| Year |
Citation |
Score |
| 2013 |
Munro TA, Xu W, Ho DM, Liu-Chen LY, Cohen BM. Studies toward bivalent κ opioids derived from salvinorin A: heteromethylation of the furan ring reduces affinity. Beilstein Journal of Organic Chemistry. 9: 2916-24. PMID 24454571 DOI: 10.3762/Bjoc.9.328 |
0.435 |
|
| 2013 |
Munro TA, Huang XP, Inglese C, Perrone MG, Van't Veer A, Carroll FI, Béguin C, Carlezon WA, Colabufo NA, Cohen BM, Roth BL. Selective κ opioid antagonists nor-BNI, GNTI and JDTic have low affinities for non-opioid receptors and transporters. Plos One. 8: e70701. PMID 23976952 DOI: 10.1371/Journal.Pone.0070701 |
0.463 |
|
| 2013 |
Schmid CL, Streicher JM, Groer CE, Munro TA, Zhou L, Bohn LM. Functional selectivity of 6'-guanidinonaltrindole (6'-GNTI) at κ-opioid receptors in striatal neurons. The Journal of Biological Chemistry. 288: 22387-98. PMID 23775075 DOI: 10.1074/Jbc.M113.476234 |
0.304 |
|
| 2012 |
Munro TA, Ho DM, Cohen BM. Salvinorin B meth-oxy-methyl ether. Acta Crystallographica. Section E, Structure Reports Online. 68: o3225-6. PMID 23284529 DOI: 10.1107/S1600536812043449 |
0.434 |
|
| 2012 |
Munro TA, Berry LM, Van't Veer A, Béguin C, Carroll FI, Zhao Z, Carlezon WA, Cohen BM. Long-acting κ opioid antagonists nor-BNI, GNTI and JDTic: pharmacokinetics in mice and lipophilicity. Bmc Pharmacology. 12: 5. PMID 22642416 DOI: 10.1186/1471-2210-12-5 |
0.318 |
|
| 2011 |
Mendelson JE, Coyle JR, Lopez JC, Baggott MJ, Flower K, Everhart ET, Munro TA, Galloway GP, Cohen BM. Lack of effect of sublingual salvinorin A, a naturally occurring kappa opioid, in humans: a placebo-controlled trial. Psychopharmacology. 214: 933-9. PMID 21140258 DOI: 10.1007/S00213-010-2103-5 |
0.335 |
|
| 2009 |
Béguin C, Duncan KK, Munro TA, Ho DM, Xu W, Liu-Chen LY, Carlezon WA, Cohen BM. Modification of the furan ring of salvinorin A: identification of a selective partial agonist at the kappa opioid receptor. Bioorganic & Medicinal Chemistry. 17: 1370-80. PMID 19147366 DOI: 10.1016/J.Bmc.2008.12.012 |
0.486 |
|
| 2008 |
Munro TA, Duncan KK, Xu W, Wang Y, Liu-Chen LY, Carlezon WA, Cohen BM, Béguin C. Standard protecting groups create potent and selective kappa opioids: salvinorin B alkoxymethyl ethers. Bioorganic & Medicinal Chemistry. 16: 1279-86. PMID 17981041 DOI: 10.1016/J.Bmc.2007.10.067 |
0.41 |
|
| 2008 |
Béguin C, Potter DN, Dinieri JA, Munro TA, Richards MR, Paine TA, Berry L, Zhao Z, Roth BL, Xu W, Liu-Chen LY, Carlezon WA, Cohen BM. N-methylacetamide analog of salvinorin A: a highly potent and selective kappa-opioid receptor agonist with oral efficacy. The Journal of Pharmacology and Experimental Therapeutics. 324: 188-95. PMID 17951511 DOI: 10.1124/Jpet.107.129023 |
0.41 |
|
| 2007 |
Munro TA, Duncan KK, Staples RJ, Xu W, Liu-Chen LY, Béguin C, Carlezon WA, Cohen BM. 8-epi-Salvinorin B: crystal structure and affinity at the kappa opioid receptor. Beilstein Journal of Organic Chemistry. 3: 1. PMID 17212822 DOI: 10.1186/1860-5397-3-1 |
0.458 |
|
| 2005 |
Munro TA, Goetchius GW, Roth BL, Vortherms TA, Rizzacasa MA. Autoxidation of salvinorin A under basic conditions. The Journal of Organic Chemistry. 70: 10057-61. PMID 16292839 DOI: 10.1021/Jo051813E |
0.573 |
|
| 2005 |
Munro TA, Rizzacasa MA, Roth BL, Toth BA, Yan F. Studies toward the pharmacophore of salvinorin A, a potent kappa opioid receptor agonist. Journal of Medicinal Chemistry. 48: 345-8. PMID 15658846 DOI: 10.1021/Jm049438Q |
0.569 |
|
| 2003 |
Bigham AK, Munro TA, Rizzacasa MA, Robins-Browne RM. Divinatorins A-C, new neoclerodane diterpenoids from the controlled sage Salvia divinorum. Journal of Natural Products. 66: 1242-4. PMID 14510607 DOI: 10.1021/Np030313I |
0.526 |
|
| 2003 |
Munro TA, Rizzacasa MA. Salvinorins D-F, new neoclerodane diterpenoids from Salvia divinorum, and an improved method for the isolation of salvinorin A. Journal of Natural Products. 66: 703-5. PMID 12762813 DOI: 10.1021/Np0205699 |
0.511 |
|
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