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Science (New York, N.Y.)
|
January 21, 1994
Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitors
P Y Lam, P K Jadhav, C J Eyermann, et al.
The Journal of Biological Chemistry
|
January 20, 2001
Potent and selective cathepsin L inhibitors do not inhibit human osteoclast resorption in vitro
I E James, R W Marquis, S M Blake, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 5, 2001
Potent and selective inhibition of human cathepsin K leads to inhibition of bone resorption in vivo in a nonhuman primate
G B Stroup, M W Lark, D F Veber, et al.
Bone
|
May 9, 2002
A potent small molecule, nonpeptide inhibitor of cathepsin K (SB 331750) prevents bone matrix resorption in the ovariectomized rat
Michael W Lark, G B Stroup, I E James, et al.
Journal of Medicinal Chemistry
|
September 11, 1998
Conformationally constrained 1,3-diamino ketones: a series of potent inhibitors of the cysteine protease cathepsin K
R W Marquis, D S Yamashita, Y Ru, et al.
Chemistry & Biology
|
November 18, 1998
Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitors
J D Rodgers, P Y Lam, B L Johnson, et al.
Bioorganic & Medicinal Chemistry
|
June 3, 1999
Potent dipeptidylketone inhibitors of the cysteine protease cathepsin K
R W Marquis, Y Ru, D S Yamashita, et al.
Journal of Medicinal Chemistry
|
March 23, 2001
Cyclic ketone inhibitors of the cysteine protease cathepsin K
R W Marquis, Y Ru, J Zeng, et al.
Journal of Medicinal Chemistry
|
August 30, 1996
Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas
P Y Lam, Y Ru, P K Jadhav, et al.
Journal of Medicinal Chemistry
|
April 20, 2001
Azepanone-based inhibitors of human and rat cathepsin K
R W Marquis, Y Ru, S M LoCastro, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 30 results.
Science (New York, N.Y.)
|
January 21, 1994
Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitors
P Y Lam, P K Jadhav, C J Eyermann, et al.
The Journal of Biological Chemistry
|
January 20, 2001
Potent and selective cathepsin L inhibitors do not inhibit human osteoclast resorption in vitro
I E James, R W Marquis, S M Blake, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 5, 2001
Potent and selective inhibition of human cathepsin K leads to inhibition of bone resorption in vivo in a nonhuman primate
G B Stroup, M W Lark, D F Veber, et al.
Bone
|
May 9, 2002
A potent small molecule, nonpeptide inhibitor of cathepsin K (SB 331750) prevents bone matrix resorption in the ovariectomized rat
Michael W Lark, G B Stroup, I E James, et al.
Journal of Medicinal Chemistry
|
September 11, 1998
Conformationally constrained 1,3-diamino ketones: a series of potent inhibitors of the cysteine protease cathepsin K
R W Marquis, D S Yamashita, Y Ru, et al.
Chemistry & Biology
|
November 18, 1998
Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitors
J D Rodgers, P Y Lam, B L Johnson, et al.
Bioorganic & Medicinal Chemistry
|
June 3, 1999
Potent dipeptidylketone inhibitors of the cysteine protease cathepsin K
R W Marquis, Y Ru, D S Yamashita, et al.
Journal of Medicinal Chemistry
|
March 23, 2001
Cyclic ketone inhibitors of the cysteine protease cathepsin K
R W Marquis, Y Ru, J Zeng, et al.
Journal of Medicinal Chemistry
|
August 30, 1996
Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas
P Y Lam, Y Ru, P K Jadhav, et al.
Journal of Medicinal Chemistry
|
April 20, 2001
Azepanone-based inhibitors of human and rat cathepsin K
R W Marquis, Y Ru, S M LoCastro, et al.
Page
of 3