Solid-Supported Synthesis and 5-HT7 /5-HT1A Receptor Affinity of Arylpiperazinylbutyl Derivatives of 4,5-dihydro-1,2,4-triazine-6-(1H)-one.

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Solid-Supported Synthesis and 5-HT7 /5-HT1A Receptor Affinity of Arylpiperazinylbutyl Derivatives of 4,5-dihydro-1,2,4-triazine-6-(1H)-one.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

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2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Solid-Supported Synthesis and ...... dro-1,2,4-triazine-6-(1H)-one.

@ast

Solid-Supported Synthesis and ...... dro-1,2,4-triazine-6-(1H)-one.

@en

type

Item

label

Solid-Supported Synthesis and ...... dro-1,2,4-triazine-6-(1H)-one.

@ast

Solid-Supported Synthesis and ...... dro-1,2,4-triazine-6-(1H)-one.

@en

prefLabel

Solid-Supported Synthesis and ...... dro-1,2,4-triazine-6-(1H)-one.

@ast

Solid-Supported Synthesis and ...... dro-1,2,4-triazine-6-(1H)-one.

@en

P1476

Solid-Supported Synthesis and ...... dro-1,2,4-triazine-6-(1H)-one.

@en

P2093

Gilles Subra

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Katarzyna Grychowska

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Maciej Pawłowski

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Nicolas Masurier

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Paweł Zajdel

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P2860

Serotonin 5-HT7 receptor agents: Structure-activity relationships and potential therapeutic applications in central nervous system disorders

Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction

Tetrahydrobenzindoles: selective antagonists of the 5-HT7 receptor

Solid-phase synthetic route to multiple derivatives of a fundamental peptide unit.

The 5-HT7 receptor and disorders of the nervous system: an overview.

The rise, fall and reinvention of combinatorial chemistry.

Role of the 5-HT7 receptor in the central nervous system: from current status to future perspectives.

The multiobjective based design, synthesis and evaluation of the arylsulfonamide/amide derivatives of aryloxyethyl- and arylthioethyl- piperidines and pyrrolidines as a novel class of potent 5-HT₇ receptor antagonists.

(Phenylpiperazinyl-butyl)oxindoles as selective 5-HT7 receptor antagonists.

The influence of modifications in imide fragment structure on 5-HT(1A) and 5-HT(7) receptor affinity and in vivo pharmacological properties of some new 1-(m-trifluoromethylphenyl)piperazines.

P304

697-703

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P31

scholarly article

P356

10.1111/CBDD.12539

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P433

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P478

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P577

2015-02-12T00:00:00Z

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P5875

272200997

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P698

25684690

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