Loading…
SYNTHESIS AND ANTIOXIDANT EVALUATION OF NOVEL PHENOTHIAZINE LINKED SUBSTITUTEDBENZYLIDENEAMINO-1,2,4-TRIAZOLE DERIVATIVES
A series of novel 5-((10H-phenothiazin-10yl)methyl)-4-(substitutedbenzylideneamino)-4H-1,2,4-triazole-3-thiol derivatives (6a-i) have been synthesized from compound (1) through a multi-step reaction. The key intermediate (5) afforded a series of title compounds (6a-i) on condensation with various su...
Saved in:
Published in: | Journal of the Chilean Chemical Society 2015-06, Vol.60 (2), p.2919-2923 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c345t-eaad8780319fe39380efe1aab2fe2096bfb0af83fb355bb87386ea13bb3421b93 |
---|---|
cites | |
container_end_page | 2923 |
container_issue | 2 |
container_start_page | 2919 |
container_title | Journal of the Chilean Chemical Society |
container_volume | 60 |
creator | MADDILA, SURESH MOMIN, MEHBUB GORLE, SRIDEVI PALAKONDU, LAVANYA JONNALAGADDA, SREEKANTH B |
description | A series of novel 5-((10H-phenothiazin-10yl)methyl)-4-(substitutedbenzylideneamino)-4H-1,2,4-triazole-3-thiol derivatives (6a-i) have been synthesized from compound (1) through a multi-step reaction. The key intermediate (5) afforded a series of title compounds (6a-i) on condensation with various suitable aldehydes in the presence of H2SO4. The structures of novel compounds were characterized based on their elemental analysis, IR, ¹H-NMR, 13C-NMR and MS spectral data. All these novel compounds were screened for their in vitro antioxidant activity by employing nitric oxide, hydrogen peroxide, and DPPH radical scavenging assays. The compounds 6d, 6e and 6i demonstrated potent antioxidant activity as these contain the electron-releasing groups. |
doi_str_mv | 10.4067/S0717-97072015000200012 |
format | article |
fullrecord | <record><control><sourceid>scielo_cross</sourceid><recordid>TN_cdi_scielo_journals_S0717_97072015000200012</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><scielo_id>S0717_97072015000200012</scielo_id><sourcerecordid>S0717_97072015000200012</sourcerecordid><originalsourceid>FETCH-LOGICAL-c345t-eaad8780319fe39380efe1aab2fe2096bfb0af83fb355bb87386ea13bb3421b93</originalsourceid><addsrcrecordid>eNp1kF9LwzAUxYMoOKefwXyAdeZP27SP3ZrZYE1lTYfbS0lmAhvTSasP-_ZGJyKID4dzL5ffuXAAuMZoHKKY3dSIYRakDDGCcIQQIl6YnIDBz-H013wOLvp-ixAlURwPwKFeSlXwWtQwk7mXEtWjyL1DvsjKJvO7hNUMymrBS_hQcFmpQmQrITkshbzjOaybSa2EahTPJ1yulqXIueTZvZBVgEdkFAZq7omq5DDnc7HwmQteX4Izp3e9vfr2IWhmXE2LoKxuxTQrgzUNo7fAav2UsARRnDpLU5og6yzW2hBnCUpj4wzSLqHO0CgyJmE0ia3G1BgaEmxSOgTjY26_3tjdvt3u37sX_7D9Kq79U5wH2BFYd_u-76xrX7vNs-4OLUbtZ-X_kh8RXGji</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>SYNTHESIS AND ANTIOXIDANT EVALUATION OF NOVEL PHENOTHIAZINE LINKED SUBSTITUTEDBENZYLIDENEAMINO-1,2,4-TRIAZOLE DERIVATIVES</title><source>SciELO</source><creator>MADDILA, SURESH ; MOMIN, MEHBUB ; GORLE, SRIDEVI ; PALAKONDU, LAVANYA ; JONNALAGADDA, SREEKANTH B</creator><creatorcontrib>MADDILA, SURESH ; MOMIN, MEHBUB ; GORLE, SRIDEVI ; PALAKONDU, LAVANYA ; JONNALAGADDA, SREEKANTH B</creatorcontrib><description>A series of novel 5-((10H-phenothiazin-10yl)methyl)-4-(substitutedbenzylideneamino)-4H-1,2,4-triazole-3-thiol derivatives (6a-i) have been synthesized from compound (1) through a multi-step reaction. The key intermediate (5) afforded a series of title compounds (6a-i) on condensation with various suitable aldehydes in the presence of H2SO4. The structures of novel compounds were characterized based on their elemental analysis, IR, ¹H-NMR, 13C-NMR and MS spectral data. All these novel compounds were screened for their in vitro antioxidant activity by employing nitric oxide, hydrogen peroxide, and DPPH radical scavenging assays. The compounds 6d, 6e and 6i demonstrated potent antioxidant activity as these contain the electron-releasing groups.</description><identifier>ISSN: 0717-9707</identifier><identifier>EISSN: 0717-9707</identifier><identifier>DOI: 10.4067/S0717-97072015000200012</identifier><language>eng</language><publisher>Sociedad Chilena de Química</publisher><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><ispartof>Journal of the Chilean Chemical Society, 2015-06, Vol.60 (2), p.2919-2923</ispartof><rights>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-eaad8780319fe39380efe1aab2fe2096bfb0af83fb355bb87386ea13bb3421b93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,24151,27924,27925</link.rule.ids></links><search><creatorcontrib>MADDILA, SURESH</creatorcontrib><creatorcontrib>MOMIN, MEHBUB</creatorcontrib><creatorcontrib>GORLE, SRIDEVI</creatorcontrib><creatorcontrib>PALAKONDU, LAVANYA</creatorcontrib><creatorcontrib>JONNALAGADDA, SREEKANTH B</creatorcontrib><title>SYNTHESIS AND ANTIOXIDANT EVALUATION OF NOVEL PHENOTHIAZINE LINKED SUBSTITUTEDBENZYLIDENEAMINO-1,2,4-TRIAZOLE DERIVATIVES</title><title>Journal of the Chilean Chemical Society</title><addtitle>J. Chil. Chem. Soc</addtitle><description>A series of novel 5-((10H-phenothiazin-10yl)methyl)-4-(substitutedbenzylideneamino)-4H-1,2,4-triazole-3-thiol derivatives (6a-i) have been synthesized from compound (1) through a multi-step reaction. The key intermediate (5) afforded a series of title compounds (6a-i) on condensation with various suitable aldehydes in the presence of H2SO4. The structures of novel compounds were characterized based on their elemental analysis, IR, ¹H-NMR, 13C-NMR and MS spectral data. All these novel compounds were screened for their in vitro antioxidant activity by employing nitric oxide, hydrogen peroxide, and DPPH radical scavenging assays. The compounds 6d, 6e and 6i demonstrated potent antioxidant activity as these contain the electron-releasing groups.</description><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><issn>0717-9707</issn><issn>0717-9707</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1kF9LwzAUxYMoOKefwXyAdeZP27SP3ZrZYE1lTYfbS0lmAhvTSasP-_ZGJyKID4dzL5ffuXAAuMZoHKKY3dSIYRakDDGCcIQQIl6YnIDBz-H013wOLvp-ixAlURwPwKFeSlXwWtQwk7mXEtWjyL1DvsjKJvO7hNUMymrBS_hQcFmpQmQrITkshbzjOaybSa2EahTPJ1yulqXIueTZvZBVgEdkFAZq7omq5DDnc7HwmQteX4Izp3e9vfr2IWhmXE2LoKxuxTQrgzUNo7fAav2UsARRnDpLU5og6yzW2hBnCUpj4wzSLqHO0CgyJmE0ia3G1BgaEmxSOgTjY26_3tjdvt3u37sX_7D9Kq79U5wH2BFYd_u-76xrX7vNs-4OLUbtZ-X_kh8RXGji</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>MADDILA, SURESH</creator><creator>MOMIN, MEHBUB</creator><creator>GORLE, SRIDEVI</creator><creator>PALAKONDU, LAVANYA</creator><creator>JONNALAGADDA, SREEKANTH B</creator><general>Sociedad Chilena de Química</general><scope>AAYXX</scope><scope>CITATION</scope><scope>GPN</scope></search><sort><creationdate>201506</creationdate><title>SYNTHESIS AND ANTIOXIDANT EVALUATION OF NOVEL PHENOTHIAZINE LINKED SUBSTITUTEDBENZYLIDENEAMINO-1,2,4-TRIAZOLE DERIVATIVES</title><author>MADDILA, SURESH ; MOMIN, MEHBUB ; GORLE, SRIDEVI ; PALAKONDU, LAVANYA ; JONNALAGADDA, SREEKANTH B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-eaad8780319fe39380efe1aab2fe2096bfb0af83fb355bb87386ea13bb3421b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>CHEMISTRY, MULTIDISCIPLINARY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MADDILA, SURESH</creatorcontrib><creatorcontrib>MOMIN, MEHBUB</creatorcontrib><creatorcontrib>GORLE, SRIDEVI</creatorcontrib><creatorcontrib>PALAKONDU, LAVANYA</creatorcontrib><creatorcontrib>JONNALAGADDA, SREEKANTH B</creatorcontrib><collection>CrossRef</collection><collection>SciELO</collection><jtitle>Journal of the Chilean Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MADDILA, SURESH</au><au>MOMIN, MEHBUB</au><au>GORLE, SRIDEVI</au><au>PALAKONDU, LAVANYA</au><au>JONNALAGADDA, SREEKANTH B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SYNTHESIS AND ANTIOXIDANT EVALUATION OF NOVEL PHENOTHIAZINE LINKED SUBSTITUTEDBENZYLIDENEAMINO-1,2,4-TRIAZOLE DERIVATIVES</atitle><jtitle>Journal of the Chilean Chemical Society</jtitle><addtitle>J. Chil. Chem. Soc</addtitle><date>2015-06</date><risdate>2015</risdate><volume>60</volume><issue>2</issue><spage>2919</spage><epage>2923</epage><pages>2919-2923</pages><issn>0717-9707</issn><eissn>0717-9707</eissn><abstract>A series of novel 5-((10H-phenothiazin-10yl)methyl)-4-(substitutedbenzylideneamino)-4H-1,2,4-triazole-3-thiol derivatives (6a-i) have been synthesized from compound (1) through a multi-step reaction. The key intermediate (5) afforded a series of title compounds (6a-i) on condensation with various suitable aldehydes in the presence of H2SO4. The structures of novel compounds were characterized based on their elemental analysis, IR, ¹H-NMR, 13C-NMR and MS spectral data. All these novel compounds were screened for their in vitro antioxidant activity by employing nitric oxide, hydrogen peroxide, and DPPH radical scavenging assays. The compounds 6d, 6e and 6i demonstrated potent antioxidant activity as these contain the electron-releasing groups.</abstract><pub>Sociedad Chilena de Química</pub><doi>10.4067/S0717-97072015000200012</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0717-9707 |
ispartof | Journal of the Chilean Chemical Society, 2015-06, Vol.60 (2), p.2919-2923 |
issn | 0717-9707 0717-9707 |
language | eng |
recordid | cdi_scielo_journals_S0717_97072015000200012 |
source | SciELO |
subjects | CHEMISTRY, MULTIDISCIPLINARY |
title | SYNTHESIS AND ANTIOXIDANT EVALUATION OF NOVEL PHENOTHIAZINE LINKED SUBSTITUTEDBENZYLIDENEAMINO-1,2,4-TRIAZOLE DERIVATIVES |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T16%3A20%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-scielo_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=SYNTHESIS%20AND%20ANTIOXIDANT%20EVALUATION%20OF%20NOVEL%20PHENOTHIAZINE%20LINKED%20SUBSTITUTEDBENZYLIDENEAMINO-1,2,4-TRIAZOLE%20DERIVATIVES&rft.jtitle=Journal%20of%20the%20Chilean%20Chemical%20Society&rft.au=MADDILA,%20SURESH&rft.date=2015-06&rft.volume=60&rft.issue=2&rft.spage=2919&rft.epage=2923&rft.pages=2919-2923&rft.issn=0717-9707&rft.eissn=0717-9707&rft_id=info:doi/10.4067/S0717-97072015000200012&rft_dat=%3Cscielo_cross%3ES0717_97072015000200012%3C/scielo_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c345t-eaad8780319fe39380efe1aab2fe2096bfb0af83fb355bb87386ea13bb3421b93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_scielo_id=S0717_97072015000200012&rfr_iscdi=true |