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Journal of Medicinal Chemistry
|
August 1, 1988
Dicarbavasopressin antagonist analogues exhibit reduced in vivo agonist activity
M L Moore, C Albrightson, B Brickson, et al.
Journal of Medicinal Chemistry
|
December 1, 1986
Potent antagonists of vasopressin antidiuretic activity that lack the beta,beta-cyclopentamethylene-beta-mercaptopropionic acid substitution at position 1
N C Yim, M L Moore, W F Huffman, et al.
Biochemistry
|
November 6, 1992
Proteolysis of an active site peptide of lactate dehydrogenase by human immunodeficiency virus type 1 protease
T A Tomaszek, M L Moore, J E Strickler, et al.
Journal of Medicinal Chemistry
|
August 18, 1995
A check on rational drug design: crystal structure of a complex of human immunodeficiency virus type 1 protease with a novel gamma-turn mimetic inhibitor
S S Hoog, B Zhao, E Winborne, et al.
Journal of Medicinal Chemistry
|
April 1, 1989
A minor modification of residue 1 in potent vasopressin antagonists dramatically reduces agonist activity
W F Huffman, C Albrightson-Winslow, B Brickson, et al.
Journal of Medicinal Chemistry
|
April 1, 1988
Design, synthesis, and biological activity of a peptide mimic of vasopressin
W M Bryan, J C Hempel, W F Huffman, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
January 1, 1991
Vasopressin antidiuretic agonist and antagonist activity in dogs: structural and stereochemical relationship between bridge and carboxyl terminus
C R Albrightson-Winslow, B Brickson, D P Brooks, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1989
Human immunodeficiency virus 1 protease expressed in Escherichia coli behaves as a dimeric aspartic protease
T D Meek, B D Dayton, B W Metcalf, et al.
Nature
|
January 14, 1990
Inhibition of HIV-1 protease in infected T-lymphocytes by synthetic peptide analogues
T D Meek, D M Lambert, G B Dreyer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
Inhibition of human immunodeficiency virus 1 protease in vitro: rational design of substrate analogue inhibitors
G B Dreyer, B W Metcalf, T A Tomaszek, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 108) with videos related to
Sort By:
Page
of 11
Journal of Medicinal Chemistry
|
August 1, 1988
Dicarbavasopressin antagonist analogues exhibit reduced in vivo agonist activity
M L Moore, C Albrightson, B Brickson, et al.
Journal of Medicinal Chemistry
|
December 1, 1986
Potent antagonists of vasopressin antidiuretic activity that lack the beta,beta-cyclopentamethylene-beta-mercaptopropionic acid substitution at position 1
N C Yim, M L Moore, W F Huffman, et al.
Biochemistry
|
November 6, 1992
Proteolysis of an active site peptide of lactate dehydrogenase by human immunodeficiency virus type 1 protease
T A Tomaszek, M L Moore, J E Strickler, et al.
Journal of Medicinal Chemistry
|
August 18, 1995
A check on rational drug design: crystal structure of a complex of human immunodeficiency virus type 1 protease with a novel gamma-turn mimetic inhibitor
S S Hoog, B Zhao, E Winborne, et al.
Journal of Medicinal Chemistry
|
April 1, 1989
A minor modification of residue 1 in potent vasopressin antagonists dramatically reduces agonist activity
W F Huffman, C Albrightson-Winslow, B Brickson, et al.
Journal of Medicinal Chemistry
|
April 1, 1988
Design, synthesis, and biological activity of a peptide mimic of vasopressin
W M Bryan, J C Hempel, W F Huffman, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
January 1, 1991
Vasopressin antidiuretic agonist and antagonist activity in dogs: structural and stereochemical relationship between bridge and carboxyl terminus
C R Albrightson-Winslow, B Brickson, D P Brooks, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1989
Human immunodeficiency virus 1 protease expressed in Escherichia coli behaves as a dimeric aspartic protease
T D Meek, B D Dayton, B W Metcalf, et al.
Nature
|
January 14, 1990
Inhibition of HIV-1 protease in infected T-lymphocytes by synthetic peptide analogues
T D Meek, D M Lambert, G B Dreyer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
Inhibition of human immunodeficiency virus 1 protease in vitro: rational design of substrate analogue inhibitors
G B Dreyer, B W Metcalf, T A Tomaszek, et al.
Page
of 11