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Akt Protein kinase B

Cat.No.  Name Information
M1837 MK-2206 2HCl MK-2206 is a novel allosteric inhibitor of Akt with IC50 values of 8 nM, 12 nM and 65 nM for Akt1, Akt2 and Akt3, respectively.
M3068 TIC10 TIC10 (ONC-201) is a potent, orally active, and stable small molecule that transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.
M5167 Calpeptin Calpeptin is a potent, cell-permeable inhibitor of the Ca2+-dependent protease, calpain.
M1823 Perifosine Perifosine is an orally active Akt inhibitor, the antiproliferative properties of Perifosine with an IC50 of 0.6–8.9 µM.
M2303 Capivasertib (AZD5363) Capivasertib (AZD5363) is a potentially first-in-class, orally effective pan-AKT inhibitor with strong inhibition against all three AKT isomers (AKT1/2/3) at an IC50 of 3 nM/8 nM/8 nM. It also showed similar inhibitory effect on P70S6K/PKA and low inhibitory activity on ROCK1/2.
M5153 SC79 SC79 is a specific and BBB permeable Akt activator used to enhance Akt activity. SC79 activates Akt in the cytosol and inhibits Akt membrane translocation. SC79 specifically binds to the PH domain of Akt. *The compound is unstable in solutions, freshly prepared is recommended
M22523 Recilisib sodium Recilisib (ON 01210) sodium is a radioprotectant, which can activate AKT, PI3K activities in cells.
M4988 AKT inhibitor VIII Akt Inhibitor VIII is a cell-permeable quinoxaline compound that has been shown to potently, selectively, allosterically, and reversibly inhibit Akt1, Akt2, and Akt3 activity (IC50 = 58 nM, 210 nM, and 2.12 μM; respectively).
M54588 LY2780301 LY2780301 is an oral dual-target inhibitor of AKT/RSK that binds to and inhibits the activity of Akt, thereby inhibiting the PI3K/Akt signaling pathway, which in turn inhibits cell proliferation and induces apoptosis in tumor cells, and possesses antitumor activity.
M50436 Akt/SKG Substrate Peptide Akt/SKG Substrate Peptide is a synthetic peptide suitable as a substrate for Akt/PKB, which is not phosphorylated by p70S6K or MAPK1.
M50434 Apoptin-derived peptide Apoptin-derived peptide is an antitumor polypeptide with cytotoxicity.
M50433 TAT-TCL1-Akt-in TAT-TCL1-Akt-in is an Akt inhibitor.
M50432 TCL1(10-24) TCL1(10-24) is a encompassing the betaA strand of human TCL1.
M49821 IPL344 IPL344 is a bioactive peptide that activates Akt pathway cell signaling and can be used in studies related to amyotrophic lateral sclerosis (ALS).
M49782 Larixol Larixol is an fMLP inhibitor and also inhibits Src kinase, ERK1/2, p38 and AKT phosphorylation signals in immune regulation.
M49744 Hu7691 hydrochloride Hu7691 hydrochloride is an orally active, selective Akt inhibitor with IC50s of 4.0 nM, 97.5 nM, 28 nM for Akt1, Akt2 and Akt3, respectively.
M49743 Hu7691 Hu7691 is an orally active, selective Akt inhibitor with IC50s of 4.0 nM, 97.5 nM, 28 nM for Akt1, Akt2 and Akt3, respectively.
M49742 AKT-IN-11 AKT-IN-11 is one of the most effective antibacterial agents against human hepatoma BEL-7402 cell line with an IC50 value of 1.15μM.
M43375 AKT-IN-17 AKT-IN-17 is a AKt inhibitor.
M43374 Dehydrovomifoliol Dehydrovomifoliol is a AKT/mTOR dual inhibitor.
M43373 Reptoside Reptoside, an iridoid glucoside, is a DNA damaging active agent.
M43372 PI3K-IN-48 PI3K-IN-48 is a PI3K inhibitor with IC50 value of 1.55 ± 0.18 μM for A549 cells.
M43371 2-Chlorophenoxazine 2-Chlorophenoxazine is a Akt inhibitor with an IC50 value of 2-5 μM for in vitro.
M43370 AKT-IN-18 AKT-IN-18, an inhibitor of Akt, inhibits Akt with an IC50 of 69.45 μΜ in A549 cells.
M43369 Tubulin/AKT1-IN-1 Tubulin/AKT1-IN-1 is an inhibitor of tubulin polymerization and AKT pathway activation.
M43368 NSC45586 NSC45586 is an inhibitor of pleckstrin homology domain and leucine-rich repeat protein phosphatase (PHLPP).
M43367 AKT-IN-14 AKT-IN-14 is a potent AKTinhibitor with the IC50 values of <0.01 nM, 1.06 nM and 0.66 nM for AKT1, AKT2, AKT3, respectively.
M43366 AKT-IN-14 free base AKT-IN-14 free baseis a potent AKTinhibitor with the IC50 values of <0.01 nM, 1.06 nM and 0.66 nM for AKT1, AKT2, AKT3, respectively.




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