Search Results - "Cuny, Gregory"
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RIPK protein kinase family: Atypical lives of typical kinases
Published in Seminars in cell & developmental biology (01-01-2021)“…Receptor Interacting Protein Kinases (RIPKs) are a family of Ser/Thr/Tyr kinases whose functions, regulation and pathophysiologic roles have remained an enigma…”
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2
A Mild, One-Pot Stadler-Ziegler Synthesis of Arylsulfides Facilitated by Photoredox Catalysis in Batch and Continuous-Flow
Published in Angewandte Chemie International Edition (22-07-2013)“…Visible advance: A mild, one‐pot Stadler–Ziegler process for CS bond formation has been developed. The method employs the photoredox catalyst [Ru(bpy)3Cl2]⋅6…”
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3
Syntheses of Gymnothespirolignans B and C and Non-natural Isomer 9‑Epi-gymnothespirolignan B
Published in Journal of organic chemistry (06-08-2021)“…Syntheses of polycyclic spiro lignans gymnothespirolignans B and C as well as the unnatural isomer 9-epi-gymnothespirolignan B were accomplished using…”
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4
A new class of small molecule inhibitor of BMP signaling
Published in PloS one (30-04-2013)“…Growth factor signaling pathways are tightly regulated by phosphorylation and include many important kinase targets of interest for drug discovery. Small…”
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5
8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities
Published in Molecules (Basel, Switzerland) (27-07-2021)“…Aporphines, a major group of aporphinoid alkaloids, exhibit interesting and diverse pharmacological activities. A set of dimeric aporphines with an aryloxy…”
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6
Microwave assisted copper-free Sonogashira coupling/5-exo- dig cycloisomerization domino reaction: access to 3-(phenylmethylene)isoindolin-1-ones and related heterocycles
Published in Tetrahedron letters (19-10-2011)“…An efficient microwave assisted one-pot synthesis of substituted 3-(phenylmethylene)isoindolin-1-ones is reported via a copper-free Sonogashira coupling and a…”
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7
Structure Guided Design of Potent and Selective Ponatinib-Based Hybrid Inhibitors for RIPK1
Published in Cell reports (Cambridge) (24-03-2015)“…RIPK1 and RIPK3, two closely related RIPK family members, have emerged as important regulators of pathologic cell death and inflammation. In the current work,…”
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8
Identification of RIP1 kinase as a specific cellular target of necrostatins
Published in Nature chemical biology (01-05-2008)“…Necroptosis is a cellular mechanism of necrotic cell death induced by apoptotic stimuli in the form of death domain receptor engagement by their respective…”
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9
Inhibitor of the tyrosine phosphatase STEP reverses cognitive deficits in a mouse model of Alzheimer's disease
Published in PLoS biology (01-08-2014)“…STEP (STriatal-Enriched protein tyrosine Phosphatase) is a neuron-specific phosphatase that regulates N-methyl-D-aspartate receptor (NMDAR) and…”
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10
Pharmacologic Inhibition of the Anaphase-Promoting Complex Induces A Spindle Checkpoint-Dependent Mitotic Arrest in the Absence of Spindle Damage
Published in Cancer cell (19-10-2010)“…Microtubule inhibitors are important cancer drugs that induce mitotic arrest by activating the spindle assembly checkpoint (SAC), which, in turn, inhibits the…”
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11
Genetic ablation of purine salvage in Cryptosporidium parvum reveals nucleotide uptake from the host cell
Published in Proceedings of the National Academy of Sciences - PNAS (15-10-2019)“…The apicomplexan parasite Cryptosporidium is a leading global cause of severe diarrheal disease and an important contributor to early-childhood mortality…”
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12
Design of pyrido[2,3-d]pyrimidin-7-one inhibitors of receptor interacting protein kinase-2 (RIPK2) and nucleotide-binding oligomerization domain (NOD) cell signaling
Published in European journal of medicinal chemistry (05-04-2021)“…Receptor interacting protein kinase-2 (RIPK2) is an enzyme involved in the transduction of pro-inflammatory nucleotide-binding oligomerization domain (NOD)…”
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13
Small-molecule inhibitors of USP1 target ID1 degradation in leukemic cells
Published in Molecular cancer therapeutics (01-12-2013)“…Inhibitor of DNA binding 1 (ID1) transcription factor is essential for the proliferation and progression of many cancer types, including leukemia. However, the…”
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14
A small molecule exerts selective antiviral activity by targeting the human cytomegalovirus nuclear egress complex
Published in PLoS pathogens (17-11-2023)“…Human cytomegalovirus (HCMV) is an important pathogen for which new antiviral drugs are needed. HCMV, like other herpesviruses, encodes a nuclear egress…”
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15
Development of Rofecoxib-Based Fluorescent Probes and Investigations on Their Solvatochromism, AIE Activity, Mechanochromism, and COX-2-Targeted Bioimaging
Published in Analytical chemistry (Washington) (07-09-2021)“…Cyclooxygenase-2 (COX-2) fluorescent probes are promising tools for early diagnosis of cancer. Traditionally, COX-2 probes were designed by connecting two…”
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16
Restored glial glutamate transporter EAAT2 function as a potential therapeutic approach for Alzheimer's disease
Published in The Journal of experimental medicine (09-03-2015)“…Glutamatergic systems play a critical role in cognitive functions and are known to be defective in Alzheimer's disease (AD) patients. Previous literature has…”
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17
BMP type I receptor inhibition reduces heterotopic ossification
Published in Nature medicine (01-12-2008)“…Ectopic ossification often involves the transformation of soft tissue into bone. In this new study, Paul Yu et al. show that inflammation is a key step in…”
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18
Necroptosis, a novel form of caspase-independent cell death, contributes to neuronal damage in a retinal ischemia-reperfusion injury model
Published in Journal of neuroscience research (15-05-2010)“…Necroptosis is programmed necrosis triggered by death receptor signaling. We investigated whether necroptosis contributes to neuronal damage and functional…”
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Akt Regulates TNFα synthesis downstream of RIP1 kinase activation during necroptosis
Published in PloS one (01-03-2013)“…Necroptosis is a regulated form of necrotic cell death that has been implicated in the pathogenesis of various diseases including intestinal inflammation and…”
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20
Structure–Activity Relationship of 3,5-Diaryl-2-aminopyridine ALK2 Inhibitors Reveals Unaltered Binding Affinity for Fibrodysplasia Ossificans Progressiva Causing Mutants
Published in Journal of medicinal chemistry (09-10-2014)“…There are currently no effective therapies for fibrodysplasia ossificans progressiva (FOP), a debilitating and progressive heterotopic ossification disease…”
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