Source:http://linkedlifedata.com/resource/pubmed/id/12538024
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2003-1-22
|
pubmed:abstractText |
SAR studies in a series of related 3-(heteroarylthio)cephems determined that a relatively high chemical reactivity of the beta-lactam ring, modulated by electronic effects of substituents at C-3 and C-7, is necessary to achieve high in vitro activity against methicillin-resistant Staphylococcus aureus (MRSA). Such high reactivity results in lowered hydrolytic stability and concomitantly increases susceptibility to beta-lactam ring opening mediated by serum enzymes. Therefore, optimization of anti-MRSA activity versus stability toward serum-mediated degradation required a fine balance of substituent effects. Serum stability studies (measured as percentage of parent drug degraded after 60 min incubation) revealed up to 80-fold difference in degradation rate in a series of closely related (3-heteroarylthio)cephems. Of the compounds evaluated, RWJ-333441 (MC-04,546) possessed the best balance of serum stability (6% degradation after 60 min incubation) and in vitro activity versus MRSA (S. aureus COL MIC=1 microgram/mL). Accordingly, RWJ-333441 displayed excellent in vivo efficacy versus methicillin-susceptible Staphylococcus aureus (MSSA, ED(50)=0.39 mg/kg in mouse sepsis model with S. aureus Smith) and good pharmacokinetic properties in the rat (Cl(total)=0.39 L/h/kg).
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Bacterial Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Cephalosporins,
http://linkedlifedata.com/resource/pubmed/chemical/Indicators and Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Lactams,
http://linkedlifedata.com/resource/pubmed/chemical/RWJ-333441
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0968-0896
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
20
|
pubmed:volume |
11
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
591-600
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:12538024-Animals,
pubmed-meshheading:12538024-Anti-Bacterial Agents,
pubmed-meshheading:12538024-Cephalosporins,
pubmed-meshheading:12538024-Drug Design,
pubmed-meshheading:12538024-Humans,
pubmed-meshheading:12538024-Indicators and Reagents,
pubmed-meshheading:12538024-Lactams,
pubmed-meshheading:12538024-Male,
pubmed-meshheading:12538024-Methicillin Resistance,
pubmed-meshheading:12538024-Mice,
pubmed-meshheading:12538024-Microbial Sensitivity Tests,
pubmed-meshheading:12538024-Rats,
pubmed-meshheading:12538024-Rats, Sprague-Dawley,
pubmed-meshheading:12538024-Staphylococcal Infections,
pubmed-meshheading:12538024-Staphylococcus aureus,
pubmed-meshheading:12538024-Structure-Activity Relationship
|
pubmed:year |
2003
|
pubmed:articleTitle |
Relationships between structure, antibacterial activity, serum stability, pharmacokinetics and efficacy in 3-(heteroarylthio)cephems. Discovery of RWJ-333441 (MC-04,546).
|
pubmed:affiliation |
Essential Therapeutics, Inc., 850Maude Ave., CA 94043, Mountain View, USA. tglinka@etrx.com
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|