RU2008113588A - 2-Ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate possessing anti-ischemic, cerebroprotective, neurotropic and lipid-regulating activity, pharmaceuticals - Google Patents
2-Ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate possessing anti-ischemic, cerebroprotective, neurotropic and lipid-regulating activity, pharmaceuticals Download PDFInfo
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- RU2008113588A RU2008113588A RU2008113588/04A RU2008113588A RU2008113588A RU 2008113588 A RU2008113588 A RU 2008113588A RU 2008113588/04 A RU2008113588/04 A RU 2008113588/04A RU 2008113588 A RU2008113588 A RU 2008113588A RU 2008113588 A RU2008113588 A RU 2008113588A
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- Prior art keywords
- hydroxybutanedioate
- hydroxypyridinium
- ethyl
- methyl
- pharmaceutical composition
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- YNPMMSJOLPPHGM-UHFFFAOYSA-N OC(CC([O-])=O)C([O-])=O.CCc1[nH+]c(C)ccc1O.CCc1[nH+]c(C)ccc1O Chemical compound OC(CC([O-])=O)C([O-])=O.CCc1[nH+]c(C)ccc1O.CCc1[nH+]c(C)ccc1O YNPMMSJOLPPHGM-UHFFFAOYSA-N 0.000 title claims abstract 6
- 230000002253 anti-ischaemic effect Effects 0.000 title claims abstract 3
- 230000001966 cerebroprotective effect Effects 0.000 title claims abstract 3
- 230000000694 effects Effects 0.000 title claims abstract 3
- 230000002276 neurotropic effect Effects 0.000 title claims abstract 3
- 239000003814 drug Substances 0.000 title claims 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims abstract 10
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims abstract 10
- -1 compounds 2-ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate Chemical class 0.000 claims abstract 9
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract 9
- 239000000654 additive Substances 0.000 claims abstract 7
- 239000013543 active substance Substances 0.000 claims abstract 6
- 239000007787 solid Substances 0.000 claims abstract 6
- 239000004471 Glycine Substances 0.000 claims abstract 5
- 229920002785 Croscarmellose sodium Polymers 0.000 claims abstract 4
- 229920002678 cellulose Polymers 0.000 claims abstract 4
- 239000001913 cellulose Substances 0.000 claims abstract 4
- 229910002012 Aerosil® Inorganic materials 0.000 claims abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract 3
- 229920002472 Starch Polymers 0.000 claims abstract 3
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims abstract 3
- 229960001681 croscarmellose sodium Drugs 0.000 claims abstract 3
- 235000010947 crosslinked sodium carboxy methyl cellulose Nutrition 0.000 claims abstract 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims abstract 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims abstract 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- 239000008107 starch Substances 0.000 claims abstract 3
- 235000019698 starch Nutrition 0.000 claims abstract 3
- 239000000126 substance Substances 0.000 claims abstract 3
- KSMRODHGGIIXDV-YFKPBYRVSA-N N-acetyl-L-glutamine Chemical compound CC(=O)N[C@H](C(O)=O)CCC(N)=O KSMRODHGGIIXDV-YFKPBYRVSA-N 0.000 claims abstract 2
- 235000021355 Stearic acid Nutrition 0.000 claims abstract 2
- 239000002253 acid Substances 0.000 claims abstract 2
- 235000010980 cellulose Nutrition 0.000 claims abstract 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000008117 stearic acid Substances 0.000 claims abstract 2
- 235000000346 sugar Nutrition 0.000 claims abstract 2
- 150000008163 sugars Chemical class 0.000 claims abstract 2
- RFMMMVDNIPUKGG-YFKPBYRVSA-N N-acetyl-L-glutamic acid Chemical compound CC(=O)N[C@H](C(O)=O)CCC(O)=O RFMMMVDNIPUKGG-YFKPBYRVSA-N 0.000 claims 6
- 239000007788 liquid Substances 0.000 claims 3
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 claims 2
- 239000013589 supplement Substances 0.000 claims 2
- 201000006474 Brain Ischemia Diseases 0.000 claims 1
- 206010008120 Cerebral ischaemia Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 206010008118 cerebral infarction Diseases 0.000 claims 1
- 230000002526 effect on cardiovascular system Effects 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 208000020016 psychiatric disease Diseases 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 abstract 1
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 abstract 1
- 229960005168 croscarmellose Drugs 0.000 abstract 1
- 239000001767 crosslinked sodium carboxy methyl cellulose Substances 0.000 abstract 1
- 235000013922 glutamic acid Nutrition 0.000 abstract 1
- 239000004220 glutamic acid Substances 0.000 abstract 1
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Abstract
1. 2-Этил-6-метил-3-гидроксипиридинийгидроксибутандиоат формулы ! ! 2. Применение соединения 2-этил-6-метил-3-гидроксипиридинийгидроксибутандиоат, отличающееся тем, что оно обладает противоишемической активностью. ! 3. Применение соединения 2-этил-6-метил-3-гидроксипиридинийгидроксибутандиоат, отличающееся тем, что оно обладает церебропротекторной активностью. ! 4. Применение соединения 2-этил-6-метил-3-гидроксипиридинийгидроксибутандиоат, отличающееся тем, что оно обладает нейротропной активностью. ! 5. Применение соединения 2-этил-6-метил-3-гидроксипиридинийгидроксибутандиоат, отличающееся тем, что оно обладает липидрегулирующей активностью. ! 6. Твердая дозированная фармацевтическая композиция, отличающаяся тем, что она содержит соединение 2-этил-6-метил-3-гидроксипиридинийгидроксибутандиоат. ! 7. Твердая дозированная фармацевтическая композиция по п.6, отличающаяся тем, что она выполнена в виде таблетки при соотношении действующего вещества и целевых добавок, маc. %: ! действующее вещество0,05-40,0целевые добавки60,0-99,95 ! 8. Твердая дозированная фармацевтическая композиция по любому из пп.6 и 7, отличающаяся тем, что в качестве целевых добавок она содержит необязательно одновременно крахмал, натрия кроскармеллозу, поливинилпирролидоны, сахара, производные целлюлозы, аэросил, глицин, N-ацетил-L-глутаминовую кислоту, 2-(диметиламино)этанол, соли стеариновой кислоты, коррегирующие вещества при следующем соотношении компонентов, мас.%: ! крахмал0,0-15,0натрия кроскармеллоза0,0-10,0поливинилпирролидоны0,0-10,0сахара0,0-20,0производные целлюлозы0,0-50,0аэросил0,0-10,0глицин0,0-10,0N-ацетил-L-глутаминовая кислота0,0-15,02-(диметиламино)этанол0,0-10,0соли с�1. 2-Ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate of the formula! ! 2. The use of compounds 2-ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate, characterized in that it has anti-ischemic activity. ! 3. The use of compounds 2-ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate, characterized in that it has cerebroprotective activity. ! 4. The use of compounds 2-ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate, characterized in that it has neurotropic activity. ! 5. The use of compounds 2-ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate, characterized in that it has lipid-regulating activity. ! 6. A solid dosage pharmaceutical composition, characterized in that it contains a compound of 2-ethyl-6-methyl-3-hydroxypyridinium hydroxybutanedioate. ! 7. The solid dosage pharmaceutical composition according to claim 6, characterized in that it is made in the form of a tablet with a ratio of active substance and target additives, wt. %:! active substance 0.05-40.0 target additives 60.0-99.95! 8. A solid dosage pharmaceutical composition according to any one of claims 6 and 7, characterized in that as target additives it optionally contains simultaneously starch, croscarmellose sodium, polyvinylpyrrolidones, sugars, cellulose derivatives, aerosil, glycine, N-acetyl-L-glutamine acid, 2- (dimethylamino) ethanol, salts of stearic acid, corrective substances in the following ratio of components, wt.%:! starch0.0-15.0 croscarmellose sodium0.0-10.0 polyvinylpyrrolidones0.0-10.0sugar0.0-20.0 cellulose derivatives glutamic acid 0.0-15.02- (dimethylamino) ethanol 0.0-10.0 salts with
Claims (12)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2008113588/04A RU2377237C1 (en) | 2008-04-10 | 2008-04-10 | 2-ethyl-6-methyl-3-hydroxyliridiniumhydroxybutanedioat expressing anti-ishemic, cerebroprotective, neurotropic and lipid-regulating activity, pharmaceutical compositions and medical product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2008113588/04A RU2377237C1 (en) | 2008-04-10 | 2008-04-10 | 2-ethyl-6-methyl-3-hydroxyliridiniumhydroxybutanedioat expressing anti-ishemic, cerebroprotective, neurotropic and lipid-regulating activity, pharmaceutical compositions and medical product |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2008113588A true RU2008113588A (en) | 2009-10-20 |
| RU2377237C1 RU2377237C1 (en) | 2009-12-27 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2008113588/04A RU2377237C1 (en) | 2008-04-10 | 2008-04-10 | 2-ethyl-6-methyl-3-hydroxyliridiniumhydroxybutanedioat expressing anti-ishemic, cerebroprotective, neurotropic and lipid-regulating activity, pharmaceutical compositions and medical product |
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| RU (1) | RU2377237C1 (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2433486C1 (en) * | 2010-03-22 | 2011-11-10 | Государственное образовательное учреждение высшего профессионального образования "Курский государственный медицинский университет Федерального агентства по здравоохранению и социальному развитию" | Method of correcting endothelial dysfunction by medication "etoxydol" in case of l-name induced nitrogen oxide deficiency |
| RU2454406C2 (en) * | 2010-07-09 | 2012-06-27 | Государственное образовательное учреждение высшего профессионального образования "Мордовский государственный университет им. Н.П. Огарева" | 2-ethyl-6-methyl-3-hydroxypyridine and nicotinic acid salt, having hypoglycemic, hypolipidemic and neuroprotective activity and synthesis method thereof |
| RU2461379C2 (en) * | 2010-12-09 | 2012-09-20 | Закрытое акционерное общество "ФАРМ-ЦЕНТР" (ЗАО "ФАРМ-ЦЕНТР") | Pharmaceutical combination possessing antiaggregant and lipid-regulating activities, pharmaceutical composition |
| EA024773B1 (en) * | 2013-06-24 | 2016-10-31 | Закрытое акционерное общество "Медимэкс" (ЗАО "Медимэкс") | Liquid pharmaceutical composition, comprising hydroxybutanedioate 2-ethyl-6-methyl-3-hydroxypyridine |
| RU2526185C1 (en) * | 2013-07-30 | 2014-08-20 | Федеральное государственное бюджетное учреждение "Научный центр экспертизы средств медицинского применения" Министерства здравоохранения Российской Федерации (ФГБУ "НЦЭСМП" Минздрава России) | Method of increasing oxygen tension in blood of patients with chronic heart failure |
| RU2671200C2 (en) * | 2015-12-07 | 2018-10-30 | Закрытое Акционерное Общество "Фармфирма "Сотекс" | Method of obtaining 6-methyl-2-ethylpyridine-3-ol salt of (2s)-2-acetaminopentanedioic acid |
| RU2657820C1 (en) * | 2017-03-13 | 2018-06-15 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Волгоградский государственный медицинский университет" Министерства здравоохранения Российской Федерации ФГБОУ ВО ВолгГМУ МЗ РФ | 4-(4-acetoxybenzoylamino)butanoylglycine, which has a cerebroprotective action in cerebral ischemia |
| RU2663836C1 (en) * | 2017-12-14 | 2018-08-10 | Акционерное общество "Мадмит трейд" | L-enantymer of 2-ethyl-6-methyl-3-hydroxypiridinium hydroxybutandioate possessing cerebroprotective activity |
| GEP20227421B (en) | 2017-12-14 | 2022-10-10 | Valenta Intellekt Ltd | L-enantiomer 2-ethyl-6-methyl-3-hydroxypyridinium l-hydroxybutandioate with cerebroprotective, hepatoprotective, lipid-regulating, anti-ischemic and neurotropic activities |
| RU2705575C1 (en) * | 2018-10-25 | 2019-11-08 | Общество С Ограниченной Ответственностью "Валента-Интеллект" | Agent exhibiting hepatoprotective, lipid-regulating, antiischemic and neurotropic activity |
| RU2696203C1 (en) * | 2018-09-10 | 2019-07-31 | Федеральное государственное автономное образовательное учреждение высшего образования "Белгородский государственный национальный исследовательский университет" (НИУ "БелГУ") | Method for preventing cerebral ischemia |
| CN111228263A (en) * | 2020-03-13 | 2020-06-05 | 北京克诺腾达贸易有限公司 | Application of ethylmethyl hydroxypyridine malate or pharmaceutical composition thereof in preventing and/or treating type II diabetes |
| RU2743923C1 (en) * | 2020-05-29 | 2021-03-01 | Общество с ограниченной ответственностью "Мадмит" | Novel 3-hydroxypyridine derivative having lipid regulating activity |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2058145C1 (en) * | 1988-12-28 | 1996-04-20 | Центр по химии лекарственных средств | Agent showing antishock activity |
| RU2065299C1 (en) * | 1994-07-15 | 1996-08-20 | Акционерное общество закрытого типа "Олвик" | Nootropic and tranquilizing agent |
| RU2145855C1 (en) * | 1999-05-26 | 2000-02-27 | Смирнов Леонид Дмитриевич | Drug showing anxiolytic, antialcoholic and cerebroprotective effects |
| RU2210568C1 (en) * | 2001-12-14 | 2003-08-20 | Промоненков Виктор Кириллович | Method for preparing derivatives of 2-ethyl-6- -methyl-3- hydroxypyridine |
| RU2284993C2 (en) * | 2002-06-14 | 2006-10-10 | Леонид Дмитриевич Смирнов | 2-ethyl-6-methyl-3-oxypyrodine salts with organic carboxylic acids possessing anxiolytic, antidepressive, antihypoxic, anti-amnestic and anti-oxidative activity and method for their preparing |
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- 2008-04-10 RU RU2008113588/04A patent/RU2377237C1/en active
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| Publication number | Publication date |
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| RU2377237C1 (en) | 2009-12-27 |
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