CN1020194C - 二氟核苷衍生物的制备方法 - Google Patents
二氟核苷衍生物的制备方法 Download PDFInfo
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- CN1020194C CN1020194C CN85109409A CN85109409A CN1020194C CN 1020194 C CN1020194 C CN 1020194C CN 85109409 A CN85109409 A CN 85109409A CN 85109409 A CN85109409 A CN 85109409A CN 1020194 C CN1020194 C CN 1020194C
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- deoxidation
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- difluoro
- amino
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- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- NMXNYNNDVPJWDP-UHFFFAOYSA-N trifluorosilyl methanesulfonate Chemical compound CS(=O)(=O)O[Si](F)(F)F NMXNYNNDVPJWDP-UHFFFAOYSA-N 0.000 description 1
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
- MDTPTXSNPBAUHX-UHFFFAOYSA-M trimethylsulfanium;hydroxide Chemical compound [OH-].C[S+](C)C MDTPTXSNPBAUHX-UHFFFAOYSA-M 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 229960004528 vincristine Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 125000000969 xylosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)CO1)* 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- FBTUMDXHSRTGRV-ALTNURHMSA-N zorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(\C)=N\NC(=O)C=1C=CC=CC=1)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 FBTUMDXHSRTGRV-ALTNURHMSA-N 0.000 description 1
- 229960000641 zorubicin Drugs 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
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67778384A | 1984-12-04 | 1984-12-04 | |
| US677,783 | 1984-12-04 | ||
| US78641985A | 1985-10-10 | 1985-10-10 | |
| US786,419 | 1985-10-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN85109409A CN85109409A (zh) | 1986-08-27 |
| CN1020194C true CN1020194C (zh) | 1993-03-31 |
Family
ID=27101898
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN85109409A Expired - Lifetime CN1020194C (zh) | 1984-12-04 | 1985-12-03 | 二氟核苷衍生物的制备方法 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US5464826A (enExample) |
| EP (1) | EP0184365B1 (enExample) |
| JP (1) | JPH0637394B2 (enExample) |
| KR (2) | KR890003439B1 (enExample) |
| CN (1) | CN1020194C (enExample) |
| AT (1) | ATE92499T1 (enExample) |
| AU (1) | AU581269B2 (enExample) |
| CA (1) | CA1264738A (enExample) |
| CY (1) | CY1806A (enExample) |
| DE (1) | DE3587500T2 (enExample) |
| DK (1) | DK162965C (enExample) |
| EG (1) | EG17765A (enExample) |
| ES (1) | ES8801546A1 (enExample) |
| GR (1) | GR852858B (enExample) |
| HK (1) | HK113693A (enExample) |
| HU (1) | HU194273B (enExample) |
| IE (1) | IE60328B1 (enExample) |
| IL (1) | IL77133A (enExample) |
| NZ (1) | NZ214364A (enExample) |
| PH (1) | PH23172A (enExample) |
| PT (1) | PT81559B (enExample) |
Families Citing this family (156)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1269659A (en) * | 1984-08-06 | 1990-05-29 | Brigham Young University | Method for the production of 2'-deoxyadenosine compounds |
| CA1295998C (en) * | 1985-07-29 | 1992-02-18 | Sai P. Sunkara | Nucleosides and their use as antineoplastic agents |
| US4994558A (en) * | 1986-12-24 | 1991-02-19 | Eli Lilly And Company | Immunoglobulin conjugates |
| US4814438A (en) * | 1986-12-24 | 1989-03-21 | Eli Lilly And Company | Immunoglobulin conjugates of 2',2'-difluronucleosides |
| IL84842A0 (en) * | 1986-12-24 | 1988-06-30 | Lilly Co Eli | Immunoglobulin conjugates |
| US4965374A (en) * | 1987-08-28 | 1990-10-23 | Eli Lilly And Company | Process for and intermediates of 2',2'-difluoronucleosides |
| US5223608A (en) * | 1987-08-28 | 1993-06-29 | Eli Lilly And Company | Process for and intermediates of 2',2'-difluoronucleosides |
| IL87517A (en) * | 1987-08-28 | 1993-05-13 | Lilly Co Eli | Process for preparing an enantiomeric mixture of erythro and threo lactones |
| US4914028A (en) * | 1988-02-10 | 1990-04-03 | Eli Lilly And Company | Method of preparing beta-2',2'-difluoronucleosides |
| IL89258A0 (en) * | 1988-02-16 | 1989-09-10 | Lilly Co Eli | 2',3'-dideoxy-2',2'-difluoro-nucleosides |
| US5644043A (en) * | 1988-02-16 | 1997-07-01 | Eli Lilly And Company | 2',3'-dideoxy-2',2'-difluoronucleosides and intermediates |
| US4996308A (en) * | 1988-03-25 | 1991-02-26 | Merrell Dow Pharmaceuticals Inc. | Derivatives with unsaturated substitutions for the 5'-hydroxymethyl group |
| JPH0232093A (ja) * | 1988-06-08 | 1990-02-01 | Merrell Dow Pharmaceut Inc | 抗レトロウィルスジフルオロ化ヌクレオシド類 |
| CA2004695C (en) * | 1988-12-12 | 1999-08-10 | Rosanne Bonjouklian | Phospholipid nucleosides |
| AU4134793A (en) * | 1992-06-22 | 1993-12-23 | Eli Lilly And Company | 2'-deoxy-2',2'-difluoro(2,6,8-substituted) purine nucleosides having anti-viral and anti-cancer activity and intermediates |
| YU43193A (sh) * | 1992-06-22 | 1997-01-08 | Eli Lilly And Company | 2'-deoksi-2',2'-difluoro(4-supstituisani)pirimidinski nukleozidi antivirusnog i antikancerogenog dejstva i međuproizvodi |
| AU671491B2 (en) * | 1992-12-18 | 1996-08-29 | F. Hoffmann-La Roche Ag | N-oxycarbonyl substituted 5'-deoxy-5-fluorcytidines |
| US5424416A (en) * | 1993-08-25 | 1995-06-13 | Eli Lilly And Company | Process for preparation of 2-deoxy-2,2-difluoro-D-ribofuranosyl-3,5-hydroxy protected-1-alkyl and aryl sulfonates and their use in preparation of 2',2'-difluoro-2'-deoxy nucleosides |
| US5480992A (en) * | 1993-09-16 | 1996-01-02 | Eli Lilly And Company | Anomeric fluororibosyl amines |
| US5637688A (en) * | 1994-12-13 | 1997-06-10 | Eli Lilly And Company | Process for preparing 1-(2'-deoxy-2'-difluoro-d-ribofuranosyl)-4-aminopyrimidin-2-one hydrochloride |
| US5559222A (en) * | 1995-02-03 | 1996-09-24 | Eli Lilly And Company | Preparation of 1-(2'-deoxy-2',2'-difluoro-D-ribo-pentofuranosyl)-cytosine from 2-deoxy-2,2-difluoro-β-D-ribo-pentopyranose |
| ATE236188T1 (de) * | 1997-01-24 | 2003-04-15 | Conpharma As | Gemcitabin-derivate |
| CA2284263A1 (en) * | 1997-03-24 | 1998-10-01 | Eli Lilly And Company | Difluoronucleoside phosphonic acids and derivatives thereof |
| TW466112B (en) * | 1998-04-14 | 2001-12-01 | Lilly Co Eli | Novel use of 2'-deoxy-2',2'-difluorocytidine for immunosuppressive therapy and pharmaceutical composition comprising the same |
| US6326507B1 (en) * | 1998-06-19 | 2001-12-04 | Trustees Of Dartmouth College | Therapeutic compounds and methods of use |
| US20050281821A1 (en) * | 1999-01-06 | 2005-12-22 | Flavia Pernasetti | Method and composition for angiogenesis inhibition |
| ATE324888T1 (de) * | 1999-06-14 | 2006-06-15 | Cancer Rec Tech Ltd | Krebstherapie |
| AU2001282717A1 (en) * | 2000-07-28 | 2002-02-13 | Cancer Research Technology Limited | Cancer treatment by combination therapy |
| GB0019124D0 (en) * | 2000-08-03 | 2000-09-27 | Pfizer | Novel process |
| EP1506962B1 (en) * | 2000-10-20 | 2008-07-02 | Eisai R&D Management Co., Ltd. | Nitrogen-containing aromatic heterocycles |
| US20050250854A1 (en) * | 2000-11-03 | 2005-11-10 | Amgen Inc. | Combination therapy using pentafluorobenzenesulfonamides and antineoplastic agents |
| US6822001B2 (en) * | 2000-11-03 | 2004-11-23 | Tularik Inc. | Combination therapy using pentafluorobenzenesulfonamides and antineoplastic agents |
| US7435755B2 (en) | 2000-11-28 | 2008-10-14 | The Trustees Of Dartmouth College | CDDO-compounds and combination therapies thereof |
| GB0121285D0 (en) * | 2001-09-03 | 2001-10-24 | Cancer Res Ventures Ltd | Anti-cancer combinations |
| US20030139373A1 (en) * | 2001-11-20 | 2003-07-24 | Breimer Lars Holger | Method for cancer therapy |
| US7365167B2 (en) * | 2001-11-26 | 2008-04-29 | Cell Matrix, Inc. | Humanized collagen antibodies and related methods |
| US7390885B2 (en) * | 2001-11-26 | 2008-06-24 | Cell Matrix, Inc. | Humanized collagen antibodies and related methods |
| CN1615136A (zh) * | 2002-01-14 | 2005-05-11 | 诺瓦提斯公司 | 包含埃坡霉素和抗代谢物的组合 |
| US7176237B2 (en) * | 2002-01-15 | 2007-02-13 | The Trustees Of Dartmouth College | Tricyclic-bis-enone derivatives and methods of use thereof |
| MXPA04007876A (es) * | 2002-02-14 | 2005-06-20 | Pharmasset Ltd | Analogos de nucleosido fluorado modificados. |
| GB2386836B (en) * | 2002-03-22 | 2006-07-26 | Cancer Res Ventures Ltd | Anti-cancer combinations |
| GB0223380D0 (en) * | 2002-10-09 | 2002-11-13 | Astrazeneca Ab | Combination therapy |
| GB2394658A (en) * | 2002-11-01 | 2004-05-05 | Cancer Rec Tech Ltd | Oral anti-cancer composition |
| EP1604665B1 (en) * | 2003-03-10 | 2011-05-11 | Eisai R&D Management Co., Ltd. | C-kit kinase inhibitor |
| WO2004105747A1 (en) * | 2003-05-20 | 2004-12-09 | Aronex Pharmaceuticals, Inc | Combination chemotherapy comprising capecitabine and a liposomal platinum complex |
| CA2525952A1 (en) * | 2003-05-20 | 2004-12-09 | Aronex Pharmaceuticals, Inc. | Combination chemotherapy comprising gemcitabine and a liposomal platinum complex |
| DE10323279A1 (de) * | 2003-05-21 | 2004-12-16 | Stada Arzneimittel Ag | Gebrauchsfertige Gemcitabin-Lösungen |
| GB0321999D0 (en) * | 2003-09-19 | 2003-10-22 | Cancer Rec Tech Ltd | Anti-cancer combinations |
| JP4303726B2 (ja) * | 2003-11-11 | 2009-07-29 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ウレア誘導体およびその製造方法 |
| KR20120117943A (ko) * | 2004-02-06 | 2012-10-24 | 쓰레솔드 파마슈티컬스, 인코포레이티드 | 항암 치료 방법 |
| PL1913947T3 (pl) * | 2004-04-22 | 2012-05-31 | Lilly Co Eli | Terapia skojarzona do leczenia raka |
| KR100578616B1 (ko) * | 2004-07-23 | 2006-05-10 | 한미약품 주식회사 | D-에리트로-2,2-다이플루오로-2-데옥시-1-옥소라이보스화합물의 제조방법 |
| ATE428421T1 (de) | 2004-09-17 | 2009-05-15 | Eisai R&D Man Co Ltd | Medizinische zusammensetzung mit verbesserter stabilität und reduzierten gelierungseigenschaften |
| US20060089329A1 (en) * | 2004-10-22 | 2006-04-27 | Edgar Schridde | Ready-to-use gemcitabine solution concentrates |
| US20060089328A1 (en) * | 2004-10-22 | 2006-04-27 | Edgar Schridde | Ready-to-use gemcitabine solutions |
| US7563570B2 (en) * | 2004-10-29 | 2009-07-21 | Pangaea Biotech | Method of determining a chemotherapeutic regimen for non small cell lung cancer based on BRCA1 expression |
| CN101076535A (zh) * | 2004-12-08 | 2007-11-21 | 西科尔公司 | 二氟核苷及其制备方法 |
| DE102004063347A1 (de) * | 2004-12-23 | 2006-07-13 | Stada Arzneimittel Ag | Gebrauchsfertige Gemcitabinlösungen und Gemcitabinlösungskonzentrate |
| TW200637870A (en) | 2005-01-31 | 2006-11-01 | Taiho Pharmaceutical Co Ltd | Novel pyrimidine nucleoside compound and salt thereof |
| DE602005019626D1 (de) * | 2005-03-04 | 2010-04-08 | Fresenius Kabi Oncology Ltd | Zwischenprodukt und verfahren zur herstellung von an beta-anomeren angereicherten 2'-desoxy,2',2'-difluor-d-ribufuranosylnukleosiden |
| TWI368621B (en) | 2005-05-02 | 2012-07-21 | Leyoung Biotech Co Ltd | Stereoselective synthesis of β-nucleosides |
| JP5066446B2 (ja) * | 2005-08-01 | 2012-11-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 血管新生阻害物質の効果を予測する方法 |
| EP2281901B1 (en) | 2005-08-02 | 2013-11-27 | Eisai R&D Management Co., Ltd. | Anti-tumour pharmaceutical composition with angiogenesis inhibitors |
| EP1928497A2 (en) * | 2005-08-24 | 2008-06-11 | Cell-Matrix, Inc. | Combination therapies for inhibiting integrin-extracellular matrix interactions |
| BRPI0614965A2 (pt) * | 2005-08-26 | 2016-09-13 | Antisoma Plc | método para a modulação de crescimento neoplástico, usos de um composto ou, um sal, éster ou pró-droga farmaceuticamente aceitável do mesmo, de um aglutinante do fator de crescimento endotelial vascular, e de um taxano, formulação farmacêutica, e, kit |
| CA2627598C (en) | 2005-11-07 | 2013-06-25 | Eisai R & D Management Co., Ltd. | Use of combination of anti-angiogenic substance and c-kit kinase inhibitor |
| WO2007061130A1 (ja) * | 2005-11-22 | 2007-05-31 | Eisai R & D Management Co., Ltd. | 多発性骨髄腫に対する抗腫瘍剤 |
| WO2007136103A1 (ja) | 2006-05-18 | 2007-11-29 | Eisai R & D Management Co., Ltd. | 甲状腺癌に対する抗腫瘍剤 |
| EP2044939A1 (en) * | 2006-06-29 | 2009-04-08 | Eisai R&D Management Co., Ltd. | Therapeutic agent for liver fibrosis |
| TW200817426A (en) | 2006-07-21 | 2008-04-16 | Taiho Pharmaceutical Co Ltd | 2'-cyanopyrimidine nucleoside compound |
| BRPI0714705A2 (pt) | 2006-07-24 | 2013-05-14 | Taiho Pharmaceutical Co Ltd | derivado de 3'-etinilcitidina |
| KR101472600B1 (ko) * | 2006-08-28 | 2014-12-15 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 미분화형 위암에 대한 항종양제 |
| US7714012B2 (en) * | 2006-11-17 | 2010-05-11 | Trustees Of Dartmouth University | Synthesis and biological activities of new tricyclic-bis-enones (TBEs) |
| US8299046B2 (en) * | 2006-11-17 | 2012-10-30 | Trustees Of Dartmouth College | Synthetic triterpenoids and tricyclic-bis-enones for use in stimulating bone and cartilage growth |
| US8921340B2 (en) | 2006-11-17 | 2014-12-30 | Trustees Of Dartmouth College | Methods for using synthetic triterpenoids in the treatment of bone or cartilage diseases or conditions |
| EP2116246A1 (en) | 2007-01-19 | 2009-11-11 | Eisai R&D Management Co., Ltd. | Composition for treatment of pancreatic cancer |
| KR101445892B1 (ko) * | 2007-01-29 | 2014-09-29 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 미분화형 위암 치료용 조성물 |
| US8765690B2 (en) * | 2007-04-05 | 2014-07-01 | Threshold Pharmaceuticals, Inc. | Treatment of cancer with glufosfamide in patients not receiving insulin therapy |
| US20090048205A1 (en) * | 2007-08-15 | 2009-02-19 | Colin Meyer | Combination therapy with synthetic triterpenoids and gemcitabine |
| JO2778B1 (en) | 2007-10-16 | 2014-03-15 | ايساي انك | Certain Compounds, Compositions and Methods |
| WO2009061894A1 (en) | 2007-11-06 | 2009-05-14 | Pharmaessentia Corporation | Novel synthesis of beta-nucleosides |
| AR069198A1 (es) | 2007-11-07 | 2010-01-06 | Schering Corp | Derivados de ribosil pirimidinas moduladores de quinasas de control chk1,y composiciones farmaceuticas que los comprenden utiles en el tratamiento del cancer. |
| KR101513326B1 (ko) | 2007-11-09 | 2015-04-17 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 혈관 신생 저해 물질과 항종양성 백금 착물의 병용 |
| SG187464A1 (en) * | 2008-01-11 | 2013-02-28 | Reata Pharmaceuticals Inc | Synthetic triterpenoids and methods of use in the treatment of disease |
| CN102036962B (zh) * | 2008-01-29 | 2013-08-07 | 卫材R&D管理有限公司 | 血管生成抑制剂和紫杉烷的组合使用 |
| BRPI0911208B1 (pt) | 2008-04-18 | 2021-05-25 | Reata Pharmaceuticals, Inc | Compostos moduladores inflamatórios antioxidantes, seu uso, e composição farmacêutica |
| US8071632B2 (en) * | 2008-04-18 | 2011-12-06 | Reata Pharmaceuticals, Inc. | Antioxidant inflammation modulators: novel derivatives of oleanolic acid |
| TW201006474A (en) * | 2008-04-18 | 2010-02-16 | Reata Pharmaceuticals Inc | Natural products including an anti-flammatory pharmacore and methods of use |
| HRP20182060T1 (hr) | 2008-04-18 | 2019-03-22 | Reata Pharmaceuticals, Inc. | Antioksidantni modulatori upale: derivati oleanolne kiseline s amino i drugim modifikacijama na c-17 |
| ES2613964T3 (es) | 2008-04-18 | 2017-05-29 | Reata Pharmaceuticals, Inc. | Moduladores de inflamación antioxidantes: Derivados de ácido oleanólico homologado C-17 |
| US9198893B2 (en) | 2008-05-22 | 2015-12-01 | Galera Labs, Llc | Combination antitumor therapy |
| WO2010011782A1 (en) * | 2008-07-22 | 2010-01-28 | Trustees Of Dartmouth College | Monocyclic cyanoenones and methods of use thereof |
| US20110207680A1 (en) * | 2008-08-13 | 2011-08-25 | Curd John G | Administration of Glufosfamide For The Treatment of Cancer |
| US8329665B2 (en) * | 2009-04-06 | 2012-12-11 | Eisai Inc. | Compositions and methods for treating cancer |
| US8609631B2 (en) | 2009-04-06 | 2013-12-17 | Eisai Inc. | Compositions and methods for treating cancer |
| JP5730854B2 (ja) * | 2009-04-06 | 2015-06-10 | 大塚製薬株式会社 | デシタビンとシチジンデアミナーゼ阻害剤との組合せ、およびがんの治療におけるその使用 |
| AR076262A1 (es) * | 2009-04-06 | 2011-06-01 | Eisai Inc | Derivados heterociclicos de diazepin-2-ona, composiciones farmaceuticas y sus usos en el tratamiento del cancer |
| GB0907551D0 (en) | 2009-05-01 | 2009-06-10 | Univ Dundee | Treatment or prophylaxis of proliferative conditions |
| ES2564797T3 (es) | 2009-08-19 | 2016-03-29 | Eisai R&D Management Co., Ltd. | Composición farmacéutica con contenido en un derivado de quinolina |
| EP2473041B1 (en) | 2009-09-04 | 2018-03-07 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| WO2011101644A1 (en) | 2010-02-18 | 2011-08-25 | Centro Nacional De Investigaciones Oncologicas (Cnio) | Triazolo [4, 5 - b] pyridin derivatives |
| ES2575160T3 (es) | 2010-03-15 | 2016-06-24 | The Board Of Trustees Of The University Of Illinois | Inhibidores de las interacciones que unen la subunidad alfa de la beta integrina-proteína G |
| WO2011143590A1 (en) | 2010-05-14 | 2011-11-17 | Cornerstone Pharmaceuticals, Inc. | Combination therapy compositions and methods using lipoic acid derivatives and an anti-proliferation agent |
| WO2011143593A1 (en) | 2010-05-14 | 2011-11-17 | Cornerstone Pharmaceuticals, Inc. | Conjugates of a lipoic acid derivative and anti-proliferation agent and medical uses thereof |
| US9192680B2 (en) | 2010-06-01 | 2015-11-24 | Aposense Ltd. | Pharmaceutical compounds |
| US8530444B2 (en) * | 2010-06-01 | 2013-09-10 | Aposense Ltd. | Pharmaceutical compounds |
| KR101677790B1 (ko) | 2010-06-25 | 2016-11-18 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 키나제 저해 작용을 갖는 화합물의 병용에 의한 항종양제 |
| WO2012069972A1 (en) | 2010-11-19 | 2012-05-31 | Piramal Life Sciences Limited | A pharmaceutical combination for the treatment of breast cancer |
| WO2012087943A2 (en) | 2010-12-20 | 2012-06-28 | The Regents Of The University Of Michigan | Inhibitors of the epidermal growth factor receptor-heat shock protein 90 binding interaction |
| TW201242597A (en) | 2011-03-14 | 2012-11-01 | Piramal Life Sciences Ltd | A synergistic pharmaceutical combination for the treatment of pancreatic cancer |
| CN103857395A (zh) | 2011-04-01 | 2014-06-11 | 基因泰克公司 | Akt抑制剂化合物和阿比特龙的组合及使用方法 |
| KR101762999B1 (ko) | 2011-04-18 | 2017-07-28 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 종양 치료제 |
| ES2705950T3 (es) | 2011-06-03 | 2019-03-27 | Eisai R&D Man Co Ltd | Biomarcadores para predecir y valorar la capacidad de respuesta de sujetos con cáncer de tiroides y de riñón a compuestos de lenvatinib |
| LT2833905T (lt) | 2012-04-04 | 2018-07-10 | Halozyme, Inc. | Derinių terapija su hialuronidaze ir į naviką nukreiptu taksanu |
| US8921419B2 (en) | 2012-05-08 | 2014-12-30 | Trustees Of Dartmouth College | Triterpenoids and compositions containing the same |
| EP2858666B1 (en) | 2012-06-08 | 2019-09-04 | F.Hoffmann-La Roche Ag | Mutant selectivity and combinations of a phosphoinositide 3 kinase inhibitor compound and chemotherapeutic agents for the treatment of cancer |
| JP6148729B2 (ja) | 2012-07-04 | 2017-06-14 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 共有結合している抗原−抗体結合体 |
| EP2711008A1 (en) | 2012-09-19 | 2014-03-26 | Institut Univ. de Ciència i Tecnologia, S.A. | N6,N6-dimethyladenosine for use in treating or preventing primary and metastatic breast cancer |
| EP2711007A1 (en) | 2012-09-19 | 2014-03-26 | Institut Univ. de Ciència i Tecnologia, S.A. | 4-Aminopyrazolo[3,4-d]pyrimidine for use in treating or preventing primary and metastatic breast and prostate cancer |
| EP2711009A1 (en) | 2012-09-19 | 2014-03-26 | Institut Univ. de Ciència i Tecnologia, S.A. | Compounds for use in treating or preventing primary and metastatic breast and prostate cancer |
| US9757432B2 (en) | 2012-11-14 | 2017-09-12 | Ohio State Innovation Foundation | Materials and methods useful for treating glioblastorna |
| BR112015009004A8 (pt) | 2012-12-21 | 2021-07-20 | Eisai R&D Man Co Ltd | forma amorfa de derivado de quinolina e método de produção da mesma |
| SG11201509278XA (en) | 2013-05-14 | 2015-12-30 | Eisai R&D Man Co Ltd | Biomarkers for predicting and assessing responsiveness of endometrial cancer subjects to lenvatinib compounds |
| WO2015191563A1 (en) | 2014-06-09 | 2015-12-17 | Lipomedix Pharmaceuticals Ltd. | Combination chemotherapy comprising a liposomal prodrug of mitomycin c |
| RU2705299C2 (ru) | 2014-06-26 | 2019-11-06 | Ф. Хоффманн-Ля Рош Аг | Антитела против 5-бром-2'-дезоксиуридина и способы применения |
| SMT202200367T1 (it) | 2014-08-28 | 2022-11-18 | Eisai R&D Man Co Ltd | Derivato di chinolina a elevata purezza e metodo per la produzione dello stesso |
| WO2016078160A1 (zh) * | 2014-11-17 | 2016-05-26 | 常州方圆制药有限公司 | 胞苷衍生物及其应用 |
| JP7264592B2 (ja) | 2015-01-26 | 2023-04-25 | ザ ユニバーシティー オブ シカゴ | IL13Rα2結合剤及び癌治療におけるその使用 |
| CN107835820B (zh) | 2015-01-26 | 2021-10-15 | 芝加哥大学 | 识别癌症特异性IL13Rα2的CAR T细胞 |
| DK3263106T3 (da) | 2015-02-25 | 2024-01-08 | Eisai R&D Man Co Ltd | Fremgangsmåde til undertrykkelse af bitterhed af quinolinderivat |
| KR20250020678A (ko) | 2015-03-04 | 2025-02-11 | 머크 샤프 앤드 돔 엘엘씨 | 암을 치료하기 위한 pd-1 길항제 및 vegfr/fgfr/ret 티로신 키나제 억제제의 조합 |
| ES2886107T3 (es) | 2015-06-16 | 2021-12-16 | Prism Biolab Co Ltd | Antineoplásico |
| CN106317147B (zh) * | 2015-07-06 | 2018-11-27 | 扬州硒瑞恩生物医药科技有限公司 | 核苷类化合物及其制备方法 |
| CA2994925C (en) | 2015-08-20 | 2023-08-29 | Eisai R&D Management Co., Ltd. | Tumor therapeutic agent |
| US20200306254A1 (en) | 2016-06-29 | 2020-10-01 | Eli Lilly And Company | Combination of erk1/2 inhibitor compound with gemcitabine or with gemcitabine and nab-paclitaxel for use in treatment of pancreatic cancer |
| US20180169120A1 (en) | 2016-11-21 | 2018-06-21 | Bexion Pharmaceuticals, Inc. | Combination therapy including sapc-dops for the treatment of pancreatic cancer |
| US11584733B2 (en) | 2017-01-09 | 2023-02-21 | Shuttle Pharmaceuticals, Inc. | Selective histone deacetylase inhibitors for the treatment of human disease |
| ES2914123T3 (es) | 2017-01-09 | 2022-06-07 | Shuttle Pharmaceuticals Inc | Inhibidores selectivos de la histona desacetilasa para el tratamiento de una enfermedad humana |
| RU2750539C2 (ru) | 2017-02-08 | 2021-06-29 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Фармацевтическая композиция для лечения опухоли |
| CA3061888A1 (en) | 2017-05-16 | 2018-11-22 | Eisai R&D Management Co., Ltd. | Treatment of hepatocellular carcinoma |
| MX2020001451A (es) | 2017-08-07 | 2020-08-06 | Amgen Inc | Tratamiento de cancer de mama triple negativo o cancer colorrectal con metastasis hepaticas con un anticuerpo anti-pd-l1 y un virus oncolitico. |
| HUE067603T2 (hu) | 2017-09-18 | 2024-10-28 | Univ California | Klaudin-6 antitestek és rákkezelési eljárások |
| US12480162B2 (en) | 2017-10-06 | 2025-11-25 | The Regents Of The University Of Michigan | Detection of metastatic disease and related methods |
| WO2019139921A1 (en) | 2018-01-09 | 2019-07-18 | Shuttle Pharmaceuticals, Inc. | Selective histone deacetylase inhibitors for the treatment of human disease |
| KR20200118827A (ko) | 2018-02-02 | 2020-10-16 | 마베릭스 온콜로지, 잉크. | 젬시타빈 모노포스페이트의 소분자 약물 컨쥬게이트 |
| US20190351031A1 (en) | 2018-05-16 | 2019-11-21 | Halozyme, Inc. | Methods of selecting subjects for combination cancer therapy with a polymer-conjugated soluble ph20 |
| MA53140A (fr) | 2018-06-29 | 2021-05-19 | Shanghai Changchengyiyaokeji Company Ltd | Promédicaments contenant du phosphore de gemcitabine |
| EP3853224A1 (en) | 2018-09-20 | 2021-07-28 | Basilea Pharmaceutica International AG | Pharmaceutical combinations for use in the treatment of neoplastic diseases |
| EP3908261A1 (en) | 2019-01-11 | 2021-11-17 | Lipomedix Pharmaceuticals Ltd. | Liposome composition comprising liposomal prodrug of mitomycin c and method of manufacture |
| ES3017207T3 (en) | 2019-03-20 | 2025-05-12 | Univ California | Claudin-6 antibodies and drug conjugates |
| WO2020191344A1 (en) | 2019-03-20 | 2020-09-24 | The Regents Of The University Of California | Claudin-6 bispecific antibodies |
| MX2021013271A (es) | 2019-04-30 | 2022-01-06 | Inst De Medicina Molecular Joao Lobo Antunes | Inhibidores de la via rank en combinacion con inhibidores de cdk. |
| US20220396794A1 (en) | 2019-06-04 | 2022-12-15 | Apterna Limited | APTAMERS AGAINST TRANSFERRIN RECEPTOR (TfR) |
| JP7763666B2 (ja) | 2019-06-24 | 2025-11-04 | アムジェン インコーポレイテッド | 癌治療のためのSIRPγの阻害 |
| CN110684062B (zh) * | 2019-10-18 | 2022-12-13 | 大连大学 | 一种治疗非小细胞肺癌的药物及其制备方法 |
| GB202019692D0 (en) | 2020-12-14 | 2021-01-27 | Apterna Ltd | Aptamer-sirna fusions |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE147774C (enExample) * | ||||
| US3705147A (en) * | 1969-08-22 | 1972-12-05 | Univ Utah | 3-deazapyrimidine nucleosides and method of preparation thereof |
| US3870700A (en) * | 1973-05-29 | 1975-03-11 | Miles Lab | 2-halogeno-2-deoxy-5-(substituted)uridines |
| JPS5136467A (en) * | 1974-09-20 | 1976-03-27 | Tanabe Seiyaku Co | 11 beetaa dd2** harogeno 2** deokishiribofuranoshirurashirujudotai no seiho |
| DE2628202A1 (de) * | 1976-06-23 | 1977-12-29 | Max Planck Gesellschaft | Verfahren zur herstellung von 2'-substituierten-d-ribofuranosylpurinderivaten |
| US4058602A (en) * | 1976-08-09 | 1977-11-15 | The United States Of America As Represented By The Department Of Health, Education And Welfare | Synthesis, structure, and antitumor activity of 5,6-dihydro-5-azacytidine |
| 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 |
| US4526988A (en) * | 1983-03-10 | 1985-07-02 | Eli Lilly And Company | Difluoro antivirals and intermediate therefor |
| ZA859008B (en) * | 1984-12-04 | 1987-07-29 | Lilly Co Eli | The treatment of tumors in mammals |
| CA1295998C (en) * | 1985-07-29 | 1992-02-18 | Sai P. Sunkara | Nucleosides and their use as antineoplastic agents |
| US4914028A (en) * | 1988-02-10 | 1990-04-03 | Eli Lilly And Company | Method of preparing beta-2',2'-difluoronucleosides |
| US4983724A (en) * | 1988-02-16 | 1991-01-08 | Eli Lilly And Company | Inversion of 2,2-difluororibose to a 2,2-difluoroxylose and intermediates therefor |
| JPH0232093A (ja) * | 1988-06-08 | 1990-02-01 | Merrell Dow Pharmaceut Inc | 抗レトロウィルスジフルオロ化ヌクレオシド類 |
-
1985
- 1985-11-25 AT AT85308547T patent/ATE92499T1/de not_active IP Right Cessation
- 1985-11-25 IL IL77133A patent/IL77133A/xx not_active IP Right Cessation
- 1985-11-25 EP EP85308547A patent/EP0184365B1/en not_active Expired - Lifetime
- 1985-11-25 DE DE85308547T patent/DE3587500T2/de not_active Expired - Lifetime
- 1985-11-25 CA CA000496077A patent/CA1264738A/en not_active Expired - Lifetime
- 1985-11-26 PT PT81559A patent/PT81559B/pt unknown
- 1985-11-27 GR GR852858A patent/GR852858B/el unknown
- 1985-11-28 NZ NZ214364A patent/NZ214364A/xx unknown
- 1985-11-28 PH PH33109A patent/PH23172A/en unknown
- 1985-11-28 DK DK549685A patent/DK162965C/da not_active IP Right Cessation
- 1985-12-02 AU AU50555/85A patent/AU581269B2/en not_active Expired
- 1985-12-03 CN CN85109409A patent/CN1020194C/zh not_active Expired - Lifetime
- 1985-12-03 EG EG771/85A patent/EG17765A/xx active
- 1985-12-03 JP JP60273161A patent/JPH0637394B2/ja not_active Expired - Lifetime
- 1985-12-03 KR KR1019850009042A patent/KR890003439B1/ko not_active Expired
- 1985-12-03 HU HU854620A patent/HU194273B/hu unknown
- 1985-12-03 IE IE303885A patent/IE60328B1/en not_active IP Right Cessation
- 1985-12-03 ES ES549547A patent/ES8801546A1/es not_active Expired
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1989
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1993
- 1993-10-21 HK HK1136/93A patent/HK113693A/en not_active IP Right Cessation
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1994
- 1994-07-26 US US08/280,687 patent/US5464826A/en not_active Expired - Lifetime
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1995
- 1995-09-08 CY CY180695A patent/CY1806A/xx unknown
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| JPH0637394B2 (ja) | 1994-05-18 |
| KR890003426B1 (ko) | 1989-09-20 |
| KR890003439B1 (ko) | 1989-09-21 |
| DK162965C (da) | 1992-06-01 |
| CA1264738A (en) | 1990-01-23 |
| DK549685A (da) | 1986-06-05 |
| EG17765A (en) | 1990-08-30 |
| DE3587500T2 (de) | 1993-12-16 |
| HK113693A (en) | 1993-10-29 |
| DK162965B (da) | 1992-01-06 |
| CY1806A (en) | 1995-09-08 |
| GR852858B (enExample) | 1986-03-28 |
| IE60328B1 (en) | 1994-06-29 |
| ATE92499T1 (de) | 1993-08-15 |
| HU194273B (en) | 1988-01-28 |
| CN85109409A (zh) | 1986-08-27 |
| PH23172A (en) | 1989-05-19 |
| JPS61148193A (ja) | 1986-07-05 |
| US5464826A (en) | 1995-11-07 |
| EP0184365B1 (en) | 1993-08-04 |
| ES549547A0 (es) | 1987-08-01 |
| ES8801546A1 (es) | 1987-08-01 |
| IE853038L (en) | 1986-06-04 |
| DK549685D0 (da) | 1985-11-28 |
| PT81559B (pt) | 1988-03-03 |
| DE3587500D1 (de) | 1993-09-09 |
| EP0184365A2 (en) | 1986-06-11 |
| AU581269B2 (en) | 1989-02-16 |
| AU5055585A (en) | 1986-06-12 |
| IL77133A (en) | 1991-01-31 |
| HUT39188A (en) | 1986-08-28 |
| KR860004920A (ko) | 1986-07-16 |
| EP0184365A3 (en) | 1988-01-27 |
| NZ214364A (en) | 1988-11-29 |
| PT81559A (en) | 1985-12-01 |
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