Search Results - "Taylor, Merry"
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Discovery of Potent and Selective SH2 Inhibitors of the Tyrosine Kinase ZAP-70
Published in Journal of medicinal chemistry (07-10-1999)“…A series of 1,2,4-oxadiazole analogues has been shown to be potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70, a potential therapeutic target…”
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Early Point-of-Care Testing at Triage Reduces Care Time in Stable Adult Emergency Department Patients
Published in The Journal of emergency medicine (01-08-2018)“…Core laboratory testing may increase length of stay and delay care. We compared length of emergency department (ED) care in patients receiving point-of-care…”
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Diagnostic Characteristics of a Clinical Screening Tool in Combination With Measuring Bedside Lactate Level in Emergency Department Patients With Suspected Sepsis
Published in Academic emergency medicine (01-08-2014)“…Background Early identification of sepsis and initiation of aggressive treatment saves lives. However, the diagnosis of sepsis may be delayed in patients…”
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Structure-Based Design of an Osteoclast-Selective, Nonpeptide Src Homology 2 Inhibitor with in vivo Antiresorptive Activity
Published in Proceedings of the National Academy of Sciences - PNAS (15-08-2000)“…Targeted disruption of the pp60src(Src) gene has implicated this tyrosine kinase in osteoclast-mediated bone resorption and as a therapeutic target for the…”
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Bone-Targeted Src kinase inhibitors: novel pyrrolo- and pyrazolopyrimidine analogues
Published in Bioorganic & medicinal chemistry letters (15-09-2003)“…Src tyrosine kinase is a therapeutic target for bone diseases that has been validated by gene knockout studies. Furthermore, in vitro cellular studies…”
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X-ray Structure of Citrate Bound to Src SH2 Leads to a High-Affinity, Bone-Targeted Src SH2 Inhibitor
Published in Journal of medicinal chemistry (01-03-2001)“…Numerous studies provide compelling evidence that the protein tyrosine kinase pp60 super(c-Src) (Src) plays a crucial role in osteoclast-mediated bone…”
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Bone-Targeted pyrido[2,3- d]pyrimidin-7-ones: potent inhibitors of Src tyrosine kinase as novel antiresorptive agents
Published in Bioorganic & medicinal chemistry letters (15-09-2003)“…The design of bone-targeted pyrido[2,3- d]pyrimidin-7-ones as Src tyrosine kinase inhibitors is described. Leveraging SAR from known compounds and using…”
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Structure-based design of novel nonpeptide inhibitors of the Src SH2 domain: Phosphotyrosine mimetics exploiting multifunctional group replacement chemistry
Published in Biopolymers (2003)“…A series of novel nonpeptide inhibitors of the pp60c‐Src (Src) SH2 domain is described that exploit multifunctional group replacement of the phenylphosphate…”
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Structure-activity relationships of a novel class of Src SH2 inhibitors
Published in Bioorganic & medicinal chemistry letters (16-08-1999)“…The structure-activity relationships (SAR) of a novel class of Src SH2 inhibitors are described. Variation at the pY+1 and pY+3 side chain positions using 2,4-…”
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A novel phosphotyrosine mimetic 4'-carboxymethyloxy-3'-phosphonophenylalanine (Cpp): exploitation in the design of nonpeptide inhibitors of pp60(Src) SH2 domain
Published in Bioorganic & medicinal chemistry letters (03-09-2001)“…The novel phosphotyrosine (pTyr) mimetic 4'-carboxymethyloxy-3'-phosphonophenylalanine (Cpp) has been designed and incorporated into a series of nonpeptide…”
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A novel phosphotyrosine mimetic 4′-carboxymethyloxy-3′-phosphonophenylalanine (cpp): exploitation in the design of nonpeptide inhibitors of pp60 Src SH2 domain
Published in Bioorganic & medicinal chemistry letters (2001)“…The novel phosphotyrosine (pTyr) mimetic 4′-carboxymethyloxy-3′-phosphonophenylalanine (Cpp) has been designed and incorporated into a series of nonpeptide…”
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Novel phosphate ester-linked resins: The solid-phase generation of phenyl phosphate-containing compounds for SH2 inhibition
Published in Tetrahedron letters (21-05-1998)“…An efficient method for the preparation of protected phosphate ester-linked resins in high yield and purity is presented. Variation in tether…”
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