Search Results - "Qi, Ziping"
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Heat shock proteins: Biological functions, pathological roles, and therapeutic opportunities
Published in MedComm (2020) (01-09-2022)“…The heat shock proteins (HSPs) are ubiquitous and conserved protein families in both prokaryotic and eukaryotic organisms, and they maintain cellular…”
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Inhibition of the deubiquitinating enzyme USP47 as a novel targeted therapy for hematologic malignancies expressing mutant EZH2
Published in Leukemia (01-04-2022)“…Activating mutations in EZH2, the catalytic component of PRC2, promote cell proliferation, tumorigenesis, and metastasis through enzymatic or non-enzymatic…”
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Nintedanib overcomes drug resistance from upregulation of FGFR signalling and imatinib‐induced KIT mutations in gastrointestinal stromal tumours
Published in Molecular oncology (01-04-2022)“…Drug resistance remains a major challenge in the clinical treatment of gastrointestinal stromal tumours (GISTs). While acquired on‐target mutations of…”
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Discovery of a novel and highly selective CDK9 kinase inhibitor (JSH-009) with potent antitumor efficacy in preclinical acute myeloid leukemia models
Published in Investigational new drugs (01-10-2020)“…Summary Acute myeloid leukemia (AML) is reported to be vulnerable to transcription disruption due to transcriptional addiction. Cyclin-dependent kinase 9…”
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Selectively targeting FLT3-ITD mutants over FLT3-wt by a novel inhibitor for acute myeloid leukemia
Published in Haematologica (Roma) (01-02-2021)Get full text
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Discovery of a highly selective VEGFR2 kinase inhibitor CHMFL-VEGFR2-002 as a novel anti-angiogenesis agent
Published in Acta pharmaceutica Sinica. B (01-03-2020)“…Angiogenesis is an essential process in tumor growth, invasion and metastasis. VEGF receptor 2 (VEGFR2) inhibitors targeting tumor angiogenic pathway have been…”
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Infiltrating neutrophils aggravate metabolic liver failure in fah-deficient mice
Published in Liver international (01-03-2015)“…Background & Aims Mice deficient in tyrosine catabolic enzyme fumarylacetoacetate hydrolase (fah−/−) was a useful animal model for studying liver failure…”
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Irreversible inhibition of BTK kinase by a novel highly selective inhibitor CHMFL-BTK-11 suppresses inflammatory response in rheumatoid arthritis model
Published in Scientific reports (28-03-2017)“…BTK plays a critical role in the B cell receptor mediated inflammatory signaling in the rheumatoid arthritis (RA). Through a rational design approach we…”
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Discovery of IHMT-MST1-39 as a novel MST1 kinase inhibitor and AMPK activator for the treatment of diabetes mellitus
Published in Signal transduction and targeted therapy (05-04-2023)“…Insulin-producing pancreatic β cell death is the fundamental cause of type 1 diabetes (T1D) and a contributing factor to type 2 diabetes (T2D). Moreover,…”
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Low dose of emetine as potential anti-SARS-CoV-2 virus therapy: preclinical in vitro inhibition and in vivo pharmacokinetic evidences
Published in Molecular biomedicine (30-11-2020)“…The global pandemic of COVID-19 has attracted extensive drug searching interets for the new coronavirus SARS-CoV-2. Although currently several of clinically…”
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Bone marrow transplantation concurrently reconstitutes donor liver and immune system across host species barrier in mice
Published in PloS one (05-09-2014)“…Liver immunopathologic mechanisms during hepatotropic infection, malignant transformation, and autoimmunity are still unclear. Establishing a chimeric mouse…”
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Discovery of a highly selective KIT kinase primary V559D mutant inhibitor for gastrointestinal stromal tumors (GISTs)
Published in Oncotarget (19-12-2017)“…KIT kinase V559D mutation is the most prevalent primary gain-of-function mutation in Gastrointestinal Stromal Tumors (GISTs). Here we reported a highly…”
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Discovery of Pyrazolo1,5-apyridine Derivatives as Potent and Selective PI3Kγ/δ Inhibitors
Published in Journal of medicinal chemistry (12-09-2024)“…PI3Kγ and PI3Kδ plays critical roles in exerting immunosuppression by targeting regulatory T cells and myeloid cells. Dual inhibition of PI3Kγ and PI3Kδ has…”
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Discovery of Pyrazolo[1,5- a ]pyridine Derivatives as Potent and Selective PI3Kγ/δ Inhibitors
Published in Journal of medicinal chemistry (20-08-2024)“…PI3Kγ and PI3Kδ plays critical roles in exerting immunosuppression by targeting regulatory T cells and myeloid cells. Dual inhibition of PI3Kγ and PI3Kδ has…”
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Magnetosome-inspired synthesis of soft ferrimagnetic nanoparticles for magnetic tumor targeting
Published in Proceedings of the National Academy of Sciences - PNAS (08-11-2022)“…Magnetic targeting is one of the most promising approaches for improving the targeting efficiency by which magnetic drug carriers are directed using external…”
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Discovery of Pyrazolo[1,5-a]pyrimidine derivative as a potent and selective PI3Kγ/δ dual inhibitor
Published in European journal of medicinal chemistry (15-11-2023)“…Phosphoinositol 3-kinases (PI3Ks) γ and δ are primarily expressed in leukocytes and play crucial roles in regulation of the immune system. Dual inhibition of…”
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Discovery of a highly potent pan-RAF inhibitor IHMT-RAF-128 for cancer treatment
Published in European journal of pharmacology (05-08-2023)“…Although rat sarcoma viral oncogene homolog (RAS) mutations occur in about 30% of solid tumors, targeting RAS mutations other than KRAS-G12C is still…”
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Discovery of IHMT-MST1-58 as a Novel, Potent, and Selective MST1 Inhibitor for the Treatment of Type 1/2 Diabetes
Published in Journal of medicinal chemistry (08-09-2022)“…The critical pathogenesis of type 1 diabetes (T1D)/type 2 diabetes (T2D) is the physical status, mass, and function of pancreatic β cells. Mammalian STE20-like…”
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Discovery of (S)‑2-(1-(4-Amino-3-(3-fluoro-4-methoxyphenyl)‑1H‑pyrazolo[3,4‑d]pyrimidin-1-yl)propyl)-3-cyclopropyl-5-fluoroquinazolin-4(3H)‑one (IHMT-PI3Kδ-372) as a Potent and Selective PI3Kδ Inhibitor for the Treatment of Chronic Obstructive Pulmonary Disease
Published in Journal of medicinal chemistry (25-11-2020)“…Accumulated pieces of evidence have shown that PI3Kδ plays a critical role in chronic obstructive pulmonary disease (COPD). Using a fragment-hybrid approach,…”
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