S. Baker

发表

The discovery of LY293111, a novel, potent and orally active leukotriene B4 receptor antagonist of the biphenylphenol class.

W. Jackson, M. Sofia, S. Silbaugh, 1997, Advances in experimental medicine and biology.

The comparative in vitro pharmacology of leukotriene D4 and its isomers.

J. Boot, D. J. Osborne, S. Baker, 1981, Biochemical and biophysical research communications.

Effects of leukotriene B4 inhalation. Airway sensitization and lung granulocyte infiltration in the guinea pig.

S. Silbaugh, D. K. Herron, P. Stengel, 1987, The American review of respiratory disease.

PIPERAZINE-2,3,5-TRIONES IN THE SYNTHESIS OF CONSTRAINED PEPTIDES

G. Rosair, P. Bailey, A. N. Boa, 1999 .

Evidence for multiple leukotriene D4 receptors in smooth muscle.

J. Fleisch, L. Rinkema, S. Baker, 1982, Life sciences.

Aerosolized LTB4 produces delayed onset increases in pulmonary gas trapping.

A. Bendele, W. Jackson, M. Sofia, 1996, Prostaglandins, leukotrienes, and essential fatty acids.

Identification and Pharmacological Profile of a New Class of Selective Nicotinic Acetylcholine Receptor Potentiators

E. Sher, L. Wallace, L. Broad, 2006, Journal of Pharmacology and Experimental Therapeutics.

A comparative study of the physical properties and enzymatic reactions of slow reacting substance of anaphylaxis and some leukotriene D4 isomers.

J. Boot, D. J. Osborne, S. Baker, 1982, Prostaglandins.

Effects of diatrizoate and iopamidol on spermatogenesis.

V. Yaghmai, Y. Patel, R. S. Harapanhalli, 1993, Investigative radiology.

Separation of the N-trifluoroacetldimethyl esters of leukotriene D and E isomers by semi-preparative high-performance liquid chromatography

J. M. Smith, S. Baker, R. Koenigsberger, 1981 .

The Synthesis of Biphenyl Amino Acids and Related 2,3- Dihydroimidazo[1,2-a]dibenz[c,e]azepines

S. Baker, J. Goldsworthy, 1994 .

Structural analogues of LY292728, a highly potent xanthone dicarboxylic acid leukotriene B4 receptor antagonist: spatial positioning of the secondary acid group

W. Jackson, J. S. Sawyer, L. L. Froelich, 1994 .

PALLADIUM CATALYSIS IN CEPHALOSPORIN CHEMISTRY : GENERAL METHODOLOGY FOR THE SYNTHESIS OF CEPHEM SIDE CHAINS

V. Farina, S. Hauck, C. Sapino, 1990 .

Palladium-catalyzed coupling between cephalosporin derivatives and unsaturated stannanes: A new ligand for palladium chemistry

V. Farina, C. Sapino, D. Benigni, 1988 .

A Convenient Synthesis of Some 1,4-Disubstituted 7-Oxabicyclo[2.2.1]heptanes

J. R. Harris, S. Baker, 1991 .

The synthesis of [2.2.2]bicyclooctane and [3.1.1]bicycloheptane based amino acids as constrained glutamate analogues

T. Hancox, S. Baker, 1999 .

Enantiospecific synthesis of (1S,2S,5R,6S)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid by a modified Corey-Link reaction

C. Domínguez, J. Ezquerra, S. Baker, 1998 .

Palladium in Cephalosporin Chemistry: Mild Triflate Couplings in the Absence of Phosphines and Halide Donors

G. Roth, C. Sapino, S. Baker, 1990 .

Palladium catalysis in cephalosporin chemistry: A versatile new approach to 3-substituted cephems

V. Farina, C. Sapino, S. Baker, 1988 .

Reactions of organocuprates with vinyl-triflates and related cephems: A novel approach to 3-substituted cephalosporins

J. Kant, C. Sapino, S. Baker, 1990 .

Synthesis of leukotriene A4 methyl ester from D-glucose

A. Mckillop, D. Clissold, S. Baker, 1988 .

(+)-2-Methyl-4-carboxyphenylglycine (LY367385) selectively antagonises metabotropic glutamate mGluR1 receptors

B. Clark, A. Kingston, J. R. Harris, 1997 .

Synthesis of 8,9-leukotriene C3 and D3

W. J. Ross, J. Boot, D. J. Osborne, 1984 .

7-(α-AMINOPHENYLACETAMIDO)-3-AZIDOMETHYL-3-CEPHEM-4-CARBOXYLIG ACID

D. Willner, S. Baker, L. C. Cheney, 1972 .

3,5‐Dihydroxyphenylglycine Is a Highly Selective Agonist for Phosphoinositide‐Linked Metabotropic Glutamate Receptors in the Rat Hippocampus

D. Schoepp, D D Schoepp, B G Johnson, 1994, Journal of neurochemistry.

Maximizing the use of food emulsifiers

S. Baker, 2010 .

The crystal structure of free radical salts and complexes. VI. [l,4-Di-(N-pyridiniummethyl)benzene]2+ (7,7,8,8-tetracyanoquinodimethane)42−

G. Ashwell, S. Wallwork, P. Berthier, 1975 .

Glycosphingolipid synthesis and tumorigenesis. A role for the Golgi apparatus in the origin of specific receptor molecules of the mammalian cell surface.

C. Richardson, T. W. Keenan, D. Morré, 1975, Biochimica et biophysica acta.

Glycosaminoglycans and other carbohydrate groups bound to proteins of control and transformed cells.

C. Buck, D. Blithe, L. Warren, 1980, The Journal of biological chemistry.

Glycopeptides derived from individual membrane glycoproteins from control and Rous sarcoma virus-transformed hamster fibroblasts.

G. Tuszynski, C. Buck, L. Warren, 1978, The Journal of biological chemistry.

The role of carbohydrates bound to proteins.

C. Buck, D. Blithe, L. Warren, 1983, Biomembranes.

4-Alkyl- and 4-cinnamylglutamic acid analogues are potent GluR5 kainate receptor agonists.

B. Ballyk, C. Dominguez, D. Bleakman, 2000, Journal of medicinal chemistry.

(2S,4S)-amino-4-(2,2-diphenylethyl)pentanedioic acid selective group 2 metabotropic glutamate receptor antagonist.

D. Schoepp, C. Pedregal, B. Johnson, 1998, Bioorganic & medicinal chemistry letters.

Ornithine carbamoyltransferase activity and embryogenesis in a carrot cell suspension culture

L. H. Jones, R. J. Yon, S. Baker, 1983 .

Characterization of ornithine carbamoyltransferase from cultured carrot cells of low embryogenic potential

R. J. Yon, S. Baker, 1983 .

Synthesis and Pharmacological Characterization of C4-(Thiotriazolyl)-substituted-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylates. Identification of (1R,2S,4R,5R,6R)-2-Amino-4-(1H-1,2,4-triazol-3-ylsulfanyl)bicyclo[3.1.0]hexane-2,6-dicarboxylic Acid (LY2812223), a Highly Potent, Functionally Selective

D. McKinzie, D. Clawson, S. Atwell, 2015, Journal of medicinal chemistry.

Synthesis and pharmacological characterization of C4-disubstituted analogs of 1S,2S,5R,6S-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate: identification of a potent, selective metabotropic glutamate receptor agonist and determination of agonist-bound human mGlu2 and mGlu3 amino terminal domain struct

D. McKinzie, D. Clawson, S. Atwell, 2015, Journal of medicinal chemistry.

Extensive calcification in the inferior vena cava in an adult.

V. Yaghmai, S. Baker, 1993, AJR. American journal of roentgenology.

A general route to 3-functionalized 3-norcephalosporins

V. Farina, S. Hauck, S. Baker, 1989 .

Comparison of values for standardized total tract digestibility and relative bioavailability of phosphorus in dicalcium phosphate and distillers dried grains with solubles fed to growing pigs.

H. Stein, B. G. Kim, S. Baker, 2013, Journal of animal science.

Leukotrienes (LTB4 and LTD4): in vitro effects on human lymphocyte proliferation and transformation.

D. K. Herron, E. Ades, A. Tilden, 1984, Journal of clinical & laboratory immunology.

Synthetic and structure/activity studies on acid-substituted 2-arylphenols: discovery of 2-[2-propyl-3-[3-[2-ethyl-4-(4-fluorophenyl)-5- hydroxyphenoxy]-propoxy]phenoxy]benzoic acid, a high-affinity leukotriene B4 receptor antagonist.

W. Jackson, J. S. Sawyer, P. Floreancig, 1995, Journal of medicinal chemistry.

Synthetic and Structure-Activity Studies on Acid-Substituted 2- Arylphenols: Discovery of 2-(2-Propyl-3-(3-(2-ethyl-4-(4-fluorophenyl)- 5-hydroxyphenoxy)propoxy)phenoxy)benzoic Acid, a High-Affinity Leukotriene B4 Receptor Antagonist.

W. Jackson, M. Sofia, S. Silbaugh, 1996 .

Disodium D-6-[alpha-(1,2,4-triazine-3,5-dione-6-carboxamido)-4-hydroxyphenylacetamido]penicillanate, BL-P1908.

D. N. Mcgregor, S. Baker, C. T. Holdrege, 1979, The Journal of antibiotics.

Allosteric Potentiators of Neuronal Nicotinic Cholinergic Receptors: Potential Treatments for Neurodegenerative Disorders

E. Sher, L. Wallace, L. Broad, 2008 .

4-Alkylidenyl glutamic acids, potent and selective GluR5 agonists.

B. Ballyk, C. Dominguez, D. Bleakman, 2000, Bioorganic & medicinal chemistry letters.

Second-messenger responses in brain slices to elucidate novel glutamate receptors

D. Schoepp, Bryan G. Johnson, R. Wright, 1995, Journal of Neuroscience Methods.

Leukotriene receptor on U-937 cells: discriminatory responses to leukotrienes C4 and D4.

J. Drazen, D. K. Herron, H. Feldman, 1991, The American journal of physiology.

Recent progress in the development of subtype selective nicotinic acetylcholine receptor ligands.

J. Boot, L. Broad, P. Astles, 2002, Current drug targets. CNS and neurological disorders.

PSAB-OFP, a selective alpha 7 nicotinic receptor agonist, is also a potent agonist of the 5-HT3 receptor.

E. Sher, L. Wallace, J. Boot, 2002, European journal of pharmacology.

Enzymatic resolution and pharmacological activity of the enantiomers of 3,5-dihydroxyphenylglycine, a metabotropic glutamate receptor agonist

D. Schoepp, C. Salhoff, R. C. Harden, 1995 .

Enzymatic Resolution and Pharmacological Activity of the Enantiomers of 3,5-Dihydroxyphenylglycine, a Metabotropic Glutamate Receptor Agonist.

D. Schoepp, C. Salhoff, R. C. Harden, 1995 .

High affinity ligands for the alpha7 nicotinic receptor that show no cross-reactivity with the 5-HT3 receptor.

L. Wallace, J. Boot, D. Dobson, 2005, Bioorganic & medicinal chemistry letters.

The pharmacology of N-methyl LTC4; a metabolically stable LTC4-mimetic.

J. Boot, M. Ward, R. Gooderham, 1990, Prostaglandins.

Biarylpropylsulfonamides as novel, potent potentiators of 2-amino-3- (5-methyl-3-hydroxyisoxazol-4-yl)- propanoic acid (AMPA) receptors.

P. Ornstein, D. Bleakman, B. Cantrell, 2000, Journal of medicinal chemistry.

Excitotoxic profile of LY339434, a GluR5 agonist, in cultured murine cortical neurons

P. Beart, N. Cheung, C. Pedregal, 2000, Brain Research.

(+)-2-Methyl-4-carboxyphenylglycine (LY367385) Selectively Antagonises Metabotropic Glutamate mGluR1 Receptors.

B. Clark, A. Kingston, J. R. Harris, 1998 .

Semi-preparative high-performance liquid chromatography and spectroscopic characterisation of eight geometric isomers of leukotriene A methyl ester

W. J. Ross, J. M. Smith, S. Morgan, 1981 .