http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NO-20076076-L

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24e76490bed88751680a5fef9bc73892
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02A50-30
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-429
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-52
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-424
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filingDate 2007-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e0b9509efe4a4c35528ac9fbb5a339e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_198a34864813377b660eefb82cf18f70
publicationDate 2008-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NO-20076076-L
titleOfInvention Bicyclic 6-alkylidene penems as class D beta-lactamase inhibitors
abstract The present invention relates to certain biscyclic 6-alkylidene penems which act as an inhibitor of class D enzymes. Lactamases hydrolyze? -lactam antibiotics and serve as such as the primary cause of bacterial resistance. The compounds of the present invention when combined with lactam antibiotics will provide effective treatment against life-threatening bacterial infections. In accordance with the present invention, compounds of the general formula I or a pharmaceutically acceptable salt or in vivo hydrolyzable ester R5 thereof are provided: wherein: one of A and B represents hydrogen and the other an optionally substituted condensed bicyclic heteroaryl group; and X = O or S. (I)
priorityDate 2005-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451

Total number of triples: 24.