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首页-小分子抑制剂&激动剂-PI3K/Akt/mTOR Pathway-PI3K-GSK1059615
GSK1059615

Chemical Structure : GSK1059615

CAS No.: 958852-01-2

GSK1059615 (GSK 1059615;GSK-1059615)

货号: PC-42850Not For Human Use, Lab Use Only.

GSK1059615 is a highly potent, dual PI3K/mTOR inhibitor with IC50 of 0.4 nM/0.6 nM/2 nM/5 nM and 12 nM for PI3Kα/β/δ/γ and mTOR, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

GSK1059615 is a highly potent, dual PI3K/mTOR inhibitor with IC50 of 0.4 nM/0.6 nM/2 nM/5 nM and 12 nM for PI3Kα/β/δ/γ and mTOR, respectively.
GSK1059615 inhibits survival and proliferation of established (SCC-9, SQ20B and A253 lines) and primary human HNSCC cells.
GSK1059615 blocks PI3K-AKT-mTOR activation in HNSCC cells, induces programmed necrosis but not apoptosis, suppresses SCC-9 tumor growth in nude mice.
GSK1059615 strongly reduces neutrophil-sperm interaction with IC50 of <10 nM in cattle.

物理化学性质&存储条件

分子量 333.3638
分子式 C18H11N3O2S
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

2,4-Thiazolidinedione, 5-[[4-(4-pyridinyl)-6-quinolinyl]methylene]-, (5Z)-

参考文献

1. Carnero A. et al. Expert Opin Investig Drugs. 2009 Sep;18(9):1265-77.

2. Xie J, et al. Oncotarget. 2017 Feb 7;8(31):50814-50823.

3. Leontieva OV, et al. Aging (Albany NY). 2016 Dec 30;8(12):3535-3551.

4. Hong J, et al. Biol Reprod. 2017 Nov 1;97(5):671-687.

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