Application of highly sensitive UPLC-MS to determine biodistribution at tracer doses: validation with the 5-HT1A ligand [(18)F]FPWAY.

about

Evaluation of fluorine-labeled gastrin-releasing peptide receptor (GRPR) agonists and antagonists by LC/MS.Applications of LC-MS in PET radioligand development and metabolic elucidation Design and development of molecular imaging probes.

P2860

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P2860

Application of highly sensitive UPLC-MS to determine biodistribution at tracer doses: validation with the 5-HT1A ligand [(18)F]FPWAY.

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http://www.wikidata.org/entity/Q36817982

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2009 nî lūn-bûn

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Application of highly sensitiv ...... he 5-HT1A ligand [(18)F]FPWAY.

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Application of highly sensitiv ...... he 5-HT1A ligand [(18)F]FPWAY.

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Application of highly sensitiv ...... he 5-HT1A ligand [(18)F]FPWAY.

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Application of highly sensitiv ...... he 5-HT1A ligand [(18)F]FPWAY.

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Application of highly sensitiv ...... he 5-HT1A ligand [(18)F]FPWAY.

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Application of highly sensitiv ...... he 5-HT1A ligand [(18)F]FPWAY.

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P1476

Application of highly sensitiv ...... he 5-HT1A ligand [(18)F]FPWAY.

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P2093

Elaine M Jagoda

http://www.w3.org/2001/XMLSchema#string

Joji Tokugawa

http://www.w3.org/2001/XMLSchema#string

Larry Reyes

http://www.w3.org/2001/XMLSchema#string

Lixin Lang

http://www.w3.org/2001/XMLSchema#string

Ying Ma

http://www.w3.org/2001/XMLSchema#string

P2860

First delineation of 5-HT1A receptors in human brain with PET and [11C]WAY-100635

PET evaluation of [(18)F]FCWAY, an analog of the 5-HT(1A) receptor antagonist, WAY-100635.

Fluoro analogs of WAY-100635 with varying pharmacokinetics properties.

Synthesis and in vivo biodistribution of F-18 labeled 3-cis-, 3-trans-, 4-cis-, and 4-trans-fluorocyclohexane derivatives of WAY 100635.

[11C]WAY 100635: a radioligand for imaging 5-HT1A receptors with positron emission tomography.

Application of LC-MS to the analysis of new radiopharmaceuticals.

Use of LC/MS to assess brain tracer distribution in preclinical, in vivo receptor occupancy studies: dopamine D2, serotonin 2A and NK-1 receptors as examples.

Comparison of rat dopamine D2 receptor occupancy for a series of antipsychotic drugs measured using radiolabeled or nonlabeled raclopride tracer.

Development of fluorine-18-labeled 5-HT1A antagonists.

Species differences in metabolites of PET ligands: serotonergic 5-HT1A receptor antagonists 3-trans-FCWAY and 3-cis-FCWAY.

P304

389-393

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scholarly article

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10.1016/J.NUCMEDBIO.2009.01.002

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Dale O Kiesewetter

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2009-03-26T00:00:00Z

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24409005

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19423006

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3644855

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Application of highly sensitive UPLC-MS to determine biodistribution at tracer doses: validation with the 5-HT1A ligand [(18)F]FPWAY.

about

P2860

P2860

Application of highly sensitive UPLC-MS to determine biodistribution at tracer doses: validation with the 5-HT1A ligand [(18)F]FPWAY.

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