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Refinado por: assunto: Life Sciences & Biomedicine remover British Journal Of Pharmacology remover
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1
1‐(3‐(9H‐Carbazol‐9‐yl)‐1‐propyl)‐4‐(2‐methoxyphenyl)‐4‐piperidinol, a novel subtype selective inhibitor of the mouse type II GABA‐transporter
1‐(3‐(9H‐Carbazol‐9‐yl)‐1‐propyl)‐4‐(2‐methoxyphenyl)‐4‐piperidinol, a novel subtype selective inhibitor of the mouse type II GABA‐transporter
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1‐(3‐(9H‐Carbazol‐9‐yl)‐1‐propyl)‐4‐(2‐methoxyphenyl)‐4‐piperidinol, a novel subtype selective inhibitor of the mouse type II GABA‐transporter

Thomsen, Christian ; Sørensen, Per Olaf ; Egebjerg, Jan

British journal of pharmacology, 1997-03, Vol.120 (6), p.983-985 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
(−)1‐(Benzofuran‐2‐yl)‐2‐propylaminopentane, [(−)BPAP], a selective enhancer of the impulse propagation mediated release of catecholamines and serotonin in the brain
(−)1‐(Benzofuran‐2‐yl)‐2‐propylaminopentane, [(−)BPAP], a selective enhancer of the impulse propagation mediated release of catecholamines and serotonin in the brain
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(−)1‐(Benzofuran‐2‐yl)‐2‐propylaminopentane, [(−)BPAP], a selective enhancer of the impulse propagation mediated release of catecholamines and serotonin in the brain

Knoll, Joseph ; Yoneda, Fumio ; Knoll, Berta ; Ohde, Hironori ; Miklya, Ildikó

British journal of pharmacology, 1999-12, Vol.128 (8), p.1723-1732 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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3
1‐Dehydro‐[10]‐gingerdione from ginger inhibits IKKβ activity for NF‐κB activation and suppresses NF‐κB‐regulated expression of inflammatory genes
1‐Dehydro‐[10]‐gingerdione from ginger inhibits IKKβ activity for NF‐κB activation and suppresses NF‐κB‐regulated expression of inflammatory genes
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1‐Dehydro‐[10]‐gingerdione from ginger inhibits IKKβ activity for NF‐κB activation and suppresses NF‐κB‐regulated expression of inflammatory genes

Lee, Hwa Young ; Park, Sun Hong ; Lee, Misoon ; Kim, Hye‐Jin ; Ryu, Shi Yong ; Kim, Nam Doo ; Hwang, Bang Yeon ; Hong, Jin Tae ; Han, Sang‐Bae ; Kim, Youngsoo

British journal of pharmacology, 2012-09, Vol.167 (1), p.128-140 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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4
1‐Hydroxy‐3‐amino‐pyrrolidone‐2 (HA‐966): a new GABA‐like compound, with potential use in extrapyramidal diseases
1‐Hydroxy‐3‐amino‐pyrrolidone‐2 (HA‐966): a new GABA‐like compound, with potential use in extrapyramidal diseases
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1‐Hydroxy‐3‐amino‐pyrrolidone‐2 (HA‐966): a new GABA‐like compound, with potential use in extrapyramidal diseases

BONTA, I. L. ; VOS, C. J. ; GRIJSEN, H. ; HILLEN, F. C. ; NOACH, E. L. ; SIM, A. W.

British journal of pharmacology, 1971-11, Vol.43 (3), p.514-535 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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5
1‐Hydroxypyrene mediates renal fibrosis through aryl hydrocarbon receptor signalling pathway
1‐Hydroxypyrene mediates renal fibrosis through aryl hydrocarbon receptor signalling pathway
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1‐Hydroxypyrene mediates renal fibrosis through aryl hydrocarbon receptor signalling pathway

Miao, Hua ; Wu, Xia‐Qing ; Wang, Yan‐Ni ; Chen, Dan‐Qian ; Chen, Lin ; Vaziri, Nosratola D. ; Zhuang, Shougang ; Guo, Yan ; Su, Wei ; Ma, Shi‐Xing ; Zhang, Huan‐Qiao ; Shang, You‐Quan ; Yu, Xiao‐Yong ; Zhao, Yan‐Long ; Mao, Jia‐Rong ; Gao, Ming ; Zhang, Jin‐Hua ; Zhao, Jin ; Zhang, Yuan ; Zhang, Li ; Zhao, Ying‐Yong ; Cao, Gang

British journal of pharmacology, 2022-01, Vol.179 (1), p.103-124 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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6
1‐Methylnicotinamide (MNA), a primary metabolite of nicotinamide, exerts anti‐thrombotic activity mediated by a cyclooxygenase‐2/prostacyclin pathway
1‐Methylnicotinamide (MNA), a primary metabolite of nicotinamide, exerts anti‐thrombotic activity mediated by a cyclooxygenase‐2/prostacyclin pathway
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1‐Methylnicotinamide (MNA), a primary metabolite of nicotinamide, exerts anti‐thrombotic activity mediated by a cyclooxygenase‐2/prostacyclin pathway

Chlopicki, S ; Swies, J ; Mogielnicki, A ; Buczko, W ; Bartus, M ; Lomnicka, M ; Adamus, J ; Gebicki, J

British journal of pharmacology, 2007-09, Vol.152 (2), p.230-239 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
1‐O‐hexadecyl‐2‐acetyl‐sn‐glycero‐3‐phospho (N,N,N trimethyl) hexanolamine: an analogue of platelet‐activating factor with partial agonist activity
1‐O‐hexadecyl‐2‐acetyl‐sn‐glycero‐3‐phospho (N,N,N trimethyl) hexanolamine: an analogue of platelet‐activating factor with partial agonist activity
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1‐O‐hexadecyl‐2‐acetyl‐sn‐glycero‐3‐phospho (N,N,N trimethyl) hexanolamine: an analogue of platelet‐activating factor with partial agonist activity

Grigoriadis, George ; Stewart, Alastair G.

British journal of pharmacology, 1991-09, Vol.104 (1), p.171-177 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
1,2,3,4,6‐Penta‐O‐galloyl‐β‐d‐glucose modulates perivascular inflammation and prevents vascular dysfunction in angiotensin II‐induced hypertension
1,2,3,4,6‐Penta‐O‐galloyl‐β‐d‐glucose modulates perivascular inflammation and prevents vascular dysfunction in angiotensin II‐induced hypertension
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1,2,3,4,6‐Penta‐O‐galloyl‐β‐d‐glucose modulates perivascular inflammation and prevents vascular dysfunction in angiotensin II‐induced hypertension

Mikolajczyk, Tomasz P. ; Nosalski, Ryszard ; Skiba, Dominik S. ; Koziol, Joanna ; Mazur, Magdalena ; Justo‐Junior, Amauri S. ; Kowalczyk, Paulina ; Kusmierczyk, Zofia ; Schramm‐Luc, Agata ; Luc, Kevin ; Maffia, Pasquale ; Graham, Delyth ; Kiss, Anna K. ; Naruszewicz, Marek ; Guzik, Tomasz J.

British journal of pharmacology, 2019-06, Vol.176 (12), p.1951-1965 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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9
1,3,6,7‐Tetrahydroxy‐8‐prenylxanthone ameliorates inflammatory responses resulting from the paracrine interaction of adipocytes and macrophages
1,3,6,7‐Tetrahydroxy‐8‐prenylxanthone ameliorates inflammatory responses resulting from the paracrine interaction of adipocytes and macrophages
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1,3,6,7‐Tetrahydroxy‐8‐prenylxanthone ameliorates inflammatory responses resulting from the paracrine interaction of adipocytes and macrophages

Li, Dan ; Liu, Qianyu ; Sun, Wen ; Chen, Xiuping ; Wang, Ying ; Sun, Yuxiang ; Lin, Ligen

British journal of pharmacology, 2018-05, Vol.175 (10), p.1590-1606 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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10
14 beta-Hydroxyprogesterone binds to the digitalis receptor, inhibits the sodium pump and enhances cardiac contractility
14 beta-Hydroxyprogesterone binds to the digitalis receptor, inhibits the sodium pump and enhances cardiac contractility
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14 beta-Hydroxyprogesterone binds to the digitalis receptor, inhibits the sodium pump and enhances cardiac contractility

Bose, D ; Elliott, D ; Kobayashi, T ; Templeton, J F ; Kumar, V P ; LaBella, F S

British journal of pharmacology, 1988-02, Vol.93 (2), p.453-461 [Periódico revisado por pares]

England

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