медицинска химия
154 проекта
FP7Реинтеграция2010–2014Гърция
COMPUT DRUG DESIGN · Targeting the mutated PI3Kα isoform for the development of novel anti-cancer agents
FP7Докторантска мрежа2009–2013Нидерландия
STARS · Scientific Training in Antimicrobial Research Strategies
7 партньори · 5 държави
FP7Индивидуална стипендия2009–2011Португалия
CYCLOTIDE MECHANISM · Elucidating the mechanism of action of cyclotides: ultra-stable proteins from plants
FP7Индивидуална стипендия2009–2010Швейцария
STOADA · Synthesis of Targeted Organometallic Anticancer Drugs and their mode of Action
FP7Обмен на изследователи2009–2013Португалия
PEP2BRAIN · Selected peptides as drug candidates directed to pain and neurodegeneration
5 партньори · 3 държави
FP7Реинтеграция2009–2013Испания
AR BF3 BINDERS · Identification of the protein binders of the androgen receptor BF3 pocket, an allosteric modulator of AF2 coactivator recruitment
FP7Обмен на изследователи2008–2012Гърция
TOPCRYST · Novel tools for crystallisation of macromolecules
3 партньори · 2 държави
FP6Индивидуална стипендия2007–2008Франция
MTDI-DNA · Molecular Theory of Drug Intercalation into DNA
FP6Индивидуална стипендия2007–2008Обединеното кралство
DRUG-DISCOVERY · Synthesis and screening of new small molecules with antibacterial activity: Discovery of novel biological targets
FP6Индивидуална стипендия2006–2008Германия
PHYTOPHARM · Phytochemical and Pharmacological Study of Plants Used in Traditional Medicine in Cameroon
FP6Индивидуална стипендия2006–2008Дания
MODELING PH-DEPENCE · Modelling pH-Dependence in rational drug design
FP6Индивидуална стипендия2006–2009Обединеното кралство
SPIROTENUIPESINES · Total Synthesis of the Potent Neurotrophic Factors Spirotenuipesine A and B
2 партньори · 2 държави
FP6Индивидуална стипендия2006–2008Обединеното кралство
P53MUT. REACTIVATORS · Computer-assisted drug discovery and biophysical characterisation of mutant re-activators of the transcription factor p53 as putative tumour therapeutics
FP6Реинтеграция2006–2008Литва
PLK1 INHIBITION · Inhibition of Cancer by Disrupting Interaction Between Polo-like Kinase 1 Polo-box Domain and Spindle Targets
FP6Докторантска мрежа2006–2010Франция
BIOMEDCHEM · Training for new approaches in anti-parasite and anti-tumour drug discovery
FP6Индивидуална стипендия2006–2010Обединеното кралство
MEDCHEM AT QUB/GSK · New methodologies to synthetise unnatural nucleosides, known and putative antiproliferative agents
FP6Индивидуална стипендия2005–2007Германия
COMBINE-ENGINEER · A software tool for molecular design using protein structure-based quantitative structure activity relationships
FP6Друго2005–2007Италия
PHARMAMAL · Investigation of the mechanism of action of antimalarial agents, by means of computational methods. Bases for the rational design of new antimalarial drugs
FP6Индивидуална стипендия2005–2007Обединеното кралство
POLYKETOMACROCYCLES · Transannular Macrocyclisation and the concise total synthesis of Antifungal natural products
FP6Докторантска мрежа2005–2009Италия
FOLDAMERS · Design, synthesis, Structural Characterization and biological evaluation of new peptidomimetics with a defined secondary structure
3 партньори · 3 държави
FP6Обмен на изследователи2004–2008Германия
SMARTSCREEN · Magnetic resonance in drug screening
4 партньори · 4 държави
FP6Обмен на изследователи2004–2008Франция
MET-CANCER THERAPY · Animal models and drug design for therapy of cancers induced by the oncogene, met
FP6Индивидуална стипендия2004–2008Дания
NAC-DRUG · Nucleic Acid Based Drug Design Training Center
FP6Индивидуална стипендия2004–2006Обединеното кралство