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Bioorganic & Medicinal Chemistry Letters
|
July 29, 2000
Difluoroketones as inhibitors of matrix metalloprotease-13
L A Reiter, G J Martinelli, L A Reeves, et al.
Annals of the New York Academy of Sciences
|
September 6, 1994
Inhibition of interleukin-1-stimulated collagen degradation in cartilage explants
P G Mitchell, L Lopresti-Morrow, S A Yocum, et al.
Journal of Medicinal Chemistry
|
February 1, 1990
Antiulcer agents. 4-substituted 2-guanidinothiazoles: reversible, competitive, and selective inhibitors of gastric H+,K(+)-ATPase
J L LaMattina, P A McCarthy, L A Reiter, et al.
Digestive Diseases and Sciences
|
December 1, 1991
CP-66,948: an antisecretory histamine H2-receptor antagonist with mucosal protective properties
J P Hakkinen, W F Holt, C J Goddard, et al.
Journal of Medicinal Chemistry
|
September 30, 1994
(+)-1-(3S,4R)-[3-(4-phenylbenzyl)-4-hydroxychroman-7-yl]cyclopentane carboxylic acid, a highly potent, selective leukotriene B4 antagonist with oral activity in the murine collagen-induced arthritis model
K Koch, L S Melvin, L A Reiter, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
trans-3-Benzyl-4-hydroxy-7-chromanylbenzoic acid derivatives as antagonists of the leukotriene B4 (LTB4) receptor
L A Reiter, K Koch, A D Piscopio, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 17, 1998
The preclinical pharmacological profile of the potent and selective leukotriene B4 antagonist CP-195543
H J Showell, M J Conklyn, R Alpert, et al.
Journal of Medicinal Chemistry
|
January 5, 1996
Discovery of the hemifumarate and (alpha-L-alanyloxy)methyl ether as prodrugs of an antirheumatic oxindole: prodrugs for the enolic OH group
R P Robinson, L A Reiter, W E Barth, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 18, 1999
Inhibition of MMP-1 and MMP-13 with phosphinic acids that exploit binding in the S2 pocket
L A Reiter, J P Rizzi, J Pandit, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 19 results.
Bioorganic & Medicinal Chemistry Letters
|
July 29, 2000
Difluoroketones as inhibitors of matrix metalloprotease-13
L A Reiter, G J Martinelli, L A Reeves, et al.
Annals of the New York Academy of Sciences
|
September 6, 1994
Inhibition of interleukin-1-stimulated collagen degradation in cartilage explants
P G Mitchell, L Lopresti-Morrow, S A Yocum, et al.
Journal of Medicinal Chemistry
|
February 1, 1990
Antiulcer agents. 4-substituted 2-guanidinothiazoles: reversible, competitive, and selective inhibitors of gastric H+,K(+)-ATPase
J L LaMattina, P A McCarthy, L A Reiter, et al.
Digestive Diseases and Sciences
|
December 1, 1991
CP-66,948: an antisecretory histamine H2-receptor antagonist with mucosal protective properties
J P Hakkinen, W F Holt, C J Goddard, et al.
Journal of Medicinal Chemistry
|
September 30, 1994
(+)-1-(3S,4R)-[3-(4-phenylbenzyl)-4-hydroxychroman-7-yl]cyclopentane carboxylic acid, a highly potent, selective leukotriene B4 antagonist with oral activity in the murine collagen-induced arthritis model
K Koch, L S Melvin, L A Reiter, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
trans-3-Benzyl-4-hydroxy-7-chromanylbenzoic acid derivatives as antagonists of the leukotriene B4 (LTB4) receptor
L A Reiter, K Koch, A D Piscopio, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 17, 1998
The preclinical pharmacological profile of the potent and selective leukotriene B4 antagonist CP-195543
H J Showell, M J Conklyn, R Alpert, et al.
Journal of Medicinal Chemistry
|
January 5, 1996
Discovery of the hemifumarate and (alpha-L-alanyloxy)methyl ether as prodrugs of an antirheumatic oxindole: prodrugs for the enolic OH group
R P Robinson, L A Reiter, W E Barth, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 18, 1999
Inhibition of MMP-1 and MMP-13 with phosphinic acids that exploit binding in the S2 pocket
L A Reiter, J P Rizzi, J Pandit, et al.
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of 2