KR20130094710A - Jak 키나아제의 억제제로서 5,7-치환된-이미다조[1,2-c]피리미딘 - Google Patents
Jak 키나아제의 억제제로서 5,7-치환된-이미다조[1,2-c]피리미딘 Download PDFInfo
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- KR20130094710A KR20130094710A KR1020127029826A KR20127029826A KR20130094710A KR 20130094710 A KR20130094710 A KR 20130094710A KR 1020127029826 A KR1020127029826 A KR 1020127029826A KR 20127029826 A KR20127029826 A KR 20127029826A KR 20130094710 A KR20130094710 A KR 20130094710A
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- compound
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- 0 C*c1cnc(C)[s]1 Chemical compound C*c1cnc(C)[s]1 0.000 description 7
- NYWHQLGDZDUFKO-UHFFFAOYSA-N CC(C)(C)NC(c1cc2ncc[n]2c(-c2c[n](C(CN)C3CC3)nc2)n1)=O Chemical compound CC(C)(C)NC(c1cc2ncc[n]2c(-c2c[n](C(CN)C3CC3)nc2)n1)=O NYWHQLGDZDUFKO-UHFFFAOYSA-N 0.000 description 1
- BDRCVPQUYMUUDX-UHFFFAOYSA-N CC(C)(C)OC(N(C1)CC1(CC#N)[n](cc1)nc1C1=NC(c2c[n](C)nc2)=CC2=N[I]=CN12)=O Chemical compound CC(C)(C)OC(N(C1)CC1(CC#N)[n](cc1)nc1C1=NC(c2c[n](C)nc2)=CC2=N[I]=CN12)=O BDRCVPQUYMUUDX-UHFFFAOYSA-N 0.000 description 1
- KZNCBQULUUIOLT-UHFFFAOYSA-N CC(C)(C)OC(N(C1)CC1(CC#N)[n]1ncc(B2OC(C)(C)C(C)(C)O2)c1)=O Chemical compound CC(C)(C)OC(N(C1)CC1(CC#N)[n]1ncc(B2OC(C)(C)C(C)(C)O2)c1)=O KZNCBQULUUIOLT-UHFFFAOYSA-N 0.000 description 1
- YYCZRZLRVYDTPC-UHFFFAOYSA-N CC(C)OCC[n]1ncc(C)c1 Chemical compound CC(C)OCC[n]1ncc(C)c1 YYCZRZLRVYDTPC-UHFFFAOYSA-N 0.000 description 1
- HXTKDDGTKRUJOQ-UHFFFAOYSA-N CC(C)[n]1cnc(C)c1 Chemical compound CC(C)[n]1cnc(C)c1 HXTKDDGTKRUJOQ-UHFFFAOYSA-N 0.000 description 1
- XBHHKVWZNGPYQD-UHFFFAOYSA-N CC(C)[n]1ncc(C)c1 Chemical compound CC(C)[n]1ncc(C)c1 XBHHKVWZNGPYQD-UHFFFAOYSA-N 0.000 description 1
- OLGOTNLCPQXGLS-UHFFFAOYSA-N CC[n]1ncc(C)c1 Chemical compound CC[n]1ncc(C)c1 OLGOTNLCPQXGLS-UHFFFAOYSA-N 0.000 description 1
- CCRSMXNAFIESDO-UHFFFAOYSA-N CN(C=CC(c1cc2ncc[n]2c(-c2n[n](C3(CC#N)CN(CC(F)(F)F)C3)cc2)n1)=C1)C1=O Chemical compound CN(C=CC(c1cc2ncc[n]2c(-c2n[n](C3(CC#N)CN(CC(F)(F)F)C3)cc2)n1)=C1)C1=O CCRSMXNAFIESDO-UHFFFAOYSA-N 0.000 description 1
- NMCAPQALCZHNRH-UHFFFAOYSA-N CS(CC[n]1ncc(-c2cc3ncc[n]3c(-c3n[n](C4(CC#N)CN(CC(F)(F)F)C4)cc3)n2)c1)(=O)=O Chemical compound CS(CC[n]1ncc(-c2cc3ncc[n]3c(-c3n[n](C4(CC#N)CN(CC(F)(F)F)C4)cc3)n2)c1)(=O)=O NMCAPQALCZHNRH-UHFFFAOYSA-N 0.000 description 1
- JAZNQCLYKJCNEB-UHFFFAOYSA-N C[n]1ncc(-c2cc3ncc[n]3c(-c3c[nH]nc3)n2)c1 Chemical compound C[n]1ncc(-c2cc3ncc[n]3c(-c3c[nH]nc3)n2)c1 JAZNQCLYKJCNEB-UHFFFAOYSA-N 0.000 description 1
- RIKMMFOAQPJVMX-UHFFFAOYSA-N Cc1c[nH]nc1 Chemical compound Cc1c[nH]nc1 RIKMMFOAQPJVMX-UHFFFAOYSA-N 0.000 description 1
- SZQCPPRPWDXLMM-UHFFFAOYSA-N Cc1c[n](C)nc1 Chemical compound Cc1c[n](C)nc1 SZQCPPRPWDXLMM-UHFFFAOYSA-N 0.000 description 1
- UVDPUOLEZAYLKE-UHFFFAOYSA-N Cc1c[n](C2CCOCC2)nc1 Chemical compound Cc1c[n](C2CCOCC2)nc1 UVDPUOLEZAYLKE-UHFFFAOYSA-N 0.000 description 1
- NOYVYANICCCMRE-UHFFFAOYSA-N Cc1c[n](C2COC2)nc1 Chemical compound Cc1c[n](C2COC2)nc1 NOYVYANICCCMRE-UHFFFAOYSA-N 0.000 description 1
- CTYIVIRELNXMMO-UHFFFAOYSA-N Cc1c[n](CC(F)(F)F)nc1 Chemical compound Cc1c[n](CC(F)(F)F)nc1 CTYIVIRELNXMMO-UHFFFAOYSA-N 0.000 description 1
- IWEBOUOPAKMFBO-UHFFFAOYSA-N Cc1c[n](CCN2CCN(C)CC2)nc1 Chemical compound Cc1c[n](CCN2CCN(C)CC2)nc1 IWEBOUOPAKMFBO-UHFFFAOYSA-N 0.000 description 1
- QULROBIBSBEIPI-UHFFFAOYSA-N Cc1c[n](COCC[Si+](C)(C)C)nc1 Chemical compound Cc1c[n](COCC[Si+](C)(C)C)nc1 QULROBIBSBEIPI-UHFFFAOYSA-N 0.000 description 1
- HTHYHGNQXCBPTD-UHFFFAOYSA-N Cc1c[n](Cc2cccnc2)nc1 Chemical compound Cc1c[n](Cc2cccnc2)nc1 HTHYHGNQXCBPTD-UHFFFAOYSA-N 0.000 description 1
- RLYUNPNLXMSXAX-UHFFFAOYSA-N Cc1cnc[s]1 Chemical compound Cc1cnc[s]1 RLYUNPNLXMSXAX-UHFFFAOYSA-N 0.000 description 1
- PYCGKPPQQAMQSP-PBDHUSIKSA-N Cc1n[n](C2(CC#N)CN(CC(F)(F)F)C2)cc1-c1nc(/C(/C=N)=C/NC)cc2ncc[n]12 Chemical compound Cc1n[n](C2(CC#N)CN(CC(F)(F)F)C2)cc1-c1nc(/C(/C=N)=C/NC)cc2ncc[n]12 PYCGKPPQQAMQSP-PBDHUSIKSA-N 0.000 description 1
- JXQGICFGPUAVLJ-UHFFFAOYSA-N Cc1nnc(C)[s]1 Chemical compound Cc1nnc(C)[s]1 JXQGICFGPUAVLJ-UHFFFAOYSA-N 0.000 description 1
- KSZLICPKISEJCA-UHFFFAOYSA-N N#CCC(C1)(CN1S(C(F)(F)F)(=O)=O)[n]1ncc(-c2nc(-c3ccc(C(F)(F)F)cc3)cc3ncc[n]23)c1 Chemical compound N#CCC(C1)(CN1S(C(F)(F)F)(=O)=O)[n]1ncc(-c2nc(-c3ccc(C(F)(F)F)cc3)cc3ncc[n]23)c1 KSZLICPKISEJCA-UHFFFAOYSA-N 0.000 description 1
- CDGWLOBEPYFSQW-UHFFFAOYSA-N N#CCC(C1CCCC1)[n]1ncc(-c2nc(-c(cc3)ccc3N3CCOCC3)cc3ncc[n]23)c1 Chemical compound N#CCC(C1CCCC1)[n]1ncc(-c2nc(-c(cc3)ccc3N3CCOCC3)cc3ncc[n]23)c1 CDGWLOBEPYFSQW-UHFFFAOYSA-N 0.000 description 1
- IZRUVVZILHUJBC-UHFFFAOYSA-N N#CCC1(CN(CC(F)(F)F)C1)[n]1ncc(-c2nc(-c3c[n](C4COC4)nc3)cc3ncc[n]23)c1 Chemical compound N#CCC1(CN(CC(F)(F)F)C1)[n]1ncc(-c2nc(-c3c[n](C4COC4)nc3)cc3ncc[n]23)c1 IZRUVVZILHUJBC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- 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
- C07D498/02—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 two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32418610P | 2010-04-14 | 2010-04-14 | |
| US61/324,186 | 2010-04-14 | ||
| PCT/US2011/031896 WO2011130146A1 (en) | 2010-04-14 | 2011-04-11 | 5, 7-substituted-imidazo [1, 2-c] pyrimidines as inhibitors of jak kinases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20130094710A true KR20130094710A (ko) | 2013-08-26 |
Family
ID=43984073
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127029826A Withdrawn KR20130094710A (ko) | 2010-04-14 | 2011-04-11 | Jak 키나아제의 억제제로서 5,7-치환된-이미다조[1,2-c]피리미딘 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US8962596B2 (https=) |
| EP (1) | EP2558468B1 (https=) |
| JP (2) | JP2013523884A (https=) |
| KR (1) | KR20130094710A (https=) |
| CN (1) | CN102985424B (https=) |
| AR (1) | AR081075A1 (https=) |
| AU (1) | AU2011240808B2 (https=) |
| CA (1) | CA2796388A1 (https=) |
| CL (1) | CL2012002882A1 (https=) |
| CO (1) | CO6630187A2 (https=) |
| CR (1) | CR20120572A (https=) |
| MX (1) | MX2012011941A (https=) |
| NZ (1) | NZ603446A (https=) |
| PH (1) | PH12012502046A1 (https=) |
| RU (1) | RU2012148246A (https=) |
| SG (1) | SG184870A1 (https=) |
| TW (1) | TWI494314B (https=) |
| UA (1) | UA109131C2 (https=) |
| UY (1) | UY33328A (https=) |
| WO (1) | WO2011130146A1 (https=) |
| ZA (1) | ZA201208544B (https=) |
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| EP2455382B1 (en) | 2005-12-13 | 2016-10-26 | Incyte Holdings Corporation | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors |
| EP3070090B1 (en) | 2007-06-13 | 2018-12-12 | Incyte Holdings Corporation | Use of salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h- pyrazol-1-yl)-3- cyclopentylpropanenitrile |
| JP5775070B2 (ja) | 2009-05-22 | 2015-09-09 | インサイト・コーポレイションIncyte Corporation | ヤヌスキナーゼ阻害剤としてのピラゾール−4−イル−ピロロ[2,3−d]ピリミジンおよびピロール−3−イル−ピロロ[2,3−d]ピリミジンのN−(ヘテロ)アリール−ピロリジン誘導体 |
| SG176111A1 (en) | 2009-05-22 | 2011-12-29 | Incyte Corp | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors |
| RS57869B1 (sr) | 2009-06-17 | 2018-12-31 | Vertex Pharma | Inhibitori replikacije virusa gripa |
| AR078012A1 (es) | 2009-09-01 | 2011-10-05 | Incyte Corp | Derivados heterociclicos de las pirazol-4-il- pirrolo (2,3-d) pirimidinas como inhibidores de la quinasa janus |
| PT3354652T (pt) | 2010-03-10 | 2020-07-20 | Incyte Holdings Corp | Derivados de piperidin-4-ilazetidina como inibidores de jak1 |
| RS54824B1 (sr) | 2010-05-21 | 2016-10-31 | Incyte Holdings Corp | Topikalna formulacija za inhibiciju jak-a |
| CA2818542A1 (en) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
| WO2012068440A1 (en) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors |
| AU2011343642A1 (en) | 2010-12-16 | 2013-05-02 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
| MY165963A (en) | 2011-06-20 | 2018-05-18 | Incyte Holdings Corp | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors |
| UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
| TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為jak抑制劑之環己基氮雜環丁烷衍生物 |
| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| US20140228349A1 (en) * | 2011-10-12 | 2014-08-14 | Array Biopharma Inc. | 5,7-substituted-imidazo[1,2-c]pyrimidines |
| CA2854879A1 (en) * | 2011-11-07 | 2013-05-16 | Vertex Pharmaceuticals Incorporated | Methods for treating inflammatory diseases and pharmaceutical combinations useful therefor |
| TW201406761A (zh) | 2012-05-18 | 2014-02-16 | Incyte Corp | 做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物 |
| EP2912031B1 (en) | 2012-10-24 | 2017-05-31 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| CN113384546A (zh) | 2012-11-15 | 2021-09-14 | 因赛特公司 | 鲁索利替尼的缓释剂型 |
| EP2951590A1 (en) | 2013-02-04 | 2015-12-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for assaying jak2 activity in red blood cells and uses thereof |
| WO2014138168A1 (en) | 2013-03-06 | 2014-09-12 | Incyte Corporation | Processes and intermediates for making a jak inhibitor |
| WO2014146249A1 (en) | 2013-03-19 | 2014-09-25 | Merck Sharp & Dohme Corp. | Geminally substituted cyanoethylpyrazolo pyridones as janus kinase inhibitors |
| EA201591881A1 (ru) * | 2013-03-28 | 2016-04-29 | Такеда Фармасьютикал Компани Лимитед | Гетероциклическое соединение |
| WO2014172639A1 (en) * | 2013-04-19 | 2014-10-23 | Ruga Corporation | Raf kinase inhibitors |
| SMT201900223T1 (it) * | 2013-05-17 | 2019-07-11 | Incyte Corp | Sale di bipirazolo come inibitore di jak |
| SG10201801069QA (en) | 2013-08-07 | 2018-03-28 | Incyte Corp | Sustained release dosage forms for a jak1 inhibitor |
| RS59144B1 (sr) | 2013-11-13 | 2019-09-30 | Vertex Pharma | Inhibitori replikacije virusa influence |
| HRP20181272T1 (hr) | 2013-11-13 | 2018-10-05 | Vertex Pharmaceuticals Incorporated | Postupci priprave inhibitora replikacije virusa influence |
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| HUE054371T2 (hu) | 2014-12-05 | 2021-09-28 | Array Biopharma Inc | 4,6-szubsztituált pirazolo[l,5-A]pirazinok mint janus kináz inhibitorok |
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| JP6770580B2 (ja) * | 2016-01-26 | 2020-10-14 | 杭州華東医薬集団生物医薬有限公司Hangzhou Huadong Medicine Group Biopharmaceutical Co., Ltd. | ピロロピリミジン5員環アザ環状誘導体およびその利用 |
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| WO2018167283A1 (en) | 2017-03-17 | 2018-09-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the diagnosis and treatment of pancreatic ductal adenocarcinoma associated neural remodeling |
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| IL311485B1 (en) | 2018-02-16 | 2026-01-01 | Incyte Corp | JAK1 pathway inhibitors for the treatment of cytokine-related disorders |
| MD3773593T2 (ro) | 2018-03-30 | 2024-10-31 | Incyte Corp | Tratament hidradenitei supurative utilizând inhibitori ai JAK |
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| TW202136261A (zh) | 2018-10-31 | 2021-10-01 | 美商基利科學股份有限公司 | 經取代之6-氮雜苯并咪唑化合物 |
| TWI721623B (zh) | 2018-10-31 | 2021-03-11 | 美商基利科學股份有限公司 | 經取代之6-氮雜苯并咪唑化合物 |
| WO2020092015A1 (en) | 2018-11-02 | 2020-05-07 | University Of Rochester | Therapeutic mitigation of epithelial infection |
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| US11453681B2 (en) | 2019-05-23 | 2022-09-27 | Gilead Sciences, Inc. | Substituted eneoxindoles and uses thereof |
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| US5728536A (en) | 1993-07-29 | 1998-03-17 | St. Jude Children's Research Hospital | Jak kinases and regulation of Cytokine signal transduction |
| US6313129B1 (en) | 1998-08-21 | 2001-11-06 | Hughes Institute | Therapeutic compounds |
| JP2001302667A (ja) * | 2000-04-28 | 2001-10-31 | Bayer Ag | イミダゾピリミジン誘導体およびトリアゾロピリミジン誘導体 |
| ATE479687T1 (de) * | 2004-10-15 | 2010-09-15 | Takeda Pharmaceutical | Kinaseinhibitoren |
| EP2455382B1 (en) * | 2005-12-13 | 2016-10-26 | Incyte Holdings Corporation | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors |
| ME02372B (me) * | 2006-11-22 | 2016-06-20 | Incyte Holdings Corp | Imidazotriazini i imidazopiramidini kao inhibitori kinaze |
| DE102007012645A1 (de) * | 2007-03-16 | 2008-09-18 | Bayer Healthcare Ag | Substituierte Imidazo- und Triazolopyrimidine |
| CL2008001709A1 (es) * | 2007-06-13 | 2008-11-03 | Incyte Corp | Compuestos derivados de pirrolo [2,3-b]pirimidina, moduladores de quinasas jak; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como cancer, psoriasis, artritis reumatoide, entre otras. |
| US8158616B2 (en) | 2008-03-11 | 2012-04-17 | Incyte Corporation | Azetidine and cyclobutane derivatives as JAK inhibitors |
| CA3121743A1 (en) | 2009-01-15 | 2010-07-22 | Incyte Holdings Corporation | Processes for preparing jak inhibitors and related intermediate compounds |
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| UA109131C2 (ru) | 2015-07-27 |
| EP2558468A1 (en) | 2013-02-20 |
| CN102985424A (zh) | 2013-03-20 |
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| CA2796388A1 (en) | 2011-10-20 |
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| US20130131039A1 (en) | 2013-05-23 |
| TWI494314B (zh) | 2015-08-01 |
| UY33328A (es) | 2012-10-31 |
| PH12012502046A1 (en) | 2017-07-26 |
| EP2558468B1 (en) | 2015-04-01 |
| ZA201208544B (en) | 2015-04-29 |
| SG184870A1 (en) | 2012-11-29 |
| CL2012002882A1 (es) | 2013-02-08 |
| AR081075A1 (es) | 2012-06-06 |
| US8962596B2 (en) | 2015-02-24 |
| AU2011240808A1 (en) | 2012-11-29 |
| CN102985424B (zh) | 2015-03-11 |
| CR20120572A (es) | 2013-02-20 |
| NZ603446A (en) | 2014-05-30 |
| RU2012148246A (ru) | 2014-05-20 |
| WO2011130146A1 (en) | 2011-10-20 |
| JP2015205905A (ja) | 2015-11-19 |
| CO6630187A2 (es) | 2013-03-01 |
| MX2012011941A (es) | 2013-08-27 |
| AU2011240808B2 (en) | 2015-01-22 |
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