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3. Stereoisomeric probes for the D1 dopamine receptor: synthesis and characterization of R-(+) and S-(-) enantiomers of 3-allyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine and its 6-bromo analogue. Neumeyer JL; Kula NS; Baldessarini RJ; Baindur N J Med Chem; 1992 Apr; 35(8):1466-71. PubMed ID: 1533424 [TBL] [Abstract][Full Text] [Related]
4. Synthesis, conformation, and dopaminergic activity of 5,6-ethano-bridged derivatives of selective dopaminergic 3-benzazepines. Weinstock J; Oh HJ; DeBrosse CW; Eggleston DS; Wise M; Flaim KE; Gessner GW; Sawyer JL; Kaiser C J Med Chem; 1987 Aug; 30(8):1303-8. PubMed ID: 2886663 [TBL] [Abstract][Full Text] [Related]
5. (+/-)-3-Allyl-6-bromo-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3- benzazepin, a new high-affinity D1 dopamine receptor ligand: synthesis and structure-activity relationship. Neumeyer JL; Baindur N; Niznik HB; Guan HC; Seeman P J Med Chem; 1991 Dec; 34(12):3366-71. PubMed ID: 1684995 [TBL] [Abstract][Full Text] [Related]
6. Identification of the enantiomers of SK&F 83566 as specific and stereoselective antagonists at the striatal D-1 dopamine receptor: comparisons with the D-2 enantioselectivity of Ro 22-1319. O'Boyle KM; Waddington JL Eur J Pharmacol; 1984 Oct; 106(1):219-20. PubMed ID: 6241567 [No Abstract] [Full Text] [Related]
7. Selective and stereospecific interactions of R-SK & F 38393 with [3H]piflutixol but not [3H]spiperone binding to striatal D1 and D2 dopamine receptors: comparisons with SCH 23390. O'Boyle KM; Waddington JL Eur J Pharmacol; 1984 Mar; 98(3-4):433-6. PubMed ID: 6144559 [TBL] [Abstract][Full Text] [Related]
8. Synthesis, resolution, absolute stereochemistry, and enantioselectivity of 3',4'-dihydroxynomifensine. Dandridge PA; Kaiser C; Brenner M; Gaitanopoulos D; Davis LD; Webb RL; Foley JJ; Sarau HM J Med Chem; 1984 Jan; 27(1):28-35. PubMed ID: 6317860 [TBL] [Abstract][Full Text] [Related]
9. A study on the contribution of the 1-phenyl substituent to the molecular electrostatic potentials of some benzazepines in relation to selective dopamine D-1 receptor activity. Pettersson I; Gundertofte K; Palm J; Liljefors T J Med Chem; 1992 Feb; 35(3):502-7. PubMed ID: 1531365 [TBL] [Abstract][Full Text] [Related]
10. Conformational analysis and structure-activity relationships of selective dopamine D-1 receptor agonists and antagonists of the benzazepine series. Pettersson I; Liljefors T; Bøgesø K J Med Chem; 1990 Aug; 33(8):2197-204. PubMed ID: 1973733 [TBL] [Abstract][Full Text] [Related]
11. Conformational analysis and molecular modeling of 1-phenyl-, 4-phenyl-, and 1-benzyl-1,2,3,4-tetrahydroisoquinolines as D1 dopamine receptor ligands. Charifson PS; Bowen JP; Wyrick SD; Hoffman AJ; Cory M; McPhail AT; Mailman RB J Med Chem; 1989 Sep; 32(9):2050-8. PubMed ID: 2527994 [TBL] [Abstract][Full Text] [Related]
12. Dihydrexidine, a novel selective high potency full dopamine D-1 receptor agonist. Lovenberg TW; Brewster WK; Mottola DM; Lee RC; Riggs RM; Nichols DE; Lewis MH; Mailman RB Eur J Pharmacol; 1989 Jul; 166(1):111-3. PubMed ID: 2572425 [No Abstract] [Full Text] [Related]
13. Synthesis and dopamine receptor affinities of 6-amino-5,6,7,8-tetrahydroquinoline derivatives. Claudi F; Cingolani GM; Giorgioni G; Cattabeni F; Cimino M; Di Luca M Drug Des Deliv; 1989 Jun; 4(4):279-87. PubMed ID: 2570592 [TBL] [Abstract][Full Text] [Related]
14. Synthesis and renal vasodilator activity of some dopamine agonist 1-aryl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diols: halogen and methyl analogues of fenoldopam. Weinstock J; Ladd DL; Wilson JW; Brush CK; Yim NC; Gallagher G; McCarthy ME; Silvestri J; Sarau HM; Flaim KE J Med Chem; 1986 Nov; 29(11):2315-25. PubMed ID: 2878077 [TBL] [Abstract][Full Text] [Related]
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16. Structural determinants of selective affinity for brain D-1 dopamine receptors within a series of 1-phenyl-1H-3-benzazepine analogues of SK&F 38393 and SCH 23390. O'Boyle KM; Waddington JL Eur J Pharmacol; 1985 Sep; 115(2-3):291-5. PubMed ID: 2866103 [TBL] [Abstract][Full Text] [Related]
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