Phytochemical investigations of Campsis radicans L

Petroleum ether, dichloromethane and ethyl acetate soluble fractions were obtained through partitioning the crude methanolic extract of the leaves of Campsis radicans L. (Family. Bignoniaceae) followed by the chromatographic separation of secondary metabolites from them. A total of five triterpene c...

Full description

Saved in:
Bibliographic Details
Published in:Journal of applied pharmaceutical research 2020-08, Vol.8 (3), p.55-59
Main Authors: Mirazul Islam, Md Ruhul Kuddus, Mohammad Abdur Rashid, Mohammad Rashedul Haque
Format: Article
Language:English
Subjects:
arjunolic acid
bignoniaceae
campsis radicans
corosolic acid
maslinic acid
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-c1760-357df17c10ad847f854f2e552b0af06a7d7a37b320d3be243df11b60c81549533
cites
container_end_page 59
container_issue 3
container_start_page 55
container_title Journal of applied pharmaceutical research
container_volume 8
creator Mirazul Islam
Md Ruhul Kuddus
Mohammad Abdur Rashid
Mohammad Rashedul Haque
description Petroleum ether, dichloromethane and ethyl acetate soluble fractions were obtained through partitioning the crude methanolic extract of the leaves of Campsis radicans L. (Family. Bignoniaceae) followed by the chromatographic separation of secondary metabolites from them. A total of five triterpene compounds i.e., corosolic acid methyl ester (1), β-amyrin (2), arjunolic acid (3), maslinic acid (4) and 28-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]-2α,3α,19α-trihydroxy-12-en-28-ursolic acid (5) were isolated from the dichloromethane fractions and their structures were characterized by 1H NMR spectroscopy and compared the NMR data with published values.
doi_str_mv 10.18231/j.joapr.2020.v.8.i.3.55.59
format article
fullrecord <record><control><sourceid>doaj</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_6f7f1a070ce64ff097e29234bbd45ae0</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_6f7f1a070ce64ff097e29234bbd45ae0</doaj_id><sourcerecordid>oai_doaj_org_article_6f7f1a070ce64ff097e29234bbd45ae0</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1760-357df17c10ad847f854f2e552b0af06a7d7a37b320d3be243df11b60c81549533</originalsourceid><addsrcrecordid>eNotj8tqwzAUREWh0JDmHwxdW73SlSx7WUwfgUC6aNfmWo9EJomMZQL5-5q2q4HDYYZh7EkAF7VE8TzwIdE4cQkS-JXXPHLkWnPd3LGVRFWXgKgf2CbnAQCE0VpLtWLy83ibkz36c7R0KuLl6vMcDzTHdMlFCkVL5zHHXEzkFmNhu0d2H-iU_eY_1-z77fWr_Sh3-_dt-7IrrTAVlKiNC8JYAeRqZUKtVZB-We2BAlRknCE0PUpw2HupcLFFX4GthVaNRlyz7V-vSzR04xTPNN26RLH7BWk6dDTN0Z58VwUTBIEB6ysVAjTGy2Z53fdOafKAP4TRVS0</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Phytochemical investigations of Campsis radicans L</title><source>DOAJ Directory of Open Access Journals</source><creator>Mirazul Islam ; Md Ruhul Kuddus ; Mohammad Abdur Rashid ; Mohammad Rashedul Haque</creator><creatorcontrib>Mirazul Islam ; Md Ruhul Kuddus ; Mohammad Abdur Rashid ; Mohammad Rashedul Haque</creatorcontrib><description>Petroleum ether, dichloromethane and ethyl acetate soluble fractions were obtained through partitioning the crude methanolic extract of the leaves of Campsis radicans L. (Family. Bignoniaceae) followed by the chromatographic separation of secondary metabolites from them. A total of five triterpene compounds i.e., corosolic acid methyl ester (1), β-amyrin (2), arjunolic acid (3), maslinic acid (4) and 28-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]-2α,3α,19α-trihydroxy-12-en-28-ursolic acid (5) were isolated from the dichloromethane fractions and their structures were characterized by 1H NMR spectroscopy and compared the NMR data with published values.</description><identifier>EISSN: 2348-0335</identifier><identifier>DOI: 10.18231/j.joapr.2020.v.8.i.3.55.59</identifier><language>eng</language><publisher>Creative Pharma Assent</publisher><subject>arjunolic acid ; bignoniaceae ; campsis radicans ; corosolic acid ; maslinic acid</subject><ispartof>Journal of applied pharmaceutical research, 2020-08, Vol.8 (3), p.55-59</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1760-357df17c10ad847f854f2e552b0af06a7d7a37b320d3be243df11b60c81549533</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,2102,27924,27925</link.rule.ids></links><search><creatorcontrib>Mirazul Islam</creatorcontrib><creatorcontrib>Md Ruhul Kuddus</creatorcontrib><creatorcontrib>Mohammad Abdur Rashid</creatorcontrib><creatorcontrib>Mohammad Rashedul Haque</creatorcontrib><title>Phytochemical investigations of Campsis radicans L</title><title>Journal of applied pharmaceutical research</title><description>Petroleum ether, dichloromethane and ethyl acetate soluble fractions were obtained through partitioning the crude methanolic extract of the leaves of Campsis radicans L. (Family. Bignoniaceae) followed by the chromatographic separation of secondary metabolites from them. A total of five triterpene compounds i.e., corosolic acid methyl ester (1), β-amyrin (2), arjunolic acid (3), maslinic acid (4) and 28-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]-2α,3α,19α-trihydroxy-12-en-28-ursolic acid (5) were isolated from the dichloromethane fractions and their structures were characterized by 1H NMR spectroscopy and compared the NMR data with published values.</description><subject>arjunolic acid</subject><subject>bignoniaceae</subject><subject>campsis radicans</subject><subject>corosolic acid</subject><subject>maslinic acid</subject><issn>2348-0335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNotj8tqwzAUREWh0JDmHwxdW73SlSx7WUwfgUC6aNfmWo9EJomMZQL5-5q2q4HDYYZh7EkAF7VE8TzwIdE4cQkS-JXXPHLkWnPd3LGVRFWXgKgf2CbnAQCE0VpLtWLy83ibkz36c7R0KuLl6vMcDzTHdMlFCkVL5zHHXEzkFmNhu0d2H-iU_eY_1-z77fWr_Sh3-_dt-7IrrTAVlKiNC8JYAeRqZUKtVZB-We2BAlRknCE0PUpw2HupcLFFX4GthVaNRlyz7V-vSzR04xTPNN26RLH7BWk6dDTN0Z58VwUTBIEB6ysVAjTGy2Z53fdOafKAP4TRVS0</recordid><startdate>20200831</startdate><enddate>20200831</enddate><creator>Mirazul Islam</creator><creator>Md Ruhul Kuddus</creator><creator>Mohammad Abdur Rashid</creator><creator>Mohammad Rashedul Haque</creator><general>Creative Pharma Assent</general><scope>DOA</scope></search><sort><creationdate>20200831</creationdate><title>Phytochemical investigations of Campsis radicans L</title><author>Mirazul Islam ; Md Ruhul Kuddus ; Mohammad Abdur Rashid ; Mohammad Rashedul Haque</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1760-357df17c10ad847f854f2e552b0af06a7d7a37b320d3be243df11b60c81549533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>arjunolic acid</topic><topic>bignoniaceae</topic><topic>campsis radicans</topic><topic>corosolic acid</topic><topic>maslinic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mirazul Islam</creatorcontrib><creatorcontrib>Md Ruhul Kuddus</creatorcontrib><creatorcontrib>Mohammad Abdur Rashid</creatorcontrib><creatorcontrib>Mohammad Rashedul Haque</creatorcontrib><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of applied pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mirazul Islam</au><au>Md Ruhul Kuddus</au><au>Mohammad Abdur Rashid</au><au>Mohammad Rashedul Haque</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phytochemical investigations of Campsis radicans L</atitle><jtitle>Journal of applied pharmaceutical research</jtitle><date>2020-08-31</date><risdate>2020</risdate><volume>8</volume><issue>3</issue><spage>55</spage><epage>59</epage><pages>55-59</pages><eissn>2348-0335</eissn><abstract>Petroleum ether, dichloromethane and ethyl acetate soluble fractions were obtained through partitioning the crude methanolic extract of the leaves of Campsis radicans L. (Family. Bignoniaceae) followed by the chromatographic separation of secondary metabolites from them. A total of five triterpene compounds i.e., corosolic acid methyl ester (1), β-amyrin (2), arjunolic acid (3), maslinic acid (4) and 28-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]-2α,3α,19α-trihydroxy-12-en-28-ursolic acid (5) were isolated from the dichloromethane fractions and their structures were characterized by 1H NMR spectroscopy and compared the NMR data with published values.</abstract><pub>Creative Pharma Assent</pub><doi>10.18231/j.joapr.2020.v.8.i.3.55.59</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier EISSN: 2348-0335
ispartof Journal of applied pharmaceutical research, 2020-08, Vol.8 (3), p.55-59
issn 2348-0335
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_6f7f1a070ce64ff097e29234bbd45ae0
source DOAJ Directory of Open Access Journals
subjects arjunolic acid
bignoniaceae
campsis radicans
corosolic acid
maslinic acid
title Phytochemical investigations of Campsis radicans L
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T09%3A17%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-doaj&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Phytochemical%20investigations%20of%20Campsis%20radicans%20L&rft.jtitle=Journal%20of%20applied%20pharmaceutical%20research&rft.au=Mirazul%20Islam&rft.date=2020-08-31&rft.volume=8&rft.issue=3&rft.spage=55&rft.epage=59&rft.pages=55-59&rft.eissn=2348-0335&rft_id=info:doi/10.18231/j.joapr.2020.v.8.i.3.55.59&rft_dat=%3Cdoaj%3Eoai_doaj_org_article_6f7f1a070ce64ff097e29234bbd45ae0%3C/doaj%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1760-357df17c10ad847f854f2e552b0af06a7d7a37b320d3be243df11b60c81549533%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true