Studies on adrenal phenylethanolamine N- methyltransferase (PNMT) with S K & F 64139, a selective inhibitor
- PMID: 6786
Studies on adrenal phenylethanolamine N- methyltransferase (PNMT) with S K & F 64139, a selective inhibitor
Abstract
SK&F 64139 is a potent, reversible inhibitor of phenylethanolamine N-methyltransferase; its IC50 concentration in our standard assay system was 1 X 10(-7) M. Kinetically, the compound is a competitive inhibitor with respect to norepinephrine but is uncompetitive when S-adenosylmethionine is the variable substrate. In contrast to a previously reported compound (SK&F 7698), the drug is only a weak alpha receptor antagonist (KB = 6 X 10(-6) M). In both the rat and squirrel monkey, SK&F 64139 produced dose-dependent decreases in the adrenal epinephrine content coupled with stoichiometrically equivalent increases in the norepinephrine pool(s). Further evidence for in vivo phenylethanolamine N-methyltransferase inhibitory activity was that the drug markedly inhibited the conversion of a tracer dose of 3H-norepinephrine to 3H-epinephrine in the rat adrenal gland after unit oral doses as low as 5 mg/kg.
Similar articles
-
Studies on SK&F 29661, an organ-specific inhibitor of phenylethanolamine N-methyltransferase.J Pharmacol Exp Ther. 1979 Jan;208(1):24-30. J Pharmacol Exp Ther. 1979. PMID: 215747
-
The effect of phenylethanolamine n-methyltransferase concentration and species difference on the inhibitory potency of SK&F 64139.Res Commun Chem Pathol Pharmacol. 1977 Jun;17(2):201-13. Res Commun Chem Pathol Pharmacol. 1977. PMID: 406652
-
Assessment of the functional role of brain adrenergic neurons: chronic effects of phenylethanolamine N-methyltransferase inhibitors and alpha adrenergic receptor antagonists on brain norepinephrine metabolism.J Pharmacol Exp Ther. 1984 Sep;230(3):577-86. J Pharmacol Exp Ther. 1984. PMID: 6147403
-
Pharmacology of brain epinephrine neurons.Annu Rev Pharmacol Toxicol. 1982;22:31-55. doi: 10.1146/annurev.pa.22.040182.000335. Annu Rev Pharmacol Toxicol. 1982. PMID: 6805416 Review.
-
Inhibitors of phenylethanolamine N-methyltransferase and epinephrine biosynthesis: a potential source of new drugs.Drug Metab Rev. 1983;14(4):709-21. doi: 10.3109/03602538308991406. Drug Metab Rev. 1983. PMID: 6352222 Review. No abstract available.
Cited by
-
Noncompetitive inhibition of indolethylamine-N-methyltransferase by N,N-dimethyltryptamine and N,N-dimethylaminopropyltryptamine.Biochemistry. 2014 May 13;53(18):2956-65. doi: 10.1021/bi500175p. Epub 2014 Apr 28. Biochemistry. 2014. PMID: 24730580 Free PMC article.
-
Synthesis of 4,5,6,7-tetrahydrothieno[3,2-c]pyridines and comparison with their isosteric 1,2,3,4-tetrahydroisoquinolines as inhibitors of phenylethanolamine N-methyltransferase.Bioorg Med Chem. 2008 Jan 1;16(1):542-59. doi: 10.1016/j.bmc.2007.08.066. Epub 2007 Oct 11. Bioorg Med Chem. 2008. PMID: 18024134 Free PMC article.
-
Target Class Profiling of Small-Molecule Methyltransferases.ACS Chem Biol. 2023 Apr 21;18(4):969-981. doi: 10.1021/acschembio.3c00124. Epub 2023 Mar 28. ACS Chem Biol. 2023. PMID: 36976909 Free PMC article.
-
The Adrenal Medulla Modulates Mechanical Allodynia in a Rat Model of Neuropathic Pain.Int J Mol Sci. 2020 Nov 6;21(21):8325. doi: 10.3390/ijms21218325. Int J Mol Sci. 2020. PMID: 33171955 Free PMC article.
-
Exploring the active site of phenylethanolamine N-methyltransferase with 1,2,3,4-tetrahydrobenz[h]isoquinoline inhibitors.Bioorg Med Chem. 2007 Feb 1;15(3):1298-310. doi: 10.1016/j.bmc.2006.11.010. Epub 2006 Nov 10. Bioorg Med Chem. 2007. PMID: 17126018 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Research Materials
Miscellaneous