Title : 7-Benzylamino-6-chloro-2-piperazino-4-pyrrolidino-pteridine, a potent inhibitor of cAMP-specific phosphodiesterase, enhancing nuclear protein binding to the CRE consensus sequence in human tumour cells.

Pub. Date : 2002 Feb 15

PMID : 11992633






4 Functional Relationships(s)
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1 7-Benzylamino-6-chloro-2-piperazino-4-pyrrolidino-pteridine, a potent inhibitor of cAMP-specific phosphodiesterase, enhancing nuclear protein binding to the CRE consensus sequence in human tumour cells. 8-chloro-cyclic adenosine monophosphate regulating synaptic membrane exocytosis 2 Homo sapiens
2 The cAMP-specific phosphodiesterase isoenzyme family PDE4 represents the highest cAMP-hydrolysing activity in many human cancer cell lines including the human large cell lung carcinoma cell line LXFL529L. 8-chloro-cyclic adenosine monophosphate phosphodiesterase 4A Homo sapiens
3 The cAMP-specific phosphodiesterase isoenzyme family PDE4 represents the highest cAMP-hydrolysing activity in many human cancer cell lines including the human large cell lung carcinoma cell line LXFL529L. 8-chloro-cyclic adenosine monophosphate phosphodiesterase 4A Homo sapiens
4 DC-TA-46 mediated inhibition of PDE4 activity in LXFL529L cells resulted in an increase of the intracellular cAMP level and significant induction of the activity of protein kinase A (PKA). 8-chloro-cyclic adenosine monophosphate phosphodiesterase 4A Homo sapiens