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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