticulin), prevented completion of folding, and promoted aggregate formation | EMBO J. 1997 Sep 1;16(17):5420-32 | |
Peripheral blood mononuclear cells (PBMCs) | 169-339 μM | 14 days | Inhibited HIV-1 and HIV-2 replication, but the effects were less persistent compared to H9 cells | Antimicrob Agents Chemother. 1989 Jan;33(1):53-7 |
H9 cells | 42-339 μM | 12 days | Inhibited HIV-1 replication, reduced gp120 cell surface expression, and blocked virus spread | Antimicrob Agents Chemother. 1989 Jan;33(1):53-7 |
Huh-7 cells | 85.7 μM (IC50) | 24 h | Evaluate the inhibitory effect of Castanospermine on DEN-2 in Huh-7 cells, showing an IC50 of 85.7 μM. | J Virol. 2005 Jul;79(14):8698-706 |
BHK-21 cells | 1 μM (IC50) | 72 h | Evaluate the inhibitory effect of Castanospermine on DEN-2, showing an IC50 of 1 μM in BHK-21 cells. | J Virol. 2005 Jul;79(14):8698-706 |
2B4 T hybridoma cells | 100 μg/ml | 3 h | Inhibition of glucosidase activity severely impaired the assembly of clonotypic TCRα with TCRβ, leading to accelerated degradation of TCRα proteins and failure to form αβ dimers. | EMBO J. 1994 Aug 15;13(16):3678-86 |
BW5147 T cells | 100 μg/ml | 3 h | Inhibition of glucosidase activity resulted in markedly accelerated degradation of nascent TCRα proteins with a half-life of ~20 min, while TCRβ protein stability was unaffected. | EMBO J. 1994 Aug 15;13(16):3678-86 |
canine pancreas microsomes | 1 mM | 1 h | To study the effect of CST on the binding of HA to CNX and CRT, results showed that CST inhibited the binding of HA to CNX and CRT. | EMBO J. 1996 Jun 17;15(12):2961-8 |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
5.29mL 1.06mL 0.53mL |
26.43mL 5.29mL 2.64mL |
52.85mL 10.57mL 5.29mL |
CAS号 | 79831-76-8 |
分子式 | C8H15NO4 |
分子量 | 189.21 |
SMILES Code | O[C@@H]1[C@@H](O)[C@H](O)[C@]([C@@H](O)CC2)([H])N2C1 |
MDL No. | MFCD00017555 |
别名 | 栗精胺 ;6,7-Diepicastanospermine; NSC 625381; 1,6,7,8-Tetrahydroxyoctahydroindolizine; 6-Epicastanospermine |
运输 | 蓝冰 |
InChI Key | JDVVGAQPNNXQDW-TVNFTVLESA-N |
Pubchem ID | 54445 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
溶解方案 |
DMSO: 105 mg/mL(554.94 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 H2O: 100 mg/mL(528.52 mM),配合低频超声助溶 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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