0000000001310403

AUTHOR

Josefa Badia

showing 6 related works from this author

Luminescent Pt-II and Pt-IV Platinacycles with Anticancer Activity Against Multiplatinum-Resistant Metastatic CRC and CRPC Cell Models

2020

Platinum-based chemotherapy persists to be the only effective therapeutic option against a wide variety of tumours. Nevertheless, the acquisition of platinum resistance is utterly common, ultimately cornering conventional platinum drugs to only palliative in many patients. Thus, encountering alternatives that are both effective and non-cross-resistant is urgent. In this work, we report the synthesis, reduction studies, and luminescent properties of a series of cyclometallated (C,N,N')PtIV compounds derived from amine- imine ligands, and their remarkable efficacy at the high nanomolar range and complete lack of cross57 resistance, as an intrinsic property of the platinacycle, against multipl…

Colorectal cancermedicine.medical_treatment010402 general chemistry01 natural sciencesCatalysisProstate cancermedicineLung cancerCàncerPlatíPlatinumCancerCisplatinChemotherapybiology010405 organic chemistryChemistryPhosphorescenceTopoisomeraseOrganic ChemistryCancerGeneral Chemistrymedicine.disease0104 chemical sciencesCancer cellbiology.proteinCancer researchFosforescènciamedicine.drug
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Luminescent PtII and PtIV Platinacycles with Anticancer Activity Against Multiplatinum‐Resistant Metastatic CRC and CRPC Cell Models

2020

Abstract: Platinum‐based chemotherapy persists to be the only effective therapeutic option against a wide variety of tumours. Nevertheless, the acquisition of platinum resistance is utterly common, ultimately cornering conventional platinum drugs to only palliative in many patients. Thus, encountering alternatives that are both effective and non‐cross‐resistant is urgent. In this work, we report the synthesis, reduction studies and luminescent properties of a series of cyclometallated (C,N,N’) PtIV compounds derived from amine‐imine ligands, and their remarkable efficacy at the high nanomolar range and complete lack of cross‐resistance, as an intrinsic property of the platinacycle, against …

platinaluminesenssibiologinen aktiivisuuslääkehoitosyöpätauditresistenssi
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CCDC 1957891: Experimental Crystal Structure Determination

2020

Related Article: Ariadna Lázaro, Cristina Balcells, Josefina Quirante, Josefa Badia, Laura Baldomà, Jas S. Ward, Kari Rissanen, Mercè Font‐Bardia, Laura Rodríguez, Margarita Crespo, Marta Cascante|2020|Chem.-Eur.J.|26|1947|doi:10.1002/chem.201905325

Space GroupCrystallographyCrystal SystemCrystal Structurechloro-[2-({[2-(dimethylamino)ethyl]imino}methyl)-5-fluorophenyl]-platinumCell ParametersExperimental 3D Coordinates
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CCDC 1958053: Experimental Crystal Structure Determination

2020

Related Article: Ariadna Lázaro, Cristina Balcells, Josefina Quirante, Josefa Badia, Laura Baldomà, Jas S. Ward, Kari Rissanen, Mercè Font‐Bardia, Laura Rodríguez, Margarita Crespo, Marta Cascante|2020|Chem.-Eur.J.|26|1947|doi:10.1002/chem.201905325

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterstribromo-[2-({[2-(dimethylamino)ethyl]imino}methyl)-5-fluorophenyl]-platinumExperimental 3D Coordinates
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CCDC 1958051: Experimental Crystal Structure Determination

2020

Related Article: Ariadna Lázaro, Cristina Balcells, Josefina Quirante, Josefa Badia, Laura Baldomà, Jas S. Ward, Kari Rissanen, Mercè Font‐Bardia, Laura Rodríguez, Margarita Crespo, Marta Cascante|2020|Chem.-Eur.J.|26|1947|doi:10.1002/chem.201905325

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbromo-[2-({[2-(dimethylamino)ethyl]imino}methyl)-5-fluorophenyl]-platinumExperimental 3D Coordinates
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CCDC 1958052: Experimental Crystal Structure Determination

2020

Related Article: Ariadna Lázaro, Cristina Balcells, Josefina Quirante, Josefa Badia, Laura Baldomà, Jas S. Ward, Kari Rissanen, Mercè Font‐Bardia, Laura Rodríguez, Margarita Crespo, Marta Cascante|2020|Chem.-Eur.J.|26|1947|doi:10.1002/chem.201905325

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatestrichloro-[2-({[2-(dimethylamino)ethyl]imino}methyl)-5-fluorophenyl]-platinum
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