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Journal of Medicinal Chemistry
|
May 26, 2006
Tumor-cell-targeted methionine-enkephalin analogues containing unnatural amino acids: design, synthesis, and in vitro antitumor activity
Stefica Horvat, Kata Mlinarić-Majerski, Ljubica Glavas-Obrovac, et al.
Journal of Medicinal Chemistry
|
September 30, 1994
(E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4- methoxyphenyl)octyl]oxy]-2-pyridinyl]-methyl]thio]methyl]benzoic acid and related compounds: high affinity leukotriene B4 receptor antagonists
R A Daines, P A Chambers, D S Eggleston, et al.
Journal of Medicinal Chemistry
|
January 1, 1991
Synthesis of water-soluble (aminoalkyl)camptothecin analogues: inhibition of topoisomerase I and antitumor activity
W D Kingsbury, J C Boehm, D R Jakas, et al.
Journal of Medicinal Chemistry
|
March 1, 1989
Modification of the hydroxy lactone ring of camptothecin: inhibition of mammalian topoisomerase I and biological activity
R P Hertzberg, M J Caranfa, K G Holden, et al.
The Journal of Antibiotics
|
January 1, 1976
Orally active 7-phenylglycyl cephalosporins. Structure-activity studies related to cefatrizine (SK&F 60771)
G L Dunn, J R Hoover, D A Berges, et al.
Antimicrobial Agents and Chemotherapy
|
October 18, 2002
Defining and combating the mechanisms of triclosan resistance in clinical isolates of Staphylococcus aureus
Frank Fan, Kang Yan, Nicola G Wallis, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Discovery of an imidazopyridine-containing 1,4-benzodiazepine nonpeptide vitronectin receptor (alpha v beta 3) antagonist with efficacy in a restenosis model
R M Keenan, M A Lago, W H Miller, et al.
Journal of Medicinal Chemistry
|
April 18, 2003
Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK
Mark A Seefeld, William H Miller, Kenneth A Newlander, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
October 26, 1999
Preclinical pharmacokinetics and interspecies scaling of a novel vitronectin receptor antagonist
K W Ward, L M Azzarano, W E Bondinell, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
September 7, 1999
In vitro and in vivo pharmacological characterization of SB 201993, an eicosanoid-like LTB4 receptor antagonist with anti-inflammatory activity
H M Sarau, J J Foley, D B Schmidt, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
Journal of Medicinal Chemistry
|
May 26, 2006
Tumor-cell-targeted methionine-enkephalin analogues containing unnatural amino acids: design, synthesis, and in vitro antitumor activity
Stefica Horvat, Kata Mlinarić-Majerski, Ljubica Glavas-Obrovac, et al.
Journal of Medicinal Chemistry
|
September 30, 1994
(E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4- methoxyphenyl)octyl]oxy]-2-pyridinyl]-methyl]thio]methyl]benzoic acid and related compounds: high affinity leukotriene B4 receptor antagonists
R A Daines, P A Chambers, D S Eggleston, et al.
Journal of Medicinal Chemistry
|
January 1, 1991
Synthesis of water-soluble (aminoalkyl)camptothecin analogues: inhibition of topoisomerase I and antitumor activity
W D Kingsbury, J C Boehm, D R Jakas, et al.
Journal of Medicinal Chemistry
|
March 1, 1989
Modification of the hydroxy lactone ring of camptothecin: inhibition of mammalian topoisomerase I and biological activity
R P Hertzberg, M J Caranfa, K G Holden, et al.
The Journal of Antibiotics
|
January 1, 1976
Orally active 7-phenylglycyl cephalosporins. Structure-activity studies related to cefatrizine (SK&F 60771)
G L Dunn, J R Hoover, D A Berges, et al.
Antimicrobial Agents and Chemotherapy
|
October 18, 2002
Defining and combating the mechanisms of triclosan resistance in clinical isolates of Staphylococcus aureus
Frank Fan, Kang Yan, Nicola G Wallis, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Discovery of an imidazopyridine-containing 1,4-benzodiazepine nonpeptide vitronectin receptor (alpha v beta 3) antagonist with efficacy in a restenosis model
R M Keenan, M A Lago, W H Miller, et al.
Journal of Medicinal Chemistry
|
April 18, 2003
Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK
Mark A Seefeld, William H Miller, Kenneth A Newlander, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
October 26, 1999
Preclinical pharmacokinetics and interspecies scaling of a novel vitronectin receptor antagonist
K W Ward, L M Azzarano, W E Bondinell, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
September 7, 1999
In vitro and in vivo pharmacological characterization of SB 201993, an eicosanoid-like LTB4 receptor antagonist with anti-inflammatory activity
H M Sarau, J J Foley, D B Schmidt, et al.
Page
of 5