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0.125% Ropivacaine is similar to 0.125% bupivacaine for labor analgesia using patient-controlled epidural infusion
0.125% Ropivacaine is similar to 0.125% bupivacaine for labor analgesia using patient-controlled epidural infusion
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0.125% Ropivacaine is similar to 0.125% bupivacaine for labor analgesia using patient-controlled epidural infusion

OWEN, M. D ; D'ANGELO, R ; GERANCHER, J. C ; THOMPSON, J. M ; FOSS, M. L ; BABB, J. D ; EISENACH, J. C

Anesthesia and analgesia, 1998-03, Vol.86 (3), p.527-531 [Periódico revisado por pares]

Hagerstown, MD: Lippincott

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2
0.2% ropivacaine with or without Fentanyl for Patient-Controlled Epidural Analgesia after Major abdominal Surgery: a Double-Blind Study
0.2% ropivacaine with or without Fentanyl for Patient-Controlled Epidural Analgesia after Major abdominal Surgery: a Double-Blind Study
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0.2% ropivacaine with or without Fentanyl for Patient-Controlled Epidural Analgesia after Major abdominal Surgery: a Double-Blind Study

Berti, Marco ; Casati, Andrea ; Fanelli, Guido ; Albertin, Andrea ; Palmisano, Sara ; Danelli, Giorgio ; Comotti, Laura ; Torri, Giorgio

Journal of clinical anesthesia, 2000-06, Vol.12 (4), p.292-297 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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3
1-[1-(2-Benzo[ b]thiopheneyl)cyclohexyl]piperidine hydrochloride (BTCP) yields two active primary metabolites in vivo : Identification and quantification of BTCP primary metabolites in mice plasma, urine, and brain and their affinity for the neuronal dopamine transporter
1-[1-(2-Benzo[ b]thiopheneyl)cyclohexyl]piperidine hydrochloride (BTCP) yields two active primary metabolites in vivo : Identification and quantification of BTCP primary metabolites in mice plasma, urine, and brain and their affinity for the neuronal dopamine transporter
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1-[1-(2-Benzo[ b]thiopheneyl)cyclohexyl]piperidine hydrochloride (BTCP) yields two active primary metabolites in vivo : Identification and quantification of BTCP primary metabolites in mice plasma, urine, and brain and their affinity for the neuronal dopamine transporter

Deleuze-Masquefa, Carine ; Michaud-Dutreilh, Martine ; Vignon, Jacques ; Kamenka, Jean-Marc

European journal of pharmaceutical sciences, 2000-02, Vol.9 (4), p.345-354 [Periódico revisado por pares]

Shannon: Elsevier B.V

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4
1-[1-(2-Benzo[b]thiopheneyl)cyclohexyl]piperidine Hydrochloride (BTCP) Yields Two Active Primary Metabolites in Vitro:  Synthesis, Identification from Rat Liver Microsome Extracts, and Affinity for the Neuronal Dopamine Transporter
1-[1-(2-Benzo[b]thiopheneyl)cyclohexyl]piperidine Hydrochloride (BTCP) Yields Two Active Primary Metabolites in Vitro:  Synthesis, Identification from Rat Liver Microsome Extracts, and Affinity for the Neuronal Dopamine Transporter
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1-[1-(2-Benzo[b]thiopheneyl)cyclohexyl]piperidine Hydrochloride (BTCP) Yields Two Active Primary Metabolites in Vitro:  Synthesis, Identification from Rat Liver Microsome Extracts, and Affinity for the Neuronal Dopamine Transporter

Deleuze-Masquefa, Carine ; Michaud, Martine ; Vignon, Jacques ; Kamenka, Jean-Marc

Journal of medicinal chemistry, 1997-12, Vol.40 (25), p.4019-4025 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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5
1-(1-naphthyl)-piperazine, a mixed 5-HT1A and 5-HT2A/2C receptor ligand, elicits an anxiolytic-like effect in the open-field test without changes in 5-HT metabolism
1-(1-naphthyl)-piperazine, a mixed 5-HT1A and 5-HT2A/2C receptor ligand, elicits an anxiolytic-like effect in the open-field test without changes in 5-HT metabolism
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1-(1-naphthyl)-piperazine, a mixed 5-HT1A and 5-HT2A/2C receptor ligand, elicits an anxiolytic-like effect in the open-field test without changes in 5-HT metabolism

PRUUS, K ; RUDISAAR, R ; VAARMANN, A ; MATTO, V ; ALLIKMETS, L

Methods and findings in experimental and clinical pharmacology, 2002-04, Vol.24 (3), p.151-157 [Periódico revisado por pares]

Barcelona: Prous

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6
1-(1-Naphthyl)piperazine as a novel template for 5-HT6 serotonin receptor ligands
1-(1-Naphthyl)piperazine as a novel template for 5-HT6 serotonin receptor ligands
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1-(1-Naphthyl)piperazine as a novel template for 5-HT6 serotonin receptor ligands

LEE, Mase ; RANGISETTY, Jagadeesh B ; PULLAGURLA, Manik R ; DUKAT, Małgorzata ; SETOLA, Vince ; ROTH, Bryan L ; GLENNON, Richard A

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (6), p.1707-1711 [Periódico revisado por pares]

Oxford: Elsevier

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7
1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists:  Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives
1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists:  Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives
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1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists:  Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives

Jeppesen, Lone ; Olesen, Preben H ; Hansen, Lena ; Sheardown, Malcolm J ; Thomsen, Christian ; Rasmussen, Thøger ; Jensen, Anders Fink ; Christensen, Michael S ; Rimvall, Karin ; Ward, John S ; Whitesitt, Celia ; Calligaro, David O ; Bymaster, Frank P ; Delapp, Neil W ; Felder, Christian C ; Shannon, Harlan E ; Sauerberg, Per

Journal of medicinal chemistry, 1999-06, Vol.42 (11), p.1999-2006 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
1-[2-(4-Nitrophenoxy)acetyl]pyrrolidin-2-one: an antiamnesic agent
1-[2-(4-Nitrophenoxy)acetyl]pyrrolidin-2-one: an antiamnesic agent
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1-[2-(4-Nitrophenoxy)acetyl]pyrrolidin-2-one: an antiamnesic agent

THAMOTHARAN, S ; PARTHASARATHI, V ; MALIK, R ; JINDAL, D. P ; PIPLANI, P ; LINDEN, Anthony

Acta crystallographica. Section C, Crystal structure communications, 2003-09, Vol.59 (Pt 9), p.o514-o515 [Periódico revisado por pares]

Oxford: Blackwell

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9
1,1-Diphenyl-3-dialkylamino-1-silacyclopentane derivatives: a new class of potent and selective 5-HT1A antagonists
1,1-Diphenyl-3-dialkylamino-1-silacyclopentane derivatives: a new class of potent and selective 5-HT1A antagonists
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1,1-Diphenyl-3-dialkylamino-1-silacyclopentane derivatives: a new class of potent and selective 5-HT1A antagonists

DAMOUR, D ; BARREAU, M ; DUTRUC-ROSSET, G ; DOBLE, A ; PIOT, O ; MIGNANI, S

Bioorganic & medicinal chemistry letters, 1994, Vol.4 (3), p.415-420 [Periódico revisado por pares]

Oxford: Elsevier

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10
1,1'-Disubstituted Ferrocenes as Molecular Hinges in Mono- and Bivalent Dopamine Receptor Ligand
1,1'-Disubstituted Ferrocenes as Molecular Hinges in Mono- and Bivalent Dopamine Receptor Ligand
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1,1'-Disubstituted Ferrocenes as Molecular Hinges in Mono- and Bivalent Dopamine Receptor Ligand

HUBER, Daniela ; HUBNER, Harald ; GMEINER, Peter

Journal of medicinal chemistry, 2009, Vol.52 (21), p.6860-6870 [Periódico revisado por pares]

Columbus, OH: American Chemical Society

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