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AKT Inhibitor
MK-2206 2HCl 是一种高度选择性的 Akt1/2/3 抑制剂,其 IC50 分别为 8 nM/12 nM/65 nM。- Bopei Cui, .et al. , Signal Transduct Target Ther, 2023, Sep 25;8(1):366 PMID: 37743418
- Yi-Ru Pan, .et al. , Int J Biol Sci, 2023, May 21;19(9):2772-2786 PMID: 37324940
- Giorgio Caratti, .et al. , EMBO Rep, 2023, Feb 6;24(2):e55363 PMID: 36520372
- Ming-Chun Hung, .et al. , Cell Biosci, 2022, 12: 122 PMID: 35918763
- Yusuke Murase, .et al. , Oncol Rep, 2022, Apr;47(4):61 PMID: 35088890
- Majid Momeny, .et al. , Life Sci, 2021, Dec 15;287:120100 PMID: 34715143
- Ali Nasrollahzadeh, .et al. , Biochim Biophys Acta Mol Cell Res, 2021, Jun 26;1868(10):119087 PMID: 34182011
- Rona Aviram, .et al. , PLoS Biol, 2021, Dec 30;19(12):e3001492 PMID: 34968386
- Cristina Rosell??-Busquets, .et al. , Front Mol Neurosci, 2020, 13: 56 PMID: 32317932
- Dai-Chi Liu, .et al. , eNeuro, 2020, Mar 27;7(2):ENEURO.0438-19.2020 PMID: 32161037
- Nishihama K, .et al. , Metabolism, 2018, May;82:88-99 PMID: 29366755
- J Wei, .et al. , bioRxiv, 2018, 2018
- Joo Sang Lee, .et al. , Nat Commun, 2018, 9: 2546 PMID: 29959327
- Wan-Ting Hu, .et al. , Am J Cancer Res, 2018, 8(9): 1739-1751 PMID: 30323967
- Angela M. Gocher, .et al. , J Biol Chem, 2017, Aug 25; 292(34): 14188-14204 PMID: 28634229
- Kusuyama J, .et al. , Biochem J, 2017, Oct 5;474(20):3421-3437 PMID: 28887384
- Pi-Lin Sung, .et al. , Oncotarget, 2016, Jan 26; 7(4): 4036-4047 PMID: 26716408
- Mikaël M. Martino, .et al. , Nat Commun, 2016, 7: 11051 PMID: 27001940
- Dominik Schulz, .et al. , Am J Cancer Res, 2016, 6(9): 1963-1975 PMID: 27725902
- Jewett KA, .et al. , J Neurochem., 2015, Oct;135(2):226-33 PMID: 26250624
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Akt inhibitor
AT7867 二盐酸盐是一种强效的 ATP-竞争性抑制剂,针对 Akt1/2/3 和 p70S6K/PKA,其 IC50 分别为 32 nM/17 nM/47 nM 和 85 nM/20 nM,除 AGC激酶家族 外几乎没有活性。 -
Akt inhibitor
Akt 抑制剂 GSK2141795 与 Akt 结合并抑制其活性,这可能导致抑制 PI3K/Akt 信号通路和肿瘤细胞增殖,并诱导肿瘤细胞凋亡。 -
AKT inhibitor
ARQ 092 是一种口服活性、高效和选择性的 AKT 抑制剂,其 IC50 值分别为:5.0 nM(AKT1);4.5 nM(AKT2);16 nM(AKT3)。 -
Akt inhibitor
Afuresertib 是一种效力强大的口服生物利用度 Akt 抑制剂,其 Ki 分别为 Akt1 0.08 nM、Akt2 2 nM 和 Akt3 2.6 nM。目前处于 第二阶段 临床试验。