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filingDate 1993-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3ec9d6d8eb80ea7ffe7017ae99c4bab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36c50312373d4b742c8f62a7e8e9f33e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7513bb8fd9a6495f5a3e9b5b8baf0deb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_372a63115f083183900a899f0b139dea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_630e4fdcc1355331eb5a7ec2077a27b1
publicationDate 1999-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2125043-C1
titleOfInvention Derivatives of octahydronaphthalene oxime, pharmaceutical composition, method of their synthesis, method of patient treatment
abstract FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to derivatives of octahydronaphthalene oxime of the formula (I) where X is C 1 -C 10 -alkyl; A is C 1 -C 10 -alkylene; R - hydrogen; Y - hydrogen, phenyl possibly substituted with substituents including: halogen, C 1 -C 4 -alkoxy or means heterocyclic group with 5 or 6 ring atoms, 1-3 of which are nitrogen and/or oxygen, and/or sulfur. Heterocyclic group can be substituted with at least a single C 1 -C 5 -alkyl. Invention describes a pharmaceutical composition for inhibition of cholesterol biosynthesis where an active component has a compound of the formula (I) or its pharmaceutically acceptable salts or esters taken at effective amount. Invention proposes a method of suppression of disorders as a result of cholesterol balance disturbance by administration to mammalian a compound of the formula (I) at the dose 1-10 mg/day. Invention proposes also a method of synthesis of derivatives of octahydronaphthalene oxime of the formula (I) by oxidation of compound of the formula (II) where R, X, Y and A are indicated above and R a - a lower alkyl, lower alkenyl or phenyl resulting to synthesis of compound of the formula (III) where R, Y, R a and A are indicated above followed by if necessary its deesterification or conversion to salt. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 19 cl, 1 dwg, 4 tbl, 23 ex
priorityDate 1992-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449166076
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451839851
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422132752
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID25041
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393276
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422112114
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154064598
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88385194
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516176
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID439242
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394753
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429375560
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411558474
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449779460
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419507953
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID457786
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71437401
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Total number of triples: 347.