SG10201510347QA - Tricyclic pi3k inhibitor compounds and methods of use - Google Patents
Tricyclic pi3k inhibitor compounds and methods of useInfo
- Publication number
- SG10201510347QA SG10201510347QA SG10201510347QA SG10201510347QA SG10201510347QA SG 10201510347Q A SG10201510347Q A SG 10201510347QA SG 10201510347Q A SG10201510347Q A SG 10201510347QA SG 10201510347Q A SG10201510347Q A SG 10201510347QA SG 10201510347Q A SG10201510347Q A SG 10201510347QA
- Authority
- SG
- Singapore
- Prior art keywords
- methods
- inhibitor compounds
- pi3k inhibitor
- tricyclic pi3k
- tricyclic
- Prior art date
Links
Classifications
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- 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
- 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
- A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
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- 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
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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- A—HUMAN NECESSITIES
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- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
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- 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
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- C07D487/14—Ortho-condensed systems
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- 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
- C07D491/12—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 three hetero rings
- C07D491/14—Ortho-condensed systems
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- 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
- C07D491/12—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 three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
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- 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
- C07D495/12—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 three hetero rings
- C07D495/14—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/20—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- 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
- C07D471/22—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 systems contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Virology (AREA)
- Gastroenterology & Hepatology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Biomedical Technology (AREA)
- Communicable Diseases (AREA)
- Emergency Medicine (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US42369410P | 2010-12-16 | 2010-12-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG10201510347QA true SG10201510347QA (en) | 2016-01-28 |
Family
ID=45478511
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG2013040563A SG190890A1 (en) | 2010-12-16 | 2011-12-15 | Tricyclic pi3k inhibitor compounds and methods of use |
SG10201510347QA SG10201510347QA (en) | 2010-12-16 | 2011-12-15 | Tricyclic pi3k inhibitor compounds and methods of use |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG2013040563A SG190890A1 (en) | 2010-12-16 | 2011-12-15 | Tricyclic pi3k inhibitor compounds and methods of use |
Country Status (32)
Country | Link |
---|---|
US (5) | US8883799B2 (en) |
EP (3) | EP2651951B1 (en) |
JP (1) | JP5775171B2 (en) |
KR (2) | KR20140099556A (en) |
CN (2) | CN103313989B (en) |
AR (2) | AR084312A1 (en) |
AU (1) | AU2011343712B2 (en) |
BR (1) | BR112013014914B8 (en) |
CA (1) | CA2820078C (en) |
CL (1) | CL2013001093A1 (en) |
CO (1) | CO6710942A2 (en) |
CR (1) | CR20130247A (en) |
DK (1) | DK2651951T3 (en) |
EA (1) | EA026134B1 (en) |
EC (1) | ECSP13012692A (en) |
ES (1) | ES2530545T3 (en) |
HK (1) | HK1185871A1 (en) |
HR (1) | HRP20150127T1 (en) |
IL (1) | IL225778A (en) |
MX (1) | MX2013006858A (en) |
MY (1) | MY164910A (en) |
NZ (1) | NZ609448A (en) |
PE (1) | PE20140314A1 (en) |
PL (1) | PL2651951T3 (en) |
PT (1) | PT2651951E (en) |
RS (1) | RS53768B1 (en) |
SG (2) | SG190890A1 (en) |
SI (1) | SI2651951T1 (en) |
TW (2) | TW201500358A (en) |
UA (1) | UA109688C2 (en) |
WO (1) | WO2012082997A1 (en) |
ZA (1) | ZA201304128B (en) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9346817B2 (en) | 2012-08-30 | 2016-05-24 | Genentech, Inc. | Dioxino- and oxazin-[2,3-D]pyrimidine PI3K inhibitor compounds and methods of use |
JP6329958B2 (en) | 2012-11-07 | 2018-05-23 | カルス セラピューティクス リミテッド | Novel histone deacetylase inhibitors and their use in therapy |
AR095443A1 (en) * | 2013-03-15 | 2015-10-14 | Fundación Centro Nac De Investig Oncológicas Carlos Iii | HEREROCICLES CONDENSED WITH ACTION ON ATR |
KR20160007577A (en) | 2013-05-10 | 2016-01-20 | 카루스 떼라퓨틱스 리미티드 | Novel histone deacetylase inhibitors |
TW201520215A (en) * | 2013-05-13 | 2015-06-01 | Daiichi Sankyo Co Ltd | Method for preparation of morpholinopurine derivatives |
CN104557955B (en) * | 2013-10-23 | 2017-05-03 | 上海汇伦生命科技有限公司 | Tricyclic compound as PI3K/mTOR inhibitor as well as preparation method and application of tricyclic compound |
MA39211B1 (en) * | 2013-12-24 | 2019-01-31 | Bristol Myers Squibb Co | Tricyclic compounds as anti-cancer agents |
CA2946538A1 (en) | 2014-04-04 | 2015-10-08 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
GB201419228D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
GB201419264D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
BR112017007662B1 (en) * | 2014-12-18 | 2021-11-03 | F. Hoffmann-La Roche Ag | COMPOUND, PHARMACEUTICAL COMPOSITION AND USE OF A COMPOUND |
JP6038111B2 (en) * | 2014-12-27 | 2016-12-07 | ヤマサ醤油株式会社 | 2,6-Dichloro-8-iodo-7-deazapurine for the synthesis of polysubstituted 7-deazapurine derivatives |
EP3539967A1 (en) * | 2015-02-11 | 2019-09-18 | Sunovion Pharmaceuticals Inc. | Process for the preparation of fused dihydro-4h-pyrazolo[5,1-c][1,4]oxazinyl compounds |
JP6701225B2 (en) * | 2015-03-09 | 2020-05-27 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Tricyclic DLK inhibitors and uses thereof |
MX2017012390A (en) | 2015-03-30 | 2018-01-26 | Daiichi Sankyo Co Ltd | 6-morpholinyl-2-pyrazolyl-9h-purine derivatives and their use as pi3k inhibitors. |
WO2017004133A1 (en) * | 2015-06-29 | 2017-01-05 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
GB201514751D0 (en) * | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
CA3004534C (en) | 2015-11-23 | 2023-11-07 | Council Of Scientific & Industrial Research | Fused pyrimidines as isoform selective phosphoinositide-3-kinase-alpha inhibitors and process for preparation thereof |
AU2016369528B2 (en) * | 2015-12-16 | 2021-04-22 | Genentech, Inc. | Process for the preparation of tricyclic PI3K inhibitor compounds and methods for using the same for the treatment of cancer |
EP3464295B1 (en) * | 2016-05-24 | 2020-02-05 | Merck Patent GmbH | Tricyclic heterocylic derivatives |
CA3028751A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Pyrimidine-based antiproliferative agents |
CN106008528A (en) * | 2016-07-28 | 2016-10-12 | 安徽赛迪生物科技有限公司 | Method for synthesizing 4-chlorine-5,7-dihydro-6H-pyrrolo[2,3-D] pyrimidine-6-ketone |
EA201990400A1 (en) | 2016-07-29 | 2019-07-31 | Суновион Фармасьютикалз, Инк. | COMPOUNDS AND COMPOSITIONS AND THEIR APPLICATION |
MA45795A (en) | 2016-07-29 | 2019-06-05 | Sunovion Pharmaceuticals Inc | COMPOUNDS AND COMPOSITIONS, AND ASSOCIATED USES |
TW201825465A (en) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
TW201815787A (en) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
TW201813963A (en) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
WO2018062382A1 (en) * | 2016-09-29 | 2018-04-05 | 第一三共株式会社 | Crystals of [2-(1-methyl-1h-pyrazol-4-yl)-6-(morpholin-4-yl)-9h-purin-8-yl][4-(morpholin-4-yl)piperidin-1-yl]methanone and pharmaceutically acceptable salt thereof |
WO2018075937A1 (en) | 2016-10-21 | 2018-04-26 | Nimbus Lakshmi, Inc. | Tyk2 inhibitors and uses thereof |
ES2911522T3 (en) | 2016-12-02 | 2022-05-19 | Daiichi Sankyo Co Ltd | Novel endo-ß-n-acetylglucosaminidase |
EP3661929B1 (en) | 2017-08-02 | 2021-07-14 | Sunovion Pharmaceuticals Inc. | Isochroman compounds and uses thereof |
EA202190654A1 (en) * | 2018-09-07 | 2021-05-27 | Оцука Фармасьютикал Ко., Лтд. | HETEROCYCLIC CONNECTION |
BR112021006225A2 (en) | 2018-10-02 | 2021-07-06 | Syngenta Participations Ag | pesticide-active benzene- and azine-amide compounds |
CN109134480A (en) * | 2018-10-19 | 2019-01-04 | 辽宁大学 | A kind of novel 4- phenylamino benzofuran simultaneously [2,3-d] pyrimidines and its application |
US11136304B2 (en) | 2019-03-14 | 2021-10-05 | Sunovion Pharmaceuticals Inc. | Salts of a heterocyclic compound and crystalline forms, processes for preparing, therapeutic uses, and pharmaceutical compositions thereof |
UY38623A (en) | 2019-03-29 | 2020-10-30 | Syngenta Crop Protection Ag | DIAZINE-AMIDE COMPOUNDS ACTIVE AS PESTICIDES |
WO2020201398A1 (en) | 2019-04-05 | 2020-10-08 | Syngenta Crop Protection Ag | Pesticidally active diazine-amide compounds |
US20220169629A1 (en) | 2019-04-11 | 2022-06-02 | Syngenta Crop Protection Ag | Pesticidally active diazine-amide compounds |
EP4017851A1 (en) | 2019-08-23 | 2022-06-29 | Syngenta Crop Protection AG | Pesticidally active pyrazine-amide compounds |
GB201913921D0 (en) * | 2019-09-26 | 2019-11-13 | Sentinel Oncology Ltd | Pharmaceutical compounds |
CN113004303A (en) * | 2019-12-18 | 2021-06-22 | 江苏恒瑞医药股份有限公司 | Pyrimido-oxazine tricyclic derivative, preparation method and application thereof in medicine |
CN115698014A (en) | 2020-05-19 | 2023-02-03 | G1治疗公司 | Cyclin dependent kinase inhibiting compounds for the treatment of medical conditions |
WO2022258481A1 (en) | 2021-06-09 | 2022-12-15 | Syngenta Crop Protection Ag | Pesticidally active diazine-amide compounds |
WO2022268025A1 (en) * | 2021-06-22 | 2022-12-29 | 成都苑东生物制药股份有限公司 | Atr inhibitor and use thereof |
WO2023072849A1 (en) | 2021-10-27 | 2023-05-04 | Syngenta Crop Protection Ag | Pesticidally active pyridazinone compounds |
WO2023104714A1 (en) | 2021-12-10 | 2023-06-15 | Syngenta Crop Protection Ag | Pesticidally active pyridazinone compounds |
KR20230115493A (en) | 2022-01-27 | 2023-08-03 | 인제대학교 산학협력단 | Composition for preventing or treating stathmin1 related diseases comprising the selective PI3K p110δ inhibitor |
CN115413669B (en) * | 2022-06-14 | 2024-03-15 | 湖南大学 | Kinase inhibitor and application of composition thereof in improving bacterial wilt resistance of plants |
CN115403593B (en) * | 2022-09-22 | 2024-02-02 | 河南师范大学 | Method for synthesizing chiral purine [3,2-c ] oxazole compound by cycloaddition |
WO2024110554A1 (en) | 2022-11-23 | 2024-05-30 | Syngenta Crop Protection Ag | N-[(1 -[2-[6-(pyridazin-3-yl]-1,2,4-triazol-3-yl]ethyl]-quinazolin-4-amine and n-[1-[3-(6-(pyridazin-3-yl)pyrazin-2-yl]ethyl]-8-quinazolin-4-amine derivatives as pesticides |
WO2024133551A1 (en) | 2022-12-21 | 2024-06-27 | Syngenta Crop Protection Ag | Pesticidally active pyridazine compounds |
Family Cites Families (89)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3016378A (en) | 1959-07-01 | 1962-01-09 | Thomae Gmbh Dr K | Amino-substituted purine derivatives |
US3773919A (en) | 1969-10-23 | 1973-11-20 | Du Pont | Polylactide-drug mixtures |
JPS4872196U (en) | 1971-12-11 | 1973-09-10 | ||
JPS4872196A (en) | 1971-12-27 | 1973-09-29 | ||
GB1570494A (en) | 1975-11-28 | 1980-07-02 | Ici Ltd | Thienopyrimidine derivatives and their use as pesticides |
US4510144A (en) * | 1981-08-26 | 1985-04-09 | Newport Pharmaceuticals International | Methods of imparting immunomodulating activity with dihydrothiazolo purine derivatives |
JPS60260579A (en) | 1984-01-13 | 1985-12-23 | Yoshitomi Pharmaceut Ind Ltd | Purine derivative |
DE3406533A1 (en) | 1984-02-23 | 1985-08-29 | Boehringer Mannheim Gmbh, 6800 Mannheim | USE OF ADENOSINE DERIVATIVES AS ANTIALLERGICA AND MEDICINAL PRODUCTS CONTAINING THEM |
JPS6216477A (en) | 1985-07-15 | 1987-01-24 | Maruishi Seiyaku Kk | 2-(4-pyridylaminomethyl)-benzimidazole derivative having antiviral activity |
US4740230A (en) | 1985-09-13 | 1988-04-26 | Idemitsu Kosan Company Limited | Triazine derivatives, and herbicides containing the derivatives as the effective component |
US5583024A (en) | 1985-12-02 | 1996-12-10 | The Regents Of The University Of California | Recombinant expression of Coleoptera luciferase |
CA1279648C (en) | 1986-07-11 | 1991-01-29 | Haruo Kuriyama | 2-(4-pyridylaminometyl)-benzimidazole derivatives having antiviral activity |
US4932998A (en) | 1986-09-30 | 1990-06-12 | Idemitsu Kosan Company Limited | Triazine derivatives, and herbicides comprising the same as the effective ingredient |
US5332744A (en) | 1989-05-30 | 1994-07-26 | Merck & Co., Inc. | Substituted imidazo-fused 6-membered heterocycles as angiotensin II antagonists |
US5846824A (en) | 1994-02-07 | 1998-12-08 | Ludwig Institute For Cancer Research | Polypeptides having kinase activity, their preparation and use |
GB9208135D0 (en) | 1992-04-13 | 1992-05-27 | Ludwig Inst Cancer Res | Polypeptides having kinase activity,their preparation and use |
US6274327B1 (en) | 1992-04-13 | 2001-08-14 | Ludwig Institute For Cancer Research | Polypeptides having kinase activity, their preparation and use |
JP3093112B2 (en) | 1994-09-01 | 2000-10-03 | 新日本製鐵株式会社 | Painted steel driving members |
US5543523A (en) | 1994-11-15 | 1996-08-06 | Regents Of The University Of Minnesota | Method and intermediates for the synthesis of korupensamines |
JPH08336393A (en) | 1995-04-13 | 1996-12-24 | Mitsubishi Chem Corp | Production of optically active gamma-substituted-beta-hydroxybutyric ester |
US5866702A (en) | 1996-08-02 | 1999-02-02 | Cv Therapeutics, Incorporation | Purine inhibitors of cyclin dependent kinase 2 |
US6602677B1 (en) | 1997-09-19 | 2003-08-05 | Promega Corporation | Thermostable luciferases and methods of production |
DE19920936A1 (en) | 1999-05-07 | 2000-11-09 | Basf Ag | Heterocyclically substituted benzimidazoles, their preparation and use |
US6608053B2 (en) | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
ES2360933T3 (en) | 2000-04-27 | 2011-06-10 | Astellas Pharma Inc. | CONDENSED HETEROARILO DERIVATIVES. |
EP1409125B1 (en) | 2001-07-12 | 2016-04-20 | Reaxa Limited | Microencapsulated catalyst, methods of preparation and methods of use thereof |
EP1427413A2 (en) | 2001-09-13 | 2004-06-16 | Synta Pharmaceuticals Corporation | 2-aroylimidazole compounds for treating cancer |
JP2005512972A (en) | 2001-10-12 | 2005-05-12 | アイアールエム エルエルシー | Kinase inhibitor scaffolds and methods for their preparation |
US6949644B2 (en) | 2001-10-12 | 2005-09-27 | Irm Llc | Methods for the synthesis of substituted purines |
US7354932B2 (en) | 2001-12-21 | 2008-04-08 | Anormed, Inc. | Chemokine receptor binding heterocyclic compounds with enhanced efficacy |
US20030139427A1 (en) | 2002-08-23 | 2003-07-24 | Osi Pharmaceuticals Inc. | Bicyclic pyrimidinyl derivatives and methods of use thereof |
US20050288503A1 (en) | 2002-09-06 | 2005-12-29 | Adams Jerry L | Novel compounds |
AU2003284142A1 (en) | 2002-10-15 | 2004-05-04 | Synta Pharmaceuticals Corp | Aromatic bicyclic heterocyles to modulate 1L-12 production |
EP1626725A4 (en) | 2003-05-29 | 2006-06-14 | Synta Pharmaceuticals Corp | Heterocyclic compounds for preventing and treating disorders associated with excessive bone loss |
TW200521119A (en) | 2003-08-05 | 2005-07-01 | Vertex Pharma | Compositions useful as inhibitors of voltage-gated ion channels |
US20060074124A1 (en) | 2003-09-12 | 2006-04-06 | Andrew Napper | Methods of treating a disorder |
BRPI0414533A (en) | 2003-09-18 | 2006-11-07 | Conforma Therapeutics Corp | compound, pharmaceutical composition, and methods for inhibiting an hsp90 and treating an individual having an hsp90 mediated disorder |
CA2541989C (en) | 2003-10-24 | 2013-10-01 | Exelixis, Inc. | P70s6 kinase modulators and method of use |
WO2005069865A2 (en) | 2004-01-13 | 2005-08-04 | Ambit Biosciences Corporation | Pyrrolopyrimidine derivatives and analogs and their use in the treatment and prevention of diseases |
EP1778231A4 (en) | 2004-08-02 | 2009-06-03 | Smithkline Beecham Corp | Chemical compounds |
GB0423653D0 (en) | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
CA2586316A1 (en) | 2004-11-11 | 2006-05-18 | Argenta Discovery Ltd. | Pyrimidine compounds as histamine modulators |
EP1934174B1 (en) | 2005-10-07 | 2011-04-06 | Exelixis, Inc. | Azetidines as mek inhibitors for the treatment of proliferative diseases |
GB2431156A (en) | 2005-10-11 | 2007-04-18 | Piramed Ltd | 1-cyclyl-3-substituted- -benzenes and -azines as inhibitors of phosphatidylinositol 3-kinase |
KR101402474B1 (en) | 2006-04-26 | 2014-06-19 | 제넨테크, 인크. | Phosphoinositide 3-kinase inhibitor compounds and pharmaceutical compositions containing them |
US8252792B2 (en) | 2006-04-26 | 2012-08-28 | F. Hoffman-La Roche Ag | Pyrimidine derivatives as PI3K inhibitors |
DK2024372T3 (en) | 2006-04-26 | 2010-09-20 | Hoffmann La Roche | Thieno [3,2-d] pyrimidine derivative suitable as P13K inhibitor |
JP5546240B2 (en) | 2006-04-26 | 2014-07-09 | ジェネンテック, インコーポレイテッド | Pharmaceutical compounds |
GB0608820D0 (en) | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
HUE033894T2 (en) | 2006-08-23 | 2018-01-29 | Kudos Pharm Ltd | 2-methylmorpholine pyrido-,pyrazo- and pyrimido-pyrimidine derivatives as mtor inhibitors |
JP4718637B2 (en) | 2006-09-15 | 2011-07-06 | ファイザー・プロダクツ・インク | Pyrido (2,3-D) pyrimidinone compounds and their use as PI3 inhibitors |
WO2008039882A1 (en) | 2006-09-30 | 2008-04-03 | Sanofi-Aventis U.S. Llc | A combination of niacin and a prostaglandin d2 receptor antagonist |
CL2007002866A1 (en) | 2006-10-04 | 2008-07-04 | Pharmacopeia Inc | COMPOUNDS DERIVED FROM 6-SUBSTITUTES-2- (BENCIMIDAZOLIL) PURINA AND PURINONA; PHARMACEUTICAL COMPOSITION THAT INCLUDES SUCH COMPOUND; AND USE OF THE COMPOUND IN THE TREATMENT OF AUTOIMMUNE DISEASES, INFLAMMATORY DISEASE, DISEASE MEDIATED BY M |
ES2559521T3 (en) | 2006-10-16 | 2016-02-12 | Thesan Pharmaceuticals, Inc. | Therapeutic pyrazolyl thienopyridines |
MY180595A (en) | 2006-12-07 | 2020-12-03 | Genentech Inc | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
MX2009005925A (en) | 2006-12-07 | 2009-08-12 | Genentech Inc | Phosphoinositide 3-kinase inhibitor compounds and methods of use. |
US20080233127A1 (en) | 2007-03-21 | 2008-09-25 | Wyeth | Imidazolopyrimidine analogs and their use as pi3 kinase and mtor inhibitors |
WO2008116909A1 (en) | 2007-03-28 | 2008-10-02 | Neurosearch A/S | Purinyl derivatives and their use as potassium channel modulators |
CN101765597A (en) | 2007-04-12 | 2010-06-30 | 霍夫曼-拉罗奇有限公司 | Pyrimidine derivatives as inhibitors of phosphatidylinositol-3-kinase |
WO2008152394A1 (en) | 2007-06-12 | 2008-12-18 | F.Hoffmann-La Roche Ag | Pharmaceutical compounds |
US7893060B2 (en) | 2007-06-12 | 2011-02-22 | F. Hoffmann-La Roche Ag | Thiazolopyrimidines and their use as inhibitors of phosphatidylinositol-3 kinase |
WO2008152387A1 (en) | 2007-06-12 | 2008-12-18 | F.Hoffmann-La Roche Ag | Quinazoline derivatives as pi3 kinase inhibitors |
KR20100033484A (en) * | 2007-06-26 | 2010-03-30 | 사노피-아벤티스 | A regioselective metal catalyzed synthesis of annelated benzimidazoles and azabenzimidazoles |
WO2009034386A1 (en) | 2007-09-13 | 2009-03-19 | Astrazeneca Ab | Derivatives of adenine and 8-aza-adenine and uses thereof-796 |
EP2207781B1 (en) | 2007-09-24 | 2012-11-28 | Genentech, Inc. | Thiazolopyrimidine p13k inhibitor compounds and methods of use |
US20110009403A1 (en) | 2007-10-05 | 2011-01-13 | S*Bio Pte Ltd. | 2-morpholinylpurines as inhibitors of pi3k |
GB0721095D0 (en) | 2007-10-26 | 2007-12-05 | Piramed Ltd | Pharmaceutical compounds |
JP5638955B2 (en) | 2007-10-26 | 2014-12-10 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Purine derivatives useful as PI3 kinase inhibitors |
GB0725218D0 (en) | 2007-12-24 | 2008-02-06 | Syngenta Ltd | Chemical compounds |
JP5608099B2 (en) | 2008-01-30 | 2014-10-15 | ジェネンテック, インコーポレイテッド | Pyrazolopyrimidine PI3K inhibitor compounds and methods of use |
WO2009146406A1 (en) | 2008-05-30 | 2009-12-03 | Genentech, Inc. | Purine pi3k inhibitor compounds and methods of use |
MX2010014230A (en) | 2008-06-20 | 2011-03-29 | Astrazeneca Ab | Compositions with and process for methylmorpholin-subsituted pyrido [2, 3-d] pyrimidines. |
WO2010014939A1 (en) | 2008-07-31 | 2010-02-04 | Genentech, Inc. | Pyrimidine compounds, compositions and methods of use |
AU2009296931A1 (en) | 2008-09-26 | 2010-04-01 | Merck Sharp & Dohme Corp. | Oxazolobenzimidazole derivatives |
TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
GB2465405A (en) * | 2008-11-10 | 2010-05-19 | Univ Basel | Triazine, pyrimidine and pyridine analogues and their use in therapy |
JP5689069B2 (en) | 2008-11-20 | 2015-03-25 | ジェネンテック, インコーポレイテッド | Pyrazolopyridine PI3K inhibitor compounds and methods of use |
WO2010136491A1 (en) | 2009-05-27 | 2010-12-02 | F. Hoffmann-La Roche Ag | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
CN102459272B (en) | 2009-05-27 | 2014-08-06 | 健泰科生物技术公司 | Bicyclic pyrimidine PI3K inhibitor compounds selective for P110 delta, and methods of use |
EP2445346A4 (en) | 2009-06-24 | 2012-12-05 | Genentech Inc | Oxo-heterocycle fused pyrimidine compounds, compositions and methods of use |
ES2534326T3 (en) * | 2009-08-20 | 2015-04-21 | Karus Therapeutics Limited | Heterocyclic tricyclic compounds as phosphoinositide 3-kinase inhibitors |
CN102020657A (en) * | 2009-09-11 | 2011-04-20 | 上海艾力斯医药科技有限公司 | Condensed heteroaryl derivative, and preparation method and application thereof |
AU2010300719A1 (en) | 2009-09-29 | 2012-05-03 | Xcovery Holding Company Llc | PI3K (delta) selective inhibitors |
BR112012019635A2 (en) | 2010-02-22 | 2016-05-03 | Hoffmann La Roche | pyrido [3,2-d] pyrimidine pi3k delta inhibitor compounds and methods of use |
UY33304A (en) | 2010-04-02 | 2011-10-31 | Amgen Inc | HETEROCYCLIC COMPOUNDS AND THEIR USES |
US9062055B2 (en) | 2010-06-21 | 2015-06-23 | Incyte Corporation | Fused pyrrole derivatives as PI3K inhibitors |
JP5555378B2 (en) | 2010-07-14 | 2014-07-23 | エフ.ホフマン−ラ ロシュ アーゲー | Purine compounds selective for PI3KP110 delta and methods of use thereof |
US8653089B2 (en) | 2011-02-09 | 2014-02-18 | F. Hoffmann-La Roche Ag | Heterocyclic compounds and methods of use |
AR086647A1 (en) | 2011-06-03 | 2014-01-15 | Hoffmann La Roche | METHODS TO TREAT MESOTELIOMA WITH A PI3K INHIBITING COMPOUND |
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