Synthesis of simplified Tetrahydropyran Hybrids with potential Antiproliferative Activity

Quintana, Vanesa - Padrón, Juan Ignacio - Martín, Víctor Sotero - Padrón, José Manuel - Davyt, Danilo - Valdomir, Guillermo

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.


Detalles Bibliográficos
2023
Agencia Nacional de Investigación e Innovación
Alexander von Humboldt Foundation
Hybrids
Tetrahydropyran
Antiproliferative
Ciencias Naturales y Exactas
Ciencias Químicas
Química Orgánica
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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- 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/