Giulia Bianchini

University of Cambridge — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

8h-index212citations18works0.02yr avg
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Research Topics

Cancer therapeutics and mechanisms(5), Bioactive Compounds and Antitumor Agents(4), Crystallization and Solubility Studies(3), X-ray Diffraction in Crystallography(3), Synthesis and Biological Evaluation(3)

Publications18 total

Straightforward, scalable, solution-phase synthesis of peptide bonds in flow
Journal of Flow Chemistry·2025Open Access
Il paziente oncologico e i meccanismi di cardiotossicità
Cardiologia Ambulatoriale·2023Open Access
Bifunctional carbazole derivatives for simultaneous therapy and fluorescence imaging in prion disease murine cell models
European Journal of Medicinal Chemistry·2022· 14 citedOpen Access
D-Ring-Modified Analogues of Luotonin A with Reduced Planarity: Design, Synthesis, and Evaluation of Their Topoisomerase Inhibition-Associated Cytotoxicity
BioMed Research International·2019· 9 citedOpen Access
Front Cover: Rearrangement Reactions in Aza‐Vinylogous Povarov Products: Metal‐Free Synthesis of C<sup>3</sup>‐Functionalized Quinolines and Studies on their Synthetic Application (Eur. J. Org. Chem. 38/2019)
European Journal of Organic Chemistry·2019Open Access
Rearrangement Reactions in Aza‐Vinylogous Povarov Products: Metal‐Free Synthesis of C<sup>3</sup>‐Functionalized Quinolines and Studies on their Synthetic Application
European Journal of Organic Chemistry·2019· 5 cited
Design and synthesis of A- and D ring-modified analogues of luotonin A with reduced planarity
Tetrahedron Letters·2019· 11 cited
CCDC 1537459: Experimental Crystal Structure Determination
The Cambridge Structural Database·2019Open Access
Crassiflorone derivatives that inhibit Trypanosoma brucei glyceraldehyde-3-phosphate dehydrogenase ( Tb GAPDH) and Trypanosoma cruzi trypanothione reductase ( Tc TR) and display trypanocidal activity
European Journal of Medicinal Chemistry·2017· 31 citedOpen Access
Design, synthesis and antiproliferative activity of decarbonyl luotonin analogues
European Journal of Medicinal Chemistry·2017· 42 cited
Development and applications of the aza-vinylogous Povarov reaction of α-ketoimines
LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)·2017Open Access
CCDC 1439465: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
CCDC 997064: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
ChemInform Abstract: Efficient Synthesis of 2‐Acylquinolines Based on an Aza‐Vinylogous Povarov Reaction.
ChemInform·2016
Tetrahydroisoquinoline-Derived Urea and 2,5-Diketopiperazine Derivatives as Selective Antagonists of the Transient Receptor Potential Melastatin 8 (TRPM8) Channel Receptor and Antiprostate Cancer Agents
Journal of Medicinal Chemistry·2016· 31 citedOpen Access
Efficient synthesis of 2-acylquinolines based on an aza-vinylogous Povarov reaction
Organic Chemistry Frontiers·2016· 46 cited
一過性受容体電位メラスタチン8(TRPM8)チャンネル受容体の選択的アンタゴニストおよび抗前立腺腫瘍薬としてのテトラヒドロキノリン誘導尿素および2,5‐ジケトピペラジン誘導体
Journal of Medicinal Chemistry·2016
B-Ring-Aryl Substituted Luotonin A Analogues with a New Binding Mode to the Topoisomerase 1-DNA Complex Show Enhanced Cytotoxic Activity
PLoS ONE·2014· 23 citedOpen Access

Frequent Co-authors

J. Carlos Menéndez(14), Abdulrahman I. Almansour(6), Natarajan Arumugam(6), Raju Suresh Kumar(6), Mohammad Altaf(6), Pascual Ribelles(5), M. Teresa Ramos(5), Sakkarapalayam M. Mahalingam(3), Samaresh Sau(3), Hazem A. Ghabbour(3), M. Antonia Martín(3), Diana Becerra(2), María Laura Bolognesi(2), Pierangelo Orlando(2), Pilar López‐Alvarado(2), Dhaifallah M. Al‐thamili(2), Govindasami Periyasami(2), José Clerigué(2), Tomás Tejero(2), Pedro Merino(2)