HK1210956A1 - 作為 激酶調節劑的雜芳環化合物及使用方法 - Google Patents
作為 激酶調節劑的雜芳環化合物及使用方法Info
- Publication number
- HK1210956A1 HK1210956A1 HK15111830.4A HK15111830A HK1210956A1 HK 1210956 A1 HK1210956 A1 HK 1210956A1 HK 15111830 A HK15111830 A HK 15111830A HK 1210956 A1 HK1210956 A1 HK 1210956A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- methods
- heteroaromatic compounds
- kinase modulators
- modulators
- kinase
- Prior art date
Links
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 title 1
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 title 1
- 150000002390 heteroarenes Chemical class 0.000 title 1
Classifications
-
- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261726139P | 2012-11-14 | 2012-11-14 | |
PCT/US2013/069366 WO2014078211A1 (en) | 2012-11-14 | 2013-11-10 | Heteroaromatic compounds as pi3 kinase modulators and methods of use |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1210956A1 true HK1210956A1 (zh) | 2016-05-13 |
Family
ID=50681898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK15111830.4A HK1210956A1 (zh) | 2012-11-14 | 2015-12-02 | 作為 激酶調節劑的雜芳環化合物及使用方法 |
Country Status (16)
Country | Link |
---|---|
US (1) | US9926324B2 (zh) |
EP (2) | EP3299019B1 (zh) |
JP (1) | JP6268183B2 (zh) |
KR (1) | KR102148679B1 (zh) |
CN (1) | CN104755085B (zh) |
AU (1) | AU2013345107B2 (zh) |
BR (1) | BR112015006726B1 (zh) |
CA (1) | CA2889346C (zh) |
ES (1) | ES2661380T3 (zh) |
HK (1) | HK1210956A1 (zh) |
MY (1) | MY180641A (zh) |
RU (1) | RU2665036C9 (zh) |
SG (1) | SG11201502725TA (zh) |
TW (1) | TWI574962B (zh) |
WO (1) | WO2014078211A1 (zh) |
ZA (1) | ZA201502575B (zh) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104496994B (zh) * | 2014-01-06 | 2016-12-07 | 广东东阳光药业有限公司 | 一种炔类杂芳基化合物的新晶型 |
CA2952992C (en) * | 2014-06-17 | 2019-05-07 | Cisen Pharmaceutical Co., Ltd. | Pyridino[1,2-a]pyrimidone analogue used as mtor/pi3k inhibitor |
CN105503877A (zh) | 2014-09-24 | 2016-04-20 | 和记黄埔医药(上海)有限公司 | 咪唑并哒嗪类化合物及其用途 |
JP6586463B2 (ja) * | 2014-12-19 | 2019-10-02 | ヤンセン ファーマシューティカ エヌ.ベー. | PI3Kβ阻害剤としての複素環連結イミダゾピリダジン誘導体 |
BR112017012930A2 (pt) | 2014-12-19 | 2018-01-09 | Janssen Pharmaceutica Nv | derivados de imidazopiridazina como inibidores de pi3kbeta. |
CA3025594C (en) * | 2016-06-16 | 2024-06-18 | Janssen Pharmaceutica Nv | Bicyclic pyridine, pyrazine, and pyrimidine derivatives as pi3k beta inhibitors |
US20190292179A1 (en) | 2016-07-21 | 2019-09-26 | Bristol-Myers Squibb Company | TGF Beta RECEPTOR ANTAGONISTS |
US10906905B2 (en) | 2016-10-14 | 2021-02-02 | Jiangsu Hengrui Medicine Co., Ltd. | Five-membered heteroaryl ring bridged ring derivative, preparation method therefor and medical use thereof |
CN108164525B (zh) * | 2016-12-08 | 2020-09-08 | 沈阳药科大学 | 一种抗肿瘤化合物的制备方法和用途 |
JP7300394B2 (ja) | 2017-01-17 | 2023-06-29 | ヘパリジェニックス ゲーエムベーハー | 肝再生の促進又は肝細胞死の低減もしくは予防のためのプロテインキナーゼ阻害 |
FR3064364A1 (fr) * | 2017-03-27 | 2018-09-28 | S.P.C.M. Sa | Methode de dosage de polymeres cationiques |
CN118201896A (zh) * | 2021-09-10 | 2024-06-14 | 传达治疗有限公司 | PI3K-α抑制剂和其使用方法 |
TW202400175A (zh) * | 2022-05-10 | 2024-01-01 | 美商傳達治療有限公司 | PI3Kα抑制劑及其使用方法 |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2036924C1 (ru) * | 1989-01-31 | 1995-06-09 | Такеда Кемикал Индастриз ЛТД | Способ получения производных имидазо (1,2-b)пиридазина или их солей и производные имидазо (1,2-b)пиридазина или их соли |
US5304121A (en) | 1990-12-28 | 1994-04-19 | Boston Scientific Corporation | Drug delivery system making use of a hydrogel polymer coating |
US5716981A (en) | 1993-07-19 | 1998-02-10 | Angiogenesis Technologies, Inc. | Anti-angiogenic compositions and methods of use |
KR100392057B1 (ko) | 1993-11-30 | 2003-10-30 | 맥길 유니버시티 | 세포의 CpG 디뉴클레오티드 내의 시토신의 메틸화를 감소하는 방법 |
US5578716A (en) | 1993-12-01 | 1996-11-26 | Mcgill University | DNA methyltransferase antisense oligonucleotides |
US6099562A (en) | 1996-06-13 | 2000-08-08 | Schneider (Usa) Inc. | Drug coating with topcoat |
US6268137B1 (en) | 1996-05-22 | 2001-07-31 | Methylgene, Inc. | Specific inhibitors of DNA methyl transferase |
AU8125098A (en) | 1997-05-30 | 1998-12-30 | Mcgill University | Dna methyltransferase genomic sequences and antisense oligonucleotides |
US6020318A (en) | 1997-05-30 | 2000-02-01 | Methylgene, Inc. | DNA methyltransferase genomic sequences and antisense oligonucleotides |
US6066625A (en) | 1998-02-03 | 2000-05-23 | Methylgene, Inc. | Optimized antisense oligonucleotides complementary to DNA methyltransferase sequences |
US6953783B1 (en) | 1998-10-19 | 2005-10-11 | Methylgene, Inc. | Modulation of gene expression by combination therapy |
EP1173562A2 (en) | 1999-05-03 | 2002-01-23 | Methylgene, Inc. | Inhibition of histone deacetylase |
CA2391952C (en) | 1999-11-23 | 2012-01-31 | Methylgene Inc. | Inhibitors of histone deacetylase |
AU2001248701A1 (en) | 2000-03-24 | 2001-10-03 | Methylgene, Inc. | Inhibitors of histone deacetylase |
WO2003006652A2 (en) | 2000-03-24 | 2003-01-23 | Methylgene, Inc. | Inhibition of specific histone deacetylase isoforms |
US6723733B2 (en) * | 2000-05-19 | 2004-04-20 | Guilford Pharmaceuticals, Inc. | Sulfonamide and carbamide derivatives of 6(5H)phenanthridinones and their uses |
US6897220B2 (en) | 2001-09-14 | 2005-05-24 | Methylgene, Inc. | Inhibitors of histone deacetylase |
US7868204B2 (en) | 2001-09-14 | 2011-01-11 | Methylgene Inc. | Inhibitors of histone deacetylase |
EP1429765A2 (en) | 2001-09-14 | 2004-06-23 | Methylgene, Inc. | Inhibitors of histone deacetylase |
US7282608B2 (en) | 2002-10-17 | 2007-10-16 | Methylgene, Inc. | Inhibitors of histone deacetylase |
CA2539117A1 (en) | 2003-09-24 | 2005-04-07 | Methylgene Inc. | Inhibitors of histone deacetylase |
JP5319113B2 (ja) | 2004-03-26 | 2013-10-16 | メチルジーン インコーポレイテッド | ヒストンデアセチラーゼの阻害剤 |
RU2007107167A (ru) | 2004-07-30 | 2008-09-10 | Метилджин, Инк. (Ca) | Ингибиторы передачи сигнала рецептора vegf и рецептора hgf |
JP5200939B2 (ja) | 2005-12-23 | 2013-06-05 | アリアド・ファーマシューティカルズ・インコーポレイテッド | 二環式ヘテロアリール化合物 |
RU2009107705A (ru) * | 2006-08-04 | 2010-09-10 | Такеда Фармасьютикал Компани Лимитед (Jp) | Конденсированное гетероциклическое соединение и его применение |
WO2009039140A1 (en) * | 2007-09-17 | 2009-03-26 | Smithkline Beecham Corporation | Pyridopyrimidine derivatives as pi3 kinase inhibitors |
US20100311736A1 (en) | 2007-10-22 | 2010-12-09 | Glaxosmithkline Llc | Pyridosulfonamide derivatives as p13 kinase inhibitors |
AU2008343813B2 (en) * | 2007-12-19 | 2012-04-12 | Amgen Inc. | Inhibitors of PI3 kinase |
CA2716947A1 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Imidazo [4,5-b] pyridine derivatives used as raf inhibitors |
AR071523A1 (es) * | 2008-04-30 | 2010-06-23 | Merck Serono Sa | Compuestos biciclicos fusionados, un proceso para su preparacion, el compuesto para ser utilizado como medicamento en el tratamiento y profilaxis de enfermedades, una composicion farmaceutica y un conjunto que comprende paquetes separados del compuesto y de un ingrediente activo del medicamento |
IN2012DN01961A (zh) | 2009-08-17 | 2015-08-21 | Intellikine Llc | |
EP2571357B1 (en) * | 2010-05-21 | 2016-07-06 | Infinity Pharmaceuticals, Inc. | Chemical compounds, compositions and methods for kinase modulation |
UY33597A (es) * | 2010-09-09 | 2012-04-30 | Irm Llc | Compuestos y composiciones como inhibidores de la trk |
EP2710018B8 (en) | 2011-05-19 | 2022-02-23 | Fundación del Sector Público Estatal Centro Nacional de Investigaciones Oncológicas Carlos III (F.S.P. CNIO) | Macrocyclic compounds as protein kinase inhibitors |
WO2012174312A2 (en) | 2011-06-15 | 2012-12-20 | Glaxosmithkline Llc | Benzimidazole derivatives as antiviral agents |
KR101274986B1 (ko) | 2011-07-27 | 2013-06-17 | 한국과학기술원 | 이미다조피리딘 유도체, 이를 포함하는 PI3K 및/또는 mTOR 저해제용 약학 조성물 및 PI3K 및/또는 mTOR과 연관된 질환 치료용 약학 조성물 |
GB201205669D0 (en) | 2012-03-30 | 2012-05-16 | Agency Science Tech & Res | Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof |
-
2013
- 2013-11-08 TW TW102140742A patent/TWI574962B/zh active
- 2013-11-10 AU AU2013345107A patent/AU2013345107B2/en active Active
- 2013-11-10 BR BR112015006726-3A patent/BR112015006726B1/pt not_active IP Right Cessation
- 2013-11-10 SG SG11201502725TA patent/SG11201502725TA/en unknown
- 2013-11-10 CN CN201380054625.XA patent/CN104755085B/zh active Active
- 2013-11-10 ES ES13855522.2T patent/ES2661380T3/es active Active
- 2013-11-10 EP EP17192050.7A patent/EP3299019B1/en active Active
- 2013-11-10 JP JP2015541973A patent/JP6268183B2/ja active Active
- 2013-11-10 WO PCT/US2013/069366 patent/WO2014078211A1/en active Application Filing
- 2013-11-10 EP EP13855522.2A patent/EP2919784B1/en active Active
- 2013-11-10 RU RU2015116102A patent/RU2665036C9/ru active
- 2013-11-10 CA CA2889346A patent/CA2889346C/en active Active
- 2013-11-10 KR KR1020157008264A patent/KR102148679B1/ko active IP Right Grant
- 2013-11-10 US US14/076,256 patent/US9926324B2/en active Active
- 2013-11-10 MY MYPI2015701411A patent/MY180641A/en unknown
-
2015
- 2015-04-16 ZA ZA2015/02575A patent/ZA201502575B/en unknown
- 2015-12-02 HK HK15111830.4A patent/HK1210956A1/zh unknown
Also Published As
Publication number | Publication date |
---|---|
EP2919784B1 (en) | 2017-12-20 |
BR112015006726A2 (pt) | 2017-08-22 |
US9926324B2 (en) | 2018-03-27 |
CA2889346C (en) | 2018-09-25 |
AU2013345107B2 (en) | 2016-02-25 |
SG11201502725TA (en) | 2015-05-28 |
MY180641A (en) | 2020-12-04 |
EP3299019B1 (en) | 2019-10-09 |
US20140134133A1 (en) | 2014-05-15 |
AU2013345107A1 (en) | 2015-04-30 |
JP6268183B2 (ja) | 2018-01-24 |
EP2919784A4 (en) | 2016-07-06 |
EP3299019A1 (en) | 2018-03-28 |
RU2665036C9 (ru) | 2018-11-12 |
ZA201502575B (en) | 2016-11-30 |
ES2661380T3 (es) | 2018-03-28 |
BR112015006726B1 (pt) | 2021-11-23 |
CN104755085B (zh) | 2018-05-01 |
WO2014078211A1 (en) | 2014-05-22 |
KR20150083833A (ko) | 2015-07-20 |
CA2889346A1 (en) | 2014-05-22 |
TWI574962B (zh) | 2017-03-21 |
KR102148679B1 (ko) | 2020-08-27 |
TW201422615A (zh) | 2014-06-16 |
RU2665036C2 (ru) | 2018-08-27 |
CN104755085A (zh) | 2015-07-01 |
JP2015536994A (ja) | 2015-12-24 |
RU2015116102A (ru) | 2017-01-10 |
EP2919784A1 (en) | 2015-09-23 |
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