MA38678A1 - Dérivés nucléosidiques 4'-azido, 3'désoxy-3'-fluoro substitués - Google Patents
Dérivés nucléosidiques 4'-azido, 3'désoxy-3'-fluoro substituésInfo
- Publication number
- MA38678A1 MA38678A1 MA38678A MA38678A MA38678A1 MA 38678 A1 MA38678 A1 MA 38678A1 MA 38678 A MA38678 A MA 38678A MA 38678 A MA38678 A MA 38678A MA 38678 A1 MA38678 A1 MA 38678A1
- Authority
- MA
- Morocco
- Prior art keywords
- azido
- deoxy
- nucleoside derivatives
- fluoro substituted
- vhc
- Prior art date
Links
- 150000003833 nucleoside derivatives Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000010076 replication Effects 0.000 abstract 1
Classifications
-
- 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
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
- A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
-
- 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
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- 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
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- 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
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Virology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne les dérivés nucléosidiques 4'-azido, 3'désoxy-3'-fluoro substitués qui sont utiles en tant qu'inhibiteurs de la réplication d'arn du réplicon du vhc. L'invention concerne également des compositions pharmaceutiques comprenant de tels composés et des méthodes d'utilisation desdits composés pour le traitement du vhc.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361824034P | 2013-05-16 | 2013-05-16 | |
| PCT/US2014/038288 WO2014193663A1 (fr) | 2013-05-16 | 2014-05-15 | Dérivés nucléosidiques 4'-azido, 3'désoxy-3'-fluoro substitués |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA38678A1 true MA38678A1 (fr) | 2017-07-31 |
Family
ID=51895939
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA38678A MA38678A1 (fr) | 2013-05-16 | 2014-05-15 | Dérivés nucléosidiques 4'-azido, 3'désoxy-3'-fluoro substitués |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US9249176B2 (fr) |
| EP (1) | EP2996696A4 (fr) |
| JP (1) | JP2016519146A (fr) |
| KR (1) | KR20160039154A (fr) |
| CN (1) | CN105307661A (fr) |
| AU (1) | AU2014272055A1 (fr) |
| BR (1) | BR112015028765A2 (fr) |
| CA (1) | CA2912684A1 (fr) |
| CL (1) | CL2015003358A1 (fr) |
| CR (1) | CR20150649A (fr) |
| EA (1) | EA201592185A1 (fr) |
| HK (2) | HK1219901A1 (fr) |
| MA (1) | MA38678A1 (fr) |
| MX (1) | MX2015015781A (fr) |
| PE (1) | PE20160119A1 (fr) |
| PH (1) | PH12015502589A1 (fr) |
| SG (1) | SG11201509427RA (fr) |
| WO (1) | WO2014193663A1 (fr) |
| ZA (1) | ZA201509055B (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2015015781A (es) * | 2013-05-16 | 2016-06-02 | Riboscience Llc | Derivados de nucleósido 4'-azido, 3'-deoxi-3'-fluoro sustituido. |
| AU2017239338B2 (en) * | 2016-03-25 | 2020-08-27 | Jiangsu Tasly Diyi Pharmaceutical Co., Ltd. | Uridine phosphoramide prodrug, preparation method therefor, and medicinal uses thereof |
| CN109562113A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的螺环降解决定子体 |
| CN109562107A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的杂环降解决定子体 |
| CN121974842A (zh) | 2016-05-10 | 2026-05-05 | C4医药公司 | 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体 |
| WO2017197046A1 (fr) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Dégronimères de type glutarimide liés au carbone c3 pour la dégradation de protéines cibles |
| EP4717317A3 (fr) | 2017-06-20 | 2026-06-03 | C4 Therapeutics, Inc. | Dégrons et dégrons liés à n/o pour dégradation protéique |
| EP3684374B1 (fr) * | 2017-09-21 | 2025-07-30 | Riboscience LLC | Dérivés nucléosidiques à substitution 4'-fluoro-2'-méthyle utilisés comme inhibiteurs de la réplication de l'arn du vhc |
Family Cites Families (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU498131B2 (en) | 1974-02-26 | 1979-02-15 | Ciba-Geigy Ag | Production of cephems by cyclization |
| US4147864A (en) | 1975-02-20 | 1979-04-03 | Ciba-Geigy Corporation | Process for the manufacture of 7β-amino-3-cephem-3-ol-4 carboxylic acid compounds |
| US4322347A (en) | 1978-04-03 | 1982-03-30 | Bristol-Myers Company | 2-Carbamoyloxymethyl-penicillin derivatives |
| WO1986006380A1 (fr) | 1985-04-30 | 1986-11-06 | Takeda Chemical Industries, Ltd. | Composes antibacteriens, utilisation et preparation |
| JPS6422823A (en) * | 1987-07-17 | 1989-01-25 | Asahi Glass Co Ltd | Antiulcer agent |
| US5449664A (en) | 1988-11-21 | 1995-09-12 | Syntex (U.S.A.) Inc. | Antiviral agents |
| US5807876A (en) | 1996-04-23 | 1998-09-15 | Vertex Pharmaceuticals Incorporated | Inhibitors of IMPDH enzyme |
| US6054472A (en) | 1996-04-23 | 2000-04-25 | Vertex Pharmaceuticals, Incorporated | Inhibitors of IMPDH enzyme |
| PL192628B1 (pl) | 1996-04-23 | 2006-11-30 | Vertex Pharma | Pochodne mocznika, kompozycje farmaceutyczne i zastosowanie związku i kompozycji |
| NZ335276A (en) | 1996-10-18 | 2000-09-29 | Vertex Pharma | Inhibitors of serine proteases, particularly hepatitis C virus (HCV) NS3 (Non Structural Protein 3) protease |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| ATE244717T1 (de) | 1997-03-14 | 2003-07-15 | Vertex Pharma | Inhibitoren des impdh-enzyms |
| US6010848A (en) | 1997-07-02 | 2000-01-04 | Smithkline Beecham Corporation | Screening methods using an atpase protein from hepatitis C virus |
| PT1012180E (pt) | 1997-08-11 | 2005-04-29 | Boehringer Ingelheim Ca Ltd | Analogos de peptidos inibidores da hepatite c |
| CA2338490A1 (fr) | 1998-07-27 | 2000-02-10 | Sergio Altamura | Derives de dicetoacides utilises comme inhibiteurs de polymerases |
| US6323180B1 (en) | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| IL141456A0 (en) | 1998-08-21 | 2002-03-10 | Viropharma Inc | Rhodanine derivatives and pharmaceutical compositions containing the same |
| WO2000013708A1 (fr) | 1998-09-04 | 2000-03-16 | Viropharma Incorporated | Methodes de traitement ou de prevention des infections virales et des maladies associees |
| BR9913935A (pt) | 1998-09-25 | 2001-06-19 | Viropharma Inc | Métodos de tratamento e prevenção de infecção causada por pelo menos um vìrus da famìlia dos flaviviridae e doença associada com a dita infecção em um hospedeiro vivo |
| CZ301802B6 (cs) | 1999-03-19 | 2010-06-30 | Vertex Pharmaceuticals Incorporated | Deriváty mocoviny jako inhibitory IMPDH a farmaceutické prostredky s jejich obsahem |
| CA2389745C (fr) | 1999-11-04 | 2010-03-23 | Shire Biochem Inc. | Procede de traitement ou de prevention de l'infection virale par flaviviridae faisant appel a des analogues des nucleosides |
| WO2001085172A1 (fr) | 2000-05-10 | 2001-11-15 | Smithkline Beecham Corporation | Nouveaux anti-infectieux |
| US6448281B1 (en) | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| WO2002051425A1 (fr) * | 2000-12-26 | 2002-07-04 | Mitsubishi Pharma Corporation | Remedes pour l'hepatite c |
| EP2363396A1 (fr) | 2001-06-11 | 2011-09-07 | Virochem Pharma Inc. | Dérivés de thiophène comme agents antivirales contre des infections par flavivirus |
| EP1395571A1 (fr) | 2001-06-11 | 2004-03-10 | Shire Biochem Inc. | Composes et methodes de traitement ou de prevention d'infections a i flavivirus /i |
| GB0114286D0 (en) | 2001-06-12 | 2001-08-01 | Hoffmann La Roche | Nucleoside Derivatives |
| AR035543A1 (es) | 2001-06-26 | 2004-06-16 | Japan Tobacco Inc | Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con |
| CA2448737C (fr) | 2001-07-20 | 2010-06-01 | Boehringer Ingelheim (Canada) Ltd. | Inhibiteurs de polymerase virale |
| EP2335700A1 (fr) | 2001-07-25 | 2011-06-22 | Boehringer Ingelheim (Canada) Ltd. | Inhibiteurs de la polymerase du virus hepatitis C avec une structure heterobicylic |
| WO2003037893A1 (fr) | 2001-11-02 | 2003-05-08 | Glaxo Group Limited | Derives d'acyl-dihydro-pyrrole utilises comme inhibiteurs du vhc |
| US20050043545A1 (en) | 2001-11-02 | 2005-02-24 | Gianpalol Bravi | 4-(5-Membered)-heteroaryl acyl pyrrolidine derivatives as hcv inhibitors |
| DE60221875T2 (de) | 2001-11-02 | 2007-12-20 | Glaxo Group Ltd., Greenford | 4-(6-gliedrige)-heteroaryl-acyl-pyrrolidinderivate als hcv-inhibitoren |
| AU2003269890A1 (en) | 2002-06-21 | 2004-01-06 | Isis Pharmaceuticals, Inc. | Nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase |
| AU2003259735A1 (en) | 2002-08-08 | 2004-02-25 | Sirna Therapeutics, Inc. | Small-mer compositions and methods of use |
| EP1617848A2 (fr) | 2003-04-25 | 2006-01-25 | Gilead Sciences, Inc. | Conjugues phosphonate anti-cancereux |
| US20040259934A1 (en) | 2003-05-01 | 2004-12-23 | Olsen David B. | Inhibiting Coronaviridae viral replication and treating Coronaviridae viral infection with nucleoside compounds |
| WO2004099241A1 (fr) * | 2003-05-09 | 2004-11-18 | Boehringer Ingelheim International Gmbh | Poche de liaison de l'inhibiteur de la polymerase ns5b du virus de l'hepatite c |
| GB0317009D0 (en) | 2003-07-21 | 2003-08-27 | Univ Cardiff | Chemical compounds |
| ES2336009T3 (es) | 2004-01-30 | 2010-04-07 | Medivir Ab | Inhibidores de la ns-3 serina proteasa del vhc. |
| EP1828145A4 (fr) | 2004-12-10 | 2009-08-19 | Univ Emory | Analogues de nucleosides de cyclobutyle a substitution 2' et 3' pour le traitement des infections virales et de la proliferation cellulaire anormale |
| CN101287472B (zh) | 2005-08-15 | 2011-10-12 | 弗·哈夫曼-拉罗切有限公司 | 抗病毒的4'-取代前核苷酸的氨基磷酸酯类化合物 |
| EP1987050A2 (fr) | 2006-02-14 | 2008-11-05 | Merck & Co., Inc. | Phosphoramidates d'aryle nucleosidiques pour le traitement d'infections ribovirales dependantes de l'arn |
| US8329159B2 (en) | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| GB2442001A (en) | 2006-08-11 | 2008-03-26 | Chembiotech | Nanoparticle - i-motif nucleic acid bioconjugates |
| AU2007342367B2 (en) | 2007-01-05 | 2012-12-06 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Nucleoside aryl phosphoramidates for the treatment of RNA-dependent RNA viral infection |
| GB0709791D0 (en) | 2007-05-22 | 2007-06-27 | Angeletti P Ist Richerche Bio | Antiviral agents |
| EA025311B1 (ru) | 2010-07-19 | 2016-12-30 | Гайлид Сайэнсиз, Инк. | Способы получения диастереомерно чистых фосфорамидатных пролекарств |
| AU2011305652B2 (en) | 2010-09-22 | 2016-10-20 | Janssen Biopharma, Inc. | Azido nucleosides and nucleotide analogs |
| WO2012040127A1 (fr) * | 2010-09-22 | 2012-03-29 | Alios Biopharma, Inc. | Analogues nucléotidiques substitués |
| WO2012048013A2 (fr) | 2010-10-06 | 2012-04-12 | Inhibitex, Inc. | Dérivés phosphorodiamidate de composés nucléosidiques à base de guanosine destinés à traiter des infections virales |
| IN2014CN04530A (fr) * | 2011-12-20 | 2015-09-11 | Hoffmann La Roche | |
| MX2015015781A (es) * | 2013-05-16 | 2016-06-02 | Riboscience Llc | Derivados de nucleósido 4'-azido, 3'-deoxi-3'-fluoro sustituido. |
-
2014
- 2014-05-15 MX MX2015015781A patent/MX2015015781A/es unknown
- 2014-05-15 EP EP14804722.8A patent/EP2996696A4/fr not_active Withdrawn
- 2014-05-15 CN CN201480033073.9A patent/CN105307661A/zh active Pending
- 2014-05-15 EA EA201592185A patent/EA201592185A1/ru unknown
- 2014-05-15 AU AU2014272055A patent/AU2014272055A1/en not_active Abandoned
- 2014-05-15 JP JP2016514105A patent/JP2016519146A/ja active Pending
- 2014-05-15 SG SG11201509427RA patent/SG11201509427RA/en unknown
- 2014-05-15 CA CA2912684A patent/CA2912684A1/fr not_active Abandoned
- 2014-05-15 HK HK16108066.4A patent/HK1219901A1/zh unknown
- 2014-05-15 US US14/279,188 patent/US9249176B2/en active Active
- 2014-05-15 KR KR1020157035496A patent/KR20160039154A/ko not_active Withdrawn
- 2014-05-15 MA MA38678A patent/MA38678A1/fr unknown
- 2014-05-15 PE PE2015002404A patent/PE20160119A1/es not_active Application Discontinuation
- 2014-05-15 BR BR112015028765A patent/BR112015028765A2/pt not_active IP Right Cessation
- 2014-05-15 WO PCT/US2014/038288 patent/WO2014193663A1/fr not_active Ceased
- 2014-05-15 HK HK16105295.3A patent/HK1217295A1/zh unknown
-
2015
- 2015-11-13 CL CL2015003358A patent/CL2015003358A1/es unknown
- 2015-11-16 PH PH12015502589A patent/PH12015502589A1/en unknown
- 2015-12-08 CR CR20150649A patent/CR20150649A/es unknown
- 2015-12-11 ZA ZA2015/09055A patent/ZA201509055B/en unknown
-
2016
- 2016-02-02 US US15/013,173 patent/US9694028B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2996696A1 (fr) | 2016-03-23 |
| HK1219901A1 (zh) | 2017-04-21 |
| US9249176B2 (en) | 2016-02-02 |
| EA201592185A1 (ru) | 2016-05-31 |
| US20160220596A1 (en) | 2016-08-04 |
| JP2016519146A (ja) | 2016-06-30 |
| AU2014272055A1 (en) | 2015-12-24 |
| US20140341848A1 (en) | 2014-11-20 |
| CR20150649A (es) | 2016-03-09 |
| CN105307661A (zh) | 2016-02-03 |
| KR20160039154A (ko) | 2016-04-08 |
| PE20160119A1 (es) | 2016-02-24 |
| MX2015015781A (es) | 2016-06-02 |
| SG11201509427RA (en) | 2015-12-30 |
| US9694028B2 (en) | 2017-07-04 |
| WO2014193663A1 (fr) | 2014-12-04 |
| ZA201509055B (en) | 2017-03-29 |
| CA2912684A1 (fr) | 2014-12-04 |
| CL2015003358A1 (es) | 2016-10-14 |
| PH12015502589A1 (en) | 2016-02-29 |
| HK1217295A1 (zh) | 2017-01-06 |
| EP2996696A4 (fr) | 2016-12-21 |
| BR112015028765A2 (pt) | 2017-07-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA46490A1 (fr) | Dérivés de nucléosides 4'- fluoro-2' - méthyle substitués | |
| PH12018502747A1 (en) | Boronic acid derivatives and therapeutic uses thereof | |
| MA35750B1 (fr) | Dérivés de nucléoside substitué 2',4'-difluoro-2'-méthyle en tant qu'inhibiteurs de la réplication de l'arn du vhc (virus de l'hépatite c) | |
| EA201590748A1 (ru) | Противовирусные соединения против rsv | |
| EA201890592A1 (ru) | Жидкие фармацевтические композиции, содержащие ингибиторы sglt-2 | |
| MA39317A1 (fr) | Dérivés de nucléosides à substitution 4'-difluorométhyle utilisés en tant qu'inhibiteurs de la réplication de l'arn du virus de la grippe | |
| MA41251B1 (fr) | Dérivés de thiéno[2,3-c]pyrrol-4-one comme inhibiteurs erk | |
| EA201491579A1 (ru) | Соединения оксазолидин-2-она и их применения в качестве ингибиторов pi3k | |
| EA201692301A1 (ru) | Производные бороновой кислоты и их терапевтическое применение | |
| MX2019003618A (es) | Inhibidores de pirimidinil tirosina cinasa. | |
| MX383124B (es) | Compuestos tricíclicos fusionados de piridazinona útiles para tratar infecciones de orthomyxovirus. | |
| MA50406B1 (fr) | Inhibiteurs pyrazole de magl | |
| MA47356B1 (fr) | Dérivés d'isochromène utiles en tant qu'inhibiteurs des phosphoinositide 3-kinases | |
| MX389724B (es) | Compuestos de fenil-2-hidroxi-acetilamino-2-metil-fenilo | |
| MA47736B1 (fr) | Pyrimidopyrimidinones utiles en tant qu'inhibiteurs de la kinase wee-1 | |
| GEAP202215599A (en) | Boron containing pde4 inhibitors | |
| EA201790289A1 (ru) | Оксазолидин-2-онпиримидиновые производные | |
| MA40366A (fr) | Dérivés de tétrahydroquinoline à titre d'inhibiteurs des bromodomaines | |
| EA201501123A1 (ru) | Новые (циано-диметил-метил)-изоксазолы и -[1,3,4]тиадиазолы | |
| EA201692474A1 (ru) | Производные 1-(циклопент-2-ен-1-ил)-3-(2-гидрокси-3-(арилсульфонил)фенил)мочевины в качестве ингибиторов cxcr2 | |
| MA39337A1 (fr) | Modulateurs de pyrazines de gpr6 | |
| MX373162B (es) | Piridopirimidinonas y utilización de las mismas como moduladores de receptores de n-metil-d-aspartato (nmda). | |
| PH12015502589A1 (en) | 4`-azido, 3`-deoxy-3`-fluoro substituted nucleoside derivatives | |
| MA40149A1 (fr) | Dérivés de nucléoside 4'-vinyle substitués utiles en tant qu'inhibiteurs de la réplication due l'arn du virus respiratoire syncytial | |
| EA201790699A1 (ru) | Стабилизированные производные адреномедуллина и их применение |