APY0201
目录号: PL09847 纯度: ≥98.0%
CAS No. :1232221-74-7
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中文名称
APY0201
中文别名
(E)-4-(5-(2-(3-甲基亚苄基)肼基)-2-(吡啶-4-基)吡唑并[1,5-a]嘧啶-7-基)吗啉;N-(3-甲基苄亚基)-N'-[7-(吗啉-4-基)-2-(吡啶-4-基)吡唑并[1,5-a]嘧啶-5-基]肼;APY0201
英文名称
APY0201
英文别名
APY0201;(E)-4-(5-(2-(3-methylbenzylidene)hydrazinyl)-2-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-7-yl)morpholine;APY-0201;4-(5-{2-[(3-methylphenyl)methylidene]hydrazin-1-yl}-2-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-7-yl)morpholine
Cas No.
1232221-74-7
分子式
C23H23N7O
分子量
413.48
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
APY0201 是一种有效的 PIKfyve 抑制剂,抑制 PtdIns3P 转化为PtdIns(3,5)P2,IC50 为 5.2 nM。 APY0201 还抑制 IL-12/IL-23 产生。
生物活性
APY0201 is a potent PIKfyve inhibitor, which inhibits the conversion of PtdIns3P to PtdIns(3,5)P 2 in the presence of in the presence of [P]ATP with an IC 50 of 5.2 nM. APY0201 also inhibits IL-12/IL-23 production.
性状
Solid
IC50 & Target[1][2]
IL-12 IL-23
体外研究(In Vitro)
APY0201 works differently from anti-IL-12/23 antibodies and acts by inhibiting production of these proinflammatory cytokines with characteristic selectivity over other cytokines, including tumor necrosis factor-alpha (TNF-α). In stimulated thioglycollate-induced mouse peritoneal exudate cells (TG-PEC), APY0201 strongly inhibits IL-12p70 and IL-12p40 production, with IC50s of 8.4 and 16 nM, respectively. APY0201 also inhibits IL-12p40 at 99 nM in human PBMC. APY0201 shows significant selectivity for the production of IL-12p70 and IL-12p40 over TNF-α, and this selectivity is maintained across species. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Oral APY0201 at a 30 mg/kg dose shows significant reduction of IL-12p70 production (78% inhibition relative to that of the vehicle control), which implys that the inhibitory potential of APY0201 against IL-12 is confirmed in the animal experiment. 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]. Hayakawa N, et al. Structure-activity relationship study, target identification, and pharmacological characterization of a small molecular IL-12/23 inhibitor, APY0201. Bioorg Med Chem. 2014 Jun 1;22(11):3021-9.
溶解度数据
In Vitro: DMSO : ≥ 35 mg/mL (84.65 mM)配制储备液
搜索质检报告(COA)

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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