Loading…

Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds

Betulinic acid (BA) and its natural analogues betulin (BN), betulonic (BoA), and 23-hydroxybetulinic (HBA) acids are lupane-type pentacyclic triterpenoids. They are present in many plants and display important biological activities. This review focuses on the chemical transformations used to functio...

Full description

Saved in:
Bibliographic Details
Published in:Molecules (Basel, Switzerland) Switzerland), 2019-01, Vol.24 (2), p.355
Main Authors: Sousa, Joana L C, Freire, Carmen S R, Silvestre, Armando J D, Silva, Artur M S
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-c493t-81e56d47ce78721c3c9326219846cc41f426828a295fb3f8a7ee3dbbfc5603e43
cites cdi_FETCH-LOGICAL-c493t-81e56d47ce78721c3c9326219846cc41f426828a295fb3f8a7ee3dbbfc5603e43
container_end_page
container_issue 2
container_start_page 355
container_title Molecules (Basel, Switzerland)
container_volume 24
creator Sousa, Joana L C
Freire, Carmen S R
Silvestre, Armando J D
Silva, Artur M S
description Betulinic acid (BA) and its natural analogues betulin (BN), betulonic (BoA), and 23-hydroxybetulinic (HBA) acids are lupane-type pentacyclic triterpenoids. They are present in many plants and display important biological activities. This review focuses on the chemical transformations used to functionalize BA/BN/BoA/HBA in order to obtain new derivatives with improved biological activity, covering the period since 2013 to 2018. It is divided by the main chemical transformations reported in the literature, including amination, esterification, alkylation, sulfonation, copper(I)-catalyzed alkyne-azide cycloaddition, palladium-catalyzed cross-coupling, hydroxylation, and aldol condensation reactions. In addition, the synthesis of heterocycle-fused BA/HBA derivatives and polymer‒BA conjugates are also addressed. The new derivatives are mainly used as antitumor agents, but there are other biological applications such as antimalarial activity, drug delivery, bioimaging, among others.
doi_str_mv 10.3390/molecules24020355
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_faa5daf2106c41c98c7788c87c8b7881</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_faa5daf2106c41c98c7788c87c8b7881</doaj_id><sourcerecordid>2179418967</sourcerecordid><originalsourceid>FETCH-LOGICAL-c493t-81e56d47ce78721c3c9326219846cc41f426828a295fb3f8a7ee3dbbfc5603e43</originalsourceid><addsrcrecordid>eNplkktvEzEUhUcIREvhB7BBlth0E_D7wQIpDRQiVUWqYG05njupI884jD1BIH48TlOqFlY-ss_95Ht0muYlwW8YM_htnyL4KUKmHFPMhHjUHBNO8Yxhbh7f00fNs5w3GFPCiXjaHDEspeGKHje_r8DDUNAH2EFM277qjMKAyjWg82nwJaTBxfDL7QVKHTqDMsUwBI_mPrTIDS1a1pFLV6bRRTSv7rSeIL9Dc3SVpgKoJHQJP9BZSK7idoAWqd-maWjz8-ZJ52KGF7fnSfPt_OPXxefZxZdPy8X8Yua5YWWmCQjZcuVBaUWJZ94wKikxmkvvOek4lZpqR43oVqzTTgGwdrXqvJCYAWcnzfLAbZPb2O0Yejf-tMkFe3ORxrV1Ywk-gu2cE63rKMGykr3RXimtvVZer6oglfX-wNpOqx7afXh17wfQhy9DuLbrtLOSCYOlqoDTW8CYvtegiu1D9hCjGyBN2VKiDCfa3Fhf_2PdpGmsCVeX4AZzIoWsLnJw-THlPEJ39xmC7b4n9r-e1JlX97e4m_hbDPYH6L68Ow</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2549041656</pqid></control><display><type>article</type><title>Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central (Open access)</source><creator>Sousa, Joana L C ; Freire, Carmen S R ; Silvestre, Armando J D ; Silva, Artur M S</creator><creatorcontrib>Sousa, Joana L C ; Freire, Carmen S R ; Silvestre, Armando J D ; Silva, Artur M S</creatorcontrib><description>Betulinic acid (BA) and its natural analogues betulin (BN), betulonic (BoA), and 23-hydroxybetulinic (HBA) acids are lupane-type pentacyclic triterpenoids. They are present in many plants and display important biological activities. This review focuses on the chemical transformations used to functionalize BA/BN/BoA/HBA in order to obtain new derivatives with improved biological activity, covering the period since 2013 to 2018. It is divided by the main chemical transformations reported in the literature, including amination, esterification, alkylation, sulfonation, copper(I)-catalyzed alkyne-azide cycloaddition, palladium-catalyzed cross-coupling, hydroxylation, and aldol condensation reactions. In addition, the synthesis of heterocycle-fused BA/HBA derivatives and polymer‒BA conjugates are also addressed. The new derivatives are mainly used as antitumor agents, but there are other biological applications such as antimalarial activity, drug delivery, bioimaging, among others.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules24020355</identifier><identifier>PMID: 30669472</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>23-hydroxybetulinic acid ; Acids ; Aldehydes ; Alkylation ; Alkynes ; Amination ; Antimalarial activity ; Antimalarial agents ; betulin ; Betulinic acid ; betulonic acid ; Bioactive compounds ; Biological activity ; Cancer ; Chemical reactions ; Chloride ; Cross coupling ; Cycloaddition ; Cytotoxicity ; derivatization ; Drug delivery ; Drug resistance ; Esterification ; functionalization ; HIV ; Human immunodeficiency virus ; Hydroxylation ; Medical imaging ; Methods ; Palladium ; Pentacyclic triterpenoids ; Polymers ; Review ; Sulfonation ; synthesis ; triterpenes ; Triterpenoids</subject><ispartof>Molecules (Basel, Switzerland), 2019-01, Vol.24 (2), p.355</ispartof><rights>2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-81e56d47ce78721c3c9326219846cc41f426828a295fb3f8a7ee3dbbfc5603e43</citedby><cites>FETCH-LOGICAL-c493t-81e56d47ce78721c3c9326219846cc41f426828a295fb3f8a7ee3dbbfc5603e43</cites><orcidid>0000-0003-2861-8286</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2549041656/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2549041656?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30669472$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sousa, Joana L C</creatorcontrib><creatorcontrib>Freire, Carmen S R</creatorcontrib><creatorcontrib>Silvestre, Armando J D</creatorcontrib><creatorcontrib>Silva, Artur M S</creatorcontrib><title>Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>Betulinic acid (BA) and its natural analogues betulin (BN), betulonic (BoA), and 23-hydroxybetulinic (HBA) acids are lupane-type pentacyclic triterpenoids. They are present in many plants and display important biological activities. This review focuses on the chemical transformations used to functionalize BA/BN/BoA/HBA in order to obtain new derivatives with improved biological activity, covering the period since 2013 to 2018. It is divided by the main chemical transformations reported in the literature, including amination, esterification, alkylation, sulfonation, copper(I)-catalyzed alkyne-azide cycloaddition, palladium-catalyzed cross-coupling, hydroxylation, and aldol condensation reactions. In addition, the synthesis of heterocycle-fused BA/HBA derivatives and polymer‒BA conjugates are also addressed. The new derivatives are mainly used as antitumor agents, but there are other biological applications such as antimalarial activity, drug delivery, bioimaging, among others.</description><subject>23-hydroxybetulinic acid</subject><subject>Acids</subject><subject>Aldehydes</subject><subject>Alkylation</subject><subject>Alkynes</subject><subject>Amination</subject><subject>Antimalarial activity</subject><subject>Antimalarial agents</subject><subject>betulin</subject><subject>Betulinic acid</subject><subject>betulonic acid</subject><subject>Bioactive compounds</subject><subject>Biological activity</subject><subject>Cancer</subject><subject>Chemical reactions</subject><subject>Chloride</subject><subject>Cross coupling</subject><subject>Cycloaddition</subject><subject>Cytotoxicity</subject><subject>derivatization</subject><subject>Drug delivery</subject><subject>Drug resistance</subject><subject>Esterification</subject><subject>functionalization</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Hydroxylation</subject><subject>Medical imaging</subject><subject>Methods</subject><subject>Palladium</subject><subject>Pentacyclic triterpenoids</subject><subject>Polymers</subject><subject>Review</subject><subject>Sulfonation</subject><subject>synthesis</subject><subject>triterpenes</subject><subject>Triterpenoids</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkktvEzEUhUcIREvhB7BBlth0E_D7wQIpDRQiVUWqYG05njupI884jD1BIH48TlOqFlY-ss_95Ht0muYlwW8YM_htnyL4KUKmHFPMhHjUHBNO8Yxhbh7f00fNs5w3GFPCiXjaHDEspeGKHje_r8DDUNAH2EFM277qjMKAyjWg82nwJaTBxfDL7QVKHTqDMsUwBI_mPrTIDS1a1pFLV6bRRTSv7rSeIL9Dc3SVpgKoJHQJP9BZSK7idoAWqd-maWjz8-ZJ52KGF7fnSfPt_OPXxefZxZdPy8X8Yua5YWWmCQjZcuVBaUWJZ94wKikxmkvvOek4lZpqR43oVqzTTgGwdrXqvJCYAWcnzfLAbZPb2O0Yejf-tMkFe3ORxrV1Ywk-gu2cE63rKMGykr3RXimtvVZer6oglfX-wNpOqx7afXh17wfQhy9DuLbrtLOSCYOlqoDTW8CYvtegiu1D9hCjGyBN2VKiDCfa3Fhf_2PdpGmsCVeX4AZzIoWsLnJw-THlPEJ39xmC7b4n9r-e1JlX97e4m_hbDPYH6L68Ow</recordid><startdate>20190119</startdate><enddate>20190119</enddate><creator>Sousa, Joana L C</creator><creator>Freire, Carmen S R</creator><creator>Silvestre, Armando J D</creator><creator>Silva, Artur M S</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-2861-8286</orcidid></search><sort><creationdate>20190119</creationdate><title>Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds</title><author>Sousa, Joana L C ; Freire, Carmen S R ; Silvestre, Armando J D ; Silva, Artur M S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-81e56d47ce78721c3c9326219846cc41f426828a295fb3f8a7ee3dbbfc5603e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>23-hydroxybetulinic acid</topic><topic>Acids</topic><topic>Aldehydes</topic><topic>Alkylation</topic><topic>Alkynes</topic><topic>Amination</topic><topic>Antimalarial activity</topic><topic>Antimalarial agents</topic><topic>betulin</topic><topic>Betulinic acid</topic><topic>betulonic acid</topic><topic>Bioactive compounds</topic><topic>Biological activity</topic><topic>Cancer</topic><topic>Chemical reactions</topic><topic>Chloride</topic><topic>Cross coupling</topic><topic>Cycloaddition</topic><topic>Cytotoxicity</topic><topic>derivatization</topic><topic>Drug delivery</topic><topic>Drug resistance</topic><topic>Esterification</topic><topic>functionalization</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Hydroxylation</topic><topic>Medical imaging</topic><topic>Methods</topic><topic>Palladium</topic><topic>Pentacyclic triterpenoids</topic><topic>Polymers</topic><topic>Review</topic><topic>Sulfonation</topic><topic>synthesis</topic><topic>triterpenes</topic><topic>Triterpenoids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sousa, Joana L C</creatorcontrib><creatorcontrib>Freire, Carmen S R</creatorcontrib><creatorcontrib>Silvestre, Armando J D</creatorcontrib><creatorcontrib>Silva, Artur M S</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sousa, Joana L C</au><au>Freire, Carmen S R</au><au>Silvestre, Armando J D</au><au>Silva, Artur M S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2019-01-19</date><risdate>2019</risdate><volume>24</volume><issue>2</issue><spage>355</spage><pages>355-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>Betulinic acid (BA) and its natural analogues betulin (BN), betulonic (BoA), and 23-hydroxybetulinic (HBA) acids are lupane-type pentacyclic triterpenoids. They are present in many plants and display important biological activities. This review focuses on the chemical transformations used to functionalize BA/BN/BoA/HBA in order to obtain new derivatives with improved biological activity, covering the period since 2013 to 2018. It is divided by the main chemical transformations reported in the literature, including amination, esterification, alkylation, sulfonation, copper(I)-catalyzed alkyne-azide cycloaddition, palladium-catalyzed cross-coupling, hydroxylation, and aldol condensation reactions. In addition, the synthesis of heterocycle-fused BA/HBA derivatives and polymer‒BA conjugates are also addressed. The new derivatives are mainly used as antitumor agents, but there are other biological applications such as antimalarial activity, drug delivery, bioimaging, among others.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>30669472</pmid><doi>10.3390/molecules24020355</doi><orcidid>https://orcid.org/0000-0003-2861-8286</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1420-3049
ispartof Molecules (Basel, Switzerland), 2019-01, Vol.24 (2), p.355
issn 1420-3049
1420-3049
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_faa5daf2106c41c98c7788c87c8b7881
source Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central (Open access)
subjects 23-hydroxybetulinic acid
Acids
Aldehydes
Alkylation
Alkynes
Amination
Antimalarial activity
Antimalarial agents
betulin
Betulinic acid
betulonic acid
Bioactive compounds
Biological activity
Cancer
Chemical reactions
Chloride
Cross coupling
Cycloaddition
Cytotoxicity
derivatization
Drug delivery
Drug resistance
Esterification
functionalization
HIV
Human immunodeficiency virus
Hydroxylation
Medical imaging
Methods
Palladium
Pentacyclic triterpenoids
Polymers
Review
Sulfonation
synthesis
triterpenes
Triterpenoids
title Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T13%3A35%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Recent%20Developments%20in%20the%20Functionalization%20of%20Betulinic%20Acid%20and%20Its%20Natural%20Analogues:%20A%20Route%20to%20New%20Bioactive%20Compounds&rft.jtitle=Molecules%20(Basel,%20Switzerland)&rft.au=Sousa,%20Joana%20L%20C&rft.date=2019-01-19&rft.volume=24&rft.issue=2&rft.spage=355&rft.pages=355-&rft.issn=1420-3049&rft.eissn=1420-3049&rft_id=info:doi/10.3390/molecules24020355&rft_dat=%3Cproquest_doaj_%3E2179418967%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c493t-81e56d47ce78721c3c9326219846cc41f426828a295fb3f8a7ee3dbbfc5603e43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2549041656&rft_id=info:pmid/30669472&rfr_iscdi=true