Search Results - "Barreca, Marilia"
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HSV-1 Glycoprotein D and Its Surface Receptors: Evaluation of Protein-Protein Interaction and Targeting by Triazole-Based Compounds through In Silico Approaches
Published in International journal of molecular sciences (01-04-2023)“…Protein-protein interactions (PPI) represent attractive targets for drug design. Thus, aiming at a deeper insight into the HSV-1 envelope glycoprotein D (gD),…”
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2
Marine Anticancer Agents: An Overview with a Particular Focus on Their Chemical Classes
Published in Marine drugs (04-12-2020)“…The marine environment is a rich source of biologically active molecules for the treatment of human diseases, especially cancer. The adaptation to unique…”
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3
Evaluation of Fused Pyrrolothiazole Systems as Correctors of Mutant CFTR Protein
Published in Molecules (Basel, Switzerland) (26-02-2021)“…Cystic fibrosis (CF) is a genetic disease caused by mutations that impair the function of the CFTR chloride channel. The most frequent mutation, F508del,…”
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Insight on [1,3]thiazolo[4,5-e]isoindoles as tubulin polymerization inhibitors
Published in European journal of medicinal chemistry (15-02-2021)“…A series of [1,3]thiazolo[4,5-e]isoindoles has been synthesized through a versatile and high yielding multistep sequence. Evaluation of the antiproliferative…”
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The New Microtubule-Targeting Agent SIX2G Induces Immunogenic Cell Death in Multiple Myeloma
Published in International journal of molecular sciences (06-09-2022)“…Microtubule-targeting agents (MTAs) are effective drugs for cancer treatment. A novel diaryl [1,2]oxazole class of compounds binding the colchicine site was…”
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6
Novel tricyclic pyrrolo-quinolines as pharmacological correctors of the mutant CFTR chloride channel
Published in Scientific reports (10-05-2023)“…F508del, the most frequent mutation in cystic fibrosis (CF), impairs the stability and folding of the CFTR chloride channel, thus resulting in intracellular…”
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Recurrence of the oxazole motif in tubulin colchicine site inhibitors with anti-tumor activity
Published in European journal of medicinal chemistry reports (01-07-2021)“…Because of its wide spectrum of targets and biological activities, the oxazole ring is a valuable heterocyclic scaffold in the design of new therapeutic agents…”
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Editorial: Emerging heterocycles as bioactive compounds
Published in Frontiers in chemistry (26-04-2023)Get full text
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9
Antibody-drug conjugates for lymphoma patients: preclinical and clinical evidences
Published in Exploration of targeted anti-tumor therapy (2022)“…Antibody-drug conjugates (ADCs) are a recent, revolutionary approach for malignancies treatment, designed to provide superior efficacy and specific targeting…”
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10
Pharmacologic screen identifies active combinations with BET inhibitors and LRRK2 as a novel putative target in lymphoma
Published in EJHaem (01-08-2022)“…Inhibitors of the Bromo‐ and Extra‐Terminal domain (BET) family proteins have strong preclinical antitumor activity in multiple tumor models, including…”
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An overview on anti-tubulin agents for the treatment of lymphoma patients
Published in Pharmacology & therapeutics (Oxford) (01-07-2020)“…Anti-tubulin agents constitute a large class of compounds with broad activity both in solid tumors and hematologic malignancies, due to the interference with…”
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12
New strategies to hit hematological cancers
Published in European journal of medicinal chemistry (15-04-2024)Get full text
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13
Advances in developing noncovalent small molecules targeting Keap1
Published in Drug discovery today (01-12-2023)“…Kelch-like ECH-associated protein 1 (Keap1) is a drug target for diseases involving oxidative stress and inflammation. There are three covalent Keap1-binding…”
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Insight on pyrimido[5,4-g]indolizine and pyrimido[4,5-c]pyrrolo[1,2-a]azepine systems as promising photosensitizers on malignant cells
Published in European journal of medicinal chemistry (05-07-2022)“…Searching for new small molecules as photosensitizing agents, we have developed a class of twenty-five pyrimido[5,4-g]indolizine and…”
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Novel insights on [1,2]oxazolo[5,4‐e]isoindoles on multidrug resistant acute myeloid leukemia cell line
Published in Drug development research (01-09-2022)“…A series of [1,2]oxazolo[5,4‐e]isoindole derivatives was evaluated against HL‐60 cell line and its multidrug resistance (MDR) variant, HL‐60R, resistant to…”
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Synthesis of 2H-Imidazo[2′,1':2,3] [1,3]thiazolo[4,5-e]isoindol-8-yl-phenylureas with promising therapeutic features for the treatment of acute myeloid leukemia (AML) with FLT3/ITD mutations
Published in European journal of medicinal chemistry (05-05-2022)“…Despite progressive advances in understanding the molecular biology of acute myeloid leukemia (AML), the conventional therapeutic approach has not changed…”
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Insight into non-nucleoside triazole-based systems as viral polymerases inhibitors
Published in European journal of medicinal chemistry (05-03-2023)“…Viruses have been recognized as the etiological agents responsible for many pathological conditions ranging from asymptomatic infections to serious diseases,…”
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Pyrrolo[2′,3′:3,4]cyclohepta[1,2‑d][1,2]oxazoles, a New Class of Antimitotic Agents Active against Multiple Malignant Cell Types
Published in Journal of medicinal chemistry (22-10-2020)“…A new class of pyrrolo[2′,3′:3,4]cyclohepta[1,2-d][1,2]oxazoles was synthesized for the treatment of hyperproliferative pathologies, including neoplasms…”
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Identification of pyrrolo[3′,4’:3,4]cyclohepta[1,2-d][1,2]oxazoles as promising new candidates for the treatment of lymphomas
Published in European journal of medicinal chemistry (05-06-2023)“…Unsatisfactory outcomes for relapsed/refractory lymphoma patients prompt continuing efforts to develop new therapeutic strategies. Our previous studies on…”
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Current development of CFTR potentiators in the last decade
Published in European journal of medicinal chemistry (15-10-2020)“…Cystic fibrosis (CF) is a genetic disorder produced by the loss of function of CFTR, a main chloride channel involved in transepithelial salt and water…”
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