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      <dc:title>A chemical biology approach to control endocannabinoid biosynthesis</dc:title>
      <dc:creator>Van der Selt, Marcelis</dc:creator>
      <dc:subject>Receptores de neurotransmisores</dc:subject>
      <dc:description>Endocannabinoids play an essential role in human health and disease, regulating processes such as immunomodulation, energy balance and neurotransmission. Diacylglycerollipase-α (DAGL-α) is responsible for the production of the endocannabinoid 2-arachidonoylglycerol (2-AG) in the central nervous system. It is a potential drug target for the treatment of obesity and neurodegenerative diseases. Currently, there are no selective inhibitors and activity-based probes available for its study. The identification of selective DAGL- inhibitors is hampered by a lack of assays that make use of endogenous DAGL- activity in proteomes. Determination of the selectivity of the inhibitors in native tissues is important, because DAGL- belongs to the class of serine hydrolases, containing more than 200 members with various physiological functions. Here, I will present a chemical biology approach to identify and characterize highly selective chemical probes to study the function of this protein both in vitro and in vivo.</dc:description>
      <dc:date>2015-04-15T09:58:39Z</dc:date>
      <dc:date>2015-04-15T09:58:39Z</dc:date>
      <dc:date>2015-04-15</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>http://hdl.handle.net/10630/9658</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>Dpt. Psicobiología y Metodología de las Ciencias del Comportamiento</dc:relation>
      <dc:relation>Málaga, España</dc:relation>
      <dc:relation>26/06/2015</dc:relation>
      <dc:rights>open access</dc:rights>
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