Camizestrant (Synonyms: AZD-9833)
目录号: PL03570 纯度: ≥98%
CAS No. :2222844-89-3
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中文名称
Camizestrant
英文名称
Camizestrant
英文别名
N-[1-(3-Fluoropropyl)azetidin-3-yl]-6-[(6S,8R)-8-methyl-7-(2,2,2-trifluoroethyl)-3,6,8,9-tetrahydrop;AZD9833;JUP57A8EPZ;Camizestrant;Camizestrant [USAN];NSC828717;WHO 11592;AZ14066724;3-Pyridinamine, N-(1-(3-fluoropropyl)-3-azetidinyl)-6-((6S,8R)-6,7,8,9-tetrahydro-8-methyl-7-(2,2,2-trifluoroethyl)-3H-pyrazolo(4,3-F)isoquinolin-6-yl)-;Unii-jup57A8epz;AZD-9833
Cas No.
2222844-89-3
分子式
C24H28F4N6
分子量
476.51
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Camizestrant (AZD-9833) 是一种有效的口服活性雌激素受体 (ER) 拮抗剂。Camizestrant 可以用于 ER+ HER2-乳腺癌的相关研究。
生物活性
Camizestrant (AZD-9833) is a potent and orally active estrogen receptor (ER) antagonist. Camizestrant is used for the study of ER HER2-advanced breast cancer.
性状
Solid
IC50 & Target[1][2]
IC50: estrogen receptor (ER)
体外研究(In Vitro)
Camizestrant is extracted from patent US20180111931A1, example 17. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Camizestrant (oral administration; 0.2-50 mg/kg; 20 days) exhibits anti-tumour efficacy as a dose-dependent manner in human parental MCF7 mice xenograft.
Camizestrant (oral administration; 0.8-40 mg/kg; 30 days) decreases tumor growth as a dose-dependent manner. It gives almost complete tumour growth inhibition at the doses >10 mg/kg in mice.
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
ClinicalTrial
参考文献
[1]. Bernard Christophe Barlaam, etal. Chemical compounds. Patent US20180111931.
溶解度数据
In Vitro: DMSO : 100 mg/mL (209.86 mM; Need ultrasonic)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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