CN101679409B - 双环杂环衍生化合物、其医药组合物和其用途 - Google Patents
双环杂环衍生化合物、其医药组合物和其用途 Download PDFInfo
- Publication number
- CN101679409B CN101679409B CN200780047742.8A CN200780047742A CN101679409B CN 101679409 B CN101679409 B CN 101679409B CN 200780047742 A CN200780047742 A CN 200780047742A CN 101679409 B CN101679409 B CN 101679409B
- Authority
- CN
- China
- Prior art keywords
- phenyl
- pyridin
- group
- base
- imidazo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 CC1=C2N=CC(*=C)=CN2CC=C1 Chemical compound CC1=C2N=CC(*=C)=CN2CC=C1 0.000 description 7
- OHTQHZVNZWWYFD-UHFFFAOYSA-N Brc(cn1)ncc1I Chemical compound Brc(cn1)ncc1I OHTQHZVNZWWYFD-UHFFFAOYSA-N 0.000 description 1
- OASOJRLJBDCVNU-UHFFFAOYSA-N Brc1cc2ncc[n]2cc1 Chemical compound Brc1cc2ncc[n]2cc1 OASOJRLJBDCVNU-UHFFFAOYSA-N 0.000 description 1
- NYPYPOZNGOXYSU-UHFFFAOYSA-N Brc1cnccc1 Chemical compound Brc1cnccc1 NYPYPOZNGOXYSU-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N C1CCCCC1 Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- VOPRIKIKYHNQPE-UHFFFAOYSA-N CC([n]1c(ccc(C)c2)c2nc1)=O Chemical compound CC([n]1c(ccc(C)c2)c2nc1)=O VOPRIKIKYHNQPE-UHFFFAOYSA-N 0.000 description 1
- YMXIIVIQLHYKOT-UHFFFAOYSA-N CC1(C)OB(c2cc(N)ccc2)OC1(C)C Chemical compound CC1(C)OB(c2cc(N)ccc2)OC1(C)C YMXIIVIQLHYKOT-UHFFFAOYSA-N 0.000 description 1
- OQZVMYHXMPXXDO-UHFFFAOYSA-N CC1(C)OB(c2cc(Nc3ncc[n]3C)ccc2)OC1(C)C Chemical compound CC1(C)OB(c2cc(Nc3ncc[n]3C)ccc2)OC1(C)C OQZVMYHXMPXXDO-UHFFFAOYSA-N 0.000 description 1
- DPXKWJRFFFMQIE-UHFFFAOYSA-N CN1CCN(Cc2cc(-c3cc4ncc[n]4cc3)ccc2)CC1 Chemical compound CN1CCN(Cc2cc(-c3cc4ncc[n]4cc3)ccc2)CC1 DPXKWJRFFFMQIE-UHFFFAOYSA-N 0.000 description 1
- BANOTGHIHYMTDL-UHFFFAOYSA-N C[n]1c(Br)ncc1 Chemical compound C[n]1c(Br)ncc1 BANOTGHIHYMTDL-UHFFFAOYSA-N 0.000 description 1
- MEQBJJUWDCYIAB-UHFFFAOYSA-N Nc(cccn1)c1Cl Chemical compound Nc(cccn1)c1Cl MEQBJJUWDCYIAB-UHFFFAOYSA-N 0.000 description 1
- OLQLKEGDKARDNO-UHFFFAOYSA-N Nc1c(Nc2ccccc2)nccc1 Chemical compound Nc1c(Nc2ccccc2)nccc1 OLQLKEGDKARDNO-UHFFFAOYSA-N 0.000 description 1
- IHEYHMWRLSPJOC-UHFFFAOYSA-N O=Cc1cc(-c2cc3ncc[n]3cc2)ccc1 Chemical compound O=Cc1cc(-c2cc3ncc[n]3cc2)ccc1 IHEYHMWRLSPJOC-UHFFFAOYSA-N 0.000 description 1
- ONGHBSNRFQKFCR-UHFFFAOYSA-N [AlH2][n]1c(ccc(Br)c2)c2nc1 Chemical compound [AlH2][n]1c(ccc(Br)c2)c2nc1 ONGHBSNRFQKFCR-UHFFFAOYSA-N 0.000 description 1
- YWWQIEUNFFAQBD-UHFFFAOYSA-N [AlH2]c1c(cnc([AlH2])c2)[n]2nc1 Chemical compound [AlH2]c1c(cnc([AlH2])c2)[n]2nc1 YWWQIEUNFFAQBD-UHFFFAOYSA-N 0.000 description 1
- MIYAGMGZOUGESO-UHFFFAOYSA-N [AlH2]c1c[n]2ncc(I)c2cn1 Chemical compound [AlH2]c1c[n]2ncc(I)c2cn1 MIYAGMGZOUGESO-UHFFFAOYSA-N 0.000 description 1
- FMXKGGRGLUTJLQ-UHFFFAOYSA-N [AlH2]c1c[n]2nccc2cn1 Chemical compound [AlH2]c1c[n]2nccc2cn1 FMXKGGRGLUTJLQ-UHFFFAOYSA-N 0.000 description 1
- FGCYBOOOROJQAY-UHFFFAOYSA-N [AlH2]c1cc2ncc[n]2cc1 Chemical compound [AlH2]c1cc2ncc[n]2cc1 FGCYBOOOROJQAY-UHFFFAOYSA-N 0.000 description 1
- UQEANKGXXSENNF-UHFFFAOYSA-N [O-][N+](c(cc(cc1)Br)c1F)=O Chemical compound [O-][N+](c(cc(cc1)Br)c1F)=O UQEANKGXXSENNF-UHFFFAOYSA-N 0.000 description 1
- AGQWNWPWJSILEU-UHFFFAOYSA-N c([n]1-c2ccccc2)nc2c1nccc2 Chemical compound c([n]1-c2ccccc2)nc2c1nccc2 AGQWNWPWJSILEU-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
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)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87153806P | 2006-12-22 | 2006-12-22 | |
| US60/871,538 | 2006-12-22 | ||
| GB0625827A GB0625827D0 (en) | 2006-12-22 | 2006-12-22 | New compounds |
| GB0625827.1 | 2006-12-22 | ||
| US97958207P | 2007-10-12 | 2007-10-12 | |
| GB0719998A GB0719998D0 (en) | 2007-10-12 | 2007-10-12 | New compounds |
| US60/979,582 | 2007-10-12 | ||
| GB0719998.7 | 2007-10-12 | ||
| PCT/GB2007/004960 WO2008078100A2 (en) | 2006-12-22 | 2007-12-21 | Tricyclic amine derivatives as protein tyrosine kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101679409A CN101679409A (zh) | 2010-03-24 |
| CN101679409B true CN101679409B (zh) | 2014-11-26 |
Family
ID=39322759
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200780047742.8A Expired - Fee Related CN101679409B (zh) | 2006-12-22 | 2007-12-21 | 双环杂环衍生化合物、其医药组合物和其用途 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8513276B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2121687B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5442449B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN101679409B (cg-RX-API-DMAC7.html) |
| AU (1) | AU2007337895C1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2672213C (cg-RX-API-DMAC7.html) |
| CY (1) | CY1117319T1 (cg-RX-API-DMAC7.html) |
| HR (1) | HRP20151398T1 (cg-RX-API-DMAC7.html) |
| MX (1) | MX2009006704A (cg-RX-API-DMAC7.html) |
| NO (1) | NO342865B1 (cg-RX-API-DMAC7.html) |
| PL (1) | PL2121687T3 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2008078100A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (90)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| AR059898A1 (es) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2 |
| JP5442449B2 (ja) | 2006-12-22 | 2014-03-12 | アステックス、セラピューティックス、リミテッド | 新規化合物 |
| MX2009006706A (es) | 2006-12-22 | 2009-07-02 | Astex Therapeutics Ltd | Compuestos heterociclicos biciclicos como inhibidores del receptor del factor de crecimiento de fibroblastos. |
| TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| RS51660B (sr) | 2007-09-14 | 2011-10-31 | Ortho-Mcneil-Janssen Pharmaceuticals Inc. | 1`,3`-disupstituisani-4-fenil-3,4,5,6-tetrahidro-2h, 1`h-[1,4`] bipiridinil-2`-oni |
| WO2009033703A1 (en) | 2007-09-14 | 2009-03-19 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | 1,3-disubstituted-4-phenyl-1 h-pyridin-2-ones |
| ATE516272T1 (de) | 2007-09-14 | 2011-07-15 | Ortho Mcneil Janssen Pharm | 1,3-disubstituierte 4-(aryl-x-phenyl)-1h-pyridin- 2-one |
| GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
| GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
| EP2220083B1 (en) | 2007-11-14 | 2017-07-19 | Janssen Pharmaceuticals, Inc. | Imidazo[1,2-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| KR20100108390A (ko) | 2007-12-19 | 2010-10-06 | 버텍스 파마슈티칼스 인코포레이티드 | JAK2 억제제로서 유용한 피라졸로[1,5-a]피리미딘 |
| GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
| WO2010017047A1 (en) * | 2008-08-05 | 2010-02-11 | Merck & Co., Inc. | Therapeutic compounds |
| US8518911B2 (en) | 2008-08-05 | 2013-08-27 | Merck Sharp & Dohme Corp. | Pyrazolo[1,5-a]pyridines as MARK inhibitors |
| EP2344470B1 (en) | 2008-09-02 | 2013-11-06 | Janssen Pharmaceuticals, Inc. | 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors |
| AU2009304293B2 (en) | 2008-10-16 | 2012-04-26 | Addex Pharma S.A. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
| JP5690277B2 (ja) * | 2008-11-28 | 2015-03-25 | ジャンセン ファーマシューティカルズ, インコーポレイテッド. | 代謝型グルタミン酸受容体の調節因子としてのインドールおよびベンゾオキサジン誘導体 |
| GB0906470D0 (en) * | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| GB0906472D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| KR20120035158A (ko) | 2009-05-12 | 2012-04-13 | 얀센 파마슈티칼즈, 인코포레이티드 | 1,2,4?트리아졸로[4,3?a]피리딘 유도체 및 mGluR2 수용체의 양성 알로스테릭 조절자로서의 그의 용도 |
| US8937060B2 (en) | 2009-05-12 | 2015-01-20 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo [4,3-A] pyridine derivatives and their use for the treatment of prevention of neurological and psychiatric disorders |
| EP2475428B1 (en) * | 2009-09-11 | 2015-07-01 | Probiodrug AG | Heterocylcic derivatives as inhibitors of glutaminyl cyclase |
| FR2950345B1 (fr) * | 2009-09-18 | 2011-09-23 | Sanofi Aventis | Derives acetyleniques de 5-phenyl-pyrazolopyridine, leur preparation et leur application en therapeutique |
| FR2950344B1 (fr) * | 2009-09-18 | 2011-11-25 | Sanofi Aventis | Derives de 5-phenyl-pyrazolopyridine, leur preparation et leur aplication en therapeutique. |
| EP2496574A1 (en) * | 2009-11-02 | 2012-09-12 | Abbott Laboratories | Imidazopyridines as a novel scaffold for multi-targeted kinase inhibition |
| FR2953520B1 (fr) * | 2009-12-04 | 2011-11-25 | Sanofi Aventis | Derives de diphenyl-pyrazolopyridines, leur preparation et leur application en therapeutique |
| EP2338888A1 (en) * | 2009-12-24 | 2011-06-29 | Almirall, S.A. | Imidazopyridine derivatives as JAK inhibitors |
| EP2360158A1 (en) * | 2010-02-18 | 2011-08-24 | Almirall, S.A. | Pyrazole derivatives as jak inhibitors |
| UY33213A (es) * | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
| CA2791020A1 (en) * | 2010-04-28 | 2011-11-03 | Daiichi Sankyo Company, Limited | [5,6] heterocyclic compound |
| AU2011320565A1 (en) * | 2010-10-28 | 2013-05-23 | Innocrin Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
| CA2814996C (en) | 2010-11-08 | 2019-10-01 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| EP2643320B1 (en) | 2010-11-08 | 2015-03-04 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
| CN103298809B (zh) | 2010-11-08 | 2016-08-31 | 杨森制药公司 | 1,2,4-三唑并[4,3-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途 |
| EP2463289A1 (en) | 2010-11-26 | 2012-06-13 | Almirall, S.A. | Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors |
| AU2011344001B2 (en) | 2010-12-13 | 2016-06-30 | Array Biopharma Inc. | Substituted N-(1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide compounds as type III receptor tyrosine kinase inhibitors |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| EP2554544A1 (en) | 2011-08-01 | 2013-02-06 | Almirall, S.A. | Pyridin-2(1h)-one derivatives as jak inhibitors |
| UY34305A (es) | 2011-09-01 | 2013-04-30 | Novartis Ag | Derivados de heterociclos bicíclicos para el tratamiento de la hipertensión arterial pulmonar |
| UA111382C2 (uk) | 2011-10-10 | 2016-04-25 | Оріон Корпорейшн | Інгібітори протеїнкінази |
| EP3495367B1 (en) | 2012-06-13 | 2020-09-30 | Incyte Holdings Corporation | Substituted tricyclic compounds as fgfr inhibitors |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| AU2013324396B2 (en) | 2012-09-28 | 2018-10-04 | Vanderbilt University | Fused heterocyclic compounds as selective BMP inhibitors |
| CN102898426B (zh) * | 2012-11-15 | 2015-04-22 | 江苏先声药业有限公司 | 抑制igf-1r酪氨酸激酶活性的吡啶并吡唑类衍生物 |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
| TWI628176B (zh) * | 2013-04-04 | 2018-07-01 | 奧利安公司 | 蛋白質激酶抑制劑 |
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| WO2014176259A1 (en) | 2013-04-22 | 2014-10-30 | Icahn School Of Medicine At Mount Sinai | Mutations in pdgfrb and notch3 as causes of autosomal dominant infantile myofibromatosis |
| JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
| JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
| MY176049A (en) * | 2013-12-06 | 2020-07-22 | Genentech Inc | Serine/threonine kinase inhibitors |
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| HRP20191646T1 (hr) | 2014-01-21 | 2019-12-13 | Janssen Pharmaceutica Nv | Kombinacije koje sadržavaju pozitivne alosteričke modulatore ili ortosteričke agoniste metabotropnog glutamatergičnog receptora podtip 2 i njihova uporaba |
| US10513521B2 (en) * | 2014-07-15 | 2019-12-24 | The Brigham And Women's Hospital, Inc. | Compositions and methods for inhibiting BMP |
| RU2658821C1 (ru) | 2014-08-18 | 2018-06-25 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Соль моноциклического производного пиридина и ее кристалл |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
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| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
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| EP3765460A1 (en) | 2018-03-14 | 2021-01-20 | Vanderbilt University | Inhibition of bmp signaling, compounds, compositions and uses thereof |
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| CA2672213A1 (en) | 2008-07-03 |
| NO20092658L (no) | 2009-09-17 |
| AU2007337895B2 (en) | 2014-01-30 |
| PL2121687T3 (pl) | 2016-03-31 |
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| EP2121687B1 (en) | 2015-10-14 |
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| CY1117319T1 (el) | 2017-04-26 |
| CN101679409A (zh) | 2010-03-24 |
| EP2121687A2 (en) | 2009-11-25 |
| US20100093718A1 (en) | 2010-04-15 |
| WO2008078100A3 (en) | 2008-11-13 |
| WO2008078100A2 (en) | 2008-07-03 |
| AU2007337895C1 (en) | 2014-07-31 |
| JP5442449B2 (ja) | 2014-03-12 |
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