Continuous flow biocatalysis: synthesis of purine nucleoside esters catalyzed by lipase TL IM from Thermomyces lanuginosus
Purine nucleoside ester is one of the derivatives of purine nucleoside, which has antiviral and anticancer activities. In this work, a continuous flow synthesis of purine nucleoside esters catalyzed by lipase TL IM from was successfully achieved. Various parameters including solvent, reaction temper...
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creator | Zhang, Shi-Yi Fu, Guo-Neng Du, Li-Hua Lin, Hang Zhang, Ao-Ying Xie, Han-Jia Sheng, Zhi-Kai Xue, Miao-Miao Yan, Bing-Lin Liu, Yi Ruan, Zhi-Xuan Pan, Bing-Le Zhou, Tong-Yao Luo, Xi-Ping |
description | Purine nucleoside ester is one of the derivatives of purine nucleoside, which has antiviral and anticancer activities. In this work, a continuous flow synthesis of purine nucleoside esters catalyzed by lipase TL IM from
was successfully achieved. Various parameters including solvent, reaction temperature, reaction time/flow rate and substrate ratio were investigated. The best yields were obtained with a continuous flow microreactor for 35 min at 50 °C with the substrate ratio of 1 : 5 (nucleosides to vinyl esters) in the solvent of
-amyl alcohol. 12 products were efficiently synthesized with yields of 78-93%. Here we reported for the first time the use of lipase TL IM from
in the synthesis of purine nucleoside esters. The significant advantages of this methodology are a green solvent and mild conditions, a simple work-up procedure and the highly reusable biocatalyst. This research provides a new technique for rapid synthesis of anticancer and antiviral nucleoside drugs and is helpful for further screening of drug activity. |
doi_str_mv | 10.1039/d4ra00097h |
format | Article |
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was successfully achieved. Various parameters including solvent, reaction temperature, reaction time/flow rate and substrate ratio were investigated. The best yields were obtained with a continuous flow microreactor for 35 min at 50 °C with the substrate ratio of 1 : 5 (nucleosides to vinyl esters) in the solvent of
-amyl alcohol. 12 products were efficiently synthesized with yields of 78-93%. Here we reported for the first time the use of lipase TL IM from
in the synthesis of purine nucleoside esters. The significant advantages of this methodology are a green solvent and mild conditions, a simple work-up procedure and the highly reusable biocatalyst. This research provides a new technique for rapid synthesis of anticancer and antiviral nucleoside drugs and is helpful for further screening of drug activity.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/d4ra00097h</identifier><identifier>PMID: 38577433</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Anticancer properties ; Cancer ; Chemical synthesis ; Chemistry ; Continuous flow ; Esters ; Lipase ; Microreactors ; Nucleosides ; Solvents ; Substrates</subject><ispartof>RSC advances, 2024-04, Vol.14 (16), p.10953-10961</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2024</rights><rights>This journal is © The Royal Society of Chemistry 2024 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c366t-665023de2ab37a1d8a8971e001e6f55f7f9ccf7369fae7c7362926201e449ec93</cites><orcidid>0000-0001-6767-2248</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10993233/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10993233/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38577433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Shi-Yi</creatorcontrib><creatorcontrib>Fu, Guo-Neng</creatorcontrib><creatorcontrib>Du, Li-Hua</creatorcontrib><creatorcontrib>Lin, Hang</creatorcontrib><creatorcontrib>Zhang, Ao-Ying</creatorcontrib><creatorcontrib>Xie, Han-Jia</creatorcontrib><creatorcontrib>Sheng, Zhi-Kai</creatorcontrib><creatorcontrib>Xue, Miao-Miao</creatorcontrib><creatorcontrib>Yan, Bing-Lin</creatorcontrib><creatorcontrib>Liu, Yi</creatorcontrib><creatorcontrib>Ruan, Zhi-Xuan</creatorcontrib><creatorcontrib>Pan, Bing-Le</creatorcontrib><creatorcontrib>Zhou, Tong-Yao</creatorcontrib><creatorcontrib>Luo, Xi-Ping</creatorcontrib><title>Continuous flow biocatalysis: synthesis of purine nucleoside esters catalyzed by lipase TL IM from Thermomyces lanuginosus</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>Purine nucleoside ester is one of the derivatives of purine nucleoside, which has antiviral and anticancer activities. In this work, a continuous flow synthesis of purine nucleoside esters catalyzed by lipase TL IM from
was successfully achieved. Various parameters including solvent, reaction temperature, reaction time/flow rate and substrate ratio were investigated. The best yields were obtained with a continuous flow microreactor for 35 min at 50 °C with the substrate ratio of 1 : 5 (nucleosides to vinyl esters) in the solvent of
-amyl alcohol. 12 products were efficiently synthesized with yields of 78-93%. Here we reported for the first time the use of lipase TL IM from
in the synthesis of purine nucleoside esters. The significant advantages of this methodology are a green solvent and mild conditions, a simple work-up procedure and the highly reusable biocatalyst. This research provides a new technique for rapid synthesis of anticancer and antiviral nucleoside drugs and is helpful for further screening of drug activity.</description><subject>Anticancer properties</subject><subject>Cancer</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Continuous flow</subject><subject>Esters</subject><subject>Lipase</subject><subject>Microreactors</subject><subject>Nucleosides</subject><subject>Solvents</subject><subject>Substrates</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkV9rFDEUxYMottS--AEk4IsIq_k3ycYXKWu1hRVB1ueQzdx0U2aSNZko00_f1K2l-pQD95fDPfcg9JKSd5Rw_b4X2RJCtNo9QceMCLlgROqnj_QROi3lujFEdpRJ-hwd8WWnlOD8GN2sUpxCrKkW7If0G29Dcnayw1xC-YDLHKcdNImTx_uaQwQcqxsgldADhjJBLvjw4QZ6vJ3xEPa2AN6s8eVX7HMa8WYHeUzj7KDgwcZ6FWIqtbxAz7wdCpzevyfox-fzzepisf725XJ1tl44LuW0kLIjjPfA7JYrS_ulXWpFgRAK0nedV1475xWX2ltQrgmmmWRtLIQGp_kJ-njw3dftCL2DOGU7mH0Oo82zSTaYfycx7MxV-mUo0ZozzpvDm3uHnH7WFtqMoTgYWhhohzOccMEE7Rht6Ov_0OtUc2z57ijNFBWSNertgXI5lZLBP2xDibmr1XwS38_-1HrR4FeP939A_5bIbwHa4p-h</recordid><startdate>20240403</startdate><enddate>20240403</enddate><creator>Zhang, Shi-Yi</creator><creator>Fu, Guo-Neng</creator><creator>Du, Li-Hua</creator><creator>Lin, Hang</creator><creator>Zhang, Ao-Ying</creator><creator>Xie, Han-Jia</creator><creator>Sheng, Zhi-Kai</creator><creator>Xue, Miao-Miao</creator><creator>Yan, Bing-Lin</creator><creator>Liu, Yi</creator><creator>Ruan, Zhi-Xuan</creator><creator>Pan, Bing-Le</creator><creator>Zhou, Tong-Yao</creator><creator>Luo, Xi-Ping</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6767-2248</orcidid></search><sort><creationdate>20240403</creationdate><title>Continuous flow biocatalysis: synthesis of purine nucleoside esters catalyzed by lipase TL IM from Thermomyces lanuginosus</title><author>Zhang, Shi-Yi ; Fu, Guo-Neng ; Du, Li-Hua ; Lin, Hang ; Zhang, Ao-Ying ; Xie, Han-Jia ; Sheng, Zhi-Kai ; Xue, Miao-Miao ; Yan, Bing-Lin ; Liu, Yi ; Ruan, Zhi-Xuan ; Pan, Bing-Le ; Zhou, Tong-Yao ; Luo, Xi-Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-665023de2ab37a1d8a8971e001e6f55f7f9ccf7369fae7c7362926201e449ec93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anticancer properties</topic><topic>Cancer</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Continuous flow</topic><topic>Esters</topic><topic>Lipase</topic><topic>Microreactors</topic><topic>Nucleosides</topic><topic>Solvents</topic><topic>Substrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Shi-Yi</creatorcontrib><creatorcontrib>Fu, Guo-Neng</creatorcontrib><creatorcontrib>Du, Li-Hua</creatorcontrib><creatorcontrib>Lin, Hang</creatorcontrib><creatorcontrib>Zhang, Ao-Ying</creatorcontrib><creatorcontrib>Xie, Han-Jia</creatorcontrib><creatorcontrib>Sheng, Zhi-Kai</creatorcontrib><creatorcontrib>Xue, Miao-Miao</creatorcontrib><creatorcontrib>Yan, Bing-Lin</creatorcontrib><creatorcontrib>Liu, Yi</creatorcontrib><creatorcontrib>Ruan, Zhi-Xuan</creatorcontrib><creatorcontrib>Pan, Bing-Le</creatorcontrib><creatorcontrib>Zhou, Tong-Yao</creatorcontrib><creatorcontrib>Luo, Xi-Ping</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Shi-Yi</au><au>Fu, Guo-Neng</au><au>Du, Li-Hua</au><au>Lin, Hang</au><au>Zhang, Ao-Ying</au><au>Xie, Han-Jia</au><au>Sheng, Zhi-Kai</au><au>Xue, Miao-Miao</au><au>Yan, Bing-Lin</au><au>Liu, Yi</au><au>Ruan, Zhi-Xuan</au><au>Pan, Bing-Le</au><au>Zhou, Tong-Yao</au><au>Luo, Xi-Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Continuous flow biocatalysis: synthesis of purine nucleoside esters catalyzed by lipase TL IM from Thermomyces lanuginosus</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2024-04-03</date><risdate>2024</risdate><volume>14</volume><issue>16</issue><spage>10953</spage><epage>10961</epage><pages>10953-10961</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>Purine nucleoside ester is one of the derivatives of purine nucleoside, which has antiviral and anticancer activities. In this work, a continuous flow synthesis of purine nucleoside esters catalyzed by lipase TL IM from
was successfully achieved. Various parameters including solvent, reaction temperature, reaction time/flow rate and substrate ratio were investigated. The best yields were obtained with a continuous flow microreactor for 35 min at 50 °C with the substrate ratio of 1 : 5 (nucleosides to vinyl esters) in the solvent of
-amyl alcohol. 12 products were efficiently synthesized with yields of 78-93%. Here we reported for the first time the use of lipase TL IM from
in the synthesis of purine nucleoside esters. The significant advantages of this methodology are a green solvent and mild conditions, a simple work-up procedure and the highly reusable biocatalyst. This research provides a new technique for rapid synthesis of anticancer and antiviral nucleoside drugs and is helpful for further screening of drug activity.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38577433</pmid><doi>10.1039/d4ra00097h</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6767-2248</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anticancer properties Cancer Chemical synthesis Chemistry Continuous flow Esters Lipase Microreactors Nucleosides Solvents Substrates |
title | Continuous flow biocatalysis: synthesis of purine nucleoside esters catalyzed by lipase TL IM from Thermomyces lanuginosus |
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