AR247217A1 - Un procedimiento para la preparacion de nuevos derivados de 5'-deoxi-fluorocitidina. - Google Patents
Un procedimiento para la preparacion de nuevos derivados de 5'-deoxi-fluorocitidina.Info
- Publication number
- AR247217A1 AR247217A1 AR88312471A AR31247188A AR247217A1 AR 247217 A1 AR247217 A1 AR 247217A1 AR 88312471 A AR88312471 A AR 88312471A AR 31247188 A AR31247188 A AR 31247188A AR 247217 A1 AR247217 A1 AR 247217A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- formula
- methyl
- cyclic
- deoxi
- Prior art date
Links
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical group [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 3
- -1 3-INDOLYLMETHYL Chemical class 0.000 abstract 3
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- 235000010650 Hyssopus officinalis Nutrition 0.000 abstract 1
- 240000001812 Hyssopus officinalis Species 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000005676 cyclic carbonates Chemical class 0.000 abstract 1
- RXPRRQLKFXBCSJ-UHFFFAOYSA-N dl-Vincamin Natural products C1=CC=C2C(CCN3CCC4)=C5C3C4(CC)CC(O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 230000004962 physiological condition Effects 0.000 abstract 1
- 230000001012 protector Effects 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- RXPRRQLKFXBCSJ-GIVPXCGWSA-N vincamine Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C[C@](O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-GIVPXCGWSA-N 0.000 abstract 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
- C07H19/06—Pyrimidine radicals
- C07H19/067—Pyrimidine radicals with ribosyl as the saccharide radical
-
- 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
-
- 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)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
PRODUCCION DE DERIVADOS DE 5'-DEOXI-5-FLUOROCITINA DE FORMULA (I), DONDE R1, R2, Y R3 SON H Y/O AL MENOS UN RADICAL FACILMENTE HIDROLIZABLE BAJO CONDICIONES FISIOLOGICAS, DE FORMULA: R4CO-R5OCO-O R6SCO-, DONDE R4 ES HIDROGENO, ALQUILO, CICLOALQUILO, OXOALQUILO, BENCILO SUSTITUIDO O NO, FENETILO, PICOLILO Y 3-INDOLILMETILO, O FENILO SUSTITUIDO O NO, NAFTILO, DIFENILILO, TIENILO, METILTIENILO, FURILO, NITROFURILO, PIRROLILO, METILPIRROLILO, IMIDAZOLILO PIRAZOLILO, PIRIDILO, METILPIRIDILO O PIRACINILO, Y R5 Y R6 SON ALQUILO O BENCILO SUSTITUIDO O NO, 1-FENILETILO, PICOLILO O 3-INDLILMETILO,ASI COMO HIDRATOS O SOLVATOS DE LOS COMPUESTOS DE FORMULA (II), DONDE R7 ES HIDROGENO O BENCILOXICARBONILO, FENICARBONILO, 2,2,2-TRICLOROETO-XI-CARBONILO, R8 Y R9 SON HIDROGENO O BENCILO SUSTITUIDO O NO, SILILO SUSTITUIDO O NO,ALILO,METOXIMETILO,(2-METOXIETOXI)METILO Y TETRAHIDROPIRANILO O R8 Y R9 JUNTOS,FORMAN ACETAL CICLIICO, CETAL CICLICO, CARBONATO CICLICO, ORTOESTER CICLICO Y 1,3-(1,1,3,3-TETR ISOPROPIL)DISILOXANDIILO CICLICO CON UN COMPUESTO DE FORMULA (III): XCOR4, DONDE X ES HALOGENO, ACILOXI, ALQUILOXICARBONILOXI, SUCCINIMIDOOXI, FTALIMIDOOXI, 4-NITROFENILO, AZIDO, 2,4,6-TRIISOPROPILBENCENSULFONILO Y DIETILOXIFOSFORILOXI Y R4 ES HIDROGENO, ALQUILO, 1-FENILETILO, BENCILO SUSTITUIDO O NO, FENETILO, PICOLILO Y 3-INDOLILMETILO, O FENILO, SUSTITUIDO O NO,NAFTILO,DIFENILILO, TIENILO, METILPIRROLILO, IMIDAZOLILO, PIRAZOLILO, PIRIDILO, METILPIRIDILO Y PIRACINILO O CON UN COMPUESTO DE FORMULA (IV): YCOR10, DONDE Y ES HALOGENO, Y R10 TIENE FORMULA:R5O-O R6S-, DONDE R5 Y R6 ES ALQUILO O BENCILO SUSTITUIDO O NO 1-FENILETILO, FENETILO, PICOLILO Y 3- INDOLILMETILO, SEGUIDO DE SER NECESARIO, DE SEPARACION DE UN RADICAL PROTECTOR.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP87116926 | 1987-11-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR247217A1 true AR247217A1 (es) | 1994-11-30 |
Family
ID=8197450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AR88312471A AR247217A1 (es) | 1987-11-17 | 1988-11-16 | Un procedimiento para la preparacion de nuevos derivados de 5'-deoxi-fluorocitidina. |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US4966891A (es) |
| EP (1) | EP0316704B1 (es) |
| JP (1) | JPH0678350B2 (es) |
| KR (1) | KR970000241B1 (es) |
| CN (1) | CN1022688C (es) |
| AR (1) | AR247217A1 (es) |
| AT (1) | ATE124951T1 (es) |
| AU (1) | AU619220B2 (es) |
| CA (1) | CA1327358C (es) |
| CS (1) | CS274486B2 (es) |
| DE (2) | DE10199027I2 (es) |
| DK (1) | DK170893B1 (es) |
| DZ (1) | DZ1270A1 (es) |
| ES (1) | ES2074429T3 (es) |
| FI (1) | FI89804C (es) |
| GR (1) | GR3017686T3 (es) |
| HU (1) | HU199866B (es) |
| IE (1) | IE883430L (es) |
| IL (1) | IL88363A0 (es) |
| IS (1) | IS1895B (es) |
| LT (1) | LT2185B (es) |
| LU (1) | LU90769I2 (es) |
| LV (1) | LV5624A3 (es) |
| MC (1) | MC1992A1 (es) |
| MX (1) | MX173347B (es) |
| NL (1) | NL300045I2 (es) |
| NO (2) | NO171167C (es) |
| NZ (1) | NZ226923A (es) |
| PH (1) | PH25641A (es) |
| PT (1) | PT89009B (es) |
| SU (1) | SU1736342A3 (es) |
| UA (1) | UA19333A (es) |
| YU (1) | YU47122B (es) |
| ZA (1) | ZA888428B (es) |
Families Citing this family (90)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6258360B1 (en) * | 1989-05-04 | 2001-07-10 | Igen International, Inc. | Prodrugs activated by targeted catalytic proteins |
| US5527782A (en) * | 1990-03-13 | 1996-06-18 | Acic (Canada) Inc. | 5-halo-2,3'-O-cyclocytidines |
| TW254946B (es) * | 1992-12-18 | 1995-08-21 | Hoffmann La Roche | |
| AU671491B2 (en) * | 1992-12-18 | 1996-08-29 | F. Hoffmann-La Roche Ag | N-oxycarbonyl substituted 5'-deoxy-5-fluorcytidines |
| US5476932A (en) * | 1994-08-26 | 1995-12-19 | Hoffmann-La Roche Inc. | Process for producing N4-acyl-5'-deoxy-5-fluorocytidine derivatives |
| IT1291983B1 (it) * | 1997-05-23 | 1999-01-25 | Pro Bio Sint Srl | Prodcedimento per la preparazione di un derivato della desossiuridina |
| NZ330360A (en) * | 1997-06-02 | 1999-03-29 | Hoffmann La Roche | 5'-deoxy-cytidine derivatives, their manufacture and use as antitumoral agents |
| EP0882734B1 (en) * | 1997-06-02 | 2009-08-26 | F. Hoffmann-La Roche Ag | 5'-Deoxy-cytidine derivatives |
| US6005098A (en) * | 1998-02-06 | 1999-12-21 | Hoffmann-La Roche Inc. | 5'deoxycytidine derivatives |
| US20080113025A1 (en) * | 1998-11-02 | 2008-05-15 | Elan Pharma International Limited | Compositions comprising nanoparticulate naproxen and controlled release hydrocodone |
| US20010051348A1 (en) * | 2000-01-28 | 2001-12-13 | Lee Chee Wee | Novel ligands and methods for preparing same |
| SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
| CA2477088A1 (en) | 2002-02-22 | 2003-10-02 | New River Pharmaceuticals Inc. | Active agent delivery systems and methods for protecting and administering active agents |
| US6774758B2 (en) * | 2002-09-11 | 2004-08-10 | Kalyan P. Gokhale | Low harmonic rectifier circuit |
| GB0226930D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| EP1631278A4 (en) * | 2003-05-20 | 2006-09-20 | Aronex Pharmaceuticals Inc | COMBINED CHEMOTHERAPY COMPRISING CAPECITABINE AND A COMPLEX BASED ON LIPOSOMIC PLATINUM |
| DK1706414T3 (da) | 2003-12-22 | 2008-10-13 | Hoffmann La Roche | Fremgangsmåde til fluorcytidinderivater |
| US20080280872A1 (en) * | 2004-02-18 | 2008-11-13 | Craig Johnstone | Benzamide Derivatives and Their Use as Glucokinase Activating Agents |
| CA2554686A1 (en) * | 2004-02-18 | 2005-09-01 | Astrazeneca Ab | Compounds |
| CN100383128C (zh) * | 2004-02-23 | 2008-04-23 | 上海迪赛诺医药发展有限公司 | N4-氧羰基胞嘧啶衍生物及制备方法与应用 |
| TW200600086A (en) * | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
| KR101061850B1 (ko) | 2004-09-08 | 2011-09-02 | 삼성전자주식회사 | 박막 트랜지스터 표시판 및 그 제조방법 |
| GB0421294D0 (en) * | 2004-09-24 | 2004-10-27 | Angiogene Pharm Ltd | Bioreductively-activated prodrugs |
| KR20070085371A (ko) | 2004-10-16 | 2007-08-27 | 아스트라제네카 아베 | 페녹시 벤즈아미드 화합물의 제조 방법 |
| GB0423043D0 (en) * | 2004-10-16 | 2004-11-17 | Astrazeneca Ab | Compounds |
| DK1848414T3 (da) | 2005-02-03 | 2011-07-25 | Gen Hospital Corp | Fremgangsmåde til behandling af gefitinib-resistent cancer |
| NO322682B1 (no) * | 2005-03-18 | 2006-11-27 | Clavis Pharma Asa | Anvendelse av gemcitabinderivater for fremstilling av orale doseringsformer ved kreftbehandling, samt slike orale doseringsformer |
| WO2006103187A2 (en) * | 2005-04-01 | 2006-10-05 | F. Hoffmann-La Roche Ag | Method for administration of capecitabine |
| JP2008542247A (ja) * | 2005-05-24 | 2008-11-27 | アストラゼネカ アクチボラグ | グルコキナーゼモジュレーターとしての2−フェニル置換イミダゾール[4,5b]ピリジン/ピラジンおよびプリン誘導体 |
| TW200714597A (en) | 2005-05-27 | 2007-04-16 | Astrazeneca Ab | Chemical compounds |
| NZ575512A (en) | 2005-07-09 | 2009-11-27 | Astrazeneca Ab | Heteroaryl benzamide derivatives for use as GLK activators in the treatment of diabetes |
| US20080234273A1 (en) * | 2005-07-09 | 2008-09-25 | Mckerrecher Darren | Heteroaryl Benzamide Derivatives for Use as Glk Activators in the Treatment of Diabetes |
| US20110053910A1 (en) * | 2005-07-09 | 2011-03-03 | Mckerrecher Darren | 2 -heterocyclyloxybenzoyl amino heterocyclyl compounds as modulators of glucokinase for the treatment of type 2 diabetes |
| CN100569790C (zh) * | 2005-07-15 | 2009-12-16 | 上海奥锐特国际贸易有限公司 | 合成n4-酰基-5'-脱氧-5-氟胞苷衍生物的方法 |
| ES2384267T3 (es) * | 2005-07-21 | 2012-07-03 | Nuvo Research Ag | Soluciones de clorito estabilizadas en combinación con fluoropirimidinas para el tratamiento del cáncer |
| US9202182B2 (en) * | 2005-08-11 | 2015-12-01 | International Business Machines Corporation | Method and system for analyzing business architecture |
| AU2006311877A1 (en) | 2005-11-04 | 2007-05-18 | Wyeth Llc | Antineoplastic combinations with mTOR inhibitor, herceptin, and/orHKI-272 |
| TW200738621A (en) | 2005-11-28 | 2007-10-16 | Astrazeneca Ab | Chemical process |
| US20080085310A1 (en) * | 2006-10-06 | 2008-04-10 | Maria Oksana Bachynsky | Capecitabine rapidly disintegrating tablets |
| TW200825063A (en) | 2006-10-23 | 2008-06-16 | Astrazeneca Ab | Chemical compounds |
| SA07280576B1 (ar) | 2006-10-26 | 2011-06-22 | استرازينيكا ايه بي | مركبات بنزويل أمينو سيكليل غير متجانسة بأعتبارها عوامل منشطة للجلوكوكيناز |
| 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 |
| AR064625A1 (es) | 2006-12-21 | 2009-04-15 | Astrazeneca Ab | Forma cristalina de 3-{[5-(azetidin-1-ilcarbonil)pirazin-2-il]oxi}-5-[(1-metiletil)oxi]-n-1h-pirazol-3-ilbenzamida |
| ITMI20070435A1 (it) | 2007-03-05 | 2008-09-06 | Innovate Biotechnology Srl | 2',3'-di-o-acil-5-fluoronucleosidi |
| MX2009011255A (es) * | 2007-04-20 | 2009-11-23 | Reddys Lab Ltd Dr | Proceso para preparar capecitabina. |
| WO2008145403A1 (en) * | 2007-06-01 | 2008-12-04 | Synthon B.V. | Processes related to making 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 |
| WO2009088989A1 (en) * | 2008-01-03 | 2009-07-16 | Plus Chemicals, S.A. | Process for the preparation of capecitabine |
| SI2310011T1 (sl) | 2008-06-17 | 2013-10-30 | Wyeth Llc | Antineoplastične kombinacije, ki vsebujejo HKI-272 in vinorelbin |
| MX2011001333A (es) | 2008-08-04 | 2011-03-15 | Astrazeneca Ab | Derivados de pirazolo [3, 4] pirimidin-4-ilo y sus usos para tratar la diabetes y obesidad. |
| BRPI0916694B1 (pt) | 2008-08-04 | 2021-06-08 | Wyeth Llc | uso de neratinibe em combinação com capecitabina para tratar câncer de mama metastático de erbb-2 positivo, kit e produto compreendendo os mesmos |
| EP2370414A4 (en) * | 2008-12-02 | 2012-11-14 | Reddys Lab Ltd Dr | PREPARATION OF CAPECITABINE |
| WO2010063080A1 (en) | 2008-12-05 | 2010-06-10 | Commonwealth Scientific And Industrial Research Organisation | Amphiphile prodrugs |
| CN101787066B (zh) * | 2009-01-23 | 2013-07-31 | 高峰 | 阿糖胞苷衍生物及其在抗癌抗肿瘤中的用途 |
| GB0902406D0 (en) | 2009-02-13 | 2009-04-01 | Astrazeneca Ab | Crystalline polymorphic form |
| GB0902434D0 (en) | 2009-02-13 | 2009-04-01 | Astrazeneca Ab | Chemical process |
| CA2755789C (en) | 2009-04-06 | 2016-01-19 | Wyeth Llc | Treatment regimen utilizing neratinib for breast cancer |
| AR076220A1 (es) | 2009-04-09 | 2011-05-26 | Astrazeneca Ab | Derivados de pirazol [4,5 - e] pirimidina |
| AR076221A1 (es) * | 2009-04-09 | 2011-05-26 | Astrazeneca Ab | Derivado de pirazol [4,5-e] pirimidina y su uso para tratar diabetes y obesidad |
| CN101875680B (zh) * | 2009-04-28 | 2012-07-25 | 上海信旗医药科技有限公司 | 一种核苷类化合物及其制备方法和应用 |
| CN102858791A (zh) * | 2009-07-23 | 2013-01-02 | 台湾神隆股份有限公司 | 制备氟胞苷衍生物的方法 |
| SI2835053T1 (sl) | 2010-03-12 | 2016-09-30 | Genzyme Corporation | Kombinirana terapija za zdravljenje raka dojke |
| AU2013243952A1 (en) | 2012-04-02 | 2014-10-30 | Modernatx, Inc. | Modified polynucleotides for the production of cytoplasmic and cytoskeletal proteins |
| HK1206612A1 (en) | 2012-04-02 | 2016-01-15 | Moderna Therapeutics, Inc. | Modified polynucleotides for the production of secreted proteins |
| PT2900657T (pt) | 2012-09-26 | 2020-05-07 | Hoffmann La Roche | Compostos cíclicos de éter-pirazol-4-il-heterociclil-carboxamida e métodos de utilização |
| CA2890359A1 (en) | 2012-11-07 | 2014-05-15 | Zucai SUO | Substituted gemcitabine aryl amide analogs and treatment methods using same |
| US10000521B2 (en) | 2013-03-15 | 2018-06-19 | Nucorion Pharmaceuticals, Inc. | Substituted gemcitabine bicyclic amide analogs and treatment methods using same |
| WO2014152027A1 (en) | 2013-03-15 | 2014-09-25 | Moderna Therapeutics, Inc. | Manufacturing methods for production of rna transcripts |
| EP3041938A1 (en) | 2013-09-03 | 2016-07-13 | Moderna Therapeutics, Inc. | Circular polynucleotides |
| AU2014315287A1 (en) | 2013-09-03 | 2015-03-12 | Moderna Therapeutics, Inc. | Chimeric polynucleotides |
| CN103450301B (zh) * | 2013-09-09 | 2015-09-09 | 南通大学 | 法尼基硫代水杨酸-核苷缀合物、其制备方法及其医药用途 |
| US10323076B2 (en) | 2013-10-03 | 2019-06-18 | Modernatx, Inc. | Polynucleotides encoding low density lipoprotein receptor |
| MX384144B (es) * | 2016-06-28 | 2025-03-14 | Cellix Bio Private Ltd | Composiciones y métodos para el tratamiento del cáncer. |
| 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 |
| WO2018200859A1 (en) | 2017-04-26 | 2018-11-01 | Kalman Thomas I | Multitargeted nucleoside derivatives |
| US10435429B2 (en) | 2017-10-03 | 2019-10-08 | Nucorion Pharmaceuticals, Inc. | 5-fluorouridine monophosphate cyclic triester compounds |
| ES2983284T3 (es) | 2018-01-09 | 2024-10-22 | Shuttle Pharmaceuticals Inc | Inhibidores selectivos de histona deacetilasa para el tratamiento de enfermedades humanas |
| WO2019139920A1 (en) | 2018-01-10 | 2019-07-18 | Nucorion Pharmaceuticals, Inc. | Phosphor(n)amidatacetal and phosph(on)atalcetal compounds |
| WO2019143860A1 (en) * | 2018-01-19 | 2019-07-25 | Nucorion Pharmaceuticals, Inc. | 5-fluorouracil compounds |
| US11427550B2 (en) | 2018-01-19 | 2022-08-30 | Nucorion Pharmaceuticals, Inc. | 5-fluorouracil compounds |
| KR20210057025A (ko) * | 2018-08-03 | 2021-05-20 | 셀릭스 바이오 프라이빗 리미티드 | 암의 치료를 위한 조성물 및 방법 |
| CN109651467A (zh) * | 2019-01-15 | 2019-04-19 | 齐鲁天和惠世制药有限公司 | 一种卡培他滨杂质及其制备方法 |
| AU2020315394A1 (en) | 2019-07-17 | 2022-02-17 | Nucorion Pharmaceuticals, Inc. | Cyclic deoxyribonucleotide compounds |
| CN115605492B (zh) | 2020-04-21 | 2025-09-16 | 配体制药股份有限公司 | 核苷酸前药化合物 |
| WO2022020811A1 (en) | 2020-07-24 | 2022-01-27 | Strand Therapeutics, Inc. | Lipidnanoparticle comprising modified nucleotides |
| TW202241931A (zh) | 2021-01-08 | 2022-11-01 | 美商斯特蘭德治療股份有限公司 | 表現構築體及其用途 |
| AU2023262576A1 (en) | 2022-04-26 | 2024-10-10 | Strand Therapeutics Inc. | Lipid nanoparticles comprising venezuelan equine encephalitis (vee) replicon and uses thereof |
| WO2025193628A2 (en) | 2024-03-09 | 2025-09-18 | Aadigen, Llc | Compositions for treating cancer with kras mutations and uses thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3404144A (en) * | 1965-12-23 | 1968-10-01 | Research Corp | 1-beta-d-arabinofuranosyl-5-fluorocytosine compounds |
| GB1379410A (en) * | 1971-06-08 | 1975-01-02 | Upjohn Co | 1-beta-d-arabino-furanosyl-n4-alpha-aminoacylcytosines |
| JPS52153977A (en) * | 1976-06-11 | 1977-12-21 | Daikin Ind Ltd | Synthesis of 5-fluorouracil and its derivatives |
| US4071680A (en) * | 1976-12-20 | 1978-01-31 | Hoffmann-La Roche Inc. | 5'-Deoxy-5-fluoropyrimidine nucleosides |
| CH633810A5 (en) * | 1978-01-01 | 1982-12-31 | Hoffmann La Roche | Novel nucleosides and process for their preparation |
| FR2528311B1 (fr) * | 1982-06-14 | 1985-06-14 | Synthelabo | Compositions pharmaceutiques a base de xylosides et lyxosides de bases puriques et pyrimidiques |
| JPS61112093A (ja) * | 1984-11-05 | 1986-05-30 | Wakunaga Seiyaku Kk | ヌクレオチド誘導体 |
-
1988
- 1988-11-02 CA CA000581964A patent/CA1327358C/en not_active Expired - Lifetime
- 1988-11-07 EP EP88118515A patent/EP0316704B1/de not_active Expired - Lifetime
- 1988-11-07 AT AT88118515T patent/ATE124951T1/de active
- 1988-11-07 DE DE2001199027 patent/DE10199027I2/de active Active
- 1988-11-07 DE DE3854148T patent/DE3854148D1/de not_active Expired - Lifetime
- 1988-11-07 ES ES88118515T patent/ES2074429T3/es not_active Expired - Lifetime
- 1988-11-08 US US07/268,437 patent/US4966891A/en not_active Expired - Lifetime
- 1988-11-10 YU YU209188A patent/YU47122B/sh unknown
- 1988-11-10 ZA ZA888428A patent/ZA888428B/xx unknown
- 1988-11-10 NZ NZ226923A patent/NZ226923A/xx unknown
- 1988-11-11 IL IL88363A patent/IL88363A0/xx not_active IP Right Cessation
- 1988-11-14 MC MC882015A patent/MC1992A1/fr unknown
- 1988-11-14 JP JP63285940A patent/JPH0678350B2/ja not_active Expired - Lifetime
- 1988-11-14 HU HU885799A patent/HU199866B/hu unknown
- 1988-11-15 CS CS747588A patent/CS274486B2/cs not_active IP Right Cessation
- 1988-11-15 KR KR1019880014983A patent/KR970000241B1/ko not_active Expired - Lifetime
- 1988-11-16 CN CN88107886A patent/CN1022688C/zh not_active Expired - Lifetime
- 1988-11-16 AU AU25168/88A patent/AU619220B2/en not_active Expired
- 1988-11-16 NO NO885106A patent/NO171167C/no not_active IP Right Cessation
- 1988-11-16 PH PH37820A patent/PH25641A/en unknown
- 1988-11-16 IS IS3412A patent/IS1895B/is unknown
- 1988-11-16 UA UA4356869A patent/UA19333A/uk unknown
- 1988-11-16 IE IE883430A patent/IE883430L/xx not_active IP Right Cessation
- 1988-11-16 DK DK640388A patent/DK170893B1/da not_active IP Right Cessation
- 1988-11-16 DZ DZ880179A patent/DZ1270A1/fr active
- 1988-11-16 SU SU884356869A patent/SU1736342A3/ru active
- 1988-11-16 AR AR88312471A patent/AR247217A1/es active
- 1988-11-16 PT PT89009A patent/PT89009B/pt not_active IP Right Cessation
- 1988-11-17 FI FI885329A patent/FI89804C/fi not_active IP Right Cessation
- 1988-11-17 MX MX013836A patent/MX173347B/es unknown
-
1993
- 1993-06-08 LV LV930507A patent/LV5624A3/xx unknown
- 1993-07-20 LT LTRP802A patent/LT2185B/xx not_active IP Right Cessation
-
1995
- 1995-10-10 GR GR950402791T patent/GR3017686T3/el unknown
-
2001
- 2001-05-02 LU LU90769C patent/LU90769I2/fr unknown
- 2001-05-17 NL NL300045C patent/NL300045I2/nl unknown
- 2001-07-17 NO NO2001013C patent/NO2001013I2/no unknown
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