LT2000029A - N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio kompleksai su metalais - Google Patents

N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio kompleksai su metalais Download PDF

Info

Publication number: LT2000029A
Authority: LT; Lithuania
Prior art keywords: aspartyl; dimethylbutyl; phenylalanine; methyl ester; chloride
Prior art date: 1997-09-11

Application number

LT2000029A

Other languages

English (en)

Lithuanian (lt)

Inventor

Indra Prakash

Zhi Guo

Original Assignee

The Nutrasweet Company

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.)

1997-09-11

Filing date

2000-04-06

Publication date

2000-12-27

2000-04-06 Application filed by The Nutrasweet Company filed Critical The Nutrasweet Company

2000-12-27 Publication of LT2000029A publication Critical patent/LT2000029A/lt

Links

229910052751 metal Inorganic materials 0.000 title claims description 24
239000002184 metal Substances 0.000 title claims description 24
235000010357 aspartame Nutrition 0.000 title description 27
229960005190 phenylalanine Drugs 0.000 title description 20
FGOJCPKOOGIRPA-UHFFFAOYSA-N 1-o-tert-butyl 4-o-ethyl 5-oxoazepane-1,4-dicarboxylate Chemical compound CCOC(=O)C1CCN(C(=O)OC(C)(C)C)CCC1=O FGOJCPKOOGIRPA-UHFFFAOYSA-N 0.000 title description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
HLIAVLHNDJUHFG-UHFFFAOYSA-N neotame Chemical compound CC(C)(C)CCNC(CC(O)=O)C(=O)NC(C(=O)OC)CC1=CC=CC=C1 HLIAVLHNDJUHFG-UHFFFAOYSA-N 0.000 claims description 16
IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 claims description 14
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
239000007788 liquid Substances 0.000 claims description 10
235000013615 non-nutritive sweetener Nutrition 0.000 claims description 9
239000002904 solvent Substances 0.000 claims description 9
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical group [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 8
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical group Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 6
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical group [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 5
239000001110 calcium chloride Substances 0.000 claims description 5
229910001628 calcium chloride Inorganic materials 0.000 claims description 5
150000004696 coordination complex Chemical class 0.000 claims description 5
229910001629 magnesium chloride Inorganic materials 0.000 claims description 4
239000000203 mixture Substances 0.000 claims description 4
NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical group [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 4
229910021577 Iron(II) chloride Inorganic materials 0.000 claims description 3
NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical group Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 claims description 3
229910000368 zinc sulfate Chemical group 0.000 claims description 2
229960001763 zinc sulfate Drugs 0.000 claims description 2
125000000896 monocarboxylic acid group Chemical group 0.000 claims 2
101100168904 Schizosaccharomyces pombe (strain 972 / ATCC 24843) cul3 gene Proteins 0.000 claims 1
239000011686 zinc sulphate Chemical group 0.000 claims 1
235000009529 zinc sulphate Nutrition 0.000 claims 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
-1 3,3-DIMETHYL-BUTYL Chemical class 0.000 description 20
235000003599 food sweetener Nutrition 0.000 description 14
239000003765 sweetening agent Substances 0.000 description 14
150000002739 metals Chemical class 0.000 description 10
150000003839 salts Chemical class 0.000 description 10
108010011485 Aspartame Proteins 0.000 description 9
239000000605 aspartame Substances 0.000 description 9
229960003438 aspartame Drugs 0.000 description 9
238000004090 dissolution Methods 0.000 description 8
239000000243 solution Substances 0.000 description 7
150000001875 compounds Chemical class 0.000 description 4
238000000034 method Methods 0.000 description 4
HLIAVLHNDJUHFG-HOTGVXAUSA-N neotame Chemical compound CC(C)(C)CCN[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 HLIAVLHNDJUHFG-HOTGVXAUSA-N 0.000 description 4
230000000007 visual effect Effects 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
229960002713 calcium chloride Drugs 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
108010016626 Dipeptides Proteins 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
239000004384 Neotame Substances 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
235000013361 beverage Nutrition 0.000 description 2
229940079593 drug Drugs 0.000 description 2
239000003814 drug Substances 0.000 description 2
239000000428 dust Substances 0.000 description 2
235000013305 food Nutrition 0.000 description 2
229960002337 magnesium chloride Drugs 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
235000019412 neotame Nutrition 0.000 description 2
108010070257 neotame Proteins 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 2
238000002798 spectrophotometry method Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
206010011224 Cough Diseases 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
229940024606 amino acid Drugs 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000006399 behavior Effects 0.000 description 1
239000004067 bulking agent Substances 0.000 description 1
LLSDKQJKOVVTOJ-UHFFFAOYSA-L calcium chloride dihydrate Chemical compound O.O.[Cl-].[Cl-].[Ca+2] LLSDKQJKOVVTOJ-UHFFFAOYSA-L 0.000 description 1
229940052299 calcium chloride dihydrate Drugs 0.000 description 1
235000012174 carbonated soft drink Nutrition 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
235000009508 confectionery Nutrition 0.000 description 1
238000010410 dusting Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000037406 food intake Effects 0.000 description 1
235000012631 food intake Nutrition 0.000 description 1
238000004108 freeze drying Methods 0.000 description 1
235000015203 fruit juice Nutrition 0.000 description 1
235000015270 fruit-flavoured drink Nutrition 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
229940050906 magnesium chloride hexahydrate Drugs 0.000 description 1
DHRRIBDTHFBPNG-UHFFFAOYSA-L magnesium dichloride hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-] DHRRIBDTHFBPNG-UHFFFAOYSA-L 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000005244 neohexyl group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000014594 pastries Nutrition 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
235000021395 porridge Nutrition 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
102000004196 processed proteins & peptides Human genes 0.000 description 1
235000013599 spices Nutrition 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000005728 strengthening Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
235000019605 sweet taste sensations Nutrition 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
239000006188 syrup Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1
RZLVQBNCHSJZPX-UHFFFAOYSA-L zinc sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Zn+2].[O-]S([O-])(=O)=O RZLVQBNCHSJZPX-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
- C07K5/06113—Asp- or Asn-amino acid
- 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
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/31—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives
- A23L27/32—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives containing dipeptides or derivatives

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Biochemistry (AREA)
Food Science & Technology (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Biophysics (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Medicinal Chemistry (AREA)
Molecular Biology (AREA)
Nutrition Science (AREA)
Seasonings (AREA)
Peptides Or Proteins (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

LT2000029A 1997-09-11 2000-04-06 N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio kompleksai su metalais LT2000029A (lt)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US5850897P	1997-09-11	1997-09-11

Publications (1)

Publication Number	Publication Date
LT2000029A true LT2000029A (lt)	2000-12-27

Family

ID=22017244

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LT2000029A LT2000029A (lt)	1997-09-11	2000-04-06	N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio kompleksai su metalais

Country Status (18)

Country	Link
US (1)	US6146680A (fr)
EP (1)	EP1012170A1 (fr)
CN (1)	CN1278826A (fr)
AU (1)	AU9567998A (fr)
BG (1)	BG104320A (fr)
BR (1)	BR9812767A (fr)
CA (1)	CA2303433A1 (fr)
EE (1)	EE200000115A (fr)
HU (1)	HUP0003574A3 (fr)
ID (1)	ID27125A (fr)
IL (1)	IL134915A0 (fr)
LT (1)	LT2000029A (fr)
NO (1)	NO20001272L (fr)
PL (1)	PL339190A1 (fr)
SI (1)	SI20329A (fr)
SK (1)	SK3252000A3 (fr)
TR (1)	TR200000732T2 (fr)
WO (1)	WO1999012955A1 (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU3904800A (en) *	1999-03-22	2000-10-09	Nutrasweet Company, The	Cereals and cereal-based food sweetened with n-(9n-(3,3- dimethylbutyl) -l-alpha- aspartyl) -l-phenylalanine 1-methyl ester
US6365216B1 (en)	1999-03-26	2002-04-02	The Nutrasweet Company	Particles of N-[N-(3,3-dimethylbutyl)-L-α-aspartyl]-L-phenylalanine 1-methyl ester
WO2000069282A1 (fr) *	1999-05-13	2000-11-23	The Nutrasweet Company	Modification du gout et des proprietes physico-chimiques de neotame, a l'aide d'additifs d'acide hydrophobe
US20030008047A1 (en) *	2000-03-17	2003-01-09	Schroeder Steve A.	Stability enhancement of sweeteners using salts containing divalent or trivalent cations
US7326430B2 (en) *	2000-07-18	2008-02-05	The Nutrasweet Company	Method of preparing liquid compositions for delivery of N-[N- (3,3-dimethylbutyl-L-α-aspartyl]-L-phenylalanine 1-methyl ester in food and beverage systems
US6225493B1 (en) *	2000-08-21	2001-05-01	The Nutrasweet Company	Metal ion assisted N-[N-(3,3-dimethylbutyl)-L-α-aspartyl]-L-phenylalanine 1-methyl ester isomer resolution
US20110097449A1 (en) *	2006-06-30	2011-04-28	Conagra Foods Rdm, Inc.	Seasoning and method for seasoning a food product while reducing dietary sodium intake
US20080008790A1 (en) *	2006-06-30	2008-01-10	Michael Jensen	Seasoned food, seasoning, and method for seasoning a food product
US7923047B2 (en) *	2006-06-30	2011-04-12	Conagra Foods Rdm, Inc.	Seasoning and method for seasoning a food product while reducing dietary sodium intake
US20080038411A1 (en) *	2006-06-30	2008-02-14	Michael Jensen	Seasoning and method for enhancing and potentiating food flavor
CA2664585C (fr) *	2006-09-27	2015-04-14	Conagra Foods Rdm, Inc.	Assaisonnement et procede d'amelioration et de renforcement des saveurs alimentaires par microencapsulation, associes a une reduction de l'apport en sodium par l'alimentation
WO2012026499A1 (fr) *	2010-08-25	2012-03-01	味の素株式会社	Procédé de conservation et agent stabilisant pour dérivé d'ester dipeptidique d'aspartyle
FR3102041B1 (fr)	2019-10-22	2025-02-14	Aroma Sens	Edulcorant pour liquides de cigarette électronique
BR112022023597A2 (pt) *	2020-06-01	2023-02-07	Balchem Corp	Quelatos de di-aminoácido de metal ou quelatos de tri-aminoácido de metal

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4031258A (en) *	1972-03-30	1977-06-21	General Foods Corporation	Inorganic salts of dipeptide sweeteners
CA1028197A (fr) *	1973-04-02	1978-03-21	Jeffrey H. Berg	Edulcorant concentre a faible teneur en calories
US4448716A (en) *	1982-03-04	1984-05-15	G. D. Searle & Co.	Dipeptide sweetener-metal complexes
FR2697844B1 (fr) *	1992-11-12	1995-01-27	Claude Nofre	Nouveaux composés dérivés de dipeptides ou d'analogues dipeptidiques utiles comme agents édulcorants, leur procédé de préparation.
FR2719590B1 (fr) *	1994-05-09	1996-07-26	Claude Nofre	Procédé perfectionné de préparation d'un composé dérivé de l'aspartame utile comme agent édulcorant.
US5728862A (en) *	1997-01-29	1998-03-17	The Nutrasweet Company	Method for preparing and purifying an N-alkylated aspartame derivative

1998
- 1998-09-04 US US09/146,965 patent/US6146680A/en not_active Expired - Lifetime
- 1998-09-11 ID IDW20000469A patent/ID27125A/id unknown
- 1998-09-11 PL PL98339190A patent/PL339190A1/xx unknown
- 1998-09-11 CN CN98811052A patent/CN1278826A/zh active Pending
- 1998-09-11 SK SK325-2000A patent/SK3252000A3/sk unknown
- 1998-09-11 EE EEP200000115A patent/EE200000115A/xx unknown
- 1998-09-11 BR BR9812767-5A patent/BR9812767A/pt not_active Application Discontinuation
- 1998-09-11 CA CA002303433A patent/CA2303433A1/fr not_active Abandoned
- 1998-09-11 SI SI9820061A patent/SI20329A/sl unknown
- 1998-09-11 EP EP98949335A patent/EP1012170A1/fr not_active Withdrawn
- 1998-09-11 HU HU0003574A patent/HUP0003574A3/hu unknown
- 1998-09-11 IL IL13491598A patent/IL134915A0/xx unknown
- 1998-09-11 AU AU95679/98A patent/AU9567998A/en not_active Abandoned
- 1998-09-11 WO PCT/US1998/018901 patent/WO1999012955A1/fr not_active Ceased
- 1998-09-11 TR TR2000/00732T patent/TR200000732T2/xx unknown
2000
- 2000-03-10 NO NO20001272A patent/NO20001272L/no not_active Application Discontinuation
- 2000-04-06 LT LT2000029A patent/LT2000029A/lt unknown
- 2000-04-10 BG BG104320A patent/BG104320A/xx unknown

Also Published As

Publication number	Publication date
NO20001272L (no)	2000-05-10
EE200000115A (et)	2000-12-15
HUP0003574A2 (hu)	2001-05-28
ID27125A (id)	2001-03-01
CN1278826A (zh)	2001-01-03
IL134915A0 (en)	2001-05-20
CA2303433A1 (fr)	1999-03-18
TR200000732T2 (tr)	2001-06-21
PL339190A1 (en)	2000-12-04
BG104320A (en)	2001-02-28
US6146680A (en)	2000-11-14
SK3252000A3 (en)	2000-10-09
BR9812767A (pt)	2000-12-12
SI20329A (sl)	2001-02-28
NO20001272D0 (no)	2000-03-10
EP1012170A1 (fr)	2000-06-28
WO1999012955A1 (fr)	1999-03-18
AU9567998A (en)	1999-03-29
HUP0003574A3 (en)	2001-08-28

Publication	Publication Date	Title
LT2000028A (lt)	2000-12-27	N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio druskos su bazėmis
FI71465B (fi)	1986-10-10	Synergistisk sammansaettning som innehaoller en blandning av olika soetningsmedel
US4448716A (en)	1984-05-15	Dipeptide sweetener-metal complexes
EP1221448A1 (fr)	2002-07-10	Compositions d'edulcorants a fort pouvoir sucrant a pouvoir sucrant accru, correcteurs de gout et leur utilisation
LT2000027A (lt)	2000-12-27	N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio druskos su saldikliais
US6146680A (en)	2000-11-14	Metal complexes of N-[N-(3,3-dimethylbutyl)-L-α-aspartyl]-L-phenylalanine 1-methyl ester
US4153737A (en)	1979-05-08	Concentrated liquid low calorie sweetner
LT4759B (lt)	2001-02-26	N-[n-(3,3-dimetilbutil)-l-alfa-aspartil)-l-fenilalanino 1-metilo esterio druskos
MXPA00002552A (en)	2001-11-21	METAL COMPLEXES OF N-[N-(3,3-DIMETHYLBUTYL) -L-&agr;-ASPARTYL]-L-PHENYLALANINE 1-METHYL ESTER
CZ2000818A3 (cs)	2000-10-11	Komplexy 1-metylesteru N-[N-(3,3-dimetylbutyl)- L-alfa-aspartyl]-L-fenylalaninu s kovy
CZ2000815A3 (cs)	2000-10-11	Kyselé soli 1-metylesteru N-[N-(3,3- dimetylbutyl)-L-alfa-aspartyl]-L-fenylalaninu
CZ2000814A3 (cs)	2000-10-11	Zásadité soli 1-metylesteru N-[N-(3,3- dimetylbutyl)-L-alfa-aspartyl]-L-fenylalaninu
MXPA00002539A (en)	2001-11-21	BASIC SALTS OF N-[N-(3,3-DIMETHYLBUTYL)-L-&agr;-ASPARTYL]-L-PHENYLALANINE 1-METHYL ESTER
MXPA00002540A (en)	2001-11-21	ACID SALTS OF N-[N-(3,3-DIMETHYLBUTYL)-L-&agr;-ASPARTYL]-L-PHENYLALANINE 1-METHYL ESTER
CZ2000819A3 (cs)	2000-10-11	Soli sladidla 1-metylesteru N-[N-(3,3- dimetylbutyl)-L-alfa-aspartyl]-L-fenylalaninu