CA2873403A1 - Composition energetique comestible renfermant de la xanthine methylatee et un derive de choline - Google Patents

Composition energetique comestible renfermant de la xanthine methylatee et un derive de choline Download PDF

Info

Publication number: CA2873403A1
Authority: CA; Canada
Prior art keywords: amount; energy composition; composition; present; vitamin
Prior art date: 2012-05-14
Legal status (The legal status 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 status listed.): Abandoned

Application number

CA2873403A

Other languages

English (en)

Inventor

Manoj Bhargava

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

International IP Holdings LLC

Original Assignee

International IP Holdings LLC

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.)

2012-05-14

Filing date

2013-05-14

Publication date

2013-11-21

2012-05-14 Priority claimed from US13/470,462 external-priority patent/US9049879B2/en

2013-05-14 Application filed by International IP Holdings LLC filed Critical International IP Holdings LLC

2013-11-21 Publication of CA2873403A1 publication Critical patent/CA2873403A1/fr

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 88
LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical class O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 title claims description 19
150000003248 quinolines Chemical class 0.000 title claims description 16
OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 claims description 40
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims description 35
LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 claims description 32
RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 claims description 26
235000019152 folic acid Nutrition 0.000 claims description 24
239000011724 folic acid Substances 0.000 claims description 24
229940024606 amino acid Drugs 0.000 claims description 23
150000001413 amino acids Chemical class 0.000 claims description 23
COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims description 21
239000000796 flavoring agent Substances 0.000 claims description 21
235000019634 flavors Nutrition 0.000 claims description 21
235000019158 vitamin B6 Nutrition 0.000 claims description 21
239000011726 vitamin B6 Substances 0.000 claims description 21
229960003080 taurine Drugs 0.000 claims description 18
229940088594 vitamin Drugs 0.000 claims description 18
229930003231 vitamin Natural products 0.000 claims description 18
235000013343 vitamin Nutrition 0.000 claims description 18
239000011782 vitamin Substances 0.000 claims description 18
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 17
OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 claims description 16
229960000304 folic acid Drugs 0.000 claims description 16
RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 claims description 16
229940011671 vitamin b6 Drugs 0.000 claims description 16
235000005152 nicotinamide Nutrition 0.000 claims description 15
239000011570 nicotinamide Substances 0.000 claims description 15
229960003966 nicotinamide Drugs 0.000 claims description 15
235000019163 vitamin B12 Nutrition 0.000 claims description 15
239000011715 vitamin B12 Substances 0.000 claims description 15
UYUXSRADSPPKRZ-UHFFFAOYSA-N D-glucuronic acid gamma-lactone Natural products O=CC(O)C1OC(=O)C(O)C1O UYUXSRADSPPKRZ-UHFFFAOYSA-N 0.000 claims description 13
UYUXSRADSPPKRZ-SKNVOMKLSA-N D-glucurono-6,3-lactone Chemical compound O=C[C@H](O)[C@H]1OC(=O)[C@@H](O)[C@H]1O UYUXSRADSPPKRZ-SKNVOMKLSA-N 0.000 claims description 13
LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 claims description 13
229960001948 caffeine Drugs 0.000 claims description 13
VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 claims description 13
229950002441 glucurolactone Drugs 0.000 claims description 13
229960001682 n-acetyltyrosine Drugs 0.000 claims description 13
CAHKINHBCWCHCF-JTQLQIEISA-N N-acetyl-L-tyrosine Chemical compound CC(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 CAHKINHBCWCHCF-JTQLQIEISA-N 0.000 claims description 12
229960005190 phenylalanine Drugs 0.000 claims description 12
RZZPDXZPRHQOCG-OJAKKHQRSA-M CDP-choline(1-) Chemical compound O[C@@H]1[C@H](O)[C@@H](COP([O-])(=O)OP([O-])(=O)OCC[N+](C)(C)C)O[C@H]1N1C(=O)N=C(N)C=C1 RZZPDXZPRHQOCG-OJAKKHQRSA-M 0.000 claims description 10
229930003779 Vitamin B12 Natural products 0.000 claims description 10
229960001284 citicoline Drugs 0.000 claims description 10
239000003755 preservative agent Substances 0.000 claims description 10
PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 9
229960003512 nicotinic acid Drugs 0.000 claims description 8
235000001968 nicotinic acid Nutrition 0.000 claims description 7
239000011664 nicotinic acid Substances 0.000 claims description 7
230000002335 preservative effect Effects 0.000 claims description 7
150000003722 vitamin derivatives Chemical class 0.000 claims description 5
150000003862 amino acid derivatives Chemical class 0.000 claims 5
FDJOLVPMNUYSCM-WZHZPDAFSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+3].N#[C-].N([C@@H]([C@]1(C)[N-]\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C(\C)/C1=N/C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO FDJOLVPMNUYSCM-WZHZPDAFSA-L 0.000 claims 3
QDGAVODICPCDMU-UHFFFAOYSA-N 2-amino-3-[3-[bis(2-chloroethyl)amino]phenyl]propanoic acid Chemical compound OC(=O)C(N)CC1=CC=CC(N(CCCl)CCCl)=C1 QDGAVODICPCDMU-UHFFFAOYSA-N 0.000 claims 2
230000008901 benefit Effects 0.000 abstract description 12
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235000001014 amino acid Nutrition 0.000 description 17
239000002243 precursor Substances 0.000 description 13
FFFHZYDWPBMWHY-VKHMYHEASA-N L-homocysteine Chemical compound OC(=O)[C@@H](N)CCS FFFHZYDWPBMWHY-VKHMYHEASA-N 0.000 description 10
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150000001875 compounds Chemical class 0.000 description 10
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BAQAVOSOZGMPRM-QBMZZYIRSA-N sucralose Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](CO)O[C@@H]1O[C@@]1(CCl)[C@@H](O)[C@H](O)[C@@H](CCl)O1 BAQAVOSOZGMPRM-QBMZZYIRSA-N 0.000 description 10
239000000126 substance Substances 0.000 description 9
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 8
229940014144 folate Drugs 0.000 description 8
230000036626 alertness Effects 0.000 description 7
OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 7
229960001231 choline Drugs 0.000 description 7
AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 description 7
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238000003786 synthesis reaction Methods 0.000 description 7
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 6
CHHHXKFHOYLYRE-UHFFFAOYSA-M 2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- Chemical compound [K+].CC=CC=CC([O-])=O CHHHXKFHOYLYRE-UHFFFAOYSA-M 0.000 description 6
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 6
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OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 6
BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 6
229940088598 enzyme Drugs 0.000 description 6
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 6
239000001630 malic acid Substances 0.000 description 6
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WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 6
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QUNWUDVFRNGTCO-UHFFFAOYSA-N 1,7-dimethylxanthine Chemical compound N1C(=O)N(C)C(=O)C2=C1N=CN2C QUNWUDVFRNGTCO-UHFFFAOYSA-N 0.000 description 4
OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 4
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BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 4
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IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 2
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- 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
- 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
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/322—Foods, ingredients or supplements having a functional effect on health having an effect on the health of the nervous system or on mental function
- 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
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/33—High-energy foods and drinks, sports drinks
- 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
- A23V2250/00—Food ingredients
- A23V2250/02—Acid
- A23V2250/06—Amino acid
- A23V2250/0644—Taurine
- 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
- A23V2250/00—Food ingredients
- A23V2250/02—Acid
- A23V2250/06—Amino acid
- A23V2250/0652—Tyrosine
- 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
- A23V2250/00—Food ingredients
- A23V2250/20—Natural extracts
- A23V2250/21—Plant extracts
- A23V2250/2108—Caffeine, coffee extract
- 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
- A23V2250/00—Food ingredients
- A23V2250/30—Other Organic compounds
- A23V2250/304—Choline
- 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
- A23V2250/00—Food ingredients
- A23V2250/70—Vitamins
- A23V2250/704—Vitamin B

Landscapes

Life Sciences & Earth Sciences (AREA)
Polymers & Plastics (AREA)
Nutrition Science (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Food Science & Technology (AREA)
Health & Medical Sciences (AREA)
Mycology (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Coloring Foods And Improving Nutritive Qualities (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicinal Preparation (AREA)

CA2873403A 2012-05-14 2013-05-14 Composition energetique comestible renfermant de la xanthine methylatee et un derive de choline Abandoned CA2873403A1 (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US13/470,462		2012-05-14
US13/470,462 US9049879B2 (en)	2008-06-13	2012-05-14	Edible energy composition
PCT/US2013/040842 WO2013173265A1 (fr)	2012-05-14	2013-05-14	Composition d'énergie comestible

Publications (1)

Publication Number	Publication Date
CA2873403A1 true CA2873403A1 (fr)	2013-11-21

Family

ID=49584195

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA2873403A Abandoned CA2873403A1 (fr)	2012-05-14	2013-05-14	Composition energetique comestible renfermant de la xanthine methylatee et un derive de choline

Country Status (7)

Country	Link
AU (1)	AU2013263025B2 (fr)
CA (1)	CA2873403A1 (fr)
IL (1)	IL235535A0 (fr)
MX (1)	MX345908B (fr)
SG (1)	SG11201407298TA (fr)
WO (1)	WO2013173265A1 (fr)
ZA (1)	ZA201409135B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA3214950A1 (fr)	2021-04-07	2022-10-13	Ralf Jager	Composition bioactive a base de 1-methylxanthine et son procede d'utilisation
JP2024527056A (ja)	2021-07-27	2024-07-19	ピーエックス・アイエヌジー，エルエルシー	生物活性組成物およびそれを使用する方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20090074936A1 (en) *	2007-09-17	2009-03-19	Schmidt James C	Energy beverage
US8187647B2 (en) *	2008-06-13	2012-05-29	BioClinical Development, Inc.	Edible energy composition
US8993033B2 (en) *	2007-11-16	2015-03-31	International Ip Holdings, Llc	Edible energy composition with low caffeine
US20090162483A1 (en) *	2007-12-20	2009-06-25	Wendy Lynn Constantine	Sports beverage and method of making
US20090162488A1 (en) *	2007-12-21	2009-06-25	The Concentrate Manufacturing Company Of Ireland	Beverage products and flavor systems having a non-sweetening amount of monatin

2013
- 2013-05-14 CA CA2873403A patent/CA2873403A1/fr not_active Abandoned
- 2013-05-14 MX MX2014013800A patent/MX345908B/es active IP Right Grant
- 2013-05-14 WO PCT/US2013/040842 patent/WO2013173265A1/fr not_active Ceased
- 2013-05-14 AU AU2013263025A patent/AU2013263025B2/en active Active
- 2013-05-14 SG SG11201407298TA patent/SG11201407298TA/en unknown
2014
- 2014-11-06 IL IL235535A patent/IL235535A0/en active IP Right Grant
- 2014-12-11 ZA ZA2014/09135A patent/ZA201409135B/en unknown

Also Published As

Publication number	Publication date
WO2013173265A1 (fr)	2013-11-21
AU2013263025A1 (en)	2015-01-15
ZA201409135B (en)	2016-07-27
SG11201407298TA (en)	2015-01-29
MX345908B (es)	2017-02-22
MX2014013800A (es)	2015-01-26
IL235535A0 (en)	2015-01-29
AU2013263025B2 (en)	2017-03-30

Publication	Publication Date	Title
US9937195B2 (en)	2018-04-10	Edible energy composition
US6420342B1 (en)	2002-07-16	Nutritional preparation comprising ribose and medical use thereof
US20060115556A1 (en)	2006-06-01	Nutritional supplement drink containing xanthone extracts
CA2704481C (fr)	2015-12-22	Composition energetique comestible a faible teneur en cafeine, comprenant de la choline
US20060115555A1 (en)	2006-06-01	Nutritional supplements containing xanthone extracts
US20100124587A1 (en)	2010-05-20	Creatine-containing vitamin and mineral composition
AU2013263025B2 (en)	2017-03-30	Edible energy composition
US10881661B2 (en)	2021-01-05	Edible energy composition
EP3449252B1 (fr)	2020-05-06	Procédé d'évaluation de la capacité d'une composition à prévenir la fatigue et les dommages musculaires
US20030148016A1 (en)	2003-08-07	Energy fitness water
US20240350502A1 (en)	2024-10-24	Edible Energy Composition
US20210077517A1 (en)	2021-03-18	Edible Energy Composition
US20040258674A1 (en)	2004-12-23	Quercetin supplementation to treat hypertenstion
US20150086654A1 (en)	2015-03-26	Nutritional energy and focus supplement
WO2017059035A1 (fr)	2017-04-06	Composition comestible contenant une protéine
IT202200002357U1 (it)	2024-01-25	Composizione di un integratore alimentare in gel multivitaminico per la riduzione della stanchezza e affaticamento
CA2903803A1 (fr)	2014-09-18	Preparation hypocalorique pour nourrissons
WO2005016268A2 (fr)	2005-02-24	Compositions alimentaires et procedes pour moduler un metabolisme
Peralta	2012	Vitamins in Diets: Metabolism Relationship
Liepa et al.	2009	7 B-Vitamins
HK1038163B (en)	2004-07-23	Beverage for increasing the body's capacity to break down alcohol

Legal Events

Date	Code	Title	Description
2014-12-10	EEER	Examination request	Effective date: 20141112
2018-09-19	FZDE	Discontinued	Effective date: 20180807