Teh MT - Search Results

1

Mapping the melatonin receptor. 7. Subtype selective ligands based on beta-substituted N-acyl-5-methoxytryptamines and beta-substituted N-acyl-5-methoxy-1-methyltryptamines.

Tsotinis A, Vlachou M, Papahatjis DP, Calogeropoulou T, Nikas SP, Garratt PJ, Piccio V, Vonhoff S, Davidson K, Teh MT, Sugden D. Tsotinis A, et al. Among authors: teh mt. J Med Chem. 2006 Jun 15;49(12):3509-19. doi: 10.1021/jm0512544. J Med Chem. 2006. PMID: 16759094

2

7-Substituted-melatonin and 7-substituted-1-methylmelatonin analogues: effect of substituents on potency and binding affinity.

Faust R, Garratt PJ, Trujillo Pérez MA, Piccio VJ, Madsen C, Stenstrøm A, Frølund B, Davidson K, Teh MT, Sugden D. Faust R, et al. Among authors: teh mt. Bioorg Med Chem. 2007 Jul 1;15(13):4543-51. doi: 10.1016/j.bmc.2007.04.013. Epub 2007 Apr 10. Bioorg Med Chem. 2007. PMID: 17459711

3

Mapping the melatonin receptor. 5. Melatonin agonists and antagonists derived from tetrahydrocyclopent[b]indoles, tetrahydrocarbazoles and hexahydrocyclohept[b]indoles.

Davies DJ, Garratt PJ, Tocher DA, Vonhoff S, Davies J, Teh MT, Sugden D. Davies DJ, et al. Among authors: teh mt. J Med Chem. 1998 Feb 12;41(4):451-67. doi: 10.1021/jm970246n. J Med Chem. 1998. PMID: 9484496

4

Mapping the melatonin receptor. 6. Melatonin agonists and antagonists derived from 6H-isoindolo[2,1-a]indoles, 5,6-dihydroindolo[2,1-a]isoquinolines, and 6,7-dihydro-5H-benzo[c]azepino[2,1-a]indoles.

Faust R, Garratt PJ, Jones R, Yeh LK, Tsotinis A, Panoussopoulou M, Calogeropoulou T, Teh MT, Sugden D. Faust R, et al. Among authors: teh mt. J Med Chem. 2000 Mar 23;43(6):1050-61. doi: 10.1021/jm980684+. J Med Chem. 2000. PMID: 10737738

5

Desensitization of pigment granule aggregation in Xenopus leavis melanophores: melatonin degradation rather than receptor down-regulation is responsible.

Teh MT, Sugden D. Teh MT, et al. J Neurochem. 2002 May;81(4):719-27. doi: 10.1046/j.1471-4159.2002.00885.x. J Neurochem. 2002. PMID: 12065631 Free article.

6

Binding affinity and biological activity of oxygen and sulfur isosteres at melatonin receptors as a function of their hydrogen bonding capability.

Davies DJ, Faust R, Garratt PJ, Marivingt-Mounir C, Kathryn Davidson, Teh MT, Sugden D. Davies DJ, et al. Among authors: teh mt. Bioorg Chem. 2004 Feb;32(1):1-12. doi: 10.1016/j.bioorg.2003.09.004. Bioorg Chem. 2004. PMID: 14700558

7

Melatonin receptor pharmacology: toward subtype specificity.

Sugden D, Pickering H, Teh MT, Garratt PJ. Sugden D, et al. Among authors: teh mt. Biol Cell. 1997 Nov;89(8):531-7. doi: 10.1016/s0248-4900(98)80009-9. Biol Cell. 1997. PMID: 9618903

8

Comparison of the structure-activity relationships of melatonin receptor agonists and antagonists: lengthening the N-acyl side-chain has differing effects on potency on Xenopus melanophores.

Teh MT, Sugden D. Teh MT, et al. Naunyn Schmiedebergs Arch Pharmacol. 1998 Nov;358(5):522-8. doi: 10.1007/pl00005288. Naunyn Schmiedebergs Arch Pharmacol. 1998. PMID: 9840420

9

Design of subtype selective melatonin receptor agonists and antagonists.

Sugden D, Yeh LK, Teh MT. Sugden D, et al. Among authors: teh mt. Reprod Nutr Dev. 1999 May-Jun;39(3):335-44. doi: 10.1051/rnd:19990306. Reprod Nutr Dev. 1999. PMID: 10420436 Free article.

10

The putative melatonin receptor antagonist GR128107 is a partial agonist on Xenopus laevis melanophores.

Teh MT, Sugden D. Teh MT, et al. Br J Pharmacol. 1999 Mar;126(5):1237-45. doi: 10.1038/sj.bjp.0702404. Br J Pharmacol. 1999. PMID: 10205014 Free PMC article.

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