 
                Chemical Structure : KT5720
CAS No.: 108068-98-0
Catalog No.: PC-23453Not For Human Use, Lab Use Only.
KT5720 is a potent, cell-permeable, specific, reversible and ATP-competitive PKA inhibitor with IC50 of 3.3 uM.
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|---|---|---|---|
| 50 ug | $138 | In stock | |
| 100 ug | $238 | In stock | |
| 500 ug | $598 | In stock | |
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                        KT5720 is a potent, cell-permeable, specific, reversible and ATP-competitive PKA inhibitor with IC50 of 3.3 uM.
KT5720 is effective in reversing MDR1-mediated multidrug resistance.
KT5720 also reduces the excitability of dorsal root ganglion (DRG) neurons by attenuating Hyperpolarization-activated cyclic nucleotide-gated (HCN) channel activity and reducing intracellular Ca2+ concentrations.
| M.Wt | 537.62 | |
| Formula | C32H31N3O5 | |
| Appearance | Solid | |
| Storage | 
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| Solubility | 10 mM in DMSO | |
| Chemical Name/SMILES | 9,12-Epoxy-1H-diindolo[1,2,3-fg:3′,2′,1′-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid, 2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-, hexyl ester, (9R,10S,12S)- | |
1. Davies SP, et al. Biochem J. 2000 Oct 1;351(Pt 1):95-105.
2. Galski H, et al. Leuk Res. 2006 Sep;30(9):1151-8.

 
                 
                 
                 
                 
                 
                 
                 
                 
            
            
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