HK1212207A1 - 經取代吡咯並嘧啶化合物、其組合物及其治療方法 - Google Patents
經取代吡咯並嘧啶化合物、其組合物及其治療方法Info
- Publication number
- HK1212207A1 HK1212207A1 HK16100005.5A HK16100005A HK1212207A1 HK 1212207 A1 HK1212207 A1 HK 1212207A1 HK 16100005 A HK16100005 A HK 16100005A HK 1212207 A1 HK1212207 A1 HK 1212207A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- compositions
- methods
- treatment therewith
- pyrrolopyrimidine compounds
- substituted pyrrolopyrimidine
- Prior art date
Links
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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361753259P | 2013-01-16 | 2013-01-16 | |
PCT/US2014/011612 WO2014113429A2 (en) | 2013-01-16 | 2014-01-15 | Substituted pyrrolopyrimidine compounds, compositions thereof, and methods of treatment therewith |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1212207A1 true HK1212207A1 (zh) | 2016-06-10 |
Family
ID=50031611
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK16100005.5A HK1212207A1 (zh) | 2013-01-16 | 2016-01-04 | 經取代吡咯並嘧啶化合物、其組合物及其治療方法 |
Country Status (24)
Country | Link |
---|---|
US (3) | US9346812B2 (zh) |
EP (2) | EP3202403A1 (zh) |
JP (1) | JP2016505041A (zh) |
KR (1) | KR20150108389A (zh) |
CN (1) | CN105188704B (zh) |
AR (1) | AR094494A1 (zh) |
AU (1) | AU2014207641A1 (zh) |
BR (1) | BR112015016997A2 (zh) |
CA (1) | CA2897985A1 (zh) |
CL (1) | CL2015001990A1 (zh) |
EA (1) | EA201591327A1 (zh) |
EC (1) | ECSP15030799A (zh) |
ES (1) | ES2638179T3 (zh) |
HK (1) | HK1212207A1 (zh) |
IL (1) | IL239901A0 (zh) |
MX (1) | MX2015009209A (zh) |
NI (1) | NI201500094A (zh) |
NZ (1) | NZ630467A (zh) |
PE (1) | PE20151995A1 (zh) |
PH (1) | PH12015501576A1 (zh) |
SG (1) | SG11201505446WA (zh) |
TW (1) | TW201441227A (zh) |
WO (1) | WO2014113429A2 (zh) |
ZA (1) | ZA201505011B (zh) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PH12017500997A1 (en) | 2012-04-04 | 2018-02-19 | Samumed Llc | Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof |
CA2897985A1 (en) | 2013-01-16 | 2014-07-24 | Signal Pharmaceuticals, Llc | Substituted pyrrolopyrimidine compounds, compositions thereof, and methods of treatment therewith |
CA2955009A1 (en) * | 2014-07-14 | 2016-01-21 | Signal Pharmaceuticals, Llc | Methods of treating a cancer using substituted pyrrolopyrimidine compounds, compositions thereof |
NZ629796A (en) | 2014-07-14 | 2015-12-24 | Signal Pharm Llc | Amorphous form of 4-((4-(cyclopentyloxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7h-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-3-methoxy-n-methylbenzamide, compositions thereof and methods of their use |
WO2016073771A2 (en) * | 2014-11-06 | 2016-05-12 | Ohio State Innovation Foundation | Pyrrolopyrimidine derivatives as mps1/ttk kinase inhibitors |
CN107801397B (zh) | 2015-02-13 | 2021-07-30 | 达纳-法伯癌症研究所公司 | Lrrk2抑制剂及其制备和使用方法 |
CN105906630B (zh) * | 2015-04-06 | 2018-10-23 | 四川百利药业有限责任公司 | 用作fgfr抑制剂的n-(1h-吡唑-5-基)嘧啶并吡唑-4,6-二取代胺类化合物 |
EP3312182B9 (en) | 2015-06-22 | 2022-06-29 | Ono Pharmaceutical Co., Ltd. | Brk inhibitory compound |
WO2017011720A1 (en) * | 2015-07-16 | 2017-01-19 | Signal Pharmaceuticals, Llc | Solod forms 4-((4-(cyclopentyloxy)-5-(2-methylbenzo[d] oxazol-6-yl)17h-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-3-methoxy-n-methylbenzamide, compositions thereof and methods of their use |
US10562902B2 (en) | 2015-08-13 | 2020-02-18 | Beijing Hanmi Pharmaceutical Co., Ltd. | IRAK4 inhibitor and use thereof |
US10603322B2 (en) | 2015-10-13 | 2020-03-31 | The Scripps Research Institute | Therapeutic targeting of casein kinase 1δ in breast cancer |
BR112018009252A2 (pt) | 2015-11-06 | 2018-11-06 | Samumed Llc | tratamento da osteoartrite |
CN105646496B (zh) * | 2016-01-20 | 2018-07-20 | 华侨大学 | 一种7H-吡咯并[2,3-d]嘧啶衍生物、其合成方法及应用 |
SI3464285T1 (sl) | 2016-06-01 | 2023-02-28 | Biosplice Therapeutics, Inc. | Postopek za pripravo N-(5-(3-(7-(3-fluorofenil)-3H-imidazo(4,5-C)piridin-2-il)-1H-indazol-5- il)piridin-3-il)-3-metilbutanamida |
CN108727400B (zh) * | 2017-05-24 | 2021-07-09 | 四川晶华生物科技有限公司 | 一种治疗肿瘤的化合物 |
EA202091003A1 (ru) * | 2017-10-27 | 2020-09-11 | Байер Акциенгезельшафт | Новые производные пиразолопирролопиримидиндиона в качестве ингибиторов p2x3 |
CN112203659A (zh) * | 2017-12-28 | 2021-01-08 | 财团法人生物技术开发中心 | 作为tyro3、axl和mertk(tam)家族受体酪氨酸激酶抑制剂的杂环化合物 |
KR102577242B1 (ko) | 2017-12-28 | 2023-09-11 | 주식회사 대웅제약 | 카이네이즈 저해제로서의 아미노-메틸피페리딘 유도체 |
JP6995428B2 (ja) | 2017-12-28 | 2022-01-14 | デウン ファーマシューティカル カンパニー リミテッド | キナーゼ阻害剤としてのオキシ-フルオロピペリジン誘導体 |
UA125551C2 (uk) * | 2018-05-15 | 2022-04-13 | Юніверсіті Оф Теннессі Рісерч Фаундейшн | Спосіб лікування тричі негативного раку молочної залози або раку яєчника |
US20230000842A1 (en) | 2019-01-17 | 2023-01-05 | Samumed, Llc | Methods of treating cartilage disorders through inhibition of clk and dyrk |
MX2023012491A (es) * | 2021-04-30 | 2023-11-03 | Wigen Biomedicine Tech Shanghai Co Ltd | Compuesto ciclico condensado como inhibidor de wee-1, metodo para su preparacion y uso de este. |
WO2022235054A1 (ko) * | 2021-05-03 | 2022-11-10 | 주식회사 제이비케이랩 | 2,6-디클로로-4-(4-(4-하이드록시사이클로헥실아미노)-7h-피롤로[2,3-d]피리미딘-5-일)페놀을 유효성분으로 포함하는 암의 예방, 개선 또는 치료용 약학적 조성물 |
Family Cites Families (74)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3507866A (en) | 1967-08-08 | 1970-04-21 | Merck & Co Inc | 1h - imidazo(4,5-b)pyrazin - 2 - one and processes for their preparation |
US3567725A (en) | 1968-11-20 | 1971-03-02 | Merck & Co Inc | Process for preparation of 1h-imidazo-(4,5-b)pyrazin-2-ones |
US4294837A (en) | 1980-03-28 | 1981-10-13 | Sterling Drug Inc. | 1,3-Dihydro-6-(pyridinyl)-2H-imidazo[4,5-b]pyridin-2-ones and -imidazo[4,5-b]pyridine-2-thiones and their cardiotonic use |
US4294836A (en) | 1980-03-24 | 1981-10-13 | Sterling Drug Inc. | 1,3-Dihydro-6-(pyridinyl)-2H-imidazo[4,5-b]pyridin-2-ones and -imidazo[4,5-b]-pyridine-2-thiones and their cardiotonic use |
US4317909A (en) | 1980-03-24 | 1982-03-02 | Sterling Drug Inc. | Preparation of 1,3-dihydro-5-(pyridinyl)-2H-imidazo[4,5-b]pyridin-2-ones |
US4309537A (en) | 1980-03-28 | 1982-01-05 | Sterling Drug Inc. | Production of imidazo[4,5-b]pyridin-2-ones or thiones |
GB8709448D0 (en) | 1987-04-21 | 1987-05-28 | Pfizer Ltd | Heterobicyclic quinoline derivatives |
JPS63275582A (ja) | 1987-05-02 | 1988-11-14 | Naade Kenkyusho:Kk | 2−アミノイミダゾ〔4,5−b〕ピリジン誘導体の製造方法 |
DD262026A1 (de) | 1987-07-10 | 1988-11-16 | Akad Wissenschaften Ddr | Verfahren zur herstellung von 4-substituierten 6-(pyrid-4-yl)-2,4-dihydro-1h-imidazo[4,5-b]pyrid-2-onen |
FR2643903A1 (fr) | 1989-03-03 | 1990-09-07 | Union Pharma Scient Appl | Nouveaux derives de benzimidazole, leurs procedes de preparation, intermediaires de synthese, compositions pharmaceutiques les contenant, utiles notamment pour le traitement des maladies cardiovasculaires, et des ulceres duodenaux |
US4963561A (en) | 1990-02-28 | 1990-10-16 | Sterling Drug Inc. | Imidazopyridines, their preparation and use |
TW274550B (zh) | 1992-09-26 | 1996-04-21 | Hoechst Ag | |
DE19601627A1 (de) | 1996-01-18 | 1997-07-24 | Bayer Ag | Heteroatomhaltige Cyclopentanopyridyl-Oxazolidinone |
US6031105A (en) | 1996-04-09 | 2000-02-29 | Pfizer Inc | Substituted pyridines |
UA72448C2 (en) | 1997-09-26 | 2005-03-15 | Zentaris Gmbh | Azabenzimidazole-based compounds, methods for their synthesis and pharmaceutical composition, method for modulating function of serine/threonine protein kinases with azabenzimidazole-based compounds, method for identifying compounds modulating functioning of serine/threonine protein kinase, method for preventing and treating serine/threonine protein kinase-related abnormal conditions with azabenzimidazole-based compounds |
ZA9810490B (en) | 1997-12-03 | 1999-05-20 | Dainippon Pharmaceutical Co | 2-Aryl-8-oxodihydropurine derivative process for the preparation thereof pharmaceutical composition containing the same and intermediate therefor |
JP2003146987A (ja) | 1999-05-31 | 2003-05-21 | Dainippon Pharmaceut Co Ltd | 2−アリールプリン−9−アセトアミド誘導体 |
JP3814125B2 (ja) | 1999-06-02 | 2006-08-23 | 大日本住友製薬株式会社 | 2−アリール−8−オキソジヒドロプリン誘導体からなる医薬 |
JP2002100363A (ja) | 2000-09-25 | 2002-04-05 | Mitsubishi Chemicals Corp | リチウム二次電池用正極材料、リチウム二次電池用正極及びリチウム二次電池 |
JP2002167387A (ja) | 2000-11-29 | 2002-06-11 | Dainippon Pharmaceut Co Ltd | 2−(7,8−ジヒドロ−8−オキソ−9h−プリン−9−イル)酢酸誘導体 |
MXPA03004245A (es) | 2000-12-12 | 2003-09-22 | Neurogen Corp | Espiro[isobenzofuran-1,4'piperidin]-3-onas y 3h-espiroisobenzofuran-1,4'-piperidinas. |
WO2002076954A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
PT1427730E (pt) | 2001-09-04 | 2006-11-30 | Boehringer Ingelheim Pharma | Novas di-hidropteridinonas, processo para sua preparação e sua utilização como medicamento |
CA2462441A1 (en) | 2001-10-18 | 2003-04-24 | Pier F. Cirillo | 1,4-disubstituted benzo-fused urea compounds as cytokine inhibitors |
US7247621B2 (en) | 2002-04-30 | 2007-07-24 | Valeant Research & Development | Antiviral phosphonate compounds and methods therefor |
EP1501850A2 (en) | 2002-05-06 | 2005-02-02 | Genelabs Technologies, Inc. | Nucleoside derivatives for treating hepatitis c virus infection |
US20040204420A1 (en) | 2002-08-05 | 2004-10-14 | Rana Tariq M. | Compounds for modulating RNA interference |
EP1556053A4 (en) | 2002-10-31 | 2006-04-19 | Amgen Inc | ANTI-INFLAMMATORY AGENTS |
MXPA05007503A (es) | 2003-01-17 | 2005-09-21 | Warner Lambert Co | Heterociclicos 2-aminopiridina sustituidos como inhibidores de proliferacion celular. |
RS52386B (en) | 2003-02-26 | 2013-02-28 | Boehringer Ingelheim Pharma Gmbh & Co.Kg. | DIHYDROPTERIDINONE, PROCEDURE FOR THEIR PREPARATION AND THEIR APPLICATION AS A MEDICINE |
GB2400101A (en) | 2003-03-28 | 2004-10-06 | Biofocus Discovery Ltd | Compounds capable of binding to the active site of protein kinases |
TW200503737A (en) | 2003-04-23 | 2005-02-01 | Wyeth Corp | Water soluble wortmannin derivatives |
CA2734052A1 (en) | 2003-05-30 | 2005-01-13 | Pharmasset, Inc. | Modified fluorinated nucleoside analogues |
AU2004263080B2 (en) | 2003-06-26 | 2008-12-18 | Merck Sharp & Dohme Corp. | Benzodiazepine CGRP receptor antagonists |
CA2569406A1 (en) | 2004-06-04 | 2005-12-22 | Icos Corporation | Methods for treating mast cell disorders |
DE102004029784A1 (de) | 2004-06-21 | 2006-01-05 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue 2-Benzylaminodihydropteridinone, Verfahren zur deren Herstellung und deren Verwendung als Arzneimittel |
WO2006001266A1 (ja) | 2004-06-23 | 2006-01-05 | Banyu Pharmaceutical Co., Ltd. | 2-アリールプリン誘導体の製造方法 |
GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
US7608622B2 (en) | 2004-09-24 | 2009-10-27 | Janssen Pharmaceutica Nv | Imidazo[4,5-b]pyrazinone inhibitors of protein kinases |
US7855205B2 (en) | 2004-10-29 | 2010-12-21 | Janssen Pharmaceutica Nv | Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders |
JP5118972B2 (ja) | 2004-10-29 | 2013-01-16 | テイボテク・フアーマシユーチカルズ | Hiv阻害性二環式ピリミジン誘導体 |
SE0403006D0 (sv) | 2004-12-09 | 2004-12-09 | Biovitrum Ab | New compounds |
JP5111113B2 (ja) | 2004-12-13 | 2012-12-26 | サネシス ファーマシューティカルズ, インコーポレイテッド | Rafキナーゼ阻害剤として有用なピリドピリミジノン、ジヒドロピリミドピリミジノンおよびプテリジノン |
PT1853588E (pt) | 2005-02-16 | 2008-08-25 | Astrazeneca Ab | Compostos químicos |
WO2006091737A1 (en) | 2005-02-24 | 2006-08-31 | Kemia, Inc. | Modulators of gsk-3 activity |
WO2006108103A1 (en) | 2005-04-05 | 2006-10-12 | Pharmacopeia, Inc. | Purine and imidazopyridine derivatives for immunosuppression |
US20090281075A1 (en) | 2006-02-17 | 2009-11-12 | Pharmacopeia, Inc. | Isomeric purinones and 1h-imidazopyridinones as pkc-theta inhibitors |
PT2583970E (pt) | 2006-08-02 | 2016-02-08 | Cytokinetics Inc | Certas entidades químicas, composições e métodos compreendendo imidazopirimidinas |
CA2662677C (en) | 2006-09-05 | 2016-05-31 | Emory University | Kinase inhibitors for preventing or treating pathogen infection and method of use thereof |
WO2008030744A2 (en) | 2006-09-05 | 2008-03-13 | Board Of Regents, The University Of Texas System | Inhibitors of c-met and uses thereof |
US7902187B2 (en) | 2006-10-04 | 2011-03-08 | Wyeth Llc | 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression |
CL2007002866A1 (es) | 2006-10-04 | 2008-07-04 | Pharmacopeia Inc | Compuestos derivados de 6-sustituidos-2-(bencimidazolil) purina y purinona; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto en el tratamiento de enfermedades autoinmunes, enfermedad inflamatoria, enfermedad mediada por m |
KR20140104060A (ko) | 2006-10-19 | 2014-08-27 | 시그날 파마소티칼 엘엘씨 | 헤테로아릴 화합물, 이들의 조성물 그리고 단백질 키나아제 억제제로서의 이들의 용도 |
CN101679432B (zh) | 2006-10-19 | 2015-04-22 | 西格诺药品有限公司 | 杂芳基化合物、其组合物及其作为蛋白激酶抑制剂的用途 |
JP2011507910A (ja) | 2007-12-21 | 2011-03-10 | ユニバーシティー オブ ロチェスター | 真核生物の寿命を変更するための方法 |
EP2285392A4 (en) | 2008-04-11 | 2012-06-06 | Bionovo Inc | PROCEDURE AGAINST CANCER WITH EXTRACTS FROM GLEDITSIA SINENSIS LAM |
AU2009238590A1 (en) * | 2008-04-22 | 2009-10-29 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
US8110578B2 (en) | 2008-10-27 | 2012-02-07 | Signal Pharmaceuticals, Llc | Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway |
AU2009324894B2 (en) | 2008-11-25 | 2015-04-09 | University Of Rochester | MLK inhibitors and methods of use |
RU2557242C2 (ru) | 2009-10-26 | 2015-07-20 | СИГНАЛ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи | Способы получения и очистки гетероарильных соединений |
KR20120123513A (ko) | 2010-02-03 | 2012-11-08 | 시그날 파마소티칼 엘엘씨 | Tor 키나제 억제자에 대한 민감성 예측 바이오마커로서 lkb1 돌연변이의 동정 |
US20120028972A1 (en) | 2010-07-30 | 2012-02-02 | Lilly Wong | Biomarker assays for detecting or measuring inhibition of tor kinase activity |
CN103857804A (zh) | 2011-08-03 | 2014-06-11 | 西格诺药品有限公司 | 作为lkb1状态的预测性生物标志物的基因表达谱的鉴定 |
CN103814030A (zh) | 2011-09-22 | 2014-05-21 | 辉瑞大药厂 | 吡咯并嘧啶及嘌呤衍生物 |
CA2852921C (en) | 2011-10-19 | 2023-10-10 | Signal Pharmaceuticals, Llc | Treatment of cancer with tor kinase inhibitors |
BR112014013332B1 (pt) | 2011-12-02 | 2022-09-06 | Signal Pharmaceuticals, Llc | Composições farmacêuticas de 7-(6-(2-hidroxi-propan-2-il)piridin-3-il)-1-((trans)-4- metoxicicloexil)-3,4-diidropirazino [2,3-b]pirazin-2(1h)-ona, uma forma sólida dessa e métodos de seu uso |
AU2013202305B2 (en) | 2012-02-24 | 2015-03-12 | Signal Pharmaceuticals, Llc | Methods for treating cancer using TOR kinase inhibitor combination therapy |
UA114194C2 (uk) | 2012-03-15 | 2017-05-10 | Сігнал Фармасьютікалз, Елелсі | Лікування раку інгібітором тоr кінази |
CN108992446A (zh) | 2012-03-15 | 2018-12-14 | 西格诺药品有限公司 | 用tor激酶抑制剂治疗癌症 |
AU2013203156C1 (en) | 2012-03-15 | 2016-02-18 | Signal Pharmaceuticals, Llc | Treatment of cancer with TOR kinase inhibitors |
CN103748096B (zh) * | 2012-08-06 | 2017-10-20 | 美国艾森生物科学公司 | 作为蛋白激酶抑制剂的吡咯并嘧啶化合物 |
AU2013203714B2 (en) | 2012-10-18 | 2015-12-03 | Signal Pharmaceuticals, Llc | Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity |
AU2013202768B2 (en) | 2012-10-18 | 2015-11-05 | Signal Pharmaceuticals, Llc | Treatment of cancer with TOR kinase inhibitors |
CA2897985A1 (en) | 2013-01-16 | 2014-07-24 | Signal Pharmaceuticals, Llc | Substituted pyrrolopyrimidine compounds, compositions thereof, and methods of treatment therewith |
-
2014
- 2014-01-15 CA CA2897985A patent/CA2897985A1/en not_active Abandoned
- 2014-01-15 MX MX2015009209A patent/MX2015009209A/es unknown
- 2014-01-15 EA EA201591327A patent/EA201591327A1/ru unknown
- 2014-01-15 EP EP17152166.9A patent/EP3202403A1/en not_active Withdrawn
- 2014-01-15 SG SG11201505446WA patent/SG11201505446WA/en unknown
- 2014-01-15 WO PCT/US2014/011612 patent/WO2014113429A2/en active Application Filing
- 2014-01-15 PE PE2015001346A patent/PE20151995A1/es not_active Application Discontinuation
- 2014-01-15 BR BR112015016997A patent/BR112015016997A2/pt not_active IP Right Cessation
- 2014-01-15 CN CN201480015876.1A patent/CN105188704B/zh not_active Expired - Fee Related
- 2014-01-15 JP JP2015553794A patent/JP2016505041A/ja active Pending
- 2014-01-15 US US14/155,498 patent/US9346812B2/en active Active
- 2014-01-15 EP EP14702393.1A patent/EP2945636B1/en not_active Not-in-force
- 2014-01-15 AU AU2014207641A patent/AU2014207641A1/en not_active Abandoned
- 2014-01-15 NZ NZ630467A patent/NZ630467A/en not_active IP Right Cessation
- 2014-01-15 US US14/155,485 patent/US9428509B2/en active Active
- 2014-01-15 TW TW103101537A patent/TW201441227A/zh unknown
- 2014-01-15 KR KR1020157022134A patent/KR20150108389A/ko not_active Application Discontinuation
- 2014-01-15 AR ARP140100151A patent/AR094494A1/es unknown
- 2014-01-15 ES ES14702393T patent/ES2638179T3/es active Active
-
2015
- 2015-07-12 IL IL239901A patent/IL239901A0/en unknown
- 2015-07-13 ZA ZA2015/05011A patent/ZA201505011B/en unknown
- 2015-07-15 PH PH12015501576A patent/PH12015501576A1/en unknown
- 2015-07-15 CL CL2015001990A patent/CL2015001990A1/es unknown
- 2015-07-15 NI NI201500094AA patent/NI201500094A/es unknown
- 2015-07-16 EC ECIEPI201530799A patent/ECSP15030799A/es unknown
-
2016
- 2016-01-04 HK HK16100005.5A patent/HK1212207A1/zh unknown
- 2016-07-21 US US15/215,728 patent/US9795607B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
CN105188704B (zh) | 2017-09-19 |
US9428509B2 (en) | 2016-08-30 |
EP2945636B1 (en) | 2017-06-28 |
BR112015016997A2 (pt) | 2017-07-11 |
US20160324861A1 (en) | 2016-11-10 |
ZA201505011B (en) | 2016-11-30 |
US20140200207A1 (en) | 2014-07-17 |
AU2014207641A1 (en) | 2015-08-06 |
CL2015001990A1 (es) | 2016-01-22 |
CA2897985A1 (en) | 2014-07-24 |
KR20150108389A (ko) | 2015-09-25 |
ECSP15030799A (es) | 2015-11-30 |
WO2014113429A2 (en) | 2014-07-24 |
TW201441227A (zh) | 2014-11-01 |
IL239901A0 (en) | 2015-08-31 |
SG11201505446WA (en) | 2015-08-28 |
AR094494A1 (es) | 2015-08-05 |
EA201591327A1 (ru) | 2015-12-30 |
PE20151995A1 (es) | 2016-01-13 |
PH12015501576A1 (en) | 2016-02-01 |
US20140200206A1 (en) | 2014-07-17 |
US9346812B2 (en) | 2016-05-24 |
WO2014113429A3 (en) | 2014-10-09 |
CN105188704A (zh) | 2015-12-23 |
NZ630467A (en) | 2017-02-24 |
US9795607B2 (en) | 2017-10-24 |
ES2638179T3 (es) | 2017-10-19 |
EP3202403A1 (en) | 2017-08-09 |
JP2016505041A (ja) | 2016-02-18 |
NI201500094A (es) | 2015-09-21 |
EP2945636A2 (en) | 2015-11-25 |
MX2015009209A (es) | 2016-03-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HK1212207A1 (zh) | 經取代吡咯並嘧啶化合物、其組合物及其治療方法 | |
IL246252A0 (en) | Diaminopyrimidyl derivative compounds, their compositions and methods of treatment | |
IL277069B (en) | Modified aminopurine compounds, their compositions and methods of treatment with them | |
IL245184B (en) | Prostacyclin compounds, preparations and methods of using them | |
IL273090B (en) | Methods and preparations for the treatment of cancer | |
EP2986140A4 (en) | COMPOSITIONS, PROCESSES AND KIT FOR TREATMENT OF PETS | |
HUE048666T2 (hu) | Mezõgazdasági endofita-növény kompozíciók és alkalmazási eljárások | |
HK1220324A1 (zh) | 用於治療血管緊張素相關疾病的方法、化合物和組合物 | |
HK1222398A1 (zh) | 治療伯克霍爾德氏菌感染症的組合物及方法 | |
GB201320723D0 (en) | Composition and methods of treatment | |
IL244066A0 (en) | Triazolopyridine compounds, preparations and methods for their use | |
SG11201510594YA (en) | Mixtures of compounds, their preparation, and uses | |
SG10201705899XA (en) | Prevention & treatment of neuropathy | |
HK1220374A1 (zh) | 用於治療碳氧血紅蛋白血症的組合物和方法 | |
EP2967055A4 (en) | BIOCIDAL COMPOSITIONS, METHODS OF MAKING, AND METHODS OF USE | |
EP3089745A4 (en) | Compounds, compositions, and methods for the treatment of cancers | |
EP2800568A4 (en) | COMPOSITIONS, USE METHOD AND TREATMENT METHOD THEREFOR | |
HK1217715A1 (zh) | 治療中風的組合物及方法 | |
EP2994156A4 (en) | Compounds, compositions and methods for the treatment of diseases through inhibiting tgf- activity |