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Refinado por: Título de revista: European Journal Of Pharmacology eliminar
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1
(−)-1-(Benzofuran-2-yl)-2-propylaminopentane enhances locomotor activity in rats due to its ability to induce dopamine release
(−)-1-(Benzofuran-2-yl)-2-propylaminopentane enhances locomotor activity in rats due to its ability to induce dopamine release
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(−)-1-(Benzofuran-2-yl)-2-propylaminopentane enhances locomotor activity in rats due to its ability to induce dopamine release

Shimazu, Seiichiro ; Takahata, Kazue ; Katsuki, Hiroshi ; Tsunekawa, Hiroko ; Tanigawa, Akie ; Yoneda, Fumio ; Knoll, Joseph ; Akaike, Akinori

European journal of pharmacology, 2001-06, Vol.421 (3), p.181-189 [Revista revisada por pares]

Amsterdam: Elsevier B.V

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2
1-(3-Trifluoromethylphenyl)piperazine (TFMPP) in the central tegmental area reduces the effect of desipramine in the forced swimming test in rats: possible role of serotonin receptors
1-(3-Trifluoromethylphenyl)piperazine (TFMPP) in the central tegmental area reduces the effect of desipramine in the forced swimming test in rats: possible role of serotonin receptors
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1-(3-Trifluoromethylphenyl)piperazine (TFMPP) in the central tegmental area reduces the effect of desipramine in the forced swimming test in rats: possible role of serotonin receptors

CERVO, L ; GRIGNASCHI, G ; NOWAKOWSKA, E ; SAMANIN, R

European journal of pharmacology, 1989, Vol.171 (1), p.119-125 [Revista revisada por pares]

Amsterdam: Elsevier

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3
1-(5-bromo-2-hydroxy-4-methoxyphenyl)ethanone [SE1] suppresses pro-inflammatory responses by blocking NF-κB and MAPK signaling pathways in activated microglia
1-(5-bromo-2-hydroxy-4-methoxyphenyl)ethanone [SE1] suppresses pro-inflammatory responses by blocking NF-κB and MAPK signaling pathways in activated microglia
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1-(5-bromo-2-hydroxy-4-methoxyphenyl)ethanone [SE1] suppresses pro-inflammatory responses by blocking NF-κB and MAPK signaling pathways in activated microglia

Himaya, S.W.A. ; Ryu, BoMi ; Qian, Zhong-Ji ; Li, Yong ; Kim, Se-Kwon

European journal of pharmacology, 2011-11, Vol.670 (2-3), p.608-616 [Revista revisada por pares]

Amsterdam: Elsevier B.V

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4
1-5-hydroxytryptophan-induced flat body posture in the rat antagonism by ritanserin and potentiation after 5,7-dihydroxytryptamine
1-5-hydroxytryptophan-induced flat body posture in the rat antagonism by ritanserin and potentiation after 5,7-dihydroxytryptamine
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1-5-hydroxytryptophan-induced flat body posture in the rat antagonism by ritanserin and potentiation after 5,7-dihydroxytryptamine

COLPAERT, F. C ; KOEK, W ; LATEGAN, A

European journal of pharmacology, 1989-10, Vol.169 (1), p.175-178 [Revista revisada por pares]

Amsterdam: Elsevier

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5
1-Aminocyclobutane-1-carboxylate (ACBC): a specific antagonist of the N-methyl-D-aspartate receptor coupled glycine receptor
1-Aminocyclobutane-1-carboxylate (ACBC): a specific antagonist of the N-methyl-D-aspartate receptor coupled glycine receptor
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1-Aminocyclobutane-1-carboxylate (ACBC): a specific antagonist of the N-methyl-D-aspartate receptor coupled glycine receptor

Hood, William F. ; Sun, Eric T. ; Compton, Robert P. ; Monahan, Joseph B.

European journal of pharmacology, 1989-02, Vol.161 (2), p.281-282 [Revista revisada por pares]

Amsterdam: Elsevier B.V

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6
1-Aminocyclopropane-1-carboxylic acid (ACC) mimics the effects of glycine on the NMDA receptor ion channel
1-Aminocyclopropane-1-carboxylic acid (ACC) mimics the effects of glycine on the NMDA receptor ion channel
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1-Aminocyclopropane-1-carboxylic acid (ACC) mimics the effects of glycine on the NMDA receptor ion channel

Nadler, Varda ; Kloog, Yoel ; Sokolovsky, Mordechai

European journal of pharmacology, 1988-11, Vol.157 (1), p.115-116 [Revista revisada por pares]

Amsterdam: Elsevier B.V

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7
1-aminocyclopropanecarboxylates exhibit antdepressant and anxiolytic actions in animal models
1-aminocyclopropanecarboxylates exhibit antdepressant and anxiolytic actions in animal models
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1-aminocyclopropanecarboxylates exhibit antdepressant and anxiolytic actions in animal models

TRULLAS, R ; FOLIO, T ; YOUNG, A ; MILLER, R ; BOJE, K ; SKOLNICK, P

European journal of pharmacology, 1991, Vol.203 (3), p.379-385 [Revista revisada por pares]

Amsterdam: Elsevier

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8
1-Aminocyclopropanecarboxylic acid protects against dynorphin A-induced spinal injury
1-Aminocyclopropanecarboxylic acid protects against dynorphin A-induced spinal injury
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1-Aminocyclopropanecarboxylic acid protects against dynorphin A-induced spinal injury

Long, Joseph B. ; Skolnick, Phil

European journal of pharmacology, 1994-08, Vol.261 (3), p.295-301 [Revista revisada por pares]

Amsterdam: Elsevier B.V

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9
1-Benzyl-N-[3-[spiroisobenzofuran-1(3H),4′-piperidin-1-yl]propyl]pyrrolidine-2-carboxamide (Compound 24) antagonizes NOP receptor-mediated potassium channel activation in rat periaqueductal gray slices
1-Benzyl-N-[3-[spiroisobenzofuran-1(3H),4′-piperidin-1-yl]propyl]pyrrolidine-2-carboxamide (Compound 24) antagonizes NOP receptor-mediated potassium channel activation in rat periaqueductal gray slices
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1-Benzyl-N-[3-[spiroisobenzofuran-1(3H),4′-piperidin-1-yl]propyl]pyrrolidine-2-carboxamide (Compound 24) antagonizes NOP receptor-mediated potassium channel activation in rat periaqueductal gray slices

Liao, Yan-Yu ; Trapella, Claudio ; Chiou, Lih-Chu

European journal of pharmacology, 2009-03, Vol.606 (1), p.84-89 [Revista revisada por pares]

Amsterdam: Elsevier B.V

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10
1-furan -2 -yl -3 -pyridin -2 -yl -propenone inhibits the invasion and migration of ΗΤ1080 human fibrosarcoma cells through the inhibition of proΜΜP-2 activation and down regulation of MMP-9 and MT1-MMP
1-furan -2 -yl -3 -pyridin -2 -yl -propenone inhibits the invasion and migration of ΗΤ1080 human fibrosarcoma cells through the inhibition of proΜΜP-2 activation and down regulation of MMP-9 and MT1-MMP
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1-furan -2 -yl -3 -pyridin -2 -yl -propenone inhibits the invasion and migration of ΗΤ1080 human fibrosarcoma cells through the inhibition of proΜΜP-2 activation and down regulation of MMP-9 and MT1-MMP

BYUNG CHUL PARK ; THAPA, Dinesh ; LEE, Yoon-Seok ; KWAK, Mi-Kyoung ; LEE, Eung-Seok ; HAN GON CHOI ; CHUL SOON YONG ; KIM, Jung-Ae

European journal of pharmacology, 2007, Vol.567 (3), p.193-197 [Revista revisada por pares]

Amsterdam: Elsevier

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