GB1277394A - Glycol phosphatides and a method of producing the same from cephalins - Google Patents
Glycol phosphatides and a method of producing the same from cephalinsInfo
- Publication number
- GB1277394A GB1277394A GB45747/70A GB4574770A GB1277394A GB 1277394 A GB1277394 A GB 1277394A GB 45747/70 A GB45747/70 A GB 45747/70A GB 4574770 A GB4574770 A GB 4574770A GB 1277394 A GB1277394 A GB 1277394A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phosphatides
- acid
- cephalin
- glycol
- phosphatide
- 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
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 title abstract 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- CFWRDBDJAOHXSH-SECBINFHSA-N 2-azaniumylethyl [(2r)-2,3-diacetyloxypropyl] phosphate Chemical compound CC(=O)OC[C@@H](OC(C)=O)COP(O)(=O)OCCN CFWRDBDJAOHXSH-SECBINFHSA-N 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical class [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 abstract 2
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 abstract 1
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 abstract 1
- 235000010469 Glycine max Nutrition 0.000 abstract 1
- 244000068988 Glycine max Species 0.000 abstract 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 238000005576 amination reaction Methods 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 1
- 238000006193 diazotization reaction Methods 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- CEYULKASIQJZGP-UHFFFAOYSA-L disodium;2-(carboxymethyl)-2-hydroxybutanedioate Chemical compound [Na+].[Na+].[O-]C(=O)CC(O)(C(=O)O)CC([O-])=O CEYULKASIQJZGP-UHFFFAOYSA-L 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000001804 emulsifying effect Effects 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 230000007717 exclusion Effects 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 238000001990 intravenous administration Methods 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 abstract 1
- 235000019799 monosodium phosphate Nutrition 0.000 abstract 1
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 abstract 1
- 229910017604 nitric acid Inorganic materials 0.000 abstract 1
- 239000012299 nitrogen atmosphere Substances 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- -1 phosphatidyl colamine Chemical compound 0.000 abstract 1
- IWZKICVEHNUQTL-UHFFFAOYSA-M potassium hydrogen phthalate Chemical compound [K+].OC(=O)C1=CC=CC=C1C([O-])=O IWZKICVEHNUQTL-UHFFFAOYSA-M 0.000 abstract 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 abstract 1
- 235000010288 sodium nitrite Nutrition 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/10—Phosphatides, e.g. lecithin
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19691949399 DE1949399C (de) | 1969-09-30 | Glycolphosphatidgemische und deren Herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1277394A true GB1277394A (en) | 1972-06-14 |
Family
ID=5746972
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB45747/70A Expired GB1277394A (en) | 1969-09-30 | 1970-09-25 | Glycol phosphatides and a method of producing the same from cephalins |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3681412A (tr) |
| JP (1) | JPS4843336B1 (tr) |
| AT (1) | AT296506B (tr) |
| BE (1) | BE756778A (tr) |
| CH (1) | CH553220A (tr) |
| DK (1) | DK138183C (tr) |
| ES (1) | ES384039A1 (tr) |
| FR (1) | FR2070098B1 (tr) |
| GB (1) | GB1277394A (tr) |
| NL (1) | NL7014221A (tr) |
| SE (1) | SE368017B (tr) |
| TR (1) | TR16587A (tr) |
| ZA (1) | ZA706676B (tr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4104403A (en) * | 1976-12-21 | 1978-08-01 | Witco Chemical Corporation | Water-oil emulsions and method of preparing same |
| US4408052A (en) * | 1980-02-27 | 1983-10-04 | Takeda Chemical Industries, Ltd. | Phospholipid carbamates |
| US4370319A (en) * | 1980-06-19 | 1983-01-25 | The Procter & Gamble Company | Skin conditioning compositions |
| US4469635A (en) * | 1980-12-24 | 1984-09-04 | The Procter & Gamble Company | Polyol esters of alpha-hydroxy carboxylic acids |
| US6878532B1 (en) | 2003-04-28 | 2005-04-12 | Sioux Biochemical, Inc. | Method of producing phosphatidylserine |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3532724A (en) * | 1967-05-31 | 1970-10-06 | Robert R Smeby | Renin inhibitor and process to make same |
| US3577446A (en) * | 1968-09-09 | 1971-05-04 | American Home Prod | Phosphatidylalkanolamine derivatives |
-
0
- BE BE756778D patent/BE756778A/xx unknown
-
1970
- 1970-04-30 DK DK493670A patent/DK138183C/da active
- 1970-09-21 JP JP45082036A patent/JPS4843336B1/ja active Pending
- 1970-09-25 GB GB45747/70A patent/GB1277394A/en not_active Expired
- 1970-09-28 SE SE13138/70A patent/SE368017B/xx unknown
- 1970-09-28 ES ES384039A patent/ES384039A1/es not_active Expired
- 1970-09-28 US US76231A patent/US3681412A/en not_active Expired - Lifetime
- 1970-09-28 NL NL7014221A patent/NL7014221A/xx unknown
- 1970-09-28 AT AT874870A patent/AT296506B/de not_active IP Right Cessation
- 1970-09-28 CH CH1432370A patent/CH553220A/xx not_active IP Right Cessation
- 1970-09-29 FR FR7035146A patent/FR2070098B1/fr not_active Expired
- 1970-09-30 ZA ZA706676*A patent/ZA706676B/xx unknown
- 1970-09-30 TR TR16587A patent/TR16587A/tr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK138183C (da) | 1979-01-08 |
| BE756778A (fr) | 1971-03-01 |
| US3681412A (en) | 1972-08-01 |
| DE1949399A1 (de) | 1971-04-01 |
| JPS4843336B1 (tr) | 1973-12-18 |
| AT296506B (de) | 1972-02-25 |
| CH553220A (de) | 1974-08-30 |
| FR2070098A1 (tr) | 1971-09-10 |
| TR16587A (tr) | 1973-01-01 |
| ES384039A1 (es) | 1972-12-16 |
| FR2070098B1 (tr) | 1975-04-18 |
| ZA706676B (en) | 1971-06-30 |
| NL7014221A (tr) | 1971-04-01 |
| DK138183B (da) | 1978-07-24 |
| SE368017B (tr) | 1974-06-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |