PL80960B1 - Complex of inosine with dialkyl-aminoalkanol[us3646007a] - Google Patents
Complex of inosine with dialkyl-aminoalkanol[us3646007a] Download PDFInfo
- Publication number
- PL80960B1 PL80960B1 PL1970142795A PL14279570A PL80960B1 PL 80960 B1 PL80960 B1 PL 80960B1 PL 1970142795 A PL1970142795 A PL 1970142795A PL 14279570 A PL14279570 A PL 14279570A PL 80960 B1 PL80960 B1 PL 80960B1
- Authority
- PL
- Poland
- Prior art keywords
- inosine
- complex compound
- complex
- dimethylaminoisopropanol
- dialkylaminoethanol
- Prior art date
Links
- UGQMRVRMYYASKQ-KQYNXXCUSA-N Inosine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C2=NC=NC(O)=C2N=C1 UGQMRVRMYYASKQ-KQYNXXCUSA-N 0.000 title claims abstract description 126
- 229930010555 Inosine Natural products 0.000 title claims abstract description 124
- 229960003786 inosine Drugs 0.000 title claims abstract description 124
- 239000000203 mixture Substances 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 91
- POIVWEXWFKSJHL-UHFFFAOYSA-N 2-(dimethylamino)propan-2-ol Chemical compound CN(C)C(C)(C)O POIVWEXWFKSJHL-UHFFFAOYSA-N 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
- 241000124008 Mammalia Species 0.000 claims description 10
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 10
- 229960002887 deanol Drugs 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 6
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 3
- 229960004050 aminobenzoic acid Drugs 0.000 claims description 2
- 238000011065 in-situ storage Methods 0.000 claims description 2
- 241000712461 unidentified influenza virus Species 0.000 abstract description 7
- 241001529453 unidentified herpesvirus Species 0.000 abstract description 6
- 239000003814 drug Substances 0.000 abstract description 4
- 230000000840 anti-viral effect Effects 0.000 abstract description 3
- 229940079593 drug Drugs 0.000 abstract 1
- 206010022000 influenza Diseases 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 description 33
- 241000700159 Rattus Species 0.000 description 21
- 230000000694 effects Effects 0.000 description 21
- IWSZDQRGNFLMJS-UHFFFAOYSA-N 2-(dibutylamino)ethanol Chemical compound CCCCN(CCO)CCCC IWSZDQRGNFLMJS-UHFFFAOYSA-N 0.000 description 19
- 150000001414 amino alcohols Chemical class 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000000243 solution Substances 0.000 description 13
- 210000004556 brain Anatomy 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- -1 for example Substances 0.000 description 8
- 238000002329 infrared spectrum Methods 0.000 description 8
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- 241000699670 Mus sp. Species 0.000 description 7
- 230000009471 action Effects 0.000 description 7
- QCXJEYYXVJIFCE-UHFFFAOYSA-N 4-acetamidobenzoic acid Chemical class CC(=O)NC1=CC=C(C(O)=O)C=C1 QCXJEYYXVJIFCE-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000012266 salt solution Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 230000037396 body weight Effects 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 5
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- 238000004458 analytical method Methods 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 230000001771 impaired effect Effects 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 102000006382 Ribonucleases Human genes 0.000 description 3
- 108010083644 Ribonucleases Proteins 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
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- 229920002477 rna polymer Polymers 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 230000008925 spontaneous activity Effects 0.000 description 3
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 241000282887 Suidae Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000004075 alteration Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000034994 death Effects 0.000 description 2
- 231100000517 death Toxicity 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000006735 deficit Effects 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 2
- 244000144993 groups of animals Species 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- 210000002729 polyribosome Anatomy 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
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- 208000024891 symptom Diseases 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- LSRUBRSFDNKORM-UHFFFAOYSA-N 1,1-diaminopropan-1-ol Chemical compound CCC(N)(N)O LSRUBRSFDNKORM-UHFFFAOYSA-N 0.000 description 1
- VKKTUDKKYOOLGG-UHFFFAOYSA-N 1-(diethylamino)propan-1-ol Chemical compound CCC(O)N(CC)CC VKKTUDKKYOOLGG-UHFFFAOYSA-N 0.000 description 1
- RPPCFYFWGVIQFS-UHFFFAOYSA-N 1-(dimethylamino)butan-1-ol Chemical compound CCCC(O)N(C)C RPPCFYFWGVIQFS-UHFFFAOYSA-N 0.000 description 1
- NCXUNZWLEYGQAH-UHFFFAOYSA-N 1-(dimethylamino)propan-2-ol Chemical compound CC(O)CN(C)C NCXUNZWLEYGQAH-UHFFFAOYSA-N 0.000 description 1
- NHJUPEHXTLQRLI-UHFFFAOYSA-N 2-(dimethylamino)propan-2-ol;hydrochloride Chemical compound Cl.CN(C)C(C)(C)O NHJUPEHXTLQRLI-UHFFFAOYSA-N 0.000 description 1
- HZLYGAQNCRJBDT-UHFFFAOYSA-N 2-(ethylamino)propan-2-ol Chemical compound CCNC(C)(C)O HZLYGAQNCRJBDT-UHFFFAOYSA-N 0.000 description 1
- QZXIXSZVEYUCGM-UHFFFAOYSA-N 2-aminopropan-2-ol Chemical compound CC(C)(N)O QZXIXSZVEYUCGM-UHFFFAOYSA-N 0.000 description 1
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-UHFFFAOYSA-N 0.000 description 1
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 description 1
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- 101100283604 Caenorhabditis elegans pigk-1 gene Proteins 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 102000053602 DNA Human genes 0.000 description 1
- 108020004414 DNA Proteins 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 1
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- 229920000877 Melamine resin Polymers 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 1
- 206010062519 Poor quality sleep Diseases 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000700157 Rattus norvegicus Species 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
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- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
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- 210000000805 cytoplasm Anatomy 0.000 description 1
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- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 231100000234 hepatic damage Toxicity 0.000 description 1
- 210000004276 hyalin Anatomy 0.000 description 1
- 229960000443 hydrochloric acid Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
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- 230000002401 inhibitory effect Effects 0.000 description 1
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- 238000007912 intraperitoneal administration Methods 0.000 description 1
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- 229940077810 liceall Drugs 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 230000008818 liver damage Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229940098895 maleic acid Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
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- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000037023 motor activity Effects 0.000 description 1
- KYVXIDYFPYFKTM-UHFFFAOYSA-N n-methylmethanamine;propan-2-ol Chemical compound CNC.CC(C)O KYVXIDYFPYFKTM-UHFFFAOYSA-N 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
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- 230000001988 toxicity Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005199 ultracentrifugation Methods 0.000 description 1
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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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Fodder In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85386469A | 1969-08-28 | 1969-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL80960B1 true PL80960B1 (en) | 1975-08-30 |
Family
ID=25317098
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1970142795A PL80960B1 (en) | 1969-08-28 | 1970-08-20 | Complex of inosine with dialkyl-aminoalkanol[us3646007a] |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US3646007A (OSRAM) |
| JP (2) | JPS493999B1 (OSRAM) |
| AT (1) | AT299457B (OSRAM) |
| BE (1) | BE755361A (OSRAM) |
| BR (1) | BR6915483D0 (OSRAM) |
| CA (1) | CA920125A (OSRAM) |
| CH (1) | CH530998A (OSRAM) |
| CS (1) | CS183616B2 (OSRAM) |
| DE (2) | DE1965431C3 (OSRAM) |
| DK (1) | DK137801B (OSRAM) |
| ES (1) | ES375387A1 (OSRAM) |
| FR (1) | FR2068522B1 (OSRAM) |
| GB (1) | GB1252401A (OSRAM) |
| HU (1) | HU162297B (OSRAM) |
| IL (1) | IL35135A (OSRAM) |
| LU (1) | LU61603A1 (OSRAM) |
| NL (1) | NL140735B (OSRAM) |
| NO (1) | NO126800B (OSRAM) |
| PH (2) | PH9221A (OSRAM) |
| PL (1) | PL80960B1 (OSRAM) |
| SE (1) | SE384866B (OSRAM) |
| SU (1) | SU381216A3 (OSRAM) |
| YU (1) | YU36188B (OSRAM) |
| ZA (1) | ZA705913B (OSRAM) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2260331B1 (OSRAM) * | 1974-02-08 | 1978-01-13 | Mauvernay Centre Europ Rech | |
| US4221909A (en) * | 1978-09-15 | 1980-09-09 | Sloan-Kettering Institute For Cancer Research | P-Acetamidobenzoic acid salts of 9-(hydroxyalkyl) purines |
| US4387226A (en) * | 1981-08-26 | 1983-06-07 | Newport Pharmaceuticals International, Inc. | Purine-dihydrothiazoles |
| US4510144A (en) * | 1981-08-26 | 1985-04-09 | Newport Pharmaceuticals International | Methods of imparting immunomodulating activity with dihydrothiazolo purine derivatives |
| JPS5994567U (ja) * | 1982-12-15 | 1984-06-27 | 松下電工株式会社 | 折り畳みドアのラツチ構造 |
| US4512981A (en) * | 1982-12-20 | 1985-04-23 | Newport Pharmaceuticals International, Inc. | Method of treating inflammation using inosiplex |
| DE3404315C1 (de) * | 1984-02-08 | 1985-05-09 | Newport AG, Zug | Verwendung von Inosin-haltigen Wirkstoffen zur Wachstumsfoerderung bei der Mast von Nutztieren |
| FR2652003A1 (fr) * | 1989-09-20 | 1991-03-22 | Delalande Sa | Utilisation d'un complexe de l'inosine avec un n,n-dialkylamino alcanol ou un sel de celui-ci avec un acide pharmacologiquement acceptable pour le traitement de certaines infections helminthiques. |
| US7585850B2 (en) * | 2004-02-10 | 2009-09-08 | Adenobio N.V. | Stable and active complexes of adenosine and adenosine phosphates with aminoalcohols for the treatment of pulmonary artery hypertension, cardiac failure and other diseases |
| JP2015536940A (ja) | 2012-10-29 | 2015-12-24 | シプラ・リミテッド | 抗ウイルス性ホスホネート類似体及びその製造方法 |
| CN104744541A (zh) * | 2014-05-05 | 2015-07-01 | 深圳信立泰药业股份有限公司 | 一种异丙肌苷新晶型、其制备方法及含有该新晶型的药物组合物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB879259A (en) * | 1956-11-20 | 1961-10-11 | Riker Laboratories Inc | Acid addition salts of 2-dimethylaminoethanol and central nervous system stimulant compositions containing them |
| US3438968A (en) * | 1966-06-23 | 1969-04-15 | Int Chem & Nuclear Corp | Substituted ammonium basic addition salts of ribonucleic acid |
-
0
- BE BE755361D patent/BE755361A/xx not_active IP Right Cessation
-
1969
- 1969-08-28 US US853864A patent/US3646007A/en not_active Expired - Lifetime
- 1969-10-07 JP JP44079730A patent/JPS493999B1/ja active Pending
- 1969-12-11 CA CA069661A patent/CA920125A/en not_active Expired
- 1969-12-17 SE SE6917421A patent/SE384866B/xx unknown
- 1969-12-19 BR BR215483/69A patent/BR6915483D0/pt unknown
- 1969-12-30 DE DE1965431A patent/DE1965431C3/de not_active Expired
- 1969-12-30 DE DE1967073A patent/DE1967073C2/de not_active Expired
-
1970
- 1970-01-08 NO NO00067/70A patent/NO126800B/no unknown
- 1970-01-13 ES ES375387A patent/ES375387A1/es not_active Expired
- 1970-01-13 GB GB1252401D patent/GB1252401A/en not_active Expired
- 1970-01-15 NL NL707000574A patent/NL140735B/xx not_active IP Right Cessation
- 1970-01-23 CH CH97170A patent/CH530998A/de not_active IP Right Cessation
- 1970-08-18 DK DK422770AA patent/DK137801B/da not_active IP Right Cessation
- 1970-08-20 IL IL35135A patent/IL35135A/xx unknown
- 1970-08-20 PL PL1970142795A patent/PL80960B1/pl unknown
- 1970-08-25 YU YU2145/70A patent/YU36188B/xx unknown
- 1970-08-25 FR FR7030995A patent/FR2068522B1/fr not_active Expired
- 1970-08-26 AT AT776070A patent/AT299457B/de not_active IP Right Cessation
- 1970-08-26 PH PH11764*UA patent/PH9221A/en unknown
- 1970-08-28 LU LU61603D patent/LU61603A1/xx unknown
- 1970-08-28 SU SU1482906A patent/SU381216A3/ru active
- 1970-08-28 CS CS7000005929A patent/CS183616B2/cs unknown
- 1970-08-28 HU HUPA1074A patent/HU162297B/hu unknown
-
1971
- 1971-03-26 ZA ZA705913A patent/ZA705913B/xx unknown
- 1971-12-07 JP JP46098967A patent/JPS4921765B1/ja active Pending
-
1973
- 1973-05-28 PH PH14658*A patent/PH10011A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH530998A (de) | 1972-11-30 |
| SU381216A3 (OSRAM) | 1973-05-15 |
| PH9221A (en) | 1975-07-10 |
| YU214570A (en) | 1981-04-30 |
| DE1965431C3 (de) | 1979-01-04 |
| NL140735B (nl) | 1974-01-15 |
| FR2068522A1 (OSRAM) | 1971-08-27 |
| DK137801C (OSRAM) | 1978-10-16 |
| DE1965431A1 (de) | 1971-04-08 |
| CS183616B2 (en) | 1978-07-31 |
| LU61603A1 (OSRAM) | 1971-08-05 |
| GB1252401A (OSRAM) | 1971-11-03 |
| BR6915483D0 (pt) | 1973-03-13 |
| ZA705913B (en) | 1971-04-28 |
| DE1965431B2 (de) | 1978-05-18 |
| AT299457B (de) | 1972-06-26 |
| SE384866B (sv) | 1976-05-24 |
| CA920125A (en) | 1973-01-30 |
| ES375387A1 (es) | 1972-05-01 |
| IL35135A0 (en) | 1970-10-30 |
| DE1967073A1 (de) | 1976-12-02 |
| DE1967073C2 (de) | 1986-04-17 |
| IL35135A (en) | 1974-07-31 |
| FR2068522B1 (OSRAM) | 1974-08-30 |
| HU162297B (OSRAM) | 1973-01-29 |
| BE755361A (fr) | 1971-03-01 |
| YU36188B (en) | 1982-02-25 |
| JPS4921765B1 (OSRAM) | 1974-06-04 |
| JPS493999B1 (OSRAM) | 1974-01-29 |
| PH10011A (en) | 1976-07-13 |
| DK137801B (da) | 1978-05-08 |
| NL7000574A (OSRAM) | 1971-03-02 |
| NO126800B (OSRAM) | 1973-03-26 |
| US3646007A (en) | 1972-02-29 |
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