S. Hall

发表

Mapping of epitopes, glycosylation sites, and complement regulatory domains in human decay accelerating factor.

T. Fujita, T. Kinoshita, K. Coyne, 1992, Journal of immunology.

Recent advances in solid phase synthesis

S. Hall, Steven E. Hall, 2010, Molecular Diversity.

Chemoproteomics-driven drug discovery: addressing high attrition rates.

S. Hall, Steven E Hall, 2006, Drug discovery today.

Discovery of novel 2-aminobenzamide inhibitors of heat shock protein 90 as potent, selective and orally active antitumor agents.

Laura G. Dubois, Philip F. Hughes, J. Strachan, 2009, Journal of medicinal chemistry.

Discovery of novel aminoquinazolin-7-yl 6,7-dihydro-indol-4-ones as potent, selective inhibitors of heat shock protein 90.

Philip F. Hughes, J. Veal, S. Hall, 2012, Bioorganic & medicinal chemistry letters.

Discovery of benzamide tetrahydro-4H-carbazol-4-ones as novel small molecule inhibitors of Hsp90.

J. Veal, S. Hall, J. Rice, 2008, Bioorganic & medicinal chemistry letters.

Small molecule inhibitors of Hsp90 potently affect inflammatory disease pathways and exhibit activity in models of rheumatoid arthritis.

Laura G. Dubois, J. Veal, P. Fadden, 2008, Arthritis and rheumatism.

Interphenylene 7-oxabicyclo[2.2.1]heptane oxazoles. Highly potent, selective, and long-acting thromboxane A2 receptor antagonists.

O. Kocy, J. Barrish, R. Misra, 1993, Journal of medicinal chemistry.

Purification of the human blood platelet thromboxane A2/prostaglandin H2 receptor protein.

G. L. Le Breton, S. O. Kim, S. Hall, 1992, Biochemical pharmacology.

Lung type II cell and macrophage annexin I release: differential effects of two glucocorticoids.

P. Barnes, S. Hall, S. Lim, 1999, American journal of physiology. Lung cellular and molecular physiology.

Thromboxane A2 receptor antagonists

S. Hall, 1991, Medicinal research reviews.

Interphenylene 7-oxabicyclo[2.2.1]heptane thromboxane A2 antagonists. Semicarbazone omega-chains.

M. Webb, R. Misra, W. Han, 1991, Journal of medicinal chemistry.

(S)-13-[(dimethylamino)methyl]-10,11,14,15-tetrahydro-4,9:16, 21-dimetheno-1H, 13H-dibenzo[e,k]pyrrolo[3,4-h][1,4,13]oxadiazacyclohexadecene-1,3(2H)-d ione (LY333531) and related analogues: isozyme selective inhibitors of protein kinase C beta.

M. Faul, L. L. Winneroski, S. Hall, 1996, Journal of medicinal chemistry.

Stereoselective syntheses of substituted methyl (Z,E,E)-deca-2,7.9-trienoates and substituted methyl (Z,E,E)-undeca-2,8,10-trienoates

S. Hall, W. Roush, H. Gillis, 1980 .

1,2-Dibenzamidobenzene inhibitors of human factor Xa.

J. A. Kyle, J. Wikel, B. Eastwood, 2000, Journal of medicinal chemistry.

1,2-Dibenzamidobenzene inhibitors of human factor Xa.

J. A. Kyle, J. Wikel, B. Eastwood, 2000, Journal of medicinal chemistry.

Molecular design and structure--activity relationships leading to the potent, selective, and orally active thrombin active site inhibitor BMS-189664.

R. Moquin, James Lin, E. Iwanowicz, 2002, Bioorganic & medicinal chemistry letters.

A polymer-bound iminophosphorane approach for the synthesis of quinazolines.

J. Mayer, S. Hall, W. Zhang, 2001, Journal of combinatorial chemistry.

Novel carbazole and acyl-indole antimitotics.

J. Veal, S. Hall, J. Rice, 2009, Bioorganic & medicinal chemistry letters.

A new ligation method for N-terminal tryptophan-containing peptides using the Pictet–Spengler reaction

J. Tam, S. Hall, Lianshan Zhang, 2000 .

Synthesis of the bottom half of chlorothricolide

S. Hall, W. Roush, 1982 .

Studies on the total synthesis of chlorothricolide: stereochemical aspects of the intramolecular Diels-Alder reactions of methyl undeca-2,8,10-trienoates

S. Hall, W. Roush, 1981 .

Solid-phase synthesis of C-terminal peptide hydroxamic acids.

J. Mayer, S. Hall, W. Zhang, 2001, Journal of combinatorial chemistry.

9,11-Epoxy-9-homo-14-oxaprosta-5-enoic acid derivatives. Novel inhibitors of fatty acid cyclooxygenase.

W. Han, S. Hall, M. Ogletree, 1986, Journal of medicinal chemistry.

Thromboxane receptor antagonist BMS-180291: A new pre-clinical lead

J. Barrish, P. Sprague, R. Morrison, 1992 .

STUDIES ON THE TOTAL SYNTHESIS OF CHLOROTHRICOLIDE: STEREOCHEMICAL ASPECTS OF THE INTRAMOLECULAR DIELS‐ALDER REACTIONS OF METHYL UNDECA‐2,8,10‐TRIENOATES

S. Hall, W. Roush, 1981 .

Synthesis and protein kinase C inhibitory activities of balanol analogs with replacement of the perhydroazepine moiety.

W. Janzen, C. K. Biggers, J. Mendoza, 1997, Journal of medicinal chemistry.

Synthesis and protein kinase C inhibitory activities of indane analogs of balanol

S. Hall, L. M. Ballas, S. Hollinshead, 1996 .

SNX2112, a Synthetic Heat Shock Protein 90 Inhibitor, Has Potent Antitumor Activity against HER Kinase–Dependent Cancers

Sarat Chandarlapaty, Neal Rosen, David B. Solit, 2008, Clinical Cancer Research.

SNX-2112, a selective Hsp90 inhibitor, potently inhibits tumor cell growth, angiogenesis, and osteoclastogenesis in multiple myeloma and other hematologic tumors by abrogating signaling via Akt and ERK.

Hiroshi Yasui, Ken Huang, N. Raje, 2009, Blood.

Application of chemoproteomics to drug discovery: identification of a clinical candidate targeting hsp90.

Briana Foley, Laura G. Dubois, Philip F. Hughes, 2010, Chemistry & biology.

Characterization of [5,6-3H]SQ 29,548 as a high affinity radioligand, binding to thromboxane A2/prostaglandin H2-receptors in human platelets.

E. Liu, S. Hall, M. Ogletree, 1988, The Journal of pharmacology and experimental therapeutics.

Inhibition of prostaglandin biosynthesis by SQ 28,852, a 7-oxabicyclo[2.2.1]heptane analog.

S. Hall, M. Ogletree, D. Harris, 1986, Prostaglandins.

RING SIZE EFFECT IN THE PKC INHIBITORY ACTIVITIES OF PERHYDROAZEPINE ANALOGS OF BALANOL

S. Hall, Y. Lai, G. E. Jagdmann, 1995 .

D-Ala-D-X ligases: evaluation of D-alanyl phosphate intermediate by MIX, PIX and rapid quench studies.

C. Walsh, F. Raushel, L. S. Mullins, 2000, Chemistry & biology.

Synthesis and protein kinase inhibitory activity of balanol analogues with modified benzophenone subunits.

M. G. Johnson, M. P. Lynch, Philip F. Hughes, 2002, Journal of medicinal chemistry.

Synthesis and protein kinase C inhibitory activities of acyclic balanol analogs that are highly selective for protein kinase C over protein kinase A.

J. Mendoza, T. Mitchell, S. Hall, 1996, Journal of medicinal chemistry.

545 POSTER SNX-2112: a novel, selective, potent small molecule inhibitor of Hsp90 with unique pharmacodynamic properties

P. Fadden, S. Hall, A. Barbasz, 2006 .

Lung type II cell and macrophage annexin I release: differential effects of two glucocorticoids.

P. Barnes, S. Hall, A. Kamal, 1999, The American journal of physiology.

Novel PKC inhibitory analogs of balanol with replacement of the ester functionality

S. Hall, Hong Hu, Y. Lai, 1995 .

Targeting of multiple signaling pathways by the Hsp90 inhibitor SNX-2112 in EGFR resistance models as a single agent or in combination with erlotinib.

J. Veal, P. Fadden, S. Hall, 2009, Oncology research.

Fragmentations and reactions of protonated O,O-dimethyl ethylphosphonate and some isotopomers produced by electrospray ionisation in an ion trap mass spectrometer

F. Ferrante, S. Hall, V. Mikhailov, 2008 .

Solid-phase synthesis of 1,2,3, 4-tetrahydro-beta-carboline-containing peptidomimetics.

J. Tam, S. Hall, L. Zhang, 2000, Organic letters.