Homology and Pharmacophore Modeling, High Throughput Virtual Screening and Molecular Docking Studies to Iden!fy Poten!al Inhibitors of the Two-pore-Domain Potassium Channel K2P9.1 (TASK-3)

dc.creatorRamírez, David
dc.creatorCaballero, Julio
dc.creatorArevalo, Barbara
dc.creatorConcha, G
dc.creatorZúñiga, Leandro
dc.creatorGonzález-Díaz, Wendy
dc.date2019-03-27T15:58:59Z
dc.date2022-06-18T20:07:46Z
dc.date2019-03-27T15:58:59Z
dc.date2022-06-18T20:07:46Z
dc.date2014
dc.date2017
dc.date2014
dc.date.accessioned2023-08-22T03:52:14Z
dc.date.available2023-08-22T03:52:14Z
dc.identifier1140624
dc.identifierhttps://hdl.handle.net/10533/234678
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8317014
dc.descriptionTwo-pore domain potassium channels (K2P) give rise to leak potassium currents, which control the excitability of the cells. The human genome contains 15 KCNK genes coding for proteins able to form K2P channels subdivided into 6 subfamilies on the basis of
dc.descriptionFONDECYT
dc.descriptionFONDECYT
dc.languageeng
dc.relationReunión Anual de la Sociedad de Bioquímica y Biología Molecular de Chile
dc.relation37°
dc.relationinfo:eu-repo/grantAgreement/Fondecyt/1140624
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleHomology and Pharmacophore Modeling, High Throughput Virtual Screening and Molecular Docking Studies to Iden!fy Poten!al Inhibitors of the Two-pore-Domain Potassium Channel K2P9.1 (TASK-3)
dc.typePonencia
dc.coveragePuerto Varas


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