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Journal of Medicinal Chemistry
|
June 20, 1998
Macrocyclic amino carboxylates as selective MMP-8 inhibitors
R J Cherney, L Wang, D T Meyer, et al.
Journal of Medicinal Chemistry
|
March 12, 1999
Corticotropin-releasing hormone receptor antagonists: framework design and synthesis guided by ligand conformational studies
C N Hodge, P E Aldrich, Z R Wasserman, et al.
Journal of Medicinal Chemistry
|
October 5, 2001
Discovery of macrocyclic hydroxamic acids containing biphenylmethyl derivatives at P1', a series of selective TNF-alpha converting enzyme inhibitors with potent cellular activity in the inhibition of TNF-alpha release
C B Xue, X He, R L Corbett, et al.
Journal of Medicinal Chemistry
|
October 5, 2001
Design and synthesis of a series of (2R)-N(4)-hydroxy-2-(3-hydroxybenzyl)-N(1)- [(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]butanediamide derivatives as potent, selective, and orally bioavailable aggrecanase inhibitors
W Yao, Z R Wasserman, M Chao, et al.
Journal of Medicinal Chemistry
|
March 12, 1999
Synthesis, corticotropin-releasing factor receptor binding affinity, and pharmacokinetic properties of triazolo-, imidazo-, and pyrrolopyrimidines and -pyridines
R J Chorvat, R Bakthavatchalam, J P Beck, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Journal of Medicinal Chemistry
|
June 20, 1998
Macrocyclic amino carboxylates as selective MMP-8 inhibitors
R J Cherney, L Wang, D T Meyer, et al.
Journal of Medicinal Chemistry
|
March 12, 1999
Corticotropin-releasing hormone receptor antagonists: framework design and synthesis guided by ligand conformational studies
C N Hodge, P E Aldrich, Z R Wasserman, et al.
Journal of Medicinal Chemistry
|
October 5, 2001
Discovery of macrocyclic hydroxamic acids containing biphenylmethyl derivatives at P1', a series of selective TNF-alpha converting enzyme inhibitors with potent cellular activity in the inhibition of TNF-alpha release
C B Xue, X He, R L Corbett, et al.
Journal of Medicinal Chemistry
|
October 5, 2001
Design and synthesis of a series of (2R)-N(4)-hydroxy-2-(3-hydroxybenzyl)-N(1)- [(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]butanediamide derivatives as potent, selective, and orally bioavailable aggrecanase inhibitors
W Yao, Z R Wasserman, M Chao, et al.
Journal of Medicinal Chemistry
|
March 12, 1999
Synthesis, corticotropin-releasing factor receptor binding affinity, and pharmacokinetic properties of triazolo-, imidazo-, and pyrrolopyrimidines and -pyridines
R J Chorvat, R Bakthavatchalam, J P Beck, et al.
Page
of 2