Randall WC - Search Results

1

Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase.

Scholz TH, Sondey JM, Randall WC, Schwam H, Thompson WJ, Mallorga PJ, Sugrue MF, Graham SL. Scholz TH, et al. Among authors: randall wc. J Med Chem. 1993 Jul 23;36(15):2134-41. doi: 10.1021/jm00067a012. J Med Chem. 1993. PMID: 8340917

2

4-substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors.

Hartman GD, Halczenko W, Smith RL, Sugŕue MF, Mallorga PJ, Michelson SR, Randall WC, Schwam H, Sondey JM. Hartman GD, et al. Among authors: randall wc. J Med Chem. 1992 Oct 16;35(21):3822-31. doi: 10.1021/jm00099a010. J Med Chem. 1992. PMID: 1433194

3

Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitors.

Hartman GD, Halczenko W, Prugh JD, Smith RL, Sugrue MF, Mallorga P, Michelson SR, Randall WC, Schwam H, Sondey JM. Hartman GD, et al. Among authors: randall wc. J Med Chem. 1992 Aug 7;35(16):3027-33. doi: 10.1021/jm00094a016. J Med Chem. 1992. PMID: 1501230

4

Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucoma.

Baldwin JJ, Ponticello GS, Anderson PS, Christy ME, Murcko MA, Randall WC, Schwam H, Sugrue MF, Springer JP, Gautheron P, et al. Baldwin JJ, et al. Among authors: randall wc. J Med Chem. 1989 Dec;32(12):2510-3. doi: 10.1021/jm00132a003. J Med Chem. 1989. PMID: 2585439 No abstract available.

5

Thienothiopyran-2-sulfonamides: a novel class of water-soluble carbonic anhydrase inhibitors.

Ponticello GS, Freedman MB, Habecker CN, Lyle PA, Schwam H, Varga SL, Christy ME, Randall WC, Baldwin JJ. Ponticello GS, et al. Among authors: randall wc. J Med Chem. 1987 Apr;30(4):591-7. doi: 10.1021/jm00387a002. J Med Chem. 1987. PMID: 3560154

6

Quantitative structure-activity relationships involving the inhibition of glycolic acid oxidase by derivatives of glycolic and glyoxylic acids.

Randall WC, Streeter KB, Cresson EL, Schwam H, Michelson SR, Anderson PS, Cragoe EJ Jr, Williams HW, Eichler E, Rooney CS. Randall WC, et al. J Med Chem. 1979 Jun;22(6):608-14. doi: 10.1021/jm00192a002. J Med Chem. 1979. PMID: 458816

7

Inhibitors of glycolic acid oxidase. 4-Substituted 3-hydroxy-1H-pyrrole-2,5-dione derivatives.

Rooney CS, Randall WC, Streeter KB, Ziegler C, Cragoe EJ Jr, Schwam H, Michelson SR, Williams HW, Eichler E, Duggan DE, Ulm EH, Noll RM. Rooney CS, et al. Among authors: randall wc. J Med Chem. 1983 May;26(5):700-14. doi: 10.1021/jm00359a015. J Med Chem. 1983. PMID: 6341589

8

Inhibitors of glycolic acid oxidase. 4-substituted 2,4-dioxobutanoic acid derivatives.

Williams HW, Eichler E, Randall WC, Rooney CS, Cragoe EJ Jr, Streeter KB, Schwam H, Michelson SR, Patchett AA, Taub D. Williams HW, et al. Among authors: randall wc. J Med Chem. 1983 Aug;26(8):1196-200. doi: 10.1021/jm00362a020. J Med Chem. 1983. PMID: 6348285

9

Positions of His-64 and a bound water in human carbonic anhydrase II upon binding three structurally related inhibitors.

Smith GM, Alexander RS, Christianson DW, McKeever BM, Ponticello GS, Springer JP, Randall WC, Baldwin JJ, Habecker CN. Smith GM, et al. Among authors: randall wc. Protein Sci. 1994 Jan;3(1):118-25. doi: 10.1002/pro.5560030115. Protein Sci. 1994. PMID: 8142888 Free PMC article.

10

Structure-affinity relationships of arylquinolizines at alpha-adrenoceptors.

Huff JR, Baldwin JJ, deSolms SJ, Guare JP Jr, Hunt CA, Randall WC, Sanders WS, Smith SJ, Vacca JP, Zrada MM. Huff JR, et al. Among authors: randall wc. J Med Chem. 1988 Mar;31(3):641-5. doi: 10.1021/jm00398a025. J Med Chem. 1988. PMID: 2831365

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