Title : Regulation of chloride channel trafficking by cyclic AMP via protein kinase A-independent pathway in A6 renal epithelial cells.

Pub. Date : 1996 Jun 14

PMID : 8670265






3 Functional Relationships(s)
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1 8-bromo-cAMP (Br-cAMP) increased the open probability of 3 pS Cl- channel and this action was inhibited by pretreatment with H89, an inhibitor of cAMP-dependent protein kinase (PKA). N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide cathelicidin antimicrobial peptide Homo sapiens
2 8-bromo-cAMP (Br-cAMP) increased the open probability of 3 pS Cl- channel and this action was inhibited by pretreatment with H89, an inhibitor of cAMP-dependent protein kinase (PKA). N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide cathelicidin antimicrobial peptide Homo sapiens
3 8-bromo-cAMP (Br-cAMP) increased the open probability of 3 pS Cl- channel and this action was inhibited by pretreatment with H89, an inhibitor of cAMP-dependent protein kinase (PKA). N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide cathelicidin antimicrobial peptide Homo sapiens