Category: Investigación Cs Qs

Investigadores de Ciencias Químicas (UCC-CONICET) logran mejorar la formulación de los insecticidas naturales

By , 12/06/2019 17:51

Investigadores del CONICET y de la Universidad Católica de Córdoba descubrieron que una proporción adecuada de compuestos vegetales puede potenciar su capacidad para eliminar insectos que son plaga.

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Invitación a Conferencias – Facultad de Ciencias Químicas

By , 24/10/2017 16:32

Conferencias:

  • Targeting drug resistance in cancer stem cells – Hedgehog pathway inhibitors – Taepeenin D.

  • Abietane diterpenes – high value natural precursors for the development of new antimicrobial agents.

Disertante:

Dr. Constantinos Athanassopoulos de la Universidad de Patras, Grecia. 

Fecha y horario:

Martes 31 de octubre a las 10 hs.

Lugar:

Aula de Postgrado B,  Edificio de Ciencias Políticas, Campus UCC

Resúmenes:

  • Targeting drug resistance in cancer stem cells – Hedgehog pathway inhibitors – Taepeenin D

Cancer stem cells (CSCs) are a subpopulation of cancer cells with high clonogenic capacity and ability to reform parental tumors upon transplantation. Several types of CSCs have shown resistance to chemotherapy and therefore they have been “accused” for causing tumor relapse. In the last decade many efforts have been made to design molecules, able to specifically target CSCs and to differentiate them or sensitize them to therapy. Among the different potential targets a special attention has been payed to the “Hedgehog pathway (Hh)”, which has emerged as a favourable target to address drug resistance in CSCs. Up to now a variety of natural, natural-derived (e.g. Cyclopamine) and synthetic origin molecules (e.g. Sonidegib, Vismodegib) have shown Hh inhibitory activity. Inhibitors of Gli1, the terminal effector of the pathway, are anticipated to evade drug resistance and to display fewer side effects than inhibitors targeting Smothened protein (Smo). Inspired by the Gli-mediated transcription inhibitor Taepeenin D we performed synthesis and evaluation of a series of analogues, which has led to key structure–activity relationships for this natural product. The information derived from this research will be discussed in the lecture.

 

  • Abietane diterpenes – high value natural precursors for the development of new antimicrobial agents

Abietanes are a family of naturally occurring diterpenoids with a highly diverse repertoire of associated bioactivities. They have generated significant interest from the medicinal and pharmacological communities since they exhibit anticancer, antiviral, antifungal and antibacterial activity. Especially the latter is potentially valuable in the battle against the antimicrobial resistance and imminent antibiotic shortage. Recent results of Prof. Carpinella’s group demonstrated that an extract from Lepechinia meyenii exhibited an outstanding selectivity against a panel of  methicillin-resistant Staphylococcus aureus (MRSA) strains. Bioguided fractionation led to the isolation of carnosol and rosmanol as its active principles. Prompted from these results and aiming at the development of new and more effective antimicrobial agents we synthesised a library of abietane analogues, using carnosic and abietic acid as the natural precursors, suitable for structure-activity relationship studies (SARS). Two promising compounds with MIC values against multi-resistant bacteria lower than that observed for the lead compounds, were identified from the abietic acid derivatives. Very interesting results regarding the structural elements responsible for the activity improvement were obtained. A second generation of derivatives, as well as, the evaluation of the carnosic acid derivatives are in progress. The results obtained will be discussed in detail.

Seminarios Externos Facultad de Ciencias Químicas

By , 19/09/2016 21:04

Mañana martes 20 de Septiembre tendremos como invitada a la Dra. Belkys Maletto, a las 12 hs en el Aula Común 2.

El Tema del Seminario Externo es: “Vacuna nanoformulada con un cristal líquido: nuestra experiencia“.
La Dra.  Maletto es Bioquimica y Farmaceutica, Doctora en Bioquimica de la FCQ de la UNC, y Profesora Adjunta en el CIBICI de la FCQ-UNC.
Los esperamos!