Inhibition of stimulated Jurkat cell adenosine 3′,5′-cyclic monophosphate synthesis by the immunomodulatory compound HR32577Abbreviations: PGE2, prostaglandin E2; FKN, forskolin; CTX, cholera toxin; cAMP, adenosine 3′,5′-cyclic monophosphate; IBMX, 3-isobutyl-1-methylxanthine; NCA, niclosamide; FCCP, carbonyl cyanide p-trifluoromethoxyphenyl hydrazone; DHO-DH, dihydroorotate dehydrogenase; IL-2, interleukin-2; and HBSS, Hanks’ balanced salt solution
Curnock, Adam P., Thomson, T.Andrew, Westwood, Robert, Kuo, Elizabeth A., Williamson, Richard A., Yea, Christopher M., Ruuthb, Erik
Published in Biochemical pharmacology (01.01.2001)
Published in Biochemical pharmacology (01.01.2001)
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Journal Article
Inhibition of stimulated Jurkat cell adenosine 3′,5′-cyclic monophosphate synthesis by the immunomodulatory compound HR325
Curnock, Adam P., Thomson, T.Andrew, Westwood, Robert, Kuo, Elizabeth A., Williamson, Richard A., Yea, Christopher M., Ruuthb, Erik
Published in Biochemical pharmacology (15.01.2001)
Published in Biochemical pharmacology (15.01.2001)
Get full text
Journal Article