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首页-小分子抑制剂&激动剂-Epigenetics-Bromodomain-MDP5
MDP5

Chemical Structure : MDP5

CAS No.: 3030921-41-3

MDP5

货号: PC-26515Not For Human Use, Lab Use Only.

MDP5 is a potent BRD4 and PI3K dual inhibitor, exhibits strong binding to BD1 and BD2.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

MDP5 is a potent BRD4 and PI3K dual inhibitor, exhibits strong binding to BD1 and BD2.
MDP5 significantly inhibits the proliferation in both cell lines with IC50 values of 5.57 μM and 5.14 μM, respectively.
MDP5 inhibits cell cycle progression, colony formation, and apoptosis in MB cells.
MDP5 treatment decreases target gene expression at mRNA and protein levels.
MDP5 (20 mg/kg) decreases xenograft tumor burden in MB xenograft mice.
When combined with the KRAS G12D inhibitor MRTX1133, MDP5 resensitized resistant cancer cells.

物理化学性质&存储条件

分子量 365.39
分子式 C21H19NO5
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

8-(2,3-dihydrobenzo[b] [1, 4] dioxin-6-yl)-2-morpholino-4H-chromen-4-one

参考文献

1. Sethi B, et al. J Control Release. 2023 Feb;354:80-90.

2. Ghanwatkar Y, et al. Acta Biomater. 2026 Mar;212:637-654.

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