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Showing 1 to 5 of 5 for “"SHIP inhibitors"”.
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CONVENIENT ETHERIFICATION USING TRICHLOROACETIMIDATES AND SYNTHESIS OF AMINOSTEROID SHIP INHIBITORS
… by the kinase PI3K and the phosphatases PTEN and SHIP.</p> <p>SHIP1 is an SH2-containing inositol 5’-phosphatase found in blood cells that is responsible for the hydrolysis of phosphatidylinositol-3,4,5-trisphosphate to phosphatidylinositol-4,5-bisphosphate. This enzyme is part of a major cellular …
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A Modular Approach to Highly Functionalized Indole Derivatives and Syntheses of Tryptamine-based SHIP Inhibitors
… with their analogs, are recognized as potent SHIP inhibitors and are considered privileged structures due their binding properties and diverse biological targeting. Also, the pyrrolo[2,3-a]indoline frameworks have been recognized as key structural motifs in many anticancer and psychoactive …
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Trichloroacetimidates as Alkylating Reagents in C-N Bond Formation and Synthesis of Aminosteroid and Quinoline Inhibitors of Src Homology 2 Domain-Containing Inositol Phosphatase (SHIP)
… of the SH2-containing inositol 5’-phosphatase (SHIP) can modulate the dephosphorylation of phosphoinositols. These molecules act as second messengers in a signal transduction cascade, with the placement of phosphorylation on the inositol acting to convey information in the transmission of …
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Trichloroacetimidates as Alkylating Reagents and Their Application in the Synthesis of Pyrroloindoline Natural Products and Synthesis of Small Molecule Inhibitors of Src Homology 2 Domain- Containing Inositol Phosphatase (SHIP)
… to the above work, synthesis of small molecule inhibitors of Src Homology 2 Domain-Containing Inositol Phosphatase (SHIP) has also been described. Aberrations in the phosphoinositide 3-kinase (PI3K) cellular signaling pathway can lead to diseased cellular states like cancer. Herein we have …
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Synthesis, Design, and Biological Evaluation of Inhibitors and Activators of Src Homology 2 Domain-Containing Inositol Phosphatase (SHIP) and Synthetic Studies of Apicularen A and Maoecrystal V
… and biological evaluation of aminosteroids as inhibitors for the SH2-containing inositol phosphatase 1 (SHIP1). SHIP1, a 145 kDa protein, is involved in regulating the formation of new blood cells. High- throughput screening identified several SHIP inhibitors including NSC23922, a mixture of …