KR950032082A - Composition for preventing or treating aldehyde disorders containing amino acids - Google Patents
Composition for preventing or treating aldehyde disorders containing amino acids Download PDFInfo
- Publication number
- KR950032082A KR950032082A KR1019940033990A KR19940033990A KR950032082A KR 950032082 A KR950032082 A KR 950032082A KR 1019940033990 A KR1019940033990 A KR 1019940033990A KR 19940033990 A KR19940033990 A KR 19940033990A KR 950032082 A KR950032082 A KR 950032082A
- Authority
- KR
- South Korea
- Prior art keywords
- histidine
- aldehyde
- composition
- mixture
- glutamine
- Prior art date
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- 150000001413 amino acids Chemical class 0.000 title claims abstract description 10
- 239000000203 mixture Substances 0.000 title claims abstract 39
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 title 1
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims abstract description 14
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims abstract description 12
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000001299 aldehydes Chemical class 0.000 claims abstract 26
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 claims abstract 13
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims abstract 13
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 claims abstract 13
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 claims abstract 13
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims abstract 13
- 229960001230 asparagine Drugs 0.000 claims abstract 13
- 235000009582 asparagine Nutrition 0.000 claims abstract 13
- 235000018417 cysteine Nutrition 0.000 claims abstract 13
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims abstract 13
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 claims abstract 13
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims abstract 13
- 150000002410 histidine derivatives Chemical class 0.000 claims abstract 13
- FFFHZYDWPBMWHY-VKHMYHEASA-N L-homocysteine Chemical compound OC(=O)[C@@H](N)CCS FFFHZYDWPBMWHY-VKHMYHEASA-N 0.000 claims abstract 12
- 150000003839 salts Chemical class 0.000 claims abstract 10
- 229940024606 amino acid Drugs 0.000 claims abstract 6
- 235000001014 amino acid Nutrition 0.000 claims abstract 6
- 238000000034 method Methods 0.000 claims abstract 6
- 239000000126 substance Substances 0.000 claims abstract 4
- 235000002639 sodium chloride Nutrition 0.000 claims 9
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 3
- 235000000346 sugar Nutrition 0.000 claims 3
- 244000046052 Phaseolus vulgaris Species 0.000 claims 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims 2
- 235000013399 edible fruits Nutrition 0.000 claims 2
- 239000000284 extract Substances 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 2
- 150000007524 organic acids Chemical class 0.000 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- 235000013311 vegetables Nutrition 0.000 claims 2
- 235000014101 wine Nutrition 0.000 claims 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims 1
- 244000144730 Amygdalus persica Species 0.000 claims 1
- 244000003416 Asparagus officinalis Species 0.000 claims 1
- 235000005340 Asparagus officinalis Nutrition 0.000 claims 1
- 108010011485 Aspartame Proteins 0.000 claims 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 1
- 229930091371 Fructose Natural products 0.000 claims 1
- 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 1
- 239000005715 Fructose Substances 0.000 claims 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 1
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims 1
- 244000141359 Malus pumila Species 0.000 claims 1
- 235000006040 Prunus persica var persica Nutrition 0.000 claims 1
- 241000220324 Pyrus Species 0.000 claims 1
- UEDUENGHJMELGK-HYDKPPNVSA-N Stevioside Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O UEDUENGHJMELGK-HYDKPPNVSA-N 0.000 claims 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 claims 1
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims 1
- 235000021016 apples Nutrition 0.000 claims 1
- 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 1
- 229960003438 aspartame Drugs 0.000 claims 1
- 235000010357 aspartame Nutrition 0.000 claims 1
- 239000000605 aspartame Substances 0.000 claims 1
- 235000013405 beer Nutrition 0.000 claims 1
- 235000015165 citric acid Nutrition 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 claims 1
- 230000006866 deterioration Effects 0.000 claims 1
- 235000021107 fermented food Nutrition 0.000 claims 1
- 235000019990 fruit wine Nutrition 0.000 claims 1
- 235000013922 glutamic acid Nutrition 0.000 claims 1
- 239000004220 glutamic acid Substances 0.000 claims 1
- 229960002989 glutamic acid Drugs 0.000 claims 1
- -1 homocyshine Chemical compound 0.000 claims 1
- 238000001990 intravenous administration Methods 0.000 claims 1
- 229960000310 isoleucine Drugs 0.000 claims 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 claims 1
- 229960003136 leucine Drugs 0.000 claims 1
- 239000001630 malic acid Substances 0.000 claims 1
- 235000011090 malic acid Nutrition 0.000 claims 1
- 229920001542 oligosaccharide Polymers 0.000 claims 1
- 150000002482 oligosaccharides Chemical class 0.000 claims 1
- 235000005985 organic acids Nutrition 0.000 claims 1
- 235000021017 pears Nutrition 0.000 claims 1
- 235000019991 rice wine Nutrition 0.000 claims 1
- 235000020083 shōchū Nutrition 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 229940013618 stevioside Drugs 0.000 claims 1
- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 claims 1
- 235000019202 steviosides Nutrition 0.000 claims 1
- 239000001384 succinic acid Substances 0.000 claims 1
- 235000011044 succinic acid Nutrition 0.000 claims 1
- 150000008163 sugars Chemical class 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 230000000451 tissue damage Effects 0.000 claims 1
- 231100000827 tissue damage Toxicity 0.000 claims 1
- 239000004474 valine Substances 0.000 claims 1
- 229960004295 valine Drugs 0.000 claims 1
- 235000013343 vitamin Nutrition 0.000 claims 1
- 229940088594 vitamin Drugs 0.000 claims 1
- 229930003231 vitamin Natural products 0.000 claims 1
- 239000011782 vitamin Substances 0.000 claims 1
- 235000015041 whisky Nutrition 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000001727 in vivo Methods 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cosmetics (AREA)
Abstract
본 발명은 아스파라긴, 글루타민, 호모시스테인, 시스테인, 히스티딘, 히스티딘 유도체 또는 그의 염의 새로운 용도를 제공한다. 본 발명에 따르면 이들 아미노산은 아세트알데히드를 비롯한 포름알데히드 또는 프로피온알데히드 등의 탄소수 1 내지 5의 저급 알데히드류를 효과적으로 제거할 수 있다.The present invention provides new uses of asparagine, glutamine, homocysteine, cysteine, histidine, histidine derivatives or salts thereof. According to the present invention, these amino acids can effectively remove lower aldehydes having 1 to 5 carbon atoms such as formaldehyde or propionaldehyde including acetaldehyde.
따라서, 본 발명은 상기 아미노산들을 이용하여 생체내에서 여러가지 독성의 큰 요인이 되는 알데히드를 효과적으로 제거하는 방법, 알데히드에 기인한 여러 장해를 예방 또는 치료하기 위한 조성물, 알데히드를 포함하고 있거나 알데히드를 발생할 수 있는 화학적 제품에의 첨가방법을 제공하며, 이러한 아미노산들이 정상적으로 체내에 존재하는 아미노산들임을 감안할 때 그 안전성, 안정성 및 효율성이 높을 것이며, 그 응용의 범위 또한 매우 클 것으로 예측된다.Accordingly, the present invention provides a method for effectively removing aldehydes, which are a major cause of various toxicity in vivo using the amino acids, a composition for preventing or treating various disorders caused by aldehydes, including aldehydes or generating aldehydes. It provides a method of addition to a chemical product, and considering that these amino acids are amino acids normally present in the body, their safety, stability and efficiency will be high, and the scope of their application is also expected to be very large.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음As this is a public information case, the full text was not included.
제1도는 pH7.4의 완충액내에서 포름알데히드를 각종 아미노산과 반응시킨 경우 시간 경과에 따른 포름알데히드의 양의 변화를 보여주는 그래프이다. 제2도는 pH7.4의 완충액내에서 아세트알데히드를 각종 아미노산과 반응시킨 경우 시간 경과에 따른 아세트알데히드의 양의 변화를 보여주는 그래프이다. 제3도는 pH7.4의 완충액내에서 프로피온알데히드를 각종 아미노산과 반응시킨 경우 시간 경과에 따른 프로피온알데히드의 양의 변화를 보여주는 그래프이다.FIG. 1 is a graph showing the change in the amount of formaldehyde over time when formaldehyde is reacted with various amino acids in a buffer of pH 7.4. 2 is a graph showing the change of the amount of acetaldehyde over time when acetaldehyde is reacted with various amino acids in a buffer of pH 7.4. 3 is a graph showing the change in the amount of propionaldehyde over time when propionaldehyde is reacted with various amino acids in a buffer of pH 7.4.
Claims (23)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019940033990A KR0162674B1 (en) | 1994-05-03 | 1994-12-13 | Composition for preventing or treating aldehyde disorders containing amino acids |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1994-9719 | 1994-05-03 | ||
KR19940009719 | 1994-05-03 | ||
KR1019940033990A KR0162674B1 (en) | 1994-05-03 | 1994-12-13 | Composition for preventing or treating aldehyde disorders containing amino acids |
Publications (2)
Publication Number | Publication Date |
---|---|
KR950032082A true KR950032082A (en) | 1995-12-20 |
KR0162674B1 KR0162674B1 (en) | 1999-01-15 |
Family
ID=66818722
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019940033990A Expired - Fee Related KR0162674B1 (en) | 1994-05-03 | 1994-12-13 | Composition for preventing or treating aldehyde disorders containing amino acids |
Country Status (1)
Country | Link |
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KR (1) | KR0162674B1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100753251B1 (en) * | 2006-02-16 | 2007-08-30 | 신호상 | Alcohol, food and water prepared from aldehyde compounds or mixtures thereof and food and water prepared therefrom |
-
1994
- 1994-12-13 KR KR1019940033990A patent/KR0162674B1/en not_active Expired - Fee Related
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Publication number | Publication date |
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KR0162674B1 (en) | 1999-01-15 |
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