Loading…
Screening of Ursolic Acid Analogs with HIF-1α and COX-2-Inhibiting Effects
Three novel series of derivatives by introducing a 1,2,3-triazoles moiety, 1,2,4-triazoles moiety or a nitroimidazoles ring to the ursolic acid (UA) nucleus were designed and synthesized. The biological activity of these compounds was evaluated to assess their hypoxia-inducible factor-1α (HIF-1α) an...
Saved in:
Published in: | Chemistry of natural compounds 2022-09, Vol.58 (5), p.882-887 |
---|---|
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-c319t-adcc315692ebe5ff0b2ed0eeca071bf062b3e347e016287385bc55a8e0c7c52a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c319t-adcc315692ebe5ff0b2ed0eeca071bf062b3e347e016287385bc55a8e0c7c52a3 |
container_end_page | 887 |
container_issue | 5 |
container_start_page | 882 |
container_title | Chemistry of natural compounds |
container_volume | 58 |
creator | Li, Chunshi Zhang, Tianyi Zhang, Qiaosi Liu, Xin Zou, Jixin Bai, Xueqian |
description | Three novel series of derivatives by introducing a 1,2,3-triazoles moiety, 1,2,4-triazoles moiety or a nitroimidazoles ring to the ursolic acid (UA) nucleus were designed and synthesized. The biological activity of these compounds was evaluated to assess their hypoxia-inducible factor-1α (HIF-1α) and cyclooxygenase-2 (COX-2) inhibitory activities along with HIF-1α inhibitory and anti-inflammatory effects. Compound
7e
exhibited the highest activity of all the synthesized compounds, which was higher activity than observed for the positive control UA. |
doi_str_mv | 10.1007/s10600-022-03821-8 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2719458826</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2719458826</sourcerecordid><originalsourceid>FETCH-LOGICAL-c319t-adcc315692ebe5ff0b2ed0eeca071bf062b3e347e016287385bc55a8e0c7c52a3</originalsourceid><addsrcrecordid>eNp9kM9KAzEQh4MoWP-8gKeA5-gkaTbZYymtLRZ60IK3kM1O2i11tyZbxMfyRXwmt67gzdPMwO_7MXyE3HC44wD6PnHIABgIwUAawZk5IQOutGRGGnNKBgCQM8klnJOLlLbdabLMDMjjk4-IdVWvaRPoKqZmV3k68lVJR7XbNetE36t2Q2fzKeNfn9TVJR0vX5hg83pTFVV7JCchoG_TFTkLbpfw-ndektV08jyescXyYT4eLZiXPG-ZK323qCwXWKAKAQqBJSB6B5oXATJRSJRDjcAzYbQ0qvBKOYPgtVfCyUty2_fuY_N2wNTabXOI3bfJCs3zoTJGZF1K9Ckfm5QiBruP1auLH5aDPUqzvTTbSbM_0qzpINlDqQvXa4x_1f9Q3yRwbgQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2719458826</pqid></control><display><type>article</type><title>Screening of Ursolic Acid Analogs with HIF-1α and COX-2-Inhibiting Effects</title><source>Springer Nature</source><creator>Li, Chunshi ; Zhang, Tianyi ; Zhang, Qiaosi ; Liu, Xin ; Zou, Jixin ; Bai, Xueqian</creator><creatorcontrib>Li, Chunshi ; Zhang, Tianyi ; Zhang, Qiaosi ; Liu, Xin ; Zou, Jixin ; Bai, Xueqian</creatorcontrib><description>Three novel series of derivatives by introducing a 1,2,3-triazoles moiety, 1,2,4-triazoles moiety or a nitroimidazoles ring to the ursolic acid (UA) nucleus were designed and synthesized. The biological activity of these compounds was evaluated to assess their hypoxia-inducible factor-1α (HIF-1α) and cyclooxygenase-2 (COX-2) inhibitory activities along with HIF-1α inhibitory and anti-inflammatory effects. Compound
7e
exhibited the highest activity of all the synthesized compounds, which was higher activity than observed for the positive control UA.</description><identifier>ISSN: 0009-3130</identifier><identifier>EISSN: 1573-8388</identifier><identifier>DOI: 10.1007/s10600-022-03821-8</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Biological activity ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Hypoxia ; Organic Chemistry ; Plant Sciences ; Synthesis ; Triazoles</subject><ispartof>Chemistry of natural compounds, 2022-09, Vol.58 (5), p.882-887</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-adcc315692ebe5ff0b2ed0eeca071bf062b3e347e016287385bc55a8e0c7c52a3</citedby><cites>FETCH-LOGICAL-c319t-adcc315692ebe5ff0b2ed0eeca071bf062b3e347e016287385bc55a8e0c7c52a3</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></links><search><creatorcontrib>Li, Chunshi</creatorcontrib><creatorcontrib>Zhang, Tianyi</creatorcontrib><creatorcontrib>Zhang, Qiaosi</creatorcontrib><creatorcontrib>Liu, Xin</creatorcontrib><creatorcontrib>Zou, Jixin</creatorcontrib><creatorcontrib>Bai, Xueqian</creatorcontrib><title>Screening of Ursolic Acid Analogs with HIF-1α and COX-2-Inhibiting Effects</title><title>Chemistry of natural compounds</title><addtitle>Chem Nat Compd</addtitle><description>Three novel series of derivatives by introducing a 1,2,3-triazoles moiety, 1,2,4-triazoles moiety or a nitroimidazoles ring to the ursolic acid (UA) nucleus were designed and synthesized. The biological activity of these compounds was evaluated to assess their hypoxia-inducible factor-1α (HIF-1α) and cyclooxygenase-2 (COX-2) inhibitory activities along with HIF-1α inhibitory and anti-inflammatory effects. Compound
7e
exhibited the highest activity of all the synthesized compounds, which was higher activity than observed for the positive control UA.</description><subject>Biological activity</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Hypoxia</subject><subject>Organic Chemistry</subject><subject>Plant Sciences</subject><subject>Synthesis</subject><subject>Triazoles</subject><issn>0009-3130</issn><issn>1573-8388</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kM9KAzEQh4MoWP-8gKeA5-gkaTbZYymtLRZ60IK3kM1O2i11tyZbxMfyRXwmt67gzdPMwO_7MXyE3HC44wD6PnHIABgIwUAawZk5IQOutGRGGnNKBgCQM8klnJOLlLbdabLMDMjjk4-IdVWvaRPoKqZmV3k68lVJR7XbNetE36t2Q2fzKeNfn9TVJR0vX5hg83pTFVV7JCchoG_TFTkLbpfw-ndektV08jyescXyYT4eLZiXPG-ZK323qCwXWKAKAQqBJSB6B5oXATJRSJRDjcAzYbQ0qvBKOYPgtVfCyUty2_fuY_N2wNTabXOI3bfJCs3zoTJGZF1K9Ckfm5QiBruP1auLH5aDPUqzvTTbSbM_0qzpINlDqQvXa4x_1f9Q3yRwbgQ</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Li, Chunshi</creator><creator>Zhang, Tianyi</creator><creator>Zhang, Qiaosi</creator><creator>Liu, Xin</creator><creator>Zou, Jixin</creator><creator>Bai, Xueqian</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20220901</creationdate><title>Screening of Ursolic Acid Analogs with HIF-1α and COX-2-Inhibiting Effects</title><author>Li, Chunshi ; Zhang, Tianyi ; Zhang, Qiaosi ; Liu, Xin ; Zou, Jixin ; Bai, Xueqian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-adcc315692ebe5ff0b2ed0eeca071bf062b3e347e016287385bc55a8e0c7c52a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biological activity</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Hypoxia</topic><topic>Organic Chemistry</topic><topic>Plant Sciences</topic><topic>Synthesis</topic><topic>Triazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Chunshi</creatorcontrib><creatorcontrib>Zhang, Tianyi</creatorcontrib><creatorcontrib>Zhang, Qiaosi</creatorcontrib><creatorcontrib>Liu, Xin</creatorcontrib><creatorcontrib>Zou, Jixin</creatorcontrib><creatorcontrib>Bai, Xueqian</creatorcontrib><collection>CrossRef</collection><jtitle>Chemistry of natural compounds</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Chunshi</au><au>Zhang, Tianyi</au><au>Zhang, Qiaosi</au><au>Liu, Xin</au><au>Zou, Jixin</au><au>Bai, Xueqian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening of Ursolic Acid Analogs with HIF-1α and COX-2-Inhibiting Effects</atitle><jtitle>Chemistry of natural compounds</jtitle><stitle>Chem Nat Compd</stitle><date>2022-09-01</date><risdate>2022</risdate><volume>58</volume><issue>5</issue><spage>882</spage><epage>887</epage><pages>882-887</pages><issn>0009-3130</issn><eissn>1573-8388</eissn><abstract>Three novel series of derivatives by introducing a 1,2,3-triazoles moiety, 1,2,4-triazoles moiety or a nitroimidazoles ring to the ursolic acid (UA) nucleus were designed and synthesized. The biological activity of these compounds was evaluated to assess their hypoxia-inducible factor-1α (HIF-1α) and cyclooxygenase-2 (COX-2) inhibitory activities along with HIF-1α inhibitory and anti-inflammatory effects. Compound
7e
exhibited the highest activity of all the synthesized compounds, which was higher activity than observed for the positive control UA.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10600-022-03821-8</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-3130 |
ispartof | Chemistry of natural compounds, 2022-09, Vol.58 (5), p.882-887 |
issn | 0009-3130 1573-8388 |
language | eng |
recordid | cdi_proquest_journals_2719458826 |
source | Springer Nature |
subjects | Biological activity Chemistry Chemistry and Materials Science Chemistry/Food Science Hypoxia Organic Chemistry Plant Sciences Synthesis Triazoles |
title | Screening of Ursolic Acid Analogs with HIF-1α and COX-2-Inhibiting Effects |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T21%3A57%3A07IST&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=Screening%20of%20Ursolic%20Acid%20Analogs%20with%20HIF-1%CE%B1%20and%20COX-2-Inhibiting%20Effects&rft.jtitle=Chemistry%20of%20natural%20compounds&rft.au=Li,%20Chunshi&rft.date=2022-09-01&rft.volume=58&rft.issue=5&rft.spage=882&rft.epage=887&rft.pages=882-887&rft.issn=0009-3130&rft.eissn=1573-8388&rft_id=info:doi/10.1007/s10600-022-03821-8&rft_dat=%3Cproquest_cross%3E2719458826%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c319t-adcc315692ebe5ff0b2ed0eeca071bf062b3e347e016287385bc55a8e0c7c52a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2719458826&rft_id=info:pmid/&rfr_iscdi=true |