Search Results - "Stanczak, Paulina"
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A Novel Oral Arginase 1/2 Inhibitor Enhances the Antitumor Effect of PD-1 Inhibition in Murine Experimental Gliomas by Altering the Immunosuppressive Environment
Published in Frontiers in oncology (24-08-2021)“…Glioblastomas (GBM) are the common and aggressive primary brain tumors that are incurable by conventional therapies. Immunotherapy with immune checkpoint…”
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Discovery and Pharmacokinetics of Sulfamides and Guanidines as Potent Human Arginase 1 Inhibitors
Published in ACS medicinal chemistry letters (09-04-2020)“…We designed and synthesized a series of arginase inhibitors as derivatives of the well-known 2-(S)-amino-6-boronohexanoic acid (ABH) with basic and neutral…”
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Inhibition of arginase modulates T-cell response in the tumor microenvironment of lung carcinoma
Published in Oncoimmunology (01-01-2021)“…Immunotherapy has demonstrated significant activity in a broad range of cancer types, but still the majority of patients receiving it do not maintain durable…”
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Discovery and optimization of novel pyrazole-benzimidazole CPL304110, as a potent and selective inhibitor of fibroblast growth factor receptors FGFR (1–3)
Published in European journal of medicinal chemistry (15-01-2021)“…The FGFR family is characterized by four receptors (FGFR 1–4), binding to 18 ligands called fibroblast growth factors (FGFs). Aberrant activation of FGFs and…”
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Preclinical characterization of CPL304110 as a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3 for gastric, bladder, and squamous cell lung cancer
Published in Frontiers in oncology (2023)“…Fibroblast Growth Factor Receptors (FGFRs) are a family of receptor tyrosine kinases expressed on a plethora of cell membranes. They play crucial roles in both…”
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Design, Synthesis, and Development of pyrazolo[1,5-a]pyrimidine Derivatives as a Novel Series of Selective PI3Kδ Inhibitors: Part I—Indole Derivatives
Published in Pharmaceuticals (Basel, Switzerland) (30-07-2022)“…Phosphoinositide 3-kinase δ (PI3Kδ), a member of the class I PI3K family, is an essential signaling biomolecule that regulates the differentiation,…”
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Arginase 1/2 Inhibitor OATD-02: From Discovery to First-in-man Setup in Cancer Immunotherapy
Published in Molecular cancer therapeutics (05-07-2023)“…Pharmacologic inhibition of the controlling immunity pathway enzymes arginases 1 and 2 (ARG1 and ARG2) is a promising strategy for cancer immunotherapy. Here,…”
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Abstract B003: Development of OAT-1746, a novel arginase 1 and 2 inhibitor for cancer immunotherapy
Published in Molecular cancer therapeutics (01-01-2018)“…Abstract Depletion of arginine represents an important mechanism of immunosuppression, and high plasma and tumor arginase (ARG) activity has been demonstrated…”
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OATD-02 Validates the Benefits of Pharmacological Inhibition of Arginase 1 and 2 in Cancer
Published in Cancers (01-08-2022)“…Background: Arginases play essential roles in metabolic pathways, determining the fitness of both immune and tumour cells. Along with the previously validated…”
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Design, Synthesis, and Development of pyrazolo[1,5-Ia/I]pyrimidine Derivatives as a Novel Series of Selective PI3KIδ/I Inhibitors: Part I—Indole Derivatives
Published in Pharmaceuticals (Basel, Switzerland) (01-07-2022)“…Phosphoinositide 3-kinase δ (PI3Kδ), a member of the class I PI3K family, is an essential signaling biomolecule that regulates the differentiation,…”
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