Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity

Bibliographic Details
Main Author: Durães, F
Publication Date: 2021
Other Authors: Silva, PMA, Novais, P, Amorim, I, Gales, L, Esteves, CIC, Guieu, S, Bousbaa, H, Pinto, M, Sousa, E
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10216/152526
Summary: Thioxanthones are bioisosteres of the naturally occurring xanthones. They have been described for multiple activities, including antitumor. As such, the synthesis of a library of thioxanthones was pursued, but unexpectedly, four tetracyclic thioxanthenes with a quinazoline– chromene scaffold were obtained. These compounds were studied for their human tumor cell growth inhibition activity, in the cell lines A375-C5, MCF-7 and NCI-H460. Photophysical studies were also performed. Two of the compounds displayed GI50 values below 10 µM for the three tested cell lines, and structure–activity relationship studies were established. Three compounds presented similar wavelengths of absorption and emission, characteristic of dyes with a push-pull character. The structures of two compounds were elucidated by X-ray crystallography. Two tetracyclic thioxanthenes emerged as hit compounds. One of the two compounds accumulated intracellularly as a bright fluorescent dye in the green channel, as analyzed by both fluorescence microscopy and flow cytometry, making it a promising theranostic cancer drug candidate.
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spelling Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activityAntitumor activityPhotophysicsTheranosticThioxanthenesThioxanthones are bioisosteres of the naturally occurring xanthones. They have been described for multiple activities, including antitumor. As such, the synthesis of a library of thioxanthones was pursued, but unexpectedly, four tetracyclic thioxanthenes with a quinazoline– chromene scaffold were obtained. These compounds were studied for their human tumor cell growth inhibition activity, in the cell lines A375-C5, MCF-7 and NCI-H460. Photophysical studies were also performed. Two of the compounds displayed GI50 values below 10 µM for the three tested cell lines, and structure–activity relationship studies were established. Three compounds presented similar wavelengths of absorption and emission, characteristic of dyes with a push-pull character. The structures of two compounds were elucidated by X-ray crystallography. Two tetracyclic thioxanthenes emerged as hit compounds. One of the two compounds accumulated intracellularly as a bright fluorescent dye in the green channel, as analyzed by both fluorescence microscopy and flow cytometry, making it a promising theranostic cancer drug candidate.MDPI20212021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/152526eng1420-304910.3390/molecules26113315Durães, FSilva, PMANovais, PAmorim, IGales, LEsteves, CICGuieu, SBousbaa, HPinto, MSousa, Einfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-27T19:22:04Zoai:repositorio-aberto.up.pt:10216/152526Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T23:16:07.283930Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
title Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
spellingShingle Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
Durães, F
Antitumor activity
Photophysics
Theranostic
Thioxanthenes
title_short Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
title_full Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
title_fullStr Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
title_full_unstemmed Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
title_sort Tetracyclic thioxanthene derivatives: Studies on fluorescence and antitumor activity
author Durães, F
author_facet Durães, F
Silva, PMA
Novais, P
Amorim, I
Gales, L
Esteves, CIC
Guieu, S
Bousbaa, H
Pinto, M
Sousa, E
author_role author
author2 Silva, PMA
Novais, P
Amorim, I
Gales, L
Esteves, CIC
Guieu, S
Bousbaa, H
Pinto, M
Sousa, E
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Durães, F
Silva, PMA
Novais, P
Amorim, I
Gales, L
Esteves, CIC
Guieu, S
Bousbaa, H
Pinto, M
Sousa, E
dc.subject.por.fl_str_mv Antitumor activity
Photophysics
Theranostic
Thioxanthenes
topic Antitumor activity
Photophysics
Theranostic
Thioxanthenes
description Thioxanthones are bioisosteres of the naturally occurring xanthones. They have been described for multiple activities, including antitumor. As such, the synthesis of a library of thioxanthones was pursued, but unexpectedly, four tetracyclic thioxanthenes with a quinazoline– chromene scaffold were obtained. These compounds were studied for their human tumor cell growth inhibition activity, in the cell lines A375-C5, MCF-7 and NCI-H460. Photophysical studies were also performed. Two of the compounds displayed GI50 values below 10 µM for the three tested cell lines, and structure–activity relationship studies were established. Three compounds presented similar wavelengths of absorption and emission, characteristic of dyes with a push-pull character. The structures of two compounds were elucidated by X-ray crystallography. Two tetracyclic thioxanthenes emerged as hit compounds. One of the two compounds accumulated intracellularly as a bright fluorescent dye in the green channel, as analyzed by both fluorescence microscopy and flow cytometry, making it a promising theranostic cancer drug candidate.
publishDate 2021
dc.date.none.fl_str_mv 2021
2021-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/10216/152526
url https://hdl.handle.net/10216/152526
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1420-3049
10.3390/molecules26113315
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reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
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