Search Results - "Ponticello, GS"

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    Pyridazine based inhibitors of p38 MAPK by McIntyre, Charles J, Ponticello, Gerald S, Liverton, Nigel J, O’Keefe, Stephen J, O’Neill, Edward A, Pang, Margaret, Schwartz, Cheryl D, Claremon, David A

    Published in Bioorganic & medicinal chemistry letters (25-02-2002)
    “…Trisubstituted pyridazines were synthesized and evaluated as in vitro inhibitors of p38 MAPK. The most active isomers were those possessing an aryl group α and…”
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    Identification and SAR for a selective, nonpeptidyl thrombin inhibitor by Naylor-Olsen, Adel M., Ponticello, Gerald S., Lewis, S.Dale, Mulichak, Anne M., Chen, Zhonguo, Habecker, Charles N., Phillips, Brian T., Sanders, William M., Tucker, Thomas J., Shafer, Jules A., Vacca, Joseph P.

    Published in Bioorganic & medicinal chemistry letters (07-07-1998)
    “…A novel, nonpeptidyl thrombin inhibitor, L-636,619 ( 1), was identified via topological similarity searching over the Merck Corporate Sample Database. X-ray…”
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    Topically active carbonic anhydrase inhibitors. 2. Benzo[b]thiophenesulfonamide derivatives with ocular hypotensive activity by Graham, Samuel L, Shepard, Kenneth L, Anderson, Paul S, Baldwin, John J, Best, Darryl B, Christy, Marcia E, Freedman, Mark B, Gautheron, Pierre, Habecker, Charles N

    Published in Journal of medicinal chemistry (01-12-1989)
    “…Derivatives of benzo[b]thiophene-2-sulfonamide were prepared to investigate their potential utility as topically active inhibitors of ocular carbonic…”
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    Thienothiopyran-2-sulfonamides: a novel class of water-soluble carbonic anhydrase inhibitors by Ponticello, Gerald S, Freedman, Mark B, Habecker, Charles N, Lyle, Paulette A, Schwam, Harvey, Varga, Sandor L, Christy, Marcia E, Randall, William C, Baldwin, John J

    Published in Journal of medicinal chemistry (01-04-1987)
    “…An attempt to develop a water-soluble carbonic anhydrase inhibitor focused on exploring structure-activity relationships in the thienothiopyransulfonamide…”
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    A short radiosynthesis of 6-[C3H3]-dorzolamide at very high specific activity and optical purity by Eng, W.-s., Burns, H. D., Ponticello, G. S., Selnick, H. G.

    “…6‐[C3H3]‐Dorzolamide was prepared starting from N, N′‐bis‐Boc‐6‐desmethyl‐dorzolamide. An efficient radiosynthesis was developed involving a regioselective and…”
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    Beta 1-selective adrenoceptor antagonists: examples of the 2-[4-[3-(substituted amino)-2-hydroxypropoxy]phenyl]imidazole class. 2 by Baldwin, J J, Christy, M E, Denny, G H, Habecker, C N, Freedman, M B, Lyle, P A, Ponticello, G S, Varga, S L, Gross, D M, Sweet, C S

    Published in Journal of medicinal chemistry (01-06-1986)
    “…An attempt to develop a highly cardioselective beta-adrenoceptor antagonist devoid of intrinsic sympathomimetic activity (ISA) focused on exploring…”
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    L-653,328: an ocular hypotensive agent with modest beta receptor blocking activity by Sugrue, MF, Gautheron, P, Grove, J, Mallorga, P, Viader, MP, Baldwin, JJ, Ponticello, GS, Varga, SL

    “…L-653,328 is the acetate ester of L-652,698 ((S)-3-tert-butylamino-1-[4-[2(hydroxy)ethyl]phenoxy]2-propanol). The penetration of L-652,698 into the albino…”
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    MK-927: a topically active ocular hypotensive carbonic anhydrase inhibitor by Sugrue, M F, Gautheron, P, Grove, J, Mallorga, P, Viader, M P, Schwam, H, Baldwin, J J, Christy, M E, Ponticello, G S

    Published in Journal of ocular pharmacology (1990)
    “…MK-927 (dl-5,6-dihydro-4-(2-methylpropylamino)-4H-thieno(2,3b)thiopyra n-2-sulfonamide-7,7-dioxide hydrochloride) is a water soluble, carbonic anhydrase…”
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    Heterocyclic analogs of the antihypertensive .beta.-adrenergic blocking agent (S)-2-[3-(tert-butylamino)-2-hydroxypropoxy]-3-cyanopyridine by Baldwin, John J, Engelhardt, Edward L, Hirschmann, Ralph, Ponticello, Gerald S, Atkinson, Joseph G, Wasson, Burton K, Sweet, Charles S, Scriabine, Alexander

    Published in Journal of medicinal chemistry (01-01-1980)
    “…The synthesis of a series of isoelectronic analogues of (S)-2-[3-(tert-butylamino)-2-hydroxypropoxy]-3-cyanopyridine (1) are described; included in this group…”
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    Beta 1-selective adrenoceptor antagonists: examples of the 2-[4-[3-(substituted-amino)-2-hydroxypropoxy]phenyl]imidazole class by Baldwin, J J, Denny, G H, Hirschmann, R, Freedman, M B, Ponticello, G S, Gross, D M, Sweet, C S

    Published in Journal of medicinal chemistry (01-07-1983)
    “…A series of 2-[4-[3-(substituted-amino)-2-hydroxypropoxy]phenyl]imidazoles is described. The compounds were investigated in vitro for beta-adrenoceptor…”
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