Neoglycorandomization and Chemoenzymatic Glycorandomization: Two Complementary Tools for Natural Product Diversification
In an effort to explore the contribution of the sugar constituents of pharmaceutically relevant glycosylated natural products, chemists have developed glycosylation methods that are amenable to the generation of libraries of analogues with a broad array of glycosidic attachments. Recently, two compl...
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Veröffentlicht in: | Journal of natural products (Washington, D.C.) D.C.), 2005-11, Vol.68 (11), p.1696-1711 |
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container_title | Journal of natural products (Washington, D.C.) |
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creator | Langenhan, Joseph M Griffith, Byron R Thorson, Jon S |
description | In an effort to explore the contribution of the sugar constituents of pharmaceutically relevant glycosylated natural products, chemists have developed glycosylation methods that are amenable to the generation of libraries of analogues with a broad array of glycosidic attachments. Recently, two complementary glycorandomization strategies have been described, namely, neoglycorandomization, a chemical approach based on a one-step sugar ligation reaction that does not require any prior sugar protection or activation, and chemoenzymatic glycorandomization, a biocatalytic approach that relies on the substrate promiscuity of enzymes to activate and attach sugars to natural products. Since both methods require reducing sugars, this review first highlights recent advances in monosaccharide generation and then follows with an overview of recent progress in the development of neoglycorandomization and chemoenzymatic glycorandomization. |
doi_str_mv | 10.1021/np0502084 |
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Nat. Prod</addtitle><description>In an effort to explore the contribution of the sugar constituents of pharmaceutically relevant glycosylated natural products, chemists have developed glycosylation methods that are amenable to the generation of libraries of analogues with a broad array of glycosidic attachments. Recently, two complementary glycorandomization strategies have been described, namely, neoglycorandomization, a chemical approach based on a one-step sugar ligation reaction that does not require any prior sugar protection or activation, and chemoenzymatic glycorandomization, a biocatalytic approach that relies on the substrate promiscuity of enzymes to activate and attach sugars to natural products. Since both methods require reducing sugars, this review first highlights recent advances in monosaccharide generation and then follows with an overview of recent progress in the development of neoglycorandomization and chemoenzymatic glycorandomization.</description><subject>Aldehyde-Lyases - metabolism</subject><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>Biological Products - chemistry</subject><subject>Biotechnology</subject><subject>Carbohydrates - chemistry</subject><subject>Catalysis</subject><subject>Chemistry</subject><subject>Combinatorial Chemistry Techniques</subject><subject>Exact sciences and technology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycosylation</subject><subject>Glycosyltransferases - metabolism</subject><subject>Macrolides - chemistry</subject><subject>Methods. Procedures. Technologies</subject><subject>Molecular Structure</subject><subject>Organic chemistry</subject><subject>Peptides - chemistry</subject><subject>Peptides - pharmacology</subject><issn>0163-3864</issn><issn>1520-6025</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0DFv1DAYBmALgehRGPgDyAtIDIHP8cV22NAVCqIqRYSFxfpiO-CSxIedAFeWrv2b_BIMd-oNMFn-_PiV_RJyn8ETBiV7Oq6hghLU8gZZsKqEQkBZ3SQLYIIXXInlAbmT0jkAcKir2-Qgz6HmZb0gP09d-NRvTIg42jD4C5x8GGne0NVnNwQ3XmyGPDP0-B_17NflFW2-B7oKw7p3gxsnjBvahNAn2oVIT3GaI_b0LAY7m4ke-W8uJt958_f-XXKrwz65e7v1kHx4-aJZvSpO3h6_Xj0_KZArNhXCspYLVQvbMXC8ZShbgaCsEaaUKCpXI7aWK255K4VUFTM1SmFLBLSy44fk0TZ3HcPX2aVJDz4Z1_c4ujAnLZTitSqXGT7eQhNDStF1eh39kP-kGeg_TevrprN9sAud28HZvdxVm8HDHcBksO9ydcanvZOcwbKC7Iqt82lyP67PMX7RQnJZ6ebsvX4HDTsC_kZ_3OeiSfo8zHHM3f3ngb8BbcukuQ</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Langenhan, Joseph M</creator><creator>Griffith, Byron R</creator><creator>Thorson, Jon S</creator><general>American Chemical Society</general><general>American Society of Pharmacognosy</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>20051101</creationdate><title>Neoglycorandomization and Chemoenzymatic Glycorandomization: Two Complementary Tools for Natural Product Diversification</title><author>Langenhan, Joseph M ; Griffith, Byron R ; Thorson, Jon S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-6d1b36896df10e3b1a7b6a08dc6c27a65e9aabd383d3b767851c9a76d2a0ad7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aldehyde-Lyases - metabolism</topic><topic>Bioconversions. Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>Biological Products - chemistry</topic><topic>Biotechnology</topic><topic>Carbohydrates - chemistry</topic><topic>Catalysis</topic><topic>Chemistry</topic><topic>Combinatorial Chemistry Techniques</topic><topic>Exact sciences and technology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycosylation</topic><topic>Glycosyltransferases - metabolism</topic><topic>Macrolides - chemistry</topic><topic>Methods. Procedures. Technologies</topic><topic>Molecular Structure</topic><topic>Organic chemistry</topic><topic>Peptides - chemistry</topic><topic>Peptides - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Langenhan, Joseph M</creatorcontrib><creatorcontrib>Griffith, Byron R</creatorcontrib><creatorcontrib>Thorson, Jon S</creatorcontrib><collection>Istex</collection><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>MEDLINE - Academic</collection><jtitle>Journal of natural products (Washington, D.C.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Langenhan, Joseph M</au><au>Griffith, Byron R</au><au>Thorson, Jon S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neoglycorandomization and Chemoenzymatic Glycorandomization: Two Complementary Tools for Natural Product Diversification</atitle><jtitle>Journal of natural products (Washington, D.C.)</jtitle><addtitle>J. Nat. Prod</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>68</volume><issue>11</issue><spage>1696</spage><epage>1711</epage><pages>1696-1711</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><coden>JNPRDF</coden><abstract>In an effort to explore the contribution of the sugar constituents of pharmaceutically relevant glycosylated natural products, chemists have developed glycosylation methods that are amenable to the generation of libraries of analogues with a broad array of glycosidic attachments. Recently, two complementary glycorandomization strategies have been described, namely, neoglycorandomization, a chemical approach based on a one-step sugar ligation reaction that does not require any prior sugar protection or activation, and chemoenzymatic glycorandomization, a biocatalytic approach that relies on the substrate promiscuity of enzymes to activate and attach sugars to natural products. 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subjects | Aldehyde-Lyases - metabolism Bioconversions. Hemisynthesis Biological and medical sciences Biological Products - chemistry Biotechnology Carbohydrates - chemistry Catalysis Chemistry Combinatorial Chemistry Techniques Exact sciences and technology Fundamental and applied biological sciences. Psychology Glycosylation Glycosyltransferases - metabolism Macrolides - chemistry Methods. Procedures. Technologies Molecular Structure Organic chemistry Peptides - chemistry Peptides - pharmacology |
title | Neoglycorandomization and Chemoenzymatic Glycorandomization: Two Complementary Tools for Natural Product Diversification |
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