CL2009001065A1 - Compuestos derivados de 4-pirimidinil-1,3-tiazol (o 1,3-oxazol) sulfonamidas sustituidas, inhibidores de quinasas raf; composicion farmaceutica; procedimiento de preparacion; y uso para tratar un neoplasma susceptible, seleccionado de adenocarcinoma de barret, carcinomas del tracto biliar y cancer de seno, entre otros. - Google Patents
Compuestos derivados de 4-pirimidinil-1,3-tiazol (o 1,3-oxazol) sulfonamidas sustituidas, inhibidores de quinasas raf; composicion farmaceutica; procedimiento de preparacion; y uso para tratar un neoplasma susceptible, seleccionado de adenocarcinoma de barret, carcinomas del tracto biliar y cancer de seno, entre otros.Info
- Publication number
- CL2009001065A1 CL2009001065A1 CL2009001065A CL2009001065A CL2009001065A1 CL 2009001065 A1 CL2009001065 A1 CL 2009001065A1 CL 2009001065 A CL2009001065 A CL 2009001065A CL 2009001065 A CL2009001065 A CL 2009001065A CL 2009001065 A1 CL2009001065 A1 CL 2009001065A1
- Authority
- CL
- Chile
- Prior art keywords
- pyrimidinyl
- sulfonamides
- barret
- carcinomas
- adenocarcinoma
- Prior art date
Links
- 206010006187 Breast cancer Diseases 0.000 title abstract 2
- 208000026310 Breast neoplasm Diseases 0.000 title abstract 2
- 201000009030 Carcinoma Diseases 0.000 title abstract 2
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 208000009956 adenocarcinoma Diseases 0.000 title abstract 2
- 210000003445 biliary tract Anatomy 0.000 title abstract 2
- 201000009036 biliary tract cancer Diseases 0.000 title abstract 2
- 208000020790 biliary tract neoplasm Diseases 0.000 title abstract 2
- 208000035269 cancer or benign tumor Diseases 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- ABJCBMWSMZOAOH-UHFFFAOYSA-N 4-pyrimidin-2-yl-1,3-thiazole Chemical class S1C=NC(C=2N=CC=CN=2)=C1 ABJCBMWSMZOAOH-UHFFFAOYSA-N 0.000 title 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 102000009929 raf Kinases Human genes 0.000 title 1
- 108010077182 raf Kinases Proteins 0.000 title 1
- 229940124530 sulfonamide Drugs 0.000 title 1
- 150000003456 sulfonamides Chemical class 0.000 title 1
- -1 4-pyrimidinyl-1,3-thiazole sulfonamides Chemical class 0.000 abstract 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Compuestos derivados de 4-pirimidinil-1,3-tiazol sulfonamidas o 4-pirimidinil-1,3-oxazol sulfonamidas sustituidas; composición farmacéutica que los comprende; proceso para prepararlos; y su uso para tratar un neoplasma susceptible seleccionado de adenocarcinoma de barret, carcinomas del tracto biliar y cáncer de seno, entre otros.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5074408P | 2008-05-06 | 2008-05-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2009001065A1 true CL2009001065A1 (es) | 2010-12-31 |
Family
ID=41265326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2009001065A CL2009001065A1 (es) | 2008-05-06 | 2009-05-04 | Compuestos derivados de 4-pirimidinil-1,3-tiazol (o 1,3-oxazol) sulfonamidas sustituidas, inhibidores de quinasas raf; composicion farmaceutica; procedimiento de preparacion; y uso para tratar un neoplasma susceptible, seleccionado de adenocarcinoma de barret, carcinomas del tracto biliar y cancer de seno, entre otros. |
Country Status (34)
| Country | Link |
|---|---|
| US (6) | US7994185B2 (es) |
| EP (2) | EP2282636B1 (es) |
| JP (1) | JP5426664B2 (es) |
| KR (1) | KR101628746B1 (es) |
| CN (1) | CN102083312B (es) |
| AR (1) | AR071617A1 (es) |
| AU (1) | AU2009244491B2 (es) |
| BR (1) | BRPI0912541B8 (es) |
| CA (1) | CA2723396C (es) |
| CL (1) | CL2009001065A1 (es) |
| CO (1) | CO6321189A2 (es) |
| CY (1) | CY1117615T1 (es) |
| DK (1) | DK2282636T3 (es) |
| DO (1) | DOP2010000326A (es) |
| EA (1) | EA019349B1 (es) |
| ES (1) | ES2576684T3 (es) |
| HR (1) | HRP20160447T1 (es) |
| HU (1) | HUE028820T2 (es) |
| IL (1) | IL209018A (es) |
| JO (1) | JO3408B1 (es) |
| MA (1) | MA32369B1 (es) |
| MX (1) | MX2010012074A (es) |
| MY (1) | MY155317A (es) |
| NZ (1) | NZ588970A (es) |
| PE (1) | PE20091952A1 (es) |
| PL (1) | PL2282636T3 (es) |
| RS (1) | RS54725B1 (es) |
| SG (1) | SG190624A1 (es) |
| SI (1) | SI2282636T1 (es) |
| TW (1) | TWI432430B (es) |
| UA (1) | UA103319C2 (es) |
| UY (1) | UY31806A (es) |
| WO (1) | WO2009137391A2 (es) |
| ZA (1) | ZA201007960B (es) |
Families Citing this family (105)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| WO2009012283A1 (en) | 2007-07-17 | 2009-01-22 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| KR20100122505A (ko) * | 2008-02-29 | 2010-11-22 | 어레이 바이오파마 인크. | Raf 저해물질 화합물 및 이들의 이용 방법 |
| JP2011513332A (ja) * | 2008-02-29 | 2011-04-28 | アレイ バイオファーマ、インコーポレイテッド | 癌の治療のためのraf阻害剤としてのn−(6−アミノピリジン−3−イル)−3−(スルホンアミド)ベンズアミド誘導体 |
| JP2011513331A (ja) * | 2008-02-29 | 2011-04-28 | アレイ バイオファーマ、インコーポレイテッド | ピラゾール[3,4−b]ピリジンRAF阻害剤 |
| CA2716947A1 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Imidazo [4,5-b] pyridine derivatives used as raf inhibitors |
| UA103319C2 (en) * | 2008-05-06 | 2013-10-10 | Глаксосмитклайн Ллк | Thiazole- and oxazole-benzene sulfonamide compounds |
| US20110319392A1 (en) * | 2009-03-12 | 2011-12-29 | George Adjabeng | Thiazole Sulfonamide And Oxazole Sulfonamide Kinase Inhibitors |
| MY172424A (en) | 2009-04-03 | 2019-11-25 | Hoffmann La Roche | Propane- i-sulfonic acid {3- (4-chloro-phenyl)-1h-pyrrolo [2, 3-b] pyridine-3-carconyl] -2, 4-difluoro-phenyl} -amide compositions and uses thereof |
| US8329724B2 (en) | 2009-08-03 | 2012-12-11 | Hoffmann-La Roche Inc. | Process for the manufacture of pharmaceutically active compounds |
| US8242260B2 (en) * | 2009-08-28 | 2012-08-14 | Novartis Ag | Compounds and compositions as protein kinase inhibitors |
| AR077975A1 (es) | 2009-08-28 | 2011-10-05 | Irm Llc | Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina |
| JP2013507382A (ja) | 2009-10-08 | 2013-03-04 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | 組合せ |
| MX2012004140A (es) * | 2009-10-08 | 2012-09-07 | Glaxosmithkline Llc | Combinacion. |
| EP2488184A4 (en) * | 2009-10-12 | 2013-04-24 | Glaxosmithkline Llc | COMBINATION |
| HUE067723T2 (hu) * | 2009-10-16 | 2024-11-28 | Novartis Ag | MEK-inhibitort és B-Raf-inhibitort tartalmazó kombináció |
| CN106220623A (zh) | 2009-11-06 | 2016-12-14 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| EP2498608A4 (en) * | 2009-11-10 | 2013-04-24 | Glaxosmithkline Llc | BENZOLSULFONAMIDE THIAZOL AND OXAZOLE COMPOUNDS |
| CN104958294A (zh) * | 2010-01-27 | 2015-10-07 | 内尔维安诺医学科学有限公司 | 作为蛋白激酶抑制剂的3,4-二芳基吡唑的亚磺酰氨基衍生物 |
| JP2013529619A (ja) * | 2010-06-25 | 2013-07-22 | ノバルティス アーゲー | タンパク質キナーゼ阻害剤としてのヘテロアリール化合物および組成物 |
| EP2601185B1 (en) * | 2010-08-03 | 2015-10-07 | Nerviano Medical Sciences S.r.l. | Derivatives of pyrazolophenyl-benzenesulfonamide compounds and use thereof as antitumor agents |
| EP2616057A4 (en) * | 2010-09-14 | 2014-03-12 | Glaxosmithkline Ip No 2 Ltd | COMBINATION OF B-RAF AND VEGFR INHIBITORS |
| WO2012061683A2 (en) * | 2010-11-05 | 2012-05-10 | Glaxosmithkline Llc | Methods for treating cancer |
| AU2011329666A1 (en) * | 2010-11-19 | 2013-05-30 | Glaxosmithkline Intellectual Property (No.2) Limited | Method of treatment with BRaf inhibitor |
| TWI505828B (zh) | 2010-12-20 | 2015-11-01 | 葛蘭素史克智慧財產(第二)有限公司 | 新穎醫藥組成物 |
| EP2668180B1 (en) * | 2011-01-25 | 2018-08-01 | The Regents of The University of Michigan | Bcl-2/bcl-xl inhibitors for use in the treatment of cancer |
| US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| AR085279A1 (es) | 2011-02-21 | 2013-09-18 | Plexxikon Inc | Formas solidas de {3-[5-(4-cloro-fenil)-1h-pirrolo[2,3-b]piridina-3-carbonil]-2,4-difluor-fenil}-amida del acido propano-1-sulfonico |
| CN103403002B (zh) * | 2011-02-24 | 2016-06-22 | 内尔维阿诺医学科学有限公司 | 作为激酶抑制剂的噻唑基苯基-苯磺酰氨基衍生物 |
| WO2013019620A2 (en) * | 2011-07-29 | 2013-02-07 | Glaxosmithkline Llc | Method of treating cancer using combination of braf inhibitor, mek inhibitor, and anti-ctla-4 antibody |
| US8389723B1 (en) * | 2011-08-24 | 2013-03-05 | Glaxosmithkline Llc | Deuterated benzene sulfonamide thiazole compounds |
| RU2622015C2 (ru) | 2011-11-11 | 2017-06-08 | Новартис Аг | Способ лечения пролиферативного заболевания |
| SI2782557T1 (sl) | 2011-11-23 | 2019-02-28 | Array Biopharma, Inc., | Farmacevtske formulacije |
| US20130184280A1 (en) * | 2011-12-21 | 2013-07-18 | Telik, Inc. | Substituted thiazoles as vegfr2 kinase inhibitors |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| KR20190057421A (ko) | 2012-08-17 | 2019-05-28 | 에프. 호프만-라 로슈 아게 | 코비메티닙 및 베무라피닙을 투여함을 포함하는 흑색종의 조합 치료법 |
| CN104582706A (zh) | 2012-09-04 | 2015-04-29 | 葛兰素史克有限责任公司 | 辅助癌症治疗的方法 |
| WO2014066606A2 (en) * | 2012-10-25 | 2014-05-01 | Glaxosmithkline Llc | Combination |
| WO2014072486A1 (en) * | 2012-11-09 | 2014-05-15 | INSERM (Institut National de la Santé et de la Recherche Médicale) | New benzene sulfonamide thiazole compounds |
| CN103936728B (zh) * | 2013-01-18 | 2016-08-10 | 通化济达医药有限公司 | 噻唑激酶抑制剂 |
| CN103936730A (zh) * | 2013-01-22 | 2014-07-23 | 通化济达医药有限公司 | 苯磺酰胺噻唑激酶抑制剂 |
| CN103965170A (zh) * | 2013-01-24 | 2014-08-06 | 通化济达医药有限公司 | 苯磺酰胺吡唑激酶抑制剂 |
| CN103965180B (zh) * | 2013-01-24 | 2016-09-07 | 通化济达医药有限公司 | 苯磺酰胺噁唑和噻唑激酶抑制剂 |
| US9242969B2 (en) | 2013-03-14 | 2016-01-26 | Novartis Ag | Biaryl amide compounds as kinase inhibitors |
| CN104109159A (zh) * | 2013-04-17 | 2014-10-22 | 杭州普晒医药科技有限公司 | 苯磺酰胺噻唑化合物的新晶型及其制备方法 |
| TWI634114B (zh) * | 2013-05-08 | 2018-09-01 | 永恒生物科技公司 | 作為激酶抑制劑之呋喃酮化合物 |
| CN105228983A (zh) | 2013-05-30 | 2016-01-06 | 普莱希科公司 | 用于激酶调节的化合物及其适应症 |
| TN2015000444A1 (en) | 2013-06-03 | 2017-04-06 | Novartis Ag | Combinations of an anti-pd-l1 antibody and a mek inhibitor and/or a braf inhibitor |
| WO2015003571A1 (zh) | 2013-07-08 | 2015-01-15 | 杭州普晒医药科技有限公司 | 达拉菲尼甲磺酸盐的新晶型及其制备方法 |
| WO2015059677A1 (en) | 2013-10-26 | 2015-04-30 | Glaxosmithkline Intellectual Property (No.2) Limited | Methods of treating cancer |
| CN103588767B (zh) * | 2013-11-20 | 2016-01-20 | 苏州明锐医药科技有限公司 | 达拉菲尼的制备方法 |
| CN103880831A (zh) * | 2013-11-25 | 2014-06-25 | 镇江圣安医药有限公司 | N-(2-氟苯基)-2,6-二氟苯磺酰胺的衍生物及其应用 |
| EP3079698A1 (en) | 2013-12-12 | 2016-10-19 | Novartis AG | Combinations of trametinib, panitumumab and dabrafenib for the treatment of cancer |
| ES2660989T3 (es) | 2013-12-28 | 2018-03-27 | Guardant Health, Inc. | Métodos y sistemas para detectar variantes genéticas |
| WO2015105822A1 (en) * | 2014-01-07 | 2015-07-16 | Glaxosmithkline Llc | Cancer treatment method |
| UY36294A (es) | 2014-09-12 | 2016-04-29 | Novartis Ag | Compuestos y composiciones como inhibidores de quinasa |
| CN107074828B (zh) * | 2014-09-12 | 2020-05-19 | 诺华股份有限公司 | 用作raf激酶抑制剂的化合物和组合物 |
| WO2016059548A1 (en) * | 2014-10-13 | 2016-04-21 | Mylan Laboratories Ltd | Processes for the preparation of dabrafenib |
| CN105651927B (zh) * | 2014-11-14 | 2019-12-13 | 泰州复旦张江药业有限公司 | 一种伐地昔布/帕瑞昔布有关物质的rt-hplc检测方法 |
| PL3277272T3 (pl) | 2015-03-31 | 2022-01-24 | Syros Pharmaceuticals, Inc. | Sposoby stratyfikacji pacjentów do leczenia agonistami receptora kwasu retinowego |
| CN106366080A (zh) * | 2015-07-21 | 2017-02-01 | 重庆大学 | 一种抗黑色素瘤的化合物及其应用 |
| EP3355886A1 (en) * | 2015-08-28 | 2018-08-08 | Novartis AG | Pharmaceutical combination comprising the pi3k inhibitor alpelisib and the b-raf inhibitor dabrafenib; the use of such combination in the treatment or prevention of cancer |
| EP3340987A1 (en) | 2015-08-28 | 2018-07-04 | Novartis AG | Combination of ribociclib and dabrafenib for treating or preventing cancer |
| US9868994B2 (en) | 2016-04-08 | 2018-01-16 | Syros Pharmaceuticals, Inc. | Methods of stratifying patients for treatment with retinoic acid receptor-α agonists |
| AU2017329090B9 (en) | 2016-09-19 | 2019-09-05 | Novartis Ag | Therapeutic combinations comprising a RAF inhibitor and a ERK inhibitor |
| US20190263796A1 (en) | 2016-09-23 | 2019-08-29 | Cellipse | Lim kinase inhibitors, pharmaceutical composition and method of use in limk-mediated diseases |
| US20180125812A1 (en) | 2016-11-04 | 2018-05-10 | Emory University | Dehydroacetic Acid (DHAA) and Derivative for Uses in Treating Cancer |
| WO2018146253A1 (en) | 2017-02-10 | 2018-08-16 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of cancers associated with activation of the mapk pathway |
| CA3057969A1 (en) | 2017-05-02 | 2018-11-08 | Novartis Ag | Combination therapy |
| JP2019529343A (ja) | 2017-07-05 | 2019-10-17 | ノバルティス アーゲー | 新規な医薬組成物 |
| WO2019133810A1 (en) | 2017-12-28 | 2019-07-04 | Tract Pharmaceuticals, Inc. | Stem cell culture systems for columnar epithelial stem cells, and uses related thereto |
| CN108129471A (zh) * | 2018-03-20 | 2018-06-08 | 韩邦森 | 一种噻唑取代嘧啶类化合物的合成工艺 |
| MX2020010231A (es) | 2018-03-30 | 2020-10-28 | Novartis Ag | Una combinacion farmaceutica triple que comprende dabrafenib, trametinib y un inhibidor de erk. |
| EP3560516A1 (en) | 2018-04-27 | 2019-10-30 | Bergen Teknologioverforing AS | Combination therapy including beta-sitosterol in combination with at least one of a braf inhibitor, a mek inhibitor or an erk inhibitor and methods and use thereof |
| WO2019246121A1 (en) * | 2018-06-18 | 2019-12-26 | Duke University | Compositions and methods for treating disorders characterized with aberrant ras/mapk signaling |
| JP2022504905A (ja) | 2018-10-16 | 2022-01-13 | ノバルティス アーゲー | 標的化療法に対する応答を予測するためのバイオマーカーとしての単独の又は免疫マーカーと組み合わせた腫瘍突然変異負荷 |
| WO2020124397A1 (en) * | 2018-12-19 | 2020-06-25 | Inventisbio Shanghai Ltd. | C-terminal src kinase inhibitors |
| US20220040324A1 (en) | 2018-12-21 | 2022-02-10 | Daiichi Sankyo Company, Limited | Combination of antibody-drug conjugate and kinase inhibitor |
| GB201901507D0 (en) | 2019-02-04 | 2019-03-27 | St Georges Hospital Medical School | New treatment |
| EP3969449B1 (en) | 2019-05-13 | 2025-02-12 | Novartis AG | New crystalline forms of n-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methvlphenyl)-2(trifluoromethyl)isonicotinamide as raf inhibitors for the treatment of cancer |
| EP4069692A1 (en) * | 2019-12-05 | 2022-10-12 | Institut National de la Santé et de la Recherche Médicale (INSERM) | N-(3-(5-(pyrimidin-4-yl)thiazol-4-yl)phenyl)sulfonamide compounds and their uses as braf inhibitors |
| CN118767143A (zh) | 2019-12-12 | 2024-10-15 | 听治疗有限责任公司 | 用于预防和治疗听力损失的组合物和方法 |
| EP4110341A2 (en) | 2020-02-28 | 2023-01-04 | Novartis AG | A triple pharmaceutical combination comprising dabrafenib, an erk inhibitor and a raf inhibitor |
| EP4110338A1 (en) | 2020-02-28 | 2023-01-04 | Novartis AG | A triple pharmaceutical combination comprising dabrafenib, an erk inhibitor and a shp2 inhibitor |
| CN115443274B (zh) * | 2020-04-30 | 2025-04-25 | 勤浩医药(苏州)有限公司 | 含苯基并内磺酰胺的化合物 |
| NZ801119A (en) * | 2020-12-02 | 2026-02-27 | Neupharma Inc | Certain chemical entities, compositions, and methods |
| CN112724052B (zh) * | 2021-01-21 | 2021-09-07 | 南京艾美斐生物医药科技有限公司 | 一种gpr101蛋白受体抑制剂及其制备和应用 |
| CN113024384A (zh) * | 2021-03-16 | 2021-06-25 | 湖南工程学院 | 一种2-氟-3-硝基苯甲酸中间体原料的合成方法 |
| US20240310266A1 (en) | 2021-03-18 | 2024-09-19 | Novartis Ag | Biomarkers for cancer and methods of use thereof |
| WO2022259157A1 (en) | 2021-06-09 | 2022-12-15 | Novartis Ag | A triple pharmaceutical combination comprising dabrafenib, trametinib and a shp2 inhibitor |
| CN113717053B (zh) * | 2021-09-02 | 2023-10-27 | 合肥利夫生物科技有限公司 | 一种酪氨酸激酶抑制剂关键中间体的合成方法 |
| WO2023070076A1 (en) * | 2021-10-22 | 2023-04-27 | The Board Of Trustees Of The University Of Illinois | Compounds for cancers driven by braf mutation |
| CN119053595A (zh) * | 2022-03-28 | 2024-11-29 | 尼坎治疗公司 | 作为细胞周期蛋白依赖性激酶2抑制剂的磺酰氨基衍生物 |
| CN119790053A (zh) * | 2022-06-08 | 2025-04-08 | 霖康疗法公司 | 作为细胞周期蛋白依赖性激酶2抑制剂的磺酰胺衍生物 |
| CN115260179A (zh) * | 2022-08-23 | 2022-11-01 | 江苏大学 | 一种2-氨基嘧啶衍生物及其制备方法和应用 |
| WO2024084086A1 (en) * | 2022-10-20 | 2024-04-25 | Biper Therapeutics Sas | Compositions comprising a benzene sulfonamide thiazole compound |
| CN115925630B (zh) * | 2022-12-15 | 2025-03-25 | 金仓(上海)医药生物科技有限公司 | 一种吡唑硫代酰胺的制备方法 |
| WO2024189184A1 (en) | 2023-03-16 | 2024-09-19 | Hua Huang | N-[3-(5-(2-aminopyrimidin-4-yl)-2-(tert-butyl)thiazol-4-yl)-2-fluorophenyl]-2,6-difluorobenzenesulfonamide or a pharmaceutically acceptable salt thereof for use in the treatment and/or prevention of cerebral cavernous malformation |
| AU2023439518A1 (en) | 2023-04-06 | 2025-08-28 | Eisai R&D Management Co., Ltd. | Pharmaceutical composition for treating tumors |
| CN119490423A (zh) * | 2023-08-15 | 2025-02-21 | 沈阳中化农药化工研发有限公司 | 一种制备2-氟-3-氨基苯甲酸及其酯类化合物的方法 |
| WO2025072462A1 (en) * | 2023-09-27 | 2025-04-03 | Nikang Therapeutics, Inc. | Sulfonamide derivatives as cyclin-dependent kinase 2 inhibitors |
| WO2025132388A2 (en) | 2023-12-21 | 2025-06-26 | Synthon B.V | A process for making dabrafenib |
| WO2025253311A1 (en) | 2024-06-04 | 2025-12-11 | Hetero Labs Limited | 1,2-dicarboxamide compounds as kinase inhibitors |
| WO2026074526A1 (en) | 2024-10-04 | 2026-04-09 | Hetero Labs Limited | 1,2-dicarboxamide compounds as kinase inhibitors |
| CN120393011A (zh) * | 2025-04-14 | 2025-08-01 | 武汉大学人民医院(湖北省人民医院) | Smoc2的诊断和制药用途 |
Family Cites Families (207)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9015764D0 (en) | 1990-07-18 | 1990-09-05 | Fujisawa Pharmaceutical Co | Pyrazolopyridine compound and processes for preparation thereof |
| KR970069028A (ko) | 1996-04-01 | 1997-11-07 | 김은영 | 화학색전용 에멀젼의 제조방법 |
| CA2249665A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| WO1997036898A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| WO1997036876A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| AU721952B2 (en) | 1996-04-03 | 2000-07-20 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| WO1997036585A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| AU716381B2 (en) | 1996-04-03 | 2000-02-24 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| GB9609441D0 (en) | 1996-05-04 | 1996-07-10 | Zeneca Ltd | Process |
| WO1998000134A1 (en) | 1996-06-28 | 1998-01-08 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5755056A (en) | 1996-07-15 | 1998-05-26 | Remington Arms Company, Inc. | Electronic firearm and process for controlling an electronic firearm |
| US5877193A (en) * | 1996-07-19 | 1999-03-02 | Hoffmann-La Roche Inc. | Use of N-(4-aryl-thiazol-2-yl)-sulfonamides |
| DZ2376A1 (fr) | 1996-12-19 | 2002-12-28 | Smithkline Beecham Plc | Dérivés de sulfonamides nouveaux procédé pour leurpréparation et compositions pharmaceutiques les c ontenant. |
| EP0977892A1 (en) | 1997-04-24 | 2000-02-09 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Methods and compositions for use in modulating expression of matrix metalloproteinase genes |
| DK1032575T3 (da) * | 1997-09-05 | 2003-10-20 | Glaxo Group Ltd | 2,3-diaryl-pyrazol(1,5-b)pyridazinderivater, deres fremstilling og anvendelse som cyclooxygenase 2 (COX-2) inhibitor |
| KR100643419B1 (ko) * | 1998-03-27 | 2006-11-10 | 얀센 파마슈티카 엔.브이. | Hiv를 억제하는 피리미딘 유도체 |
| US6294558B1 (en) * | 1999-05-31 | 2001-09-25 | Pfizer Inc. | Sulfonylbenzene compounds as anti-inflammatory/analgesic agents |
| GB9812768D0 (en) | 1998-06-13 | 1998-08-12 | Zeneca Ltd | Methods |
| HUP0104202A3 (en) | 1998-10-22 | 2003-12-29 | Hoffmann La Roche | Thiazole-derivatives, process for their preparation and pharmaceutical compositions containing them |
| US7223772B1 (en) | 1998-11-03 | 2007-05-29 | Smithkline Beecham Corporation | Pyrazolopyridine derivatives as selective cox-2 inhibitors |
| CA2349832A1 (en) * | 1999-01-13 | 2000-07-20 | Warner-Lambert Company | Benzenesulfonamide derivatives and their use as mek inhibitors |
| FR2788770B1 (fr) | 1999-01-21 | 2001-02-16 | Oreal | Nouveaux 2-sulfonylaminophenols cationiques, leur utilisation a titre de coupleur pour la teinture d'oxydation, compositions les comprenant et procedes de teinture |
| ATE261444T1 (de) | 1999-02-27 | 2004-03-15 | Glaxo Group Ltd | Pyrazolopyridine |
| GB9904930D0 (en) * | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Thiazoloindolinone compounds |
| EP1173254A2 (en) | 1999-04-27 | 2002-01-23 | Smithkline Beecham Plc | Novel treatment of neurotraumatic conditions with a raf inhibitor |
| UA71971C2 (en) | 1999-06-04 | 2005-01-17 | Agoron Pharmaceuticals Inc | Diaminothiazoles, composition based thereon, a method for modulation of protein kinases activity, a method for the treatment of diseases mediated by protein kinases |
| KR20020063837A (ko) | 1999-07-19 | 2002-08-05 | 시오노기세이야쿠가부시키가이샤 | 아실옥시메톡시카르보닐 측쇄를 갖는 삼환 화합물 |
| BR0012697A (pt) | 1999-07-23 | 2002-04-09 | Shionogi & Co | Inibidores da diferenciação de th2 |
| WO2001007401A1 (en) | 1999-07-23 | 2001-02-01 | Shionogi & Co., Ltd. | Tricyclic compounds and drug compositions containing the same |
| ES2316383T3 (es) | 1999-09-17 | 2009-04-16 | Millennium Pharmaceuticals, Inc. | Benzamidas e inhibidores relacionados del factor xa. |
| CZ2002959A3 (cs) | 1999-09-17 | 2002-07-17 | Millennium Pharmaceuticals, Inc. | Inhibitory faktoru Xa |
| US6632815B2 (en) | 1999-09-17 | 2003-10-14 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
| AU7922900A (en) | 1999-10-27 | 2001-05-08 | Novartis Ag | Thiazole and imidazo (4,5-b) pyridine compounds and their pharmaceutical use |
| AU1529901A (en) * | 1999-11-22 | 2001-06-04 | Smithkline Beecham Plc | Compounds |
| WO2001056989A2 (en) | 2000-02-01 | 2001-08-09 | Cor Therapeutics, Inc. | Inhibitors of factor xa |
| WO2001064642A2 (en) | 2000-02-29 | 2001-09-07 | Cor Therapeutics, Inc. | Benzamides and related inhibitors of factor xa |
| CN100355751C (zh) | 2000-03-29 | 2007-12-19 | 西克拉塞尔有限公司 | 2-取代的4-杂芳基-嘧啶、其组合物及其用途 |
| KR20030009416A (ko) | 2000-04-04 | 2003-01-29 | 시오노기세이야쿠가부시키가이샤 | 고지용성 약물을 함유하는 유성 조성물 |
| AU2001244610A1 (en) | 2000-04-05 | 2001-10-23 | Shionogi And Co., Ltd. | Oil-in-water microemulsions containing tricyclic compounds or preconcentrates thereof |
| US6727267B2 (en) | 2000-04-05 | 2004-04-27 | Tularik Inc. | NS5B HVC polymerase inhibitors |
| AU2001259242A1 (en) | 2000-04-28 | 2001-11-12 | Glaxo Group Limited | Process for the preparation of chemical compounds |
| AU2001256765A1 (en) | 2000-05-16 | 2001-11-26 | Nippon Soda Co., Ltd. | Phenyloxazole compounds and fungicides for agricultural and horticultural use |
| JP2004503527A (ja) | 2000-06-13 | 2004-02-05 | イーライ・リリー・アンド・カンパニー | スルホンアミド誘導体 |
| WO2002000647A1 (en) | 2000-06-23 | 2002-01-03 | Bristol-Myers Squibb Pharma Company | Heteroaryl-phenyl substituted factor xa inhibitors |
| PE20020506A1 (es) | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | Derivados de pirazol fusionados como inhibidores de la proteina cinasa |
| US20040067938A1 (en) | 2000-09-29 | 2004-04-08 | Penglie Zhang | Quaternary amines and related inhibitors of factor xa |
| ATE301653T1 (de) | 2000-12-15 | 2005-08-15 | Glaxo Group Ltd | Pyrazolopyridine |
| JP2004515550A (ja) | 2000-12-15 | 2004-05-27 | グラクソ グループ リミテッド | 治療用化合物 |
| AU2002232919A1 (en) | 2000-12-29 | 2002-07-16 | Alteon, Inc. | Method for treating fibrotic diseases or other indications |
| US7199124B2 (en) | 2001-02-02 | 2007-04-03 | Takeda Pharmaceutical Company Limited | JNK inhibitor |
| WO2002070469A2 (en) | 2001-03-05 | 2002-09-12 | Icos Corporation | Selective pde3b inhibitors and use of the same in therapy |
| WO2002072581A2 (en) | 2001-03-08 | 2002-09-19 | Smithkline Beecham Corporation | Pyrazolopyriadine derivatives |
| WO2002078700A1 (en) | 2001-03-30 | 2002-10-10 | Smithkline Beecham Corporation | Pyralopyridines, process for their preparation and use as therapteutic compounds |
| WO2002078701A1 (en) | 2001-03-30 | 2002-10-10 | Smithkline Beecham Corporation | Use of pyrazolopyridines as therapeutic compounds |
| ES2266487T3 (es) | 2001-04-10 | 2007-03-01 | Smithkline Beecham Corporation | Compuestos de pirazolopirina antivirales. |
| CZ20032829A3 (cs) | 2001-04-16 | 2005-03-16 | Tanabe Seiyaku Co., Ltd. | Heterocyklické sloučeniny |
| ATE296826T1 (de) | 2001-04-27 | 2005-06-15 | Smithkline Beecham Corp | Pyrazolo(1,5)pyridinderivate |
| AU2002312348A1 (en) | 2001-06-06 | 2002-12-16 | Agouron Pharmaceuticals, Inc. | Non-peptide gnrh agents, pharmaceutical compositions and methods for their uses, and processes for preparing them |
| ATE337316T1 (de) | 2001-06-21 | 2006-09-15 | Smithkline Beecham Corp | Imidazo 1,2-aöpyridin-derivate zur prophylaxe und behandlung von herpes-infektionen |
| AUPR738301A0 (en) | 2001-08-30 | 2001-09-20 | Starpharma Limited | Chemotherapeutic agents |
| WO2003022832A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham P.L.C. | Pyridylfurans and pyrroles as raf kinase inhibitors |
| US20040214834A1 (en) | 2001-09-07 | 2004-10-28 | Kristjan Gudmunsson | Pyrazolo-pyridines for the treatment of herpes infections |
| GB0123589D0 (en) | 2001-10-01 | 2001-11-21 | Syngenta Participations Ag | Organic compounds |
| EP1432712B1 (en) | 2001-10-05 | 2006-05-17 | SmithKline Beecham Corporation | Imidazo-pyridine derivatives for use in the treatment of herpes viral infection |
| DE10154125A1 (de) | 2001-10-25 | 2003-05-22 | Zeiss Carl Semiconductor Mfg | Messverfahren und Messsystem zur Vermessung der Abbildungsqualität eines optischen Abbildunsgssystems |
| WO2003047523A2 (en) * | 2001-12-04 | 2003-06-12 | Onyx Pharmaceuticals, Inc. | Raf-mek-erk pathway inhibitors to treat cancer |
| JP2005516916A (ja) | 2001-12-11 | 2005-06-09 | スミスクライン ビーチャム コーポレーション | 抗ヘルペス薬としてのピラゾロ−ピリジン誘導体 |
| WO2004087941A1 (en) | 2002-02-15 | 2004-10-14 | The General Hospital Corporation | Map-kinase inhibitors as regulators of tumor-associated antigen expression |
| DE60301339T2 (de) | 2002-03-07 | 2006-03-09 | Smithkline Beecham Corp. | Pyrazolopyrimidin- und pyrazolotriazinderivate und diese enthaltende pharmazeutische zubereitungen |
| GB0205693D0 (en) | 2002-03-09 | 2002-04-24 | Astrazeneca Ab | Chemical compounds |
| AR039241A1 (es) | 2002-04-04 | 2005-02-16 | Biogen Inc | Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos |
| JP2005529889A (ja) | 2002-04-26 | 2005-10-06 | ファイザー・プロダクツ・インク | ピリミジン−2,4,6−トリオンメタロ−プロテイナーゼ阻害剤 |
| NI200300045A (es) | 2002-04-26 | 2005-07-08 | Pfizer Prod Inc | Inhibidores de triariloxiariloxipirimidin-2,4,6-triona de metaloproteinasa. |
| JP2005529919A (ja) | 2002-05-10 | 2005-10-06 | スミスクライン ビーチャム コーポレーション | 治療用化合物 |
| AU2003249369A1 (en) | 2002-06-21 | 2004-01-06 | Cellular Genomics, Inc. | Certain amino-substituted monocycles as kinase modulators |
| BR0313160A (pt) | 2002-08-08 | 2005-07-12 | Smithkline Beecham Corp | Composto, composição farmacêutica, métodos para tratar uma condição e um neoplasmo suscetìvel em um animal em um animal, processo para preparar um composto e uso de um composto |
| US20050277118A1 (en) | 2002-09-11 | 2005-12-15 | Roth Richard B | Methods for identifying subjects at risk of melanoma and treatments thereof |
| EP1575417A4 (en) | 2002-09-30 | 2007-07-04 | Bayer Pharmaceuticals Corp | CANCER FORECASTING AND PROGNOSTIC TECHNIQUES AND SURVEILLANCE OF ANTICANCER THERAPY |
| US20040157836A1 (en) * | 2002-10-08 | 2004-08-12 | Comess Kenneth M. | Sulfonamides having antiangiogenic and anticancer activity |
| AU2003295408A1 (en) | 2002-11-06 | 2004-06-03 | Smithkline Beecham Corporation | Sulfonamides |
| SE0203754D0 (sv) | 2002-12-17 | 2002-12-17 | Astrazeneca Ab | New compounds |
| WO2004058713A1 (en) | 2002-12-20 | 2004-07-15 | Irm Llc | Differential tumor cytotoxocity compounds and compositions |
| US7144911B2 (en) | 2002-12-31 | 2006-12-05 | Deciphera Pharmaceuticals Llc | Anti-inflammatory medicaments |
| US7202257B2 (en) | 2003-12-24 | 2007-04-10 | Deciphera Pharmaceuticals, Llc | Anti-inflammatory medicaments |
| US6893159B1 (en) | 2003-01-27 | 2005-05-17 | Christopher Eugene Hosmer | Lubrication free connection |
| WO2004078114A2 (en) | 2003-02-28 | 2004-09-16 | Encysive Pharmaceuticals Inc. | Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-ii receptor antagonists. |
| US8178570B2 (en) | 2003-04-09 | 2012-05-15 | Exelixis, Inc. | Tie-2 modulators and methods of use |
| US20070099250A1 (en) | 2003-04-14 | 2007-05-03 | Ping Hu | Methods for treating proliferative diseases and for monitoring the effectiveness of treatment of proliferative diseases |
| EA200501607A1 (ru) | 2003-04-14 | 2006-06-30 | ДЗЕ ИНСТИТЬЮТС ФОР ФАРМАСЬЮТИКАЛ ДИСКАВЕРИ, ЭлЭлСи | Замещённые фенилалкановые кислоты |
| EP1622886A2 (en) | 2003-04-30 | 2006-02-08 | The Institutes for Pharmaceutical Discovery, LLC | Substituted amino carboxylic acids as inhibitors of protein tyrosine phosphatase-1b |
| KR20060006954A (ko) | 2003-04-30 | 2006-01-20 | 디 인스티튜트스 포 파마슈티컬 디스커버리, 엘엘씨 | 단백질 티로신 포스파타제-1b 억제제로서의 페닐 치환된카르복실산 |
| US7329680B2 (en) | 2003-04-30 | 2008-02-12 | The Institute For Pharmaceutical Discovery, Llc | Heterocycle substituted carboxylic acids |
| BRPI0409914A (pt) | 2003-04-30 | 2006-04-25 | Inst For Pharm Discovery Inc | ácidos carboxìlicos substituìdos |
| SE0301650D0 (sv) | 2003-06-04 | 2003-06-04 | Astrazeneca Ab | Novel compounds |
| BRPI0411275A (pt) | 2003-06-10 | 2006-08-01 | Kalypsys Inc | compostos de carbonila como inibidores de histona deacetilase para tratamento de doenças; composição farmacêutica; método de modular a atividade catalìtica de hdac; método de tratar doença em um indivìduo; utilização de um composto ou composição; método de inibir hdac |
| GB0315111D0 (en) | 2003-06-27 | 2003-07-30 | Cancer Rec Tech Ltd | Substituted 5-membered ring compounds and their use |
| GB0315517D0 (en) | 2003-07-02 | 2003-08-06 | Barrett Kevin J | Earth clamp |
| WO2005007090A2 (en) | 2003-07-03 | 2005-01-27 | President And Fellows Of Harvard College | Inhibitors of the map kinase pathway |
| JP2007500178A (ja) | 2003-07-30 | 2007-01-11 | サイクラセル・リミテッド | プロテインキナーゼ阻害剤としてのピリジニルアミノ−ピリミジン誘導体 |
| WO2005047542A1 (en) | 2003-10-16 | 2005-05-26 | The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Treatments for inhibiting development and progression of nevi and melanoma having braf mutations |
| JP5164380B2 (ja) | 2003-10-21 | 2013-03-21 | サイクラセル リミテッド | ピリミジン−4−イル−3,4−チオン化合物及び治療におけるその使用 |
| GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
| WO2005070900A1 (en) | 2004-01-22 | 2005-08-04 | Altana Pharma Ag | N-4-(6- (heteo) aryl-pyrimidin-4-ylaminophenyl) -bezenesulfonamides as kinase inhibitors |
| CA2554925A1 (en) | 2004-01-30 | 2005-08-11 | Ab Science | 2-(3-substituted-aryl)amino-4-aryl-thiazoles as tyrosine kinase inhibitors |
| US8193389B2 (en) | 2004-03-11 | 2012-06-05 | Elan Pharmaceuticals, Inc. | N-substituted benzene sulfonamides |
| WO2005087236A1 (en) | 2004-03-11 | 2005-09-22 | Glaxo Group Limited | Novel m3 muscarinic acetylcholine receptor antagonists |
| BRPI0508970A (pt) | 2004-03-19 | 2007-08-21 | Penn State Res Found | método combinatórios e composições para o tratamento de melanoma |
| DE102004018198A1 (de) * | 2004-04-15 | 2005-11-03 | Merck Patent Gmbh | Sulfonamide |
| US20050267032A1 (en) | 2004-05-21 | 2005-12-01 | Icagen, Inc. | Sulfone-containing prodrugs |
| GB0411791D0 (en) | 2004-05-26 | 2004-06-30 | Cyclacel Ltd | Compounds |
| SI1761528T1 (sl) | 2004-06-11 | 2008-06-30 | Japan Tobacco Inc | 5-amino-2,4,7-triokso-3,4,7,8-tetrahidro-2H-pirido(2,3-D)pirimidinski derivati in sorodne spojine za zdravljenje raka |
| JP2007223903A (ja) | 2004-07-09 | 2007-09-06 | Takeda Chem Ind Ltd | 新規な固体分散体およびその製造方法 |
| PE20060574A1 (es) * | 2004-07-28 | 2006-06-24 | Glaxo Group Ltd | Derivados de arilpiperazina sulfonamida como agonistas de los receptores de secretagogos de la hormona del crecimiento (ghs) |
| CA2575466A1 (en) | 2004-08-13 | 2006-02-23 | Genentech, Inc. | Thiazole based inhibitors of atp-utilizing enzymes |
| AU2005280167A1 (en) | 2004-08-31 | 2006-03-09 | Biogen Idec Ma Inc. | Pyrimidinylpyrazoles as TGF-beta inhibitors |
| GB0420424D0 (en) | 2004-09-14 | 2004-10-20 | Ionix Pharmaceuticals Ltd | Therapeutic compounds |
| JP4810814B2 (ja) | 2004-09-15 | 2011-11-09 | オムロン株式会社 | 光学シート及び面光源装置 |
| JP2008514608A (ja) | 2004-09-24 | 2008-05-08 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | スルホンアミド化合物 |
| EP1640018A1 (en) | 2004-09-24 | 2006-03-29 | Universität Zürich | Combinational therapy for treating cancer |
| AU2005295734A1 (en) | 2004-10-15 | 2006-04-27 | Biogen Idec Ma Inc. | Methods of treating vascular injuries |
| CA2584794A1 (en) | 2004-10-26 | 2006-05-04 | Third-Order Nanotechnologies, Inc. | Tricyclic spacer systems for nonlinear optical devices |
| EP1805136A1 (en) | 2004-10-28 | 2007-07-11 | The Institutes for Pharmaceutical Discovery, LLC | Substituted phenylalkanoic acids |
| AU2005302409A1 (en) * | 2004-10-28 | 2006-05-11 | The Institutes For Pharmaceutical Discovery Llc | Substituted carboxylic acids |
| US20060134068A1 (en) * | 2004-11-09 | 2006-06-22 | Mount Sinai School Of Medicine Of New York University | Treatment of cancer by simultaneous inhibiton of BRAF and restoration or mimicry of p16INK4A activity |
| US7713998B2 (en) | 2004-11-10 | 2010-05-11 | Ono Pharmaceutical Co., Ltd. | Nitrogenous heterocyclic compound and pharmaceutical use thereof |
| WO2006055503A2 (en) | 2004-11-15 | 2006-05-26 | Glaxo Group Limited | Novel m3 muscarinic acetylcholine receptor antagonists |
| WO2006055553A2 (en) | 2004-11-15 | 2006-05-26 | Glaxo Group Limited | Novel m3 muscarinic acetylcholine receptor antagonists |
| JP2008520693A (ja) | 2004-11-18 | 2008-06-19 | ジ インスチチュート フォー ファーマシューティカル ディスカバリー、エルエルシー | プロテインチロシンホスファターゼ阻害剤としての置換アミノ酸 |
| JP2008520692A (ja) | 2004-11-18 | 2008-06-19 | ジ インスチチュート フォー ファーマシューティカル ディスカバリー、エルエルシー | 複素環置換カルボン酸 |
| EP1836182A2 (en) | 2004-11-18 | 2007-09-26 | The Institutes for Pharmaceutical Discovery, LLC | Heterocyclylbiphenyl derivates as protein tyrosine phosphatase inhibitors |
| WO2006064375A2 (en) | 2004-12-16 | 2006-06-22 | Ab Science | Aminoaryl substituted five-membered ring heterocyclic compounds for the treatment of diseases |
| ES2325035T3 (es) | 2004-12-21 | 2009-08-24 | Smithkline Beecham Corporation | Inhibidores de quinasa erbb de 2-pirimidinil pirazolopiridina. |
| US7812022B2 (en) | 2004-12-21 | 2010-10-12 | Glaxosmithkline Llc | 2-pyrimidinyl pyrazolopyridine ErbB kinase inhibitors |
| US7622583B2 (en) | 2005-01-14 | 2009-11-24 | Chemocentryx, Inc. | Heteroaryl sulfonamides and CCR2 |
| DK1838674T3 (da) | 2005-01-14 | 2011-06-14 | Chemocentryx Inc | Heteroarylsulfonamider og CCR2 |
| US20060235028A1 (en) | 2005-04-14 | 2006-10-19 | Li James J | Inhibitors of 11-beta hydroxysteroid dehydrogenase type I |
| GB0510139D0 (en) | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds B1 |
| JP5388574B2 (ja) | 2005-05-31 | 2014-01-15 | バーテックス ファーマシューティカルズ インコーポレイテッド | イオンチャネルのモジュレーターとして有用なヘテロ環式類 |
| UA95244C2 (ru) | 2005-06-22 | 2011-07-25 | Плексикон, Инк. | Соединения и способ модулирования активности киназ, и показания для их применения |
| EP1899695B8 (en) | 2005-06-30 | 2012-06-27 | LED Roadway Lighting Ltd. | Method and system for luminance characterization |
| GB0513702D0 (en) | 2005-07-04 | 2005-08-10 | Sterix Ltd | Compound |
| WO2007009013A2 (en) | 2005-07-13 | 2007-01-18 | University Of Utah Research Foundation | Methods and compositions related to a braf mutation and microsatellite stability |
| WO2007013997A2 (en) | 2005-07-22 | 2007-02-01 | H. Lee Moffitt Cancer Center And Research Institute | Inhibition of the raf/mek/p-erk pathway for treating cancer |
| EP2407459A1 (en) | 2005-09-27 | 2012-01-18 | Shionogi & Co., Ltd. | Synthetic intermediate in the production of a sulfonamide derivative having PGD2 receptor antagonistic activity |
| US7910742B2 (en) | 2005-09-29 | 2011-03-22 | Abbott Laboratories | Survivin inhibitors |
| US7968572B2 (en) | 2005-10-03 | 2011-06-28 | Ono Pharmaceuticals Co., Ltd. | Nitrogen-containing heterocyclic compound and pharmaceutical application thereof |
| CA2626443A1 (en) | 2005-11-07 | 2007-05-18 | Irm Llc | Oxazole and thiazole ppar modulators |
| JP2009514964A (ja) | 2005-11-07 | 2009-04-09 | アイアールエム・リミテッド・ライアビリティ・カンパニー | Pparモジュレーターとしての化合物および組成物 |
| AR056786A1 (es) | 2005-11-10 | 2007-10-24 | Smithkline Beecham Corp | Compuesto de 1h- imidazo ( 4,5-c) piridin-2-ilo, composicion farmaceutica que lo comprende, procedimiento para preparar dicha composicion, su uso para preparar unmedicamento, uso de una combinacion que omprende al compuesto y al menos un agente antineoplasico para preparar un medicamento y dicha com |
| US20070179125A1 (en) | 2005-11-16 | 2007-08-02 | Damien Fraysse | Aminopyrimidines useful as kinase inhibitors |
| US7625896B2 (en) | 2005-11-25 | 2009-12-01 | Hoffman-La Roche Inc. | Pyridylsulfonamide derivatives |
| JP5103403B2 (ja) | 2005-12-05 | 2012-12-19 | スミスクライン ビーチャム コーポレーション | 2−ピリミジニルピラゾロピリジンErbBキナーゼ阻害剤 |
| US20070135368A1 (en) | 2005-12-09 | 2007-06-14 | Knapp Pamela E | Cell-to-cell transmission of siRNA induced gene silencing in mammalian cells |
| EP2316829A1 (en) | 2005-12-21 | 2011-05-04 | Vertex Pharmaceuticals Incorporated | Heterocyclic derivatives as modulators of ion channels |
| WO2007084391A2 (en) * | 2006-01-18 | 2007-07-26 | Amgen Inc. | Thiazole compounds as protein kinase b ( pkb) inhibitors |
| DK1984353T3 (en) | 2006-01-23 | 2016-03-14 | Amgen Inc | Aurorakinasemodulatorer and method of use |
| US7560551B2 (en) * | 2006-01-23 | 2009-07-14 | Amgen Inc. | Aurora kinase modulators and method of use |
| WO2007087429A2 (en) | 2006-01-25 | 2007-08-02 | Synta Pharmaceuticals Corp. | Phenyl and pyridyl compounds for inflammation and immune-related uses |
| US20070219239A1 (en) | 2006-02-10 | 2007-09-20 | Mjalli Adnan M | Nitrogen-containing heterocycle derivatives, pharmaceutical compositions, and methods of use thereof as antiviral agents |
| PE20080176A1 (es) * | 2006-03-31 | 2008-04-25 | Glaxo Group Ltd | Compuestos de arilpiperazina sulfonamida como agonista de los receptores de secretagogos de la hormona de crecimiento (ghs) |
| US7351434B2 (en) | 2006-04-07 | 2008-04-01 | Academia Sinica | Therapeutic Gastrodia extracts |
| EP2007716A1 (en) * | 2006-04-13 | 2008-12-31 | Glaxo Group Limited | Aryl and heteroaryl sulphonamides as growth hormone secretagogue receptor agonists |
| JP2009534380A (ja) | 2006-04-20 | 2009-09-24 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | c−fmsキナーゼインヒビター |
| ES2352320T3 (es) | 2006-05-12 | 2011-02-17 | Ab Science | Nuevo procedimiento para la síntesis de compuestos de 2-aminoxazol. |
| WO2008002490A2 (en) | 2006-06-23 | 2008-01-03 | Radius Health, Inc. | Treatment of vasomotor symptoms with selective estrogen receptor modulators |
| CN101501023A (zh) | 2006-07-07 | 2009-08-05 | 贝林格尔.英格海姆国际有限公司 | 苯基取代的杂芳基衍生物及其作为抗肿瘤剂的用途 |
| US20080032990A1 (en) | 2006-07-07 | 2008-02-07 | Khalifah Raja G | Inhibitors of advanced glycation end products |
| WO2008013928A2 (en) | 2006-07-28 | 2008-01-31 | Biogen Idec Ma Inc. | Treatment of cancer with interferon gene delivery in combination with a tgf-beta inhibitor |
| DK2054397T3 (en) | 2006-08-16 | 2016-01-18 | J David Gladstone Inst A Testamentary Trust Established Under The Will Of J David Gladstone | SMALL MOLECULAR INHIBITORS OF KYNURENIN-3-MONOOXYGENASE |
| EP2054056A4 (en) * | 2006-08-16 | 2010-08-25 | J David Gladstone Inst A Testa | SMALL MOLECULAR INHIBITORS OF KYNURENINE-3-MONOOXYGENASE |
| GB0622202D0 (en) | 2006-11-07 | 2006-12-20 | Addex Pharmaceuticals Sa | Novel compounds |
| KR101472765B1 (ko) | 2006-12-08 | 2014-12-15 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | 경구용 Xa 인자 억제제를 포함하는 단위 용량 제형 및 경구용 Xa 인자 억제제를 사용하는 혈전증의 치료 방법 |
| EP2125808A2 (en) | 2006-12-15 | 2009-12-02 | Bayer Schering Pharma Aktiengesellschaft | 3-h-pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| JP5461197B2 (ja) | 2007-02-02 | 2014-04-02 | ベイラー カレッジ オブ メディスン | 代謝障害を処置するための組成物および方法 |
| EP2129791A4 (en) | 2007-02-26 | 2010-07-28 | Wayne John Cancer Inst | BENEFITS OF THE B-RAF DNA MUTATION FOR THE DIAGNOSIS AND TREATMENT OF CANCER |
| EP2137158A4 (en) | 2007-02-28 | 2012-04-18 | Methylgene Inc | LOW-MOLECULAR INHIBITORS OF PROTEINARGININE METHYLTRANSFERASES (PRMTS) |
| EP2121591A2 (en) | 2007-03-08 | 2009-11-25 | Plexxikon, Inc. | Ppar active compounds |
| WO2008120004A1 (en) | 2007-04-02 | 2008-10-09 | Astrazeneca Ab | Combination of a mek- inhibitor and a b-raf inhibitor for the treatment of cancer |
| WO2008129288A2 (en) | 2007-04-19 | 2008-10-30 | Boehringer Ingelheim International Gmbh | Disulfonamides useful in the treatment of inflammation |
| PE20090288A1 (es) * | 2007-05-10 | 2009-04-03 | Smithkline Beecham Corp | Derivados de quinoxalina como inhibidores de la pi3 quinasa |
| EP2162552A4 (en) | 2007-05-11 | 2010-06-30 | Univ Johns Hopkins | BIOMARKER FOR MELANOME |
| CN101932580B (zh) * | 2007-06-01 | 2013-05-22 | 葛兰素史密丝克莱恩有限责任公司 | 咪唑并吡啶激酶抑制剂 |
| TWI519508B (zh) | 2007-06-12 | 2016-02-01 | Achaogen Inc | 抗菌劑 |
| CA2692379A1 (en) | 2007-07-02 | 2009-01-08 | Boehringer Ingelheim International Gmbh | Antiproliferative compounds based on 5-membered heterocycles |
| WO2009010871A2 (en) | 2007-07-13 | 2009-01-22 | Addex Pharma S.A. | Pyrazole derivatives as antagonists of adenosine a3 receptor |
| WO2009011850A2 (en) | 2007-07-16 | 2009-01-22 | Abbott Laboratories | Novel therapeutic compounds |
| WO2009012283A1 (en) | 2007-07-17 | 2009-01-22 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| JP2011507801A (ja) | 2007-09-11 | 2011-03-10 | ユニバーシティ オブ マサチューセッツ | 癌の処置のためのインスリン様成長因子結合タンパク質7 |
| CL2008002793A1 (es) | 2007-09-20 | 2009-09-04 | Cgi Pharmaceuticals Inc | Compuestos derivados de amidas sustituidas, inhibidores de la actividad de btk; composicion farmaceutica que los comprende; utiles en el tratamiento del cancer, trastornos oseos, enfermedades autoinmunes, entre otras |
| US7943319B2 (en) | 2007-11-09 | 2011-05-17 | John Wayne Cancer Institute | Utility of RET mutant in diagnosis and treatment of melanoma |
| GB0722680D0 (en) | 2007-11-19 | 2007-12-27 | Topotarget As | Therapeutic compounds and their use |
| WO2009076140A1 (en) | 2007-12-13 | 2009-06-18 | Smithkline Beecham Corporation | Thiazole and oxazole kinase inhibitors |
| EP2234966B1 (fr) | 2007-12-18 | 2013-09-11 | Sanofi | Derives d'azetidines, leur preparation et leur application en therapeutique |
| WO2009096198A1 (ja) | 2008-02-01 | 2009-08-06 | Pharma Ip Limited Liability Intermediary Corporations | 新規ビアリール誘導体 |
| WO2009100214A2 (en) | 2008-02-05 | 2009-08-13 | The Johns Hopkins University | Induction of thyroid iodide-handling gene expression in human cancers |
| JP2011511056A (ja) | 2008-02-05 | 2011-04-07 | ファイザー・インク | Cns障害および代謝障害治療のためのピリジニルアミド |
| US20090275546A1 (en) | 2008-04-10 | 2009-11-05 | Istituto Superiore Di Sanita | Diagnostic tests and personalized treatment regimes for cancer stem cells |
| US8198284B2 (en) * | 2008-04-30 | 2012-06-12 | National Health Research Institutes | Treatment of neurodegenerative disorders with thiourea compounds |
| UA103319C2 (en) | 2008-05-06 | 2013-10-10 | Глаксосмитклайн Ллк | Thiazole- and oxazole-benzene sulfonamide compounds |
| US8133884B2 (en) | 2008-05-06 | 2012-03-13 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| CA2729767A1 (en) | 2008-07-07 | 2010-01-14 | Fasgen, Inc. | Novel compounds, pharmaceutical compositions containing same, methods of use for same, and methods for preparing same |
| PT2324008E (pt) | 2008-07-24 | 2012-06-25 | Nerviano Medical Sciences Srl | 3,4-diarilpirazoles como inibidores da proteína quinase |
| JP5693452B2 (ja) | 2008-08-04 | 2015-04-01 | シーエイチディーアイ ファウンデーション,インコーポレーテッド | 特定のキヌレニン−3−モノオキシゲナーゼインヒビター、医薬組成物およびそれらの使用方法 |
| WO2010018458A2 (en) | 2008-08-12 | 2010-02-18 | Crystalgenomics, Inc. | Phenol derivatives and methods of use thereof |
| CN102216775B (zh) | 2008-08-18 | 2014-04-16 | 马克斯·普朗克科学促进协会 | 对hsp90-抑制剂的易感性 |
| GB0815947D0 (en) | 2008-09-02 | 2008-10-08 | Univ Dundee | Compounds |
| US8499305B2 (en) | 2010-10-15 | 2013-07-30 | Via Technologies, Inc. | Systems and methods for performing multi-program general purpose shader kickoff |
-
2009
- 2009-04-05 UA UAA201013069A patent/UA103319C2/ru unknown
- 2009-05-04 NZ NZ588970A patent/NZ588970A/en unknown
- 2009-05-04 EP EP09743378.3A patent/EP2282636B1/en active Active
- 2009-05-04 UY UY0001031806A patent/UY31806A/es active IP Right Grant
- 2009-05-04 JP JP2011508571A patent/JP5426664B2/ja active Active
- 2009-05-04 DK DK09743378.3T patent/DK2282636T3/en active
- 2009-05-04 BR BRPI0912541A patent/BRPI0912541B8/pt active IP Right Grant
- 2009-05-04 SI SI200931416A patent/SI2282636T1/sl unknown
- 2009-05-04 PL PL09743378T patent/PL2282636T3/pl unknown
- 2009-05-04 AR ARP090101596A patent/AR071617A1/es active IP Right Grant
- 2009-05-04 HU HUE09743378A patent/HUE028820T2/en unknown
- 2009-05-04 ES ES09743378.3T patent/ES2576684T3/es active Active
- 2009-05-04 HR HRP20160447TT patent/HRP20160447T1/hr unknown
- 2009-05-04 AU AU2009244491A patent/AU2009244491B2/en active Active
- 2009-05-04 JO JOP/2009/0162A patent/JO3408B1/ar active
- 2009-05-04 WO PCT/US2009/042682 patent/WO2009137391A2/en not_active Ceased
- 2009-05-04 SG SG2013034004A patent/SG190624A1/en unknown
- 2009-05-04 CL CL2009001065A patent/CL2009001065A1/es unknown
- 2009-05-04 US US12/434,963 patent/US7994185B2/en active Active
- 2009-05-04 TW TW098114746A patent/TWI432430B/zh active
- 2009-05-04 KR KR1020107027452A patent/KR101628746B1/ko active Active
- 2009-05-04 RS RS20160291A patent/RS54725B1/sr unknown
- 2009-05-04 CA CA2723396A patent/CA2723396C/en active Active
- 2009-05-04 EP EP16159264.7A patent/EP3106462A1/en not_active Withdrawn
- 2009-05-04 CN CN200980126781.6A patent/CN102083312B/zh active Active
- 2009-05-04 EA EA201001680A patent/EA019349B1/ru not_active IP Right Cessation
- 2009-05-04 PE PE2009000600A patent/PE20091952A1/es active IP Right Grant
- 2009-05-04 US US12/991,004 patent/US8415345B2/en active Active
- 2009-05-04 MY MYPI2010005179A patent/MY155317A/en unknown
- 2009-05-04 MX MX2010012074A patent/MX2010012074A/es active IP Right Grant
-
2010
- 2010-10-28 DO DO2010000326A patent/DOP2010000326A/es unknown
- 2010-10-31 IL IL209018A patent/IL209018A/en active IP Right Grant
- 2010-11-05 ZA ZA2010/07960A patent/ZA201007960B/en unknown
- 2010-11-29 CO CO10150410A patent/CO6321189A2/es active IP Right Grant
- 2010-12-01 MA MA33384A patent/MA32369B1/fr unknown
-
2013
- 2013-01-31 US US13/755,466 patent/US8642759B2/en active Active
- 2013-11-25 US US14/088,598 patent/US9233956B2/en active Active
-
2015
- 2015-10-21 US US14/918,679 patent/US20160068523A1/en not_active Abandoned
-
2016
- 2016-06-02 CY CY20161100487T patent/CY1117615T1/el unknown
- 2016-10-26 US US15/334,457 patent/US20170073341A1/en not_active Abandoned
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CL2009001065A1 (es) | Compuestos derivados de 4-pirimidinil-1,3-tiazol (o 1,3-oxazol) sulfonamidas sustituidas, inhibidores de quinasas raf; composicion farmaceutica; procedimiento de preparacion; y uso para tratar un neoplasma susceptible, seleccionado de adenocarcinoma de barret, carcinomas del tracto biliar y cancer de seno, entre otros. | |
| CO2020016285A2 (es) | Compuestos heterocíclicos y de heteroarilo para tratar la enfermedad de huntington | |
| EA202092001A1 (ru) | Соединения для лечения болезни гентингтона | |
| MX2021013854A (es) | Compuestos para tratar enfermedad de huntington. | |
| BR112022007612A2 (pt) | Inibidores de raf quinases | |
| MX2020014315A (es) | Compuestos de heteroarilo para tratar la enfermedad de huntington. | |
| MX391850B (es) | Compuestos para usarse en el tratamiento o mejoramiento de la enfermedad de huntington | |
| CL2008002243A1 (es) | Compuestos derivados de 2-pirazolamino-1,3,5-triazina, inhibidores de kinasa jak; procedimiento de preparacion; composicion farmaceutica; y uso para el tratamiento del cancer. | |
| EA201692285A8 (ru) | Ингибиторы ezh2 для лечения лимфомы | |
| UA122528C2 (uk) | Сполуки, які модулюють fxr (nr1h4) | |
| DOP2021000017A (es) | Compuestos de pirimidina y composiciones farmaceuticas para prevenir o tratar cánceres que incluyen los mismos | |
| BR112015011760A2 (pt) | composto, uso do composto, e uso de uma composição farmacêutica | |
| MX372716B (es) | Nuevos derivados hidroxiéster, un proceso para su preparación y composiciones farmacéuticas que los contienen. | |
| BR112012016797A2 (pt) | intensificador dinâmico de baixo utilizando compressor com equalizador incorporado | |
| CL2008002430A1 (es) | Compuestos derivados de bencenosulfonamida, inhibidores de catepsina c; composicion farmaceutica que los comprende; y su uso para el tratamiento de la epoc. | |
| CL2008000862A1 (es) | Compuestos derivados de triazolonas, inhibidores no nucleosidos de transcriptasa inversa; composicion farmaceutica que contiene a dichos compuestos; y uso del compuesto para tratar la infeccion del vih-1. | |
| UY31215A1 (es) | Compuestos de morfolino pirimidina, procesos para su preparacion, composiciones farmacéuticas conteniéndolos y su uso en terapia. | |
| MX2019012847A (es) | Compuestos de c5-anilinoquinazolina y su uso en el tratamiento del cancer. | |
| CL2007002382A1 (es) | Uso de compuestos derivados de 2,5-dihidroxibenceno para el tratamiento del cancer a la piel. | |
| EA201891440A1 (ru) | Составы/композиции, содержащие ингибитор btk | |
| EA201070327A1 (ru) | Катехоламиновые производные и их пролекарства | |
| UY29360A1 (es) | Nuevos derivados de pirazol, composiciones farmacéuticas que los contienen, procedimientos de preparación y aplicaciones. | |
| MX2018008772A (es) | Formulaciones/composiciones que comprenden un inhibidor de btk. | |
| CL2008000202A1 (es) | Compuestos derivados de n-aril-acetamida, antagonista trpv1;composicion farmaceutica que los comprende, utiles en el tratamiento del dolor. | |
| CL2021001753A1 (es) | Compuestos derivados de 2,4-diaminoquinazolina; composición farmacéutica; y su uso para el tratamiento de una infección vírica, cáncer, entre otras (divisional de solicitud 202002253). |