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Antimicrobial Agents and Chemotherapy
|
August 15, 2001
Efficacies of ABT-773, a new ketolide, against experimental bacterial infections
M J Mitten, J Meulbroek, M Nukkala, 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.
The Journal of Investigative Dermatology
|
May 8, 1999
A macrolactam inhibitor of T helper type 1 and T helper type 2 cytokine biosynthesis for topical treatment of inflammatory skin diseases
K W Mollison, T A Fey, D M Gauvin, 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.
Current Pharmaceutical Design
|
April 10, 1999
Discovery of ascomycin analogs with potent topical but weak systemic activity for treatment of inflammatory skin diseases
K W Mollison, T A Fey, D M Gauvin, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Antimicrobial Agents and Chemotherapy
|
August 15, 2001
Efficacies of ABT-773, a new ketolide, against experimental bacterial infections
M J Mitten, J Meulbroek, M Nukkala, 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.
The Journal of Investigative Dermatology
|
May 8, 1999
A macrolactam inhibitor of T helper type 1 and T helper type 2 cytokine biosynthesis for topical treatment of inflammatory skin diseases
K W Mollison, T A Fey, D M Gauvin, 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.
Current Pharmaceutical Design
|
April 10, 1999
Discovery of ascomycin analogs with potent topical but weak systemic activity for treatment of inflammatory skin diseases
K W Mollison, T A Fey, D M Gauvin, et al.
Page
of 3