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Synthesis and bioactivity of novel C2-glycosyl benzofuranylthiazoles derivatives as acetylcholinesterase inhibitors
A new series of C2-glycosyl benzofuranylthiazole derivatives was synthesised by the further cyclization of glycosyl thiourea and 2-(bromoacetyl)-benzofuran via Hantzsch’s method. The corresponding 2-(bromoacetyl)-benzofuran derivatives were obtained by the reaction from various salicylaldehydes, and...
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Published in: | Journal of chemical research 2019-07, Vol.43 (7-8), p.257-261 |
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container_title | Journal of chemical research |
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creator | Wang, Lei Wu, Yu-Ran Ren, Shu-Ting Yin, Long Wang, You-Xian Liu, Shu-Hao Liu, Wei-Wei Shi, Da-Hua Cao, Zhi-Ling Sun, Hui-Min |
description | A new series of C2-glycosyl benzofuranylthiazole derivatives was synthesised by the further cyclization of glycosyl thiourea and 2-(bromoacetyl)-benzofuran via Hantzsch’s method. The corresponding 2-(bromoacetyl)-benzofuran derivatives were obtained by the reaction from various salicylaldehydes, and the glycosyl thiourea was prepared through a series of steps from D-Glucosamine. The acetylcholinesterase-inhibitory activities of the products were tested by Ellman’s method. The most active compounds were subsequently evaluated for the 50% inhibitory concentration values. N-(1,3,4,6-tetra-O-benzyl-2-deoxy-β-D-glucopyranosyl)-4-(5-methoxy-benzofuran-2-yl)-1,3-thiazole-2-amine possessed the best acetylcholinesterase-inhibition activity with a 50% inhibitory concentration of 2.03 ± 0.26 μM. |
doi_str_mv | 10.1177/1747519819856973 |
format | article |
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N-(1,3,4,6-tetra-O-benzyl-2-deoxy-β-D-glucopyranosyl)-4-(5-methoxy-benzofuran-2-yl)-1,3-thiazole-2-amine possessed the best acetylcholinesterase-inhibition activity with a 50% inhibitory concentration of 2.03 ± 0.26 μM.</description><identifier>ISSN: 1747-5198</identifier><identifier>EISSN: 2047-6507</identifier><identifier>DOI: 10.1177/1747519819856973</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Alcohol ; Chromatography ; Derivatives ; NMR ; Nuclear magnetic resonance ; Thioureas</subject><ispartof>Journal of chemical research, 2019-07, Vol.43 (7-8), p.257-261</ispartof><rights>The Author(s) 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c309t-7fe1131eafae91089396465b55758560ee0ab19b917a54a5cdf84d5cbf3260f43</citedby><cites>FETCH-LOGICAL-c309t-7fe1131eafae91089396465b55758560ee0ab19b917a54a5cdf84d5cbf3260f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1747519819856973$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1747519819856973$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21945,27830,27901,27902,44921,45309</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.1177/1747519819856973?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc></links><search><creatorcontrib>Wang, Lei</creatorcontrib><creatorcontrib>Wu, Yu-Ran</creatorcontrib><creatorcontrib>Ren, Shu-Ting</creatorcontrib><creatorcontrib>Yin, Long</creatorcontrib><creatorcontrib>Wang, You-Xian</creatorcontrib><creatorcontrib>Liu, Shu-Hao</creatorcontrib><creatorcontrib>Liu, Wei-Wei</creatorcontrib><creatorcontrib>Shi, Da-Hua</creatorcontrib><creatorcontrib>Cao, Zhi-Ling</creatorcontrib><creatorcontrib>Sun, Hui-Min</creatorcontrib><title>Synthesis and bioactivity of novel C2-glycosyl benzofuranylthiazoles derivatives as acetylcholinesterase inhibitors</title><title>Journal of chemical research</title><description>A new series of C2-glycosyl benzofuranylthiazole derivatives was synthesised by the further cyclization of glycosyl thiourea and 2-(bromoacetyl)-benzofuran via Hantzsch’s method. 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N-(1,3,4,6-tetra-O-benzyl-2-deoxy-β-D-glucopyranosyl)-4-(5-methoxy-benzofuran-2-yl)-1,3-thiazole-2-amine possessed the best acetylcholinesterase-inhibition activity with a 50% inhibitory concentration of 2.03 ± 0.26 μM.</description><subject>Alcohol</subject><subject>Chromatography</subject><subject>Derivatives</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Thioureas</subject><issn>1747-5198</issn><issn>2047-6507</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1UEtLAzEQDqJgrd49BjyvJptkszlK8QUFD-p5ye5OuilxU5O0sP31plQQBGFgBr7HzHwIXVNyS6mUd1RyKaiqc4lKSXaCZiXhsqgEkadodoCLA36OLmJcE8Izi85QfJvGNEC0Eeuxx631ukt2Z9OEvcGj34HDi7JYuanzcXK4hXHvzTbocXJpsHrvHUTcQ7A7nXV51rk6SJPrBu_sCDFB0BGwHQfb2uRDvERnRrsIVz99jj4eH94Xz8Xy9ellcb8sOkZUKqQBShkFbTQoSmrFVMUr0QohRf6RABDdUtUqKrXgWnS9qXkvutawsiKGszm6Ofpugv_a5kOatd-GMa9syrJmdU0YZ5lFjqwu-BgDmGYT7KcOU0NJc4i2-RttlhRHSdQr-DX9l_8N50l7wA</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Wang, Lei</creator><creator>Wu, Yu-Ran</creator><creator>Ren, Shu-Ting</creator><creator>Yin, Long</creator><creator>Wang, You-Xian</creator><creator>Liu, Shu-Hao</creator><creator>Liu, Wei-Wei</creator><creator>Shi, Da-Hua</creator><creator>Cao, Zhi-Ling</creator><creator>Sun, Hui-Min</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>EHMNL</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201907</creationdate><title>Synthesis and bioactivity of novel C2-glycosyl benzofuranylthiazoles derivatives as acetylcholinesterase inhibitors</title><author>Wang, Lei ; 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The corresponding 2-(bromoacetyl)-benzofuran derivatives were obtained by the reaction from various salicylaldehydes, and the glycosyl thiourea was prepared through a series of steps from D-Glucosamine. The acetylcholinesterase-inhibitory activities of the products were tested by Ellman’s method. The most active compounds were subsequently evaluated for the 50% inhibitory concentration values. N-(1,3,4,6-tetra-O-benzyl-2-deoxy-β-D-glucopyranosyl)-4-(5-methoxy-benzofuran-2-yl)-1,3-thiazole-2-amine possessed the best acetylcholinesterase-inhibition activity with a 50% inhibitory concentration of 2.03 ± 0.26 μM.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><doi>10.1177/1747519819856973</doi><tpages>5</tpages></addata></record> |
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subjects | Alcohol Chromatography Derivatives NMR Nuclear magnetic resonance Thioureas |
title | Synthesis and bioactivity of novel C2-glycosyl benzofuranylthiazoles derivatives as acetylcholinesterase inhibitors |
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