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. 2010 Sep;62(3):343–380. doi: 10.1124/pr.110.002832

TABLE 1.

IUPHAR melatonin receptor nomenclature and classification

Nomenclature MT1 MT2 MT3
Previous names MEL1A, ML1A, Mel1a MEL1B, ML1B, Mel1b ML2
Structural information 7TM 7TM
Gene/chromosome
    Human 350 aa,a P48039; chr 4q 35.1 362 aa,b P49286; chr 11q21–22
    Mouse 353 aa,c Q61184; chr 8 365 aa,d U57554; chr 9
Selective agonists S 26284e IIK7 (10.3)f N-Acetylserotonin,gk 5MCA-NATk
Selective antagonists S 26131e 4P-ADOT,l,m 4P-PDOT (8.8),l,m GR 128107l, K185 (9.3)f Prazosinh
Radioligands [3H]MLT,n 2- [125I]IMLTo [3H]MLT,n 2-[125I]IMLT,o [3H]4P-PDOTp 2-[125I]5MCA-NAT,k 2-[125I]IMLTn
Tissue Functions Vascular vasoconstriction,qu inhibition neuronal firing,v phase-shift circadian activity rhythmsu Vascular vasodilation,t inhibition retinal dopamine release,l phase-shift circadian rhythms of neuronal firingm,w,v,x Leukocyte adhesionu
Comments MT1 full-length cDNAs were cloned from human (350 aa),a mouse (353 aa),c sheep (366 aa),a rat (353 aa),y hamster (353 aa),z monkey (352),aa and partial cDNAs from cattle (257 aa) and pig (154 aa).bb MT2 cDNA was cloned from human (362 aa),z rat (364 aa),y mouse (365 aa),d sheep (376 aa),cc monkey (362 aa),aa and partial cDNA from hamster.z Endogenous ligands are MLT and N-acetylserotonin. A recent report identifies an MT3 binding site in hamster kidney as the enzyme quinone reductase-2.dd Antagonist potencies have not yet been established.