Loading…
Antifungal dimeric chalcone derivative kamalachalcone E from Mallotus philippinensis
From the red coloured extract (Kamala) prepared through acetone extraction of the fresh whole uncrushed fruits of Mallotus philippinensis, one new dimeric chalcone (1) along with three known compounds 1-(5,7-dihydroxy-2,2,6-trimethyl-2H-1-benzopyran-8-yl)-3-phenyl-2-propen-1-one (2), rottlerin (3) a...
Saved in:
Published in: | Natural product research 2014-02, Vol.28 (4), p.245-250 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites 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-c396t-7f9bd40d4b83c7f5109c5012eed412c3fea6afbc7828ab10bd2548ff1289d0863 |
---|---|
cites | cdi_FETCH-LOGICAL-c396t-7f9bd40d4b83c7f5109c5012eed412c3fea6afbc7828ab10bd2548ff1289d0863 |
container_end_page | 250 |
container_issue | 4 |
container_start_page | 245 |
container_title | Natural product research |
container_volume | 28 |
creator | Kulkarni, Roshan R. Tupe, Santosh G. Gample, Suwarna P. Chandgude, Macchindra G. Sarkar, Dhiman Deshpande, Mukund V. Joshi, Swati P. |
description | From the red coloured extract (Kamala) prepared through acetone extraction of the fresh whole uncrushed fruits of Mallotus philippinensis, one new dimeric chalcone (1) along with three known compounds 1-(5,7-dihydroxy-2,2,6-trimethyl-2H-1-benzopyran-8-yl)-3-phenyl-2-propen-1-one (2), rottlerin (3) and 4′-hydroxyrottlerin (4) were isolated. The structure of compound 1 was elucidated by 1D and 2D NMR analyses that included HSQC, HMBC, COSY and ROESY experiments along with the literature comparison. Compounds 1-4 were evaluated for antifungal activity against different human pathogenic yeasts and filamentous fungi. The antiproliferative activity of the compounds was evaluated against Thp-1 cell lines. Compounds 1 and 2 both exhibited IC
50
of 8, 4 and 16 μg/mL against Cryptococcus neoformans PRL518, C. neoformans ATCC32045 and Aspergillus fumigatus, respectively. Compound 4, at 100 μg/mL, showed 54% growth inhibition of Thp-1 cell lines. |
doi_str_mv | 10.1080/14786419.2013.843178 |
format | article |
fullrecord | <record><control><sourceid>proquest_infor</sourceid><recordid>TN_cdi_proquest_miscellaneous_1506789873</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1520377953</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-7f9bd40d4b83c7f5109c5012eed412c3fea6afbc7828ab10bd2548ff1289d0863</originalsourceid><addsrcrecordid>eNqNkElLAzEUgIMo7v9AZI5eWrNOkpOU4gaKFz2HTBaNZiZjMqP039vS2qN4etv33oMPgDMEpwgKeIkoFzVFcoohIlNBCeJiBxyu2pOaYr67zZE8AEelvEOIEWNsHxxgCqVkUB6C51k3BD92rzpWNrQuB1OZNx1N6lxll-WXHsKXqz50q6PeTq4rn1NbPeoY0zCWqn8LMfR96FxXQjkBe17H4k438Ri83Fw_z-8mD0-39_PZw8QQWQ8T7mVjKbS0EcRwzxCUhkGEnbMUYUO807X2jeECC90g2FjMqPAeYSEtFDU5Bhfru31On6Mrg2pDMS5G3bk0FoUYhoRzycg_UFhzIQVfoXSNmpxKyc6rPodW54VCUK3Uq1_1aqVerdUv1843H8amdXa79Ot6CVytgdD5lFv9nXK0atCLmLLPujOhKPLnix_CCJNW</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1506789873</pqid></control><display><type>article</type><title>Antifungal dimeric chalcone derivative kamalachalcone E from Mallotus philippinensis</title><source>Taylor and Francis Science and Technology Collection</source><creator>Kulkarni, Roshan R. ; Tupe, Santosh G. ; Gample, Suwarna P. ; Chandgude, Macchindra G. ; Sarkar, Dhiman ; Deshpande, Mukund V. ; Joshi, Swati P.</creator><creatorcontrib>Kulkarni, Roshan R. ; Tupe, Santosh G. ; Gample, Suwarna P. ; Chandgude, Macchindra G. ; Sarkar, Dhiman ; Deshpande, Mukund V. ; Joshi, Swati P.</creatorcontrib><description>From the red coloured extract (Kamala) prepared through acetone extraction of the fresh whole uncrushed fruits of Mallotus philippinensis, one new dimeric chalcone (1) along with three known compounds 1-(5,7-dihydroxy-2,2,6-trimethyl-2H-1-benzopyran-8-yl)-3-phenyl-2-propen-1-one (2), rottlerin (3) and 4′-hydroxyrottlerin (4) were isolated. The structure of compound 1 was elucidated by 1D and 2D NMR analyses that included HSQC, HMBC, COSY and ROESY experiments along with the literature comparison. Compounds 1-4 were evaluated for antifungal activity against different human pathogenic yeasts and filamentous fungi. The antiproliferative activity of the compounds was evaluated against Thp-1 cell lines. Compounds 1 and 2 both exhibited IC
50
of 8, 4 and 16 μg/mL against Cryptococcus neoformans PRL518, C. neoformans ATCC32045 and Aspergillus fumigatus, respectively. Compound 4, at 100 μg/mL, showed 54% growth inhibition of Thp-1 cell lines.</description><identifier>ISSN: 1478-6419</identifier><identifier>EISSN: 1478-6427</identifier><identifier>DOI: 10.1080/14786419.2013.843178</identifier><identifier>PMID: 24099509</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>4′-hydroxyrottlerin ; antifungal ; Antifungal Agents - chemistry ; Antifungal Agents - isolation & purification ; Antifungal Agents - pharmacology ; Aspergillus fumigatus ; Aspergillus fumigatus - drug effects ; Chalcone - analogs & derivatives ; Chalcone - chemistry ; Chalcone - isolation & purification ; Chalcone - pharmacology ; Chalcones ; Cryptococcus neoformans ; Cryptococcus neoformans - drug effects ; dimeric chalcone ; Drug Screening Assays, Antitumor ; Euphorbiaceae - chemistry ; Fruit - chemistry ; Fungi - drug effects ; Humans ; India ; Inhibitory Concentration 50 ; kamalachalcone E ; Leukemia - drug therapy ; Mallotus ; Mallotus philippinensis ; Microbial Sensitivity Tests ; Molecular Structure ; Nuclear Magnetic Resonance, Biomolecular ; Plant Extracts - chemistry ; rottlerin ; Yeasts - drug effects</subject><ispartof>Natural product research, 2014-02, Vol.28 (4), p.245-250</ispartof><rights>2013 Taylor & Francis 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-7f9bd40d4b83c7f5109c5012eed412c3fea6afbc7828ab10bd2548ff1289d0863</citedby><cites>FETCH-LOGICAL-c396t-7f9bd40d4b83c7f5109c5012eed412c3fea6afbc7828ab10bd2548ff1289d0863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24099509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kulkarni, Roshan R.</creatorcontrib><creatorcontrib>Tupe, Santosh G.</creatorcontrib><creatorcontrib>Gample, Suwarna P.</creatorcontrib><creatorcontrib>Chandgude, Macchindra G.</creatorcontrib><creatorcontrib>Sarkar, Dhiman</creatorcontrib><creatorcontrib>Deshpande, Mukund V.</creatorcontrib><creatorcontrib>Joshi, Swati P.</creatorcontrib><title>Antifungal dimeric chalcone derivative kamalachalcone E from Mallotus philippinensis</title><title>Natural product research</title><addtitle>Nat Prod Res</addtitle><description>From the red coloured extract (Kamala) prepared through acetone extraction of the fresh whole uncrushed fruits of Mallotus philippinensis, one new dimeric chalcone (1) along with three known compounds 1-(5,7-dihydroxy-2,2,6-trimethyl-2H-1-benzopyran-8-yl)-3-phenyl-2-propen-1-one (2), rottlerin (3) and 4′-hydroxyrottlerin (4) were isolated. The structure of compound 1 was elucidated by 1D and 2D NMR analyses that included HSQC, HMBC, COSY and ROESY experiments along with the literature comparison. Compounds 1-4 were evaluated for antifungal activity against different human pathogenic yeasts and filamentous fungi. The antiproliferative activity of the compounds was evaluated against Thp-1 cell lines. Compounds 1 and 2 both exhibited IC
50
of 8, 4 and 16 μg/mL against Cryptococcus neoformans PRL518, C. neoformans ATCC32045 and Aspergillus fumigatus, respectively. Compound 4, at 100 μg/mL, showed 54% growth inhibition of Thp-1 cell lines.</description><subject>4′-hydroxyrottlerin</subject><subject>antifungal</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - isolation & purification</subject><subject>Antifungal Agents - pharmacology</subject><subject>Aspergillus fumigatus</subject><subject>Aspergillus fumigatus - drug effects</subject><subject>Chalcone - analogs & derivatives</subject><subject>Chalcone - chemistry</subject><subject>Chalcone - isolation & purification</subject><subject>Chalcone - pharmacology</subject><subject>Chalcones</subject><subject>Cryptococcus neoformans</subject><subject>Cryptococcus neoformans - drug effects</subject><subject>dimeric chalcone</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Euphorbiaceae - chemistry</subject><subject>Fruit - chemistry</subject><subject>Fungi - drug effects</subject><subject>Humans</subject><subject>India</subject><subject>Inhibitory Concentration 50</subject><subject>kamalachalcone E</subject><subject>Leukemia - drug therapy</subject><subject>Mallotus</subject><subject>Mallotus philippinensis</subject><subject>Microbial Sensitivity Tests</subject><subject>Molecular Structure</subject><subject>Nuclear Magnetic Resonance, Biomolecular</subject><subject>Plant Extracts - chemistry</subject><subject>rottlerin</subject><subject>Yeasts - drug effects</subject><issn>1478-6419</issn><issn>1478-6427</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkElLAzEUgIMo7v9AZI5eWrNOkpOU4gaKFz2HTBaNZiZjMqP039vS2qN4etv33oMPgDMEpwgKeIkoFzVFcoohIlNBCeJiBxyu2pOaYr67zZE8AEelvEOIEWNsHxxgCqVkUB6C51k3BD92rzpWNrQuB1OZNx1N6lxll-WXHsKXqz50q6PeTq4rn1NbPeoY0zCWqn8LMfR96FxXQjkBe17H4k438Ri83Fw_z-8mD0-39_PZw8QQWQ8T7mVjKbS0EcRwzxCUhkGEnbMUYUO807X2jeECC90g2FjMqPAeYSEtFDU5Bhfru31On6Mrg2pDMS5G3bk0FoUYhoRzycg_UFhzIQVfoXSNmpxKyc6rPodW54VCUK3Uq1_1aqVerdUv1843H8amdXa79Ot6CVytgdD5lFv9nXK0atCLmLLPujOhKPLnix_CCJNW</recordid><startdate>20140216</startdate><enddate>20140216</enddate><creator>Kulkarni, Roshan R.</creator><creator>Tupe, Santosh G.</creator><creator>Gample, Suwarna P.</creator><creator>Chandgude, Macchindra G.</creator><creator>Sarkar, Dhiman</creator><creator>Deshpande, Mukund V.</creator><creator>Joshi, Swati P.</creator><general>Taylor & Francis</general><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><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>20140216</creationdate><title>Antifungal dimeric chalcone derivative kamalachalcone E from Mallotus philippinensis</title><author>Kulkarni, Roshan R. ; Tupe, Santosh G. ; Gample, Suwarna P. ; Chandgude, Macchindra G. ; Sarkar, Dhiman ; Deshpande, Mukund V. ; Joshi, Swati P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-7f9bd40d4b83c7f5109c5012eed412c3fea6afbc7828ab10bd2548ff1289d0863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>4′-hydroxyrottlerin</topic><topic>antifungal</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - isolation & purification</topic><topic>Antifungal Agents - pharmacology</topic><topic>Aspergillus fumigatus</topic><topic>Aspergillus fumigatus - drug effects</topic><topic>Chalcone - analogs & derivatives</topic><topic>Chalcone - chemistry</topic><topic>Chalcone - isolation & purification</topic><topic>Chalcone - pharmacology</topic><topic>Chalcones</topic><topic>Cryptococcus neoformans</topic><topic>Cryptococcus neoformans - drug effects</topic><topic>dimeric chalcone</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Euphorbiaceae - chemistry</topic><topic>Fruit - chemistry</topic><topic>Fungi - drug effects</topic><topic>Humans</topic><topic>India</topic><topic>Inhibitory Concentration 50</topic><topic>kamalachalcone E</topic><topic>Leukemia - drug therapy</topic><topic>Mallotus</topic><topic>Mallotus philippinensis</topic><topic>Microbial Sensitivity Tests</topic><topic>Molecular Structure</topic><topic>Nuclear Magnetic Resonance, Biomolecular</topic><topic>Plant Extracts - chemistry</topic><topic>rottlerin</topic><topic>Yeasts - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kulkarni, Roshan R.</creatorcontrib><creatorcontrib>Tupe, Santosh G.</creatorcontrib><creatorcontrib>Gample, Suwarna P.</creatorcontrib><creatorcontrib>Chandgude, Macchindra G.</creatorcontrib><creatorcontrib>Sarkar, Dhiman</creatorcontrib><creatorcontrib>Deshpande, Mukund V.</creatorcontrib><creatorcontrib>Joshi, Swati P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Natural product research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kulkarni, Roshan R.</au><au>Tupe, Santosh G.</au><au>Gample, Suwarna P.</au><au>Chandgude, Macchindra G.</au><au>Sarkar, Dhiman</au><au>Deshpande, Mukund V.</au><au>Joshi, Swati P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antifungal dimeric chalcone derivative kamalachalcone E from Mallotus philippinensis</atitle><jtitle>Natural product research</jtitle><addtitle>Nat Prod Res</addtitle><date>2014-02-16</date><risdate>2014</risdate><volume>28</volume><issue>4</issue><spage>245</spage><epage>250</epage><pages>245-250</pages><issn>1478-6419</issn><eissn>1478-6427</eissn><abstract>From the red coloured extract (Kamala) prepared through acetone extraction of the fresh whole uncrushed fruits of Mallotus philippinensis, one new dimeric chalcone (1) along with three known compounds 1-(5,7-dihydroxy-2,2,6-trimethyl-2H-1-benzopyran-8-yl)-3-phenyl-2-propen-1-one (2), rottlerin (3) and 4′-hydroxyrottlerin (4) were isolated. The structure of compound 1 was elucidated by 1D and 2D NMR analyses that included HSQC, HMBC, COSY and ROESY experiments along with the literature comparison. Compounds 1-4 were evaluated for antifungal activity against different human pathogenic yeasts and filamentous fungi. The antiproliferative activity of the compounds was evaluated against Thp-1 cell lines. Compounds 1 and 2 both exhibited IC
50
of 8, 4 and 16 μg/mL against Cryptococcus neoformans PRL518, C. neoformans ATCC32045 and Aspergillus fumigatus, respectively. Compound 4, at 100 μg/mL, showed 54% growth inhibition of Thp-1 cell lines.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>24099509</pmid><doi>10.1080/14786419.2013.843178</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1478-6419 |
ispartof | Natural product research, 2014-02, Vol.28 (4), p.245-250 |
issn | 1478-6419 1478-6427 |
language | eng |
recordid | cdi_proquest_miscellaneous_1506789873 |
source | Taylor and Francis Science and Technology Collection |
subjects | 4′-hydroxyrottlerin antifungal Antifungal Agents - chemistry Antifungal Agents - isolation & purification Antifungal Agents - pharmacology Aspergillus fumigatus Aspergillus fumigatus - drug effects Chalcone - analogs & derivatives Chalcone - chemistry Chalcone - isolation & purification Chalcone - pharmacology Chalcones Cryptococcus neoformans Cryptococcus neoformans - drug effects dimeric chalcone Drug Screening Assays, Antitumor Euphorbiaceae - chemistry Fruit - chemistry Fungi - drug effects Humans India Inhibitory Concentration 50 kamalachalcone E Leukemia - drug therapy Mallotus Mallotus philippinensis Microbial Sensitivity Tests Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plant Extracts - chemistry rottlerin Yeasts - drug effects |
title | Antifungal dimeric chalcone derivative kamalachalcone E from Mallotus philippinensis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T00%3A59%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antifungal%20dimeric%20chalcone%20derivative%20kamalachalcone%20E%20from%20Mallotus%20philippinensis&rft.jtitle=Natural%20product%20research&rft.au=Kulkarni,%20Roshan%20R.&rft.date=2014-02-16&rft.volume=28&rft.issue=4&rft.spage=245&rft.epage=250&rft.pages=245-250&rft.issn=1478-6419&rft.eissn=1478-6427&rft_id=info:doi/10.1080/14786419.2013.843178&rft_dat=%3Cproquest_infor%3E1520377953%3C/proquest_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c396t-7f9bd40d4b83c7f5109c5012eed412c3fea6afbc7828ab10bd2548ff1289d0863%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1506789873&rft_id=info:pmid/24099509&rfr_iscdi=true |