Irsenontrine

(Synonyms: E2027)
目录号: PL09082 纯度: ≥98%
Irsenontrine (E2027) 是一种具有口服活性和选择性的磷酸二酯酶 9 (PDE9) 抑制剂。Irsenontrine (E2027) 可用于神经系统疾病的研究。
CAS No. :1429509-82-9
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中文名称
Irsenontrine
英文名称
Irsenontrine
英文别名
Irsenontrine;54QB00NNRB;E2027;Irsenontrine [USAN];WHO 11606;(S)-7-(2-methoxy-3,5-dimethylpyridin-4-yl)-1-(tetrahydrofuran-3-yl)-1H-pyrazolo[4,3-c]quinolin-4(5H)-one;4H-Pyrazolo(4,3-c)quinolin-4-one, 1,5-dihydro-7-(2-methoxy-3,5-dimethyl-4-pyridinyl)-1-((3S)-tetrahydro-3-furanyl)-;7-(2-Methoxy-3,5-dimethylpyridin-4-yl)-1-((3S)-tetrahydrofuran-3-yl)-1,5-dihydro-4H-pyrazolo(4,3-c)quinolin-4-one
Cas No.
1429509-82-9
分子式
C22H22N4O3
分子量
390.44
包装储存
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
详情描述
Irsenontrine (E2027) 是一种具有口服活性和选择性的磷酸二酯酶 9 (PDE9) 抑制剂。Irsenontrine (E2027) 可用于神经系统疾病的研究。
产品详情
Irsenontrine (E2027) 是一种具有口服活性和选择性的磷酸二酯酶 9 (PDE9) 抑制剂。Irsenontrine (E2027) 可用于神经系统疾病的研究。
生物活性
Irsenontrine (E2027) is an orally active and selective phosphodiesterase 9 (PDE9) inhibitor. Irsenontrine can be used for the research of neurological diseases.
性状
Solid
IC50 & Target[1][2]
PDE9
体外研究(In Vitro)
Irsenontrine (E2027) is an orally active and selective phosphodiesterase 9 (PDE 9) inhibitor. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Irsenontrine (0.3, 3.3 mg/kg; p.o.) exhibits a significant ameliorative effect on the percentage of exploration of the novel object at 3.3 mg/kg in Scopolamine-induced rats.
Irsenontrine (1 mg/kg; p.o.) and memantine hydrochloride (1 mg/kg; p.o.) combined treatment group exhibits a significantly higher percentage of exploration of the novel object than memantine hydrochloride (1 mg/kg) alone. 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
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
ClinicalTrial
参考文献
[1]. Miyamoto, et al. Dementia therapeutic agent combining pyrazoloquinoline derivative and memantine. WO2018221550 A1
[2]. Hershey LA, et al. Pharmacological Management of Dementia with Lewy Bodies. Drugs Aging. 2019;36(4):309-319.
[3]. Eisai to present latest research on Alzheimer’s disease / dementia pipeline at the 14th international conference on Alzhei
溶解度数据
In Vitro: DMSO : 12.5 mg/mL (32.02 mM; warming and heat to 60°C)配制储备液
搜索质检报告(COA)
[1]. Miyamoto, et al. Dementia therapeutic agent combining pyrazoloquinoline derivative and memantine. WO2018221550 A1
[2]. Hershey LA, et al. Pharmacological Management of Dementia with Lewy Bodies. Drugs Aging. 2019;36(4):309-319.
[3]. Eisai to present latest research on Alzheimer’s disease / dementia pipeline at the 14th international conference on Alzhei

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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The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2