23587424 24815322 32930582 27433555 23284529 23357481 26057692 31201990 22736766 27020718 32132923 26441647 29615341 23942594 22464684 24126281 23127545 24201308 24484985 24454571 - Search Results

Year	Number of Results
2012	4
2013	7
2014	2
2015	2
2016	2
2018	1
2019	1
2020	3
2021	1
2023	0

1

Kappa-opioid receptor-selective dicarboxylic ester-derived salvinorin A ligands.

Polepally PR, White K, Vardy E, Roth BL, Ferreira D, Zjawiony JK. Polepally PR, et al. Bioorg Med Chem Lett. 2013 May 15;23(10):2860-2. doi: 10.1016/j.bmcl.2013.03.111. Epub 2013 Apr 4. Bioorg Med Chem Lett. 2013. PMID: 23587424 Free PMC article.

2

Behavioral and cellular pharmacology characterization of 17-cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6α-(isoquinoline-3'-carboxamido)morphinan (NAQ) as a mu opioid receptor selective ligand.

Zhang Y, Braithwaite A, Yuan Y, Streicher JM, Bilsky EJ. Zhang Y, et al. Eur J Pharmacol. 2014 Aug 5;736:124-30. doi: 10.1016/j.ejphar.2014.04.041. Epub 2014 May 8. Eur J Pharmacol. 2014. PMID: 24815322 Free PMC article.

3

Natural Products for the Treatment of Pain: Chemistry and Pharmacology of Salvinorin A, Mitragynine, and Collybolide.

Chakraborty S, Majumdar S. Chakraborty S, et al. Biochemistry. 2021 May 11;60(18):1381-1400. doi: 10.1021/acs.biochem.0c00629. Epub 2020 Sep 22. Biochemistry. 2021. PMID: 32930582 Free PMC article. Review.

4

Clerodane diterpenes: sources, structures, and biological activities.

Li R, Morris-Natschke SL, Lee KH. Li R, et al. Nat Prod Rep. 2016 Oct 28;33(10):1166-226. doi: 10.1039/c5np00137d. Epub 2016 Jul 18. Nat Prod Rep. 2016. PMID: 27433555 Free PMC article. Review.

5

Salvinorin B meth-oxy-methyl ether.

Munro TA, Ho DM, Cohen BM. Munro TA, et al. Acta Crystallogr Sect E Struct Rep Online. 2012 Nov 1;68(Pt 11):o3225-6. doi: 10.1107/S1600536812043449. Epub 2012 Oct 27. Acta Crystallogr Sect E Struct Rep Online. 2012. PMID: 23284529 Free PMC article.

6

Effects of the neoclerodane Hardwickiic acid on the presynaptic opioid receptors which modulate noradrenaline and dopamine release in mouse central nervous system.

Pittaluga A, Olivero G, Di Prisco S, Merega E, Bisio A, Romussi G, Grilli M, Marchi M. Pittaluga A, et al. Neurochem Int. 2013 Mar;62(4):354-9. doi: 10.1016/j.neuint.2013.01.016. Epub 2013 Jan 26. Neurochem Int. 2013. PMID: 23357481

7

Intrinsic relative activities of κ opioid agonists in activating Gα proteins and internalizing receptor: Differences between human and mouse receptors.

DiMattio KM, Ehlert FJ, Liu-Chen LY. DiMattio KM, et al. Eur J Pharmacol. 2015 Aug 15;761:235-44. doi: 10.1016/j.ejphar.2015.05.054. Epub 2015 Jun 6. Eur J Pharmacol. 2015. PMID: 26057692 Free PMC article.

8

A Novel Mu-Delta Opioid Agonist Demonstrates Enhanced Efficacy With Reduced Tolerance and Dependence in Mouse Neuropathic Pain Models.

Lei W, Vekariya RH, Ananthan S, Streicher JM. Lei W, et al. J Pain. 2020 Jan-Feb;21(1-2):146-160. doi: 10.1016/j.jpain.2019.05.017. Epub 2019 Jun 12. J Pain. 2020. PMID: 31201990 Free PMC article.

9

6'-Guanidinonaltrindole (6'-GNTI) is a G protein-biased κ-opioid receptor agonist that inhibits arrestin recruitment.

Rives ML, Rossillo M, Liu-Chen LY, Javitch JA. Rives ML, et al. J Biol Chem. 2012 Aug 3;287(32):27050-4. doi: 10.1074/jbc.C112.387332. Epub 2012 Jun 26. J Biol Chem. 2012. PMID: 22736766 Free PMC article.

10

Diterpenes: Advances in Neurobiological Drug Research.

Islam MT, da Silva CB, de Alencar MV, Paz MF, Almeida FR, Melo-Cavalcante AA. Islam MT, et al. Phytother Res. 2016 Jun;30(6):915-28. doi: 10.1002/ptr.5609. Epub 2016 Mar 28. Phytother Res. 2016. PMID: 27020718 Review.

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