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4. Catechol O-methyltransferase. 6. Affinity labeling with N-haloacetyl-3,5-dimethoxy-4-hydroxyphenylalkylamines. Borchardt RT; Thakker DR J Med Chem; 1975 Feb; 18(2):152-8. PubMed ID: 1120981 [TBL] [Abstract][Full Text] [Related]
5. Kinetic studies on catechol O-methyltransferase. Product inhibition and the nature of the catechol binding site. Coward JK; Slixz EP; Wu FY Biochemistry; 1973 Jun; 12(12):2291-7. PubMed ID: 4736330 [No Abstract] [Full Text] [Related]
6. [Psychomimetic compounds in the urine of schizophrenics. I. Study of catechol derivatives: so-called Pink Spot and 3.4-dimethoxyphenylethylamine (DMPEA)]. Willmann PK; Bidziński A; Jakimow B; Puzyński S Psychiatr Pol; 1977; 11(2):143-9. PubMed ID: 887672 [No Abstract] [Full Text] [Related]
7. Psychoactivity of normacromerine in animals. Bourn WM; Keller WJ; Bonfiglio JF Life Sci; 1978 Sep; 23(11):1175-84. PubMed ID: 713693 [No Abstract] [Full Text] [Related]
8. Catechol O-methyltransferase. 12. Affinity labeling the active site with the oxidation products of 5,6-dihydroxyindole. Borchardt RT; Bhatia P J Med Chem; 1982 Mar; 25(3):263-71. PubMed ID: 7069705 [TBL] [Abstract][Full Text] [Related]
9. Catechol O-methyltransferase. 5. Structure-activity relationships for inhibition by flavonoids. Borchardt RT; Huber JA J Med Chem; 1975 Jan; 18(1):120-2. PubMed ID: 1109569 [No Abstract] [Full Text] [Related]
10. Haloacetyl derivatives. Wilchek M; Givol D Methods Enzymol; 1977; 46():153-7. PubMed ID: 909404 [No Abstract] [Full Text] [Related]
11. Facilitation and disruption by mescaline and 3,4-dimethoxyphenylethylamine of shock avoidance in rats. Gorelick DA; Bridger WH Psychopharmacology (Berl); 1977 Apr; 52(2):157-63. PubMed ID: 407599 [TBL] [Abstract][Full Text] [Related]
13. The effect of mescaline, 3, 4-dimethoxyphenethylamine and 2, 5-dimethoxy-4-methylamphetamine on rat plasma prolactin: evidence for serotonergic mediation. Meltzer HY; Fessler RG; Simonovic M; Fang VS Life Sci; 1978 Sep; 23(11):1185-92. PubMed ID: 152377 [No Abstract] [Full Text] [Related]
14. Catechol O-methyltransferase. 8. Structure-activity relationships for inhibtion by 8-hydroxyquinolines. Borchardt RT; Thakker DR; Warner VD; Mirth DB; Sane JN J Med Chem; 1976 Apr; 19(4):558-60. PubMed ID: 817025 [TBL] [Abstract][Full Text] [Related]
15. 4-Bromo-2,5-dimethoxyphenethylamine (2C-B) and structurally related phenylethylamines are potent 5-HT2A receptor antagonists in Xenopus laevis oocytes. Villalobos CA; Bull P; Sáez P; Cassels BK; Huidobro-Toro JP Br J Pharmacol; 2004 Apr; 141(7):1167-74. PubMed ID: 15006903 [TBL] [Abstract][Full Text] [Related]
16. Pharmacology of beta-(3,4-dimethoxyphenyl)ethyl amine: lack of peripheral and central antidopaminergic properties. Jarboe CH; Bannon MJ; Lipson SF J Pharm Pharmacol; 1978 Jul; 30(7):450-1. PubMed ID: 27614 [No Abstract] [Full Text] [Related]
17. Affinity labeling of catechol-O-methyltransferase with N-iodoacetyl-3,5-dimethoxy-4-hydroxyphenylethylamine. Borchardt RT; Thakker D Biochem Biophys Res Commun; 1973 Oct; 54(3):1233-9. PubMed ID: 4753192 [No Abstract] [Full Text] [Related]