NO861047L - Soetningsmiddel. - Google Patents

Soetningsmiddel.

Info

Publication number: NO861047L
Authority: NO; Norway
Prior art keywords: alkyl; sweetening; preparations; sweetener; formula
Prior art date: 1985-03-19

Application number

NO861047A

Other languages

English (en)

Norwegian (no)

Inventor

Claude Nofre

Jean-Marie Tinti

Original Assignee

Univ Claude Bernard Lyon

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.)

1985-03-19

Filing date

1986-03-18

Publication date

1986-09-22

1986-03-18 Application filed by Univ Claude Bernard Lyon filed Critical Univ Claude Bernard Lyon

1986-09-22 Publication of NO861047L publication Critical patent/NO861047L/no

Links

125000000217 alkyl group Chemical group 0.000 claims abstract description 31
235000003599 food sweetener Nutrition 0.000 claims abstract description 25
239000003765 sweetening agent Substances 0.000 claims abstract description 24
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 5
125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims abstract description 5
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims abstract description 5
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims abstract description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
150000001768 cations Chemical class 0.000 claims abstract description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 4
125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 claims abstract description 3
125000000753 cycloalkyl group Chemical group 0.000 claims abstract 4
150000001875 compounds Chemical class 0.000 claims description 22
229930006000 Sucrose Natural products 0.000 claims description 12
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 12
239000005720 sucrose Substances 0.000 claims description 12
238000002360 preparation method Methods 0.000 claims description 11
238000000034 method Methods 0.000 claims description 7
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
235000009508 confectionery Nutrition 0.000 claims description 6
-1 gums Substances 0.000 claims description 6
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 4
239000011734 sodium Substances 0.000 claims description 4
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 2
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 claims description 2
SGBKWNVYBHTKLV-UHFFFAOYSA-N 2,2,4,4-tetramethylthietan-3-amine Chemical compound CC1(C)SC(C)(C)C1N SGBKWNVYBHTKLV-UHFFFAOYSA-N 0.000 claims description 2
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 claims description 2
108010011485 Aspartame Proteins 0.000 claims description 2
229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 2
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 2
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 2
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
239000005715 Fructose Substances 0.000 claims description 2
229930091371 Fructose Natural products 0.000 claims description 2
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 2
239000004378 Glycyrrhizin Substances 0.000 claims description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims description 2
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 claims description 2
ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims description 2
229920002774 Maltodextrin Polymers 0.000 claims description 2
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 2
229930195725 Mannitol Natural products 0.000 claims description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
229920002472 Starch Polymers 0.000 claims description 2
TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 2
240000008042 Zea mays Species 0.000 claims description 2
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 2
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 2
239000002253 acid Substances 0.000 claims description 2
150000007513 acids Chemical class 0.000 claims description 2
239000000605 aspartame Substances 0.000 claims description 2
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 2
235000010357 aspartame Nutrition 0.000 claims description 2
229960003438 aspartame Drugs 0.000 claims description 2
235000010233 benzoic acid Nutrition 0.000 claims description 2
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 2
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
159000000007 calcium salts Chemical class 0.000 claims description 2
239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 2
239000008112 carboxymethyl-cellulose Substances 0.000 claims description 2
239000001913 cellulose Substances 0.000 claims description 2
229920002678 cellulose Polymers 0.000 claims description 2
235000010980 cellulose Nutrition 0.000 claims description 2
235000015218 chewing gum Nutrition 0.000 claims description 2
229940112822 chewing gum Drugs 0.000 claims description 2
235000015165 citric acid Nutrition 0.000 claims description 2
235000005822 corn Nutrition 0.000 claims description 2
239000002537 cosmetic Substances 0.000 claims description 2
235000013305 food Nutrition 0.000 claims description 2
229960002737 fructose Drugs 0.000 claims description 2
235000011087 fumaric acid Nutrition 0.000 claims description 2
239000008103 glucose Substances 0.000 claims description 2
LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 claims description 2
229960004949 glycyrrhizic acid Drugs 0.000 claims description 2
UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 claims description 2
235000019410 glycyrrhizin Nutrition 0.000 claims description 2
LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 claims description 2
239000008101 lactose Substances 0.000 claims description 2
239000000594 mannitol Substances 0.000 claims description 2
235000010355 mannitol Nutrition 0.000 claims description 2
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 2
229920000609 methyl cellulose Polymers 0.000 claims description 2
239000001923 methylcellulose Substances 0.000 claims description 2
235000010981 methylcellulose Nutrition 0.000 claims description 2
235000019520 non-alcoholic beverage Nutrition 0.000 claims description 2
239000001814 pectin Substances 0.000 claims description 2
235000010987 pectin Nutrition 0.000 claims description 2
229920001277 pectin Polymers 0.000 claims description 2
125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 2
235000011007 phosphoric acid Nutrition 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
150000004672 propanoic acids Chemical class 0.000 claims description 2
QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims description 2
235000019260 propionic acid Nutrition 0.000 claims description 2
BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 claims description 2
229910052708 sodium Inorganic materials 0.000 claims description 2
239000000661 sodium alginate Substances 0.000 claims description 2
235000010413 sodium alginate Nutrition 0.000 claims description 2
229940005550 sodium alginate Drugs 0.000 claims description 2
229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 2
235000017557 sodium bicarbonate Nutrition 0.000 claims description 2
235000010199 sorbic acid Nutrition 0.000 claims description 2
239000000600 sorbitol Substances 0.000 claims description 2
239000008107 starch Substances 0.000 claims description 2
235000019698 starch Nutrition 0.000 claims description 2
239000006188 syrup Substances 0.000 claims description 2
235000020357 syrup Nutrition 0.000 claims description 2
235000002906 tartaric acid Nutrition 0.000 claims description 2
239000000892 thaumatin Substances 0.000 claims description 2
235000010436 thaumatin Nutrition 0.000 claims description 2
239000000811 xylitol Substances 0.000 claims description 2
235000010447 xylitol Nutrition 0.000 claims description 2
HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 2
229960002675 xylitol Drugs 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
YGCFIWIQZPHFLU-UHFFFAOYSA-N acesulfame Chemical compound CC1=CC(=O)NS(=O)(=O)O1 YGCFIWIQZPHFLU-UHFFFAOYSA-N 0.000 claims 1
229960005164 acesulfame Drugs 0.000 claims 1
150000001559 benzoic acids Chemical class 0.000 claims 1
125000006360 carbonyl amino methylene group Chemical group [H]N(C([*:1])=O)C([H])([H])[*:2] 0.000 claims 1
150000002238 fumaric acids Chemical class 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
150000003398 sorbic acids Chemical class 0.000 claims 1
CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract description 3
125000001424 substituent group Chemical group 0.000 abstract description 2
125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 20
239000000243 solution Substances 0.000 description 18
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000000047 product Substances 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 5
150000003254 radicals Chemical class 0.000 description 5
239000007787 solid Substances 0.000 description 5
238000003786 synthesis reaction Methods 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
239000000203 mixture Substances 0.000 description 4
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
244000299461 Theobroma cacao Species 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
238000009835 boiling Methods 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
229960005261 aspartic acid Drugs 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
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238000009833 condensation Methods 0.000 description 2
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238000001816 cooling Methods 0.000 description 2
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125000001841 imino group Chemical group [H]N=* 0.000 description 2
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239000002244 precipitate Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000008256 whipped cream Substances 0.000 description 2
125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
DZFKAXLNKZXNHD-UHFFFAOYSA-N 4-isothiocyanatobenzonitrile Chemical compound S=C=NC1=CC=C(C#N)C=C1 DZFKAXLNKZXNHD-UHFFFAOYSA-N 0.000 description 1
WBZFUFAFFUEMEI-UHFFFAOYSA-M Acesulfame k Chemical compound [K+].CC1=CC(=O)[N-]S(=O)(=O)O1 WBZFUFAFFUEMEI-UHFFFAOYSA-M 0.000 description 1
244000208874 Althaea officinalis Species 0.000 description 1
235000006576 Althaea officinalis Nutrition 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
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FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
206010013911 Dysgeusia Diseases 0.000 description 1
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150000001408 amides Chemical class 0.000 description 1
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235000016213 coffee Nutrition 0.000 description 1
235000013353 coffee beverage Nutrition 0.000 description 1
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
235000015071 dressings Nutrition 0.000 description 1
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BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
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PIRFWHVVLRIJPU-UHFFFAOYSA-N methyl n-cyano-n'-(4-cyanophenyl)carbamimidothioate Chemical compound N#CN=C(SC)NC1=CC=C(C#N)C=C1 PIRFWHVVLRIJPU-UHFFFAOYSA-N 0.000 description 1
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235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
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230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
239000002324 mouth wash Substances 0.000 description 1
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RLPDHOAILQJTHX-UHFFFAOYSA-N n-(cyclopropanecarbonyl)cyclopropanecarboxamide Chemical compound C1CC1C(=O)NC(=O)C1CC1 RLPDHOAILQJTHX-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
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MBEGFNBBAVRKLK-UHFFFAOYSA-N sodium;iminomethylideneazanide Chemical compound [Na+].[NH-]C#N MBEGFNBBAVRKLK-UHFFFAOYSA-N 0.000 description 1
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VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
235000013618 yogurt Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/28—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to cyano groups, e.g. cyanoguanidines, dicyandiamides
- 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
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Engineering & Computer Science (AREA)
Food Science & Technology (AREA)
Polymers & Plastics (AREA)
Biochemistry (AREA)
Biophysics (AREA)
General Health & Medical Sciences (AREA)
Nutrition Science (AREA)
Medicinal Chemistry (AREA)
Molecular Biology (AREA)
Seasonings (AREA)
Peptides Or Proteins (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pretreatment Of Seeds And Plants (AREA)
Saccharide Compounds (AREA)
Electrically Operated Instructional Devices (AREA)
Road Signs Or Road Markings (AREA)
Medicines Containing Plant Substances (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Medicinal Preparation (AREA)
Cosmetics (AREA)

NO861047A 1985-03-19 1986-03-18 Soetningsmiddel. NO861047L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR8504241A FR2579201B1 (fr)	1985-03-19	1985-03-19	Composes chimiques perfectionnes, utilisation comme agents edulcorants et compositions contenant de tels agents

Publications (1)

Publication Number	Publication Date
NO861047L true NO861047L (no)	1986-09-22

Family

ID=9317447

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO861047A NO861047L (no)	1985-03-19	1986-03-18	Soetningsmiddel.

Country Status (15)

Country	Link
US (1)	US4673582A (de)
EP (1)	EP0195731B1 (de)
JP (1)	JPS61219353A (de)
AT (1)	ATE49700T1 (de)
AU (1)	AU571773B2 (de)
DE (1)	DE3668412D1 (de)
DK (1)	DK123486A (de)
ES (1)	ES8702882A1 (de)
FR (1)	FR2579201B1 (de)
GR (1)	GR860583B (de)
IL (1)	IL78055A0 (de)
NO (1)	NO861047L (de)
NZ (1)	NZ215514A (de)
PT (1)	PT82216B (de)
ZA (1)	ZA861844B (de)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4921939A (en) *	1985-03-19	1990-05-01	Universite Claude Bernard -Lyon 1	Sweetening agents
FR2606404B2 (fr) *	1986-04-10	1991-11-22	Univ Claude Bernard Lyon	Nouveaux composes chimiques derivant de l'acide phenylguanidinoacetique et leur utilisation comme agents edulcorants
FR2579202B1 (fr) *	1985-03-19	1988-04-29	Univ Claude Bernard Lyon	Nouveaux composes chimiques, utilisation comme agents edulcorants et compositions contenant de tels agents
FR2608379B1 (fr) *	1986-12-23	1989-03-24	Univ Claude Bernard Lyon	Agents edulcorants derives des acides n-phenylguanidinoacetique et n-phenylethanamidinoacetique, procede pour edulcorer des produits divers, et compositions contenant de tels agents edulcorants
KR870008526A (ko) *	1986-03-13	1987-10-19	원본미기재	감미료 및 그 제조방법
FR2609603B1 (fr) *	1987-01-15	1989-03-24	Univ Claude Bernard Lyon	Agents edulcorants derives des acides guanidinoacetique et ethanamidinoacetique, procede pour edulcorer des produits divers, et compositions contenant de tels agents edulcorants
JPH0655730B2 (ja) *	1987-07-17	1994-07-27	ザヌトラスウィートカンパニー	強力甘味剤
US4900740A (en) *	1987-10-02	1990-02-13	The Nutrasweet Company	N,N'-disubstituted guanidines containing a carboxyl or a tetrazolyl moiety
FR2624698A1 (fr) *	1987-12-18	1989-06-23	Bernard Lyon I Universite Clau	Derives heterocycliques de n-carbamoyl-, n-thiocarbamoyl- ou n-amidino-aminomalonyl ou aminosuccinyl amides utiles comme agents edulcorants
FR2624699B1 (fr) *	1987-12-18	1990-04-13	Bernard Lyon I Universite Clau	Derives heterocycliques de n-carbamoyl-, n-thiocarbamoyl- ou n-amidino-glycine ou beta-alanine utiles comme agents edulcorants
FR2630304B1 (fr) *	1988-04-22	1990-08-31	Bernard Lyon I Universite Clau	Derives n-hydrocarbones des acides aspartique et glutamique alpha-monoamides utiles comme agents edulcorants
NZ229828A (en) *	1988-08-09	1992-03-26	Squibb & Sons Inc	Aryl cyanoguanidine derivatives and pharmaceutical compositions
US5011837A (en) *	1988-08-09	1991-04-30	E. R. Squibb & Sons, Inc.	Aryl cyanoguanidines: potassium channel activators and method of making same
US4994490A (en) *	1989-04-03	1991-02-19	The Nutrasweet Company	Novel N-(sulfomethyl)-N'-arylureas
US5266717A (en) *	1989-04-03	1993-11-30	Glenn Roy	N-(sulfomethyl)-N'arylureas
FR2653303B1 (fr) *	1989-10-24	1992-09-18	Noffre Claude	Agents edulcorants de grande stabilite derivant des acides l-aspartique et l-glutamique n-hydrocarbones 1-oxo-2-ramifies.
US5272162A (en) *	1992-07-02	1993-12-21	G. D. Searle & Co.	Platelet aggregation inhibitors
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.
AU5679794A (en) *	1992-11-24	1994-06-22	Block Drug Company Inc., The	Pharmaceutical compositions for use in gastrointestinal washes
US5314902A (en) *	1993-01-27	1994-05-24	Monsanto Company	Urea derivatives useful as platelet aggregation inhibitors
PL194958B1 (pl) *	1998-06-05	2007-07-31	Wrigley W M Jun Co	Sposób wytwarzania gumy do żucia zawierającej fizycznie zmodyfikowaną N-podstawioną pochodną aspartamu o kontrolowanej szybkości uwalniania
US6692778B2 (en) *	1998-06-05	2004-02-17	Wm. Wrigley Jr. Company	Method of controlling release of N-substituted derivatives of aspartame in chewing gum
US20040258818A1 (en) *	2003-06-20	2004-12-23	Kraft Foods Holdings, Inc.	Reduced acidic flavor in acidified starch products
US8283338B2 (en)	2007-11-30	2012-10-09	Kao Corporation	GIP secretion inhibitor
JP5581129B2 (ja)	2009-06-17	2014-08-27	花王株式会社	肥満予防・改善剤

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3492131A (en) *	1966-04-18	1970-01-27	Searle & Co	Peptide sweetening agents
US3475403A (en) *	1967-01-20	1969-10-28	Searle & Co	Aspartic acid containing dipeptide lower alkyl esters
US3800046A (en) *	1967-04-17	1974-03-26	Searle & Co	Artificially sweetened consumable products
GB1258248A (de) *	1968-07-17	1971-12-22
US3642491A (en) *	1970-01-12	1972-02-15	Searle & Co	Artificially sweetened consumable products
DE2113251A1 (de) *	1970-03-25	1971-10-14	Squibb & Sons Inc	Suessstoffkombination
CA1027113A (en) *	1973-04-02	1978-02-28	General Foods Corporation	Sweetener solution containing saccharin and aspartane
US4287346A (en) *	1979-02-16	1981-09-01	Eisai Co., Ltd.	Cyanoguanidine derivatives
NL8005006A (nl) *	1980-09-04	1982-04-01	Stamicarbon	Dipeptide-zoetstof.
FR2533210A1 (fr) *	1982-09-17	1984-03-23	Lyon I Universite Claude	Edulcorants de synthese

1985
- 1985-03-19 FR FR8504241A patent/FR2579201B1/fr not_active Expired
1986
- 1986-03-03 GR GR860583A patent/GR860583B/el unknown
- 1986-03-05 US US06/836,383 patent/US4673582A/en not_active Expired - Fee Related
- 1986-03-06 IL IL78055A patent/IL78055A0/xx unknown
- 1986-03-07 AU AU54407/86A patent/AU571773B2/en not_active Ceased
- 1986-03-12 ZA ZA861844A patent/ZA861844B/xx unknown
- 1986-03-13 AT AT86420072T patent/ATE49700T1/de not_active IP Right Cessation
- 1986-03-13 EP EP86420072A patent/EP0195731B1/de not_active Expired - Lifetime
- 1986-03-13 DE DE8686420072T patent/DE3668412D1/de not_active Expired - Lifetime
- 1986-03-18 NO NO861047A patent/NO861047L/no unknown
- 1986-03-18 DK DK123486A patent/DK123486A/da not_active Application Discontinuation
- 1986-03-18 PT PT82216A patent/PT82216B/pt unknown
- 1986-03-18 NZ NZ215514A patent/NZ215514A/xx unknown
- 1986-03-19 JP JP61061929A patent/JPS61219353A/ja active Pending
- 1986-03-19 ES ES553155A patent/ES8702882A1/es not_active Expired

Also Published As

Publication number	Publication date
ES553155A0 (es)	1987-01-16
PT82216A (fr)	1986-04-01
DK123486A (da)	1986-09-20
IL78055A0 (en)	1986-07-31
ATE49700T1 (de)	1990-02-15
NZ215514A (en)	1988-10-28
ZA861844B (en)	1986-11-26
EP0195731B1 (de)	1990-01-24
DE3668412D1 (de)	1990-03-01
FR2579201A1 (fr)	1986-09-26
GR860583B (en)	1986-07-22
FR2579201B1 (fr)	1987-05-07
US4673582A (en)	1987-06-16
AU571773B2 (en)	1988-04-21
EP0195731A2 (de)	1986-09-24
AU5440786A (en)	1987-09-24
JPS61219353A (ja)	1986-09-29
DK123486D0 (da)	1986-03-18
ES8702882A1 (es)	1987-01-16
EP0195731A3 (en)	1987-07-01
PT82216B (fr)	1987-08-17

Publication	Publication Date	Title
NO861047L (no)	1986-09-22	Soetningsmiddel.
RU2107071C1 (ru)	1998-03-20	Производные аспартама или их физиологически приемлемые соли, способ их получения, подслащивающее средство
US4645678A (en)	1987-02-24	Sweetening agents
US4997667A (en)	1991-03-05	Pyridinyl compounds of N-carbamoyl-N-thiocarbamoyl- or N-amidino-glycine or beta-alanine useful as sweetening agents
US7935377B2 (en)	2011-05-03	Crystals of free (2R, 4R)-monatin and use thereof
CA2486015C (en)	2013-05-14	Novel amino acid derivative and sweetening agent
US4877895A (en)	1989-10-31	Glycine and β alanine derivatives as sweetening agents
JPH022326A (ja)	1990-01-08	複素環式基を持つ甘味剤
US4994490A (en)	1991-02-19	Novel N-(sulfomethyl)-N'-arylureas
RU2053239C1 (ru)	1996-01-27	Агент для подслащивания и способ его получения
WO1989000563A1 (en)	1989-01-26	High potency sweetening agents
US5968581A (en)	1999-10-19	Dipeptide derivatives and sweetening agents
AU605228B2 (en)	1991-01-10	Sweetening agents derived from guanidinoacetic and ethanamidinoacetic acids, process for sweetening various products, and compositions containing such sweetening agents
CA1251802A (en)	1989-03-28	Oxa-fenchols and oxa-fenchyl amines useful for preparing high intensity sweeteners
US4900740A (en)	1990-02-13	N,N'-disubstituted guanidines containing a carboxyl or a tetrazolyl moiety
US5272272A (en)	1993-12-21	Sweetening agents derived from L-glutamic acid
US4677126A (en)	1987-06-30	Oxa-fenchyl esters and amides of alpha-L-aspartyl-D-phenylglycine
US20030065210A1 (en)	2003-04-03	Aspartyl dipeptide ester derivatives and sweeteners
RU1834647C (ru)	1993-08-15	Состав пищевого продукта
CA1276395C (en)	1990-11-13	Oxa-fenchyl esters and amides of alpha-l-aspartyl-d- phenylglycine
US5266717A (en)	1993-11-30	N-(sulfomethyl)-N'arylureas
JPS6339896A (ja)	1988-02-20	Ｌ−アスパルチルセリンメチルエステルのｏ−フエンチルエ−テル