W. Randall

发表

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

J J Baldwin, J. Springer, G. M. Smith, 1994, Protein science : a publication of the Protein Society.

A potent cyclic hexapeptide analogue of somatostatin

Ruth F. Nutt, Roger M. Freidinger, Ralph Hirschmann, 1981, Nature.

Pharmacological profile of a new potent and specific α2-adrenoceptor antagonist, L-657,743

V. J. Lotti, J. Huff, J. Vacca, 1987, Naunyn-Schmiedeberg's Archives of Pharmacology.

Chemical synthesis of echistatin, a potent inhibitor of platelet aggregation from Echis carinatus: synthesis and biological activity of selected analogs.

D. Veber, R. Freidinger, V. Garsky, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Fructose-3-phosphate production and polyol pathway metabolism in diabetic rat hearts.

T. Brown, B. Szwergold, A. Taylor, 1997, Metabolism: clinical and experimental.

Pyridinylpiperazines, a new class of selective alpha 2-adrenoceptor antagonists.

P. Anderson, V. J. Lotti, J. Huff, 1983, Journal of medicinal chemistry.

Multiple central α2 adrenoceptors of avian and mammalian species

W. Randall, J. Baldwin, R. Tolman, 1983 .

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

P. Anderson, E. Eichler, W. Randall, 1979, Journal of medicinal chemistry.

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

G. Ponticello, W. Randall, J. Baldwin, 1987, Journal of medicinal chemistry.

Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase.

P. Mallorga, W. Randall, S. Graham, 1993, Journal of medicinal chemistry.

L-654,284 a new potent and selective α2-adrenoceptor antagonist

V. J. Lotti, J. Huff, J. Vacca, 1986, Naunyn-Schmiedeberg's Archives of Pharmacology.

Production and Metabolism of 3-Deoxyglucosone in Humans

T. Brown, B. Szwergold, P. Beisswenger, 2005 .

SYNTHESIS OF 4-SUBSTITUTED 2H-NAPHTH(1,2-B)-1,4-OXAZINES, A NEW CLASS OF DOPAMINE AGONISTS

G. F. Lundell, P. Anderson, J. Hirshfield, 1985 .

N-(1,3,4,6,7,12b-hexahydro-2H-benzo[b]furo[2,3-a]quinolizin -2-yl)-N- methyl-2-hydroxyethane-sulfonamide: a potent and selective alpha 2-adrenoceptor antagonist.

P. Anderson, V. J. Lotti, J. Huff, 1985, Journal of medicinal chemistry.

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

A. Patchett, E. Eichler, W. Randall, 1983, Journal of medicinal chemistry.

Production of fructose and fructose-3-phosphate in maturing rat lenses.

T. Brown, B. Szwergold, A. Taylor, 1995, Investigative ophthalmology & visual science.

Synthesis and antihypertensive activity of some ester progenitors of methyldopa.

W. Randall, E. Engelhardt, R. Hirschmann, 1978, Journal of medicinal chemistry.

Purification and characterization of human liver glycolate oxidase. Molecular weight, subunit, and kinetic properties.

W. Randall, R. Hirschmann, H. Schwam, 1979, Biochemistry.

Antihypertensive beta-adrenergic blocking agents: N-aralkyl analogues of 2-[3-(tert-butylamino)-2-hydroxypropoxy]-3-cyanopyridine.

G. F. Lundell, W. Randall, J. Baldwin, 1983, Journal of medicinal chemistry.

[3H]L-654,284 as a probe of the central alpha2 adrenoceptor

J. Huff, J. Vacca, W. Randall, 1988, Naunyn-Schmiedeberg's Archives of Pharmacology.

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

E. Eichler, W. Randall, E. Ulm, 1983, Journal of medicinal chemistry.

Synthesis, assignment of absolute configuration, and receptor binding studies relevant to the neuroleptic activities of a series of chiral 3-substituted cyproheptadine atropisomers.

K. Rittle, P. Anderson, J. Springer, 1979, Journal of medicinal chemistry.

Multiple central WB-4101 binding sites and the selectivity of prazosin.

W. Randall, T. Lyon, 1980, Life sciences.

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

R L Smith, P. Mallorga, W. Randall, 1992, Journal of medicinal chemistry.

Inhibitors of gastric acid secretion: 3,4-diamino-1,2,5-thiadiazole 1-oxides and 1,1-dioxides as urea equivalents in a series of histamine H2-receptor antagonists.

B. T. Phillips, P. Anderson, J. Hirshfield, 1982, Journal of medicinal chemistry.

Carbonic anhydrase inhibitors for the treatment of glaucoma

J J Baldwin, M. Murcko, P. Anderson, 2023, Медицинская этика.

The Role of 3-Deoxyglucosone and the Activity of its Degradative Pathways in the Etiology of Diabetic Microvascular Disease

T. Brown, B. Szwergold, S. Howell, 2005 .

Identification of galactitol 2-phosphate and galactitol 3-phosphate in the lens of galactose-fed rats.

T. Brown, B. Szwergold, W. Randall, 1995, Metabolism: clinical and experimental.

The kinetics of thiocyanate binding to aquocobalamin.

R. Alberty, W. Randall, 1966, Biochemistry.

Synthesis of 4-substituted 2H-naphth[1,2-b]-1,4-oxazines, a new class of dopamine agonists.

G. F. Lundell, P. Anderson, J. Hirshfield, 1984, Journal of medicinal chemistry.

SYNTHESIS AND ANTIHYPERTENSIVE ACTIVITY OF SOME ESTER PROGENITORS OF METHYLDOPA

W. Randall, E. Engelhardt, R. Hirschmann, 1978 .

Structure-affinity relationships of arylquinolizines at alpha-adrenoceptors.

J. Huff, J. Vacca, W. Randall, 1988, Journal of medicinal chemistry.

Conformational modifications of cyclic hexapeptide somatostatin analogs.

D. Veber, R. Freidinger, W. Randall, 2009, International journal of peptide and protein research.

Synthesis of (7R)-7H-indolo[3,4-gh][1,4]benzoxazines, a new class of D-heteroergolines with dopamine agonist activity.

G. F. Lundell, P. Anderson, J. Hirshfield, 1983, Journal of medicinal chemistry.

SYNTHESIS OF (7R)-7H-INDOLO(3,4-GH)(1,4)BENZOXAZINES, A NEW CLASS OF D-HETEROERGOLINES WITH DOPAMINE AGONIST ACTIVITY

G. F. Lundell, P. Anderson, J. Hirshfield, 1983 .

Piperazinylimidazo[1,2-a]pyrazines with selective affinity for in vitro alpha-adrenergic receptor subtypes.

J. Huff, W. Randall, W. C. Lumma, 1983, Journal of medicinal chemistry.

Metabolism of fructose-3-phosphate in the diabetic rat lens.

T. Brown, B. Szwergold, A. Taylor, 1995, Archives of biochemistry and biophysics.

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

J. Springer, D. Christianson, R. Alexander, 1994, Protein science : a publication of the Protein Society.

Synthesis and receptor binding studies relevant to the neuroleptic activities of some 1-methyl-4-piperidylidene-9-substituted-pyrrolo[2,1-b][3]benzazepine derivatives.

P. Anderson, W. Randall, M. Williams, 1983, Journal of medicinal chemistry.