產(chǎn)品名稱(chēng) AT 13148 dihydrochloride
產(chǎn)品貨號(hào) Axon 2166 CAS [1056901-62-2] MF C17H16ClN3O.2HClMW 386.70 Purity: 98% Soluble in DMSO Description An oral, ATP-competitive inhibitor of multi-AGC kinases with potent pharmacodynamic and antitumor activity, which shows a distinct mechanism of action from other AKT inhibitors. AT13148 caused substantial blockade of AKT, p70S6K (S6K1), PKA, ROCK, and SGK substrate phosphorylation and induced apoptosis in cancer cells, with IC50 values of 38, 402, 50, 8, 3, 6, 4, 63 nM for AKT1, AKT2, AKT3, p70S6K, PKA, ROCK1, ROCK2, and SGK3 respectively. References Certificates Categories Extra info TA Yap et al. AT13148 Is a Novel, Oral Multi-AGC Kinase Inhibitor with Potent Pharmacodynamic and Antitumor Activity. Clin. Cancer Res. 2012.? Certificate of Analysis Material Safety Data Sheet Apoptosis Cell Signaling & Oncology ROCK Akt PKA PI3K-Akt-mTOR EC 2.7.11.1 SGK ATP-competitive inhibitor of multi-AGC kinases Chemical name (S)-1-(4-(1H-pyrazol-4-yl)phenyl)-2-amino-1-(4-chlorophenyl)ethanol dihydrochloride Parent CAS No. [1056901-62-2] Order Size Unit Price Stock 2 mg €85.00 In Stock
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AT 13148 dihydrochloride

Based on 16 reference(s) in Google Scholar 9 10 16

Axon 2166

CAS [1056901-62-2]

MF C17H16ClN3O.2HCl
MW 386.70

  • Purity: 98%
  • Soluble in DMSO

AT 13148 dihydrochloride

Description

An oral, ATP-competitive inhibitor of multi-AGC kinases with potent pharmacodynamic and antitumor activity, which shows a distinct mechanism of action from other AKT inhibitors. AT13148 caused substantial blockade of AKT, p70S6K (S6K1), PKA, ROCK, and SGK substrate phosphorylation and induced apoptosis in cancer cells, with IC50 values of 38, 402, 50, 8, 3, 6, 4, 63 nM for AKT1, AKT2, AKT3, p70S6K, PKA, ROCK1, ROCK2, and SGK3 respectively.
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