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Volumn 54, Issue 24, 2011, Pages 8681-8692

Structure-activity relationship studies of sulfonylpiperazine analogues as novel negative allosteric modulators of human neuronal nicotinic receptors

Author keywords

[No Author keywords available]

Indexed keywords

1 [(4 FLUOROPHENYL)SULFONYL]PIPERAZINE; 2 [4 [(2 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL] N (1H PYRAZOL 3 YL)ACETAMIDE; 2 [4 [(2 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL] N (4 METHOXYPHENYL)ACETAMIDE; 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL] N (1H INDAZOL 5 YL)ACETAMIDE; 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL] N (1H PYRAZOL 3 YL)ACETAMIDE; 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL] N (4 METHOXYPHENYL)ACETAMIDE; 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL] N PHENYLACETAMIDE; 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETIC ACID; 2 BROMO N (2 FLUOROPHENYL)ACETAMIDE; 4 [2 [4 [(2 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDO]BENZOIC ACID; ACETAMIDE DERIVATIVE; METHYL 4 [2 [4 [(2 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDO]BENZOATE; N (1H PYRAZOL 3 YL) 2 [4 (PYRIDIN 3 YLSULFONYL)PIPERAZIN 1 YL]ACETAMIDE; N (2 FLUOROPHENYL) 2 [4 (PHENYLSULFONYL)PIPERAZIN 1 YL]ACETAMIDE; N (2 FLUOROPHENYL) 2 [4 (PYRIDIN 3 YLSULFONYL)PIPERAZIN 1 YL]ACETAMIDE; N (2 FLUOROPHENYL) 2 [4 [(2 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N (2 FLUOROPHENYL) 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N (2 FLUOROPHENYL) 2 [4 [(4 METHOXYPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N (4 FLUOROPHENYL) 2 [4 [(2 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N (4 FLUOROPHENYL) 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N (4 FLUOROPHENYL) 2 [4 [(4 METHOXYPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N (4 METHOXYPHENYL) 2 [4 (PYRIDIN 3 YLSULFONYL)PIPERAZIN 1 YL]ACETAMIDE; N [(1,1' BIPHENYL) 2 YL] 2 [4 [(2 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N [(1,1' BIPHENYL) 2 YL] 2 [4 [(4 FLUOROPHENYL)SULFONYL]PIPERAZIN 1 YL]ACETAMIDE; N PHENYL 2 [4 (PHENYLSULFONYL)PIPERAZIN 1 YL]ACETAMIDE; NICOTINIC RECEPTOR; PIPERAZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84055211763     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm201294r     Document Type: Article
Times cited : (26)

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