| Sci-Hub provides access to nearly all scholarly literature DS Himmelstein, AR Romero, JG Levernier, TA Munro, SR McLaughlin, ... eLife 7, e32822, 2018 | 248 | 2018 |
| Studies toward the pharmacophore of salvinorin A, a potent κ opioid receptor agonist TA Munro, MA Rizzacasa, BL Roth, BA Toth, F Yan Journal of Medicinal Chemistry 48 (2), 345-348, 2005 | 150 | 2005 |
| Salvinorins D-F, new neoclerodane diterpenoids from Salvia divinorum, and an improved method for the isolation of salvinorin A TA Munro, MA Rizzacasa Journal of Natural Products 66 (5), 703-705, 2003 | 115 | 2003 |
| Divinatorins A-C, new neoclerodane diterpenoids from the controlled sage Salvia divinorum AK Bigham, TA Munro, MA Rizzacasa, RM Robins-Browne Journal of Natural Products 66 (9), 1242-1244, 2003 | 101 | 2003 |
| Long-acting κ opioid antagonists nor-BNI, GNTI and JDTic: pharmacokinetics in mice and lipophilicity TA Munro, LM Berry, AV Veer, C Béguin, FI Carroll, Z Zhao, WA Carlezon, ... BMC Pharmacology 12, 5, 2012 | 97 | 2012 |
| Functional selectivity of 6′-guanidinonaltrindole (6′-GNTI) at κ-opioid receptors in striatal neurons CL Schmid, JM Streicher, CE Groer, TA Munro, L Zhou, LM Bohn Journal of Biological Chemistry 288 (31), 22,387-22,398, 2013 | 92 | 2013 |
| Standard protecting groups create potent and selective κ opioids: salvinorin B alkoxymethyl ethers TA Munro, KK Duncan, W Xu, Y Wang, LY Liu-Chen, WA Carlezon Jr, ... Bioorganic & Medicinal Chemistry 16 (3), 1279-1286, 2008 | 81 | 2008 |
| N-methylacetamide analog of salvinorin A: A highly potent and selective κ-opioid receptor agonist with oral efficacy C Beguin, DN Potter, JA DiNieri, TA Munro, MR Richards, TA Paine, ... Journal of Pharmacology and Experimental Therapeutics 324 (1), 188-195, 2008 | 58 | 2008 |
| Lack of effect of sublingual salvinorin A, a naturally occurring kappa opioid, in humans: a placebo-controlled trial JE Mendelson, JR Coyle, JC Lopez, MJ Baggott, K Flower, ET Everhart, ... Psychopharmacology 214 (4), 933-939, 2011 | 47 | 2011 |
| Salvinorin A and derivatives: protection from metabolism does not prolong short-term, whole-brain residence JM Hooker, TA Munro, C Béguin, D Alexoff, C Shea, Y Xu, BM Cohen Neuropharmacology 57 (4), 386-391, 2009 | 45 | 2009 |
| Modification of the furan ring of salvinorin A: identification of a selective partial agonist at the kappa opioid receptor C Béguin, KK Duncan, TA Munro, DM Ho, W Xu, LY Liu-Chen, ... Bioorganic & Medicinal Chemistry 17 (3), 1370-1380, 2009 | 42 | 2009 |
| Selective κ opioid antagonists nor-BNI, GNTI and JDTic have low affinities for non-opioid receptors and transporters TA Munro, XP Huang, C Inglese, MG Perrone, A Van’t Veer, FI Carroll, ... PLoS ONE 8 (8), e70701, 2013 | 35 | 2013 |
| 8-epi-Salvinorin B: crystal structure and affinity at the κ opioid receptor T Munro, K Duncan, R Staples, W Xu, LY Liu-Chen, C Béguin, ... Beilstein Journal of Organic Chemistry 3, 1, 2007 | 28 | 2007 |
| Autoxidation of salvinorin A under basic conditions TA Munro, GW Goetchius, BL Roth, TA Vortherms, MA Rizzacasa Journal of Organic Chemistry 70 (24), 10,057-10,061, 2005 | 24 | 2005 |
| The chemistry of Salvia divinorum TA Munro Dissertation Abstracts International, 2006 | 18 | 2006 |
| Studies toward bivalent κ opioids derived from salvinorin A: heteromethylation of the furan ring reduces affinity TA Munro, W Xu, DM Ho, LY Liu-Chen, BM Cohen Beilstein Journal of Organic Chemistry 9, 2916–2924, 2013 | 13 | 2013 |
| Salvinorin derivatives and uses thereof C Beguin, JS Potuzak, TA Munro, KK Duncan, WA Carlezon, BM Cohen, ... US Patent 8,492,564, 2013 | 8 | 2013 |
| Salvinorin B methoxymethyl ether TA Munro, DM Ho, BM Cohen Acta Crystallographica Section E 68 (11), o3225-o3226, 2012 | 3 | 2012 |
| Revised (β-phenyl) stereochemistry of ultrapotent μ opioid BU72 TA Munro bioRxiv, http://doi.org/dq7s, 2020 | 1 | 2020 |
| Confirmation of the NMR assignments of salvinorin A [letter to the editor] TA Munro Magnetic Resonance in Chemistry 45 (9), 801-801, 2007 | 1* | 2007 |
Bruce CohenVerified email at broadinstitute.org
