Potential Opioid Addiction Therapeutics

dc.contributor.authorParras, Isabelen
dc.contributor.authorKidd, Rachelen
dc.contributor.authorMerten, Ericen
dc.contributor.authorLewis, Stephanie N.en
dc.date.accessioned2020-02-02T03:33:56Zen
dc.date.available2020-02-02T03:33:56Zen
dc.date.issued2019-05-07en
dc.description.abstractThroughout the last thirty years, a severe opioid epidemic has arisen due to the excessive consumption and abuse of these addictive narcotics. Opioids are currently the best analgesic known to man, however the effects of opioids are not all beneficial; they are extremely addictive and are deadly when taken in high doses. Since opioids began rising in popularity in the 1990’s as a prescribed pain-reliever, opioid deaths have skyrocketed. These circumstances have caused the need for the development of both a potent, non-addictive pain reliever and also a way to treat patients with an opioid addiction. To solve this problem, we used computational methods and structural analysis to investigate the µ-opioid receptor binding cavity and its unique interactions with four different ligands: morphine, heroin, fentanyl, and naloxone. From the results, we have created a criterion of interactions that a potential opioid therapeutic should have.en
dc.description.notesThis report was composed as the final assignment for Dr. Nikki Lewis in the spring 2019 UH-4504 Honors Topics in Discovery and Innovation Studios course titled, "Drug Discovery and Design in the Digital Age". This report is a learning object and should not be treated as a peer-reviewed article on the topic.en
dc.identifier.urihttp://hdl.handle.net/10919/96655en
dc.language.isoen_USen
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectOpioiden
dc.subjectmolecular dockingen
dc.subjectopioid receptoren
dc.titlePotential Opioid Addiction Therapeuticsen
dc.typeLearning objecten
dc.typeReporten

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