NO300014B1 - Kjemiske forbindelser - Google Patents
Kjemiske forbindelser Download PDFInfo
- Publication number
- NO300014B1 NO300014B1 NO941269A NO941269A NO300014B1 NO 300014 B1 NO300014 B1 NO 300014B1 NO 941269 A NO941269 A NO 941269A NO 941269 A NO941269 A NO 941269A NO 300014 B1 NO300014 B1 NO 300014B1
- Authority
- NO
- Norway
- Prior art keywords
- acid
- ara
- connection according
- cis
- nucleoside
- Prior art date
Links
- MKUXAQIIEYXACX-UHFFFAOYSA-N aciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000002777 nucleoside Substances 0.000 claims abstract description 34
- 229960004150 aciclovir Drugs 0.000 claims abstract description 33
- -1 Fatty acid esters Chemical class 0.000 claims abstract description 27
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 22
- 229930195729 fatty acid Natural products 0.000 claims abstract description 22
- 239000000194 fatty acid Substances 0.000 claims abstract description 22
- 229940127073 nucleoside analogue Drugs 0.000 claims abstract description 17
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims abstract description 15
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 claims abstract description 15
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims abstract description 15
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000005642 Oleic acid Substances 0.000 claims abstract description 9
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 9
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims abstract description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims description 66
- 238000011282 treatment Methods 0.000 claims description 25
- 208000036142 Viral infection Diseases 0.000 claims description 15
- 150000003833 nucleoside derivatives Chemical class 0.000 claims description 15
- 230000009385 viral infection Effects 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 12
- 229940108623 eicosenoic acid Drugs 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 8
- BITHHVVYSMSWAG-KTKRTIGZSA-N (11Z)-icos-11-enoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCC(O)=O BITHHVVYSMSWAG-KTKRTIGZSA-N 0.000 claims description 7
- DWRXFEITVBNRMK-JBPTWFHOSA-N 1-[(3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione Chemical group O=C1NC(=O)C(C)=CN1C1[C@@H](O)[C@H](O)[C@@H](CO)O1 DWRXFEITVBNRMK-JBPTWFHOSA-N 0.000 claims description 7
- BITHHVVYSMSWAG-UHFFFAOYSA-N eicosenoic acid Natural products CCCCCCCCC=CCCCCCCCCCC(O)=O BITHHVVYSMSWAG-UHFFFAOYSA-N 0.000 claims description 7
- HBOMLICNUCNMMY-XLPZGREQSA-N zidovudine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](N=[N+]=[N-])C1 HBOMLICNUCNMMY-XLPZGREQSA-N 0.000 claims description 7
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 claims description 6
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Chemical compound NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 claims description 6
- UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 claims description 6
- RWQNBRDOKXIBIV-UHFFFAOYSA-N thymine Chemical compound CC1=CNC(=O)NC1=O RWQNBRDOKXIBIV-UHFFFAOYSA-N 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 229960000643 adenine Drugs 0.000 claims description 4
- 229960002555 zidovudine Drugs 0.000 claims description 4
- 229930024421 Adenine Natural products 0.000 claims description 3
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 229940104302 cytosine Drugs 0.000 claims description 3
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- IRSCQMHQWWYFCW-UHFFFAOYSA-N ganciclovir Chemical group O=C1NC(N)=NC2=C1N=CN2COC(CO)CO IRSCQMHQWWYFCW-UHFFFAOYSA-N 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
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- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical group [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
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- 229910052805 deuterium Inorganic materials 0.000 claims description 2
- 229910052731 fluorine Chemical group 0.000 claims description 2
- 239000011737 fluorine Chemical group 0.000 claims description 2
- 229960002963 ganciclovir Drugs 0.000 claims description 2
- 150000002771 monosaccharide derivatives Chemical class 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 229940113082 thymine Drugs 0.000 claims description 2
- OIRDTQYFTABQOQ-UHTZMRCNSA-N Vidarabine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O OIRDTQYFTABQOQ-UHTZMRCNSA-N 0.000 claims 5
- KDCGOANMDULRCW-UHFFFAOYSA-N Purine Natural products N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 claims 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 22
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- 231100000053 low toxicity Toxicity 0.000 abstract 1
- FIKTURVKRGQNQD-VHEBQXMUSA-N trans-2-icosenoic acid Chemical compound CCCCCCCCCCCCCCCCC\C=C\C(O)=O FIKTURVKRGQNQD-VHEBQXMUSA-N 0.000 abstract 1
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 78
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 72
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 55
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 48
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 22
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- DWRXFEITVBNRMK-UHFFFAOYSA-N Beta-D-1-Arabinofuranosylthymine Natural products O=C1NC(=O)C(C)=CN1C1C(O)C(O)C(CO)O1 DWRXFEITVBNRMK-UHFFFAOYSA-N 0.000 description 8
- DWRXFEITVBNRMK-JAGXHNFQSA-N Spongothymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 DWRXFEITVBNRMK-JAGXHNFQSA-N 0.000 description 8
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- MLQBTMWHIOYKKC-MDZDMXLPSA-N (e)-octadec-9-enoyl chloride Chemical compound CCCCCCCC\C=C\CCCCCCCC(Cl)=O MLQBTMWHIOYKKC-MDZDMXLPSA-N 0.000 description 5
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- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C07H19/06—Pyrimidine radicals
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
- External Artificial Organs (AREA)
- Mechanical Coupling Of Light Guides (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NO941269A NO300014B1 (no) | 1991-10-07 | 1994-04-07 | Kjemiske forbindelser |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9121257A GB2260319B (en) | 1991-10-07 | 1991-10-07 | Acyl derivatives of nucleosides and nucleoside analogues having anti-viral activity |
PCT/NO1992/000162 WO1993007163A1 (en) | 1991-10-07 | 1992-09-30 | Chemical compounds |
NO941269A NO300014B1 (no) | 1991-10-07 | 1994-04-07 | Kjemiske forbindelser |
Publications (3)
Publication Number | Publication Date |
---|---|
NO941269L NO941269L (no) | 1994-04-07 |
NO941269D0 NO941269D0 (no) | 1994-04-07 |
NO300014B1 true NO300014B1 (no) | 1997-03-17 |
Family
ID=10702531
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO941269A NO300014B1 (no) | 1991-10-07 | 1994-04-07 | Kjemiske forbindelser |
Country Status (27)
Country | Link |
---|---|
US (1) | US6548486B1 (xx) |
EP (1) | EP0642525B1 (xx) |
JP (1) | JP2873313B2 (xx) |
KR (1) | KR100272732B1 (xx) |
AT (1) | ATE152454T1 (xx) |
CA (1) | CA2120725C (xx) |
CH (1) | CH0642525H1 (xx) |
CZ (1) | CZ288153B6 (xx) |
DE (1) | DE69219482T2 (xx) |
DK (1) | DK0642525T3 (xx) |
FI (2) | FI105035B (xx) |
GB (1) | GB2260319B (xx) |
GR (1) | GR3024149T3 (xx) |
HK (1) | HK1007430A1 (xx) |
HU (1) | HU219400B (xx) |
IL (1) | IL103351A (xx) |
MX (1) | MX9205715A (xx) |
NO (1) | NO300014B1 (xx) |
NZ (1) | NZ244535A (xx) |
PL (1) | PL170846B1 (xx) |
RU (1) | RU2126417C1 (xx) |
SG (1) | SG47759A1 (xx) |
SK (1) | SK281903B6 (xx) |
TW (1) | TW347333B (xx) |
UA (1) | UA41296C2 (xx) |
WO (1) | WO1993007163A1 (xx) |
ZA (1) | ZA927432B (xx) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9307043D0 (en) * | 1993-04-05 | 1993-05-26 | Norsk Hydro As | Chemical compounds |
US6703394B2 (en) | 1996-02-16 | 2004-03-09 | Medivir Ab | Acyclic nucleoside derivatives |
US5869493A (en) | 1996-02-16 | 1999-02-09 | Medivir Ab | Acyclic nucleoside derivatives |
GB2321455A (en) * | 1997-01-24 | 1998-07-29 | Norsk Hydro As | Lipophilic derivatives of biologically active compounds |
GB0201179D0 (en) * | 2002-01-18 | 2002-03-06 | Angeletti P Ist Richerche Bio | Therapeutic agents |
TWI332507B (en) | 2002-11-19 | 2010-11-01 | Hoffmann La Roche | Antiviral nucleoside derivatives |
US8114847B2 (en) | 2005-03-16 | 2012-02-14 | Case Western Reserve University | Selective inhibitors of translesion DNA replication |
WO2008147454A1 (en) * | 2006-11-16 | 2008-12-04 | Case Western Reserve University | Selective inhibitors of translesion dna replication |
NO324263B1 (no) * | 2005-12-08 | 2007-09-17 | Clavis Pharma Asa | Kjemiske forbindelser, anvendelse derav ved behandling av kreft, samt farmasoytiske preparater som omfatter slike forbindelser |
US8497292B2 (en) * | 2005-12-28 | 2013-07-30 | Translational Therapeutics, Inc. | Translational dysfunction based therapeutics |
WO2008150438A1 (en) * | 2007-06-01 | 2008-12-11 | Luitpold Pharmaceuticals, Inc. | Pmea lipid conjugates |
CN101835374B (zh) | 2007-07-09 | 2014-08-27 | 东弗吉尼亚医学院 | 具有抗病毒和抗微生物性质的取代的核苷衍生物 |
UA99836C2 (xx) * | 2007-09-26 | 2012-10-10 | Маунт Синай Скул Оф Медсин | Аналоги азацитидину та їх застосування$аналоги азацитидина и их применение |
EP2825546B1 (en) | 2011-09-01 | 2017-07-12 | Case Western Reserve University | Non-natural nucleosides as theranostic agents |
US9493500B2 (en) | 2012-07-19 | 2016-11-15 | Richard Daifuku | Fluorinated pyrimidine analogs and methods of use thereof |
US9821173B2 (en) | 2013-02-08 | 2017-11-21 | Case Western Reserve University | Anti-cancer agents and methods of use |
RU2621145C2 (ru) * | 2015-11-03 | 2017-05-31 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Воронежский государственный университет" (ФГБОУ ВПО "ВГУ") | Способ получения липосом |
US20200407393A1 (en) * | 2018-03-07 | 2020-12-31 | Glaxosmithkline Intellectual Property (No. 2) Limited | Medical Use |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1325798A (en) * | 1970-09-24 | 1973-08-08 | Upjohn Co | Derivatives of 2,2-anhydro-ara-cytidine |
US3920630A (en) * | 1970-09-24 | 1975-11-18 | Upjohn Co | 2,2{40 -Anhydro-ara-cytidine compounds and process of preparation |
US4211773A (en) * | 1978-10-02 | 1980-07-08 | Sloan Kettering Institute For Cancer Research | 5-Substituted 1-(2'-Deoxy-2'-substituted-β-D-arabinofuranosyl)pyrimidine nucleosides |
DE3100478A1 (de) * | 1981-01-09 | 1982-08-12 | Dr. Thilo & Co GmbH, 8021 Sauerlach | 5'ester von pyrimidinnucleosiden mit antiviraler wirksamkeit, verfahren zur herstellung und daraus hergestellte arzneimittel |
US4355032B2 (en) | 1981-05-21 | 1990-10-30 | 9-(1,3-dihydroxy-2-propoxymethyl)guanine as antiviral agent | |
US4816447A (en) | 1981-08-26 | 1989-03-28 | Merck & Co., Inc. | Anti-viral guanine compounds |
NZ201662A (en) | 1981-08-26 | 1986-07-11 | Merck & Co Inc | 9-(1,3-(and 2,3)-dihydroxy-1-(and 2)-propoxy-methyl)guanine derivatives and methods for their preparation |
US5250535A (en) * | 1982-02-01 | 1993-10-05 | Syntex Inc. | Substituted 9-(1 or 3-monoacyloxy or 1,3-diacyloxy-2-propoxymethyl) purines as antiviral agent |
US4556659A (en) * | 1982-08-09 | 1985-12-03 | Syntex (U.S.A.) Inc. | Substituted 9-(1-0- or 3-0-monosubstituted or 1,3-Di-0-substituted propoxymethyl)-purines as antiviral agents |
JPH0655755B2 (ja) * | 1985-01-23 | 1994-07-27 | 富山化学工業株式会社 | 新規な5−フルオロ−2′−デオキシウリジン−3′−ホスフエ−ト誘導体およびその塩 |
US4684631A (en) | 1984-10-09 | 1987-08-04 | Toyama Chemical Co., Ltd. | Novel 5-fluoro-2-deoxyuridine derivatives and salts thereof, process for producing the same, and antitumor agents containing the same |
US5223263A (en) | 1988-07-07 | 1993-06-29 | Vical, Inc. | Liponucleotide-containing liposomes |
JPS6483092A (en) * | 1987-09-24 | 1989-03-28 | Arakawa Chotaro & Co | Novel n6,n6-dimethyladenosine derivative having carcinostatic activity, its production and carcinostatic agent containing said derivative as active component |
DE3856557T2 (de) * | 1987-10-28 | 2004-06-03 | Wellstat Therapeutics Corp. | Acyldeoxyribonukleosid-Derivate und Verwendungen davon |
JPH0278696A (ja) * | 1988-09-13 | 1990-03-19 | Shoichiro Ozaki | 5−フルオロウラシル誘導体 |
US5216142A (en) | 1989-04-17 | 1993-06-01 | Efamol Holdings Plc | Anti-virals |
RU2085557C1 (ru) * | 1991-09-30 | 1997-07-27 | Санкио Компани Лимитед | Производные нуклеозидов пиримидина или их фармацевтически приемлемые соли и способ их получения |
-
1991
- 1991-10-07 GB GB9121257A patent/GB2260319B/en not_active Expired - Fee Related
-
1992
- 1992-09-28 ZA ZA927432A patent/ZA927432B/xx unknown
- 1992-09-29 NZ NZ244535A patent/NZ244535A/en not_active IP Right Cessation
- 1992-09-30 KR KR1019940701120A patent/KR100272732B1/ko not_active IP Right Cessation
- 1992-09-30 RU RU94021110/04A patent/RU2126417C1/ru active
- 1992-09-30 WO PCT/NO1992/000162 patent/WO1993007163A1/en active IP Right Grant
- 1992-09-30 SK SK397-94A patent/SK281903B6/sk not_active IP Right Cessation
- 1992-09-30 HU HU9400988A patent/HU219400B/hu unknown
- 1992-09-30 CA CA002120725A patent/CA2120725C/en not_active Expired - Lifetime
- 1992-09-30 US US08/211,386 patent/US6548486B1/en not_active Expired - Lifetime
- 1992-09-30 CH CH92922008.5T patent/CH0642525H1/xx unknown
- 1992-09-30 DK DK92922008.5T patent/DK0642525T3/da active
- 1992-09-30 DE DE69219482T patent/DE69219482T2/de not_active Expired - Lifetime
- 1992-09-30 CZ CZ1994805A patent/CZ288153B6/cs not_active IP Right Cessation
- 1992-09-30 SG SG1996004250A patent/SG47759A1/en unknown
- 1992-09-30 AT AT92922008T patent/ATE152454T1/de active
- 1992-09-30 JP JP5506814A patent/JP2873313B2/ja not_active Expired - Lifetime
- 1992-09-30 PL PL92303098A patent/PL170846B1/pl unknown
- 1992-09-30 EP EP92922008A patent/EP0642525B1/en not_active Expired - Lifetime
- 1992-09-30 UA UA94005489A patent/UA41296C2/uk unknown
- 1992-10-03 TW TW081107870A patent/TW347333B/zh not_active IP Right Cessation
- 1992-10-05 IL IL10335192A patent/IL103351A/xx not_active IP Right Cessation
- 1992-10-06 MX MX9205715A patent/MX9205715A/es unknown
-
1994
- 1994-04-06 FI FI941574A patent/FI105035B/fi not_active IP Right Cessation
- 1994-04-07 NO NO941269A patent/NO300014B1/no not_active IP Right Cessation
-
1997
- 1997-07-16 GR GR970401799T patent/GR3024149T3/el unknown
-
1998
- 1998-06-17 HK HK98105563A patent/HK1007430A1/xx not_active IP Right Cessation
-
1999
- 1999-02-10 FI FI990270A patent/FI990270A0/fi unknown
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Legal Events
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MK1K | Patent expired |