MK-2206 free base structure
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Common Name | MK-2206 free base | ||
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CAS Number | 1032349-93-1 | Molecular Weight | 407.46700 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C25H21N5O | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of MK-2206 free baseMK-2206 free base is an orally active, highly potent and selective allosteric Akt inhibitor, with IC50s of 8, 12, and 65 nM for Akt1, Akt2, and Akt3, respectively. Many breast cancer cell lines, and PIK3CA-mutant and cell lines with PTEN loss are sensitive to MK-2206 free base. MK-2206 free base has anticancer activities[1][2]. |
Name | 8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3-one |
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Synonym | More Synonyms |
Description | MK-2206 free base is an orally active, highly potent and selective allosteric Akt inhibitor, with IC50s of 8, 12, and 65 nM for Akt1, Akt2, and Akt3, respectively. Many breast cancer cell lines, and PIK3CA-mutant and cell lines with PTEN loss are sensitive to MK-2206 free base. MK-2206 free base has anticancer activities[1][2]. |
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Related Catalog | |
Target |
Akt1:8 nM (IC50) Akt2:12 nM (IC50) Akt3:65 nM (IC50) |
References |
[1]. Li Yan, et al. Abstract #DDT01-1: MK-2206: A potent oral allosteric AKT inhibitor. 2009. |
Molecular Formula | C25H21N5O |
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Molecular Weight | 407.46700 |
Exact Mass | 407.17500 |
PSA | 89.33000 |
LogP | 5.35530 |
UNII-51HZG6MP1K |
MK-2206 dihydrochloride |