Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution. - Wikidata - awgldk - TriplyDB

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

http://www.wikidata.org/entity/Q43239777

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Radiolabeled Cyclic RGD Peptide Bioconjugates as Radiotracers Targeting Multiple Integrins Radiolabeled cyclic RGD peptides as radiotracers for tumor imaging Improved 18F labeling of peptides with a fluoride-aluminum-chelate complex Automated radiochemical synthesis of [18F]FBEM: a thiol reactive synthon for radiofluorination of peptides and proteins.One-pot two-step radiosynthesis of a new (18)F-labeled thiol reactive prosthetic group and its conjugate for insulinoma imaging Bombesin receptor-mediated imaging and cytotoxicity: review and current status Rapid and simple one-step F-18 labeling of peptides.Syntheses of meta-[F]Fluorobenzaldehyde and meta-[F]Fluorobenzylbromide from Phenyl(3-Formylphenyl) Iodonium Salt Precursors Fluorine-18 radiochemistry, labeling strategies and synthetic routes High-yielding aqueous 18F-labeling of peptides via Al18F chelation New lyophilized kit for rapid radiofluorination of peptides Development of a new thiol site-specific prosthetic group and its conjugation with [Cys(40)]-exendin-4 for in vivo targeting of insulinomas.Molecular Imaging of Hypoxia: Strategies for Probe Design and Application.18F labeling of arenes.RGD-based PET tracers for imaging receptor integrin αv β3 expression.Molecular imaging probes derived from natural peptides.Microwave-assisted one-pot synthesis of N-succinimidyl-4[ ¹⁸F]fluorobenzoate ([¹⁸F]SFB).Radiofluorination of PSMA-HBED via Al(18)F(2+) Chelation and Biological Evaluations In Vitro.18 F-Labeling of Sensitive Biomolecules for Positron Emission Tomography.Strain-promoted copper-free "click" chemistry for 18F radiolabeling of bombesin.Fluoride-18 radiolabeling of peptides bearing an aminooxy functional group to a prosthetic ligand via an oxime bond.4-Substituted tert-butyl phenylazocarboxylates--synthetic equivalents for the para-phenyl radical cation.Facile room temperature synthesis of fluorine-18 labeled fluoronicotinic acid-2,3,5,6-tetrafluorophenyl ester without azeotropic drying of fluorine-18.High-Affinity "Click" RGD Peptidomimetics as Radiolabeled Probes for Imaging αv β3 Integrin.A localized tolerance in the substrate specificity of the fluorinase enzyme enables "last-step" 18F fluorination of a RGD peptide under ambient aqueous conditions.Fast indirect fluorine-18 labeling of protein/peptide using the useful 6-fluoronicotinic acid-2,3,5,6-tetrafluorophenyl prosthetic group: A method comparable to direct fluorination.Development of 6-[(18) F]fluoro-carbohydrate-based prosthetic groups and their conjugation to peptides via click chemistry.Positronen-Emissions-Tomographie

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P2860

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

http://www.wikidata.org/entity/Q43239777

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh-hant

name

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

@en

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

@nl

type

label

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

@en

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

@nl

prefLabel

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

@en

Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

@nl

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P1433

Bioconjugate Chemistry

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Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.

@en

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Ananth Srinivasan

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

Dietmar Berndorff

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Jessica Becaud

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

Keith Graham

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

Linjing Mu

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

Ludger Dinkelborg

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

Lutz Lehmann

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

Mylène Karramkam

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

Pius A Schubiger

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

René Smits

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2254-2261

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scholarly article

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10.1021/BC900240Z

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12

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20

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2009-12-01T00:00:00Z

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38097548

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19921791

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