CN101675053B - 磷酸肌醇3-激酶抑制剂化合物及使用方法 - Google Patents
磷酸肌醇3-激酶抑制剂化合物及使用方法 Download PDFInfo
- Publication number
- CN101675053B CN101675053B CN200780051049.8A CN200780051049A CN101675053B CN 101675053 B CN101675053 B CN 101675053B CN 200780051049 A CN200780051049 A CN 200780051049A CN 101675053 B CN101675053 B CN 101675053B
- Authority
- CN
- China
- Prior art keywords
- pyrimidine
- methyl
- morpholino
- thieno
- aminopyrimidine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 0 *c1cc(nc(-c(cc2)cnc2N)nc2N3CCOCC3)c2[s]1 Chemical compound *c1cc(nc(-c(cc2)cnc2N)nc2N3CCOCC3)c2[s]1 0.000 description 1
- YEFYIJJGHCHMHG-UHFFFAOYSA-N CC(C)(c1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)N Chemical compound CC(C)(c1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)N YEFYIJJGHCHMHG-UHFFFAOYSA-N 0.000 description 1
- XDJIYRGGYWQYGX-AKGZTFGVSA-N CC(C1)[C@H]1c1cc(NC(NC2=O)=O)c2[s]1 Chemical compound CC(C1)[C@H]1c1cc(NC(NC2=O)=O)c2[s]1 XDJIYRGGYWQYGX-AKGZTFGVSA-N 0.000 description 1
- SDKXWODGLFETMZ-UHFFFAOYSA-N CC1(C)OB(c(cc2)cnc2N)OC1 Chemical compound CC1(C)OB(c(cc2)cnc2N)OC1 SDKXWODGLFETMZ-UHFFFAOYSA-N 0.000 description 1
- KECYTIHITLJYOB-UHFFFAOYSA-N COC(CC(COCC1)N1c1nc(Cl)nc2c1[s]cc2)=O Chemical compound COC(CC(COCC1)N1c1nc(Cl)nc2c1[s]cc2)=O KECYTIHITLJYOB-UHFFFAOYSA-N 0.000 description 1
- UTLPWTWCOSOPMX-UHFFFAOYSA-N COC(c([o]cc1)c1N)=O Chemical compound COC(c([o]cc1)c1N)=O UTLPWTWCOSOPMX-UHFFFAOYSA-N 0.000 description 1
- TWEQNZZOOFKOER-UHFFFAOYSA-N COC(c([s]cc1)c1N)=O Chemical compound COC(c([s]cc1)c1N)=O TWEQNZZOOFKOER-UHFFFAOYSA-N 0.000 description 1
- SJFBXOOPWKAOLP-UHFFFAOYSA-N Cc(cc(cc1)C(O)=O)c1-c1cc(nc(-c2cnc(N)nc2)nc2N3CCOCC3)c2[s]1 Chemical compound Cc(cc(cc1)C(O)=O)c1-c1cc(nc(-c2cnc(N)nc2)nc2N3CCOCC3)c2[s]1 SJFBXOOPWKAOLP-UHFFFAOYSA-N 0.000 description 1
- AQECFYPZMBRCIA-UHFFFAOYSA-N Clc1nc(Cl)nc2c1[s]cc2 Chemical compound Clc1nc(Cl)nc2c1[s]cc2 AQECFYPZMBRCIA-UHFFFAOYSA-N 0.000 description 1
- HRXNGIQKOWQHCX-UHFFFAOYSA-N Clc1nc(Cl)nc2c1cc[s]2 Chemical compound Clc1nc(Cl)nc2c1cc[s]2 HRXNGIQKOWQHCX-UHFFFAOYSA-N 0.000 description 1
- SJEBUPZLTNDCMP-UHFFFAOYSA-N Clc1nc(N2CCOCC2)c2[s]c(I)cc2n1 Chemical compound Clc1nc(N2CCOCC2)c2[s]c(I)cc2n1 SJEBUPZLTNDCMP-UHFFFAOYSA-N 0.000 description 1
- ONGYLSSMBGLLSH-UHFFFAOYSA-N NC(c1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)=O Chemical compound NC(c1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)=O ONGYLSSMBGLLSH-UHFFFAOYSA-N 0.000 description 1
- JGOOQALRLGHKIY-UHFFFAOYSA-N O=C(c1c(N2)[s]cc1)NC2=O Chemical compound O=C(c1c(N2)[s]cc1)NC2=O JGOOQALRLGHKIY-UHFFFAOYSA-N 0.000 description 1
- WETMINKYSXSGDJ-UHFFFAOYSA-N OC(c1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)=O Chemical compound OC(c1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)=O WETMINKYSXSGDJ-UHFFFAOYSA-N 0.000 description 1
- UJOJBFAUAVIWPP-UHFFFAOYSA-N OCc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1 Chemical compound OCc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1 UJOJBFAUAVIWPP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Immunology (AREA)
- Emergency Medicine (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87342206P | 2006-12-07 | 2006-12-07 | |
| US60/873,422 | 2006-12-07 | ||
| PCT/US2007/086533 WO2008073785A2 (en) | 2006-12-07 | 2007-12-05 | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101675053A CN101675053A (zh) | 2010-03-17 |
| CN101675053B true CN101675053B (zh) | 2014-03-12 |
Family
ID=39403189
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200780051049.8A Active CN101675053B (zh) | 2006-12-07 | 2007-12-05 | 磷酸肌醇3-激酶抑制剂化合物及使用方法 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US9487533B2 (enExample) |
| EP (1) | EP2114950B1 (enExample) |
| JP (1) | JP5500990B2 (enExample) |
| KR (1) | KR101507182B1 (enExample) |
| CN (1) | CN101675053B (enExample) |
| AR (1) | AR064154A1 (enExample) |
| AU (1) | AU2007333243B2 (enExample) |
| BR (1) | BRPI0717907A2 (enExample) |
| CA (1) | CA2671845C (enExample) |
| CL (1) | CL2007003523A1 (enExample) |
| ES (1) | ES2571028T3 (enExample) |
| IL (1) | IL199151A (enExample) |
| MX (1) | MX2009005925A (enExample) |
| NO (1) | NO342697B1 (enExample) |
| PE (1) | PE20081353A1 (enExample) |
| RU (1) | RU2470936C2 (enExample) |
| TW (1) | TW200829594A (enExample) |
| WO (1) | WO2008073785A2 (enExample) |
| ZA (1) | ZA200904531B (enExample) |
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| CA2264819C (en) * | 1996-09-04 | 2010-03-23 | Intertrust Technologies Corp. | Trusted infrastructure support systems, methods and techniques for secure electronic commerce, electronic transactions, commerce process control and automation, distributed computing, and rights management |
| AR064155A1 (es) * | 2006-12-07 | 2009-03-18 | Piramed Ltd | Compuestos de inhibidores de fosfoinositido-3 quinasa y metodos de uso |
| JP5539190B2 (ja) * | 2007-06-12 | 2014-07-02 | エフ.ホフマン−ラ ロシュ アーゲー | チアゾロピリミジン類及びホスファチジルイノシトール−3キナーゼのインヒビターとしてのそれらの使用 |
| TWI471134B (zh) * | 2007-09-12 | 2015-02-01 | Genentech Inc | 肌醇磷脂3-激酶抑制劑化合物及化療劑之組合及使用方法 |
| ES2399774T3 (es) | 2007-09-24 | 2013-04-03 | Genentech, Inc. | Compuestos de tiazolopirimidina inhibidores de PI3K y métodos de uso |
| CA2701292C (en) * | 2007-10-25 | 2015-03-24 | Genentech, Inc. | Process for making thienopyrimidine compounds |
| GB0721095D0 (en) * | 2007-10-26 | 2007-12-05 | Piramed Ltd | Pharmaceutical compounds |
| CA2710194C (en) | 2007-12-19 | 2014-04-22 | Amgen Inc. | Inhibitors of p13 kinase |
| KR20110046514A (ko) * | 2008-07-31 | 2011-05-04 | 제넨테크, 인크. | 피리미딘 화합물, 조성물 및 사용 방법 |
| WO2010027002A1 (ja) * | 2008-09-05 | 2010-03-11 | 塩野義製薬株式会社 | Pi3k阻害活性を有する縮環モルホリン誘導体 |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| WO2010042998A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1p receptors modulators |
| WO2010043000A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1p receptors modulators and their use thereof |
| ME02230B (me) * | 2009-01-08 | 2016-02-20 | Curis Inc | Inhibitori fosfoinozitid 3-kinaze sa delom koji vezuje cink |
| US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
| CA2753285A1 (en) | 2009-03-12 | 2010-09-16 | Genentech, Inc. | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents for the treatment of hematopoietic malignancies |
| CA2754890C (en) * | 2009-03-13 | 2018-01-16 | Piet Herdewijn | Bicyclic heterocycles |
| CN102361878A (zh) | 2009-03-24 | 2012-02-22 | 住友化学株式会社 | 用于制备硼酸酯化合物的方法 |
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| WO2011049625A1 (en) | 2009-10-20 | 2011-04-28 | Mansour Samadpour | Method for aflatoxin screening of products |
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| BR112012011147A2 (pt) * | 2009-11-12 | 2021-09-08 | F.Hoffmann-La Roche Ag | Composto, composição farmacêutica e uso de um composto. |
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| CN103003279B (zh) | 2010-07-14 | 2015-09-23 | 弗·哈夫曼-拉罗切有限公司 | 对PI3K P110δ具有选择性的嘌呤化合物及其使用方法 |
| DE102010049595A1 (de) * | 2010-10-26 | 2012-04-26 | Merck Patent Gmbh | Chinazolinderivate |
| EP3053925A1 (en) | 2010-12-16 | 2016-08-10 | F. Hoffmann-La Roche AG | Tricyclic pi3k inhibitor compounds and methods of use |
| JP2014505076A (ja) * | 2011-01-27 | 2014-02-27 | ザ トラスティーズ オブ プリンストン ユニバーシティ | 抗ウイルス剤としてのmTORキナーゼの阻害剤 |
| US8653089B2 (en) | 2011-02-09 | 2014-02-18 | F. Hoffmann-La Roche Ag | Heterocyclic compounds and methods of use |
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| RU2013143747A (ru) | 2011-03-21 | 2015-04-27 | Ф. Хоффманн-Ля Рош Аг | Соединения бензоксазепина, селективные в отношении pi3k p110 дельта и способы их применения |
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