AZD4573

目录号: PL01988 纯度: ≥99%
AZD4573 是一种有效且高度选择性的 CDK9 抑制剂 (IC50 值小于 4 nM),可用于血液恶性肿瘤的研究。
CAS No. :2057509-72-3
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中文名称
AZD4573
英文名称
AZD4573
英文别名
AZD4573;AZD4573 free base;(1S,3R)-3-acetamido-N-(5-chloro-4-(5,5-dimethyl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)pyridin-2-yl)cyclohexane-1-carboxamide;E5XSP3X68B;s8719;(1S,3R)-3-(Acetylamino)-N-(5-chloro-4-(5,6-dihydro-5,5-dimethyl-4H-pyrrolo(1,2-b)pyrazol-3-yl)-2-pyridinyl)cyclohexanecarboxamide
Cas No.
2057509-72-3
分子式
C22H28ClN5O2
分子量
429.94
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
AZD4573 是一种有效且高度选择性的 CDK9 抑制剂 (IC50 值小于 4 nM),可用于血液恶性肿瘤的研究。
产品详情
AZD4573 是一种有效且高度选择性的 CDK9 抑制剂 (IC50 值小于 4 nM),可用于血液恶性肿瘤的研究。
生物活性
AZD4573 is a potent and highly selective CDK9 inhibitor (IC 50 of <4 nM) that enables transient target engagement for the treatment of hematologic malignancies.
性状
Solid
IC50 & Target[1][2]
CDK9 4 nM (IC50)
体外研究(In Vitro)
Short-term treatment with AZD4573 led to a rapid dose- and time-dependent decrease in cellular pSer2-RNAPII, resulting in activation of caspase 3 and cell apoptosis in a broad range of haematological cancer cell lines (e.g. caspase activation EC50 13.7 nM in an acute myeloid leukemia model MV4-11) . has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
AZD4573 exhibits a short half-life in multiple species (less than one hour in rat, dog and monkey) and good solubility for intravenous administration. 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 Barlaam, et al. Abstract 1650: Discovery of AZD4573, a potent and selective inhibitor of CDK9 that enables transient target engagement for the treatment of hematologic malignancies. Cancer Research. July 2018. 78(13): Supplement.
溶解度数据
In Vitro: DMSO : 50 mg/mL (116.30 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Bernard Barlaam, et al. Abstract 1650: Discovery of AZD4573, a potent and selective inhibitor of CDK9 that enables transient target engagement for the treatment of hematologic malignancies. Cancer Research. July 2018. 78(13): Supplement.

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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