DE2519063A1 - Verfahren zur herstellung von adeninderivaten - Google Patents
Verfahren zur herstellung von adeninderivatenInfo
- Publication number
- DE2519063A1 DE2519063A1 DE19752519063 DE2519063A DE2519063A1 DE 2519063 A1 DE2519063 A1 DE 2519063A1 DE 19752519063 DE19752519063 DE 19752519063 DE 2519063 A DE2519063 A DE 2519063A DE 2519063 A1 DE2519063 A1 DE 2519063A1
- Authority
- DE
- Germany
- Prior art keywords
- adenine
- reaction
- adenosine
- solution
- rearrangement
- 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.)
- Withdrawn
Links
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical class NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 14
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 10
- 102000004190 Enzymes Human genes 0.000 claims description 9
- 108090000790 Enzymes Proteins 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 229930024421 Adenine Natural products 0.000 claims description 6
- 239000004593 Epoxy Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 229960000643 adenine Drugs 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
- 230000008707 rearrangement Effects 0.000 claims description 5
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- XTWYTFMLZFPYCI-KQYNXXCUSA-N 5'-adenylphosphoric acid Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O XTWYTFMLZFPYCI-KQYNXXCUSA-N 0.000 claims description 2
- XTWYTFMLZFPYCI-UHFFFAOYSA-N Adenosine diphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(O)=O)C(O)C1O XTWYTFMLZFPYCI-UHFFFAOYSA-N 0.000 claims description 2
- ZKHQWZAMYRWXGA-UHFFFAOYSA-N Adenosine triphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1O ZKHQWZAMYRWXGA-UHFFFAOYSA-N 0.000 claims description 2
- 239000002126 C01EB10 - Adenosine Substances 0.000 claims description 2
- UDMBCSSLTHHNCD-UHFFFAOYSA-N Coenzym Q(11) Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(O)=O)C(O)C1O UDMBCSSLTHHNCD-UHFFFAOYSA-N 0.000 claims description 2
- IVOMOUWHDPKRLL-KQYNXXCUSA-N Cyclic adenosine monophosphate Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=CN=C2N)=C2N=C1 IVOMOUWHDPKRLL-KQYNXXCUSA-N 0.000 claims description 2
- 229960005305 adenosine Drugs 0.000 claims description 2
- UDMBCSSLTHHNCD-KQYNXXCUSA-N adenosine 5'-monophosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O UDMBCSSLTHHNCD-KQYNXXCUSA-N 0.000 claims description 2
- LNQVTSROQXJCDD-UHFFFAOYSA-N adenosine monophosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(CO)C(OP(O)(O)=O)C1O LNQVTSROQXJCDD-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims 1
- ZKHQWZAMYRWXGA-KQYNXXCUSA-N Adenosine triphosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-N 0.000 claims 1
- XJLXINKUBYWONI-NNYOXOHSSA-N NADP zwitterion Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-NNYOXOHSSA-N 0.000 claims 1
- -1 adenine compound Chemical class 0.000 claims 1
- 229960001456 adenosine triphosphate Drugs 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 claims 1
- 229960002715 nicotine Drugs 0.000 claims 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000000243 solution Substances 0.000 description 24
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 21
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 239000000047 product Substances 0.000 description 16
- BAWFJGJZGIEFAR-NNYOXOHSSA-N NAD zwitterion Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 BAWFJGJZGIEFAR-NNYOXOHSSA-N 0.000 description 12
- 238000002211 ultraviolet spectrum Methods 0.000 description 8
- 229950006238 nadide Drugs 0.000 description 7
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 6
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 6
- 239000005515 coenzyme Substances 0.000 description 6
- 239000012154 double-distilled water Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 4
- PVEOYINWKBTPIZ-UHFFFAOYSA-N but-3-enoic acid Chemical compound OC(=O)CC=C PVEOYINWKBTPIZ-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 3
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 229920002521 macromolecule Polymers 0.000 description 3
- 230000020477 pH reduction Effects 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- ZVNYKZKUBKIIAH-UHFFFAOYSA-N 2-(oxiran-2-yl)acetic acid Chemical compound OC(=O)CC1CO1 ZVNYKZKUBKIIAH-UHFFFAOYSA-N 0.000 description 2
- NKXYQYUYJMQGII-UHFFFAOYSA-N 3-hydroxy-4-(7h-purin-6-ylamino)butanoic acid;pyridine-3-carboxamide Chemical compound NC(=O)C1=CC=CN=C1.OC(=O)CC(O)CNC1=NC=NC2=C1NC=N2 NKXYQYUYJMQGII-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- 102000007698 Alcohol dehydrogenase Human genes 0.000 description 2
- 108010021809 Alcohol dehydrogenase Proteins 0.000 description 2
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 238000001042 affinity chromatography Methods 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000008034 disappearance Effects 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 238000004108 freeze drying Methods 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 238000010405 reoxidation reaction Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
- KGLZWCCDTHHPLO-UHFFFAOYSA-N 2,3-dihydropyridine-3-carboxamide Chemical compound NC(=O)C1CN=CC=C1 KGLZWCCDTHHPLO-UHFFFAOYSA-N 0.000 description 1
- YYPNJNDODFVZLE-UHFFFAOYSA-N 3-methylbut-2-enoic acid Chemical compound CC(C)=CC(O)=O YYPNJNDODFVZLE-UHFFFAOYSA-N 0.000 description 1
- FCZOVUJWOBSMSS-UHFFFAOYSA-N 5-[(6-aminopurin-9-yl)methyl]-5-methyl-3-methylideneoxolan-2-one Chemical compound C1=NC2=C(N)N=CN=C2N1CC1(C)CC(=C)C(=O)O1 FCZOVUJWOBSMSS-UHFFFAOYSA-N 0.000 description 1
- ZKHQWZAMYRWXGA-KQYNXXCUSA-J ATP(4-) Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-J 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 101710088194 Dehydrogenase Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002152 aqueous-organic solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical compound [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 229960003966 nicotinamide Drugs 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
- C07H19/207—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids the phosphoric or polyphosphoric acids being esterified by a further hydroxylic compound, e.g. flavine adenine dinucleotide or nicotinamide-adenine dinucleotide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/48—Compounds containing oxirane rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms, e.g. ester or nitrile radicals
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
- C07F9/65616—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT22105/74A IT1017564B (it) | 1974-04-30 | 1974-04-30 | Processo per la preparazione di derivati adeninici funzionalizza ti e prodotti cosi ottenuti |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2519063A1 true DE2519063A1 (de) | 1975-11-20 |
Family
ID=11191560
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19752519063 Withdrawn DE2519063A1 (de) | 1974-04-30 | 1975-04-29 | Verfahren zur herstellung von adeninderivaten |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4008363A (en, 2012) |
| JP (1) | JPS5324960B2 (en, 2012) |
| BE (1) | BE828259A (en, 2012) |
| CA (1) | CA1058169A (en, 2012) |
| CH (1) | CH618169A5 (en, 2012) |
| CS (1) | CS199583B2 (en, 2012) |
| DD (1) | DD119789A5 (en, 2012) |
| DE (1) | DE2519063A1 (en, 2012) |
| DK (1) | DK140696B (en, 2012) |
| FR (1) | FR2269530B1 (en, 2012) |
| GB (1) | GB1510534A (en, 2012) |
| HU (1) | HU171512B (en, 2012) |
| IL (1) | IL47141A (en, 2012) |
| IT (1) | IT1017564B (en, 2012) |
| LU (1) | LU72340A1 (en, 2012) |
| NL (1) | NL7505121A (en, 2012) |
| NO (1) | NO142081C (en, 2012) |
| SE (1) | SE419551B (en, 2012) |
| YU (1) | YU79875A (en, 2012) |
| ZA (1) | ZA751831B (en, 2012) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1039756B (it) * | 1975-07-10 | 1979-12-10 | Snam Progetti | Procedimento per migliopare l at tivita di enzimi ossidoriduttasici inglobati in strutture filamentose |
| IT1065294B (it) * | 1976-12-23 | 1985-02-25 | Snam Progetti | Procedimento per la preparazione di fibre a struttura porosa,fibre porose cosi'ottenute e impieghi delle stesse |
| DE2841414C2 (de) * | 1978-09-22 | 1980-04-03 | Gesellschaft Fuer Biotechnologische Forschung Mbh (Gbf), 3300 Braunschweig | Verfahren zur Herstellung von an Makromoleküle gebundenen, ein Adeninringsystem enthaltenden Koenzymen |
| JPS5564599A (en) * | 1978-11-08 | 1980-05-15 | Unitika Ltd | Adenosine triphosphate derivative |
| US4711955A (en) * | 1981-04-17 | 1987-12-08 | Yale University | Modified nucleotides and methods of preparing and using same |
| DE3728772A1 (de) * | 1987-08-28 | 1989-03-09 | Hoechst Ag | Enzymreaktor mit polymerfixiertem cofaktor |
| US5569650A (en) * | 1993-06-11 | 1996-10-29 | Sloan-Kettering Institute For Cancer Research | C-nucleoside isosters of analogs thereof and pharmaceutical compositions |
| ATE327242T1 (de) * | 1999-12-17 | 2006-06-15 | Ariad Pharma Inc | Neue purine |
| JP2003531111A (ja) * | 1999-12-17 | 2003-10-21 | アライアッド・ファーマシューティカルズ・インコーポレーテッド | プロトンポンプインヒビター |
| EP1248790A1 (en) * | 1999-12-17 | 2002-10-16 | Ariad Pharmaceuticals, Inc. | Proton pump inhibitors |
| US20030228621A1 (en) * | 2002-05-24 | 2003-12-11 | Yong Qin | Common ligand universal enzyme assay and compositions for use therein |
| WO2005009348A2 (en) * | 2003-06-25 | 2005-02-03 | Ariad Pharmaceuticals, Inc. | Substituted purine derivatives |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3287352A (en) * | 1964-10-12 | 1966-11-22 | Upjohn Co | Nu6-(2-hydroxyethyl) tubercidin and process therefor |
| DE1545645A1 (de) * | 1965-12-06 | 1969-08-21 | Boehringer Mannheim Gmbh | Verfahren zur Herstellung von disubstituierten Adenosin-Derivaten |
-
1974
- 1974-04-30 IT IT22105/74A patent/IT1017564B/it active
-
1975
- 1975-03-24 ZA ZA00751831A patent/ZA751831B/xx unknown
- 1975-03-27 CS CS752123A patent/CS199583B2/cs unknown
- 1975-03-28 YU YU00798/75A patent/YU79875A/xx unknown
- 1975-04-09 GB GB14711/75A patent/GB1510534A/en not_active Expired
- 1975-04-22 CH CH512075A patent/CH618169A5/it not_active IP Right Cessation
- 1975-04-22 IL IL47141A patent/IL47141A/xx unknown
- 1975-04-22 FR FR7512541A patent/FR2269530B1/fr not_active Expired
- 1975-04-23 BE BE155664A patent/BE828259A/xx not_active IP Right Cessation
- 1975-04-23 LU LU72340A patent/LU72340A1/xx unknown
- 1975-04-24 HU HU75SA00002783A patent/HU171512B/hu unknown
- 1975-04-25 SE SE7504842A patent/SE419551B/xx unknown
- 1975-04-28 NO NO751510A patent/NO142081C/no unknown
- 1975-04-28 JP JP5085175A patent/JPS5324960B2/ja not_active Expired
- 1975-04-28 DD DD185736A patent/DD119789A5/xx unknown
- 1975-04-29 DE DE19752519063 patent/DE2519063A1/de not_active Withdrawn
- 1975-04-29 NL NL7505121A patent/NL7505121A/xx unknown
- 1975-04-29 US US05/572,653 patent/US4008363A/en not_active Expired - Lifetime
- 1975-04-29 DK DK186175AA patent/DK140696B/da unknown
- 1975-04-30 CA CA225,889A patent/CA1058169A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| YU79875A (en) | 1982-02-28 |
| SE7504842L (sv) | 1975-10-31 |
| JPS50149697A (en, 2012) | 1975-11-29 |
| FR2269530A1 (en, 2012) | 1975-11-28 |
| NO142081B (no) | 1980-03-17 |
| CH618169A5 (en, 2012) | 1980-07-15 |
| JPS5324960B2 (en, 2012) | 1978-07-24 |
| CS199583B2 (en) | 1980-07-31 |
| DK186175A (en, 2012) | 1975-10-31 |
| GB1510534A (en) | 1978-05-10 |
| DD119789A5 (en, 2012) | 1976-05-12 |
| IL47141A (en) | 1978-08-31 |
| CA1058169A (en) | 1979-07-10 |
| HU171512B (hu) | 1978-01-28 |
| ZA751831B (en) | 1976-06-30 |
| SE419551B (sv) | 1981-08-10 |
| FR2269530B1 (en, 2012) | 1977-04-15 |
| NL7505121A (nl) | 1975-11-03 |
| DK140696C (en, 2012) | 1980-05-05 |
| IT1017564B (it) | 1977-08-10 |
| LU72340A1 (en, 2012) | 1975-08-20 |
| NO751510L (en, 2012) | 1975-10-31 |
| US4008363A (en) | 1977-02-15 |
| DK140696B (da) | 1979-10-29 |
| AU8020675A (en) | 1976-10-21 |
| BE828259A (fr) | 1975-08-18 |
| NO142081C (no) | 1980-06-25 |
| IL47141A0 (en) | 1975-06-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1795763C3 (de) | Verfahren zur Herstellung von Vincaleukoblastin- und Leurocristinderivaten | |
| EP0574667B1 (de) | Verfahren zur Herstellung von 2,2,6,6-Tetramethylpiperidin-N-oxyl und in seiner 4-Stellung substituierten Derivaten | |
| DE2519063A1 (de) | Verfahren zur herstellung von adeninderivaten | |
| DE4219471A1 (de) | N-Oxyl-Derivate des 2,2,6,6-Tetramethylpiperidins und deren Herstellung | |
| EP0417604B1 (de) | Verfahren zur Herstellung von Riboflavin-5'-phosphat bzw. dessen Natriumsalz | |
| DE2229223C3 (de) | 2-Nitro-S-imidazol-Derivate und Verfahren zu deren Herstellung | |
| DE2160319B2 (de) | 3-Exomethylencepham-Verbindungen, Verfahren zu deren Herstellung und deren Verwendung zur Herstellung von 3-Methyl-Cephem-Derivaten | |
| DE2822876C2 (en, 2012) | ||
| EP0364875A1 (de) | Riboflavin-4'5'-cyclo-phosphorsäureesterchlorid, dessen Herstellung und Verwendung zur Herstellung von Riboflavin-5'-phosphat (5'-FMN) bzw. dessen Natriumsalz | |
| DE2841644C2 (en, 2012) | ||
| EP0608693A2 (de) | Verfahren zur Herstellung von Folsäure | |
| DD148779A5 (de) | Verfahren zur herstellung von vindesin | |
| DE3516953A1 (de) | Verfahren zur herstellung von n(pfeil hoch)6(pfeil hoch)-substituiertem 3',5'-cyclischen adenosinmonophosphat oder eines salzes davon | |
| DE2503889A1 (de) | Verfahren zur herstellung von 2,2'- cyclocytidin | |
| CH396003A (de) | Verfahren zur Herstellung von Penicillinderivaten | |
| DD213437A5 (de) | Verfahren zur herstellung von cyclopentenderivaten | |
| DE3142944C2 (de) | Verfahren zur Herstellung von Auromercaptobernsteinsäure | |
| DE1545838C3 (de) | 7-(2-Azidooctanamido)-cephalosporansäure, deren Salze und Verfahren zur Herstellung dieser Verbindungen | |
| DE1793690C3 (de) | 1 S-Hydroxy-9-oxoprosta-5-cis-10,13trans-triensäure und deren Salze sowie Verfahren zu ihrer Herstellung | |
| DE2525827C3 (de) | Verfahren zur Herstellung von a-Diol-γ-(!!oxoverbindungen | |
| DE3500029A1 (de) | Anthracyclinester | |
| AT354628B (de) | Verfahren zur debromierung von 11a-brom-6- demethyl-6-deoxy-6-methylen-5-oxytetracyclin- sulfosalicylat | |
| AT226364B (de) | Verfahren zur Herstellung von neuen Penicillinderivaten | |
| EP0690056A2 (de) | Verfahren zur Herstellung von Purinen | |
| DE2235428A1 (de) | Verfahren zur herstellung von 3(beta-dialkyl-aminoaethyl)-4-alkyl-7-carboaethoxymethoxycumarinen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8127 | New person/name/address of the applicant |
Owner name: ANIC S.P.A., PALERMO, IT |
|
| 8139 | Disposal/non-payment of the annual fee |