Artemisone (Synonyms: 青蒿酮; Artemifone; BAY 44-9585)
目录号: PL08860 纯度: ≥98.0%
CAS No. :255730-18-8
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中文名称
Artemisone
中文别名
青蒿标准品;青蒿酮
英文名称
Artemisone
英文别名
Thiomorpholine,4-[(3R,5aS,6R,8aS,9R,10R,12R,12aR)-decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-yl]-,1,1-dioxide;Artemifone;Thiomorpholine,4-[(3R,5aS,6R,8aS,9R,10R,12R,12aR)-decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10;4-[(3R,5aS,6R,8aS,9R,10R,12R,12aR)-decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-yl]thiomorpholine 1,1-dioxide;4-benzamide;Benzamide, 4-[(3-nitrophenoxy)methyl]-;CTK3C2059;10alpha-[4'-(S,S-Dioxothiomorpholin-1'-yl)]-10-deoxodihydroartemisinin;BAY 44-9585;Artemisone
Cas No.
255730-18-8
分子式
C19H31NO6S
分子量
401.52
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Artemisone (Artemifone) 是一种有效、半合成的抗疟疾剂,能够抑制多种 P. falciparum,平均 IC50 值为 0.83 nM。Artemisone 还是一种人 CMV 的有效抑制剂。
生物活性
Artemisone (Artemifone) is a potent and semi-synthetic antimalarial, inhibits P. falciparum strains, with a mean IC 50 of 0.83 nM. Artemisone is also a potent inhibitor of human CMV.
性状
Solid
IC50 & Target[1][2]
Plasmodium
体外研究(In Vitro)
Artemisone inhibits 3D7 and K1 P. falciparum , with IC50s of 0.88±0.59 and 1.23±0.64 nM, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Artemisone is effectve at inhibiting the parasitaemia in the P. berghei NY susceptible strain, with an ED 50 of 9.62 mg/kg via subcutaneous route and 11.67 mg/kg via oral administration.
Artemisone (3, 1, 0.3 and 0.1 mg/kg, s.c.) in combination with ohter antimalarials has enhanced effect against the chloroquine-resistant line P. yoelii NS has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Vivas L, et al. Antimalarial efficacy and drug interactions of the novel semi-synthetic endoperoxide artemisone in vitro and in vivo. J Antimicrob Chemother. 2007 Apr;59(4):658-65.
[2]. Ruiyuan Cao, et al. Anti-SARS-CoV-2 Potential of Artemisinins In Vitro. ACS Infect. Dis. 2020 Jul.
溶解度数据
In Vitro: DMSO : 130 mg/mL (323.77 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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