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Refinado por: Nome da Publicação: Acs Chemical Neuroscience remover
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1
Sigma 2 Receptor/Tmem97 Agonists Produce Long Lasting Antineuropathic Pain Effects in Mice
Sigma 2 Receptor/Tmem97 Agonists Produce Long Lasting Antineuropathic Pain Effects in Mice
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Sigma 2 Receptor/Tmem97 Agonists Produce Long Lasting Antineuropathic Pain Effects in Mice

Sahn, James J ; Mejia, Galo L ; Ray, Pradipta R ; Martin, Stephen F ; Price, Theodore J

ACS chemical neuroscience, 2017-08, Vol.8 (8), p.1801-1811 [Periódico revisado por pares]

United States: American Chemical Society

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2
Characterization of a Potential KOR/DOR Dual Agonist with No Apparent Abuse Liability via a Complementary Structure–Activity Relationship Study on Nalfurafine Analogues
Characterization of a Potential KOR/DOR Dual Agonist with No Apparent Abuse Liability via a Complementary Structure–Activity Relationship Study on Nalfurafine Analogues
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Characterization of a Potential KOR/DOR Dual Agonist with No Apparent Abuse Liability via a Complementary Structure–Activity Relationship Study on Nalfurafine Analogues

Li, Mengchu ; Stevens, David L. ; Arriaga, Michelle ; Townsend, E. Andrew ; Mendez, Rolando E. ; Blajkevch, Nadejda A. ; Selley, Dana E. ; Banks, Matthew L. ; Negus, S. Stevens ; Dewey, William L. ; Zhang, Yan

ACS chemical neuroscience, 2022-12, Vol.13 (24), p.3608-3628 [Periódico revisado por pares]

United States: American Chemical Society

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3
Recent Advances in the Realm of Allosteric Modulators for Opioid Receptors for Future Therapeutics
Recent Advances in the Realm of Allosteric Modulators for Opioid Receptors for Future Therapeutics
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Recent Advances in the Realm of Allosteric Modulators for Opioid Receptors for Future Therapeutics

Remesic, Michael ; Hruby, Victor J ; Porreca, Frank ; Lee, Yeon Sun

ACS chemical neuroscience, 2017-06, Vol.8 (6), p.1147-1158 [Periódico revisado por pares]

United States: American Chemical Society

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4
Molecular Docking, Molecular Dynamics, and Structure–Activity Relationship Explorations of 14-Oxygenated N‑Methylmorphinan-6-ones as Potent μ‑Opioid Receptor Agonists
Molecular Docking, Molecular Dynamics, and Structure–Activity Relationship Explorations of 14-Oxygenated N‑Methylmorphinan-6-ones as Potent μ‑Opioid Receptor Agonists
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Molecular Docking, Molecular Dynamics, and Structure–Activity Relationship Explorations of 14-Oxygenated N‑Methylmorphinan-6-ones as Potent μ‑Opioid Receptor Agonists

Noha, Stefan M ; Schmidhammer, Helmut ; Spetea, Mariana

ACS chemical neuroscience, 2017-06, Vol.8 (6), p.1327-1337 [Periódico revisado por pares]

United States: American Chemical Society

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5
Structure–Activity Relationship Studies of 6α- and 6β-Indolylacetamidonaltrexamine Derivatives as Bitopic Mu Opioid Receptor Modulators and Elaboration of the “Message-Address Concept” To Comprehend Their Functional Conversion
Structure–Activity Relationship Studies of 6α- and 6β-Indolylacetamidonaltrexamine Derivatives as Bitopic Mu Opioid Receptor Modulators and Elaboration of the “Message-Address Concept” To Comprehend Their Functional Conversion
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Structure–Activity Relationship Studies of 6α- and 6β-Indolylacetamidonaltrexamine Derivatives as Bitopic Mu Opioid Receptor Modulators and Elaboration of the “Message-Address Concept” To Comprehend Their Functional Conversion

Obeng, Samuel ; Wang, Huiqun ; Jali, Abdulmajeed ; Stevens, David L ; Akbarali, Hamid I ; Dewey, William L ; Selley, Dana E ; Zhang, Yan

ACS chemical neuroscience, 2019-03, Vol.10 (3), p.1075-1090 [Periódico revisado por pares]

United States: American Chemical Society

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6
Characterization of 17-Cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6α-(indole-7-carboxamido)morphinan (NAN) as a Novel Opioid Receptor Modulator for Opioid Use Disorder Treatment
Characterization of 17-Cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6α-(indole-7-carboxamido)morphinan (NAN) as a Novel Opioid Receptor Modulator for Opioid Use Disorder Treatment
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Characterization of 17-Cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6α-(indole-7-carboxamido)morphinan (NAN) as a Novel Opioid Receptor Modulator for Opioid Use Disorder Treatment

Obeng, Samuel ; Jali, Abdulmajeed ; Zheng, Yi ; Wang, Huiqun ; Schwienteck, Kathryn L ; Chen, Chongguang ; Stevens, David L ; Akbarali, Hamid I ; Dewey, William L ; Banks, Mathew L ; Liu-Chen, Lee-Yuan ; Selley, Dana E ; Zhang, Yan

ACS chemical neuroscience, 2019-05, Vol.10 (5), p.2518-2532 [Periódico revisado por pares]

United States: American Chemical Society

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7
Structure–Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias
Structure–Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias
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Structure–Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias

Lovell, Kimberly M ; Frankowski, Kevin J ; Stahl, Edward L ; Slauson, Stephen R ; Yoo, Euna ; Prisinzano, Thomas E ; Aubé, Jeffrey ; Bohn, Laura M

ACS chemical neuroscience, 2015-08, Vol.6 (8), p.1411-1419 [Periódico revisado por pares]

United States: American Chemical Society

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8
Identification of the First Marine-Derived Opioid Receptor “Balanced” Agonist with a Signaling Profile That Resembles the Endorphins
Identification of the First Marine-Derived Opioid Receptor “Balanced” Agonist with a Signaling Profile That Resembles the Endorphins
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Identification of the First Marine-Derived Opioid Receptor “Balanced” Agonist with a Signaling Profile That Resembles the Endorphins

Johnson, Tyler A ; Milan-Lobo, Laura ; Che, Tao ; Ferwerda, Madeline ; Lambu, Eptisam ; McIntosh, Nicole L ; Li, Fei ; He, Li ; Lorig-Roach, Nicholas ; Crews, Phillip ; Whistler, Jennifer L

ACS chemical neuroscience, 2017-03, Vol.8 (3), p.473-485 [Periódico revisado por pares]

United States: American Chemical Society

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9
Caged Naloxone: Synthesis, Characterization, and Stability of 3‑O‑(4,5-Dimethoxy-2-nitrophenyl)carboxymethyl Naloxone (CNV-NLX)
Caged Naloxone: Synthesis, Characterization, and Stability of 3‑O‑(4,5-Dimethoxy-2-nitrophenyl)carboxymethyl Naloxone (CNV-NLX)
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Caged Naloxone: Synthesis, Characterization, and Stability of 3‑O‑(4,5-Dimethoxy-2-nitrophenyl)carboxymethyl Naloxone (CNV-NLX)

Lewin, Anita H ; Fix, Scott E ; Zhong, Desong ; Mayer, Louise D ; Burgess, Jason P ; Mascarella, S. Wayne ; Reddy, P. Anantha ; Seltzman, Herbert H ; Carroll, F. Ivy

ACS chemical neuroscience, 2018-03, Vol.9 (3), p.563-567 [Periódico revisado por pares]

United States: American Chemical Society

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10
Combined Glia Inhibition and Opioid Receptor Agonism Afford Highly Potent Analgesics without Tolerance
Combined Glia Inhibition and Opioid Receptor Agonism Afford Highly Potent Analgesics without Tolerance
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Combined Glia Inhibition and Opioid Receptor Agonism Afford Highly Potent Analgesics without Tolerance

Akgün, Eyup ; Lunzer, Mary M ; Portoghese, Philip S

ACS chemical neuroscience, 2019-04, Vol.10 (4), p.2004-2011 [Periódico revisado por pares]

United States: American Chemical Society

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