The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET
- Author
- MARTARELLO, Laurent1 ; SCHAFFRATH, Christoph2 ; HAI DENG2 ; GEE, Antony D1 ; LOCKHART, Andrew1 ; O'HAGAN, David2
[1] GlaxoSmithKline Pharmaceuticals, Translational Medicine and Technology, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2GG, United Kingdom
[2] School of Chemistry, University of St Andrews, Centre for Biomolecular Sciences, North Haugh, St Andrews, Fife KY16 9ST, United Kingdom - Source
Journal of labelled compounds & radiopharmaceuticals. 2003, Vol 46, Num 13, pp 1181-1189, 9 p ; ref : 9 ref
- ISSN
- 0362-4803
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry; Pharmacology drugs
- Publisher
- Wiley, Chichester
/
Wiley, New York, NY
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Adénosylméthionine Aminoacide soufré Désoxyribonucléoside Fluor 18 Hydrogène Fluorure Marquage radioisotopique Purine nucléoside Réaction enzymatique Streptomyces Adénosine(5p-désoxy-5p-fluoro) Streptomyces cattleya Actinomycetales Actinomycetes Bactérie Streptomycetaceae
- Keyword (en)
- Adenosylmethionine Sulfur containing aminoacid Deoxyribonucleoside Fluorine 18 Hydrogen Fluorides Radiolabelling Purine nucleoside Enzymatic reaction Streptomyces Actinomycetales Actinomycetes Bacteria Streptomycetaceae
- Keyword (es)
- Adenosilmetionina Aminoácido azufrado Desoxirribonucleósido Hidrógeno Fluoruro Marcación radioisotópica Purina nucleósido Reacción enzimática Streptomyces Actinomycetales Actinomycetes Bacteria Streptomycetaceae
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A31 Biotechnology / 002A31C Methods. Procedures. Technologies / 002A31C06 Bioconversions. Hemisynthesis
- Discipline
- Biotechnology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 15314611
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
Access to the document
Install on your browser
DOI
10.1002/jlcr.779 
https://dx.doi.org/10.1002/jlcr.779
"O:13:\"PanistOpenUrl\":36:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000idc\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:16:\"10.1002\/jlcr.779\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:9:\"\u0000*\u0000jtitle\";s:52:\"Journal of labelled compounds & radiopharmaceuticals\";s:9:\"\u0000*\u0000stitle\";s:29:\"J. labelled compd. radiopharm\";s:7:\"\u0000*\u0000date\";s:4:\"2003\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:2:\"13\";s:8:\"\u0000*\u0000spage\";s:4:\"1181\";s:8:\"\u0000*\u0000epage\";s:4:\"1189\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0362-4803\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:10:\"MARTARELLO\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Laurent\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:5:{i:0;s:21:\"SCHAFFRATH, Christoph\";i:1;s:8:\"HAI DENG\";i:2;s:13:\"GEE, Antony D\";i:3;s:16:\"LOCKHART, Andrew\";i:4;s:14:\"O'HAGAN, David\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"9\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Panist access
"O:12:\"IstexOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:16:\"10.1002\/jlcr.779\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:9:\"\u0000*\u0000jtitle\";s:52:\"Journal of labelled compounds & radiopharmaceuticals\";s:9:\"\u0000*\u0000stitle\";s:29:\"J. labelled compd. radiopharm\";s:7:\"\u0000*\u0000date\";s:4:\"2003\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:2:\"13\";s:8:\"\u0000*\u0000spage\";s:4:\"1181\";s:8:\"\u0000*\u0000epage\";s:4:\"1189\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0362-4803\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:10:\"MARTARELLO\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Laurent\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:5:{i:0;s:21:\"SCHAFFRATH, Christoph\";i:1;s:8:\"HAI DENG\";i:2;s:13:\"GEE, Antony D\";i:3;s:16:\"LOCKHART, Andrew\";i:4;s:14:\"O'HAGAN, David\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"9\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Istex access
"O:16:\"UnpaywallOpenUrl\":35:{s:8:\"\u0000*\u0000email\";s:27:\"assistance-portail@inist.fr\";s:6:\"\u0000*\u0000fmt\";N;s:6:\"\u0000*\u0000doi\";s:16:\"10.1002\/jlcr.779\";s:6:\"\u0000*\u0000pii\";N;s:7:\"\u0000*\u0000pmid\";N;s:9:\"\u0000*\u0000atitle\";N;s:9:\"\u0000*\u0000jtitle\";N;s:9:\"\u0000*\u0000stitle\";N;s:7:\"\u0000*\u0000date\";N;s:9:\"\u0000*\u0000volume\";N;s:8:\"\u0000*\u0000issue\";N;s:8:\"\u0000*\u0000spage\";N;s:8:\"\u0000*\u0000epage\";N;s:8:\"\u0000*\u0000pages\";N;s:7:\"\u0000*\u0000issn\";N;s:8:\"\u0000*\u0000eissn\";N;s:9:\"\u0000*\u0000aulast\";N;s:10:\"\u0000*\u0000aufirst\";N;s:9:\"\u0000*\u0000auinit\";N;s:10:\"\u0000*\u0000auinitm\";N;s:5:\"\u0000*\u0000au\";N;s:9:\"\u0000*\u0000aucorp\";N;s:7:\"\u0000*\u0000isbn\";N;s:8:\"\u0000*\u0000coden\";N;s:8:\"\u0000*\u0000genre\";N;s:7:\"\u0000*\u0000part\";N;s:9:\"\u0000*\u0000btitle\";N;s:8:\"\u0000*\u0000title\";N;s:8:\"\u0000*\u0000place\";N;s:6:\"\u0000*\u0000pub\";N;s:10:\"\u0000*\u0000edition\";N;s:9:\"\u0000*\u0000tpages\";N;s:9:\"\u0000*\u0000series\";N;s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";N;}"
Unpaywall access
"O:16:\"EuropePMCOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:16:\"10.1002\/jlcr.779\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:9:\"\u0000*\u0000jtitle\";s:52:\"Journal of labelled compounds & radiopharmaceuticals\";s:9:\"\u0000*\u0000stitle\";s:29:\"J. labelled compd. radiopharm\";s:7:\"\u0000*\u0000date\";s:4:\"2003\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:2:\"13\";s:8:\"\u0000*\u0000spage\";s:4:\"1181\";s:8:\"\u0000*\u0000epage\";s:4:\"1189\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0362-4803\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:10:\"MARTARELLO\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Laurent\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:5:{i:0;s:21:\"SCHAFFRATH, Christoph\";i:1;s:8:\"HAI DENG\";i:2;s:13:\"GEE, Antony D\";i:3;s:16:\"LOCKHART, Andrew\";i:4;s:14:\"O'HAGAN, David\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"9\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Europe PubMed Central access
"O:12:\"ArXivOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:16:\"10.1002\/jlcr.779\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:9:\"\u0000*\u0000jtitle\";s:52:\"Journal of labelled compounds & radiopharmaceuticals\";s:9:\"\u0000*\u0000stitle\";s:29:\"J. labelled compd. radiopharm\";s:7:\"\u0000*\u0000date\";s:4:\"2003\";s:9:\"\u0000*\u0000volume\";s:2:\"46\";s:8:\"\u0000*\u0000issue\";s:2:\"13\";s:8:\"\u0000*\u0000spage\";s:4:\"1181\";s:8:\"\u0000*\u0000epage\";s:4:\"1189\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0362-4803\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:10:\"MARTARELLO\";s:10:\"\u0000*\u0000aufirst\";s:7:\"Laurent\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:5:{i:0;s:21:\"SCHAFFRATH, Christoph\";i:1;s:8:\"HAI DENG\";i:2;s:13:\"GEE, Antony D\";i:3;s:16:\"LOCKHART, Andrew\";i:4;s:14:\"O'HAGAN, David\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:0:\"\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:124:\"The first enzymatic method for C-18F bond formation: the synthesis of 5'-[18F]-fluoro-5'-deoxyadenosine for imaging with PET\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"9\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
arXiv access
