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Journal of Medicinal Chemistry
|
March 29, 2000
Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens
Y S Or, R F Clark, S Wang, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 27, 2000
Synthesis and antibacterial activity of novel 6-O-substituted erythromycin A derivatives
R F Clark, Z Ma, S Wang, et al.
Diabetologia
|
November 1, 1994
Expression of human GLUT4 in mice results in increased insulin action
R O Deems, J L Evans, R W Deacon, et al.
Journal of Medicinal Chemistry
|
May 30, 1998
Anhydrolide macrolides. 2. Synthesis and antibacterial activity of 2,3-anhydro-6-O-methyl 11,12-carbazate erythromycin A analogues
G Griesgraber, M J Kramer, R L Elliott, et al.
Journal of Medicinal Chemistry
|
October 9, 1999
Synthesis and antimicrobial activity of 4H-4-oxoquinolizine derivatives: consequences of structural modification at the C-8 position
Z Ma, D T Chu, C S Cooper, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Synthesis and structure-activity relationships of 2-pyridones: II. 8-(Fluoro-substituted pyrrolidinyl)-2-pyridones as antibacterial agents
Q Li, W Wang, K B Berst, et al.
Journal of Medicinal Chemistry
|
May 30, 1998
Anhydrolide macrolides. 1. Synthesis and antibacterial activity of 2,3-anhydro-6-O-methyl 11,12-carbamate erythromycin A analogues
R L Elliott, D Pireh, G Griesgraber, et al.
Neoplasma
|
June 25, 2013
Individualized treatment of NSCLC: from research to clinical practice
Y Wang, Z D Liu, L M Zhao, et al.
Journal of Medicinal Chemistry
|
August 2, 1996
Synthesis and structure-activity relationships of 2-pyridones: a novel series of potent DNA gyrase inhibitors as antibacterial agents
Q Li, D T Chu, A Claiborne, et al.
Journal of Medicinal Chemistry
|
November 16, 2001
Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens
Z Ma, R F Clark, A Brazzale, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 81) with videos related to
Sort By:
Page
of 9
Journal of Medicinal Chemistry
|
March 29, 2000
Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens
Y S Or, R F Clark, S Wang, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 27, 2000
Synthesis and antibacterial activity of novel 6-O-substituted erythromycin A derivatives
R F Clark, Z Ma, S Wang, et al.
Diabetologia
|
November 1, 1994
Expression of human GLUT4 in mice results in increased insulin action
R O Deems, J L Evans, R W Deacon, et al.
Journal of Medicinal Chemistry
|
May 30, 1998
Anhydrolide macrolides. 2. Synthesis and antibacterial activity of 2,3-anhydro-6-O-methyl 11,12-carbazate erythromycin A analogues
G Griesgraber, M J Kramer, R L Elliott, et al.
Journal of Medicinal Chemistry
|
October 9, 1999
Synthesis and antimicrobial activity of 4H-4-oxoquinolizine derivatives: consequences of structural modification at the C-8 position
Z Ma, D T Chu, C S Cooper, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Synthesis and structure-activity relationships of 2-pyridones: II. 8-(Fluoro-substituted pyrrolidinyl)-2-pyridones as antibacterial agents
Q Li, W Wang, K B Berst, et al.
Journal of Medicinal Chemistry
|
May 30, 1998
Anhydrolide macrolides. 1. Synthesis and antibacterial activity of 2,3-anhydro-6-O-methyl 11,12-carbamate erythromycin A analogues
R L Elliott, D Pireh, G Griesgraber, et al.
Neoplasma
|
June 25, 2013
Individualized treatment of NSCLC: from research to clinical practice
Y Wang, Z D Liu, L M Zhao, et al.
Journal of Medicinal Chemistry
|
August 2, 1996
Synthesis and structure-activity relationships of 2-pyridones: a novel series of potent DNA gyrase inhibitors as antibacterial agents
Q Li, D T Chu, A Claiborne, et al.
Journal of Medicinal Chemistry
|
November 16, 2001
Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens
Z Ma, R F Clark, A Brazzale, et al.
Page
of 9