Zobrazeno 1 - 10
of 77
pro vyhledávání: '"6-halopurine"'
Publikováno v:
Journal of Medicinal Chemistry; Nov2009, Vol. 52 Issue 22, p7284-7288, 5p
Akademický článek
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Publikováno v:
Journal of Medicinal Chemistry. 52:7284-7288
6-Bromo-7-[(11)C]methylpurine is reported to react with glutathione via glutathione S-transferases in the brain and to be converted into a substrate for multidrug resistance-associated protein 1 (MRP1), an efflux pump. The compound with a rapid conve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f960cdd5b5c2d5ec67aab7f9848bcdc
https://doi.org/10.1021/jm901332c
https://doi.org/10.1021/jm901332c
Autor:
Liu, Jiangqiong
Publikováno v:
CLICK HERE for online access.
Thesis (Ph. D.)--Brigham Young University. Dept. of Chemistry and Biochemistry, 2007.
Includes bibliographical references.
Includes bibliographical references.
Externí odkaz:
http://contentdm.lib.byu.edu/ETD/image/etd1821.pdf
Publikováno v:
The Journal of Organic Chemistry. 34:2157-2159
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c099d1255fa365122ebc58ad456696e
https://doi.org/10.1021/jo01259a028
https://doi.org/10.1021/jo01259a028
Publikováno v:
Molecules, Vol 18, Iss 5, Pp 5335-5347 (2013)
2-[18F]Fluoroethyl azide ([18F]FEA) can readily be obtained by nucleophilic substitution of 2-azidoethyl-4-toluenesulfonate with [18F]fluoride (half-life 110 min), and has become widely used as a reagent for ‘click’ labeling of PET tracers. Howev
Externí odkaz:
https://doaj.org/article/5fff6783f2d84185ab6b3bf3b2c8b611
Autor:
Liu, Jiangqiong
Publikováno v:
Theses and Dissertations.
In chapter 1, we describe development of a mild and efficient method for SNAr iodination of 6-chloropurine 2'-deoxynucleosides and nucleosides. Our studies demonstrate that 6-iodopurine nucleosides are excellent substrates for certain transition meta
Externí odkaz:
https://scholarsarchive.byu.edu/etd/892
https://scholarsarchive.byu.edu/context/etd/article/1891/viewcontent/ETD_CISOPTR_1015.pdf
https://scholarsarchive.byu.edu/context/etd/article/1891/viewcontent/ETD_CISOPTR_1015.pdf
Publikováno v:
Molecules
Volume 18
Issue 5
Pages: 5335-5347
Molecules, Vol 18, Iss 5, Pp 5335-5347 (2013)
Volume 18
Issue 5
Pages: 5335-5347
Molecules, Vol 18, Iss 5, Pp 5335-5347 (2013)
2-[18F]Fluoroethyl azide ([18F]FEA) can readily be obtained by nucleophilic substitution of 2-azidoethyl-4-toluenesulfonate with [18F]fluoride (half-life 110 min), and has become widely used as a reagent for ‘click’ labeling of PET tracers. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb80253882d37e2db52dd41b8325415c
Publikováno v:
Molecules
2-[18F]Fluoroethyl azide ([18F]FEA) can readily be obtained by nucleophilic substitution of 2-azidoethyl-4-toluenesulfonate with [18F]fluoride (half-life 110 min), and has become widely used as a reagent for ‘click’ labeling of PET tracers. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::59d33aa01c23eb8019c417c8be57a8c4
https://pubmed.ncbi.nlm.nih.gov/23666002
https://pubmed.ncbi.nlm.nih.gov/23666002
Autor:
Mairinger, Severin1,2 (AUTHOR) severin.mairinger@meduniwien.ac.at, Jackwerth, Matthias1 (AUTHOR), Soukup, Ondřej3 (AUTHOR), Blaickner, Matthias4 (AUTHOR), Decristoforo, Clemens5 (AUTHOR), Nics, Lukas2 (AUTHOR), Pahnke, Jens6,7,8,9,10 (AUTHOR), Hacker, Marcus2 (AUTHOR), Zeitlinger, Markus1 (AUTHOR), Langer, Oliver1,2 (AUTHOR)
Publikováno v:
EJNMMI Radiopharmacy & Chemistry. 4/29/2024, Vol. 9 Issue 1, p1-13. 13p.