S. Ross

发表

Discovery of orally active nonpeptide vitronectin receptor antagonists based on a 2-benzazepine Gly-Asp mimetic.

K. Ward, K. Erhard, R. Calvo, 2000, Journal of medicinal chemistry.

Multisubstrate inhibitors of dopamine beta-hydroxylase. 2. Structure-activity relationships at the phenethylamine binding site.

C. Kaiser, L I Kruse, C Kaiser, 1987, Journal of medicinal chemistry.

Multisubstrate Inhibitors of Dopamine β-Hydroxylates. Part 2. Structure-Activity Relationships at the Phenethylamine Binding Site.

E. Ohlstein, C. Kaiser, S. Ross, 1987 .

Phenylbutyrates as potent, orally bioavailable vitronectin receptor (integrin αvβ3) antagonists

K. Ward, R. Willette, T. Yue, 2003 .

Orally bioavailable nonpeptide vitronectin receptor antagonists with efficacy in an osteoporosis model.

K. Erhard, R. Keenan, M. Lark, 1999, Bioorganic & medicinal chemistry letters.

Discovery of an imidazopyridine-containing 1,4-benzodiazepine nonpeptide vitronectin receptor (αvβ3) antagonist with efficacy in a restenosis model

B. Smith, T. Yue, E. Ohlstein, 1998 .

Benzimidazole derivatives as arginine mimetics in 1,4-benzodiazepine nonpeptide vitronectin receptor (αvβ3) antagonists

B. Smith, R. Calvo, R. Keenan, 1998 .

Irreversible interaction of beta-haloalkylamine derivatives with dopamine D1 and D2 receptors.

J. Waddington, A. Cross, S. Ross, 1983, Life sciences.

Synthesis, renal vasodilator and dopamine-sensitive adenylate cyclase activities of O-Methyl derivatives of 6-chloro-2,3,4,5-tetr ahydro-1-(4-hydroxyphenyl)-1H-3-benzazepin-7,8-diol (SK&F 82526)

H. Sarau, S. Ross, R. A. Hahn, 1986 .

Enantiospecific synthesis of SB 214857, a potent, orally active, nonpeptide fibrinogen receptor antagonist

K. Erhard, R. Calvo, R. Keenan, 1995 .

Potent, selective, orally active 3-oxo-1,4-benzodiazepine GPIIb/IIIa integrin antagonists.

C. E. Peishoff, K. Erhard, R. Calvo, 1996, Journal of medicinal chemistry.

The Preparation and Reactions of Some Halophosphoranes1

D. B. Denney, S. Ross, 1962 .

Inhibitors of dopamine beta-hydroxylase. 3. Some 1-(pyridylmethyl)imidazole-2-thiones.

E. Ohlstein, B A Berkowitz, E H Ohlstein, 1987, Journal of medicinal chemistry.

Some benzyl-substituted imidazoles, triazoles, tetrazoles, pyridinethiones, and structural relatives as multisubstrate inhibitors of dopamine beta-hydroxylase. 4. Structure-activity relationships at the copper binding site.

C. Kaiser, L I Kruse, C Kaiser, 1990, Journal of medicinal chemistry.

Synthesis and antineoplastic activity of alanyl-2-glycyl peptide derivatives of nocodazole

K. Erhard, S. Ross, F. McCabe, 1989 .

Original paperSynthesis and antineoplastic activity of alanyl-2-glycyl peptide derivatives of nocodazoleSynthèse et activité antinéoplastique de dérivés alanyl-2-glycyl peptide de nocodazole

K. Erhard, S. Ross, F. McCabe, 1989 .

Regioselective alkylation at the N4 positionof a 3-oxo-1,4-benzodiazepine on solid support

C. Yuan, S. Ross, F. Ali, 2004, Molecular Diversity.

Design and characterization of orally active Arg-Gly-Asp peptidomimetic vitronectin receptor antagonist SB 265123 for prevention of bone loss in osteoporosis.

K. Erhard, B. R. Smith, M. Lark, 1999, Journal of Pharmacology and Experimental Therapeutics.

Chapter 6. Agents Affecting Appetite

S. Ross, G. C. Heil, 1973 .

Syntheses and in vitro evaluation of 4-(2-aminoethyl)-2(3H)-indolones and related compounds as peripheral prejunctional dopamine receptor agonists.

R. Hall, C. Kaiser, W. Huffman, 1986, Journal of medicinal chemistry.

Synthesis, Renal Vasodilator, and Dopamine-Sensitive Adenylate Cyclase Activities of O-Methyl Derivatives of 6-Chloro-2,3,4,5-tetrahydro-1-(4- hydroxyphenyl)-1H-3-benzazepin-7,8-diol (SK&F 82526).

H. Sarau, S. Ross, R. A. Hahn, 1987 .

Dopamine receptor agonists: 3-allyl-6-chloro-2,3,4,5-tetrahydro- 1-(4-hydroxyphenyl)-1H-3-benzazepine-7,8-diol and a series of related 3-benzazepines.

H. Sarau, J. Hieble, S. Ross, 1986, Journal of medicinal chemistry.

STRUCTURAL ASSIGNMENTS OF 2-ARYL AND 3-ARYLBENZOFURANS BY CARBON-13 NMR

S. Ross, G. Y. Kuo, 1978 .