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Synthesis, spectroscopic properties and protein labeling of water soluble 3,5-disubstituted boron dipyrromethenes
Sulfur-containing 3,5-disubstituted boron dipyrromethene (Bodipy®) fluorescent probes with improved water solubility were synthesized. A dicarboxylic acid derivative that can be excited by the 543nm HeNe laser line is very soluble in aqueous solution and retains high fluorescence quantum yield of th...
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Published in: | Bioorganic & medicinal chemistry letters 2009-12, Vol.19 (24), p.6911-6913 |
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container_title | Bioorganic & medicinal chemistry letters |
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creator | Dilek, Özlem Bane, Susan L. |
description | Sulfur-containing 3,5-disubstituted boron dipyrromethene (Bodipy®) fluorescent probes with improved water solubility were synthesized. A dicarboxylic acid derivative that can be excited by the 543nm HeNe laser line is very soluble in aqueous solution and retains high fluorescence quantum yield of the unionizable parent molecule. Conversion of the dicarboxylic acid to the succimidyl or sulfosuccinimidyl diester produces molecules capable of labeling proteins with a bright and stable fluorescence signal. |
doi_str_mv | 10.1016/j.bmcl.2009.10.080 |
format | article |
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A dicarboxylic acid derivative that can be excited by the 543nm HeNe laser line is very soluble in aqueous solution and retains high fluorescence quantum yield of the unionizable parent molecule. Conversion of the dicarboxylic acid to the succimidyl or sulfosuccinimidyl diester produces molecules capable of labeling proteins with a bright and stable fluorescence signal.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Biological and medical sciences</subject><subject>Boron Compounds - chemical synthesis</subject><subject>Boron Compounds - chemistry</subject><subject>Boron dipyrromethenes</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - chemical synthesis</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects, investigation methods</subject><subject>Protein labeling</subject><subject>Proteins</subject><subject>Proteins - chemistry</subject><subject>Solubility</subject><subject>Spectrometry, Fluorescence</subject><subject>Water - chemistry</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kUtvFSEUgInR2NvqH3Bh2Gg3nSsMzIPEmJjGV9LEhZq4IwycablhYApMzf33Mt6bqpuuCIfvPDgfQi8o2VJC2ze77TBpt60JESWwJT15hDaUt7xinDSP0YaIllS94D9P0GlKO0IoJ5w_RSdU9J2grN-g2297n28g2XSB0ww6x5B0mK3GcwwzxGwhYeXNes1gPXZqAGf9NQ4j_qUyRJyCWwYHmF00lbFpGVK2eclg8BBi8NjYeR9jmKD08ZCeoSejcgmeH88z9OPjh--Xn6urr5--XL6_qnRDm1zVrOO8obofYVRUDZqrWtDeaNqAaQlpRtMKxoUmHQwNENGPxLC206qrW0MNO0PvDnXnZZjAaPA5KifnaCcV9zIoK_9_8fZGXoc7WfesE4yUAufHAjHcLpCynGzS4JzyEJYkO8Y62tI_5OsHyZoSLhjrC1gfQF3WnCKM9-NQIlencidXp3J1usaK05L08t-P_E05SizAqyOgklZujMprm-65uqZd2_CucG8PHJS131mIMmkLXoOxsZiXJtiH5vgNIkzDiA</recordid><startdate>20091215</startdate><enddate>20091215</enddate><creator>Dilek, Özlem</creator><creator>Bane, Susan L.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20091215</creationdate><title>Synthesis, spectroscopic properties and protein labeling of water soluble 3,5-disubstituted boron dipyrromethenes</title><author>Dilek, Özlem ; Bane, Susan L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-2374451c8fefa1abc4a2918dc15ed6005fd69349c07eb5e098f0d367ca726d1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Biological and medical sciences</topic><topic>Boron Compounds - chemical synthesis</topic><topic>Boron Compounds - chemistry</topic><topic>Boron dipyrromethenes</topic><topic>Fluorescence</topic><topic>Fluorescent Dyes - chemical synthesis</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects, investigation methods</topic><topic>Protein labeling</topic><topic>Proteins</topic><topic>Proteins - chemistry</topic><topic>Solubility</topic><topic>Spectrometry, Fluorescence</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dilek, Özlem</creatorcontrib><creatorcontrib>Bane, Susan L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Bioorganic & medicinal chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dilek, Özlem</au><au>Bane, Susan L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, spectroscopic properties and protein labeling of water soluble 3,5-disubstituted boron dipyrromethenes</atitle><jtitle>Bioorganic & medicinal chemistry letters</jtitle><addtitle>Bioorg Med Chem Lett</addtitle><date>2009-12-15</date><risdate>2009</risdate><volume>19</volume><issue>24</issue><spage>6911</spage><epage>6913</epage><pages>6911-6913</pages><issn>0960-894X</issn><eissn>1464-3405</eissn><abstract>Sulfur-containing 3,5-disubstituted boron dipyrromethene (Bodipy®) fluorescent probes with improved water solubility were synthesized. 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source | ScienceDirect Freedom Collection |
subjects | Analytical, structural and metabolic biochemistry Biological and medical sciences Boron Compounds - chemical synthesis Boron Compounds - chemistry Boron dipyrromethenes Fluorescence Fluorescent Dyes - chemical synthesis Fluorescent Dyes - chemistry Fundamental and applied biological sciences. Psychology General aspects, investigation methods Protein labeling Proteins Proteins - chemistry Solubility Spectrometry, Fluorescence Water - chemistry |
title | Synthesis, spectroscopic properties and protein labeling of water soluble 3,5-disubstituted boron dipyrromethenes |
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