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Volumn 64, Issue 2, 2012, Pages 326-335

Synthesis, anticonvulsant activity and 5-HT1A/5-HT7 receptors affinity of 1-[(4-arylpiperazin-1-yl)-propyl]-succinimides

Author keywords

3,3 disubstituted pyrrolidine 2,5 diones; Anticonvulsant activity; Arylpiperazines

Indexed keywords

1 [3 (4 PHENYLPIPERAZIN 1 YL)PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (2 CHLOROPHENYL) PIPERAZIN 1 YL]PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (2 CHLOROPHENYL)PIPERAZIN 1 YL]PROPYL] 3 METHYL 3 PHENYLPYRROLIDINE 2,5, DIONE MONOHYDROCHLORIDE; 1 [3 [4 (2 FLUOROPHENYL) PIPERAZIN 1 YL]PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (2 FLUOROPHENYL)PIPERAZIN 1 YL]PROPYL] 3 METHYL 3 PHENYLPYRROLIDINE 2,5, DIONE MONOHYDROCHLORIDE; 1 [3 [4 (2 METHOXYPHENYL) PIPERAZIN 1 YL]PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (2 METHOXYPHENYL)PIPERAZIN 1 YL]PROPYL] 3 METHYL 3 PHENYLPYRROLIDINE 2,5, DIONE MONOHYDROCHLORIDE; 1 [3 [4 (3 CHLOROPHENYL) PIPERAZIN 1 YL]PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (3 CHLOROPHENYL)PIPERAZIN 1 YL]PROPYL] 3 METHYL 3 PHENYLPYRROLIDINE 2,5, DIONE MONOHYDROCHLORIDE; 1 [3 [4 (3 TRIFLUOROMETHYLPHENYL) PIPERAZIN 1 YL]PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (3 TRIFLUOROMETHYLPHENYL)PIPERAZIN 1 YL]PROPYL] 3 METHYL 3 PHENYLPYRROLIDINE 2,5, DIONE MONOHYDROCHLORIDE; 1 [3 [4 (4 CHLOROPHENYL) PIPERAZIN 1 YL]PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (4 CHLOROPHENYL)PIPERAZIN 1 YL]PROPYL] 3 METHYL 3 PHENYLPYRROLIDINE 2,5, DIONE MONOHYDROCHLORIDE; 1 [3 [4 (4 FLUOROPHENYL) PIPERAZIN 1 YL]PROPYL] 3 ETHYL 3 METHYLPYRROLIDINE 2,5 DIONE MONOHYDROCHLORIDE; 1 [3 [4 (4 FLUOROPHENYL)PIPERAZIN 1 YL]PROPYL] 3 METHYL 3 PHENYLPYRROLIDINE 2,5, DIONE MONOHYDROCHLORIDE; ANTICONVULSIVE AGENT; PHENYTOIN; SEROTONIN 1A RECEPTOR; SEROTONIN 7 RECEPTOR; UNCLASSIFIED DRUG;

EID: 84862214322     PISSN: 22995684     EISSN: 22995684     Source Type: Journal    
DOI: 10.1016/S1734-1140(12)70772-7     Document Type: Article
Times cited : (14)

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