Search Results - "Bemis, Jean E."
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protein deacetylase SIRT1 is a negative regulator of metalloproteinase-9
Published in The FASEB journal (01-09-2009)“…Inappropriate elevation of matrix metalloproteinase-9 (MMP9) is reported to be involved in the pathogenesis of chronic obstructive pulmonary disease (COPD)…”
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Crystal Structures of Human SIRT3 Displaying Substrate-induced Conformational Changes
Published in The Journal of biological chemistry (04-09-2009)“…SIRT3 is a major mitochondrial NAD+-dependent protein deacetylase playing important roles in regulating mitochondrial metabolism and energy production and has…”
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3
Biochemical characterization, localization, and tissue distribution of the longer form of mouse SIRT3
Published in Protein science (01-03-2009)“…SIRT3 is a key mitochondrial protein deacetylase proposed to play key roles in regulating mitochondrial metabolism but there has been considerable debate about…”
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Discovery of oxazolo[4,5- b]pyridines and related heterocyclic analogs as novel SIRT1 activators
Published in Bioorganic & medicinal chemistry letters (15-04-2009)“…The identification and SAR of novel small molecule activators of SIRT1, which are structurally distinct and more potent than resveratrol ( 1), are described…”
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Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes
Published in Nature (29-11-2007)“…Calorie restriction extends lifespan and produces a metabolic profile desirable for treating diseases of ageing such as type 2 diabetes. SIRT1, an…”
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Synthesis and Characterization of Fatty Acid Conjugates of Niacin and Salicylic Acid
Published in Journal of medicinal chemistry (11-02-2016)“…This report describes the synthesis and preliminary biological characterization of novel fatty acid niacin conjugates and fatty acid salicylate conjugates…”
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Discovery of Imidazo[1,2-b]thiazole Derivatives as Novel SIRT1 Activators
Published in Journal of medicinal chemistry (12-03-2009)“…A series of imidazo[1,2-b]thiazole derivatives is shown to activate the NAD+-dependent deacetylase SIRT1, a potential new therapeutic target to treat various…”
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Discovery of Aminoquinazolines as Potent, Orally Bioavailable Inhibitors of Lck: Synthesis, SAR, and in Vivo Anti-Inflammatory Activity
Published in Journal of medicinal chemistry (21-09-2006)“…The lymphocyte-specific kinase (Lck) is a cytoplasmic tyrosine kinase of the Src family expressed in T cells and natural killer (NK) cells. Genetic evidence in…”
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Discovery of 4-amino-5,6-biaryl-furo[2,3- d]pyrimidines as inhibitors of Lck: Development of an expedient and divergent synthetic route and preliminary SAR
Published in Bioorganic & medicinal chemistry letters (15-04-2007)“…4-Amino-5,6-biaryl-furo[2,3- d]pyrimidines were identified as potent non-selective inhibitors of Lck. A novel, divergent, and practical synthetic route was…”
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Discovery of novel 2,3-diarylfuro[2,3- b]pyridin-4-amines as potent and selective inhibitors of Lck: Synthesis, SAR, and pharmacokinetic properties
Published in Bioorganic & medicinal chemistry letters (15-04-2007)“…2,3-Diarylfuro[2,3- b ]pyridine-4-amines are a novel class of potent and selective inhibitors of Lck. The discovery, synthesis, and structure activity…”
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Structure-Guided Design of Aminopyrimidine Amides as Potent, Selective Inhibitors of Lymphocyte Specific Kinase: Synthesis, Structure–Activity Relationships, and Inhibition of in Vivo T Cell Activation
Published in Journal of medicinal chemistry (27-03-2008)“…The lymphocyte-specific kinase (Lck), a member of the Src family of cytoplasmic tyrosine kinases, is expressed in T cells and natural killer (NK) cells…”
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Crystal Structures of Human SIRT[subscript 3] Displaying Substrate-induced Conformational Changes
Published in The Journal of biological chemistry (04-11-2009)“…SIRT3 is a major mitochondrial NAD{sup +}-dependent protein deacetylase playing important roles in regulating mitochondrial metabolism and energy production…”
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Erratum to “Discovery of novel 2,3-diarylfuro[2,3- b]pyridin-4-amines as potent and selective inhibitors of Lck: Synthesis, SAR, and pharmacokinetic properties” [Bioorg. Med. Chem. Lett. 17 (2007) 2299–2304]
Published in Bioorganic & medicinal chemistry letters (15-09-2007)Get full text
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Erratum to “Discovery of 4-amino-5,6-biaryl-furo[2,3- d]pyrimidines as inhibitors of Lck: Development of an expedient and divergent synthetic route and preliminary SAR” [Bioorg. Med. Chem. Lett. 17 (2007) 2305–2309]
Published in Bioorganic & medicinal chemistry letters (15-09-2007)Get full text
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