???global.info.a_carregar???
I started my scientific career deeply engaged with drug discovery and with the development of innovative synthetic strategies and procedures to obtain concise and diverse-orientated chemical libraries based on natural products. The obtained libraries were screened toward several biological targets to develop enzymatic inhibitors and ligands of adenosine receptors aiming the discovery and development of new drug candidates to address multifactorial diseases such as cancer and neurodegenerative diseases. In addition, when required, I have performed the antioxidant evaluation of diverse system. Over the years I have been genuinely engaged in acquiring and developing a vast number of skills in the field of medicinal chemistry, allowing me to be aware of the importance of its transdisciplinary research and of the tools that are involved in the daily routine of the multidisciplinary R&D projects and of the overall process inherent to drug discovery and development. Currently, My research is focused on the design and development of new antimicrobial drugs based on naturally-occurring privileged structures. In this context, I collaborate with LEPABE in the group of Prof. Manuel Simões, to improve my skills in the area, and I establish an international collaboration with CO-ADD (Community for Open Antimicrobial Drug Discovery). At present more than 50 compounds were screened against several antibacterial and antifungal strains.
Read full resume ↓
Identification

Personal identification

Full name
Alexandra Maria Neves Gaspar

Citation names

  • Gaspar, Alexandra

Author identifiers

Ciência ID
1A19-6480-E6F1
ORCID iD
0000-0002-3892-4124

Email addresses

  • alexandra.gaspar@fc.up.pt (Professional)

Addresses

  • CIQ. Rua Campo Alegre, 4169-007, Porto, Porto, Portugal (Professional)

Websites

Knowledge fields

  • Exact Sciences - Chemical Sciences
  • Medical and Health Sciences - Basic Medicine - Medicinal Chemistry

Languages

Language Speaking Reading Writing Listening Peer-review
Portuguese (Mother tongue)
English Upper intermediate (B2) Upper intermediate (B2) Upper intermediate (B2) Upper intermediate (B2) Upper intermediate (B2)
Education
Degree Classification
2009/03/01 - 2013/12/09
Concluded
 Química (Doutoramento)
Major in Química Medicinal
Universidade do Porto Faculdade de Ciências, Portugal
"Chromone as a privileged scaffold in medicinal chemistry" (THESIS/DISSERTATION)
 Aprovado com distinção
2004 - 2007
Concluded
 Controlo de Qualidade e Toxicologia dos Alimentos (Mestrado)
Universidade de Lisboa Faculdade de Farmácia, Portugal
 18
2004 - 2005
Concluded
 Controlo da Qualidade e Toxicologia dos Alimentos (Especialização pós-licenciatura)
Universidade de Lisboa Faculdade de Farmácia, Portugal
 17
1996 - 2002
Concluded
 Ciências Farmacêuticas (Licenciatura)
Universidade do Porto Faculdade de Farmácia, Portugal
 12
Affiliation

Science

Category
Host institution 		Employer
2019/01/15 - Current Contracted Researcher (Research) Universidade do Porto Faculdade de Ciências, Portugal
Universidade do Porto Centro de Investigação em Química, Portugal
2014/03/01 - 2019/01/14 Postdoc (Research) Fundação para a Ciência e a Tecnologia, Portugal
Universidade do Porto Centro de Investigação em Química, Portugal
2018/09/01 - 2018/11/30 Visiting Researcher (Research) Università degli Studi di Cagliari, Italy

Teaching in Higher Education

Category
Host institution 		Employer
2010/10/01 - 2011/02/28 Assistant (University Teacher) Cooperativa de Ensino Superior Politécnico e Universitário, Portugal
Cooperativa de Ensino Superior Politécnico e Universitário, Portugal
2007/10/09 - 2007/12/31 Assistant (Polytechnic Teacher) ETGI-AESBUC (Associação para a Escola Superior de Biotecnologia da Universidade Católica), Portugal

Others

Category
Host institution 		Employer
2019/09/01 - 2025/01/05 Colaboração à Docência Universidade do Porto Faculdade de Ciências, Portugal
Universidade do Porto Centro de Investigação em Química, Portugal
2017/04/02 - 2017/07/30 Investigador Visitante Universidade de Santiago de Compostela, Spain
Projects

Contract

Designation Funders
2018 - Current Development of centrally-active and safe catechol O-methyltransferase inhibitors
POCI-01-0145-FEDER-029164
Researcher
Associação para a Inovação e Desenvolvimento da FCT
2018 - Current Development of new antibiotics for aquaculture
POCI-01-0145-FEDER-028397
Researcher
Universidade do Porto Centro de Investigação em Química, Portugal
Ongoing
2016 - Current Sustainable advanced materials
NORTE-01-0145-FEDER-000028
Researcher
Universidade do Porto Centro de Investigação em Química, Portugal
Concluded
2014 - Current Development of Functional Materials
NORTE-07-0124-FEDER-000065
Researcher
Universidade do Porto Centro de Investigação em Química, Portugal
Concluded
2022/01/02 - 2023/07/01 A estratégia do Cavalo de Troia para o desenvolvimento de antibacterianos contra microrganismos multirresistentes
EXPL/MED-QUI/1156/2021
Principal investigator
Universidade do Porto Centro de Investigação em Química, Portugal

Universidade do Porto Faculdade de Ciências, Portugal

Universidade do Porto Faculdade de Engenharia, Portugal
Fundação para a Ciência e a Tecnologia
Ongoing
2011/01/20 - 2014 BP4Brain - Benzopyrane as a privileged structure for the rational design of multi-target-directed drugs potentially useful in neurodegenerative diseases
info:eu-repo/grantAgreement/FCT/5876-PPCDTI/113687/PT
Universidade do Porto Centro de Investigação em Química, Portugal
 Fundação para a Ciência e a Tecnologia
Concluded
2009/08/01 - 2013/07/31 NEW THERAPEUTIC APROACHES IN CANCER:DESIGN AND SYNTHESIS OF NEW A3 RECEPTOR LIGANDS
SFRH/BD/43531/2008
Universidade do Porto Faculdade de Ciências, Portugal
 Fundação para a Ciência e a Tecnologia
Concluded
2008/01/01 - 2011/03/31 Novas abordagens terapêuticas no cancro: desenho racional e síntese de novos ligandos dos receptores A3 da adenosina
PTDC/QUI/70359/2006
Universidade de Coimbra Unidade de Investigação e Desenvolvimento Química-Física Molecular, Portugal

Instituto Politécnico do Porto Instituto Superior de Engenharia do Porto, Portugal

Universidade de Coimbra, Portugal
Fundação para a Ciência e a Tecnologia
Concluded
2008 - 2011 Rational design and synthesis of new adenosine A3 receptor ligands
PTDC/QUI/70359/2006
Research Fellow
Universidade do Porto Faculdade de Farmácia, Portugal
Concluded
2005/10/15 - 2007/04/15 Desenvolvimento de Novos Agentes Anticancerígenos: Derivados Fenólicos de Origem Natural ou Sintética - Relações Estrutura-Actividade
POCI/QUI/55631/2004
Universidade de Coimbra, Portugal

Universidade de Coimbra Unidade de Investigação e Desenvolvimento Química-Física Molecular, Portugal

Universidade do Porto Faculdade de Farmácia, Portugal

Instituto Politécnico do Porto Instituto Superior de Engenharia do Porto, Portugal

Universidade do Porto Faculdade de Ciências, Portugal
Fundação para a Ciência e a Tecnologia
Concluded
Outputs

Publications

Book chapter
  1. Gaspar, Alexandra. "Synthesis of p-conjugated systems using formylchromone as building block". In Comprehensive Organic Chemistry Experiments for the Laboratory Classroom. 2016.
    Published
  2. Gaspar, Alexandra. "Synthesis of 7-methoxy-4-oxo- N-phenyl- 4H-chromene-2-carboxamide". In Comprehensive Organic Chemistry Experiments for the Laboratory Classroom. Royal Chemical Society, 2016.
    Published
  3. Gaspar, Alexandra. "Molecular Physicochemistry- a Tool for the Rational Development of New Antioxidants". In New Strides in Biotechnology. 2008.
Conference abstract
  1. Gaspar, Alexandra. "Chromone as a privileged structure for lead optimization of new adenosine receptors ligands". Paper presented in Purines 2014, an International Conference on Nucleotides, Nucleosides and Nucleobases, 2014.
    10.1007/s11302-014-9430-7
  2. Volpini, Rosaria; Lambertucci, Catia; Taffi, Sara; Vittori, Sauro; Klotz, Karl-Norbert; Cristalli, Gloria. "A3 adenosine receptors: Synthesis and biological evaluation of new potent and selective ligands". Paper presented in Purinergic Signalling (2014) 10:657–854- International Conference on Nucleotides, Nucleosides and Nucleobases, Bonn, 2014.
    10.1135/css200507297
  3. Gaspar, Alexandra. "Surpassing the Pharmacokinetic Drawbacks of Natural Phenolic Antioxidants". Paper presented in XXIInd International Symposium on Medicinal Chemistry, Berlim, 2012.
    Published
  4. Gaspar, Alexandra. "Benzopyrone as a privileged scaffold for drug discovery: synthesis and structure–affinity relationships for adenosine receptors". Paper presented in ChemMedChem ISMC 2012 -XXIInd International Symposium on Medicinal Chemistry, Berlim, 2012.
    Published
  5. Gaspar, Alexandra. "Discovery of a novel class of reversible monoamine oxidase B inhibitors based on chromone scaffold". Paper presented in ChemMedChem ISMC 2012-XXIInd International Symposium on Medicinal Chemistry, Berlim, 2012.
    Published
  6. Borghesi, Marco. "Striving for success in antioxidant therapy for neurodegenerative diseases: current status and future prospects". Paper presented in ChemMedChem ISMC 2012-XXIInd International Symposium on Medicinal Chemistry, Berlim, 2012.
    Published
  7. Gaspar, Alexandra. "Exploring natural profits: Development of novel and potent galloyl-cinnamic hybrids lipophilic antioxidants". Paper presented in Free Radical Biology and Medicine-Society for Free Radical Research International 16th Biennial Meeting, Londres, 2012.
    Published • 10.1016/j.freeradbiomed.2012.08.213
  8. Gaspar, Alexandra. "Concise and diversity-oriented synthesis of novel scaffolds embedded with privileged benzopyran motif". Paper presented in Purinergic Signalling volume 6, pages49–115(2010)-Third joint Italian-German Purine Club meeting: “Purinergic receptors: new frontiers for novel therapies”, Camerino, 2010.
    Published • https://doi.org/10.1007/s11302-009-9171-1
  9. Cong, Chunyu; Sun, Pingping; Ma, Zhiqiang. "Predicting binding affinity using differential evolution". Paper presented in Purinergic Signalling (2010) -Third joint Italian-German Purine Club meeting: “Purinergic receptors: new frontiers for novel therapies”, Camerino, 2010.
    Published • 10.1007/s11302-009-9171-1
  10. Boudreau, Michael. "Development of novel systems to deliver natural antioxidants to mitochondria: MitoCIN'S as a case study". Paper presented in 47th Annual Scientific Meeting of the European Society for Clinical Investigation,, Albufeira, 2007.
    10.1109/sysose.2007.4304229
Conference poster
  1. Gaspar, Alexandra. "A rational drug discovery approach for the design and development of new antimicrobial agents.". Paper presented in MuTaLig COST ACTION CA15135, 2020.
  2. Gaspar, Alexandra. "Evaluation of benzopyrone pharmacophore features on MAO-B inhibition". Paper presented in 26th Young Research Fellows meeting, 2019.
  3. Gaspar, Alexandra. "Design and Development of Dual -Target Ligands Based on Benzopyran for the Treatment of Parkinson’s Disease". Paper presented in 3rd Annual meeting - MuTaLig COST Action, 2018.
  4. Gaspar, Alexandra. "Mapping the Pharmacophore of Benzopyrone MAO-B Inhibitors". Paper presented in VIII Meeting of the Paul Ehrlich EuroPhD Network, 2018.
  5. Gaspar, Alexandra. "Development of new antimicrobial agents based on the chromone scaffold". Paper presented in VIII Meeting of the Paul Ehrlich EuroPhD Network, 2018.
  6. Gaspar, Alexandra. "Benzopyrane as a valid scaffold for the development of multitarget ligands for neurodegenerative diseases". Paper presented in 1st annual meeting – MuTaLig COST Action, 2016.
  7. Gaspar, Alexandra. "Search of new antibacterial compounds inspired on benzopyran scaffold". Paper presented in Meeting of the Paul Ehrlich Euro-PhD Network, 2015.
  8. Hugues, Edgar. "Development of new adenosine receptors ligands based on chromone scaffold: adventures in the design and optimization process". Paper presented in Meeting of the Paul Ehrlich Euro-PhD Network, 2015.
  9. Gaspar, Alexandra. "Development of A3 adenosine receptor ligands by an analogue-based approach". Paper presented in XXII Young Research Fellow Meeting, 2015.
  10. Gaspar, Alexandra. "Discovery of new leads for old targets: insights on the lead optimization process of a new MAO-B inhibitor based on chromone scaffold". Paper presented in 4th Meeting of the Paul Ehrlich MedChem Euro–PhD Network–Hradec Králové, República Checa, 2014.
  11. Gaspar, Alexandra. "“Chromone: a valid scaffold in medicinal chemistry". Paper presented in 4th Meeting of the Paul Ehrlich MedChem Euro-PhD Network - Hradec Králové, Praga, República Checa, 2014.
  12. Gaspar, Alexandra. "MITOCIN’S - the Highway to Target Bioactive Cinnamic Molecules to Mitochondria". Paper presented in 8th World Congress on Polyphenols Applications: ISANH Polyphenols - Lisboa, Portugal, 2014.
  13. Gaspar, Alexandra. "Remaking of Dietary Antioxidants: Targeting MitoBEN’s to Mitochondria as a New Therapeutic Strategy". Paper presented in 10º Portuguese National Meeting of Organic Chemistry – 1st Portuguese– Brazilian Organic Chemistry Symposium–, 2013.
  14. Gaspar, Alexandra. "Targeted Delivery of MitoCIN’S: a New Therapeutic Approach for Oxidative Stress Related Diseases". Paper presented in 10º Portuguese National Meeting of Organic Chemistry – 1st Portuguese– Brazilian Organic Chemistry Symposium–, 2013.
  15. Gaspar, Alexandra. "Nature-Inspired Artwoark: Development of 6-(Heteroaryl/Aryl) Chromones as Novel Adenosine Receptor Ligands". Paper presented in III SEQT Summer School – Medicinal Chemistry in Drug Discovery: The Pharma Perspective–Madrid, Espanha,, 2013.
  16. Gaspar, Alexandra. "Development of new dual-target strategy for the discovery of new anti-Parkinson drugs". Paper presented in III SEQT Summer School – Medicinal Chemistry in Drug Discovery: The Pharma Perspective–Madrid, Espanha,, 2013.
  17. Gaspar, Alexandra. "Development of new dual-target MAO-B/AChE inhibitors based on chromone derivatives". Paper presented in Frontiers in Medicinal Chemistry–São Francisco, Califórnia, EUA,, 2013.
  18. Gaspar, Alexandra. "Parkinson disease and non-dopaminergic therapy: synthesis and evaluation of new adenosine receptors antagonists based on benzo-¿-pyrone scaffold". Paper presented in 6th Drug Discovery for Neurodegeneration conference: an Intensive Course on Translating Research into Drugs–Nova Iorque, EUA, 2012.
  19. Gaspar, Alexandra. "Modulating the pharmacokinetic profile of natural phenolic antioxidants with potential neuroprotective activity". Paper presented in 6th Drug Discovery for Neurodegeneration conference: an Intensive Course on Translating Research into Drugs–Nova Iorque, EUA, 2012.
  20. Gaspar, Alexandra. "Mitochondria-Targeted Cinnamic Antioxidants: Novel Promising Drugs for Treatment of Alzheimer Disease". Paper presented in 6th Drug Discovery for Neurodegeneration conference: an Intensive Course on Translating Research into Drugs–Nova Iorque, EUA, 2012.
  21. Gaspar, Alexandra. "New therapeutic approaches towards neurodegenerative diseases: targeting oxidative damage with innovative lipophilic antioxidants". Paper presented in 16th RSC_SCI Cambridge Medicinal Chemistry Symposium–Cambridge, Reino Unido, 2011.
  22. Gaspar, Alexandra. "Drug discovery for neurodegenerative diseases: development of novel potent and selective chromone based MAO-B inhibitors". Paper presented in 16th RSC_SCI Cambridge Medicinal Chemistry Symposium–Cambridge, Reino Unido, 2011.
  23. Gaspar, Alexandra. "Benzo-¿-pyrone based ligands as a privileged scaffold for drug discovery: synthesis and structure-affinity relationships for adenosines rece". Paper presented in 16th RSC_SCI Cambridge Medicinal Chemistry Symposium–Cambridge, Reino Unido, 2011.
  24. Gaspar, Alexandra. "New mitochondria-targeted antioxidants based on cinnamic scaffold for neurodegenerative disease therapy". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, Portugal,, 2011.
  25. Gaspar, Alexandra. "Chromone-based adenosine receptor ligands: a new challenge in the anticancer drug discovery scenario". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, Portugal, 2011.
  26. Gaspar, Alexandra. "Targeting phenolic antioxidants to mitochondria: synthesis and characterization of novel triphenylphosphonium-conjugated lipophilic cinnamic derivatives". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, 2011.
  27. Gaspar, Alexandra. "Design and development of a novel chemical library, based on a privileged scaffold, suitable to speed up the drug discovery process of IMAO-B”". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, 2011.
  28. Gaspar, Alexandra. "Accelerating lead optimization of MAO inhibitors throughout microwaveassisted organic synthesis". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, Portugal, 2011.
  29. Leferink, Frank; Blaj, Alex; Hogeman, Edwin; Storck, Rob. "Using preloading to protect bearings against lightning damage". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, Portugal, 2011.
    10.1109/sipda.2015.7339301
  30. Gaspar, Alexandra. "Development of novel lipophilic antioxidants based on ferulic acid". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, Portugal, 2011.
  31. Rivero, Ralph A.; Hardwicke, Mary Ann. "Abstract 2913: Identification of GSK2636771, a potent and selective, orally bioavailable inhibitor of phosphatidylinositol 3-kinase-beta (PI3Ka) for the treatment of PTEN deficient tumors". Paper presented in 2nd Iberic Meeting on Medicinal Chemistry–Porto, Portugal, 2011.
    10.1158/1538-7445.am2012-2913
  32. Sonoda, Kenzo. "Abstract C256: New therapeutic modalities by targeting RCAS1 which induces apoptosisviaectodomain shedding mediated by ADAM9". Paper presented in Frontiers in Medicinal Chemistry: Emerging Targets, Novel Candidates and Innovative Strategies–Barcelona, Espanha, 2009.
    10.1158/1535-7163.targ-09-c256
  33. Gaspar, Alexandra. "QSAR model for predicting binding affinity to adenosine A2b receptors of antagonists based on chromone scaffold". Paper presented in Third Joint Italian–German Purine Club Meeting Purinergic Receptors: New Frontiers for Novel Therapies–Camerino, Itália, 2009.
  34. Gaspar, Alexandra. "From nature to drug discovery: the chromone scaffold as a privileged structure¿ for the development of novel A3 receptor ligands". Paper presented in III EWDSy–Third European Workshop in Drug Synthesis, University of Siena– Siena, Itália,, 2009.
  35. Gaspar, Alexandra. "Biological activity of novel esters structurally based on a natural phenolic acid model". Paper presented in Metabolic Toxicology: from Pathway to Organism – International Courses on Toxicology, Cell and Molecular Toxicology Research Area, Centre for Neurosciences and Cell Biology of the University of Coimbra–Coimbra, Portugal, 2008.
  36. Gaspar, Alexandra. "Phenolic Alkyl Esters with Potential Anticancer Activity: A Raman Spectroscopy Study in the Solid State". Paper presented in 12th European Conference on the Spectroscopy of Biological Molecules (ECSBM–12)–Bobigny, Paris, França, 2007.
  37. Gaspar, Alexandra. "Phenolic Esters with Potential Anticancer Activity: Solution Equilibria Studied by Raman Spectroscopy". Paper presented in 12th European Conference on the Spectroscopy of Biological Molecules (ECSBM–12)–Bobigny, Paris, Franç, 2007.
  38. Gaspar, Alexandra. "Therapeutic anti-inflammatory strategies based on targeting adenosine receptors". Paper presented in International Symposium on Advances in Synthetic and Medicinal Chemistry (ASMC07)–St. Petersburgo, Rússia, 2007.
  39. Gaspar, Alexandra. "Novel Therapeutic approaches in cancer: design and synthesis of new adenosine A3 Receptor ligands". Paper presented in First Iberic Meeting on Medicinal Chemistry–anticancer agents–Régua, Portugal, 2007.
  40. Gaspar, Alexandra. "New insights in the therapeutic value of hydroxyl cinnamic derivatives: cytotoxic and COX-2 inhibition properties". Paper presented in First Iberic Meeting on Medicinal Chemistry–anticancer agents–Régua, Portugal, 2007.
  41. Gaspar, Alexandra; Machado, N.F.L.; Calheiros, R.; Fiuza, S.M.; Borges, F.; Gaspar, A.; Garrido, J.; Marques, M.P.. "Phenolic esters with potential anticancer activity the structural Variable". Paper presented in First Iberic Meeting on Medicinal Chemistry–anticancer agents–Régua, Portugal, 2007.
    10.1007/s00894-007-0174-y
  42. Gaspar, Alexandra. "Alkyl Phenolic Esters – A Raman Spectroscopy Study". Paper presented in IV CIE (IV Congresso Ibérico de Espectroscopia/XX Reunión Española de Espectroscopía)–Ciudad Real, Espanha,, 2006.
  43. Gaspar, Alexandra. "New Potential Nonsteroidal Aromatase Inhibitors: A Raman Spectroscopy Study". Paper presented in IV CIE (IV Congresso Ibérico de Espectroscopia/XX Reunión Española de Espectroscopía)–Ciudad Real, Espanha, 2006.
  44. Gaspar, Alexandra. "Structural Elucidation of New Potential Selective A2A Adenosine Receptor Agonists by Raman Spectroscopy". Paper presented in IV CIE (IV Congresso Ibérico de Espectroscopia/XX Reunión Española de Espectroscopía)–Ciudad Real, Espanha, 2006.
  45. Gaspar, Alexandra. "Spectroscopic Studies on Hydroxycinnamic Acid Derivatives as Potential Antiinflammatory Agents". Paper presented in IV CIE (IV Congresso Ibérico de Espectroscopia/XX Reunión Española de Espectroscopía)–Ciudad Real, Espanha, 2006.
  46. Gaspar, Alexandra. "Design and Synthesis of Novel Hydroxycinnamic Derivatives with Cytotoxic, Antioxidant and Anti-inflammatory Activities". Paper presented in 3rd International Conference on Oxidative Stress in Skin Medicine and Biology– Andros, Grécia,, 2006.
  47. Gaspar, Alexandra. "Phenolic Derivatives as Potential Anticancer Agents". Paper presented in 3rd International Conference on Oxidative Stress in Skin Medicine and Biology– Andros, Grécia, 2006.
  48. Gaspar, Alexandra. "Anticancer and Anti-inflammatory Properties of Hydroxycinnamic Derivatives". Paper presented in XXIII International Conference on Polyphenols, 2006.
  49. Gaspar, Alexandra. "Evaluation of anti-inflammatory and anti-cancer properties of synthetic hydroxycinnamic derivatives". Paper presented in 66th Intern. Pharm. Fed. Congress–Salvador Bahia, Brasil, 2006.
  50. Gaspar, Alexandra. "Synthesis of Novel Chromone Derivatives as Potential Lypophilic Antioxidants". Paper presented in International Symposium on Chemistry, Biology and Medicine–, 2006.
  51. Gaspar, Alexandra. "Enzymatic and non-enzymatic synthesis of glutathionil conjugates of cinnamic acids: an experimental and theorical study". Paper presented in International Symposium on Chemistry, Biology and Medicine, 2006.
  52. Gaspar, Alexandra. "Synthesis of promising antioxidant agents structurally based on cinnamic acid". Paper presented in International Symposium on Chemistry, Biology and Medicine, 2006.
  53. Gaspar, Alexandra. "Antioxidant versus Anticancer/Anti-inflammatory Properties of Phenolic Derivatives: A New Challenge on Structure-Activity Studies". Paper presented in Paris Anti–Inflammatory Drugs, 2005.
Journal article
  1. Mesiti, Francesco; Gaspar, Alexandra; Chavarria, Daniel; Maruca, Annalisa; Rocca, Roberta; Gil Martins, Eva; Barreiro, Sandra; et al. Corresponding author: Gaspar, Alexandra. "Mapping Chromone-3-Phenylcarboxamide Pharmacophore: Quid Est Veritas?". Journal of Medicinal Chemistry 64 15 (2021): 11169-11182. http://dx.doi.org/10.1021/acs.jmedchem.1c00510.
    10.1021/acs.jmedchem.1c00510
  2. Francesco Mesiti; Annalisa Maruca; Vera Silva; Roberta Rocca; Carlos Fernandes; Fernando Remião; Eugenio Uriarte; et al. Corresponding author: Alexandra Gaspar. "4-Oxoquinolines and monoamine oxidase: When tautomerism matters". European Journal of Medicinal Chemistry (2021): 113183-113183. https://doi.org/10.1016/j.ejmech.2021.113183.
    10.1016/j.ejmech.2021.113183
  3. Gomes, Ligia R.; Low, John Nicolson; Borges, Fernanda; Gaspar, Alexandra; Mesiti, Francesco. "The synthesis, crystal structure and Hirshfeld analysis of 4-(3,4-dimethylanilino)-N-(3,4-dimethylphenyl)quinoline-3-carboxamide". Acta Crystallographica Section E Crystallographic Communications 76 2 (2020): 201-207. http://dx.doi.org/10.1107/s2056989020000298.
    10.1107/s2056989020000298
  4. Mesiti, Francesco; Chavarria, Daniel; Gaspar, Alexandra; Alcaro, Stefano; Borges, Fernanda. Corresponding author: Gaspar, Alexandra. "The chemistry toolbox of multitarget-directed ligands for Alzheimer's disease". European Journal of Medicinal Chemistry 181 (2019): 111572. http://dx.doi.org/10.1016/j.ejmech.2019.111572.
    Published • 10.1016/j.ejmech.2019.111572
  5. Gaspar, A.; Mohabbati, M.; Cagide, F.; Razzaghi-Asl, N.; Miri, R.; Firuzi, O.; Borges, F.. "Searching for new cytotoxic agents based on chromen-4-one and chromane-2,4-dione scaffolds". Research in Pharmaceutical Sciences 14 1 (2019): 74-83. http://www.scopus.com/inward/record.url?eid=2-s2.0-85061659825&partnerID=MN8TOARS.
    10.4103/1735-5362.251855
  6. Oliveira, C.; Gaspar, A.; Gomes, L.R.; Low, J.N.; Borges, F.; Cagide, F.. "Structural elucidation of a series of benzamide derivatives". Magnetic Resonance in Chemistry 56 3 (2018): 216-223. http://www.scopus.com/inward/record.url?eid=2-s2.0-85037652503&partnerID=MN8TOARS.
    10.1002/mrc.4682
  7. Reis, J.; Cagide, F.; Chavarria, D.; Silva, T.; Fernandes, C.; Gaspar, A.; Uriarte, E.; et al. "Correction to: Discovery of New Chemical Entities for Old Targets: Insights on the Lead Optimization of Chromone-Based Monoamine Oxidase B (MAO-B) Inhibitors (Journal of Medicinal Chemistry (2016) 59 (5879-5893) DOI: 10.1021/acs.jmedchem.6b00527)". Journal of Medicinal Chemistry 61 11 (2018): 5054-5054. http://www.scopus.com/inward/record.url?eid=2-s2.0-85048642711&partnerID=MN8TOARS.
    10.1021/acs.jmedchem.8b00600
  8. Reis, J.; Gaspar, A.; Milhazes, N.; Borges, F.. "Chromone as a Privileged Scaffold in Drug Discovery: Recent Advances". Journal of Medicinal Chemistry 60 19 (2017): 7941-7957. http://www.scopus.com/inward/record.url?eid=2-s2.0-85031293351&partnerID=MN8TOARS.
    10.1021/acs.jmedchem.6b01720
  9. Low, J.N.; Gomes, L.R.; Gaspar, A.; Borges, F.. "Structure of 7-hydroxy-3-(2-methoxyphenyl)-2-trifluoromethyl-4H-chromen-4-one". Acta Crystallographica Section E: Crystallographic Communications 73 (2017): 1130-1134. http://www.scopus.com/inward/record.url?eid=2-s2.0-85029517534&partnerID=MN8TOARS.
    10.1107/S2056989017009896
  10. Borges, A.; Sousa, P.; Gaspar, A.; Vilar, S.; Borges, F.; Simões, M.. "Furvina inhibits the 3-oxo-C12-HSL-based quorum sensing system of Pseudomonas aeruginosa and QS-dependent phenotypes". Biofouling 33 2 (2017): 156-168. http://www.scopus.com/inward/record.url?eid=2-s2.0-85011301293&partnerID=MN8TOARS.
    10.1080/08927014.2017.1280732
  11. Fonseca, A.; Gaspar, A.; Matos, M.J.; Gomes, L.R.; Low, J.N.; Uriarte, E.; Borges, F.. "Structural elucidation of a series of 6-methyl-3-carboxamidocoumarins". Magnetic Resonance in Chemistry 55 4 (2017): 373-378. http://www.scopus.com/inward/record.url?eid=2-s2.0-85000471196&partnerID=MN8TOARS.
    10.1002/mrc.4541
  12. Cagide, F.; Reis, J.; Gaspar, A.; Chavarria, D.; Kachler, S.; Klotz, K.N.; Gomes, L.R.; et al. "Discovery of the first A1 adenosine receptor ligand based on the chromone scaffold". RSC Advances 6 52 (2016): 46972-46976. http://www.scopus.com/inward/record.url?eid=2-s2.0-84969939884&partnerID=MN8TOARS.
    10.1039/c6ra02347a
  13. Oliveira, J.A.S.A.; Oliveira, T.S.M.; Gaspar, A.; Borges, F.; Ribeiro da Silva, M.D.M.C.; Monte, M.J.S.. "Study on the volatility of halogenated fluorenes". Chemosphere 157 (2016): 25-32. http://www.scopus.com/inward/record.url?eid=2-s2.0-84968830414&partnerID=MN8TOARS.
    10.1016/j.chemosphere.2016.05.014
  14. Reis, J.; Cagide, F.; Chavarria, D.; Silva, T.; Fernandes, C.; Gaspar, A.; Uriarte, E.; et al. "Discovery of New Chemical Entities for Old Targets: Insights on the Lead Optimization of Chromone-Based Monoamine Oxidase B (MAO-B) Inhibitors". Journal of Medicinal Chemistry 59 12 (2016): 5879-5893. http://www.scopus.com/inward/record.url?eid=2-s2.0-84975871993&partnerID=MN8TOARS.
    10.1021/acs.jmedchem.6b00527
  15. Gonçalves, A.L.; Abreu, A.C.; Coqueiro, A.; Gaspar, A.; Borges, F.; Choi, Y.H.; Pires, J.C.M.; Simões, M.. "Co-cultivation of Synechocystis salina and Pseudokirchneriella subcapitata under varying phosphorus concentrations evidences an allelopathic competition scenario". RSC Advances 6 61 (2016): 56091-56100. http://www.scopus.com/inward/record.url?eid=2-s2.0-84975041703&partnerID=MN8TOARS.
    10.1039/c6ra07771d
  16. Fernandes, C.; Soares, P.; Gaspar, A.; Martins, D.; Gomes, L.R.; Low, J.N.; Borges, F.. "Synthesis of 6-aryl/heteroaryl-4-oxo-4H-chromene-2-carboxylic ethyl ester derivatives". Tetrahedron Letters 57 27-28 (2016): 3006-3010. http://www.scopus.com/inward/record.url?eid=2-s2.0-84973109330&partnerID=MN8TOARS.
    10.1016/j.tetlet.2016.05.096
  17. Gomes, L.R.; Low, J.N.; Fernandes, C.; Gaspar, A.; Borges, F.. "Crystal structures of ethyl 6-(4-methylphenyl)-4-oxo-4H-chromene-2-carboxylate and ethyl 6-(4-fluorophenyl)-4-oxo-4H-chromene-2-carboxylate". Acta Crystallographica Section E: Crystallographic Communications 72 (2016): http://www.scopus.com/inward/record.url?eid=2-s2.0-84954144374&partnerID=MN8TOARS.
    10.1107/S2056989015022781
  18. Cagide, F.; Silva, T.; Reis, J.; Gaspar, A.; Borges, F.; Gomes, L.R.; Low, J.N.. "Discovery of two new classes of potent monoamine oxidase-B inhibitors by tricky chemistry". Chemical Communications 51 14 (2015): 2832-2835. http://www.scopus.com/inward/record.url?eid=2-s2.0-84922432422&partnerID=MN8TOARS.
    10.1039/c4cc08798d
  19. Gaspar, A.; Milhazes, N.; Santana, L.; Uriarte, E.; Borges, F.; Matos, M.J.. "Oxidative stress and neurodegenerative diseases: Looking for a therapeutic solution inspired on benzopyran chemistry". Current Topics in Medicinal Chemistry 15 5 (2015): 432-445. http://www.scopus.com/inward/record.url?eid=2-s2.0-84930908241&partnerID=MN8TOARS.
  20. Cagide, F.; Gaspar, A.; Reis, J.; Chavarria, D.; Vilar, S.; Hripcsak, G.; Uriarte, E.; et al. "Navigating in chromone chemical space: Discovery of novel and distinct A3 adenosine receptor ligands". RSC Advances 5 96 (2015): 78572-78585. http://www.scopus.com/inward/record.url?eid=2-s2.0-84942156288&partnerID=MN8TOARS.
    10.1039/c5ra14988f
  21. Gomes, L.R.; Low, J.N.; Cagide, F.; Gaspar, A.; Borges, F.. "A comparison of the structures of some 2- and 3-substituted chromone derivatives: A structural study on the importance of the secondary carboxamide backbone for the inhibitory activity of MAO-B". Acta Crystallographica Section E: Crystallographic Communications 71 (2015): 1270-1277. http://www.scopus.com/inward/record.url?eid=2-s2.0-84948458262&partnerID=MN8TOARS.
    10.1107/S2056989015017958
  22. Reis, J.; Gaspar, A.; Borges, F.; Rebelo Gomes, L.; Low, J.N.. "Synthesis, spectroscopic characterization and X-ray structure of novel 7-methoxy-4-oxo-N-phenyl-4H-chromene-2-carboxamides". Journal of Molecular Structure 1056-1057 1 (2014): 31-37. http://www.scopus.com/inward/record.url?eid=2-s2.0-84886478757&partnerID=MN8TOARS.
    10.1016/j.molstruc.2013.09.024
  23. Gaspar, A.; Matos, M.J.; Garrido, J.; Uriarte, E.; Borges, F.. "Chromone: A valid scaffold in medicinal chemistry". Chemical Reviews 114 9 (2014): 4960-4992. http://www.scopus.com/inward/record.url?eid=2-s2.0-84900440197&partnerID=MN8TOARS.
    10.1021/cr400265z
  24. Fernandes, C.; Encarnação, I.; Gaspar, A.; Garrido, J.; Borges, F.; Garrido, E.M.. "Influence of hydroxypropyl- ß -cyclodextrin on the photostability of fungicide pyrimethanil". International Journal of Photoenergy 2014 (2014): http://www.scopus.com/inward/record.url?eid=2-s2.0-84897555260&partnerID=MN8TOARS.
    10.1155/2014/489873
  25. Teixeira, J.; Silva, T.; Benfeito, S.; Gaspar, A.; Garrido, E.M.; Garrido, J.; Borges, F.. "Exploring nature profits: Development of novel and potent lipophilic antioxidants based on galloyl-cinnamic hybrids". European Journal of Medicinal Chemistry 62 (2013): 289-296. http://www.scopus.com/inward/record.url?eid=2-s2.0-84873030904&partnerID=MN8TOARS.
    10.1016/j.ejmech.2012.12.049
  26. Helguera, A.M.; Pérez-Garrido, A.; Gaspar, A.; Reis, J.; Cagide, F.; Vina, D.; Cordeiro, M.N.D.S.; Borges, F.. "Combining QSAR classification models for predictive modeling of human monoamine oxidase inhibitors". European Journal of Medicinal Chemistry 59 (2013): 75-90. http://www.scopus.com/inward/record.url?eid=2-s2.0-84870213017&partnerID=MN8TOARS.
    10.1016/j.ejmech.2012.10.035
  27. Gomes, L.R.; Low, J.N.; Cagide, F.; Gaspar, A.; Reis, J.; Borges, F.. "Structural characterization of some N-phenyl-4-oxo-4H-2-chromone carboxamides". Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials 69 3 (2013): 294-309. http://www.scopus.com/inward/record.url?eid=2-s2.0-84881167454&partnerID=MN8TOARS.
    10.1107/S2052519213009676
  28. Teixeira, J.; Gaspar, A.; Garrido, E.M.; Garrido, J.; Borges, F.. "Hydroxycinnamic acid antioxidants: An electrochemical overview". BioMed Research International 2013 (2013): http://www.scopus.com/inward/record.url?eid=2-s2.0-84881540701&partnerID=MN8TOARS.
    10.1155/2013/251754
  29. Gaspar, A.; Cagide, F.; Quezada, E.; Reis, J.; Uriarte, E.; Borges, F.. "Synthesis and NMR studies of novel chromone-2-carboxamide derivatives". Magnetic Resonance in Chemistry 51 4 (2013): 251-254. http://www.scopus.com/inward/record.url?eid=2-s2.0-84875254988&partnerID=MN8TOARS.
    10.1002/mrc.3937
  30. Matos, M.J.; Hogger, V.; Gaspar, A.; Kachler, S.; Borges, F.; Uriarte, E.; Santana, L.; Klotz, K.-N.. "Synthesis and adenosine receptors binding affinities of a series of 3-arylcoumarins". Journal of Pharmacy and Pharmacology 65 11 (2013): 1590-1597. http://www.scopus.com/inward/record.url?eid=2-s2.0-84886085159&partnerID=MN8TOARS.
    10.1111/jphp.12135
  31. Matos, M.J.; Gaspar, A.; Kachler, S.; Klotz, K.-N.; Borges, F.; Santana, L.; Uriarte, E.. "Targeting adenosine receptors with coumarins: Synthesis and binding activities of amide and carbamate derivatives". Journal of Pharmacy and Pharmacology 65 1 (2013): 30-34. http://www.scopus.com/inward/record.url?eid=2-s2.0-84870870474&partnerID=MN8TOARS.
    10.1111/j.2042-7158.2012.01571.x
  32. Reis, J.; Gaspar, A.; Borges, F.; Gomes, L.R.; Low, J.N.. "4-Oxo-N-phenyl-4H-chromene-2-carboxamide and of a new polymorph of 7-methoxy-4-oxo-N-p-tolyl-4H-chromene-2-carboxamide and its hemihydrate". Acta Crystallographica Section C: Crystal Structure Communications 69 12 (2013): 1527-1533. http://www.scopus.com/inward/record.url?eid=2-s2.0-84890072345&partnerID=MN8TOARS.
    10.1107/S0108270113029727
  33. Teixeira, J.; Soares, P.; Benfeito, S.; Gaspar, A.; Garrido, J.; Murphy, M.P.; Borges, F.. "Rational discovery and development of a mitochondria-targeted antioxidant based on cinnamic acid scaffold". Free Radical Research 46 5 (2012): 600-611. http://www.scopus.com/inward/record.url?eid=2-s2.0-84859067775&partnerID=MN8TOARS.
    10.3109/10715762.2012.662593
  34. Gaspar, A.; Reis, J.; Matos, M.J.; Uriarte, E.; Borges, F.. "In search for new chemical entities as adenosine receptor ligands: Development of agents based on benzo-¿-pyrone skeleton". European Journal of Medicinal Chemistry 54 (2012): 914-918. http://www.scopus.com/inward/record.url?eid=2-s2.0-84864409949&partnerID=MN8TOARS.
    10.1016/j.ejmech.2012.05.033
  35. Garrido, J.; Gaspar, A.; Garrido, E.M.; Miri, R.; Tavakkoli, M.; Pourali, S.; Saso, L.; Borges, F.; Firuzi, O.. "Alkyl esters of hydroxycinnamic acids with improved antioxidant activity and lipophilicity protect PC12 cells against oxidative stress". Biochimie 94 4 (2012): 961-967. http://www.scopus.com/inward/record.url?eid=2-s2.0-84857454548&partnerID=MN8TOARS.
    10.1016/j.biochi.2011.12.015
  36. Matos, M.J.; Gaspar, A.; Borges, F.; Uriarte, E.; Santana, L.. "Improved synthesis of 3-(aminoaryl)coumarins". Organic Preparations and Procedures International 44 6 (2012): 522-526. http://www.scopus.com/inward/record.url?eid=2-s2.0-84870010404&partnerID=MN8TOARS.
    10.1080/00304948.2012.730937
  37. Gaspar, A.; Reis, J.; Kachler, S.; Paoletta, S.; Uriarte, E.; Klotz, K.-N.; Moro, S.; Borges, F.. "Discovery of novel A 3 adenosine receptor ligands based on chromone scaffold". Biochemical Pharmacology 84 1 (2012): 21-29. http://www.scopus.com/inward/record.url?eid=2-s2.0-84860664996&partnerID=MN8TOARS.
    10.1016/j.bcp.2012.03.007
  38. Borges, F.; Reis, J.; Encarnação, I.; Gaspar, A.; Morales, A.; Milhazes, N.. "Parkinson's disease management. part iidiscovery of mao-b inhibitors based on nitrogen heterocycles and analogues". Current Topics in Medicinal Chemistry 12 20 (2012): 2116-2130. http://www.scopus.com/inward/record.url?eid=2-s2.0-84874913282&partnerID=MN8TOARS.
  39. Gaspar, A.; Reis, J.; Fonseca, A.; Milhazes, N.; Viña, D.; Uriarte, E.; Borges, F.. "Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors". Bioorganic and Medicinal Chemistry Letters 21 2 (2011): 707-709. http://www.scopus.com/inward/record.url?eid=2-s2.0-78651257725&partnerID=MN8TOARS.
    10.1016/j.bmcl.2010.11.128
  40. Cagide, F.; Reis, J.; Gaspar, A.; Borges, F.. "Accelerating lead optimization of chromone carboxamide scaffold throughout microwave-assisted organic synthesis". Tetrahedron Letters 52 48 (2011): 6446-6449. http://www.scopus.com/inward/record.url?eid=2-s2.0-80255127537&partnerID=MN8TOARS.
    10.1016/j.tetlet.2011.09.095
  41. Menezes, J.C.J.M.D.S.; Kamat, S.P.; Cavaleiro, J.A.S.; Gaspar, A.; Garrido, J.; Borges, F.. "Synthesis and antioxidant activity of long chain alkyl hydroxycinnamates". European Journal of Medicinal Chemistry 46 2 (2011): 773-777. http://www.scopus.com/inward/record.url?eid=2-s2.0-79151481300&partnerID=MN8TOARS.
    10.1016/j.ejmech.2010.12.016
  42. Gaspar, A.; Silva, T.; Yáñez, M.; Vina, D.; Orallo, F.; Ortuso, F.; Uriarte, E.; et al. "Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors". Journal of Medicinal Chemistry 54 14 (2011): 5165-5173. http://www.scopus.com/inward/record.url?eid=2-s2.0-79960651250&partnerID=MN8TOARS.
    Published • 10.1021/jm2004267
  43. Gaspar, A.; Teixeira, F.; Uriarte, E.; Milhazes, N.; Melo, A.; Cordeiro, M.N.D.S.; Ortuso, F.; Alcaro, S.; Borges, F.. "Towards the Discovery of a Novel Class of Monoamine Oxidase Inhibitors: Structure-Property-Activity and Docking Studies on Chromone Amides". ChemMedChem 6 4 (2011): 628-632. http://www.scopus.com/inward/record.url?eid=2-s2.0-79953066953&partnerID=MN8TOARS.
    10.1002/cmdc.201000452
  44. Gaspar, A.; Silva, T.; Borges, F.. "Adenosine a3 receptors: A new therapeutic approach in cancer,Receptores a3 da adenosina: uma nova abordagem terapêutica no câncer". Quimica Nova 34 8 (2011): 1417-1424. http://www.scopus.com/inward/record.url?eid=2-s2.0-80054893720&partnerID=MN8TOARS.
    10.1590/S0100-40422011000800022
  45. Gaspar, A.; Martins, M.; Silva, P.; Garrido, E.M.; Garrido, J.; Firuzi, O.; Miri, R.; Saso, L.; Borges, F.. "Dietary phenolic acids and derivatives. Evaluation of the antioxidant activity of sinapic acid and its alkyl esters". Journal of Agricultural and Food Chemistry 58 21 (2010): 11273-11280. http://www.scopus.com/inward/record.url?eid=2-s2.0-78149321255&partnerID=MN8TOARS.
    10.1021/jf103075r
  46. Alcaro, S.; Gaspar, A.; Ortuso, F.; Milhazes, N.; Orallo, F.; Uriarte, E.; Yáñez, M.; Borges, F.. "Chromone-2- and -3-carboxylic acids inhibit differently monoamine oxidases A and B". Bioorganic and Medicinal Chemistry Letters 20 9 (2010): 2709-2712. http://www.scopus.com/inward/record.url?eid=2-s2.0-77950954802&partnerID=MN8TOARS.
    10.1016/j.bmcl.2010.03.081
  47. Gaspar, A.; Garrido, E.M.; Esteves, M.; Quezada, E.; Milhazes, N.; Garrido, J.; Borges, F.. "New insights into the antioxidant activity of hydroxycinnamic acids: Synthesis and physicochemical characterization of novel halogenated derivatives". European Journal of Medicinal Chemistry 44 5 (2009): 2092-2099. http://www.scopus.com/inward/record.url?eid=2-s2.0-62749186901&partnerID=MN8TOARS.
    10.1016/j.ejmech.2008.10.027
  48. Machado, N.F.L.; Calheiros, R.; Gaspar, A.; Garrido, J.; Borgesa, F.; Marques, M.P.M.. "Antioxidant phenolic esters with potential anticancer activity: Solution equilibria studied by Raman spectroscopy". Journal of Raman Spectroscopy 40 1 (2009): 80-85. http://www.scopus.com/inward/record.url?eid=2-s2.0-84962407137&partnerID=MN8TOARS.
    10.1002/jrs.2083
  49. Esteves, M.; Siquet, C.; Gaspar, A.; Rio, V.; Sousa, J.B.; Reis, S.; Marques, M.P.M.; Borges, F.. "Antioxidant versus cytotoxic properties of hydroxycinnamic acid derivatives - A new paradigm in phenolic research". Archiv der Pharmazie 341 3 (2008): 164-173. http://www.scopus.com/inward/record.url?eid=2-s2.0-44649198620&partnerID=MN8TOARS.
    10.1002/ardp.200700168
  50. Calheiros, R.; Machado, N.F.L.; Fiuza, S.M.; Gaspar, A.; Garrido, J.; Milhazes, N.; Borges, F.; Marques, M.P.M.. "Antioxidant phenolic esters with potential anticancer activity: A Raman spectroscopy study". Journal of Raman Spectroscopy 39 1 (2008): 95-107. http://www.scopus.com/inward/record.url?eid=2-s2.0-38549148538&partnerID=MN8TOARS.
    10.1002/jrs.1822
  51. Marques, M.P.M.; Borges, F.; Sousa, J.; Calheiros, R.; Garrido, J.; Gaspar, A.; Antunes, F.; Diniz, C.; Fresco, P.. "Cytotoxic and COX-2 inhibition properties of hydroxycinnamic derivatives". Letters in Drug Design and Discovery 3 5 (2006): 316-320. http://www.scopus.com/inward/record.url?eid=2-s2.0-33745603707&partnerID=MN8TOARS.
    10.2174/157018006777574212
Online resource
  1. Gaspar, Alexandra. Multi-target Design, Synthesis and Study of a Selected Series of Carbamates and Esters with Coumarin Scaffold. 2016. http://www.sciforum.net/conf/ecsoc-16/.
  2. Gaspar, Alexandra; Matos, Maria; Olea-azar, Claudio; Perez-Cruz, Fernanda; Borges, Fernanda; Gaspar, Alexandra; Santana, Lourdes; Janeiro, Patricia. Insights into the antioxidant activity of phenolic compounds: Synthesis and electrochemical study of new series of hydroxycoumarins. 2015. http://www.sciforum.net/presentation/617.
    10.3390/ecsoc-15-00617

Intellectual property

Patent
  1. Gaspar, Alexandra. 2009. "Cromonas e derivados de cromonas com actividade inibidora da monoamina oxidase e aplicações terapêuticas relacionadas". Portugal.
    Granted/Issued
  2. Gaspar, Alexandra. 2008. "Novel chromone derivatives, methods of synthesis therefor and use as antioxidants/preservatives". Portugal.
    Granted/Issued
  3. Gaspar, Alexandra. 2007. "Novos derivados de cromonas, respectivo processo de síntese e sua utilização como antioxidantes/conservantes".
    Granted/Issued

Other

Dataset
  1. Gaspar, Alexandra. CCDC 939914: Experimental Crystal Structure Determination.
    10.5517/cc10k1tf
Activities

Oral presentation

Presentation title Event name
Host (Event location)
2021/02/12 The influence of 4-oxoquinoline tautomerism in the MAOs inhibition 28th Young Research Fellows Meeting
Faculty of Pharmacy, University of Paris (Paris, France)
2020/03/05 Mapping the chromone-3-carboxamide pharmacophore: structure-activity-toxicity and efflux transport studies 4th WG meeting – MuTaLig COST Action – Final stutus of WG meeting Oral
Faculty of Pharmacy - Ege University - Izmir - Turkey (Izmir, Turkey)
2019/06 Looking for the Pharmacophore of Benzopyran MAO-B Inhibitors MedChem19 Catanzaro- IV annual COST ACTION CA15135 meeting/Paul Ehrlich Euro-PhD Network & MuTaLig COST Action meeting,
(Catanzaro, Italy)
2019/02 Design and development of new chemical entities for the treatment of Parkinson disease MuTaLig COST ACTION CA15135 3rd WG meeting
(Paris, France)
2018/05 Descoberta e desenvolvimento de novos antibacterianos contra bactérias multirresistentes 2ºEncontro Investigadores DQB-FCUP
(Porto, Portugal)
2014/06 Chromone: a valid scaffold in medicinal chemistry 4th Meeting of the Paul Ehrlich MedChem Euro-PhD Network
(Cracóvia, Czech Republic)
2014/06 “MITOCIN’S - the Highway to Target Bioactive Cinnamic Molecules to Mitochondria” World Congress on Polyphenols Applications: ISANH Polyphenols 2014
(Lisboa, Portugal)
2013/09 Discovery of dual-target agents based on chromone scaffold for Parkinson´s disease 3rd Meeting of the Paul Ehrlich MedChem Euro-PhD Network
(Calhari, Italy)
2013/04 Development of novel systems to delivery natural antioxidants to mitochondria: MitoCIN’s as a case study 47th Annual Scientific Meeting of the European Society for Clinical Investigation (ESCI)
(Albufeira, Portugal)
2013/02 Mitocondriotropic derivatives based on the natural polyphenol caffeic acid as an way out for oxidative stress related diseases IJUP13–6º Encontro de Jovens Investigadores da U. Porto–Porto
(Porto, Portugal)
2013/01 Chromone: a valid scaffold in Medicinal Chemistry 2nd Workshop on Medicinal Chemistry
(Porto)
2013/01 Bridging the gap between nature and phenolic antioxidants 2nd Workshop on Medicinal Chemistry
(Porto, Portugal)
2013/01 Development of Smart Carriers for delivering natural antioxidants to Mitochondria 2nd Workshop on Medicinal Chemistry Drug Discovery and Development: Understanding the R&D process
(Porto, Portugal)
2013 Caracterização do complexo de inclusão do fungicida pirimetanil com a 2-hidroxipropil-ß-ciclodextrina XIX Encontro Galego-Português de Química
(Vigo, Spain)
2013 Bridging the gap between nature and antioxidant therapy: development of mitochondria-targeted antioxidants based on benzoic scaffold IJUP13–6º Encontro de Jovens Investigadores da U. Porto
(Porto, Portugal)
2012 Development of innovative lipophilic hydroxycinnamic antioxidants: a solution to tackle mitochondrial oxidative damage V Encontro de Jovens Investigadores da UP (IJUP)–Porto
(Porto, Portugal)
2011/11 Striving for success in antioxidant therapy 10th Indo-Italian Workshop on Chemistry and Biology of Antioxidants
(Roma, Italy)
2011/11 New solutions for an old problem: surpassing the pharmacokinetic drawbacks of natural phenolic antioxidants 10th Indo-Italian Workshop on Chemistry and Biology of Antioxidants
(Roma, Italy)
2011/10 Toward the discovery of new lipophilic antioxidants based on cinnamic acid scaffold as mitochondria-directed neuroprotective agents 2nd World Congress on Targeting Mitochondria
(Berlim, Germany)
2011 Antioxidant therapy: in search of the magic bullet 2nd World Congress on Targeting Mitochondria
(Berlim, Germany)
2010/05 Chromones: a valid scaffold for the development of potent and selective MAO-B inhibitors III European Workshop in Drug Synthesis
(Siena, Italy)
2010 From nature to drug discovery: the chromone scaffold as a ‘privileged structure’ for the development of novel A3 receptor ligands III EWDSy- Third European Workshop in Drug Synthesis
(Siena, Italy)
2009 Searching for novel monoamine oxidase inhibitors based on chromone scaffold XXVIII Meeting of Clinical Pharmacology and IX Meeting of Toxicology
(Porto, Portugal)
2009 Adenosine receptor binding and neurotoxicity of novel chromone based ligands XL Meeting of Portuguese Society of Pharmacology, XXVIII Meeting of Clinical Pharmacology and IX Meeting of Toxicology
(Porto, Portugal)
2008/04 Metabolic Toxicology: from Synthesis to (Bio)analysis International Courses on Toxicology, Cell and Molecular Toxicology Research Area, Centre for Neurosciences and Cell Biology
(Coimbra, Portugal)
2007/12 Opening the Pandora box: The Syntab Contribution to the knowledge on the Toxic Effects of Drugs of Abuse and Their Metabolites XXXVIII Reunião Anual da Sociedade Portuguesa de Farmacologia; XXV Reunião de Farmacologia Clínica; VII Reunião de Toxicologia
(Coimbra, Portugal)
2006/10 Finding the Toxicophore: a Challenging Target in Medicinal Chemistry Medicinal Chemistry in the 21st Century
(Lisboa, Portugal)
2005/10 Phenolic Derivatives: A Study on the Relationship between Structure, Activity and Physicochemical Parameters Anti-Inflammatory Drugs
(Paris, France)

Supervision

Thesis Title
Role 		Degree Subject (Type)
Institution / Organization
2022/02 - 2022/07 Descoberta e desenvolvimento de novos antibacterianos contra microrganismos multirresistentes
Co-supervisor
 Química
Universidade do Porto Faculdade de Ciências, Portugal
2021/02 - 2021/07 síntese de novos antimicrobianos baseados em produtos naturais
Co-supervisor
 Química (Degree)
Universidade do Porto Faculdade de Ciências, Portugal
2020/01/03 - 2020/07 Síntese de novos antimicrobianos baseados em produtos naturais
Co-supervisor
 Quimica (Degree)
2020/01 - 2020/06 Desenvolvimento de novos antibióticos baseados em modelos naturais
Supervisor
 Projecto extracurricular (Degree)
Universidade do Porto Faculdade de Ciências, Portugal
2020/01 - 2020/06 Desenvolvimento de novos antibióticos baseados em modelos naturais
Supervisor
 Projecto extracurricular (Degree)
2019/01 - 2019/09 Desenvolvimento de novos agentes antimicrobianos baseados em modelos naturais
Co-supervisor
 Quimica (Degree)
2017 - 2019 Design and synthesis of chromone like derivatives as multitarget ligands: for neurodegeneratives diseases
Co-supervisor
 Doutoramento (PhD)
University “Magna Græcia, Italy
2016 - 2016 Evaluation of antioxidant activity of natural extracts
Co-supervisor
 Doutoramento (PhD)
Università degli Studi di Cagliari, Italy
2014 - 2014 Synthesis, Purification, characterization of Hydroxytirosol, Adenosine and lipoic acid derivatives and evaluation of their antioxidant profile
Co-supervisor
 Doutoramento (PhD)
Università degli Studi di Milano, Italy

Event organisation

Event name
Type of event (Role) 		Institution / Organization
2017/10/14 - Current Member of the organizing committee of the CIQUP’s workshop meeting (2017/10/17)
Meeting (Member of the Organising Committee)
 Universidade do Porto Centro de Investigação em Química, Portugal
2018/07/12 - 2018/07/14 Member of the organizing committee VIII Meeting of the Paul Ehrlich EuroPhD Network (2018/07/12 - 2018/07/14)
Congress (Member of the Organising Committee)
 Universidade do Porto Faculdade de Ciências, Portugal
2017/09/22 - 2017/09/24 Member of the organizing committee of the EpiChemBio (CM1406) and MuTaLig COST (CA15135) actions joint annual meeting :A bridge between EpiChemBio and MuTaLig COST Actions (2017/09/22)
Congress (Member of the Organising Committee)
 Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
2016/06/29 - 2016/07/01 Member of the Local Organizing Committee of the 10th World Congress on Polyphenols Applications (2016/06/29)
Congress (Member of the Organising Committee)
 Instituto Politécnico do Porto, Portugal

Jury of academic degree

Topic
Role 		Candidate name (Type of degree)
Institution / Organization
2022/02/11 Efeito de Chalconas em Células da Granulosa
(Thesis) Arguer
 Ruben Lourenço Seixas (Other)
Universidade do Porto Faculdade de Farmácia, Portugal
2019/07/18 Repurposing non-antibiotic drugs for antimicrobial purposes
(Thesis) Main arguer
 Cláudia Cristina Moreira Leão (Master)
Universidade do Porto Faculdade de Engenharia, Portugal
2019/07/10 Desenvolvimento de novos antioxidantes para o tratamento da doença de Alzheimer
(Thesis) Main arguer
 Cláudia Sofia Ferreira Pinto (Other)
Universidade do Porto Faculdade de Ciências, Portugal
2018/07/07 The use of phytochemicals with EDTA as catheter lock solutions
(Thesis) Main arguer
 João Pedro Rocha Vale (Master)
Universidade do Porto Faculdade de Engenharia, Portugal
2018/04/26 Single and multi-target agents for neurodegenerative diseases based on the chromone scaffold”
(Thesis) Arguer
 Joana Alexandra Costa Reis (PhD)
Faculdade de Ciencias Universidade do Porto, Portugal
2017/07/13 Síntese de derivados de piperazine com atividade inibitória da acetilcolinesterase como possível tratamento da Doenças de Alzheimer
(Thesis) Main arguer
 Tânia Catarina Pinto Moura (Other)
Universidade do Porto Faculdade de Ciências, Portugal
2017/07/07 Análisis y predicciones teóricas en medicamentos y alimentos
(Thesis) Main arguer
 Estela Guardado Yordi (PhD)
Universidade de Santiago de Compostela Departamento de Farmacoloxía Farmacia e Tecnoloxía Farmacéutica, Spain
2016/07/26 Desenvolvimento de novos antioxidantes tendo como base modelos naturais
(Thesis) Main arguer
 Mariana Fontoura da Fonseca Tavares Nogueira (Other)
Universidade do Porto Faculdade de Ciências, Portugal

Association member

Society Organization name Role
2016/04/18 - 2020/04/17 COST Action AGA-CA15135-1(MuTaLig) MC substitute member

Committee member

Activity description
Role 		Institution / Organization
2022 - 2022/09 Guest editor Special Issue "In Honor of Prof. Dr. Fernanda Borges’s Contribution"
Member
2020 - 2021/01/31 Guest Editor of Special Issue "New Insights into Antimicrobial Drug Discovery"
Member

Course / Discipline taught

Academic session Degree Subject (Type) Institution / Organization
2014 - Current Advances Methods in Structural Analysis Quimica e bioquimica (Mestrado) Universidade do Porto Faculdade de Ciências, Portugal
2014 - Current Métodos Avançados de análise estrutural (Mestrado) Universidade do Porto Faculdade de Ciências, Portugal

Journal scientific committee

Journal title (ISSN) Publisher
2018 - Current Current Medicinal Chemistry Bentham Science
2017 - Current MedChemComm RSC Publishing
2016 - Current Biofouling Taylor & Francis Online
2015 - Current European Journal of Medicinal Chemistry Elsevier
Distinctions

Award

2020 best oral communication" Mapping the chromone-3-phenylcarboxamide pharmacophore: structure-activity-cytotoxicity and efflux transport studies"
4th WG meeting – MuTaLig COST Action – Final stutus of WG meeting, Turkey

Other distinction

2014 Paul Ehrlich MedChem Euro-PhD award
2013 III Escuela de Verano de la SEQT “Medicinal Chemistry in Drug Discovery: The Pharma Perspective
2013 Top-10 most cited articles for the article “Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors” J. Med. Chem., 54 (14), 5165-5173.
2012 ADDF Young Investigator Scholarship
2011 Prémio Provincial al trabajo
2006 Prémio da Spectro para melhor comunicação científica