Sökning: WFRF:(Luthman Kristina) > 2,6,8-Trisubstitute...
Fältnamn | Indikatorer | Metadata |
---|---|---|
000 | 03565naa a2200421 4500 | |
001 | oai:gup.ub.gu.se/100642 | |
003 | SwePub | |
008 | 240528s2009 | |||||||||||000 ||eng| | |
009 | oai:research.chalmers.se:f047e1df-3425-4038-94fc-5122892c2e90 | |
024 | 7 | a https://gup.ub.gu.se/publication/1006422 URI |
024 | 7 | a https://doi.org/10.1002/chem.2009002792 DOI |
024 | 7 | a https://research.chalmers.se/publication/1006422 URI |
040 | a (SwePub)gud (SwePub)cth | |
041 | a eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Dyrager, Christine,d 1975u Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg4 aut0 (Swepub:gu)xdyrch |
245 | 1 0 | a 2,6,8-Trisubstituted 3-hydroxychromone derivatives as fluorophores for live-cell imaging. |
264 | 1 | b Wiley,c 2009 |
520 | a We present the synthesis and photophysical characterisation of a series of structurally diverse, fluorescent 2,6,8-trisubstituted 3-hydroxychromone derivatives with high fluorescence quantum yields and molar extinction coefficients. Two of these derivatives (9 and 10 a) have been studied as fluorophores for cellular imaging in HeLa cells and show excellent permeability and promising fluorescence properties in a cellular environment. In addition, we have demonstrated by photophysical characterisation of 3-isobutyroxychromone derivatives that esterification of the 3-hydroxyl group results in acceptable and useful fluorescence properties. | |
650 | 7 | a NATURVETENSKAPx Kemi0 (SwePub)1042 hsv//swe |
650 | 7 | a NATURAL SCIENCESx Chemical Sciences0 (SwePub)1042 hsv//eng |
700 | 1 | a Friberg, Annikau Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg4 aut0 (Swepub:gu)xfannz |
700 | 1 | a Dahlén, Kristian,d 1973u Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg4 aut0 (Swepub:gu)xdahkr |
700 | 1 | a Fridén-Saxin, Maria,d 1979u Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg4 aut |
700 | 1 | a Börjesson, Karl,d 1982u Chalmers tekniska högskola,Chalmers University of Technology4 aut0 (Swepub:cth)kb01boka |
700 | 1 | a Wilhelmsson, Marcus,d 1974u Chalmers tekniska högskola,Chalmers University of Technology4 aut0 (Swepub:cth)mawi |
700 | 1 | a Smedh, Maria,d 1968u Gothenburg University,Göteborgs universitet,Institutionen för fysik (GU),Department of Physics (GU),University of Gothenburg4 aut0 (Swepub:gu)xsmema |
700 | 1 | a Grøtli, Morten,d 1966u Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg4 aut0 (Swepub:cth)grotli |
700 | 1 | a Luthman, Kristina,d 1953u Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg4 aut0 (Swepub:gu)xlutkr |
710 | 2 | a Göteborgs universitetb Institutionen för kemi4 org |
773 | 0 | t Chemistry (Weinheim an der Bergstrasse, Germany)d : Wileyg 15:37, s. 9417-23q 15:37<9417-23x 1521-3765x 0947-6539 |
773 | 0 | t Chemistry - A European Journald : Wileyg 15:37, s. 9417-23q 15:37<9417-23x 0947-6539 |
856 | 4 | u http://dx.doi.org/10.1002/chem.200900279y FULLTEXT |
856 | 4 8 | u https://gup.ub.gu.se/publication/100642 |
856 | 4 8 | u https://doi.org/10.1002/chem.200900279 |
856 | 4 8 | u https://research.chalmers.se/publication/100642 |
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