A lipophilic, cell-permeable cAMP analog which activates cAMP- and cGMP-dependent protein kinase. More potent than cAMP and more resistant to phosphodiesterasese, with good selectivity for site B of PKA. For specific activation of the cAMP pathway the highly membrane permeable Sp-5,6-DCI-cBIMPS (Prod. No. BML-CN135).
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Last modified: May 29, 2024
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