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1
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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2
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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3
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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4
1-(2-(2,2,2-trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors
1-(2-(2,2,2-trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors
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1-(2-(2,2,2-trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

Tollefson, Michael B ; Acker, Brad A ; Jacobsen, E J ; Hughes, Robert O ; Walker, John K ; Fox, David N A ; Palmer, Michael J ; Freeman, Sandra K ; Yu, Ying ; Bond, Brian R

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (10), p.3125-3128 [Periódico revisado por pares]

England

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5
1,1-Difluoroethyl-substituted triazolothienopyrimidines as inhibitors of a human urea transport protein (UT-B): New analogs and binding model
1,1-Difluoroethyl-substituted triazolothienopyrimidines as inhibitors of a human urea transport protein (UT-B): New analogs and binding model
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1,1-Difluoroethyl-substituted triazolothienopyrimidines as inhibitors of a human urea transport protein (UT-B): New analogs and binding model

Liu, Y. ; Esteva-Font, C. ; Yao, C. ; Phuan, P.W. ; Verkman, A.S. ; Anderson, M.O.

Bioorganic & medicinal chemistry letters, 2013-06, Vol.23 (11), p.3338-3341 [Periódico revisado por pares]

England: Elsevier Ltd

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6
1,1-Dimethylallylcoumarins potently supress both lipopolysaccharide- and interferon-γ-induced nitric oxide generation in mouse macrophage RAW 264.7 cells
1,1-Dimethylallylcoumarins potently supress both lipopolysaccharide- and interferon-γ-induced nitric oxide generation in mouse macrophage RAW 264.7 cells
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1,1-Dimethylallylcoumarins potently supress both lipopolysaccharide- and interferon-γ-induced nitric oxide generation in mouse macrophage RAW 264.7 cells

MURAKAMI, A ; GUANXIN GAO ; OMURA, M ; YANO, M ; ITO, C ; FURUKAWA, H ; TAKAHASHI, D ; KOSHIMIZU, K ; OHIGASHI, H

Bioorganic & medicinal chemistry letters, 2000-01, Vol.10 (1), p.59-62 [Periódico revisado por pares]

Oxford: Elsevier

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7
1,1-diphenyl-3-dialkylamino-1-silacyclopentane derivatives: A new class of potent and selective 5-HT2A antagonists
1,1-diphenyl-3-dialkylamino-1-silacyclopentane derivatives: A new class of potent and selective 5-HT2A antagonists
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1,1-diphenyl-3-dialkylamino-1-silacyclopentane derivatives: A new class of potent and selective 5-HT2A antagonists

Damour, Dominique ; Barreau, Michel ; Dutruc-Rosset, Gilles ; Doble, Adam ; Piot, Odile ; Mignani, Serge

Bioorganic & medicinal chemistry letters, 1994-02, Vol.4 (3), p.415-420 [Periódico revisado por pares]

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8
1,10-Phenanthroline and its derivatives are novel hatching stimulants for soybean cyst nematodes
1,10-Phenanthroline and its derivatives are novel hatching stimulants for soybean cyst nematodes
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1,10-Phenanthroline and its derivatives are novel hatching stimulants for soybean cyst nematodes

Nonaka, Shiori ; Katsuyama, Tsutomu ; Kondo, Tatsuhiko ; Sasaki, Yasuyuki ; Asami, Tadao ; Yajima, Shunsuke ; Ito, Shinsaku

Bioorganic & medicinal chemistry letters, 2016-11, Vol.26 (21), p.5240-5243 [Periódico revisado por pares]

England: Elsevier Ltd

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9
1,1′-Dicyano-2-substituted ethylenes: A new class of glucose uptake inhibitors in antifilarial chemotherapy
1,1′-Dicyano-2-substituted ethylenes: A new class of glucose uptake inhibitors in antifilarial chemotherapy
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1,1′-Dicyano-2-substituted ethylenes: A new class of glucose uptake inhibitors in antifilarial chemotherapy

Tewari, Swati ; Chauhan, P.M.S. ; Bhaduri, A.P. ; Singh, S.N. ; Fatma, Nigar ; Chatterjee, R.K. ; Srivastava, V.M.L.

Bioorganic & medicinal chemistry letters, 1997-07, Vol.7 (14), p.1891-1896 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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10
1,1′-Xylyl bis-1,4,8,11-tetraaza cyclotetradecane: A new potential copper chelator agent for neuroprotection in Alzheimer’s disease. Its comparative effects with clioquinol on rat brain copper distribution
1,1′-Xylyl bis-1,4,8,11-tetraaza cyclotetradecane: A new potential copper chelator agent for neuroprotection in Alzheimer’s disease. Its comparative effects with clioquinol on rat brain copper distribution
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1,1′-Xylyl bis-1,4,8,11-tetraaza cyclotetradecane: A new potential copper chelator agent for neuroprotection in Alzheimer’s disease. Its comparative effects with clioquinol on rat brain copper distribution

Moret, Vincent ; Laras, Younes ; Pietrancosta, Nicolas ; Garino, Cédrik ; Quéléver, Gilles ; Rolland, Amandine ; Mallet, Bernard ; Norreel, Jean-Chrétien ; Kraus, Jean-Louis

Bioorganic & medicinal chemistry letters, 2006-06, Vol.16 (12), p.3298-3301 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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