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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...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2019-01, Vol.24 (2), p.355 |
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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. |
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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/). 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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 & 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 & Medical Complete (Alumni)</collection><collection>Health & 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> |
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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 |
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