RU93005182A - DERIVATIVES OF OCTAGIDRONAPTALINOXIMA, PHARMACEUTICAL COMPOSITION, METHOD OF TREATMENT, METHOD OF THEIR PREPARATION, METHODS OF OBTAINING INITIAL MATERIALS AND CULTURE OF MICROORGANISMS - Google Patents

DERIVATIVES OF OCTAGIDRONAPTALINOXIMA, PHARMACEUTICAL COMPOSITION, METHOD OF TREATMENT, METHOD OF THEIR PREPARATION, METHODS OF OBTAINING INITIAL MATERIALS AND CULTURE OF MICROORGANISMS

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Publication number
RU93005182A
RU93005182A RU93005182/04A RU93005182A RU93005182A RU 93005182 A RU93005182 A RU 93005182A RU 93005182/04 A RU93005182/04 A RU 93005182/04A RU 93005182 A RU93005182 A RU 93005182A RU 93005182 A RU93005182 A RU 93005182A
Authority
RU
Russia
Prior art keywords
treatment
octagidronaptalinoxima
microorganisms
culture
derivatives
Prior art date
Application number
RU93005182/04A
Other languages
Russian (ru)
Other versions
RU2125043C1 (en
Inventor
Хироси Коген
Телсиро Кога
Тору Комаи
Харуо Изабуси
Масааки Курабаяси
Original Assignee
Санкио Компани Лимитед
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Санкио Компани Лимитед filed Critical Санкио Компани Лимитед
Publication of RU93005182A publication Critical patent/RU93005182A/en
Application granted granted Critical
Publication of RU2125043C1 publication Critical patent/RU2125043C1/en

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Claims (1)

Соединения формулы:
Figure 00000001

в которой R представляет водород, метил или гидрокси; X представляет алкил, алкенил, циклоалкил, арил, аралкил или гетероциклическую группу; А представляет одинарную связь, или алкиленовую, алкениленовую, алкиниленовую группу или алкадиениленовую группу; Y представляет водород, арил, циклоалкил или гетероциклическую группу; обладают способностью ингибировать биосинтез холестерина, и таким образом, могут использоваться для лечения и профилактики заболеваний, связанных с высокими уровнями холестерина в крови.
The compounds of the formula:
Figure 00000001

in which R represents hydrogen, methyl or hydroxy; X represents alkyl, alkenyl, cycloalkyl, aryl, aralkyl or heterocyclic group; A represents a single bond, or an alkylene, alkenylene, alkynylene group or an alkadienylene group; Y represents hydrogen, aryl, cycloalkyl or a heterocyclic group; have the ability to inhibit cholesterol biosynthesis, and thus, can be used for the treatment and prevention of diseases associated with high levels of cholesterol in the blood.
RU93005182/04A 1992-05-15 1993-05-14 Derivatives of octahydronaphthalene oxime, pharmaceutical composition, method of their synthesis, method of patient treatment RU2125043C1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP4-122476 1992-05-15
JP12247692 1992-05-15

Publications (2)

Publication Number Publication Date
RU93005182A true RU93005182A (en) 1996-04-27
RU2125043C1 RU2125043C1 (en) 1999-01-20

Family

ID=14836794

Family Applications (1)

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RU93005182/04A RU2125043C1 (en) 1992-05-15 1993-05-14 Derivatives of octahydronaphthalene oxime, pharmaceutical composition, method of their synthesis, method of patient treatment

Country Status (22)

Country Link
US (1) US5604256A (en)
EP (1) EP0570245B1 (en)
JP (1) JPH0641040A (en)
KR (2) KR0177840B1 (en)
CN (1) CN1034498C (en)
AT (1) ATE144768T1 (en)
AU (1) AU656855B2 (en)
CA (1) CA2096281A1 (en)
CZ (1) CZ281151B6 (en)
DE (1) DE69305684T2 (en)
DK (1) DK0570245T3 (en)
ES (1) ES2096208T3 (en)
FI (1) FI932188A (en)
GR (1) GR3022095T3 (en)
HK (1) HK31797A (en)
HU (1) HU221854B1 (en)
IL (1) IL105708A (en)
MX (1) MX9302870A (en)
NO (1) NO180443C (en)
NZ (1) NZ247617A (en)
RU (1) RU2125043C1 (en)
ZA (1) ZA933359B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9320597D0 (en) * 1993-10-06 1993-11-24 Proteus Molecular Design Improvements in and realting to vaccines
US5461049A (en) * 1994-05-27 1995-10-24 Warner-Lambert Company Amide tetrazole ACAT inhibitors
WO2000056328A1 (en) * 1999-03-19 2000-09-28 Enos Pharmaceuticals, Inc. Increasing cerebral bioavailability of drugs
EP1562555A2 (en) * 2002-10-24 2005-08-17 Enos Pharmaceuticals, Inc. Sustained release l-arginine formulations and methods of manufacture and use
US20080145424A1 (en) * 2002-10-24 2008-06-19 Enos Phramaceuticals, Inc. Sustained release L-arginine formulations and methods of manufacture and use
EP1675619A4 (en) * 2003-09-29 2010-10-06 Palmetto Pharmaceuticals Llc Sustained release l-arginine formulations and methods of manufacture and use

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5612114B2 (en) 1974-06-07 1981-03-18
JPS5925599B2 (en) 1979-02-20 1984-06-19 三共株式会社 New physiologically active substance monacolin K and its production method
JPS5612114A (en) 1979-07-11 1981-02-06 Tdk Corp Manufacture of piezoelectric body resonator
MX7065E (en) 1980-06-06 1987-04-10 Sankyo Co A MICROBIOLOGICAL PROCEDURE FOR PREPARING DERIVATIVES OF ML-236B
JPS5855443A (en) * 1981-09-25 1983-04-01 Sankyo Co Ltd Octahydronaphthalene derivative and its preparation
CA1327360C (en) 1983-11-14 1994-03-01 William F. Hoffman Oxo-analogs of mevinolin-like antihypercholesterolemic agents
JPS6113699A (en) 1984-06-28 1986-01-21 三菱電機株式会社 Shield of electric device
JPH0687664B2 (en) 1987-06-22 1994-11-02 株式会社東芝 Circulating current control type cycloconverter control device
US4997848A (en) * 1987-10-27 1991-03-05 Sankyo Company, Limited Octahydronaphthalene oxime derivatives for cholesterol synthesis inhibition
JP2542429B2 (en) 1987-10-27 1996-10-09 三共株式会社 Octahydronaphthalene substituted oxime derivative

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