{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
{{facet.count}}
Restrict the search for
methicillin
to a specific field?
Status:
Investigational
Class (Stereo):
CHEMICAL (ABSOLUTE)
Targets:
Conditions:
Eperezolid is an antibiotic agent developed for the treatment of a wide range of bacterial infections. The drug exerts its action by binding to 50 S ribosome subunit causing the inhibition of protein synthesis in bacterias. Eperezolid was tested in preclinical in vivo models of different becterial diseases in which it was shown to be active.
Status:
Investigational
Class (Stereo):
CHEMICAL (ABSOLUTE)
Tomopenem (formerly CS-023) is a 1β-methylcarbapenem with improved activity against diverse hospital pathogens, including Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus (MRSA), and has a half-life about twice longer than the half-lives of other carbapenems such as imipenem (IPM) and meropenem (MEM). In vitro activity of tomopenem is comparable to that of IPM against most isolates of Gram-positive pathogens and similar to that of MEM against Gram-negative pathogens. Furthermore, tomopenem displayed improved activity against not only P. aeruginosa but also MRSA compared to IPM and MEM. In addition to the improved activity, tomopenem showed a half-life about twice longer than that of IPM or MEM in humans. The affinity of tomopenem for penicillin-binding protein (PBP) 2a might be higher than that of IPM. Tomopenem had been in phase II clinical trial for the treatment of Gram-positive and Gram-negative bacterial infection. However, this development was discontinued.
Status:
Investigational
Class (Stereo):
CHEMICAL (ABSOLUTE)
LTX109 is a synthetic antimicrobial agent and is a potent fungicide that disturbs plasma membrane integrity in a sphingolipid dependent manner. LTX109 was in clinical phase II trials for topical treatment of infections of multiresistant bacterial strains. However, the further development of this drug apparently has been discontinued.
Status:
Other
Class (Stereo):
CHEMICAL (ABSOLUTE)
