Loading…

Caesalpinflavans D-F and caesalpinnone B, hybrid flavan-chalcones and normonoterpene-chalcone heterodimer from Caesalpinia digyna

Three undescribed hybrid flavan-chalcones, caesalpinflavans D-F, and an unreported normonoterpene-chalcone heterodimer, caesalpinnone B, along with three known biflavonoids were isolated from the twigs and leaves of Caesalpinia digyna. Their structures were elucidated based on extensive spectroscopi...

Full description

Saved in:
Bibliographic Details
Published in:Phytochemistry (Oxford) 2024-01, Vol.217, p.113925-113925, Article 113925
Main Authors: Duan, Chengbao, Qin, Haobei, Bi, Dewen, Gao, Yongchun, Xie, Huiping, Dai, Qi, Wang, Liqin
Format: Article
Language:English
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c259t-e4ef3f3dd6dbe36b55ce540deb58ee903f7e0984208d57c622fbf70a7ad54eb3
container_end_page 113925
container_issue
container_start_page 113925
container_title Phytochemistry (Oxford)
container_volume 217
creator Duan, Chengbao
Qin, Haobei
Bi, Dewen
Gao, Yongchun
Xie, Huiping
Dai, Qi
Wang, Liqin
description Three undescribed hybrid flavan-chalcones, caesalpinflavans D-F, and an unreported normonoterpene-chalcone heterodimer, caesalpinnone B, along with three known biflavonoids were isolated from the twigs and leaves of Caesalpinia digyna. Their structures were elucidated based on extensive spectroscopic analysis and quantum chemical calculations. Caesalpinflavan F was identified as a bis-(hybrid flavan-chalcone), its natural occurrence was supported by HPLC-IT-TOF-MS analysis. The condensation of caesalpinflavan B with acetone was possibly a key step in the biosynthesis of caesalpinflavan F. Caesalpinnone B represents an unprecedented meroterpenoid featuring a cyclobutane central framework, which was derived from chalcone and normonoterpenoid via a key [2 + 2] cyclization reaction. Biological evaluation revealed that compounds caesalpinflavan D, oxytrodiflavanone A, and caesalpinnone B exhibited moderate cytotoxicity against HL-60, SMMC-7721, SW480, A-549 and/or MDA-MB-231 cell lines with IC values ranging from 8.051 ± 0.673 to 24.26 ± 0.61 μM. This study provided evidence for further research and possible utilization of C. digyna in the future.
doi_str_mv 10.1016/j.phytochem.2023.113925
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2891759282</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2891759282</sourcerecordid><originalsourceid>FETCH-LOGICAL-c259t-e4ef3f3dd6dbe36b55ce540deb58ee903f7e0984208d57c622fbf70a7ad54eb3</originalsourceid><addsrcrecordid>eNo9kMtOwzAQRS0EglL4BfCSBSl-xHGyhEIBqRKb7i3HHpNUiR3sFqlL_pyWlq5GmnvujHQQuqVkQgktHpaTodmsgmmgnzDC-IRSXjFxgka0lDzjkpBTNCKE06zKGbtAlyktCSFCFMU5uuCykpIJPkI_Uw1Jd0PrXae_tU_4OZth7S02_4EPHvDTPW42dWwt3nOZaXRntkn6g32IffBhBXEAD8cQN7BdBdv2ELGLocfHd63Gtv3ceH2FzpzuElwf5hgtZi-L6Vs2_3h9nz7OM8NEtcogB8cdt7awNfCiFsKAyImFWpQAFeFOAqnKnJHSCmkKxlztJNFSW5FDzcfobn92iOFrDWml-jYZ6DrtIayTYmVFpahYybao3KMmhpQiODXEttdxoyhRO_1qqY761U6_2uvfNm8OT9Z1D_bY-_fNfwEcAofq</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2891759282</pqid></control><display><type>article</type><title>Caesalpinflavans D-F and caesalpinnone B, hybrid flavan-chalcones and normonoterpene-chalcone heterodimer from Caesalpinia digyna</title><source>ScienceDirect Freedom Collection</source><creator>Duan, Chengbao ; Qin, Haobei ; Bi, Dewen ; Gao, Yongchun ; Xie, Huiping ; Dai, Qi ; Wang, Liqin</creator><creatorcontrib>Duan, Chengbao ; Qin, Haobei ; Bi, Dewen ; Gao, Yongchun ; Xie, Huiping ; Dai, Qi ; Wang, Liqin</creatorcontrib><description>Three undescribed hybrid flavan-chalcones, caesalpinflavans D-F, and an unreported normonoterpene-chalcone heterodimer, caesalpinnone B, along with three known biflavonoids were isolated from the twigs and leaves of Caesalpinia digyna. Their structures were elucidated based on extensive spectroscopic analysis and quantum chemical calculations. Caesalpinflavan F was identified as a bis-(hybrid flavan-chalcone), its natural occurrence was supported by HPLC-IT-TOF-MS analysis. The condensation of caesalpinflavan B with acetone was possibly a key step in the biosynthesis of caesalpinflavan F. Caesalpinnone B represents an unprecedented meroterpenoid featuring a cyclobutane central framework, which was derived from chalcone and normonoterpenoid via a key [2 + 2] cyclization reaction. Biological evaluation revealed that compounds caesalpinflavan D, oxytrodiflavanone A, and caesalpinnone B exhibited moderate cytotoxicity against HL-60, SMMC-7721, SW480, A-549 and/or MDA-MB-231 cell lines with IC values ranging from 8.051 ± 0.673 to 24.26 ± 0.61 μM. This study provided evidence for further research and possible utilization of C. digyna in the future.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/j.phytochem.2023.113925</identifier><identifier>PMID: 37977253</identifier><language>eng</language><publisher>England</publisher><ispartof>Phytochemistry (Oxford), 2024-01, Vol.217, p.113925-113925, Article 113925</ispartof><rights>Copyright © 2023 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c259t-e4ef3f3dd6dbe36b55ce540deb58ee903f7e0984208d57c622fbf70a7ad54eb3</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/37977253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Duan, Chengbao</creatorcontrib><creatorcontrib>Qin, Haobei</creatorcontrib><creatorcontrib>Bi, Dewen</creatorcontrib><creatorcontrib>Gao, Yongchun</creatorcontrib><creatorcontrib>Xie, Huiping</creatorcontrib><creatorcontrib>Dai, Qi</creatorcontrib><creatorcontrib>Wang, Liqin</creatorcontrib><title>Caesalpinflavans D-F and caesalpinnone B, hybrid flavan-chalcones and normonoterpene-chalcone heterodimer from Caesalpinia digyna</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>Three undescribed hybrid flavan-chalcones, caesalpinflavans D-F, and an unreported normonoterpene-chalcone heterodimer, caesalpinnone B, along with three known biflavonoids were isolated from the twigs and leaves of Caesalpinia digyna. Their structures were elucidated based on extensive spectroscopic analysis and quantum chemical calculations. Caesalpinflavan F was identified as a bis-(hybrid flavan-chalcone), its natural occurrence was supported by HPLC-IT-TOF-MS analysis. The condensation of caesalpinflavan B with acetone was possibly a key step in the biosynthesis of caesalpinflavan F. Caesalpinnone B represents an unprecedented meroterpenoid featuring a cyclobutane central framework, which was derived from chalcone and normonoterpenoid via a key [2 + 2] cyclization reaction. Biological evaluation revealed that compounds caesalpinflavan D, oxytrodiflavanone A, and caesalpinnone B exhibited moderate cytotoxicity against HL-60, SMMC-7721, SW480, A-549 and/or MDA-MB-231 cell lines with IC values ranging from 8.051 ± 0.673 to 24.26 ± 0.61 μM. This study provided evidence for further research and possible utilization of C. digyna in the future.</description><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtOwzAQRS0EglL4BfCSBSl-xHGyhEIBqRKb7i3HHpNUiR3sFqlL_pyWlq5GmnvujHQQuqVkQgktHpaTodmsgmmgnzDC-IRSXjFxgka0lDzjkpBTNCKE06zKGbtAlyktCSFCFMU5uuCykpIJPkI_Uw1Jd0PrXae_tU_4OZth7S02_4EPHvDTPW42dWwt3nOZaXRntkn6g32IffBhBXEAD8cQN7BdBdv2ELGLocfHd63Gtv3ceH2FzpzuElwf5hgtZi-L6Vs2_3h9nz7OM8NEtcogB8cdt7awNfCiFsKAyImFWpQAFeFOAqnKnJHSCmkKxlztJNFSW5FDzcfobn92iOFrDWml-jYZ6DrtIayTYmVFpahYybao3KMmhpQiODXEttdxoyhRO_1qqY761U6_2uvfNm8OT9Z1D_bY-_fNfwEcAofq</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Duan, Chengbao</creator><creator>Qin, Haobei</creator><creator>Bi, Dewen</creator><creator>Gao, Yongchun</creator><creator>Xie, Huiping</creator><creator>Dai, Qi</creator><creator>Wang, Liqin</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202401</creationdate><title>Caesalpinflavans D-F and caesalpinnone B, hybrid flavan-chalcones and normonoterpene-chalcone heterodimer from Caesalpinia digyna</title><author>Duan, Chengbao ; Qin, Haobei ; Bi, Dewen ; Gao, Yongchun ; Xie, Huiping ; Dai, Qi ; Wang, Liqin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c259t-e4ef3f3dd6dbe36b55ce540deb58ee903f7e0984208d57c622fbf70a7ad54eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duan, Chengbao</creatorcontrib><creatorcontrib>Qin, Haobei</creatorcontrib><creatorcontrib>Bi, Dewen</creatorcontrib><creatorcontrib>Gao, Yongchun</creatorcontrib><creatorcontrib>Xie, Huiping</creatorcontrib><creatorcontrib>Dai, Qi</creatorcontrib><creatorcontrib>Wang, Liqin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duan, Chengbao</au><au>Qin, Haobei</au><au>Bi, Dewen</au><au>Gao, Yongchun</au><au>Xie, Huiping</au><au>Dai, Qi</au><au>Wang, Liqin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Caesalpinflavans D-F and caesalpinnone B, hybrid flavan-chalcones and normonoterpene-chalcone heterodimer from Caesalpinia digyna</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2024-01</date><risdate>2024</risdate><volume>217</volume><spage>113925</spage><epage>113925</epage><pages>113925-113925</pages><artnum>113925</artnum><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>Three undescribed hybrid flavan-chalcones, caesalpinflavans D-F, and an unreported normonoterpene-chalcone heterodimer, caesalpinnone B, along with three known biflavonoids were isolated from the twigs and leaves of Caesalpinia digyna. Their structures were elucidated based on extensive spectroscopic analysis and quantum chemical calculations. Caesalpinflavan F was identified as a bis-(hybrid flavan-chalcone), its natural occurrence was supported by HPLC-IT-TOF-MS analysis. The condensation of caesalpinflavan B with acetone was possibly a key step in the biosynthesis of caesalpinflavan F. Caesalpinnone B represents an unprecedented meroterpenoid featuring a cyclobutane central framework, which was derived from chalcone and normonoterpenoid via a key [2 + 2] cyclization reaction. Biological evaluation revealed that compounds caesalpinflavan D, oxytrodiflavanone A, and caesalpinnone B exhibited moderate cytotoxicity against HL-60, SMMC-7721, SW480, A-549 and/or MDA-MB-231 cell lines with IC values ranging from 8.051 ± 0.673 to 24.26 ± 0.61 μM. This study provided evidence for further research and possible utilization of C. digyna in the future.</abstract><cop>England</cop><pmid>37977253</pmid><doi>10.1016/j.phytochem.2023.113925</doi><tpages>1</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0031-9422
ispartof Phytochemistry (Oxford), 2024-01, Vol.217, p.113925-113925, Article 113925
issn 0031-9422
1873-3700
language eng
recordid cdi_proquest_miscellaneous_2891759282
source ScienceDirect Freedom Collection
title Caesalpinflavans D-F and caesalpinnone B, hybrid flavan-chalcones and normonoterpene-chalcone heterodimer from Caesalpinia digyna
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T23%3A17%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Caesalpinflavans%20D-F%20and%20caesalpinnone%20B,%20hybrid%20flavan-chalcones%20and%20normonoterpene-chalcone%20heterodimer%20from%20Caesalpinia%20digyna&rft.jtitle=Phytochemistry%20(Oxford)&rft.au=Duan,%20Chengbao&rft.date=2024-01&rft.volume=217&rft.spage=113925&rft.epage=113925&rft.pages=113925-113925&rft.artnum=113925&rft.issn=0031-9422&rft.eissn=1873-3700&rft_id=info:doi/10.1016/j.phytochem.2023.113925&rft_dat=%3Cproquest_cross%3E2891759282%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c259t-e4ef3f3dd6dbe36b55ce540deb58ee903f7e0984208d57c622fbf70a7ad54eb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2891759282&rft_id=info:pmid/37977253&rfr_iscdi=true