SI2585470T1 - Novi fuzirani derivati pirimidina za inhibicijo aktivnosti tirozin kinaze - Google Patents
Novi fuzirani derivati pirimidina za inhibicijo aktivnosti tirozin kinazeInfo
- Publication number
- SI2585470T1 SI2585470T1 SI201131094A SI201131094A SI2585470T1 SI 2585470 T1 SI2585470 T1 SI 2585470T1 SI 201131094 A SI201131094 A SI 201131094A SI 201131094 A SI201131094 A SI 201131094A SI 2585470 T1 SI2585470 T1 SI 2585470T1
- Authority
- SI
- Slovenia
- Prior art keywords
- inhibition
- tyrosine kinase
- kinase activity
- pyrimidine derivatives
- fused pyrimidine
- Prior art date
Links
Classifications
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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
- C07D495/02—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
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- 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
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- 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
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—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
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- 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
- A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- 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
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20100059686 | 2010-06-23 | ||
PCT/KR2011/004482 WO2011162515A2 (en) | 2010-06-23 | 2011-06-20 | Novel fused pyrimidine derivatives for inhd3ition of tyrosine kinase activity |
EP11798350.2A EP2585470B1 (en) | 2010-06-23 | 2011-06-20 | Novel fused pyrimidine derivatives for inhibition of tyrosine kinase activity |
Publications (1)
Publication Number | Publication Date |
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SI2585470T1 true SI2585470T1 (sl) | 2017-03-31 |
Family
ID=45371929
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI201131644T SI2975042T1 (sl) | 2010-06-23 | 2011-06-20 | Novi fuzirani derivati pirimidina za inhibicijo aktivnosti tirozin kinaze |
SI201131094A SI2585470T1 (sl) | 2010-06-23 | 2011-06-20 | Novi fuzirani derivati pirimidina za inhibicijo aktivnosti tirozin kinaze |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI201131644T SI2975042T1 (sl) | 2010-06-23 | 2011-06-20 | Novi fuzirani derivati pirimidina za inhibicijo aktivnosti tirozin kinaze |
Country Status (31)
Country | Link |
---|---|
US (4) | US8957065B2 (sl) |
EP (2) | EP2975042B1 (sl) |
JP (2) | JP5834347B2 (sl) |
KR (2) | KR101587506B1 (sl) |
CN (2) | CN105061438B (sl) |
AR (2) | AR081978A1 (sl) |
AU (1) | AU2011269989B2 (sl) |
BR (2) | BR112012033253A2 (sl) |
CA (1) | CA2803056C (sl) |
CY (1) | CY1118750T1 (sl) |
DK (2) | DK2585470T3 (sl) |
ES (2) | ES2622138T3 (sl) |
HK (1) | HK1211575A1 (sl) |
HR (2) | HRP20170456T1 (sl) |
HU (2) | HUE032515T2 (sl) |
IL (2) | IL223689A (sl) |
LT (2) | LT2585470T (sl) |
MX (2) | MX342164B (sl) |
MY (2) | MY162132A (sl) |
NZ (2) | NZ627709A (sl) |
PL (2) | PL2585470T3 (sl) |
PT (2) | PT2585470T (sl) |
RS (2) | RS58265B1 (sl) |
RU (2) | RU2598852C2 (sl) |
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JP2008013527A (ja) | 2006-07-10 | 2008-01-24 | Sankyo Co Ltd | チエノ[3,2−d]ピリミジン−2,4−ジアミン誘導体 |
JP5500990B2 (ja) | 2006-12-07 | 2014-05-21 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | ホスホイノシチド3−キナーゼ阻害剤化合物及び使用方法 |
WO2008152394A1 (en) | 2007-06-12 | 2008-12-18 | F.Hoffmann-La Roche Ag | Pharmaceutical compounds |
WO2009017838A2 (en) | 2007-08-01 | 2009-02-05 | Exelixis, Inc. | Combinations of jak-2 inhibitors and other agents |
EP3109249A1 (en) | 2007-11-15 | 2016-12-28 | YM BioSciences Australia Pty Ltd | N-containing heterocyclic compounds |
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KR101892989B1 (ko) * | 2008-06-27 | 2018-08-30 | 셀젠 카르 엘엘씨 | 헤테로아릴 화합물 및 이의 용도 |
WO2010054285A2 (en) * | 2008-11-10 | 2010-05-14 | National Health Research Institutes | Fused bicyclic and tricyclic pyrimidine compounds as tyrosine kinase inhibitors |
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US8957065B2 (en) * | 2010-06-23 | 2015-02-17 | Hanmi Science Co., Ltd | Fused pyrimidine derivatives for inhibition of tyrosine kinase activity |
AU2012311184A1 (en) * | 2011-09-22 | 2014-03-06 | Pfizer Inc. | Pyrrolopyrimidine and purine derivatives |
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