Novel euglycemic and hypolipidemic agents: Part - 2 antioxidant moiety as structural motif
Several thiazolidinediones having antioxidant moities in their structural motif have been synthesised and evaluated for their euglycemic and hypolipidemic activities. A few of them have been found to be superior to troglitazone. Insertion of -N-Me-group between chroman ring and phenoxyethyl moiety l...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 1998-05, Vol.8 (9), p.999-1002 |
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creator | Reddy, K.Anji Lohray, B.B. Bhushan, Vidya Reddy, A.Sekar Kishore, P.Hari Rao, V.Venugopal Saibaba, V. Bajji, A.C. Rajesh, B.M. Reddy, K.Vivekananda Chakrabarti, Ranjan Rajagopalan, R. |
description | Several thiazolidinediones having antioxidant moities in their structural motif have been synthesised and evaluated for their euglycemic and hypolipidemic activities. A few of them have been found to be superior to troglitazone.
Insertion of -N-Me-group between chroman ring and phenoxyethyl moiety lead to improved antidiabetic and hypolipidemic activities compared to troglitazone. |
doi_str_mv | 10.1016/S0960-894X(98)00159-0 |
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Insertion of -N-Me-group between chroman ring and phenoxyethyl moiety lead to improved antidiabetic and hypolipidemic activities compared to troglitazone.</description><identifier>ISSN: 0960-894X</identifier><identifier>EISSN: 1464-3405</identifier><identifier>DOI: 10.1016/S0960-894X(98)00159-0</identifier><identifier>PMID: 9871696</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Antioxidants - chemical synthesis ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Biological and medical sciences ; Blood Glucose - metabolism ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Mellitus, Type 2 - genetics ; Drug Design ; General and cellular metabolism. Vitamins ; Hypoglycemic Agents - chemical synthesis ; Hypoglycemic Agents - chemistry ; Hypoglycemic Agents - pharmacology ; Hypolipidemic Agents - chemical synthesis ; Hypolipidemic Agents - chemistry ; Hypolipidemic Agents - pharmacology ; Indicators and Reagents ; Medical sciences ; Mice ; Mice, Mutant Strains ; Pharmacology. Drug treatments ; Structure-Activity Relationship ; Thiazoles - chemical synthesis ; Thiazoles - chemistry ; Thiazoles - pharmacology ; Triglycerides - blood</subject><ispartof>Bioorganic & medicinal chemistry letters, 1998-05, Vol.8 (9), p.999-1002</ispartof><rights>1998</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c321t-c6e3b71f9f2b47afaa247c7bda443a92e303fa9f641bba0a62394f4dd2ae7b783</citedby><cites>FETCH-LOGICAL-c321t-c6e3b71f9f2b47afaa247c7bda443a92e303fa9f641bba0a62394f4dd2ae7b783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0960894X98001590$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2248561$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9871696$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Reddy, K.Anji</creatorcontrib><creatorcontrib>Lohray, B.B.</creatorcontrib><creatorcontrib>Bhushan, Vidya</creatorcontrib><creatorcontrib>Reddy, A.Sekar</creatorcontrib><creatorcontrib>Kishore, P.Hari</creatorcontrib><creatorcontrib>Rao, V.Venugopal</creatorcontrib><creatorcontrib>Saibaba, V.</creatorcontrib><creatorcontrib>Bajji, A.C.</creatorcontrib><creatorcontrib>Rajesh, B.M.</creatorcontrib><creatorcontrib>Reddy, K.Vivekananda</creatorcontrib><creatorcontrib>Chakrabarti, Ranjan</creatorcontrib><creatorcontrib>Rajagopalan, R.</creatorcontrib><title>Novel euglycemic and hypolipidemic agents: Part - 2 antioxidant moiety as structural motif</title><title>Bioorganic & medicinal chemistry letters</title><addtitle>Bioorg Med Chem Lett</addtitle><description>Several thiazolidinediones having antioxidant moities in their structural motif have been synthesised and evaluated for their euglycemic and hypolipidemic activities. A few of them have been found to be superior to troglitazone.
Insertion of -N-Me-group between chroman ring and phenoxyethyl moiety lead to improved antidiabetic and hypolipidemic activities compared to troglitazone.</description><subject>Animals</subject><subject>Antioxidants - chemical synthesis</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - metabolism</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - genetics</subject><subject>Drug Design</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Hypoglycemic Agents - chemical synthesis</subject><subject>Hypoglycemic Agents - chemistry</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Hypolipidemic Agents - chemical synthesis</subject><subject>Hypolipidemic Agents - chemistry</subject><subject>Hypolipidemic Agents - pharmacology</subject><subject>Indicators and Reagents</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Mutant Strains</subject><subject>Pharmacology. Drug treatments</subject><subject>Structure-Activity Relationship</subject><subject>Thiazoles - chemical synthesis</subject><subject>Thiazoles - chemistry</subject><subject>Thiazoles - pharmacology</subject><subject>Triglycerides - blood</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkNtLHDEUh4O06Hr5E4Q8lFIfpiaZbGbSl1KkNxAV2kLxJZxJTmzKXNYkI-5_b3SXffXpwO9858JHyClnHznj6vwX04pVrZZ_P-j2jDG-1BXbIwsulaxqyZZvyGKHHJDDlP4XSDIp98m-bhuutFqQ26vpAXuK812_tjgES2F09N96NfVhFdwmucMxp0_0BmKmFRUFyWF6DK5UOkwB85pCoinH2eY5Ql_CHPwxeeuhT3iyrUfkz7evvy9-VJfX339efLmsbC14rqzCumu41150sgEPIGRjm86BlDVogTWrPWivJO86YKBEraWXzgnApmva-oi83-xdxel-xpTNEJLFvocRpzkZpTkXiskCLjegjVNKEb1ZxTBAXBvOzLNT8-LUPAszujUvTg0rc6fbA3M3oNtNbSWW_rttH5KF3kcYbUg7TAjZLhUv2OcNhkXGQ8Bokg04WnQhos3GTeGVR54AExWUvg</recordid><startdate>19980505</startdate><enddate>19980505</enddate><creator>Reddy, K.Anji</creator><creator>Lohray, B.B.</creator><creator>Bhushan, Vidya</creator><creator>Reddy, A.Sekar</creator><creator>Kishore, P.Hari</creator><creator>Rao, V.Venugopal</creator><creator>Saibaba, V.</creator><creator>Bajji, A.C.</creator><creator>Rajesh, B.M.</creator><creator>Reddy, K.Vivekananda</creator><creator>Chakrabarti, Ranjan</creator><creator>Rajagopalan, R.</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>7X8</scope></search><sort><creationdate>19980505</creationdate><title>Novel euglycemic and hypolipidemic agents: Part - 2 antioxidant moiety as structural motif</title><author>Reddy, K.Anji ; Lohray, B.B. ; Bhushan, Vidya ; Reddy, A.Sekar ; Kishore, P.Hari ; Rao, V.Venugopal ; Saibaba, V. ; Bajji, A.C. ; Rajesh, B.M. ; Reddy, K.Vivekananda ; Chakrabarti, Ranjan ; Rajagopalan, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c321t-c6e3b71f9f2b47afaa247c7bda443a92e303fa9f641bba0a62394f4dd2ae7b783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Antioxidants - chemical synthesis</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - metabolism</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - genetics</topic><topic>Drug Design</topic><topic>General and cellular metabolism. Vitamins</topic><topic>Hypoglycemic Agents - chemical synthesis</topic><topic>Hypoglycemic Agents - chemistry</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Hypolipidemic Agents - chemical synthesis</topic><topic>Hypolipidemic Agents - chemistry</topic><topic>Hypolipidemic Agents - pharmacology</topic><topic>Indicators and Reagents</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Mutant Strains</topic><topic>Pharmacology. 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A few of them have been found to be superior to troglitazone.
Insertion of -N-Me-group between chroman ring and phenoxyethyl moiety lead to improved antidiabetic and hypolipidemic activities compared to troglitazone.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>9871696</pmid><doi>10.1016/S0960-894X(98)00159-0</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Antioxidants - chemical synthesis Antioxidants - chemistry Antioxidants - pharmacology Biological and medical sciences Blood Glucose - metabolism Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - genetics Drug Design General and cellular metabolism. Vitamins Hypoglycemic Agents - chemical synthesis Hypoglycemic Agents - chemistry Hypoglycemic Agents - pharmacology Hypolipidemic Agents - chemical synthesis Hypolipidemic Agents - chemistry Hypolipidemic Agents - pharmacology Indicators and Reagents Medical sciences Mice Mice, Mutant Strains Pharmacology. Drug treatments Structure-Activity Relationship Thiazoles - chemical synthesis Thiazoles - chemistry Thiazoles - pharmacology Triglycerides - blood |
title | Novel euglycemic and hypolipidemic agents: Part - 2 antioxidant moiety as structural motif |
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