CN102271683B - 恶性血液病的治疗 - Google Patents
恶性血液病的治疗 Download PDFInfo
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- CN102271683B CN102271683B CN200980154097.9A CN200980154097A CN102271683B CN 102271683 B CN102271683 B CN 102271683B CN 200980154097 A CN200980154097 A CN 200980154097A CN 102271683 B CN102271683 B CN 102271683B
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- 0 CCC1Cc2c(*C(*)C(N3c4ccccc4)=NC4C=CC=C(*)[C@]4C3=CC)ncnc2*C1 Chemical compound CCC1Cc2c(*C(*)C(N3c4ccccc4)=NC4C=CC=C(*)[C@]4C3=CC)ncnc2*C1 0.000 description 4
- DOCINCLJNAXZQF-UHFFFAOYSA-N CC(C(N1c2ccccc2)=Nc(ccc(F)c2)c2C1=O)Nc1ncnc2c1nc[nH]2 Chemical compound CC(C(N1c2ccccc2)=Nc(ccc(F)c2)c2C1=O)Nc1ncnc2c1nc[nH]2 DOCINCLJNAXZQF-UHFFFAOYSA-N 0.000 description 1
- IOEVTFYPXJLXOP-VZCXRCSSSA-N CCC(C(N1c2ccccc2)=Nc(cccc2F)c2C1=O)N/C(/N=C)=C1\N=CN/C1=N/C Chemical compound CCC(C(N1c2ccccc2)=Nc(cccc2F)c2C1=O)N/C(/N=C)=C1\N=CN/C1=N/C IOEVTFYPXJLXOP-VZCXRCSSSA-N 0.000 description 1
- QTSUDTIZEHKJTN-AATRIKPKSA-N CCC/C=C/NC Chemical compound CCC/C=C/NC QTSUDTIZEHKJTN-AATRIKPKSA-N 0.000 description 1
- IFSDAJWBUCMOAH-HNNXBMFYSA-N CC[C@@H](C(N1c2ccccc2)=Nc(cccc2F)c2C1=O)Nc1ncnc2c1nc[nH]2 Chemical compound CC[C@@H](C(N1c2ccccc2)=Nc(cccc2F)c2C1=O)Nc1ncnc2c1nc[nH]2 IFSDAJWBUCMOAH-HNNXBMFYSA-N 0.000 description 1
Classifications
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- 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
- A61K31/52—Purines, e.g. adenine
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- 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
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
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- C—CHEMISTRY; METALLURGY
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- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
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- 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
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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- A61K31/745—Polymers of hydrocarbons
- A61K31/75—Polymers of hydrocarbons of ethene
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Gastroenterology & Hepatology (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Otolaryngology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410246030.0A CN104042618B (zh) | 2008-11-13 | 2009-11-13 | 恶性血液病的治疗 |
Applications Claiming Priority (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11443408P | 2008-11-13 | 2008-11-13 | |
| US61/114,434 | 2008-11-13 | ||
| US14284509P | 2009-01-06 | 2009-01-06 | |
| US61/142,845 | 2009-01-06 | ||
| US15505709P | 2009-02-24 | 2009-02-24 | |
| US61/155,057 | 2009-02-24 | ||
| US18076809P | 2009-05-22 | 2009-05-22 | |
| US61/180,768 | 2009-05-22 | ||
| US23127809P | 2009-08-04 | 2009-08-04 | |
| US61/231,278 | 2009-08-04 | ||
| US24519609P | 2009-09-23 | 2009-09-23 | |
| US61/245,196 | 2009-09-23 | ||
| PCT/US2009/064471 WO2010057048A1 (en) | 2008-11-13 | 2009-11-13 | Therapies for hematologic malignancies |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201410246030.0A Division CN104042618B (zh) | 2008-11-13 | 2009-11-13 | 恶性血液病的治疗 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102271683A CN102271683A (zh) | 2011-12-07 |
| CN102271683B true CN102271683B (zh) | 2014-07-09 |
Family
ID=41604034
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980154097.9A Expired - Fee Related CN102271683B (zh) | 2008-11-13 | 2009-11-13 | 恶性血液病的治疗 |
| CN201410246030.0A Expired - Fee Related CN104042618B (zh) | 2008-11-13 | 2009-11-13 | 恶性血液病的治疗 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201410246030.0A Expired - Fee Related CN104042618B (zh) | 2008-11-13 | 2009-11-13 | 恶性血液病的治疗 |
Country Status (13)
| Country | Link |
|---|---|
| US (5) | US20100202963A1 (enExample) |
| EP (2) | EP2355828B1 (enExample) |
| JP (3) | JP5794919B2 (enExample) |
| KR (3) | KR20170060179A (enExample) |
| CN (2) | CN102271683B (enExample) |
| AU (6) | AU2009313878B2 (enExample) |
| CA (3) | CA2975473C (enExample) |
| ES (1) | ES2674719T3 (enExample) |
| IL (1) | IL212851A0 (enExample) |
| NZ (3) | NZ611764A (enExample) |
| PT (1) | PT2355828T (enExample) |
| SG (2) | SG10201703911XA (enExample) |
| WO (1) | WO2010057048A1 (enExample) |
Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6667300B2 (en) | 2000-04-25 | 2003-12-23 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
| US20050043239A1 (en) * | 2003-08-14 | 2005-02-24 | Jason Douangpanya | Methods of inhibiting immune responses stimulated by an endogenous factor |
| ES2607804T3 (es) | 2004-05-13 | 2017-04-04 | Icos Corporation | Quinazolinones como inhibidores de la fosfatidilinositol humana 3-quinasa delta |
| EP1750714A1 (en) * | 2004-05-13 | 2007-02-14 | Vanderbilt University | Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis |
| KR101653842B1 (ko) | 2008-01-04 | 2016-09-02 | 인텔리카인, 엘엘씨 | 특정 화학 물질, 조성물 및 방법 |
| US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
| US9492449B2 (en) | 2008-11-13 | 2016-11-15 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
| CN102271683B (zh) * | 2008-11-13 | 2014-07-09 | 吉里德卡利斯托加公司 | 恶性血液病的治疗 |
| AU2010229968A1 (en) | 2009-03-24 | 2011-10-13 | Gilead Calistoga Llc | Atropisomers of2-purinyl-3-tolyl-quinazolinone derivatives and methods of use |
| EP2421536B1 (en) * | 2009-04-20 | 2015-08-26 | Gilead Calistoga LLC | Methods of treatment for solid tumors |
| PE20120493A1 (es) | 2009-06-29 | 2012-05-20 | Incyte Corp | Pirimidinonas como inhibidores de pi3k |
| US8691829B2 (en) | 2009-07-21 | 2014-04-08 | Gilead Calistoga Llc | Treatment of liver disorders with PI3K inhibitors |
| US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| AR081823A1 (es) | 2010-04-14 | 2012-10-24 | Incyte Corp | DERIVADOS FUSIONADOS COMO INHIBIDORES DE PI3Kd |
| NZ717373A (en) | 2010-06-03 | 2017-11-24 | Pharmacyclics Llc | The use of inhibitors of bruton’s tyrosine kinase (btk) |
| JP2013528228A (ja) * | 2010-06-11 | 2013-07-08 | ギリアード カリストガ エルエルシー | キナゾリノン化合物による選択した患者における血液系障害を処置する方法 |
| WO2011163195A1 (en) * | 2010-06-21 | 2011-12-29 | Incyte Corporation | Fused pyrrole derivatives as pi3k inhibitors |
| DE102010039631A1 (de) * | 2010-08-22 | 2012-02-23 | Ulrich Schubert | Pharmazeutische Zusammensetzungen mit immunmodulatorischen Eigenschaften |
| WO2012064671A1 (en) * | 2010-11-08 | 2012-05-18 | The Ohio State University Research Foundation | Compositions and methods for increasing drug efficacy in cancer |
| JP2014500259A (ja) * | 2010-11-17 | 2014-01-09 | ニーキ ファーマ インコーポレイテッド | 血液癌を処置する方法 |
| ES2764848T3 (es) | 2010-12-20 | 2020-06-04 | Incyte Holdings Corp | N-(1-(fenilo sustituido)etilo)-9H-purina-6-aminas como inhibidores de PI3K |
| AR084824A1 (es) | 2011-01-10 | 2013-06-26 | Intellikine Inc | Procesos para preparar isoquinolinonas y formas solidas de isoquinolinonas |
| WO2012121953A1 (en) * | 2011-03-08 | 2012-09-13 | The Trustees Of Columbia University In The City Of New York | Methods and pharmaceutical compositions for treating lymphoid malignancy |
| AU2012229266A1 (en) * | 2011-03-11 | 2013-05-02 | Gilead Calistoga Llc | Combination therapies for hematologic malignancies |
| WO2012125629A1 (en) | 2011-03-14 | 2012-09-20 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors |
| WO2012135009A1 (en) | 2011-03-25 | 2012-10-04 | Incyte Corporation | Pyrimidine-4,6-diamine derivatives as pi3k inhibitors |
| AU2012236834B2 (en) | 2011-03-28 | 2015-12-10 | Mei Pharma, Inc | (alpha- substituted aralkylamino and heteroarylalkylamino) pyrimidinyl and 1,3,5 -triazinyl benzimidazoles, pharmaceutical compositions containing them, and these compounds for use in treating proliferative diseases |
| KR20230038593A (ko) | 2011-09-02 | 2023-03-20 | 인사이트 홀딩스 코포레이션 | Pi3k 억제제로서 헤테로시클릴아민 |
| WO2013082540A1 (en) * | 2011-12-02 | 2013-06-06 | Gilead Calistoga Llc | Compositions and methods of treating a proliferative disease with a quinazolinone derivative |
| PL2790705T3 (pl) | 2011-12-15 | 2018-06-29 | Novartis Ag | Zastosowanie inhibitorów czynności lub funkcji PI3K |
| WO2013134288A1 (en) * | 2012-03-05 | 2013-09-12 | Gilead Calistoga Llc | Polymorphic forms of (s)-2-(1-(9h-purin-6-ylamino)propyl)-5-fluoro-3-phenylquinazolin-4(3h)-one |
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- 2014-07-03 US US14/323,925 patent/US20140323439A1/en not_active Abandoned
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2015
- 2015-04-16 JP JP2015083935A patent/JP2015155436A/ja active Pending
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2016
- 2016-03-15 AU AU2016201634A patent/AU2016201634B2/en active Active
- 2016-08-22 JP JP2016161692A patent/JP2017008088A/ja not_active Withdrawn
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2017
- 2017-02-08 AU AU2017200837A patent/AU2017200837B2/en active Active
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2018
- 2018-06-14 AU AU2018204264A patent/AU2018204264C1/en active Active
- 2018-10-12 AU AU2018247326A patent/AU2018247326B2/en active Active
- 2018-11-13 US US16/189,435 patent/US20190083498A1/en not_active Abandoned
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2019
- 2019-08-06 AU AU2019213337A patent/AU2019213337C1/en active Active
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2020
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005113556A1 (en) * | 2004-05-13 | 2005-12-01 | Icos Corporation | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
| WO2005117889A1 (en) * | 2004-05-25 | 2005-12-15 | Icos Corporation | Methods for treating and/or preventing aberrant proliferation of hematopoietic |
| WO2005120511A1 (en) * | 2004-06-04 | 2005-12-22 | Icos Corporation | Methods for treating mast cell disorders |
| WO2006089106A2 (en) * | 2005-02-17 | 2006-08-24 | Icos Corporation | Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation |
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