NO118064B - - Google Patents
Download PDFInfo
- Publication number
- NO118064B NO118064B NO155230A NO15523064A NO118064B NO 118064 B NO118064 B NO 118064B NO 155230 A NO155230 A NO 155230A NO 15523064 A NO15523064 A NO 15523064A NO 118064 B NO118064 B NO 118064B
- Authority
- NO
- Norway
- Prior art keywords
- cycloserine
- salt
- water
- alkaline earth
- antibiotic
- Prior art date
Links
- DYDCUQKUCUHJBH-UWTATZPHSA-N D-Cycloserine Chemical compound N[C@@H]1CONC1=O DYDCUQKUCUHJBH-UWTATZPHSA-N 0.000 claims description 42
- DYDCUQKUCUHJBH-UHFFFAOYSA-N D-Cycloserine Natural products NC1CONC1=O DYDCUQKUCUHJBH-UHFFFAOYSA-N 0.000 claims description 41
- 229960003077 cycloserine Drugs 0.000 claims description 41
- 230000003115 biocidal effect Effects 0.000 claims description 15
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 13
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 12
- -1 alkaline earth metal salt Chemical class 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000002002 slurry Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 9
- 238000003860 storage Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 159000000007 calcium salts Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 241000187747 Streptomyces Species 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 159000000003 magnesium salts Chemical class 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 241000186359 Mycobacterium Species 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910001617 alkaline earth metal chloride Inorganic materials 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 159000000008 strontium salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/08—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 not condensed with other rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Saccharide Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1291963A CH426783A (de) | 1963-10-21 | 1963-10-21 | Verfahren zur Herstellung von neuen Äthanoanthracenderivaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO118064B true NO118064B (enExample) | 1969-11-03 |
Family
ID=4387594
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO155230A NO118064B (enExample) | 1963-10-21 | 1964-10-20 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US3519718A (enExample) |
| AT (5) | AT252226B (enExample) |
| BE (1) | BE654587A (enExample) |
| CH (1) | CH426783A (enExample) |
| DE (2) | DE1793612A1 (enExample) |
| DK (2) | DK112029B (enExample) |
| ES (3) | ES305124A1 (enExample) |
| FI (1) | FI44627C (enExample) |
| FR (2) | FR1463791A (enExample) |
| GB (1) | GB1061869A (enExample) |
| IL (1) | IL22290A (enExample) |
| NL (1) | NL123295C (enExample) |
| NO (1) | NO118064B (enExample) |
| SE (4) | SE313303B (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1211092B (de) * | 1962-05-22 | 1966-02-17 | Prym Werke William | Halterung fuer auswechselbare Laufflecken |
| DE19742014A1 (de) * | 1997-09-24 | 1999-03-25 | Roche Diagnostics Gmbh | Neue Tetracyclen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel |
| US6995181B2 (en) * | 2002-07-18 | 2006-02-07 | Bristol-Myers Squibb Co. | Modulators of the glucocorticoid receptor and method |
-
0
- NL NL123295D patent/NL123295C/xx active
-
1963
- 1963-10-21 CH CH1291963A patent/CH426783A/de unknown
-
1964
- 1964-10-20 FI FI642206A patent/FI44627C/fi active
- 1964-10-20 NO NO155230A patent/NO118064B/no unknown
- 1964-10-20 SE SE12627/64A patent/SE313303B/xx unknown
- 1964-10-20 AT AT81066A patent/AT252226B/de active
- 1964-10-20 AT AT891064A patent/AT250940B/de active
- 1964-10-20 DE DE19641793612 patent/DE1793612A1/de active Granted
- 1964-10-20 AT AT507166A patent/AT254185B/de active
- 1964-10-20 ES ES0305124A patent/ES305124A1/es not_active Expired
- 1964-10-20 ES ES0305123A patent/ES305123A1/es not_active Expired
- 1964-10-20 BE BE654587D patent/BE654587A/xx unknown
- 1964-10-20 AT AT80866A patent/AT253492B/de active
- 1964-10-20 SE SE09816/67A patent/SE329611B/xx unknown
- 1964-10-20 IL IL22290A patent/IL22290A/xx unknown
- 1964-10-20 ES ES0305122A patent/ES305122A1/es not_active Expired
- 1964-10-20 AT AT80966A patent/AT254184B/de active
- 1964-10-20 DE DEG41822A patent/DE1291743B/de active Pending
- 1964-10-20 GB GB42638/64A patent/GB1061869A/en not_active Expired
- 1964-10-21 FR FR992103A patent/FR1463791A/fr not_active Expired
-
1965
- 1965-01-20 FR FR2558A patent/FR3989M/fr not_active Expired
- 1965-10-15 DK DK528365AA patent/DK112029B/da unknown
- 1965-10-15 DK DK528265AA patent/DK113077B/da unknown
-
1967
- 1967-06-30 SE SE09814/67A patent/SE329610B/xx unknown
- 1967-06-30 SE SE981567A patent/SE316761B/xx unknown
-
1968
- 1968-08-21 US US754452A patent/US3519718A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| FR1463791A (fr) | 1966-07-22 |
| SE316761B (enExample) | 1969-11-03 |
| DK113077B (da) | 1969-02-17 |
| DE1291743B (de) | 1969-04-03 |
| SE329610B (enExample) | 1970-10-19 |
| BE654587A (enExample) | 1965-04-20 |
| GB1061869A (en) | 1967-03-15 |
| ES305124A1 (es) | 1965-04-01 |
| US3519718A (en) | 1970-07-07 |
| AT250940B (de) | 1966-12-12 |
| AT254185B (de) | 1967-05-10 |
| DE1793612A1 (de) | 1972-02-10 |
| FR3989M (enExample) | 1966-03-07 |
| SE313303B (enExample) | 1969-08-11 |
| ES305122A1 (es) | 1965-04-01 |
| FI44627C (fi) | 1971-12-10 |
| AT254184B (de) | 1967-05-10 |
| AT253492B (de) | 1967-04-10 |
| ES305123A1 (es) | 1965-04-01 |
| DK112029B (da) | 1968-11-04 |
| IL22290A (en) | 1968-03-28 |
| CH426783A (de) | 1966-12-31 |
| NL123295C (enExample) | |
| FI44627B (enExample) | 1971-08-31 |
| SE329611B (enExample) | 1970-10-19 |
| AT252226B (de) | 1967-02-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Hutchinson et al. | On the decomposition of cellulose by an aerobic organism (Spirochaeta cytophaga, n. sp.). | |
| DK155525B (da) | Fremgangsmaade til fremstilling af (6r,7r)-7-oe(z)-2-(2-aminotiazol-4-yl)-2-(2-karboxyprop-2-oxyimino)-acetamidoaa-3-(1-pyridiniummetyl)-ceph-3-em-4-karboxylat-pentahydrat | |
| US2498574A (en) | Dihydrostreptomycin and acid addition salts | |
| DE3018767C2 (enExample) | ||
| US3027229A (en) | Method of preparing hydrated calcium phosphate gels | |
| NO132692B (enExample) | ||
| US2967802A (en) | Hydrated calcium phosphate gelantigen composition and method of preparing same | |
| US2982689A (en) | Thiostrepton, its salts, and production | |
| NO118064B (enExample) | ||
| Yonehara et al. | The detoxin complex, selective antagonists of blasticidin S | |
| Birkinshaw et al. | Studies in the biochemistry of micro-organisms: 73. Metabolic products of Aspergillus fumigatus Fresenius | |
| CA1339021C (en) | Ó-crystals of cefazolin sodium | |
| DE2040141C3 (de) | Dipeptide und Verfahren zu ihrer Herstellung | |
| US3639590A (en) | Antibacterial composition containing (-) (cis-1 2-epoxypropyl) phosphoric acid | |
| US2565653A (en) | Substantially pure dihydrostreptomycin-b base and salts thereof and method of obtaining same | |
| Heymann et al. | The preparation and some biological properties of the asparagine analog L-2-amino-2-carboxyethanesulfonamide | |
| NO115952B (enExample) | ||
| GB889769A (en) | Slowly acting insulin preparation in crystalline form | |
| US2602041A (en) | Method for the manufacture of polymyxin | |
| US2811481A (en) | Zinc neomycin | |
| US2438209A (en) | Reaction product of gramicidin and formaldehyde and method of production | |
| US2985533A (en) | Bacitracin product and processes utilizing manganese compounds | |
| RU2076722C1 (ru) | Способ получения сухой биомассы лакто-, коли- или бифидобактерий | |
| Mowat et al. | Pteroic Acid Derivatives. I. Pteroyl-α-glutamylglutamic Acid and Pteroyl-α, γ-glutamyldiglutamic Acid | |
| US3096243A (en) | Perlimycin |