Search for dissertations about: "Quinoline-3-carboxamide"
Showing result 1 - 5 of 7 swedish dissertations containing the word Quinoline-3-carboxamide.
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1. Effect of the quinoline-3-carboxamide ABR-215757 during inflammation
Abstract : ABR-215757 (5757) is a quinoline-3-carboxamide (Q-compound) currently in clinical development for systemic sclerosis. Q-compounds have shown efficacy in several different models of autoimmune diseases such as experimental autoimmune encephalomyelitis (EAE) and collagen induced arthritis. However, the mechanism of action is still poorly understood. READ MORE
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2. Metabolism of quinoline 3-carboxamide compounds, a group of synthetic immunomodulators, in various species
Abstract : Cytochrome P450 (CYP) is involved in the metabolism of the majority of clinically used drugs. We have studied the CYP mediated metabolism of quinoline 3-carboxamides, a group of synthetic immunomodulators in liver microsomal preparations from various species. READ MORE
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3. Effect of quinoline-3-carboxamides on myeloid cells in inflammation and cancer
Abstract : The quinoline-3-carboxamides (Q compounds) are a family of small molecules that ameliorate various types of murine inflammatory autoimmune disease. One such compound has also demonstrated anti-tumor effects in murine tumor models. READ MORE
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4. Tolerance and Immunity: Opposite Outcomes of Microbial Antigen Stimulation
Abstract : The immune system is remarkable in many ways. It exerts immunity to defend us from foreign pathogens, while it is also responsible for maintaining tolerance to avoid autoimmune diseases and allergy. This thesis includes three separate papers concerning both tolerance and immunity. READ MORE
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5. S100A9 in inflammatory disease: a potential target for amelioration
Abstract : The quinoline-3-carboxamides (Q compounds) are a family of small molecules with immunomodulatory functions that have shown efficacy in various murine models of inflammatory diseases. One such compound has demonstrated antitumor effects in murine models. Q compounds bind to S100A9, thereby preventing its ligation to TLR4 and RAGE. READ MORE