MX2010012583A - Compuestos inhibidores de purina pi3k y métodos de uso. - Google Patents
Compuestos inhibidores de purina pi3k y métodos de uso.Info
- Publication number
- MX2010012583A MX2010012583A MX2010012583A MX2010012583A MX2010012583A MX 2010012583 A MX2010012583 A MX 2010012583A MX 2010012583 A MX2010012583 A MX 2010012583A MX 2010012583 A MX2010012583 A MX 2010012583A MX 2010012583 A MX2010012583 A MX 2010012583A
- Authority
- MX
- Mexico
- Prior art keywords
- purin
- morpholino
- methyl
- alkylene
- compound according
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 126
- 238000000034 method Methods 0.000 title claims abstract description 90
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 title description 10
- 239000012828 PI3K inhibitor Substances 0.000 title description 2
- 229940043441 phosphoinositide 3-kinase inhibitor Drugs 0.000 title description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 27
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 24
- 201000011510 cancer Diseases 0.000 claims abstract description 21
- 238000011282 treatment Methods 0.000 claims abstract description 21
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 5
- -1 quenyl Chemical group 0.000 claims description 165
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 63
- 125000000623 heterocyclic group Chemical group 0.000 claims description 32
- 125000002947 alkylene group Chemical group 0.000 claims description 26
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
- 125000003118 aryl group Chemical group 0.000 claims description 20
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 125000001072 heteroaryl group Chemical group 0.000 claims description 17
- 229910052801 chlorine Inorganic materials 0.000 claims description 16
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 15
- 229910052794 bromium Inorganic materials 0.000 claims description 15
- 229910052731 fluorine Inorganic materials 0.000 claims description 15
- 125000004452 carbocyclyl group Chemical group 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 229910052740 iodine Inorganic materials 0.000 claims description 14
- 230000001225 therapeutic effect Effects 0.000 claims description 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 10
- 241000124008 Mammalia Species 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- LJXQPZWIHJMPQQ-UHFFFAOYSA-N pyrimidin-2-amine Chemical compound NC1=NC=CC=N1 LJXQPZWIHJMPQQ-UHFFFAOYSA-N 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 7
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 7
- 125000006736 (C6-C20) aryl group Chemical group 0.000 claims description 6
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 5
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 125000002619 bicyclic group Chemical group 0.000 claims description 5
- 230000027455 binding Effects 0.000 claims description 5
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 5
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- 238000012360 testing method Methods 0.000 claims description 5
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- 125000000304 alkynyl group Chemical group 0.000 claims description 4
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- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 3
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- 239000010426 asphalt Substances 0.000 claims 2
- DKPZUBJRAYHHQC-UHFFFAOYSA-N 1-(3-hydroxypyrrolidin-1-yl)propan-1-one Chemical compound CCC(=O)N1CCC(O)C1 DKPZUBJRAYHHQC-UHFFFAOYSA-N 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
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- RCHNSHJXCTURJD-UHFFFAOYSA-N 5-(6-morpholin-4-yl-7H-purin-2-yl)pyrimidin-2-amine Chemical compound NC1=NC=C(C=N1)C1=NC(=C2N=CNC2=N1)N1CCOCC1 RCHNSHJXCTURJD-UHFFFAOYSA-N 0.000 claims 1
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- 239000000488 activin Substances 0.000 claims 1
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- METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 claims 1
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- 125000002971 oxazolyl group Chemical group 0.000 claims 1
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- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
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- 125000000335 thiazolyl group Chemical group 0.000 claims 1
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- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 1
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D473/32—Nitrogen atom
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- 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
- A61P35/02—Antineoplastic agents specific for leukemia
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- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5755908P | 2008-05-30 | 2008-05-30 | |
| PCT/US2009/045603 WO2009146406A1 (en) | 2008-05-30 | 2009-05-29 | Purine pi3k inhibitor compounds and methods of use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2010012583A true MX2010012583A (es) | 2011-02-24 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2010012583A MX2010012583A (es) | 2008-05-30 | 2009-05-29 | Compuestos inhibidores de purina pi3k y métodos de uso. |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8158624B2 (enExample) |
| EP (1) | EP2279188B1 (enExample) |
| JP (1) | JP2011521968A (enExample) |
| KR (1) | KR20110042153A (enExample) |
| CN (1) | CN102105474B (enExample) |
| AU (1) | AU2009251291B2 (enExample) |
| BR (1) | BRPI0909614A2 (enExample) |
| CA (1) | CA2721851A1 (enExample) |
| ES (1) | ES2533788T3 (enExample) |
| IL (1) | IL208838A0 (enExample) |
| MX (1) | MX2010012583A (enExample) |
| RU (1) | RU2509081C2 (enExample) |
| WO (1) | WO2009146406A1 (enExample) |
| ZA (1) | ZA201007524B (enExample) |
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- 2009-05-29 CN CN200980129148.2A patent/CN102105474B/zh active Active
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- 2009-05-29 AU AU2009251291A patent/AU2009251291B2/en not_active Ceased
- 2009-05-29 BR BRPI0909614A patent/BRPI0909614A2/pt not_active Application Discontinuation
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- 2009-05-29 RU RU2010154428/04A patent/RU2509081C2/ru not_active IP Right Cessation
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| US20090318411A1 (en) | 2009-12-24 |
| IL208838A0 (en) | 2011-01-31 |
| EP2279188B1 (en) | 2015-01-28 |
| BRPI0909614A2 (pt) | 2015-09-22 |
| AU2009251291A1 (en) | 2009-12-03 |
| JP2011521968A (ja) | 2011-07-28 |
| RU2509081C2 (ru) | 2014-03-10 |
| CN102105474A (zh) | 2011-06-22 |
| CA2721851A1 (en) | 2009-12-03 |
| US20120135988A1 (en) | 2012-05-31 |
| CN102105474B (zh) | 2014-01-08 |
| US8158624B2 (en) | 2012-04-17 |
| ZA201007524B (en) | 2012-01-25 |
| US8445487B2 (en) | 2013-05-21 |
| ES2533788T3 (es) | 2015-04-14 |
| WO2009146406A1 (en) | 2009-12-03 |
| RU2010154428A (ru) | 2012-07-10 |
| AU2009251291B2 (en) | 2013-05-02 |
| EP2279188A1 (en) | 2011-02-02 |
| KR20110042153A (ko) | 2011-04-25 |
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