Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects

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Main Authors: Seth F. Vigneron, Shohei Ohno, Joao Braz, Joseph Y. Kim, Oh Sang Kweon, Chase Webb, Christian B. Billesbølle, Karthik Srinivasan, Karnika Bhardwaj, John J. Irwin, Aashish Manglik, Allan I. Basbaum, Jonathan A. Ellman, Brian K. Shoichet
Format: Article
Language:English
Published: American Chemical Society 2025-04-01
Series:ACS Central Science
Online Access:https://doi.org/10.1021/acscentsci.5c00052
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author Seth F. Vigneron
Shohei Ohno
Joao Braz
Joseph Y. Kim
Oh Sang Kweon
Chase Webb
Christian B. Billesbølle
Karthik Srinivasan
Karnika Bhardwaj
John J. Irwin
Aashish Manglik
Allan I. Basbaum
Jonathan A. Ellman
Brian K. Shoichet
author_facet Seth F. Vigneron
Shohei Ohno
Joao Braz
Joseph Y. Kim
Oh Sang Kweon
Chase Webb
Christian B. Billesbølle
Karthik Srinivasan
Karnika Bhardwaj
John J. Irwin
Aashish Manglik
Allan I. Basbaum
Jonathan A. Ellman
Brian K. Shoichet
author_sort Seth F. Vigneron
collection DOAJ
format Article
id doaj-art-a8f8651d36494ca6b0e29cb6047fdcc2
institution DOAJ
issn 2374-7951
language English
publishDate 2025-04-01
publisher American Chemical Society
record_format Article
series ACS Central Science
spelling doaj-art-a8f8651d36494ca6b0e29cb6047fdcc22025-08-20T03:12:12ZengAmerican Chemical SocietyACS Central Science2374-79512025-04-0111577079010.1021/acscentsci.5c00052Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal EffectsSeth F. Vigneron0Shohei Ohno1Joao Braz2Joseph Y. Kim3Oh Sang Kweon4Chase Webb5Christian B. Billesbølle6Karthik Srinivasan7Karnika Bhardwaj8John J. Irwin9Aashish Manglik10Allan I. Basbaum11Jonathan A. Ellman12Brian K. Shoichet13Department of Pharmaceutical Chemistry, University of California, San Francisco, California, United StatesDepartment of Chemistry, Yale University, New Haven, Connecticut, United StatesDepartment of Anatomy, University of California, San Francisco, California, United StatesDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United StatesDepartment of Chemistry, Yale University, New Haven, Connecticut, United StatesDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United StatesDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United StatesDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United StatesDepartment of Anatomy, University of California, San Francisco, California, United StatesDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United StatesDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United StatesDepartment of Anatomy, University of California, San Francisco, California, United StatesDepartment of Chemistry, Yale University, New Haven, Connecticut, United StatesDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United Stateshttps://doi.org/10.1021/acscentsci.5c00052
spellingShingle Seth F. Vigneron
Shohei Ohno
Joao Braz
Joseph Y. Kim
Oh Sang Kweon
Chase Webb
Christian B. Billesbølle
Karthik Srinivasan
Karnika Bhardwaj
John J. Irwin
Aashish Manglik
Allan I. Basbaum
Jonathan A. Ellman
Brian K. Shoichet
Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects
ACS Central Science
title Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects
title_full Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects
title_fullStr Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects
title_full_unstemmed Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects
title_short Docking 14 Million Virtual Isoquinuclidines against the μ and κ Opioid Receptors Reveals Dual Antagonists–Inverse Agonists with Reduced Withdrawal Effects
title_sort docking 14 million virtual isoquinuclidines against the μ and κ opioid receptors reveals dual antagonists inverse agonists with reduced withdrawal effects
url https://doi.org/10.1021/acscentsci.5c00052
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