UY23697A1 - Procedimiento para la preparacion de 5'-deoxi-5'-fluorcitidinas sustitutas del n-oxicarbonilo - Google Patents
Procedimiento para la preparacion de 5'-deoxi-5'-fluorcitidinas sustitutas del n-oxicarboniloInfo
- Publication number
- UY23697A1 UY23697A1 UY23697A UY23697A UY23697A1 UY 23697 A1 UY23697 A1 UY 23697A1 UY 23697 A UY23697 A UY 23697A UY 23697 A UY23697 A UY 23697A UY 23697 A1 UY23697 A1 UY 23697A1
- Authority
- UY
- Uruguay
- Prior art keywords
- radical
- formula
- deoxy
- integer
- protecting groups
- Prior art date
Links
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
- C07H19/06—Pyrimidine radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicinal Preparation (AREA)
Abstract
La presente invención se refiere al procedimiento para preparar un compuesto de fórmula general (I) (ver figura 1) derivados de N4-(oxicarbonil sustituidos)-5'-desoxi-5-fuorocitidina, así como también hidratos o solvatos de dichos compuestos, donde: R1 es un radical hidrocarburo saturado o insaturado; R2 es un átomo de hidrógeno o un radical fácilmente hidrolizable en condiciones fisiológicas. El procedimiento comprende la reacción de un compuesto de fórmula general (II) (figura 2), donde R4 es un radical de protección de los hidroxilos con un compuesto: R1OCOC1, y si es necesario se eliminan los radicales de protección. Ejemplo no limitante: 5'-desoxi-5-fluoro-N4-[(1,1,2-trimetilpropoxi)carbonil]citidina. Los productos según la invención son de utilidad para el tratamiento de tumores.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP92121538 | 1992-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY23697A1 true UY23697A1 (es) | 1994-06-08 |
Family
ID=8210304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY23697A UY23697A1 (es) | 1992-12-18 | 1993-12-17 | Procedimiento para la preparacion de 5'-deoxi-5'-fluorcitidinas sustitutas del n-oxicarbonilo |
Country Status (41)
Country | Link |
---|---|
US (1) | US5472949A (es) |
EP (1) | EP0602454B1 (es) |
JP (1) | JP2501297B2 (es) |
KR (1) | KR100347218B1 (es) |
CN (1) | CN1035617C (es) |
AT (1) | ATE137244T1 (es) |
AU (1) | AU671491B2 (es) |
BG (1) | BG61485B1 (es) |
BR (1) | BR9305089A (es) |
CA (1) | CA2103324C (es) |
CZ (1) | CZ284788B6 (es) |
DE (1) | DE69302360T2 (es) |
DK (1) | DK0602454T3 (es) |
EE (1) | EE03086B1 (es) |
ES (1) | ES2086856T3 (es) |
FI (1) | FI112365B (es) |
GE (1) | GEP20074251B (es) |
GR (1) | GR3020286T3 (es) |
HK (1) | HK1005875A1 (es) |
HR (1) | HRP931430B1 (es) |
HU (2) | HU218291B (es) |
IL (1) | IL108000A0 (es) |
IS (1) | IS4108A (es) |
LT (1) | LT3115B (es) |
LV (1) | LV10625B (es) |
MY (1) | MY109282A (es) |
NO (1) | NO300066B1 (es) |
NZ (1) | NZ250414A (es) |
PH (1) | PH30168A (es) |
PL (1) | PL174100B1 (es) |
RO (1) | RO112619B1 (es) |
RU (2) | RU2458932C2 (es) |
SA (1) | SA93140409B1 (es) |
SI (1) | SI9300648B (es) |
SK (1) | SK281403B6 (es) |
SV (1) | SV1993000080A (es) |
TW (1) | TW372239B (es) |
UA (1) | UA39158C2 (es) |
UY (1) | UY23697A1 (es) |
YU (1) | YU49411B (es) |
ZA (1) | ZA939293B (es) |
Families Citing this family (86)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5476932A (en) * | 1994-08-26 | 1995-12-19 | Hoffmann-La Roche Inc. | Process for producing N4-acyl-5'-deoxy-5-fluorocytidine derivatives |
EP0882734B1 (en) * | 1997-06-02 | 2009-08-26 | F. Hoffmann-La Roche Ag | 5'-Deoxy-cytidine derivatives |
NZ330360A (en) * | 1997-06-02 | 1999-03-29 | Hoffmann La Roche | 5'-deoxy-cytidine derivatives, their manufacture and use as antitumoral agents |
US6005098A (en) * | 1998-02-06 | 1999-12-21 | Hoffmann-La Roche Inc. | 5'deoxycytidine derivatives |
IL141951A0 (en) * | 1998-09-25 | 2002-03-10 | Warner Lambert Co | Chemotherapy of cancer with acetyldinaline in combination with gemcitabine, capecitabine or cisplatin |
US20080113025A1 (en) * | 1998-11-02 | 2008-05-15 | Elan Pharma International Limited | Compositions comprising nanoparticulate naproxen and controlled release hydrocodone |
US20070122481A1 (en) * | 1998-11-02 | 2007-05-31 | Elan Corporation Plc | Modified Release Compositions Comprising a Fluorocytidine Derivative for the Treatment of Cancer |
CA2401191C (en) | 2000-02-28 | 2006-05-02 | Aventis Pharma S.A. | A composition comprising camptothecin and a pyrimidine derivative for the treatment of cancer |
AU2001246863A1 (en) * | 2000-04-11 | 2001-10-23 | Sayuri Yamada | Curcumin compositions |
KR100730768B1 (ko) * | 2000-08-09 | 2007-06-21 | 코오롱생명과학 주식회사 | 5'-데옥시-n-알킬옥시카르보닐-5-플루오로사이토신-5'-카르복실산 및 그 유도체와 이들의 제조방법 |
KR100631754B1 (ko) * | 2000-08-09 | 2006-10-09 | 주식회사 코오롱 | N-알킬옥시카르보닐-5-플루오로사이토신 유도체 및 그의제조방법 |
GB0113374D0 (en) * | 2001-06-04 | 2001-07-25 | Jerram Clare | Washing line umbrella |
WO2003057217A1 (en) * | 2002-01-14 | 2003-07-17 | Novartis Ag | Combinations comprising epothilones and anti-metabolites |
JP4625637B2 (ja) | 2002-02-22 | 2011-02-02 | シャイア エルエルシー | 活性物質送達系及び活性物質を保護し投与する方法 |
MXPA05003431A (es) * | 2002-11-15 | 2005-07-05 | Warner Lambert Co | Quimioterapia de combinacion. |
AU2003233586A1 (en) * | 2003-05-20 | 2005-01-21 | Aronex Pharmaceuticals, Inc. | Combination chemotherapy comprising capecitabine and a liposomal platinum complex |
JP2007511499A (ja) * | 2003-11-13 | 2007-05-10 | ファーマ・マール・エス・アー・ウー | コンビネーション |
KR20080046752A (ko) * | 2003-12-22 | 2008-05-27 | 에프. 호프만-라 로슈 아게 | 플루오로시티딘 유도체에 대한 방법 |
DK1848414T3 (da) | 2005-02-03 | 2011-07-25 | Gen Hospital Corp | Fremgangsmåde til behandling af gefitinib-resistent cancer |
AU2006228581A1 (en) * | 2005-04-01 | 2006-10-05 | F. Hoffmann-La Roche Ag | Method for administration of capecitabine |
CN101242822B (zh) | 2005-07-18 | 2011-08-24 | 彼帕科学公司 | 治疗卵巢癌的药物 |
JP2009501734A (ja) | 2005-07-21 | 2009-01-22 | ヌボ・リサーチ・インコーポレイテッド | 癌の治療方法 |
JP2009514870A (ja) | 2005-11-04 | 2009-04-09 | ワイス | mTORインヒビター、ハーセプチン、および/またはHKI−272の抗悪性腫瘍性組み合わせ |
LT2426129T (lt) | 2005-12-13 | 2017-02-10 | Incyte Holdings Corporation | Heteroarilu pakeisti pirolo[2,3-b]piridinai ir pirolo[2,3-b]pirimidinai kaip janus kinazės inhibitoriai |
US20100160442A1 (en) * | 2006-07-18 | 2010-06-24 | Ossovskaya Valeria S | Formulations for cancer treatment |
US20080085310A1 (en) * | 2006-10-06 | 2008-04-10 | Maria Oksana Bachynsky | Capecitabine rapidly disintegrating tablets |
CN100425617C (zh) * | 2006-10-31 | 2008-10-15 | 浙江海正药业股份有限公司 | 一种含氟嘧啶类化合物烷氧羰酰化的方法 |
ITMI20070435A1 (it) | 2007-03-05 | 2008-09-06 | Innovate Biotechnology Srl | 2',3'-di-o-acil-5-fluoronucleosidi |
KR20100015568A (ko) * | 2007-04-20 | 2010-02-12 | 닥터 레디스 레보러터리즈 리미티드 | 카페시타빈의 제조 방법 |
WO2008145403A1 (en) * | 2007-06-01 | 2008-12-04 | Synthon B.V. | Processes related to making capecitabine |
RS54878B1 (sr) | 2007-06-13 | 2016-10-31 | Incyte Holdings Corp | Kristalne soli inhibitora janus kinaze (r)-3-(4-(7h-pirolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il)-3-ciklopentilpropionitril |
US7842675B2 (en) * | 2007-09-15 | 2010-11-30 | Protia, Llc | Deuterium-enriched capecitabine |
WO2009042064A2 (en) | 2007-09-21 | 2009-04-02 | Nektar Therapeutics Al, Corporation | Oligomer-nucleoside phosphate conjugates |
US8022216B2 (en) | 2007-10-17 | 2011-09-20 | Wyeth Llc | Maleate salts of (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide and crystalline forms thereof |
KR101013312B1 (ko) * | 2007-11-19 | 2011-02-09 | 한미홀딩스 주식회사 | 카페시타빈의 제조방법 및 이에 사용되는 β-아노머가강화된 트리알킬카보네이트 화합물의 제조방법 |
AR064165A1 (es) | 2007-12-06 | 2009-03-18 | Richmond Sa Com Ind Y Financie | Un procedimiento para la preparacion de capecitabina e intermediarios utilizables en dicho procedimiento |
EP2225566A1 (en) * | 2008-01-03 | 2010-09-08 | Plus Chemicals S.A. | Process for the preparation of capecitabine |
US20090311335A1 (en) * | 2008-06-12 | 2009-12-17 | Scott Jenkins | Combination of a triptan and an nsaid |
KR101922096B1 (ko) | 2008-06-17 | 2018-11-27 | 와이어쓰 엘엘씨 | Hki-272 및 비노렐빈을 함유하는 항신생물성 조합물 |
DK2326329T3 (en) | 2008-08-04 | 2017-02-20 | Wyeth Llc | Antineoplastic combinations of 4-anilino-3-cyanoquinolines and capecitabine |
WO2010065586A2 (en) * | 2008-12-02 | 2010-06-10 | Dr. Reddy's Laboratories Ltd. | Preparation of capecitabine |
EP2393472B1 (en) * | 2008-12-05 | 2019-06-05 | NanoMed Holdings Pty Ltd | Amphiphile prodrugs |
HRP20230315T1 (hr) | 2009-04-06 | 2023-05-12 | Wyeth Llc | Režim liječenja raka dojke korištenjem neratiniba |
FR2945211A1 (fr) | 2009-05-06 | 2010-11-12 | Sanofi Aventis | Combinaison antitumorale comprenant la cabazitaxel et la capecitabine |
UA106078C2 (uk) | 2009-05-22 | 2014-07-25 | Інсайт Корпорейшн | 3-[4-(7H-ПІРОЛО[2,3-d]ПІРИМІДИН-4-ІЛ)-1H-ПІРАЗОЛ-1-ІЛ]ОКТАН- АБО ГЕПТАННІТРИЛ ЯК JAK-ІНГІБІТОРИ |
JP2012533618A (ja) * | 2009-07-23 | 2012-12-27 | サイノファーム タイワン リミテッド | フルオロシチジン誘導体の製造プロセス |
WO2011067588A1 (en) | 2009-12-04 | 2011-06-09 | Generics [Uk] Limited | Cyclic sulphinyl esters of cytidine |
WO2011104540A1 (en) * | 2010-02-24 | 2011-09-01 | Generics [Uk] Limited | One step process for the preparation of capecitabine |
MX364636B (es) | 2010-03-10 | 2019-05-03 | Incyte Corp | Derivados de piperidin-4-il azetidina como inhibidores de janus cinasa 1 (jak1). |
HUE040107T2 (hu) | 2010-03-12 | 2019-02-28 | Genzyme Corp | Kombinációs terápia mellrák kezelésére |
SI2574168T1 (sl) | 2010-05-21 | 2016-07-29 | Incyte Holdings Corporation | Topična formulacija zaviralca jak |
CN102260309B (zh) * | 2010-05-24 | 2014-10-22 | 重庆福安药业(集团)股份有限公司 | 一种高纯度卡培他滨的制备方法 |
SG190839A1 (en) | 2010-11-19 | 2013-07-31 | Incyte Corp | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
CN102558262A (zh) * | 2010-12-23 | 2012-07-11 | 天津泰普药品科技发展有限公司 | 一种高纯度卡培他滨的制备方法 |
AU2012273164B2 (en) | 2011-06-20 | 2015-05-28 | Incyte Holdings Corporation | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as JAK inhibitors |
CN102266303A (zh) * | 2011-07-07 | 2011-12-07 | 程雪翔 | 一种卡培他滨药用组合物及其制备方法 |
UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
CN102516338B (zh) * | 2011-12-09 | 2014-04-02 | 海南锦瑞制药股份有限公司 | 一种卡培他滨化合物、其药物组合物及其制备方法 |
TWI560195B (en) * | 2012-01-13 | 2016-12-01 | Pharmaessentia Corp | Novel synthesis of 5-deoxy-5'-fluorocytidine compounds |
JP2015537030A (ja) | 2012-11-15 | 2015-12-24 | インサイト・コーポレイションIncyte Corporation | ルキソリチニブの徐放性投薬形態 |
KR102366356B1 (ko) | 2013-03-06 | 2022-02-23 | 인사이트 홀딩스 코포레이션 | Jak 저해제를 제조하기 위한 방법 및 중간생성물 |
EP3721873A1 (en) | 2013-08-07 | 2020-10-14 | Incyte Corporation | Sustained release dosage forms for a jak1 inhibitor |
EA201690421A1 (ru) * | 2013-08-20 | 2016-06-30 | Инсайт Корпорейшн | Положительный эффект в форме увеличения продолжительности жизни у больных с солидными опухолями с повышенными уровнями c-реактивного белка |
EP2883959A1 (en) | 2013-12-13 | 2015-06-17 | Plasmia Biotech, S.L. | Enzymatic production of cytosinic nucleoside analogues |
CN103897006A (zh) * | 2013-12-18 | 2014-07-02 | 吉林修正药业新药开发有限公司 | 一种卡培他滨异构体的制备方法 |
WO2015191576A1 (en) | 2014-06-09 | 2015-12-17 | Lipomedix Pharmaceuticals Ltd. | Combination therapy comprising a liposomal prodrug of mitomycin c and radiotherapy |
CN104530164A (zh) * | 2014-12-31 | 2015-04-22 | 辰欣药业股份有限公司 | 一种卡培他滨的合成工艺 |
KR20160117060A (ko) | 2015-03-31 | 2016-10-10 | 이승주 | 유아용 탁자 |
CN105646625B (zh) * | 2015-12-29 | 2019-06-11 | 江苏吴中医药集团有限公司 | 一种卡培他滨的制备方法 |
US11034667B2 (en) | 2017-01-09 | 2021-06-15 | Shuttle Pharmaceuticals, Inc. | Selective histone deacetylase inhibitors for the treatment of human disease |
US11584733B2 (en) | 2017-01-09 | 2023-02-21 | Shuttle Pharmaceuticals, Inc. | Selective histone deacetylase inhibitors for the treatment of human disease |
TR201702500A2 (tr) * | 2017-02-20 | 2017-07-21 | Anadolu Ueniversitesi | Serani̇b-2?ni̇n akci̇ğer kanseri̇ ve meme kanseri̇ni̇n tedavi̇si̇nde kullanimi |
US10435429B2 (en) | 2017-10-03 | 2019-10-08 | Nucorion Pharmaceuticals, Inc. | 5-fluorouridine monophosphate cyclic triester compounds |
TW201924683A (zh) | 2017-12-08 | 2019-07-01 | 美商英塞特公司 | 用於治療骨髓增生性贅瘤的低劑量組合療法 |
EP3737376B1 (en) | 2018-01-09 | 2024-04-17 | Shuttle Pharmaceuticals, Inc. | Selective histone deacetylase inhibitors for the treatment of human diseases |
AU2019207626B2 (en) | 2018-01-10 | 2023-10-05 | Nucorion Pharmaceuticals, Inc. | Phosphor(n)amidatacetal and phosph(on)atalcetal compounds |
US11427550B2 (en) | 2018-01-19 | 2022-08-30 | Nucorion Pharmaceuticals, Inc. | 5-fluorouracil compounds |
WO2019143860A1 (en) * | 2018-01-19 | 2019-07-25 | Nucorion Pharmaceuticals, Inc. | 5-fluorouracil compounds |
AR114810A1 (es) | 2018-01-30 | 2020-10-21 | Incyte Corp | Procesos e intermedios para elaborar un inhibidor de jak |
CN113768934A (zh) | 2018-03-30 | 2021-12-10 | 因赛特公司 | 使用jak抑制剂治疗化脓性汗腺炎 |
AU2020207026A1 (en) | 2019-01-11 | 2021-07-29 | Lipomedix Pharmaceuticals Ltd. | Liposome composition comprising liposomal prodrug of mitomycin C and method of manufacture |
US12110311B2 (en) | 2019-07-17 | 2024-10-08 | Nucorion Pharmaceuticals, Inc. | Cyclic deoxyribonucleotide compounds |
CN115605492A (zh) | 2020-04-21 | 2023-01-13 | 配体制药股份有限公司(Us) | 核苷酸前药化合物 |
US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
WO2023177894A1 (en) | 2022-03-18 | 2023-09-21 | Ideaya Biosciences, Inc. | Combination therapy comprising a mat2a inhibitor and an antimetabolite agent |
EP4382093A1 (en) | 2022-12-05 | 2024-06-12 | a Fine House S.A. | Oral suspensions comprising capecitabine |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1135258A (en) * | 1979-06-15 | 1982-11-09 | Richard D'souza | Process for the preparation of 5'deoxy-5-fluorouridine |
ATE92499T1 (de) * | 1984-12-04 | 1993-08-15 | Lilly Co Eli | Tumorbehandlung bei saeugetieren. |
CA1327358C (en) * | 1987-11-17 | 1994-03-01 | Morio Fujiu | Fluoro cytidine derivatives |
-
1993
- 1993-11-12 AU AU50690/93A patent/AU671491B2/en not_active Expired
- 1993-11-15 TW TW082109533A patent/TW372239B/zh not_active IP Right Cessation
- 1993-11-17 CA CA002103324A patent/CA2103324C/en not_active Expired - Lifetime
- 1993-11-23 HR HR92121538.0A patent/HRP931430B1/xx not_active IP Right Cessation
- 1993-12-01 DK DK93119349.4T patent/DK0602454T3/da active
- 1993-12-01 AT AT93119349T patent/ATE137244T1/de active
- 1993-12-01 EP EP93119349A patent/EP0602454B1/en not_active Expired - Lifetime
- 1993-12-01 ES ES93119349T patent/ES2086856T3/es not_active Expired - Lifetime
- 1993-12-01 DE DE69302360T patent/DE69302360T2/de not_active Expired - Lifetime
- 1993-12-07 SA SA93140409A patent/SA93140409B1/ar unknown
- 1993-12-10 NZ NZ250414A patent/NZ250414A/en not_active IP Right Cessation
- 1993-12-10 HU HU9303525A patent/HU218291B/hu active Protection Beyond IP Right Term
- 1993-12-10 ZA ZA939293A patent/ZA939293B/xx unknown
- 1993-12-10 SI SI9300648A patent/SI9300648B/sl unknown
- 1993-12-13 CZ CZ932731A patent/CZ284788B6/cs not_active IP Right Cessation
- 1993-12-13 IL IL10800093A patent/IL108000A0/xx not_active IP Right Cessation
- 1993-12-14 US US08/167,392 patent/US5472949A/en not_active Expired - Lifetime
- 1993-12-14 FI FI935616A patent/FI112365B/fi not_active IP Right Cessation
- 1993-12-15 PH PH47455A patent/PH30168A/en unknown
- 1993-12-15 RO RO93-01706A patent/RO112619B1/ro unknown
- 1993-12-15 YU YU77993A patent/YU49411B/sh unknown
- 1993-12-16 MY MYPI93002726A patent/MY109282A/en unknown
- 1993-12-16 BG BG98304A patent/BG61485B1/bg unknown
- 1993-12-16 BR BR9305089A patent/BR9305089A/pt not_active Application Discontinuation
- 1993-12-16 KR KR1019930027962A patent/KR100347218B1/ko not_active IP Right Cessation
- 1993-12-16 RU RU93056196/04A patent/RU2458932C2/ru active Protection Beyond IP Right Term
- 1993-12-16 JP JP5342812A patent/JP2501297B2/ja not_active Expired - Fee Related
- 1993-12-16 RU RU2012134029/04A patent/RU2493162C1/ru not_active IP Right Cessation
- 1993-12-17 NO NO934671A patent/NO300066B1/no not_active IP Right Cessation
- 1993-12-17 SK SK1444-93A patent/SK281403B6/sk not_active IP Right Cessation
- 1993-12-17 PL PL93301541A patent/PL174100B1/pl unknown
- 1993-12-17 UY UY23697A patent/UY23697A1/es not_active IP Right Cessation
- 1993-12-17 UA UA93004687A patent/UA39158C2/uk unknown
- 1993-12-17 IS IS4108A patent/IS4108A/is unknown
- 1993-12-17 CN CN93112838A patent/CN1035617C/zh not_active Expired - Lifetime
- 1993-12-17 SV SV1993000080A patent/SV1993000080A/es not_active Application Discontinuation
- 1993-12-17 LT LTIP1627A patent/LT3115B/lt not_active IP Right Cessation
- 1993-12-17 LV LVP-93-1347A patent/LV10625B/en unknown
-
1994
- 1994-11-18 EE EE9400154A patent/EE03086B1/xx not_active IP Right Cessation
-
1995
- 1995-06-19 HU HU95P/P00255P patent/HU211965A9/hu unknown
-
1996
- 1996-06-19 GR GR960401668T patent/GR3020286T3/el unknown
-
1998
- 1998-06-05 HK HK98105008A patent/HK1005875A1/xx not_active IP Right Cessation
-
2006
- 2006-07-17 GE GEAP20069525A patent/GEP20074251B/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UY23697A1 (es) | Procedimiento para la preparacion de 5'-deoxi-5'-fluorcitidinas sustitutas del n-oxicarbonilo | |
RU93056196A (ru) | N-карбонилзамещенные 5'-дезокси-5-фторцитидина | |
NZ231983A (en) | Substituted 1,3-diazoles and 1,2,4-triazoles; fungicidal compositions, methods for preparation and combating fungal disease | |
EP0368429A3 (en) | Fluor-substituted benzene derivatives | |
CA2065978A1 (en) | Organosilicon compounds containing (meth)acryloxy groups, their preparation and use | |
FR2702480B1 (fr) | Nouveaux dérivés de l'érythromycine, leur procédé de préparation et leur application comme médicaments. | |
HU9202367D0 (en) | Preparative for reducing blood pressure | |
EP0401715A3 (en) | Aminoketone compounds |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
VENC | Patent expired |
Effective date: 20131116 |