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
Descripción
Sumario: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

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