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1
0.05% clobetasol 17-propionate cream and ointment but not the corresponding 0.1% triamcinolone acetonide preparations increase skin surface roughness: a possible dissociation of unwanted epidermal and dermal effects
0.05% clobetasol 17-propionate cream and ointment but not the corresponding 0.1% triamcinolone acetonide preparations increase skin surface roughness: a possible dissociation of unwanted epidermal and dermal effects
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0.05% clobetasol 17-propionate cream and ointment but not the corresponding 0.1% triamcinolone acetonide preparations increase skin surface roughness: a possible dissociation of unwanted epidermal and dermal effects

Kerscher, M J ; Korting, H C ; Mehringer, L ; Mätzig, R

Skin pharmacology, 1996, Vol.9 (2), p.120

Switzerland

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2
07H239-A, a New Cytotoxic Eremophilane Sesquiterpene from the Marine-Derived Xylariaceous Fungus LL-07H239
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 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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3
0.9% sodium chloride injection with and without heparin for maintaining peripheral indwelling intermittent-infusion devices in infants
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 [Periódico revisado por pares]

Bethesda, MD: ASHP

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4
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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5
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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6
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
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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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 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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7
1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors
1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors
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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 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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8
1-(1-Naphthyl)piperazine, a central serotonin agonist
1-(1-Naphthyl)piperazine, a central serotonin agonist
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1-(1-Naphthyl)piperazine, a central serotonin agonist

Fuller, R W ; Mason, N R ; Snoddy, H D ; Perry, K W

Research communications in chemical pathology and pharmacology, 1986-01, Vol.51 (1), p.37

United States

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9
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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10
1-(1,3-Benzodioxol-5-ylmethyl)-3-[4-(1 H-imidazol-1-yl)phenoxy]-piperidine analogs as potent and selective inhibitors of nitric oxide formation
1-(1,3-Benzodioxol-5-ylmethyl)-3-[4-(1 H-imidazol-1-yl)phenoxy]-piperidine analogs as potent and selective inhibitors of nitric oxide formation
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1-(1,3-Benzodioxol-5-ylmethyl)-3-[4-(1 H-imidazol-1-yl)phenoxy]-piperidine analogs as potent and selective inhibitors of nitric oxide formation

Wei, Robert G. ; Adler, Marc ; Davey, David ; Ho, Elena ; Mohan, Raju ; Polokoff, Mark ; Tseng, Jih-Lie ; Whitlow, Marc ; Xu, Wei ; Yuan, Shendong ; Phillips, Gary

Bioorganic & medicinal chemistry letters, 2007-05, Vol.17 (9), p.2499-2504 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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