Watson LS - Search Results

1

2-(Aminomethyl)phenols, a new class of saluretic agents. 6. Effects of N,O-spiroannulation and subsequent quaternization.

Stokker GE, Schultz EM, Smith RL, Cragoe EJ Jr, Russo HF, Watson LS, Ludden CT, Sweet CS. Stokker GE, et al. Among authors: watson ls. J Med Chem. 1983 Apr;26(4):585-90. doi: 10.1021/jm00358a024. J Med Chem. 1983. PMID: 6834393

2

2-(Aminomethyl)phenols, a new class of saluretic agents. 5. Fused-ring analogues.

Deana AA, Stokker GE, Schultz EM, Smith RL, Cragoe EJ Jr, Russo HF, Watson LS. Deana AA, et al. Among authors: watson ls. J Med Chem. 1983 Apr;26(4):580-5. doi: 10.1021/jm00358a023. J Med Chem. 1983. PMID: 6834392

3

2-(Aminomethyl)phenols, a new class of saluretic agents. 4. Effects of oxygen and/or nitrogen substitution.

Stokker GE, Deana AA, deSolms SJ, Schultz EM, Smith RL, Cragoe EJ Jr, Baer JE, Russo HF, Watson LS. Stokker GE, et al. Among authors: watson ls. J Med Chem. 1982 Jun;25(6):735-42. doi: 10.1021/jm00348a024. J Med Chem. 1982. PMID: 7097728

4

2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.

Stokker GE, Smith RL, Cragoe EJ Jr, Ludden CT, Russo HF, Sweet CS, Watson LS. Stokker GE, et al. Among authors: watson ls. J Med Chem. 1981 Jan;24(1):115-7. doi: 10.1021/jm00133a024. J Med Chem. 1981. PMID: 7205867

5

2-(Aminomethyl)phenols, a new class of saluretic agents. 3. Effects of functional group reorientation and modification.

Stokker GE, Deana AA, deSolms SJ, Schultz EM, Smith RL, Cragoe EJ Jr, Baer JE, Russo HF, Watson LS. Stokker GE, et al. Among authors: watson ls. J Med Chem. 1981 Sep;24(9):1063-7. doi: 10.1021/jm00141a009. J Med Chem. 1981. PMID: 7288821

6

2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.

Stokker GE, Deana AA, deSolms SJ, Schultz EM, Smith RL, Cragoe EJ Jr, Baer JE, Ludden CT, Russo HF, Scriabine A, Sweet CS, Watson LS. Stokker GE, et al. Among authors: watson ls. J Med Chem. 1980 Dec;23(12):1414-27. doi: 10.1021/jm00186a024. J Med Chem. 1980. PMID: 7452697

7

(1-oxo-2-substituted-5-indanyloxy)acetic acids, a new class of potent renal agents possessing both uricosuric and saluretic activity. A reexamination of the role of sulfhydryl binding in the mode of action of acylphenoxyacetic acidsaluretics.

Cragoe EJ Jr, Schultz EM, Schneeberg JD, Stokker GE, Woltersdorf OW Jr, Fanelli GM Jr, Watson LS. Cragoe EJ Jr, et al. Among authors: watson ls. J Med Chem. 1975 Feb;18(2):225-8. doi: 10.1021/jm00236a031. J Med Chem. 1975. PMID: 1120997 No abstract available.

8

(Vinylaryloxy)acetic acids. A new class of diuretic agents. 2. (4-(3-Oxo-1-alkenyl)phenoxy)acetic acids.

Bicking JB, Robb CM, Watson LS, Cragoe EJ Jr. Bicking JB, et al. Among authors: watson ls. J Med Chem. 1976 Apr;19(4):544-7. doi: 10.1021/jm00226a020. J Med Chem. 1976. PMID: 1263208

9

(Vinylaryloxy)acetic acids. A new class of diuretic agents. 4. Various ((2-substituted and 2,2-disubstituted vinyl)aryloxy)acetic acids.

Woltersdorf OW Jr, Robb CM, Bicking JB, Watson LS, Cragoe EJ Jr. Woltersdorf OW Jr, et al. Among authors: watson ls. J Med Chem. 1976 Jul;19(7):972-5. doi: 10.1021/jm00229a024. J Med Chem. 1976. PMID: 940118

10

(Vinylaryloxy)acetic acids. A new class of diuretic agents. 3. ((2-Nitro-1-alkenyl)aryloxy)acetic acids.

Schultz EM, Bicking JB, Deana AA, Gould NP, Strobauge TP, Watson LS, Cragoe EJ Jr. Schultz EM, et al. Among authors: watson ls. J Med Chem. 1976 Jun;19(6):783-7. doi: 10.1021/jm00228a009. J Med Chem. 1976. PMID: 950646

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