SK11252003A3 - Kompozície biochemických zlúčenín zúčastňujúcich sa bioenergetického metabolizmu buniek a ich použitie - Google Patents
Kompozície biochemických zlúčenín zúčastňujúcich sa bioenergetického metabolizmu buniek a ich použitie Download PDFInfo
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- SK11252003A3 SK11252003A3 SK1125-2003A SK11252003A SK11252003A3 SK 11252003 A3 SK11252003 A3 SK 11252003A3 SK 11252003 A SK11252003 A SK 11252003A SK 11252003 A3 SK11252003 A3 SK 11252003A3
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Classifications
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- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/41—Porphyrin- or corrin-ring-containing peptides
- A61K38/415—Cytochromes
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/12—Ketones
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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/12—Ketones
- A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/194—Carboxylic acids, e.g. valproic acid having two or more carboxyl groups, e.g. succinic, maleic or phthalic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
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- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Food Science & Technology (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Nutrition Science (AREA)
- Mycology (AREA)
- Polymers & Plastics (AREA)
- Immunology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26882501P | 2001-02-14 | 2001-02-14 | |
| PCT/EP2002/001545 WO2002064129A2 (en) | 2001-02-14 | 2002-02-14 | Compositions of biochemical compounds involved in bioenergy metabolism of cells |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK11252003A3 true SK11252003A3 (sk) | 2003-12-02 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| SK1125-2003A SK11252003A3 (sk) | 2001-02-14 | 2002-02-14 | Kompozície biochemických zlúčenín zúčastňujúcich sa bioenergetického metabolizmu buniek a ich použitie |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US7056950B2 (tr) |
| EP (1) | EP1368017A2 (tr) |
| JP (1) | JP2004518712A (tr) |
| KR (1) | KR20020093906A (tr) |
| CN (1) | CN1457255A (tr) |
| AU (1) | AU2002250942B2 (tr) |
| BR (1) | BR0203902A (tr) |
| CA (1) | CA2401383A1 (tr) |
| CZ (1) | CZ20023935A3 (tr) |
| EE (1) | EE200200585A (tr) |
| HR (1) | HRP20020702A2 (tr) |
| HU (1) | HUP0302384A2 (tr) |
| IL (1) | IL151411A0 (tr) |
| MX (1) | MXPA02010149A (tr) |
| NO (1) | NO20024536D0 (tr) |
| NZ (1) | NZ528194A (tr) |
| PL (1) | PL363392A1 (tr) |
| RU (1) | RU2301665C2 (tr) |
| SK (1) | SK11252003A3 (tr) |
| TR (1) | TR200202175T1 (tr) |
| UA (1) | UA76444C2 (tr) |
| WO (1) | WO2002064129A2 (tr) |
| ZA (1) | ZA200207100B (tr) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US20050245612A1 (en) | 2004-05-03 | 2005-11-03 | Blass John P | Pharmaceutical compositions for metabolic insufficiencies |
| UA77660C2 (en) * | 2000-10-03 | 2007-01-15 | Compositions and methods for reducing plasma lipoprotein a level in human | |
| ITMI20021366A1 (it) * | 2002-06-21 | 2003-12-22 | Dietetic S P A | Composizioni nutraceutiche e integratori alimentari contenenti nadh |
| ATE380027T1 (de) | 2003-09-09 | 2007-12-15 | Fumapharm Ag | Verwendung von fumarsäure-derivaten zur behandlung von herzinsuffizienz und asthma |
| US7271099B2 (en) * | 2005-06-06 | 2007-09-18 | Ffei Limited | Forming a conductive pattern on a substrate |
| DE102005035917A1 (de) * | 2005-07-28 | 2007-02-01 | November Ag | Verwendung von Isocitrat, Isocitronensäure oder einem Derivat davon zur Herstellung eines Medikaments |
| NL1030611C2 (nl) | 2005-12-07 | 2007-06-08 | Maasland Nv | Inrichting voor het afgeven van vloeibaar voeder aan een dier en autonoom verplaatsbaar voertuig voor gebruik in een dergelijke inrichting. |
| JP5103374B2 (ja) | 2006-03-13 | 2012-12-19 | 株式会社カネカ | 心機能不良改善剤または心機能維持剤 |
| NL1034771C2 (nl) | 2007-11-29 | 2009-06-02 | Lely Patent Nv | Onbemand autonoom voertuig voor het verplaatsen van voeder. |
| WO2008007728A1 (fr) * | 2006-07-13 | 2008-01-17 | Kaneka Corporation | Préparation orale contenue dans une structure à membrane lipidique, et agent contre la fatigue comprenant une coenzyme comme ingrédient actif |
| EP3135282A1 (en) * | 2007-02-08 | 2017-03-01 | Biogen MA Inc. | Neuroprotection in demyelinating diseases |
| EP2680006A1 (en) | 2007-02-08 | 2014-01-01 | Biogen Idec MA Inc. | Treatment for Amyotrophic Lateral Sclerosis |
| FR2915381B1 (fr) * | 2007-04-27 | 2012-06-08 | Vincience | Utilisation d'un principe actif issu du soja (glycine max l) pour preparer une composition destinee a activer le cytochrome c |
| FR2915378B1 (fr) * | 2007-04-27 | 2009-08-21 | Vincience Sa | Utilisation d'un principe actif issu du soja (glycine max l.) pour preparer une composition destinee a proteger les mitochondries |
| FR2915384B1 (fr) * | 2007-04-27 | 2010-01-15 | Vincience | Utilisation d'un principe actif issu du soja (glycine maxl.) pour preparer une composition destinee a activer l'energie cellulaire et a proteger la peau des dommages oxydatifs. |
| FR2915397B1 (fr) | 2007-04-27 | 2012-01-20 | Vincience | Composition pharmaceutique et/ou cosmetique contenant des principes actifs activateurs de l'aconitase |
| US8257753B2 (en) | 2007-07-20 | 2012-09-04 | Isp Investments Inc. | Use of an active principle originating from flax in a composition intended to reinforce the barrier function of the skin and to protect the skin and the appendages against external aggressions |
| FR2918893B1 (fr) * | 2007-07-20 | 2012-10-19 | Vincience | Utilisation d'un principe actif issu du lin pour preparer une composition destinee a activer le cytochrome c |
| NL1036081C (nl) | 2008-10-16 | 2010-04-19 | Lely Patent Nv | Onbemand voertuig met beveiligingsinrichting. |
| KR100977638B1 (ko) | 2009-06-29 | 2010-08-24 | 서울대학교산학협력단 | 독성분이 있는 배출가스 혼합체에 생존하면서 온실가스를 흡수한 수생식물의 포식자를 이용하는 온실가스 제거 및 바이오 에너지 제조 방법 |
| US9271983B2 (en) | 2010-03-26 | 2016-03-01 | Bioadatp, Llc | Composition for enhancing athletic performance |
| US8344032B2 (en) * | 2010-03-26 | 2013-01-01 | Kevin Meehan | Composition for enhancing athletic performance |
| NL1037957C2 (nl) | 2010-05-12 | 2011-11-15 | Lely Patent Nv | Voertuig voor het verplaatsen van voer. |
| NL2010499C2 (en) | 2013-03-21 | 2014-09-24 | Lely Patent Nv | Vehicle for displacing feed lying on a floor in a sideward displacement direction. |
| CN103478632B (zh) * | 2013-09-17 | 2014-09-17 | 江西宇骏生物工程有限公司 | 一种果蔬保健片及其制备方法 |
| JP6129395B1 (ja) * | 2016-10-29 | 2017-05-17 | 誠一 荒木 | ミトコンドリア活性化に起因した血管内皮細胞保護回復用還元型ビタミンｂ２製剤 |
| CA3113071A1 (en) * | 2018-10-11 | 2020-04-16 | Imbria Pharmaceuticals, Inc. | Tca cycle intermediates and methods of use thereof |
| WO2021137257A1 (en) * | 2020-01-01 | 2021-07-08 | Celagenex Research (India) Pvt. Ltd. | Synergistic nutritional compositions for enhancing atp efficiency |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60100517A (ja) * | 1983-11-08 | 1985-06-04 | Eisai Co Ltd | 放射線潰瘍治療剤および方法 |
| US4981687A (en) * | 1988-07-29 | 1991-01-01 | University Of Florida | Compositions and methods for achieving improved physiological response to exercise |
| DE3943424A1 (de) * | 1989-12-30 | 1991-07-04 | Nephro Medica Pharma | Infusions- und injektionsloesung zur intravenoesen verabreichung |
| SE9201584D0 (sv) * | 1992-05-20 | 1992-05-20 | Vinnars Erik Ab | Use of alpha-ketoglutarate |
| IT1262954B (it) | 1992-07-03 | 1996-07-23 | Ist Farmacoterapico It Spa | Regioni antigeniche dei complessi tpl e anticorpi diretti contro di essi. |
| AU2330892A (en) * | 1992-07-06 | 1994-01-31 | Natalya Mikhailovna Burbenskaya | Pharmaceutical composition having anti-alcohol, radioprotecting and anti-choleraic activity and stimulating energy metabolism, stomach mucous membrane acid-generation and secretion functions |
| US5328701A (en) * | 1992-09-10 | 1994-07-12 | Peregrine Surgical Ltd. | Tissue irrigation solution |
| AU679020B2 (en) * | 1992-12-23 | 1997-06-19 | Abbott Laboratories | Medical foods for the nutritional support of infant/toddler metabolic diseases |
| SE9303691D0 (sv) * | 1993-11-09 | 1993-11-09 | Gramineer Ab | New beverage |
| DE4341000A1 (de) | 1993-12-02 | 1995-06-08 | Beiersdorf Ag | Verwendung von L-Arginin, L-Ornithin oder L-Citrullin und topischen Zubereitungen mit diesen Stoffen |
| US5378722A (en) * | 1993-12-03 | 1995-01-03 | Clintec Nutrition Co. | Nutritional compositions for management of nitrogen metabolism |
| US5707971A (en) * | 1995-06-07 | 1998-01-13 | Life Resuscitation Technologies, Inc. | Modulation of glycolytic ATP production |
| DE19520662A1 (de) * | 1995-06-07 | 1996-12-12 | Beiersdorf Ag | Mittel zur Behandlung von Kopfschuppen und zur Behandlung der Haare |
| DE19533330A1 (de) * | 1995-09-11 | 1997-03-13 | Beiersdorf Ag | Gegen Hautkrebs wirksame topische Zubereitungen |
| US6033689A (en) * | 1997-02-14 | 2000-03-07 | Milk Specialities Company | Animal feed composition of soluble sugar and dicarboxylic acid |
| US5874471A (en) * | 1997-02-27 | 1999-02-23 | Waugh; William Howard | Orthomolecular medical use of L-citrulline for vasoprotection, relaxative smooth muscle tone and cell protection |
| JPH10333335A (ja) | 1997-05-28 | 1998-12-18 | Ricoh Co Ltd | レジストパターンの形成方法 |
| ATE555780T1 (de) | 1997-10-24 | 2012-05-15 | John P Blass | Nahrungsergänzungsmittel für metabolische hirnleistungsstörungen |
| US5904924A (en) * | 1997-11-04 | 1999-05-18 | Oncologics, Inc. | Green nutritional powder composition |
| JP2000128784A (ja) * | 1998-10-20 | 2000-05-09 | Kuressendo Corporation:Kk | 二日酔い症状 |
| US20020150627A1 (en) * | 2001-01-26 | 2002-10-17 | Stout Jeffrey Ray | Composition containing creatine and phosphorus |
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- 2002-02-14 SK SK1125-2003A patent/SK11252003A3/sk not_active Application Discontinuation
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- 2002-02-14 JP JP2002563923A patent/JP2004518712A/ja active Pending
- 2002-02-14 RU RU2003125179/15A patent/RU2301665C2/ru not_active IP Right Cessation
- 2002-08-27 HR HR20020702A patent/HRP20020702A2/xx not_active Application Discontinuation
- 2002-09-04 ZA ZA200207100A patent/ZA200207100B/en unknown
- 2002-09-20 NO NO20024536A patent/NO20024536D0/no not_active Application Discontinuation
-
2006
- 2006-02-17 US US11/356,476 patent/US20060140925A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CZ20023935A3 (cs) | 2003-05-14 |
| CN1457255A (zh) | 2003-11-19 |
| UA76444C2 (en) | 2006-08-15 |
| WO2002064129A3 (en) | 2003-05-08 |
| NO20024536L (no) | 2002-09-20 |
| HUP0302384A2 (hu) | 2003-10-28 |
| RU2301665C2 (ru) | 2007-06-27 |
| JP2004518712A (ja) | 2004-06-24 |
| EE200200585A (et) | 2004-04-15 |
| US20020173546A1 (en) | 2002-11-21 |
| ZA200207100B (en) | 2003-09-04 |
| US20060140925A1 (en) | 2006-06-29 |
| WO2002064129A2 (en) | 2002-08-22 |
| EP1368017A2 (en) | 2003-12-10 |
| US7056950B2 (en) | 2006-06-06 |
| MXPA02010149A (es) | 2004-08-19 |
| CA2401383A1 (en) | 2002-08-22 |
| NZ528194A (en) | 2006-08-31 |
| PL363392A1 (en) | 2004-11-15 |
| HRP20020702A2 (en) | 2004-02-29 |
| RU2003125179A (ru) | 2005-01-20 |
| BR0203902A (pt) | 2003-01-28 |
| KR20020093906A (ko) | 2002-12-16 |
| IL151411A0 (en) | 2003-04-10 |
| TR200202175T1 (tr) | 2003-10-21 |
| NO20024536D0 (no) | 2002-09-20 |
| AU2002250942B2 (en) | 2007-04-26 |
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