Morita–Baylis–Hillman adducts: Biological activities and potentialities to the discovery of new cheaper drugs
This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new green efficient drugs. This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new...
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Veröffentlicht in: | Bioorganic & medicinal chemistry 2012-07, Vol.20 (13), p.3954-3971 |
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description | This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new green efficient drugs.
This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new cheaper and efficient drugs. Now, most these compounds can be prepared fast and on a single synthetic step (one-pot reaction) in high yields and using ecofriendly synthetic protocols. We highlight here the aromatic MBHA, which have shown diverse biological activities as anti-Leishmania chagasi and Leishmania amazonensis (parasites that cause cutaneous and visceral leishmaniasis), anti-Trypanosoma cruzi (parasite that cause Chagas disease), anti-Plasmodium falciparum and Plasmodium berghei (parasites that cause malaria), lethal against Biomphalaria glabrata (the snail transmitter of schistosomiasis), antibacterial, antifungal, herbicide and actives against some human tumor cell lines. Understanding of the biological mechanisms of action of this new class of molecules is still in the infancy stage. However, we report here which has been described to date on the possibilities of biological mechanisms of action, and we present new analyzes based on literature in this area. The academic and industrial interest in selecting green and cheaper experiments to the drugs development has been the prime mover of the growth on the subject. |
doi_str_mv | 10.1016/j.bmc.2012.04.061 |
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This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new cheaper and efficient drugs. Now, most these compounds can be prepared fast and on a single synthetic step (one-pot reaction) in high yields and using ecofriendly synthetic protocols. We highlight here the aromatic MBHA, which have shown diverse biological activities as anti-Leishmania chagasi and Leishmania amazonensis (parasites that cause cutaneous and visceral leishmaniasis), anti-Trypanosoma cruzi (parasite that cause Chagas disease), anti-Plasmodium falciparum and Plasmodium berghei (parasites that cause malaria), lethal against Biomphalaria glabrata (the snail transmitter of schistosomiasis), antibacterial, antifungal, herbicide and actives against some human tumor cell lines. Understanding of the biological mechanisms of action of this new class of molecules is still in the infancy stage. However, we report here which has been described to date on the possibilities of biological mechanisms of action, and we present new analyzes based on literature in this area. The academic and industrial interest in selecting green and cheaper experiments to the drugs development has been the prime mover of the growth on the subject.</description><identifier>ISSN: 0968-0896</identifier><identifier>EISSN: 1464-3391</identifier><identifier>DOI: 10.1016/j.bmc.2012.04.061</identifier><identifier>PMID: 22632793</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Animals ; Antibiotics ; Antiparasitic Agents - chemical synthesis ; Antiparasitic Agents - chemistry ; Antiparasitic Agents - economics ; Antiparasitic Agents - pharmacology ; bioactive properties ; Biological activities ; Biological and medical sciences ; Biomphalaria glabrata ; Cancer ; Chagas disease ; drugs ; Green Chemistry Technology ; Herbicides ; Humans ; Leishmania - drug effects ; Leishmania amazonensis ; Leishmania donovani ; malaria ; mechanism of action ; Medical sciences ; Morita–Baylis–Hillman adducts ; Negligenced disease ; parasites ; Pharmacology. Drug treatments ; Plasmodium berghei ; Plasmodium falciparum ; Plasmodium falciparum - drug effects ; schistosomiasis ; snails ; Structure-Activity Relationship ; Trypanosoma cruzi - drug effects ; visceral leishmaniasis</subject><ispartof>Bioorganic & medicinal chemistry, 2012-07, Vol.20 (13), p.3954-3971</ispartof><rights>2012 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-5f33a8b7dcd5ac8d2e5015d6ffdf72acecbd99a332060fe91b81cdb7bf2720da3</citedby><cites>FETCH-LOGICAL-c473t-5f33a8b7dcd5ac8d2e5015d6ffdf72acecbd99a332060fe91b81cdb7bf2720da3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0968089612003586$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26079222$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22632793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lima–Junior, Claudio G.</creatorcontrib><creatorcontrib>Vasconcellos, Mário L.A.A.</creatorcontrib><title>Morita–Baylis–Hillman adducts: Biological activities and potentialities to the discovery of new cheaper drugs</title><title>Bioorganic & medicinal chemistry</title><addtitle>Bioorg Med Chem</addtitle><description>This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new green efficient drugs.
This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new cheaper and efficient drugs. Now, most these compounds can be prepared fast and on a single synthetic step (one-pot reaction) in high yields and using ecofriendly synthetic protocols. We highlight here the aromatic MBHA, which have shown diverse biological activities as anti-Leishmania chagasi and Leishmania amazonensis (parasites that cause cutaneous and visceral leishmaniasis), anti-Trypanosoma cruzi (parasite that cause Chagas disease), anti-Plasmodium falciparum and Plasmodium berghei (parasites that cause malaria), lethal against Biomphalaria glabrata (the snail transmitter of schistosomiasis), antibacterial, antifungal, herbicide and actives against some human tumor cell lines. Understanding of the biological mechanisms of action of this new class of molecules is still in the infancy stage. However, we report here which has been described to date on the possibilities of biological mechanisms of action, and we present new analyzes based on literature in this area. The academic and industrial interest in selecting green and cheaper experiments to the drugs development has been the prime mover of the growth on the subject.</description><subject>Animals</subject><subject>Antibiotics</subject><subject>Antiparasitic Agents - chemical synthesis</subject><subject>Antiparasitic Agents - chemistry</subject><subject>Antiparasitic Agents - economics</subject><subject>Antiparasitic Agents - pharmacology</subject><subject>bioactive properties</subject><subject>Biological activities</subject><subject>Biological and medical sciences</subject><subject>Biomphalaria glabrata</subject><subject>Cancer</subject><subject>Chagas disease</subject><subject>drugs</subject><subject>Green Chemistry Technology</subject><subject>Herbicides</subject><subject>Humans</subject><subject>Leishmania - drug effects</subject><subject>Leishmania amazonensis</subject><subject>Leishmania donovani</subject><subject>malaria</subject><subject>mechanism of action</subject><subject>Medical sciences</subject><subject>Morita–Baylis–Hillman adducts</subject><subject>Negligenced disease</subject><subject>parasites</subject><subject>Pharmacology. Drug treatments</subject><subject>Plasmodium berghei</subject><subject>Plasmodium falciparum</subject><subject>Plasmodium falciparum - drug effects</subject><subject>schistosomiasis</subject><subject>snails</subject><subject>Structure-Activity Relationship</subject><subject>Trypanosoma cruzi - drug effects</subject><subject>visceral leishmaniasis</subject><issn>0968-0896</issn><issn>1464-3391</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1uEzEQgFcIRNPCA3ABX5B6yTK295eeaAUUqYgD9GzN2uPU0Wad2k5QbrwDb8iT4GoD3JBGmtHomx99RfGCQ8mBN2_W5bDRpQAuSqhKaPijYsGrplpK2fPHxQL6pltC1zcnxWmMawAQVc-fFidCNFK0vVwU9599cAl__fh5iYfRxVxcu3Hc4MTQmJ1O8S27dH70K6dxZKiT27vkKDKcDNv6RFNyOM6t5Fm6I2Zc1H5P4cC8ZRN9Z_qOcEuBmbBbxWfFE4tjpOfHfFbcfnj_7ep6efPl46erdzdLXbUyLWsrJXZDa7SpUXdGUA28No21xrYCNenB9D1KKaABSz0fOq7N0A5WtAIMyrPifN67Df5-RzGpTf6LxhEn8ruoOAjoZJUjo3xGdfAxBrJqG9wGwyFD6sG0WqtsWj2YVlCpbDrPvDyu3w0bMn8n_qjNwOsjgDGrswEn7eI_roG2F0Jk7tXMWfQKVyEzt1_zpRqAc5B1l4mLmaCsa-8oqKgdTZqMC6STMt7959HflcypDw</recordid><startdate>20120701</startdate><enddate>20120701</enddate><creator>Lima–Junior, Claudio G.</creator><creator>Vasconcellos, Mário L.A.A.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120701</creationdate><title>Morita–Baylis–Hillman adducts: Biological activities and potentialities to the discovery of new cheaper drugs</title><author>Lima–Junior, Claudio G. ; Vasconcellos, Mário L.A.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-5f33a8b7dcd5ac8d2e5015d6ffdf72acecbd99a332060fe91b81cdb7bf2720da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Antibiotics</topic><topic>Antiparasitic Agents - chemical synthesis</topic><topic>Antiparasitic Agents - chemistry</topic><topic>Antiparasitic Agents - economics</topic><topic>Antiparasitic Agents - pharmacology</topic><topic>bioactive properties</topic><topic>Biological activities</topic><topic>Biological and medical sciences</topic><topic>Biomphalaria glabrata</topic><topic>Cancer</topic><topic>Chagas disease</topic><topic>drugs</topic><topic>Green Chemistry Technology</topic><topic>Herbicides</topic><topic>Humans</topic><topic>Leishmania - drug effects</topic><topic>Leishmania amazonensis</topic><topic>Leishmania donovani</topic><topic>malaria</topic><topic>mechanism of action</topic><topic>Medical sciences</topic><topic>Morita–Baylis–Hillman adducts</topic><topic>Negligenced disease</topic><topic>parasites</topic><topic>Pharmacology. Drug treatments</topic><topic>Plasmodium berghei</topic><topic>Plasmodium falciparum</topic><topic>Plasmodium falciparum - drug effects</topic><topic>schistosomiasis</topic><topic>snails</topic><topic>Structure-Activity Relationship</topic><topic>Trypanosoma cruzi - drug effects</topic><topic>visceral leishmaniasis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lima–Junior, Claudio G.</creatorcontrib><creatorcontrib>Vasconcellos, Mário L.A.A.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic & medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lima–Junior, Claudio G.</au><au>Vasconcellos, Mário L.A.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morita–Baylis–Hillman adducts: Biological activities and potentialities to the discovery of new cheaper drugs</atitle><jtitle>Bioorganic & medicinal chemistry</jtitle><addtitle>Bioorg Med Chem</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>20</volume><issue>13</issue><spage>3954</spage><epage>3971</epage><pages>3954-3971</pages><issn>0968-0896</issn><eissn>1464-3391</eissn><abstract>This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new green efficient drugs.
This review aims to present by the first time the Morita–Baylis–Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new cheaper and efficient drugs. Now, most these compounds can be prepared fast and on a single synthetic step (one-pot reaction) in high yields and using ecofriendly synthetic protocols. We highlight here the aromatic MBHA, which have shown diverse biological activities as anti-Leishmania chagasi and Leishmania amazonensis (parasites that cause cutaneous and visceral leishmaniasis), anti-Trypanosoma cruzi (parasite that cause Chagas disease), anti-Plasmodium falciparum and Plasmodium berghei (parasites that cause malaria), lethal against Biomphalaria glabrata (the snail transmitter of schistosomiasis), antibacterial, antifungal, herbicide and actives against some human tumor cell lines. Understanding of the biological mechanisms of action of this new class of molecules is still in the infancy stage. However, we report here which has been described to date on the possibilities of biological mechanisms of action, and we present new analyzes based on literature in this area. The academic and industrial interest in selecting green and cheaper experiments to the drugs development has been the prime mover of the growth on the subject.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>22632793</pmid><doi>10.1016/j.bmc.2012.04.061</doi><tpages>18</tpages></addata></record> |
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subjects | Animals Antibiotics Antiparasitic Agents - chemical synthesis Antiparasitic Agents - chemistry Antiparasitic Agents - economics Antiparasitic Agents - pharmacology bioactive properties Biological activities Biological and medical sciences Biomphalaria glabrata Cancer Chagas disease drugs Green Chemistry Technology Herbicides Humans Leishmania - drug effects Leishmania amazonensis Leishmania donovani malaria mechanism of action Medical sciences Morita–Baylis–Hillman adducts Negligenced disease parasites Pharmacology. Drug treatments Plasmodium berghei Plasmodium falciparum Plasmodium falciparum - drug effects schistosomiasis snails Structure-Activity Relationship Trypanosoma cruzi - drug effects visceral leishmaniasis |
title | Morita–Baylis–Hillman adducts: Biological activities and potentialities to the discovery of new cheaper drugs |
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