BDP9066
目录号: PL10865 纯度: ≥98%
CAS No. :2226507-04-4
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中文名称
BDP9066
英文名称
BDP9066
英文别名
BDP9066;(S)-8-(3-(Pyrimidin-4-yl)-1H-pyrrolo[2,3-b]pyridin-4-yl)-1,8-diazaspiro[5.5]undecane;(6~{S})-8-(3-pyrimidin-4-yl-1~{H}-pyrrolo[2,3-b]pyridin-4-yl)-1,8-diazaspiro[5.5]undecane;A16874;AQ5
Cas No.
2226507-04-4
分子式
C20H24N6
分子量
348.44
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
BDP9066 是肌强直性肌营养不良相关 Cdc-42 结合激酶 MRCK 的选择性有效抑制剂,其在 SCC12 细胞中测得对 MRCKβ 的IC50 值为 64 nM,对 MRCKα/β 的 Ki 值分别为 0.0136 nM 和 0.0233 nM。BDP9066 可用来研究皮肤癌。
生物活性
BDP9066 is a potent and selective myotonic dystrophy-related Cdc42-binding kinase MRCK inhibitor with an IC 50 of 64 nM for MRCKβ in SCC12 cells, K i values of 0.0136 nM and 0.0233 nM for MRCKα/β in house determinations, respectively. BDP9066 has therapeutic effect on skin cancer by reducing substrate phosphorylation.
性状
Solid
IC50 & Target[1][2]
IC50: 64 nM (MRCKβ in SCC12 cells), Ki: 0.0136 nM/0.0233 nM (MRCKα/β).
体外研究(In Vitro)
BDP9066 shows antiproliferative effects with greatest activity in hematologic cancer cells. BDP9066 inhibits MLC phosphorylation and blocks SCC12 squamous cell carcinoma motility and invasion. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
BDP9066 topical application significantly decreases phosphorylated MRCKα S1003 staining and tumor volumes. 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]. Unbekandt M, et al. Discovery of Potent and Selective MRCK Inhibitors with Therapeutic Effect on Skin Cancer. Cancer Res. 2018 Apr 15;78(8):2096-2114.
溶解度数据
In Vitro: DMSO : 10 mg/mL (28.70 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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