TenBrink RE - Search Results

1

Renin inhibitors containing psi[CH2O] pseudopeptide inserts.

TenBrink RE, Pals DT, Harris DW, Johnson GA. TenBrink RE, et al. J Med Chem. 1988 Mar;31(3):671-7. doi: 10.1021/jm00398a029. J Med Chem. 1988. PMID: 3279210

2

(S)-(-)-4-[4-[2-(isochroman-1-yl)ethyl]-piperazin-1-yl] benzenesulfonamide, a selective dopamine D4 antagonist.

TenBrink RE, Bergh CL, Duncan JN, Harris DW, Huff RM, Lahti RA, Lawson CF, Lutzke BS, Martin IJ, Rees SA, Schlachter SK, Sih JC, Smith MW. TenBrink RE, et al. J Med Chem. 1996 Jun 21;39(13):2435-7. doi: 10.1021/jm960084f. J Med Chem. 1996. PMID: 8691438 No abstract available.

3

1-(alkylamino)isochromans: hypotensives with peripheral and central activities.

McCall JM, McCall RB, TenBrink RE, Kamdar BV, Humphrey SJ, Sethy VH, Harris DW, Daenzer C. McCall JM, et al. Among authors: tenbrink re. J Med Chem. 1982 Jan;25(1):75-81. doi: 10.1021/jm00343a015. J Med Chem. 1982. PMID: 6123600

4

Tetrahydro-2-benzoxepins: a novel family of hypotensives.

TenBrink RE, McCall JM, Pals DT, McCall RB, Orley J, Humphrey SJ, Wendling MG. TenBrink RE, et al. J Med Chem. 1981 Jan;24(1):64-7. doi: 10.1021/jm00133a014. J Med Chem. 1981. PMID: 7205878

5

Pharmacological characterization of U-101387, a dopamine D4 receptor selective antagonist.

Merchant KM, Gill GS, Harris DW, Huff RM, Eaton MJ, Lookingland K, Lutzke BS, Mccall RB, Piercey MF, Schreur PJ, Sethy VH, Smith MW, Svensson KA, Tang AH, Vonvoigtlander PF, Tenbrink RE. Merchant KM, et al. Among authors: tenbrink re. J Pharmacol Exp Ther. 1996 Dec;279(3):1392-403. J Pharmacol Exp Ther. 1996. PMID: 8968364

6

Inhibitors of the protease from human immunodeficiency virus: synthesis, enzyme inhibition, and antiviral activity of a series of compounds containing the dihydroxyethylene transition-state isostere.

Thaisrivongs S, Turner SR, Strohbach JW, TenBrink RE, Tarpley WG, McQuade TJ, Heinrikson RL, Tomasselli AG, Hui JO, Howe WJ. Thaisrivongs S, et al. Among authors: tenbrink re. J Med Chem. 1993 Apr 16;36(8):941-52. doi: 10.1021/jm00060a001. J Med Chem. 1993. PMID: 8478908

7

Arylformamidines with antinociceptive properties.

Gall M, McCall JM, TenBrink RE, Von Voigtlander PF, Mohrland JS. Gall M, et al. Among authors: tenbrink re. J Med Chem. 1988 Sep;31(9):1816-20. doi: 10.1021/jm00117a023. J Med Chem. 1988. PMID: 3411603

8

Antagonist, partial agonist, and full agonist imidazo[1,5-a]quinoxaline amides and carbamates acting through the GABAA/benzodiazepine receptor.

TenBrink RE, Im WB, Sethy VH, Tang AH, Carter DB. TenBrink RE, et al. J Med Chem. 1994 Mar 18;37(6):758-68. doi: 10.1021/jm00032a008. J Med Chem. 1994. PMID: 8145225

9

Piperazine imidazo[1,5-a]quinoxaline ureas as high-affinity GABAA ligands of dual functionality.

Jacobsen EJ, Stelzer LS, TenBrink RE, Belonga KL, Carter DB, Im HK, Im WB, Sethy VH, Tang AH, VonVoigtlander PF, Petke JD, Zhong WZ, Mickelson JW. Jacobsen EJ, et al. Among authors: tenbrink re. J Med Chem. 1999 Apr 8;42(7):1123-44. doi: 10.1021/jm9801307. J Med Chem. 1999. PMID: 10197957

10

High-affinity partial agonist imidazo[1,5-a]quinoxaline amides, carbamates, and ureas at the gamma-aminobutyric acid A/benzodiazepine receptor complex.

Jacobsen EJ, TenBrink RE, Stelzer LS, Belonga KL, Carter DB, Im HK, Im WB, Sethy VH, Tang AH, VonVoigtlander PF, Petke JD. Jacobsen EJ, et al. Among authors: tenbrink re. J Med Chem. 1996 Jan 5;39(1):158-75. doi: 10.1021/jm940765f. J Med Chem. 1996. PMID: 8568803

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