Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity
Resumen:
During previous studies, we have developed several hybrid compounds combining tetrahydropyrans with oxa and thiazols. These compounds exhibited interesting selective antiproliferative activity against a set of human tumour cell lines. As part of our process to produce new compounds with better activity, we decided to simplify the structures and substitute the building block less active (oxazole). Therefore, we used the on-line software LLAMA (Lead-Likeness And Molecular Analysis) to generate a library of compounds and theoretically evaluate their properties to be a potential lead compound. LLAMA software generates new compounds adding different “decorations” into a base structure. After comparing some of the compounds with anticancer products from the literature, we proposed a new series of hybrid compounds to be prepared, combining tetrahydropyrans wit different aromatic rings and N-heterocycles.
2023 | |
Agencia Nacional de Investigación e Innovación Alexander von Humboldt Foundation |
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Hybrids Tetrahydropyran Antiproliferative Ciencias Naturales y Exactas Ciencias Químicas Química Orgánica |
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Inglés | |
Agencia Nacional de Investigación e Innovación | |
REDI | |
https://hdl.handle.net/20.500.12381/3362
https://brazmedchem.org/2023/ |
|
Acceso abierto | |
Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND) |
_version_ | 1814959253053505536 |
---|---|
author | Quintana, Vanesa |
author2 | Padrón, Juan Ignacio Martín, Víctor Sotero Padrón, José Manuel Davyt, Danilo Valdomir, Guillermo |
author2_role | author author author author author |
author_facet | Quintana, Vanesa Padrón, Juan Ignacio Martín, Víctor Sotero Padrón, José Manuel Davyt, Danilo Valdomir, Guillermo |
author_role | author |
bitstream.checksum.fl_str_mv | a4ce09f01b5dd771727aa05c73851623 44588a01af9fd821c5a5361ea0b7e759 |
bitstream.checksumAlgorithm.fl_str_mv | MD5 MD5 |
bitstream.url.fl_str_mv | https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3362/2/license.txt https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3362/1/Brazmed_Application_G.Valdomir.docx |
collection | REDI |
dc.creator.none.fl_str_mv | Quintana, Vanesa Padrón, Juan Ignacio Martín, Víctor Sotero Padrón, José Manuel Davyt, Danilo Valdomir, Guillermo |
dc.date.accessioned.none.fl_str_mv | 2023-12-22T18:52:48Z |
dc.date.available.none.fl_str_mv | 2023-12-22T18:52:48Z |
dc.date.issued.none.fl_str_mv | 2023-10-28 |
dc.description.abstract.none.fl_txt_mv | During previous studies, we have developed several hybrid compounds combining tetrahydropyrans with oxa and thiazols. These compounds exhibited interesting selective antiproliferative activity against a set of human tumour cell lines. As part of our process to produce new compounds with better activity, we decided to simplify the structures and substitute the building block less active (oxazole). Therefore, we used the on-line software LLAMA (Lead-Likeness And Molecular Analysis) to generate a library of compounds and theoretically evaluate their properties to be a potential lead compound. LLAMA software generates new compounds adding different “decorations” into a base structure. After comparing some of the compounds with anticancer products from the literature, we proposed a new series of hybrid compounds to be prepared, combining tetrahydropyrans wit different aromatic rings and N-heterocycles. |
dc.description.sponsorship.none.fl_txt_mv | Agencia Nacional de Investigación e Innovación Alexander von Humboldt Foundation |
dc.identifier.anii.es.fl_str_mv | FCE_3_2020_1_162136 |
dc.identifier.uri.none.fl_str_mv | https://hdl.handle.net/20.500.12381/3362 |
dc.identifier.url.none.fl_str_mv | https://brazmedchem.org/2023/ |
dc.language.iso.none.fl_str_mv | eng |
dc.relation.uri.none.fl_str_mv | https://hdl.handle.net/20.500.12381/3363 https://hdl.handle.net/20.500.12381/3364 |
dc.rights.*.fl_str_mv | Acceso abierto |
dc.rights.license.none.fl_str_mv | Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND) |
dc.rights.none.fl_str_mv | info:eu-repo/semantics/openAccess |
dc.source.es.fl_str_mv | BrazMedChem 2023 |
dc.source.none.fl_str_mv | reponame:REDI instname:Agencia Nacional de Investigación e Innovación instacron:Agencia Nacional de Investigación e Innovación |
dc.subject.anii.none.fl_str_mv | Ciencias Naturales y Exactas Ciencias Químicas Química Orgánica |
dc.subject.es.fl_str_mv | Hybrids Tetrahydropyran Antiproliferative |
dc.title.none.fl_str_mv | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity |
dc.type.es.fl_str_mv | Documento de conferencia |
dc.type.none.fl_str_mv | info:eu-repo/semantics/conferenceObject |
dc.type.version.es.fl_str_mv | Publicado |
dc.type.version.none.fl_str_mv | info:eu-repo/semantics/publishedVersion |
description | During previous studies, we have developed several hybrid compounds combining tetrahydropyrans with oxa and thiazols. These compounds exhibited interesting selective antiproliferative activity against a set of human tumour cell lines. As part of our process to produce new compounds with better activity, we decided to simplify the structures and substitute the building block less active (oxazole). Therefore, we used the on-line software LLAMA (Lead-Likeness And Molecular Analysis) to generate a library of compounds and theoretically evaluate their properties to be a potential lead compound. LLAMA software generates new compounds adding different “decorations” into a base structure. After comparing some of the compounds with anticancer products from the literature, we proposed a new series of hybrid compounds to be prepared, combining tetrahydropyrans wit different aromatic rings and N-heterocycles. |
eu_rights_str_mv | openAccess |
format | conferenceObject |
id | REDI_53f532cb93150b5a71cc45246f63edbf |
identifier_str_mv | FCE_3_2020_1_162136 |
instacron_str | Agencia Nacional de Investigación e Innovación |
institution | Agencia Nacional de Investigación e Innovación |
instname_str | Agencia Nacional de Investigación e Innovación |
language | eng |
network_acronym_str | REDI |
network_name_str | REDI |
oai_identifier_str | oai:redi.anii.org.uy:20.500.12381/3362 |
publishDate | 2023 |
reponame_str | REDI |
repository.mail.fl_str_mv | jmaldini@anii.org.uy |
repository.name.fl_str_mv | REDI - Agencia Nacional de Investigación e Innovación |
repository_id_str | 9421 |
rights_invalid_str_mv | Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND) Acceso abierto |
spelling | Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND)Acceso abiertoinfo:eu-repo/semantics/openAccess2023-12-22T18:52:48Z2023-12-22T18:52:48Z2023-10-28https://hdl.handle.net/20.500.12381/3362FCE_3_2020_1_162136https://brazmedchem.org/2023/During previous studies, we have developed several hybrid compounds combining tetrahydropyrans with oxa and thiazols. These compounds exhibited interesting selective antiproliferative activity against a set of human tumour cell lines. As part of our process to produce new compounds with better activity, we decided to simplify the structures and substitute the building block less active (oxazole). Therefore, we used the on-line software LLAMA (Lead-Likeness And Molecular Analysis) to generate a library of compounds and theoretically evaluate their properties to be a potential lead compound. LLAMA software generates new compounds adding different “decorations” into a base structure. After comparing some of the compounds with anticancer products from the literature, we proposed a new series of hybrid compounds to be prepared, combining tetrahydropyrans wit different aromatic rings and N-heterocycles.Agencia Nacional de Investigación e InnovaciónAlexander von Humboldt Foundationenghttps://hdl.handle.net/20.500.12381/3363https://hdl.handle.net/20.500.12381/3364BrazMedChem 2023reponame:REDIinstname:Agencia Nacional de Investigación e Innovacióninstacron:Agencia Nacional de Investigación e InnovaciónHybridsTetrahydropyranAntiproliferativeCiencias Naturales y ExactasCiencias QuímicasQuímica OrgánicaSynthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative ActivityDocumento de conferenciaPublicadoinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectUniversidad de la República. Facultad de QuímicaUniversidad de La Laguna. IUBO-AG//Ciencias Naturales y Exactas/Ciencias Químicas/Química OrgánicaQuintana, VanesaPadrón, Juan IgnacioMartín, Víctor SoteroPadrón, José ManuelDavyt, DaniloValdomir, GuillermoLICENSElicense.txtlicense.txttext/plain; charset=utf-84967https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3362/2/license.txta4ce09f01b5dd771727aa05c73851623MD52ORIGINALBrazmed_Application_G.Valdomir.docxBrazmed_Application_G.Valdomir.docxapplication/vnd.openxmlformats-officedocument.wordprocessingml.document334125https://redi.anii.org.uy/jspui/bitstream/20.500.12381/3362/1/Brazmed_Application_G.Valdomir.docx44588a01af9fd821c5a5361ea0b7e759MD5120.500.12381/33622024-01-10 14:10:47.182oai:redi.anii.org.uy:20.500.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Gobiernohttps://www.anii.org.uy/https://redi.anii.org.uy/oai/requestjmaldini@anii.org.uyUruguayopendoar:94212024-01-10T17:10:47REDI - Agencia Nacional de Investigación e Innovaciónfalse |
spellingShingle | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity Quintana, Vanesa Hybrids Tetrahydropyran Antiproliferative Ciencias Naturales y Exactas Ciencias Químicas Química Orgánica |
status_str | publishedVersion |
title | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity |
title_full | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity |
title_fullStr | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity |
title_full_unstemmed | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity |
title_short | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity |
title_sort | Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity |
topic | Hybrids Tetrahydropyran Antiproliferative Ciencias Naturales y Exactas Ciencias Químicas Química Orgánica |
url | https://hdl.handle.net/20.500.12381/3362 https://brazmedchem.org/2023/ |