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Synthesis and Anti-Inflammatory Activities of Some Novel S-Pyridyl Glycosides Derivatives
A series of some new acetylated S-glycosides of pyridine-2-thione derivatives, including D-glucose, D-galactose, D-xylose and L-arabinose derivatives were synthesized. Oxidation of some formed S-glycosides derivatives with H 2 O 2 afforded the corresponding sulfones. S-Alkylation of pyridine-2-thion...
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Published in: | Phosphorus, sulfur, and silicon and the related elements sulfur, and silicon and the related elements, 2008-11, Vol.183 (12), p.3046-3062 |
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container_end_page | 3062 |
container_issue | 12 |
container_start_page | 3046 |
container_title | Phosphorus, sulfur, and silicon and the related elements |
container_volume | 183 |
creator | Khalifa, Nagy M. Ramla, Mostafa M. Amr, Abd El-Galil E. Abdulla, Mohamed M. |
description | A series of some new acetylated S-glycosides of pyridine-2-thione derivatives, including D-glucose, D-galactose, D-xylose and L-arabinose derivatives were synthesized. Oxidation of some formed S-glycosides derivatives with H
2
O
2
afforded the corresponding sulfones. S-Alkylation of pyridine-2-thione derivatives was performed to furnish the S-acyclo deazauridine derivatives. The entire tested compound showed potent anti-inflammatory activity were potent against edema and in the same time inhibited the prostaglandine formation. It is work mention that all the tested compounds showed high safety margin. The structures of the new synthesized compounds have been proved by IR,
1
HNMR, mass spectra and elemental analysis. |
doi_str_mv | 10.1080/10426500802059885 |
format | article |
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2
O
2
afforded the corresponding sulfones. S-Alkylation of pyridine-2-thione derivatives was performed to furnish the S-acyclo deazauridine derivatives. The entire tested compound showed potent anti-inflammatory activity were potent against edema and in the same time inhibited the prostaglandine formation. It is work mention that all the tested compounds showed high safety margin. The structures of the new synthesized compounds have been proved by IR,
1
HNMR, mass spectra and elemental analysis.</description><identifier>ISSN: 1042-6507</identifier><identifier>EISSN: 1563-5325</identifier><identifier>DOI: 10.1080/10426500802059885</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>5,6,7,8-Tetrahydronaphthalene ; Anti-inflammatory activity ; glycoside derivatives</subject><ispartof>Phosphorus, sulfur, and silicon and the related elements, 2008-11, Vol.183 (12), p.3046-3062</ispartof><rights>Copyright Taylor & Francis Group, LLC 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c346t-40a02dee6459ef56e625b07a4806dcf3dd499b1c7e1e076812d736774d14d6163</citedby><cites>FETCH-LOGICAL-c346t-40a02dee6459ef56e625b07a4806dcf3dd499b1c7e1e076812d736774d14d6163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Khalifa, Nagy M.</creatorcontrib><creatorcontrib>Ramla, Mostafa M.</creatorcontrib><creatorcontrib>Amr, Abd El-Galil E.</creatorcontrib><creatorcontrib>Abdulla, Mohamed M.</creatorcontrib><title>Synthesis and Anti-Inflammatory Activities of Some Novel S-Pyridyl Glycosides Derivatives</title><title>Phosphorus, sulfur, and silicon and the related elements</title><description>A series of some new acetylated S-glycosides of pyridine-2-thione derivatives, including D-glucose, D-galactose, D-xylose and L-arabinose derivatives were synthesized. Oxidation of some formed S-glycosides derivatives with H
2
O
2
afforded the corresponding sulfones. S-Alkylation of pyridine-2-thione derivatives was performed to furnish the S-acyclo deazauridine derivatives. The entire tested compound showed potent anti-inflammatory activity were potent against edema and in the same time inhibited the prostaglandine formation. It is work mention that all the tested compounds showed high safety margin. The structures of the new synthesized compounds have been proved by IR,
1
HNMR, mass spectra and elemental analysis.</description><subject>5,6,7,8-Tetrahydronaphthalene</subject><subject>Anti-inflammatory activity</subject><subject>glycoside derivatives</subject><issn>1042-6507</issn><issn>1563-5325</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqF0M9KAzEQBvAgCtbqA3jLC6xO_u-Cl1K1FooK1YOnJd0kGNndSBKq-_ZdqbeCnuaD-X5zGIQuCVwRKOGaAKdSwBgpiKosxRGaECFZIRgVx2Me98VYUKfoLKUPAKgogwl6Ww99frfJJ6x7g2d99sWyd63uOp1DHPCsyX7rs7cJB4fXobP4MWxti9fF8xC9GVq8aIcmJG_Gyq2NfqtHYdM5OnG6Tfbid07R6_3dy_yhWD0tlvPZqmgYl7ngoIEaayUXlXVCWknFBpTmJUjTOGYMr6oNaZQlFpQsCTWKSaW4IdxIItkUkf3dJoaUonX1Z_SdjkNNoP75TX3wm9Hc7I3vXYid_gqxNXXWQxuii7pvfKrZX1z9yw9Unb8z2wHXgHxb</recordid><startdate>20081107</startdate><enddate>20081107</enddate><creator>Khalifa, Nagy M.</creator><creator>Ramla, Mostafa M.</creator><creator>Amr, Abd El-Galil E.</creator><creator>Abdulla, Mohamed M.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20081107</creationdate><title>Synthesis and Anti-Inflammatory Activities of Some Novel S-Pyridyl Glycosides Derivatives</title><author>Khalifa, Nagy M. ; Ramla, Mostafa M. ; Amr, Abd El-Galil E. ; Abdulla, Mohamed M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c346t-40a02dee6459ef56e625b07a4806dcf3dd499b1c7e1e076812d736774d14d6163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>5,6,7,8-Tetrahydronaphthalene</topic><topic>Anti-inflammatory activity</topic><topic>glycoside derivatives</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khalifa, Nagy M.</creatorcontrib><creatorcontrib>Ramla, Mostafa M.</creatorcontrib><creatorcontrib>Amr, Abd El-Galil E.</creatorcontrib><creatorcontrib>Abdulla, Mohamed M.</creatorcontrib><collection>CrossRef</collection><jtitle>Phosphorus, sulfur, and silicon and the related elements</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khalifa, Nagy M.</au><au>Ramla, Mostafa M.</au><au>Amr, Abd El-Galil E.</au><au>Abdulla, Mohamed M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Anti-Inflammatory Activities of Some Novel S-Pyridyl Glycosides Derivatives</atitle><jtitle>Phosphorus, sulfur, and silicon and the related elements</jtitle><date>2008-11-07</date><risdate>2008</risdate><volume>183</volume><issue>12</issue><spage>3046</spage><epage>3062</epage><pages>3046-3062</pages><issn>1042-6507</issn><eissn>1563-5325</eissn><abstract>A series of some new acetylated S-glycosides of pyridine-2-thione derivatives, including D-glucose, D-galactose, D-xylose and L-arabinose derivatives were synthesized. Oxidation of some formed S-glycosides derivatives with H
2
O
2
afforded the corresponding sulfones. S-Alkylation of pyridine-2-thione derivatives was performed to furnish the S-acyclo deazauridine derivatives. The entire tested compound showed potent anti-inflammatory activity were potent against edema and in the same time inhibited the prostaglandine formation. It is work mention that all the tested compounds showed high safety margin. The structures of the new synthesized compounds have been proved by IR,
1
HNMR, mass spectra and elemental analysis.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/10426500802059885</doi><tpages>17</tpages></addata></record> |
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source | Taylor and Francis Science and Technology Collection |
subjects | 5,6,7,8-Tetrahydronaphthalene Anti-inflammatory activity glycoside derivatives |
title | Synthesis and Anti-Inflammatory Activities of Some Novel S-Pyridyl Glycosides Derivatives |
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