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The difference between the unsubstituted phenylpiperazine and 4-methylphenylpiperazine analogs is very small (2- to 3-fold) in terms of binding affinity based on our previous antagonist work. See:
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The difference between the unsubstituted phenylpiperazine and 4-methylphenylpiperazine analogs is very small (2- to 3-fold) in terms of binding affinity based on our previous antagonist work. See:. Chen C.W., Tran J.A., Jiang W., Tucci F.C., Arellano M., Wen J., Fleck B.A., Marinkovic D., White N.S., Pontillo J., Saunders J., Madan A., Foster A.C., and Chen C. Bioorg. Med. Chem. Lett. 16 (2006) 4800
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The difference between the unsubstituted phenylpiperazine and 4-(trifluoromethyl)phenylpiperazine analogs is very small (about 2-fold) in terms of binding affinity based on our previous antagonist work. See:
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The difference between the unsubstituted phenylpiperazine and 4-(trifluoromethyl)phenylpiperazine analogs is very small (about 2-fold) in terms of binding affinity based on our previous antagonist work. See:. Chen C.W., Tran J.A., Jiang W., Tucci F.C., Arellano M., Wen J., Fleck B.A., Marinkovic D., White N.S., Pontillo J., Saunders J., Madan A., Foster A.C., and Chen C. Bioorg. Med. Chem. Lett. 16 (2006) 4800
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