Title : Synthesis and binding affinity of bidentate phenothiazines with two different photoactive groups.

Pub. Date : 1995 Sep-Oct

PMID : 8974455






3 Functional Relationships(s)
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1 The development of targeted, bidentate photoaffinity reagents for mapping the interacting domains of calmodulin (CaM) with the enzymes that it regulates required the synthesis and evaluation of the binding affinity of various phenothiazines. Phenothiazines calmodulin 3 Homo sapiens
2 The development of targeted, bidentate photoaffinity reagents for mapping the interacting domains of calmodulin (CaM) with the enzymes that it regulates required the synthesis and evaluation of the binding affinity of various phenothiazines. Phenothiazines calmodulin 3 Homo sapiens
3 The phenothiazines that possessed photoactive 3-azido and benzophenone groups and in which one of the piperazine nitrogens in the side chain was converted to a quaternary, N-methylammonium iodide inhibited the calmodulin-mediated activation of phosphodiesterase at a level comparable to that of chlorpromazine. Phenothiazines calmodulin 3 Homo sapiens