CA1036170A - Aluminum and/or magnesium salts - Google Patents
Aluminum and/or magnesium saltsInfo
- Publication number
- CA1036170A CA1036170A CA206,631A CA206631A CA1036170A CA 1036170 A CA1036170 A CA 1036170A CA 206631 A CA206631 A CA 206631A CA 1036170 A CA1036170 A CA 1036170A
- Authority
- CA
- Canada
- Prior art keywords
- est
- dans
- produit
- sur
- générale
- Prior art date
- 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.)
- Expired
Links
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 18
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 18
- 159000000003 magnesium salts Chemical class 0.000 title abstract 2
- 239000004411 aluminium Substances 0.000 claims description 16
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 claims description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 7
- 239000000203 mixture Substances 0.000 abstract description 6
- 206010000087 Abdominal pain upper Diseases 0.000 abstract 1
- 208000007882 Gastritis Diseases 0.000 abstract 1
- 208000025865 Ulcer Diseases 0.000 abstract 1
- 150000001413 amino acids Chemical class 0.000 abstract 1
- 230000002183 duodenal effect Effects 0.000 abstract 1
- 230000002496 gastric effect Effects 0.000 abstract 1
- 230000001175 peptic effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 231100000397 ulcer Toxicity 0.000 abstract 1
- 235000010210 aluminium Nutrition 0.000 description 14
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- 239000000725 suspension Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000004472 Lysine Substances 0.000 description 4
- 238000013019 agitation Methods 0.000 description 4
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
- 240000001812 Hyssopus officinalis Species 0.000 description 2
- 235000010650 Hyssopus officinalis Nutrition 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 229940082150 encore Drugs 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229960003104 ornithine Drugs 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- 229960002447 thiram Drugs 0.000 description 2
- 101100135641 Caenorhabditis elegans par-3 gene Proteins 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 101100406879 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) par-2 gene Proteins 0.000 description 1
- 241000212342 Sium Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- TUCNEACPLKLKNU-UHFFFAOYSA-N acetyl Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/003—Compounds containing elements of Groups 2 or 12 of the Periodic Table without C-Metal linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7329163A FR2240018A1 (en) | 1973-08-09 | 1973-08-09 | Aluminium and/or magnesium salts of amino acids - prepd from diacetyl-ornithine or lysine, for ulcer treatment |
| FR7422228A FR2276034A1 (fr) | 1974-06-26 | 1974-06-26 | Sels d'aluminium et/ou de magnesium de la diacethyllysine, leur preparation et les compositions qui les contiennent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1036170A true CA1036170A (en) | 1978-08-08 |
Family
ID=26217887
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA206,631A Expired CA1036170A (en) | 1973-08-09 | 1974-08-08 | Aluminum and/or magnesium salts |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4013699A (enExample) |
| JP (1) | JPS5076216A (enExample) |
| AR (1) | AR201609A1 (enExample) |
| AT (1) | AT333718B (enExample) |
| CA (1) | CA1036170A (enExample) |
| CH (1) | CH591426A5 (enExample) |
| DE (1) | DE2438456A1 (enExample) |
| DK (1) | DK424074A (enExample) |
| ES (1) | ES429119A1 (enExample) |
| GB (1) | GB1433314A (enExample) |
| IE (1) | IE39661B1 (enExample) |
| NL (1) | NL7410373A (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2289179A1 (fr) | 1974-10-28 | 1976-05-28 | Morelle Jean | Sels metalliques de lipoaminoacides |
| US4675422A (en) * | 1985-10-23 | 1987-06-23 | Stepan Company | Organometallic compounds |
| US4900561A (en) * | 1989-01-03 | 1990-02-13 | Zinpro Corporation | Copper complexes of alpha-amino acids that contain terminal amino groups, and their use as nutritional supplements |
| US4948594A (en) * | 1989-01-03 | 1990-08-14 | Zinpro Corporation | Copper complexes of alpha-amino acids that contain terminal amino groups, and their use as nutritional supplements |
| WO2002094256A1 (en) * | 2001-05-23 | 2002-11-28 | Debatosh Datta | Lysine and/or analogues and/or polymers thereof for promoting wound healing and angiogenesis |
| AU2021248667A1 (en) * | 2020-04-03 | 2022-12-01 | Nutrition 21, Llc | Method and composition for enhancing the quality and benefits of sleep |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2480743A (en) * | 1946-05-03 | 1949-08-30 | Krantz | Basic aluminum salt of an aliphatic amino acid and method of preparing the same |
| US2588090A (en) * | 1950-04-14 | 1952-03-04 | Geza S Delmar | Process for the preparation of basic aluminum salts of alpha amino acids |
| US2907781A (en) * | 1956-06-08 | 1959-10-06 | Victor M Hermelin | Monohydroxy magnesium aluminum salt of an amino aliphatic acid and method of preparing same |
| NL127988C (enExample) * | 1965-06-04 | |||
| DE1296642B (de) * | 1965-10-01 | 1969-06-04 | Basf Ag | Verfahren zur Herstellung von ª, ªÏ-Diaminoalkancarbonsaeuren |
| FR2062873B1 (enExample) * | 1969-09-25 | 1973-07-13 | Choay Sa | |
| US3651137A (en) * | 1969-12-23 | 1972-03-21 | Atlantic Richfield Co | Selective conversion of nalpha nepsilon-diacetyllysine esters to nalpha -diacetyllysine |
| US3836551A (en) * | 1970-01-30 | 1974-09-17 | Roehm Gmbh | Method for making salts of n-acylamino carboxylic acids |
| NO131985C (enExample) * | 1970-06-05 | 1975-09-03 | Kyowa Hakko Kogyo Kk |
-
1974
- 1974-07-08 GB GB3502174A patent/GB1433314A/en not_active Expired
- 1974-08-01 NL NL7410373A patent/NL7410373A/xx not_active Application Discontinuation
- 1974-08-08 DK DK424074A patent/DK424074A/da unknown
- 1974-08-08 AR AR255110A patent/AR201609A1/es active
- 1974-08-08 CA CA206,631A patent/CA1036170A/en not_active Expired
- 1974-08-08 US US05/495,781 patent/US4013699A/en not_active Expired - Lifetime
- 1974-08-08 JP JP49090352A patent/JPS5076216A/ja active Pending
- 1974-08-08 IE IE1667/74A patent/IE39661B1/xx unknown
- 1974-08-08 CH CH1086374A patent/CH591426A5/xx not_active IP Right Cessation
- 1974-08-09 ES ES429119A patent/ES429119A1/es not_active Expired
- 1974-08-09 DE DE2438456A patent/DE2438456A1/de active Pending
- 1974-08-09 AT AT652774A patent/AT333718B/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IE39661B1 (en) | 1978-12-06 |
| DE2438456A1 (de) | 1975-02-20 |
| IE39661L (en) | 1975-02-09 |
| ES429119A1 (es) | 1976-09-01 |
| NL7410373A (nl) | 1975-02-11 |
| DK424074A (enExample) | 1975-04-21 |
| USB495781I5 (enExample) | 1976-03-23 |
| AT333718B (de) | 1976-12-10 |
| US4013699A (en) | 1977-03-22 |
| AR201609A1 (es) | 1975-03-31 |
| ATA652774A (de) | 1976-04-15 |
| GB1433314A (en) | 1976-04-28 |
| JPS5076216A (enExample) | 1975-06-21 |
| CH591426A5 (enExample) | 1977-09-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1203242A (fr) | Procede de preparation de sels derives de l'acide 3- hydroxybutanoique et d'une base organique aminee, et les sels ainsi obtenus | |
| CA2024419C (fr) | Nouveaux sels de metaux bivalents de l'acide n,n-di(carboxymethyl) amino-2cyano-3carboxymethyl-4 carboxy-5 thiophene, leur procede de preparation et les compositions pharmaceutiques les renfermant | |
| CA1181761A (fr) | Oligomeres tensio-actifs perfluores, procede pour les preparer et compositions les contenant | |
| CA1271422A (fr) | Compositions pharmaceutiques | |
| CA1036170A (en) | Aluminum and/or magnesium salts | |
| FR2672288A1 (fr) | Nouveaux amides dipeptidiques derivant de la glycyl-serine, utilisables, notamment dans des compositions cosmetiques, pharmaceutiques ou alimentaires. | |
| EP0408448A1 (fr) | Nouveaux dérivés d'uréthanne, leur préparation et leur application notamment comme agents hydratants dans des compositions cosmétiques ou pharmaceutiques destinées au traitement des peaux sèches | |
| KR900701760A (ko) | 치환된 비사이클릭 화합물의 n-이미다졸일-및 n-이마다졸일 메틸-유도체 | |
| FR2617477A1 (fr) | Nouveaux derives de la thiouree, leur preparation et leur utilisation comme medicaments | |
| EP0652209B1 (fr) | Dérivés de la lysine à groupement N-epsilon-alkoxy ou alcénoxy carbonyle, leur préparation et leur utilisation, dans des compositions cosmétiques, pharmaceutiques, hygiéniques ou alimentaires | |
| BE897492A (fr) | Derives de la xanthine procede pour les preparer compositions pharmaceutiques les contenant et leur application therapeutique | |
| CA1134824A (fr) | Compositions cosmetiques pour le traitement de l'etat gras des cheveux et de la peau, composes nouveaux et leur procede de preparation | |
| FR2529545A1 (fr) | Nouveaux sels de carnitine ainsi que leur procede de preparation | |
| CA1097684A (fr) | PROCEDE DE PREPARATION D'ACIDES.gamma.ARYL .gamma.OXO ISOVALERIQUES | |
| EP0086320B1 (de) | Panthenolderivate | |
| EP0725056B1 (fr) | Dérivés perfluoroalkyle de lysine, procédé de préparation, leur utilisation notamment en cosmétique et compositions les comprenant | |
| CA1242738A (en) | Acid salts of valproic acid | |
| CH400118A (fr) | Procédé de préparation de sels de l'acide glycyrrhétinique et de sels de semi-esters de l'acide glycyrrhétinique | |
| CA1039301A (en) | Process for preparing novel monohydroxyphenethylamines and their salts | |
| CA2036920A1 (fr) | Sels de metaux alcalinoterreux d'oxa-polyacides leur procede de preparation et les compositions pharmaceutiques qui les contiennent | |
| KR880005079A (ko) | 3-아미노카르보닐-1,4-디히드로피리딘-5-카르복실산 화합물, 그의 제조방법, 및 그를 함유하는 약학조성물 | |
| EP0725057B1 (fr) | Dérivés de lysine à groupement alkylsulfonyle ou alkylaminocarbonyle, procédé de préparation, leur utilisation notamment en cosmétique et compositions les comprenant | |
| US4070482A (en) | Prostaglandin antagonists | |
| EP0312412B1 (fr) | Nouveaux dérivés du norbornane, leur procédé de préparation et compositions cosmétique et médicamenteuse les contenant | |
| EP0738710B1 (fr) | Dérivés d'ornithine, procédé de préparation, utilisation en cosmétique et compositions les comprenant |