Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]

The following are available online, spectral and analytical data for hybrid compounds.. NMR spectroscopic and mass-spectrometric data NMR and Mass Spectra: Figure S1: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 3 Figure S2: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 3 Figure S3: HRESI-MS Spectru...

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Detalles Bibliográficos
Autores: Estévez, Francisco, Saavedra, Ester, Brouard, Ignacio, Peyrac, Jesús, Hernández-Garcés, Judith, García, Celina, Quintana, José
Tipo de recurso: conjunto de datos
Estado:Versión publicada
Fecha de publicación:2022
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/311022
Acceso en línea:http://hdl.handle.net/10261/311022
Access Level:acceso abierto
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spelling Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]Estévez, FranciscoSaavedra, EsterBrouard, IgnacioPeyrac, JesúsHernández-Garcés, JudithGarcía, CelinaQuintana, JoséEstévez, FranciscoThe following are available online, spectral and analytical data for hybrid compounds.. NMR spectroscopic and mass-spectrometric data NMR and Mass Spectra: Figure S1: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 3 Figure S2: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 3 Figure S3: HRESI-MS Spectrum of Compound 3 Figure S4: ESI-MS Spectrum of Compound 3 Figure S5: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6a Figure S6: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6a Figure S7: HRESI-MS Spectrum of Compound 6a Figure S8: ESI-MS Spectrum of Compound 6a Figure S9: 1H -NMR (500 MHz, CDCl3) Spectrum of Compound 6b Figure S10: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6b Figure S11: HRESI-MS Spectrum of Compound 6b Figure S12: ESI-MS Spectrum of Compound 6b Figure S13: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6c Figure S14: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6c Figure S15: HRESI-MS Spectrum of Compound 6c Figure S16: ESI-MS Spectrum of Compound 6c 2 Figure S17: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6d Figure S18: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6d Figure S19: HRESI-MS Spectrum of Compound 6d Figure S20: ESI-MS Spectrum of Compound 6d Figure S21: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6e Figure S22: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6e Figure S23: HRESI-MS Spectrum of Compound 6e Figure S24: ESI-MS Spectrum of Compound 6e Figure S25: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6f Figure S26: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6f Figure S27: HRESI-MS Spectrum of Compound 6f Figure S28: ESI-MS Spectrum of Compound 6f Figure S29: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6g Figure S30: 13C -NMR (125 MHz, CDCl3) Spectrum of Compound 6g Figure S31: HRESI-MS Spectrum of Compound 6g Figure S32: ESI-MS Spectrum of Compound 6g Figure S33: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6h Figure S34: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6h Figure S35: HRESI-MS Spectrum of Compound 6h Figure S36: ESI-MS Spectrum of Compound 6h Figure S37: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6i Figure S38: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6i Figure S39: HRESI-MS Spectrum of Compound 6i Figure S40: ESI-MS Spectrum of Compound 6i Figure S41: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6j Figure S42: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6j Figure S43: HRESI-MS Spectrum of Compound 6j Figure S44: ESI-MS Spectrum of Compound 6j Figure S45: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6k Figure S46: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6k Figure S47: HRESI-MS Spectrum of Compound 6k Figure S48: ESI-MS Spectrum of Compound 6kPeer reviewedMultidisciplinary Digital Publishing InstituteConsejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]202320232022info:eu-repo/semantics/datasethttp://purl.org/coar/resource_type/c_ddb1Publisher's versioninfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10261/311022reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)InglésEstévez, Francisco; Saavedra, Ester; Brouard, Ignacio; Peyrac, Jesús; Hernández-Garcés, Judith; García, Celina; Quintana, José; Estévez, Francisco. Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells. International Journal of Molecular Sciences 23(24): 15518 (2022). https://doi.org/10.3390/ijms232415518. http://hdl.handle.net/10261/296257https://doi.org/10.3390/ijms232415518Síinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/3110222026-05-22T06:33:51Z
dc.title.none.fl_str_mv Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
title Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
spellingShingle Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
Estévez, Francisco
title_short Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
title_full Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
title_fullStr Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
title_full_unstemmed Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
title_sort Supplementary files of the article: Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells [Dataset]
dc.creator.none.fl_str_mv Estévez, Francisco
Saavedra, Ester
Brouard, Ignacio
Peyrac, Jesús
Hernández-Garcés, Judith
García, Celina
Quintana, José
Estévez, Francisco
author Estévez, Francisco
author_facet Estévez, Francisco
Saavedra, Ester
Brouard, Ignacio
Peyrac, Jesús
Hernández-Garcés, Judith
García, Celina
Quintana, José
author_role author
author2 Saavedra, Ester
Brouard, Ignacio
Peyrac, Jesús
Hernández-Garcés, Judith
García, Celina
Quintana, José
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]
description The following are available online, spectral and analytical data for hybrid compounds.. NMR spectroscopic and mass-spectrometric data NMR and Mass Spectra: Figure S1: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 3 Figure S2: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 3 Figure S3: HRESI-MS Spectrum of Compound 3 Figure S4: ESI-MS Spectrum of Compound 3 Figure S5: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6a Figure S6: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6a Figure S7: HRESI-MS Spectrum of Compound 6a Figure S8: ESI-MS Spectrum of Compound 6a Figure S9: 1H -NMR (500 MHz, CDCl3) Spectrum of Compound 6b Figure S10: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6b Figure S11: HRESI-MS Spectrum of Compound 6b Figure S12: ESI-MS Spectrum of Compound 6b Figure S13: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6c Figure S14: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6c Figure S15: HRESI-MS Spectrum of Compound 6c Figure S16: ESI-MS Spectrum of Compound 6c 2 Figure S17: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6d Figure S18: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6d Figure S19: HRESI-MS Spectrum of Compound 6d Figure S20: ESI-MS Spectrum of Compound 6d Figure S21: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6e Figure S22: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6e Figure S23: HRESI-MS Spectrum of Compound 6e Figure S24: ESI-MS Spectrum of Compound 6e Figure S25: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6f Figure S26: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6f Figure S27: HRESI-MS Spectrum of Compound 6f Figure S28: ESI-MS Spectrum of Compound 6f Figure S29: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6g Figure S30: 13C -NMR (125 MHz, CDCl3) Spectrum of Compound 6g Figure S31: HRESI-MS Spectrum of Compound 6g Figure S32: ESI-MS Spectrum of Compound 6g Figure S33: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6h Figure S34: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6h Figure S35: HRESI-MS Spectrum of Compound 6h Figure S36: ESI-MS Spectrum of Compound 6h Figure S37: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6i Figure S38: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6i Figure S39: HRESI-MS Spectrum of Compound 6i Figure S40: ESI-MS Spectrum of Compound 6i Figure S41: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6j Figure S42: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6j Figure S43: HRESI-MS Spectrum of Compound 6j Figure S44: ESI-MS Spectrum of Compound 6j Figure S45: 1H-NMR (500 MHz, CDCl3) Spectrum of Compound 6k Figure S46: 13C-NMR (125 MHz, CDCl3) Spectrum of Compound 6k Figure S47: HRESI-MS Spectrum of Compound 6k Figure S48: ESI-MS Spectrum of Compound 6k
publishDate 2022
dc.date.none.fl_str_mv 2022
2023
2023
dc.type.none.fl_str_mv info:eu-repo/semantics/dataset
http://purl.org/coar/resource_type/c_ddb1
Publisher's version
info:eu-repo/semantics/publishedVersion
format dataset
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/10261/311022
url http://hdl.handle.net/10261/311022
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Estévez, Francisco; Saavedra, Ester; Brouard, Ignacio; Peyrac, Jesús; Hernández-Garcés, Judith; García, Celina; Quintana, José; Estévez, Francisco. Guanidine derivatives containing the chalcone skeleton are potent antiproliferative compounds against human leukemia cells. International Journal of Molecular Sciences 23(24): 15518 (2022). https://doi.org/10.3390/ijms232415518. http://hdl.handle.net/10261/296257
https://doi.org/10.3390/ijms232415518
Sí
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute
publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute
dc.source.none.fl_str_mv reponame:DIGITAL.CSIC. Repositorio Institucional del CSIC
instname:Consejo Superior de Investigaciones Científicas (CSIC)
instname_str Consejo Superior de Investigaciones Científicas (CSIC)
reponame_str DIGITAL.CSIC. Repositorio Institucional del CSIC
collection DIGITAL.CSIC. Repositorio Institucional del CSIC
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15.812455

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