CN102666541B - 用于治疗特别是病毒感染的嘌呤或脱氮嘌呤的衍生物 - Google Patents
用于治疗特别是病毒感染的嘌呤或脱氮嘌呤的衍生物 Download PDFInfo
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- CN102666541B CN102666541B CN201080047895.4A CN201080047895A CN102666541B CN 102666541 B CN102666541 B CN 102666541B CN 201080047895 A CN201080047895 A CN 201080047895A CN 102666541 B CN102666541 B CN 102666541B
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- 0 C*(*N(C(C(N1)=C(N)N=C(*)**)=C)C1=O)I*(*)(*)*=* Chemical compound C*(*N(C(C(N1)=C(N)N=C(*)**)=C)C1=O)I*(*)(*)*=* 0.000 description 2
- USLDCFNPHGAEKK-UHFFFAOYSA-N Brc1nc(CN2CCCC2)c[s]1 Chemical compound Brc1nc(CN2CCCC2)c[s]1 USLDCFNPHGAEKK-UHFFFAOYSA-N 0.000 description 1
- QAMUBCOGTSVDFA-UHFFFAOYSA-N Brc1ncc(CN2CCCC2)[s]1 Chemical compound Brc1ncc(CN2CCCC2)[s]1 QAMUBCOGTSVDFA-UHFFFAOYSA-N 0.000 description 1
- MTXAQFRARZGGFQ-UHFFFAOYSA-N CCCCOc(cc1N2Cc(cc3)cnc3-c3ccc(CN4CCCC4)cc3)nc(N)c1NC2=O Chemical compound CCCCOc(cc1N2Cc(cc3)cnc3-c3ccc(CN4CCCC4)cc3)nc(N)c1NC2=O MTXAQFRARZGGFQ-UHFFFAOYSA-N 0.000 description 1
- DAAJWTARFLXAFN-UHFFFAOYSA-N CCCCOc(nc1N2Cc(cc3)ccc3-c(cc(CN3CCCC3)cc3)c3OC)nc(N)c1NC2=O Chemical compound CCCCOc(nc1N2Cc(cc3)ccc3-c(cc(CN3CCCC3)cc3)c3OC)nc(N)c1NC2=O DAAJWTARFLXAFN-UHFFFAOYSA-N 0.000 description 1
- ZGUXVEOVEZASAL-UHFFFAOYSA-N CCCCOc(nc1N2Cc(cc3)cnc3-c3ccc(CN4CCCC4)cc3)nc(N)c1NC2=O Chemical compound CCCCOc(nc1N2Cc(cc3)cnc3-c3ccc(CN4CCCC4)cc3)nc(N)c1NC2=O ZGUXVEOVEZASAL-UHFFFAOYSA-N 0.000 description 1
- LJXHLCUPAZPPNB-UHFFFAOYSA-N CCCCOc(nc1N2Cc3cc(-c4ccccc4CN4CCCC4)ccc3)nc(N)c1NC2=O Chemical compound CCCCOc(nc1N2Cc3cc(-c4ccccc4CN4CCCC4)ccc3)nc(N)c1NC2=O LJXHLCUPAZPPNB-UHFFFAOYSA-N 0.000 description 1
- JOAWYSITVVKFSO-UHFFFAOYSA-N CCCCOc(nc1[n]2Cc(cc3)ccc3-c3cc(F)c(CN4CCCC4)cc3)nc(N)c1nc2OC Chemical compound CCCCOc(nc1[n]2Cc(cc3)ccc3-c3cc(F)c(CN4CCCC4)cc3)nc(N)c1nc2OC JOAWYSITVVKFSO-UHFFFAOYSA-N 0.000 description 1
- WHGYSNWXXYOABN-UHFFFAOYSA-N CCCCOc(nc1[n]2Cc(cc3)ccc3-c3ncc(CN4CCCC4)[s]3)nc(N)c1nc2OC Chemical compound CCCCOc(nc1[n]2Cc(cc3)ccc3-c3ncc(CN4CCCC4)[s]3)nc(N)c1nc2OC WHGYSNWXXYOABN-UHFFFAOYSA-N 0.000 description 1
- MQJBHNCKAPGILR-UHFFFAOYSA-N CCCCOc(nc1[n]2Cc3ncc(C4C=C(CN5CCCC5)C=CC4)cc3)nc(N)c1nc2OC Chemical compound CCCCOc(nc1[n]2Cc3ncc(C4C=C(CN5CCCC5)C=CC4)cc3)nc(N)c1nc2OC MQJBHNCKAPGILR-UHFFFAOYSA-N 0.000 description 1
- PCPOPXLXZFRCCU-UHFFFAOYSA-N CCOC(N(Cc(cc1)ccc1I)c(cc(nc1N)OCCOC)c1[N+]([O-])=O)=O Chemical compound CCOC(N(Cc(cc1)ccc1I)c(cc(nc1N)OCCOC)c1[N+]([O-])=O)=O PCPOPXLXZFRCCU-UHFFFAOYSA-N 0.000 description 1
- QKDPOOJVFFKOTP-UHFFFAOYSA-N CCOC(N(Cc(cc1)ccc1I)c1cc(Cl)nc(N)c1[N+]([O-])=O)=O Chemical compound CCOC(N(Cc(cc1)ccc1I)c1cc(Cl)nc(N)c1[N+]([O-])=O)=O QKDPOOJVFFKOTP-UHFFFAOYSA-N 0.000 description 1
- YQYJHZDLMXFYDH-UHFFFAOYSA-N CN1CCN(Cc2cccc(C3=CCC(CN(c4nc(OCCOC)nc(N)c4N4)C4=O)C=C3)c2)CC1 Chemical compound CN1CCN(Cc2cccc(C3=CCC(CN(c4nc(OCCOC)nc(N)c4N4)C4=O)C=C3)c2)CC1 YQYJHZDLMXFYDH-UHFFFAOYSA-N 0.000 description 1
- RWLLJHVZEJQVTJ-UHFFFAOYSA-N COCCOc(nc1N2Cc(cc3)cnc3-c3ccc(CN4CCCC4)cc3)nc(N)c1NC2=O Chemical compound COCCOc(nc1N2Cc(cc3)cnc3-c3ccc(CN4CCCC4)cc3)nc(N)c1NC2=O RWLLJHVZEJQVTJ-UHFFFAOYSA-N 0.000 description 1
- RPSIBPTWNIXHKT-UHFFFAOYSA-N COCCOc(nc1[n]2Cc(ccc(I)c3)c3Cl)nc(N)c1nc2OC Chemical compound COCCOc(nc1[n]2Cc(ccc(I)c3)c3Cl)nc(N)c1nc2OC RPSIBPTWNIXHKT-UHFFFAOYSA-N 0.000 description 1
- DOEXBLXBLWVXNL-UHFFFAOYSA-N COc([n](Cc(cc1C(F)(F)F)ccc1S)c1n2)nc1c(N)nc2OCC1CCOCC1 Chemical compound COc([n](Cc(cc1C(F)(F)F)ccc1S)c1n2)nc1c(N)nc2OCC1CCOCC1 DOEXBLXBLWVXNL-UHFFFAOYSA-N 0.000 description 1
- BGOOLWKAXFLUFX-UHFFFAOYSA-N Nc(nc(nc1N2CC3C=CC(c4ccc(CN5CCCC5)nc4)=CC3)OCC3CCOCC3)c1NC2=O Chemical compound Nc(nc(nc1N2CC3C=CC(c4ccc(CN5CCCC5)nc4)=CC3)OCC3CCOCC3)c1NC2=O BGOOLWKAXFLUFX-UHFFFAOYSA-N 0.000 description 1
- CYUDDQBQNRAZRG-UHFFFAOYSA-N Nc(nc(nc1N2Cc(cc3)ccc3-c3ncc(CN4CCCC4)cc3)OCC3CCOCC3)c1NC2=O Chemical compound Nc(nc(nc1N2Cc(cc3)ccc3-c3ncc(CN4CCCC4)cc3)OCC3CCOCC3)c1NC2=O CYUDDQBQNRAZRG-UHFFFAOYSA-N 0.000 description 1
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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P31/14—Antivirals for RNA viruses
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- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
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- A—HUMAN NECESSITIES
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- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
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- A—HUMAN NECESSITIES
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-
- 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
- C07D471/02—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 two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/18—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/24—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one nitrogen and one sulfur atom
-
- C—CHEMISTRY; METALLURGY
- 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
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Gastroenterology & Hepatology (AREA)
- Otolaryngology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25410309P | 2009-10-22 | 2009-10-22 | |
| US61/254,103 | 2009-10-22 | ||
| US36679010P | 2010-07-22 | 2010-07-22 | |
| US61/366,790 | 2010-07-22 | ||
| PCT/US2010/052802 WO2011049825A1 (en) | 2009-10-22 | 2010-10-15 | Derivatives of purine or deazapurine useful for the treatment of (inter alia) viral infections |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102666541A CN102666541A (zh) | 2012-09-12 |
| CN102666541B true CN102666541B (zh) | 2015-11-25 |
Family
ID=43502860
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201080047895.4A Active CN102666541B (zh) | 2009-10-22 | 2010-10-15 | 用于治疗特别是病毒感染的嘌呤或脱氮嘌呤的衍生物 |
Country Status (27)
| Country | Link |
|---|---|
| US (3) | US8507507B2 (enExample) |
| EP (1) | EP2491035B1 (enExample) |
| JP (1) | JP5694345B2 (enExample) |
| KR (1) | KR101793300B1 (enExample) |
| CN (1) | CN102666541B (enExample) |
| AP (1) | AP3103A (enExample) |
| AU (1) | AU2010310813B2 (enExample) |
| BR (1) | BR112012009329A2 (enExample) |
| CA (1) | CA2777824C (enExample) |
| CL (1) | CL2012000988A1 (enExample) |
| CO (1) | CO6531469A2 (enExample) |
| CR (1) | CR20120255A (enExample) |
| EA (1) | EA020488B1 (enExample) |
| EC (1) | ECSP12011915A (enExample) |
| ES (1) | ES2644286T3 (enExample) |
| IL (1) | IL218747A (enExample) |
| IN (1) | IN2012DN02984A (enExample) |
| MX (1) | MX2012004706A (enExample) |
| NO (1) | NO2491035T3 (enExample) |
| NZ (1) | NZ598933A (enExample) |
| PE (1) | PE20121091A1 (enExample) |
| PL (1) | PL2491035T3 (enExample) |
| PT (1) | PT2491035T (enExample) |
| SG (1) | SG10201406813RA (enExample) |
| SI (1) | SI2491035T1 (enExample) |
| WO (1) | WO2011049825A1 (enExample) |
| ZA (1) | ZA201202858B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI704916B (zh) | 2018-05-25 | 2020-09-21 | 大陸商江蘇恒瑞醫藥股份有限公司 | 一種吡唑并雜芳基類衍生物鹽酸鹽的晶型及製備方法 |
Families Citing this family (235)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2577514T3 (es) | 2005-08-22 | 2016-07-15 | The Regents Of The University Of California | Antagonistas de TLR |
| WO2007142755A2 (en) * | 2006-05-31 | 2007-12-13 | The Regents Of The University Of California | Purine analogs |
| EA019151B1 (ru) | 2007-02-07 | 2014-01-30 | Дзе Регентс Оф Дзе Юниверсити Оф Калифорния | Конъюгаты синтетических агонистов tlr и их применение |
| EP2259788A4 (en) * | 2008-02-07 | 2011-03-16 | Univ California | TREATMENT OF BLADDER DISEASES WITH A TLR7 ACTIVATOR |
| EA026557B1 (ru) | 2008-12-09 | 2017-04-28 | Джилид Сайэнс, Инк. | Промежуточные соединения для получения модуляторов толл-подобных рецепторов |
| KR20110117705A (ko) * | 2009-02-11 | 2011-10-27 | 더 리전트 오브 더 유니버시티 오브 캘리포니아 | 톨-유사 수용체 조정제 및 질병의 치료 |
| PE20120493A1 (es) | 2009-06-29 | 2012-05-20 | Incyte Corp | Pirimidinonas como inhibidores de pi3k |
| US8507507B2 (en) | 2009-10-22 | 2013-08-13 | Gilead Sciences, Inc. | Modulators of toll-like receptors |
| TW201130842A (en) * | 2009-12-18 | 2011-09-16 | Incyte Corp | Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors |
| US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| AR081823A1 (es) | 2010-04-14 | 2012-10-24 | Incyte Corp | DERIVADOS FUSIONADOS COMO INHIBIDORES DE PI3Kd |
| WO2011163195A1 (en) | 2010-06-21 | 2011-12-29 | Incyte Corporation | Fused pyrrole derivatives as pi3k inhibitors |
| ES2764848T3 (es) | 2010-12-20 | 2020-06-04 | Incyte Holdings Corp | N-(1-(fenilo sustituido)etilo)-9H-purina-6-aminas como inhibidores de PI3K |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
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