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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
filingDate 2005-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1eaee50eb912be9215118ad50bf0204e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7722e94aa32e4cb9e3422458d4f03f0e
publicationDate 2008-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-100364989-C
titleOfInvention Prazole derivative and its salt and use
abstract The present invention relates to derivates in a general formula (I) or (II) and salts thereof. In the general formula (I) or (II), R1 represents low grade alkyl or low grade alkyl substituted by a halogen atom; R2 represents straight chain alkyls or branch chain alkyls of one to four carbon atoms; R3 represents hydrogen atom or alkali metals, such as lithium, natrium, potassium, etc. or alkaline earth metals, such as magnesium, calcium, etc. The compounds of the present invention in a general formula (I) or (II) or derivates thereof or pharmacology acceptable salts and pharmacology acceptable salts visibly increase the anti-digestive tract ulcer effect and have less inhibition on gastric acid, and therefore, the risk of forming stomach cancer is largely reduced. The present invention has intra-corporeal medicine metabolizing pharmacokinetic characteristics, such as more excellent biological availability, etc.
priorityDate 2004-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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