SK283392B6 - Soľ L-karnitínu alebo alkanoyl-L-karnitínu, kompozícia s jej obsahom a použitie - Google Patents

Soľ L-karnitínu alebo alkanoyl-L-karnitínu, kompozícia s jej obsahom a použitie Download PDF

Info

Publication number: SK283392B6
Authority: SK; Slovakia
Prior art keywords: carnitine; salt; alkanoyl; composition according; formula
Prior art date: 1997-04-01

Application number

SK1350-99A

Other languages

English (en)

Slovak (sk)

Other versions

SK135099A3 (en

Inventor

Nazareno Scafetta

Maria Ornella Tinti

Original Assignee

Sigma-Tau Industrie Farmaceutiche Riunite S.P.A.

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.)

1997-04-01

Filing date

1998-03-19

Publication date

2003-07-01

1998-03-19 Application filed by Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. filed Critical Sigma-Tau Industrie Farmaceutiche Riunite S.P.A.

2000-05-16 Publication of SK135099A3 publication Critical patent/SK135099A3/sk

2003-07-01 Publication of SK283392B6 publication Critical patent/SK283392B6/sk

Links

PHIQHXFUZVPYII-ZCFIWIBFSA-N (R)-carnitine Chemical class C[N+](C)(C)C[C@H](O)CC([O-])=O PHIQHXFUZVPYII-ZCFIWIBFSA-N 0.000 title claims abstract description 31
239000000203 mixture Substances 0.000 title claims description 18
150000003839 salts Chemical class 0.000 claims abstract description 33
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims abstract description 26
229960003080 taurine Drugs 0.000 claims abstract description 13
235000015872 dietary supplement Nutrition 0.000 claims abstract description 11
230000000378 dietary effect Effects 0.000 claims abstract description 3
-1 isovaleryl Chemical group 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 7
125000001589 carboacyl group Chemical group 0.000 claims description 6
239000004480 active ingredient Substances 0.000 claims description 5
239000002775 capsule Substances 0.000 claims description 3
239000003826 tablet Substances 0.000 claims description 3
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
239000007910 chewable tablet Substances 0.000 claims description 2
239000006052 feed supplement Substances 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
239000000546 pharmaceutical excipient Substances 0.000 claims description 2
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
239000008187 granular material Substances 0.000 claims 1
239000004615 ingredient Substances 0.000 claims 1
239000000843 powder Substances 0.000 claims 1
239000008247 solid mixture Substances 0.000 abstract 1
239000013589 supplement Substances 0.000 abstract 1
238000002360 preparation method Methods 0.000 description 6
239000007787 solid Substances 0.000 description 6
230000001225 therapeutic effect Effects 0.000 description 6
235000013305 food Nutrition 0.000 description 5
235000016709 nutrition Nutrition 0.000 description 5
RDHQFKQIGNGIED-MRVPVSSYSA-N O-acetyl-L-carnitine Chemical compound CC(=O)O[C@H](CC([O-])=O)C[N+](C)(C)C RDHQFKQIGNGIED-MRVPVSSYSA-N 0.000 description 4
PHIQHXFUZVPYII-UHFFFAOYSA-N carnitine Chemical class C[N+](C)(C)CC(O)CC([O-])=O PHIQHXFUZVPYII-UHFFFAOYSA-N 0.000 description 4
230000029087 digestion Effects 0.000 description 4
239000000126 substance Substances 0.000 description 4
XOAAWQZATWQOTB-UHFFFAOYSA-M 2-aminoethanesulfonate Chemical compound NCCS([O-])(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-M 0.000 description 3
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
230000002503 metabolic effect Effects 0.000 description 3
239000002417 nutraceutical Substances 0.000 description 3
235000021436 nutraceutical agent Nutrition 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
230000005526 G1 to G0 transition Effects 0.000 description 2
208000017170 Lipid metabolism disease Diseases 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
210000004556 brain Anatomy 0.000 description 2
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
239000008116 calcium stearate Substances 0.000 description 2
235000013539 calcium stearate Nutrition 0.000 description 2
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
230000001684 chronic effect Effects 0.000 description 2
230000000295 complement effect Effects 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
238000000921 elemental analysis Methods 0.000 description 2
230000036449 good health Effects 0.000 description 2
238000004128 high performance liquid chromatography Methods 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
239000000047 product Substances 0.000 description 2
239000002994 raw material Substances 0.000 description 2
210000002027 skeletal muscle Anatomy 0.000 description 2
239000008107 starch Substances 0.000 description 2
235000019698 starch Nutrition 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical class C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 description 1
HOHIAEPXOHCCGW-UHFFFAOYSA-N 2-aminoethanesulfonic acid Chemical compound NCCS(O)(=O)=O.NCCS(O)(=O)=O HOHIAEPXOHCCGW-UHFFFAOYSA-N 0.000 description 1
206010002383 Angina Pectoris Diseases 0.000 description 1
206010019280 Heart failures Diseases 0.000 description 1
235000011002 L(+)-tartaric acid Nutrition 0.000 description 1
239000001358 L(+)-tartaric acid Substances 0.000 description 1
FEWJPZIEWOKRBE-LWMBPPNESA-N L-(+)-Tartaric acid Natural products OC(=O)[C@@H](O)[C@H](O)C(O)=O FEWJPZIEWOKRBE-LWMBPPNESA-N 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
206010025476 Malabsorption Diseases 0.000 description 1
208000004155 Malabsorption Syndromes Diseases 0.000 description 1
208000007101 Muscle Cramp Diseases 0.000 description 1
206010028372 Muscular weakness Diseases 0.000 description 1
RFDAIACWWDREDC-UHFFFAOYSA-N Na salt-Glycocholic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(=O)NCC(O)=O)C)C1(C)C(O)C2 RFDAIACWWDREDC-UHFFFAOYSA-N 0.000 description 1
208000005392 Spasm Diseases 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
WBWWGRHZICKQGZ-UHFFFAOYSA-N Taurocholic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(=O)NCCS(O)(=O)=O)C)C1(C)C(O)C2 WBWWGRHZICKQGZ-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
235000019728 animal nutrition Nutrition 0.000 description 1
206010003119 arrhythmia Diseases 0.000 description 1
230000000386 athletic effect Effects 0.000 description 1
210000000941 bile Anatomy 0.000 description 1
239000003613 bile acid Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
210000003169 central nervous system Anatomy 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
235000012000 cholesterol Nutrition 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
235000005911 diet Nutrition 0.000 description 1
230000037213 diet Effects 0.000 description 1
230000002526 effect on cardiovascular system Effects 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
RFDAIACWWDREDC-FRVQLJSFSA-N glycocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 RFDAIACWWDREDC-FRVQLJSFSA-N 0.000 description 1
238000001631 haemodialysis Methods 0.000 description 1
235000001497 healthy food Nutrition 0.000 description 1
230000000322 hemodialysis Effects 0.000 description 1
235000020256 human milk Nutrition 0.000 description 1
210000004251 human milk Anatomy 0.000 description 1
210000000936 intestine Anatomy 0.000 description 1
238000002372 labelling Methods 0.000 description 1
239000008101 lactose Substances 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
230000007774 longterm Effects 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
230000007102 metabolic function Effects 0.000 description 1
238000000034 method Methods 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
210000003205 muscle Anatomy 0.000 description 1
230000036473 myasthenia Effects 0.000 description 1
208000031225 myocardial ischemia Diseases 0.000 description 1
238000010606 normalization Methods 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
230000004962 physiological condition Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
210000001525 retina Anatomy 0.000 description 1
210000002966 serum Anatomy 0.000 description 1
WBWWGRHZICKQGZ-GIHLXUJPSA-N taurocholic acid Chemical compound C([C@@H]1C[C@H]2O)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@@H]([C@@H](CCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@H](O)C1 WBWWGRHZICKQGZ-GIHLXUJPSA-N 0.000 description 1
235000021476 total parenteral nutrition Nutrition 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/105—Aliphatic or alicyclic compounds
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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
- A23L33/17—Amino acids, peptides or proteins
- A23L33/175—Amino acids
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
- 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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
- C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C309/13—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/14—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton containing amino groups bound to the carbon skeleton

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Pharmacology & Pharmacy (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Polymers & Plastics (AREA)
Cardiology (AREA)
Heart & Thoracic Surgery (AREA)
Food Science & Technology (AREA)
Urology & Nephrology (AREA)
Mycology (AREA)
Zoology (AREA)
Animal Husbandry (AREA)
Neurology (AREA)
Orthopedic Medicine & Surgery (AREA)
Physical Education & Sports Medicine (AREA)
Nutrition Science (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Diabetes (AREA)
Pain & Pain Management (AREA)
Vascular Medicine (AREA)
Hospice & Palliative Care (AREA)
Obesity (AREA)
Hematology (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicinal Preparation (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Coloring Foods And Improving Nutritive Qualities (AREA)
Fodder In General (AREA)

SK1350-99A 1997-04-01 1998-03-19 Soľ L-karnitínu alebo alkanoyl-L-karnitínu, kompozícia s jej obsahom a použitie SK283392B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IT97RM000184A IT1291126B1 (it)	1997-04-01	1997-04-01	Composizioni solide atte alla somministrazione orale comprendenti sali non igroscopici della l-carnitina e delle alcanoil l-carnitine
PCT/IT1998/000060 WO1998043945A1 (en)	1997-04-01	1998-03-19	Solid compositions suitable for oral administration comprising non hygroscopic salts of l-carnitine and alkanoyl-l-carnitine with 2-aminoethanesulfonic acid

Publications (2)

Publication Number	Publication Date
SK135099A3 SK135099A3 (en)	2000-05-16
SK283392B6 true SK283392B6 (sk)	2003-07-01

Family

ID=11404924

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1350-99A SK283392B6 (sk)	1997-04-01	1998-03-19	Soľ L-karnitínu alebo alkanoyl-L-karnitínu, kompozícia s jej obsahom a použitie

Country Status (22)

Country	Link
US (1)	US6124360A (cs)
EP (1)	EP0971880B1 (cs)
JP (1)	JP4047935B2 (cs)
KR (1)	KR100562055B1 (cs)
CN (1)	CN1187318C (cs)
AT (1)	ATE210111T1 (cs)
AU (1)	AU733272B2 (cs)
BR (1)	BR9808461A (cs)
CA (1)	CA2285380C (cs)
CZ (1)	CZ296465B6 (cs)
DE (1)	DE69802789T2 (cs)
DK (1)	DK0971880T3 (cs)
ES (1)	ES2167878T3 (cs)
HU (1)	HU226109B1 (cs)
IL (2)	IL131956A0 (cs)
IT (1)	IT1291126B1 (cs)
NZ (1)	NZ500537A (cs)
PL (1)	PL189488B1 (cs)
PT (1)	PT971880E (cs)
SI (1)	SI0971880T1 (cs)
SK (1)	SK283392B6 (cs)
WO (1)	WO1998043945A1 (cs)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6090849A (en) *	1999-03-23	2000-07-18	The Board Of Regents For Oklahoma State University	Carnitine supplemented diet to prevent sudden death syndrome in breeder type poultry
IT1305308B1 (it) *	1999-03-26	2001-05-04	Biosint S P A	Granulato ad alto contenuto di l-carnitina o alcanoil-l-carnitina,particolarmente adatto alla produzione di compresse per compressione
IT1317924B1 (it) *	2000-10-31	2003-07-15	Sigma Tau Ind Farmaceuti	Composizioni solide atte alla somministrazione orale comprendenti salinon igroscopici della l-carnitina e delle alcanoil l-carnitine con
DE10350140A1 (de) *	2003-03-28	2004-10-14	Martin Schymura	Fruchtgummizusammensetzung
CN104276986B (zh) *	2013-07-12	2016-07-06	辽宁科硕营养科技有限公司	左旋肉碱牛磺酸盐的制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1153640A (en) *	1967-04-10	1969-05-29	Soc D Etudes Prod Chimique	A Carnitin Salt
FR2529545B1 (fr) *	1982-07-02	1985-05-31	Sanofi Sa	Nouveaux sels de carnitine ainsi que leur procede de preparation
DE3463261D1 (en) *	1983-12-28	1987-05-27	Sigma Tau Ind Farmaceuti	Salts of l-carnitine and alkanoyl l-carnitines and process for preparing same
IT1188176B (it) *	1985-07-05	1988-01-07	Bicresearch Spa	Sali della carnitina particolarmente idonei per uso orale
SE8701662L (sv) *	1987-04-22	1988-10-23	Gelder Nico M Van	Saett och medel foer att behandla neurologiska sjukdomar, exempelvis migraen genom paaverkan av nervcellerna
CA2018137C (en) *	1989-06-14	2000-01-11	Thomas Scholl	L-carnitine magnesium citrate
US5073376A (en) *	1989-12-22	1991-12-17	Lonza Ltd.	Preparations containing l-carnitine
US5571783A (en) *	1993-03-09	1996-11-05	Clintec Nutrition Company	Composition and method for treating patients with hepatic disease
IT1261688B (it) *	1993-05-28	1996-05-29	Avantgarde Spa	Uso di esteri sull'ossidrile della l-carnitina per produrre composizioni farmaceutiche per il trattamento di affezioni cutanee.
US5589468A (en) *	1995-01-13	1996-12-31	Clintec Nutrition Co.	Method for providing nutrition to elderly patients

1997
- 1997-04-01 IT IT97RM000184A patent/IT1291126B1/it active IP Right Grant
1998
- 1998-03-19 IL IL13195698A patent/IL131956A0/xx active IP Right Grant
- 1998-03-19 DK DK98912695T patent/DK0971880T3/da active
- 1998-03-19 PL PL98335937A patent/PL189488B1/pl unknown
- 1998-03-19 JP JP54137798A patent/JP4047935B2/ja not_active Expired - Lifetime
- 1998-03-19 SK SK1350-99A patent/SK283392B6/sk not_active IP Right Cessation
- 1998-03-19 CA CA002285380A patent/CA2285380C/en not_active Expired - Lifetime
- 1998-03-19 PT PT98912695T patent/PT971880E/pt unknown
- 1998-03-19 US US09/381,806 patent/US6124360A/en not_active Expired - Lifetime
- 1998-03-19 HU HU0001866A patent/HU226109B1/hu unknown
- 1998-03-19 BR BR9808461-5A patent/BR9808461A/pt not_active Application Discontinuation
- 1998-03-19 NZ NZ500537A patent/NZ500537A/xx not_active IP Right Cessation
- 1998-03-19 ES ES98912695T patent/ES2167878T3/es not_active Expired - Lifetime
- 1998-03-19 KR KR1019997008943A patent/KR100562055B1/ko not_active Expired - Lifetime
- 1998-03-19 AU AU67455/98A patent/AU733272B2/en not_active Expired
- 1998-03-19 AT AT98912695T patent/ATE210111T1/de active
- 1998-03-19 CN CNB988038471A patent/CN1187318C/zh not_active Expired - Lifetime
- 1998-03-19 DE DE69802789T patent/DE69802789T2/de not_active Expired - Lifetime
- 1998-03-19 CZ CZ0347899A patent/CZ296465B6/cs not_active IP Right Cessation
- 1998-03-19 EP EP98912695A patent/EP0971880B1/en not_active Expired - Lifetime
- 1998-03-19 WO PCT/IT1998/000060 patent/WO1998043945A1/en not_active Ceased
- 1998-03-19 SI SI9830060T patent/SI0971880T1/xx unknown
1999
- 1999-09-16 IL IL131956A patent/IL131956A/en not_active IP Right Cessation

Also Published As

Publication number	Publication date
SI0971880T1 (en)	2002-06-30
ITRM970184A1 (it)	1998-10-01
ATE210111T1 (de)	2001-12-15
PT971880E (pt)	2002-05-31
DE69802789D1 (de)	2002-01-17
IL131956A0 (en)	2001-03-19
HU226109B1 (en)	2008-04-28
CA2285380C (en)	2008-07-08
HUP0001866A3 (en)	2002-09-30
CN1187318C (zh)	2005-02-02
KR100562055B1 (ko)	2006-03-17
IL131956A (en)	2007-09-20
AU6745598A (en)	1998-10-22
ES2167878T3 (es)	2002-05-16
US6124360A (en)	2000-09-26
NZ500537A (en)	2001-03-30
IT1291126B1 (it)	1998-12-29
HK1025560A1 (en)	2000-11-17
PL189488B1 (pl)	2005-08-31
CN1251573A (zh)	2000-04-26
CZ296465B6 (cs)	2006-03-15
CZ347899A3 (cs)	2000-04-12
JP4047935B2 (ja)	2008-02-13
PL335937A1 (en)	2000-05-22
CA2285380A1 (en)	1998-10-08
SK135099A3 (en)	2000-05-16
BR9808461A (pt)	2000-05-23
DK0971880T3 (da)	2002-03-04
EP0971880A1 (en)	2000-01-19
EP0971880B1 (en)	2001-12-05
KR20010005867A (ko)	2001-01-15
HUP0001866A2 (hu)	2000-11-28
WO1998043945A1 (en)	1998-10-08
AU733272B2 (en)	2001-05-10
JP2001517227A (ja)	2001-10-02
DE69802789T2 (de)	2002-07-18

Legal Events

Date	Code	Title	Description
2018-05-02	MK4A	Patent expired	Expiry date: 20180319

Publication	Publication Date	Title
PL189602B1 (pl)	2005-08-31	Sól L-karnityny lub alkanoilo-L-karnityny i preparaty je zawierające oraz ich zastosowanie
SK283392B6 (sk)	2003-07-01	Soľ L-karnitínu alebo alkanoyl-L-karnitínu, kompozícia s jej obsahom a použitie
EP1330428B1 (en)	2005-12-14	Solid compositions suitable for oral administration containing non-hygroscopic salts of l-carnitine and the alkanoyl l-carnitines with taurine chloride
AU2001295893A1 (en)	2002-07-18	Solid compositions suitable for oral administration containing non-hygroscopic salts of L-carnitine and the alkanoyl L-carnitines with taurine chloride and glycine chloride
US6465515B2 (en)	2002-10-15	Solid compositions suitable for oral administration containing non-hydroscopic salts of L-carnitine and alkanoyl L-carnitines
HK1025560B (en)	2002-07-05	Solid compositions suitable for oral administration comprising non hygroscopic salts of l-carnitine and alkanoyl-l-carnitine with 2-aminoethanesulfonic acid
MXPA99008994A (en)	2000-02-02	Solid compositions suitable for oral administration comprising non hygroscopic salts of l-carnitine and alkanoyl-l-carnitine with 2-aminoethanesulfonic acid