Name | 8-(4-chlorophenylthio) adenosine-3',5'-cyclic monophosphorothioate, sp-isomer sodium salt |
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Description | Sp-8-CPT-cAMPS, a cAMP analog, is a potent and selective activator of the cAMP-dependent protein kinas A (PKA I and PKA II). Sp-8-CPT-cAMPS selects site A of RI compares to site A of RII by 153-fold and site B of RII compares to site B of RI by 59-fold[1][2]. |
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Related Catalog | |
Target |
PKA[1] |
In Vitro | Sp-8-CPT-cAMPS (100 μM; 24 h) enhances the IL-1β-stimulated nitrite release, and increases the release ofnitrite by vascular smooth muscle cells by 3 fold in the absence of IL-1β in vascular smooth muscle cells[2]. Sp-8-CPT-cAMPS (100 μM; 24 h) increases IL-1β-induced expression of iNOS protein in rat aortic smooth muscle cells[2]. Sp-8-CPT-cAMPS (10 μM; 30 min) exhibits anti-spasmogenic activity on ACh-induced tension development in guinea-pig trachealis[3]. |
References |
Molecular Formula | C16H14ClN5NaO5PS2 |
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Molecular Weight | 509.85900 |
Exact Mass | 508.97600 |
PSA | 207.80000 |
LogP | 3.77360 |