Lau Cheuk-Kun

发表

The discovery of a new structural class of potent orally active leukotriene D4 antagonists

R. Young, P. Prasit, A. Ford-hutchinson, 1992 .

Evolution of a series of non-quinoline leukotriene D4 receptor antagonist; synthesis and sar of benzothiazoles and thiazoles substituted benzyl alcohols as potent LTD4 antagonists

R. Young, A. Ford-hutchinson, R. Zamboni, 1995 .

The stereospecific synthesis of leukotriene A4 (LTA4), 5-epi-LTA4, 6-epi-LTA4 and 5-epi,6-epi-LTA4

R. Zamboni, J. Rokach, Y. Guindon, 1981 .

Stereospecific synthesis of leukotriene B4 (LTB4)

R. Zamboni, J. Rokach, Y. Guindon, 1982 .

From indomethacin to a selective COX-2 inhibitor: Development of indolalkanoic acids as potent and selective cyclooxygenase-2 inhibitors

C. Bayly, D. Denis, P. Prasit, 1996 .

Facile preparations of 4-fluororesorcinol

J. Scheigetz, P. Belanger, C. Dufresne, 1988 .

A C-glycoside route to leukotrienes

R. Zamboni, J. Rokach, Y. Guindon, 1981 .

SYNTHESIS AND BIOLOGICAL EVALUATION OF BOTH ENANTIOMERS OF L-761,000 AS INHIBITORS OF CYCLOOXYGENASE 1 AND 2

Yves Leblanc, Daniel Guay, Petpiboon Prasit, 1996 .

Syntheses of Quinolines, Dihydro‐ and Tetrahydroquinolines via ortho‐ Quinone Methide Imine Intermediates.

A. Caillé, L. Trimble, Lau Cheuk-Kun, 1996 .

Synthesis and Biological Evaluation of 2,3-Diarylthiophenes as Selective COX-2 Inhibitors. Part 2. Replacing the Heterocycle

D. Riendeau, P. Prasit, W. Cromlish, 1996 .

Synthetic leukotriene B4 is a potent chemotaxin but a weak secretagogue for human PMN.

R. Zamboni, J. Rokach, B. Zanolari, 1983, Prostaglandins.