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1
0.125% Ropivacaine is similar to 0.125% bupivacaine for labor analgesia using patient-controlled epidural infusion
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Article
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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 [Peer Reviewed Journal]

Hagerstown, MD: Lippincott

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2
0.2% Chlorhexidine Mouthwash With an Antidiscoloration System Versus 0.2% Chlorhexidine Mouthwash: A Prospective Clinical Comparative Study
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0.2% Chlorhexidine Mouthwash With an Antidiscoloration System Versus 0.2% Chlorhexidine Mouthwash: A Prospective Clinical Comparative Study

Solís, Carols ; Santos, Antonio ; Nart, José ; Violant, Deborah

Journal of periodontology (1970), 2011-01, Vol.82 (1), p.80-85 [Peer Reviewed Journal]

Chicago, IL: American Academy of Periodontology

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3
0.2% ropivacaine with or without Fentanyl for Patient-Controlled Epidural Analgesia after Major abdominal Surgery: a Double-Blind Study
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Article
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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 [Peer Reviewed Journal]

New York, NY: Elsevier Inc

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4
0.25% Chlorhexidine Gluconate Gel: A Protective Topical Microbicide
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Article
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0.25% Chlorhexidine Gluconate Gel: A Protective Topical Microbicide

PATTON, DOROTHY L. ; SWEENEY, YVONNE T. COSGROVE ; McKAY, TAMYRA L. ; DeMERS, SHAUNE M. ; CLARK, AGNES M. ; RABE, LORNA K. ; HILLIER, SHARON L.

Sexually transmitted diseases, 1998-09, Vol.25 (8), p.421-424 [Peer Reviewed Journal]

Hagerstown, MD: Lippincott Williams & Wilkins

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5
07H239-A, a New Cytotoxic Eremophilane Sesquiterpene from the Marine-Derived Xylariaceous Fungus LL-07H239
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07H239-A, a New Cytotoxic Eremophilane Sesquiterpene from the Marine-Derived Xylariaceous Fungus LL-07H239

McDonald, Leonard A ; Barbieri, Laurel R ; Bernan, Valerie S ; Janso, Jeffrey ; Lassota, Peter ; Carter, Guy T

Journal of natural products (Washington, D.C.), 2004-09, Vol.67 (9), p.1565-1567 [Peer Reviewed Journal]

Washington, DC: American Chemical Society

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6
0.9% sodium chloride injection with and without heparin for maintaining peripheral indwelling intermittent-infusion devices in infants
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0.9% sodium chloride injection with and without heparin for maintaining peripheral indwelling intermittent-infusion devices in infants

Nelson, TJ ; Graves, SM

American journal of health-system pharmacy, 1998-03, Vol.55 (6), p.570-573 [Peer Reviewed Journal]

Bethesda, MD: ASHP

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7
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 [Peer Reviewed Journal]

Shannon: Elsevier B.V

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8
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 [Peer Reviewed Journal]

Washington, DC: American Chemical Society

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9
1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia
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Article
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1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia

Anandan, Sampath-Kumar ; Webb, Heather Kay ; Chen, Dawn ; Wang, Yi-Xin (Jim) ; Aavula, Basker R. ; Cases, Sylvaine ; Cheng, Ying ; Do, Zung N. ; Mehra, Upasana ; Tran, Vinh ; Vincelette, Jon ; Waszczuk, Joanna ; White, Kathy ; Wong, Kenneth R. ; Zhang, Le-Ning ; Jones, Paul D. ; Hammock, Bruce D. ; Patel, Dinesh V. ; Whitcomb, Randall ; MacIntyre, D. Euan ; Sabry, James ; Gless, Richard

Bioorganic & medicinal chemistry letters, 2011-02, Vol.21 (3), p.983-988 [Peer Reviewed Journal]

Amsterdam: Elsevier Ltd

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10
1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors
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Article
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1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors

Liu, Jinbing ; Yi, Wei ; Wan, Yiqian ; Ma, Lin ; Song, Huacan

Bioorganic & medicinal chemistry, 2008-02, Vol.16 (3), p.1096-1102 [Peer Reviewed Journal]

Oxford: Elsevier Ltd

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