Antagonist interaction with the human 5-HT(7) receptor mediates the rapid and potent inhibition of non-G-protein-stimulated adenylate cyclase activity: a novel GPCR effect.
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Toward selective drug development for the human 5-hydroxytryptamine 1E receptor: a comparison of 5-hydroxytryptamine 1E and 1F receptor structure-affinity relationshipsThe arylpiperazine derivatives N-(4-cyanophenylmethyl)-4-(2-diphenyl)-1-piperazinehexanamide and N-benzyl-4-(2-diphenyl)-1-piperazinehexanamide exert a long-lasting inhibition of human serotonin 5-HT7 receptor binding and cAMP signaling.Distribution of 5-ht(1E) receptors in the mammalian brain and cerebral vasculature: an immunohistochemical and pharmacological study.
P2860
Antagonist interaction with the human 5-HT(7) receptor mediates the rapid and potent inhibition of non-G-protein-stimulated adenylate cyclase activity: a novel GPCR effect.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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2011年论文
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name
Antagonist interaction with the human 5-HT
@nl
Antagonist interaction with th ...... activity: a novel GPCR effect.
@en
type
label
Antagonist interaction with the human 5-HT
@nl
Antagonist interaction with th ...... activity: a novel GPCR effect.
@en
prefLabel
Antagonist interaction with the human 5-HT
@nl
Antagonist interaction with th ...... activity: a novel GPCR effect.
@en
P2860
P1476
Antagonist interaction with th ...... activity: a novel GPCR effect.
@en
P2093
P2860
P304
P356
10.1111/J.1476-5381.2010.01194.X
P407
P577
2011-04-01T00:00:00Z