GB1231879A - - Google Patents
Info
- Publication number
- GB1231879A GB1231879A GB1231879DA GB1231879A GB 1231879 A GB1231879 A GB 1231879A GB 1231879D A GB1231879D A GB 1231879DA GB 1231879 A GB1231879 A GB 1231879A
- Authority
- GB
- United Kingdom
- Prior art keywords
- glutamic acid
- racemic
- acid
- optically
- aqueous solution
- 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
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 abstract 11
- 239000004220 glutamic acid Substances 0.000 abstract 10
- 235000013922 glutamic acid Nutrition 0.000 abstract 8
- 239000007864 aqueous solution Substances 0.000 abstract 3
- 235000001014 amino acid Nutrition 0.000 abstract 2
- 150000001413 amino acids Chemical class 0.000 abstract 2
- 239000013078 crystal Substances 0.000 abstract 2
- 238000002425 crystallisation Methods 0.000 abstract 2
- 230000008025 crystallization Effects 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- QWCKQJZIFLGMSD-UHFFFAOYSA-N 2-Aminobutanoic acid Natural products CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 239000004475 Arginine Substances 0.000 abstract 1
- 108010076119 Caseins Proteins 0.000 abstract 1
- QWCKQJZIFLGMSD-GSVOUGTGSA-N D-alpha-aminobutyric acid Chemical compound CC[C@@H](N)C(O)=O QWCKQJZIFLGMSD-GSVOUGTGSA-N 0.000 abstract 1
- 108010010803 Gelatin Proteins 0.000 abstract 1
- 108010068370 Glutens Proteins 0.000 abstract 1
- 244000068988 Glycine max Species 0.000 abstract 1
- 235000010469 Glycine max Nutrition 0.000 abstract 1
- SNDPXSYFESPGGJ-BYPYZUCNSA-N L-2-aminopentanoic acid Chemical compound CCC[C@H](N)C(O)=O SNDPXSYFESPGGJ-BYPYZUCNSA-N 0.000 abstract 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 abstract 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 abstract 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 abstract 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 abstract 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 abstract 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 abstract 1
- SNDPXSYFESPGGJ-UHFFFAOYSA-N L-norVal-OH Natural products CCCC(N)C(O)=O SNDPXSYFESPGGJ-UHFFFAOYSA-N 0.000 abstract 1
- LRQKBLKVPFOOQJ-YFKPBYRVSA-N L-norleucine Chemical compound CCCC[C@H]([NH3+])C([O-])=O LRQKBLKVPFOOQJ-YFKPBYRVSA-N 0.000 abstract 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004472 Lysine Substances 0.000 abstract 1
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 abstract 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000001888 Peptone Substances 0.000 abstract 1
- 108010080698 Peptones Proteins 0.000 abstract 1
- 108010073771 Soybean Proteins Proteins 0.000 abstract 1
- 241000209140 Triticum Species 0.000 abstract 1
- 235000021307 Triticum Nutrition 0.000 abstract 1
- 235000004279 alanine Nutrition 0.000 abstract 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 abstract 1
- 235000009697 arginine Nutrition 0.000 abstract 1
- 235000003704 aspartic acid Nutrition 0.000 abstract 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005018 casein Substances 0.000 abstract 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 1
- 235000021240 caseins Nutrition 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 229920000159 gelatin Polymers 0.000 abstract 1
- 239000008273 gelatin Substances 0.000 abstract 1
- 235000019322 gelatine Nutrition 0.000 abstract 1
- 235000011852 gelatine desserts Nutrition 0.000 abstract 1
- -1 glutamic acid monohydrate Chemical class 0.000 abstract 1
- 235000021312 gluten Nutrition 0.000 abstract 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 abstract 1
- 235000014304 histidine Nutrition 0.000 abstract 1
- 235000018977 lysine Nutrition 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000010899 nucleation Methods 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 229960003104 ornithine Drugs 0.000 abstract 1
- 235000019319 peptone Nutrition 0.000 abstract 1
- 229920001184 polypeptide Polymers 0.000 abstract 1
- 102000004196 processed proteins & peptides Human genes 0.000 abstract 1
- 108090000765 processed proteins & peptides Proteins 0.000 abstract 1
- 239000007790 solid phase Substances 0.000 abstract 1
- 235000019710 soybean protein Nutrition 0.000 abstract 1
- 230000002269 spontaneous effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 230000007704 transition Effects 0.000 abstract 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R13/00—Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
- H01R13/64—Means for preventing incorrect coupling
Landscapes
- Peptides Or Proteins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7612467 | 1967-11-29 | ||
| JP430368 | 1968-01-26 | ||
| JP1753568 | 1968-03-19 | ||
| JP4290168 | 1968-06-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1231879A true GB1231879A (enExample) | 1971-05-12 |
Family
ID=27454061
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1231879D Expired GB1231879A (enExample) | 1967-11-29 | 1968-11-28 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3632639A (enExample) |
| DE (1) | DE1811874A1 (enExample) |
| FR (1) | FR1598230A (enExample) |
| GB (1) | GB1231879A (enExample) |
| NL (1) | NL6817170A (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2250867C3 (de) * | 1972-10-17 | 1984-01-12 | Siemens AG, 1000 Berlin und 8000 München | Röntgendiagnostikapparat mit einem Frequenzwandler, der einen Hochspannungstransformator mit einer Speisespannung in Abhängigkeit von einer Betriebsgröße der Röntgenröhre einstellbarer Frequenz speist |
-
1968
- 1968-11-28 GB GB1231879D patent/GB1231879A/en not_active Expired
- 1968-11-29 NL NL6817170A patent/NL6817170A/xx unknown
- 1968-11-29 DE DE19681811874 patent/DE1811874A1/de active Pending
- 1968-11-29 FR FR1598230D patent/FR1598230A/fr not_active Expired
- 1968-11-29 US US779928A patent/US3632639A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| FR1598230A (enExample) | 1970-07-06 |
| NL6817170A (enExample) | 1969-06-02 |
| DE1811874A1 (de) | 1969-07-17 |
| US3632639A (en) | 1972-01-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Desai et al. | Some aspects of nitrogen metabolism in the fat body of the larva of Calliphora erythrocephala | |
| MATSUBARA et al. | Crystalline bacterial proteinase ii. General properties of crystalline proteinase of Bacillus subtilis N' | |
| RO80806A (ro) | Procedeu pentru obtinerea enzimatica a peptidelor | |
| GB1399888A (en) | Injectable amino acid composition | |
| FR2623498B1 (fr) | Nouveaux composes enantiomeres derives d'amino-acides, leur procede de preparation et leurs applications therapeutiques | |
| GB1251251A (enExample) | ||
| GB1417060A (en) | Racemization of optically active n-acyl amino acids | |
| GB1231879A (enExample) | ||
| GB1158726A (en) | Amino Acid Derivatives | |
| IE38651B1 (en) | Improvements in or relating to an aqueous lipid emulsion for parenteral alimentation | |
| Friedberg | The amino acid composition of adenosine triphosphate-creatine transphosphorylase | |
| GB1469616A (en) | Optical resolution of phenyl-glycine amide | |
| ATE118470T1 (de) | Isolierung von l-phenylalanin aus dessen racemischen mischungen. | |
| ES8505932A1 (es) | Procedimiento para la preparacion de fenilalanina opticamente activa | |
| EP0321722B1 (de) | Verfahren zur Herstellung von Dipeptiden | |
| GB1211589A (en) | Enantiomer isolation process | |
| GB1389859A (en) | Salts of fluorinated amino acid with optically active acids or bases | |
| GB1245436A (en) | Process for the preparation of a salt of optically active lysine | |
| GB1250557A (enExample) | ||
| Armstrong et al. | Transamination in the human tooth | |
| GB910860A (en) | Method of crystallizing optically active glutamic acid | |
| GB1178605A (en) | A process for Crystallizing L-Glutamic Acid | |
| SU130630A1 (ru) | Питательна среда дл культивировани тканей | |
| Smekal et al. | Effect of Surface Active Agents on Biosynthesis of L-Lysine. | |
| Hecker et al. | Physiological study on the formation of heat shock proteins in Bacillus subtilis.). |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |