JP2005539012A5 - - Google Patents
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- JP2005539012A5 JP2005539012A5 JP2004526255A JP2004526255A JP2005539012A5 JP 2005539012 A5 JP2005539012 A5 JP 2005539012A5 JP 2004526255 A JP2004526255 A JP 2004526255A JP 2004526255 A JP2004526255 A JP 2004526255A JP 2005539012 A5 JP2005539012 A5 JP 2005539012A5
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 20
- 201000010099 disease Diseases 0.000 claims description 14
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- 238000000034 method Methods 0.000 claims description 7
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- 208000024172 Cardiovascular disease Diseases 0.000 claims description 6
- 208000012902 Nervous system disease Diseases 0.000 claims description 6
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- 125000001931 aliphatic group Chemical group 0.000 claims 8
- 229940079593 drug Drugs 0.000 claims 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- 239000002260 anti-inflammatory agent Substances 0.000 claims 3
- 229940121363 anti-inflammatory agent Drugs 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
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- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 229910052717 sulfur Chemical group 0.000 claims 3
- 239000011593 sulfur Chemical group 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 102000001267 GSK3 Human genes 0.000 claims 2
- 108060006662 GSK3 Proteins 0.000 claims 2
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 239000012472 biological sample Substances 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 239000003900 neurotrophic factor Substances 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 206010007572 Cardiac hypertrophy Diseases 0.000 claims 1
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- 239000002671 adjuvant Substances 0.000 claims 1
- 230000001430 anti-depressive effect Effects 0.000 claims 1
- 230000000561 anti-psychotic effect Effects 0.000 claims 1
- 239000000164 antipsychotic agent Substances 0.000 claims 1
- 229940005529 antipsychotics Drugs 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
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- 239000002552 dosage form Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 230000002757 inflammatory effect Effects 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 150000002926 oxygen Chemical class 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 208000019116 sleep disease Diseases 0.000 claims 1
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- 230000019100 sperm motility Effects 0.000 claims 1
- 210000000278 spinal cord Anatomy 0.000 claims 1
- 230000000982 vasogenic effect Effects 0.000 claims 1
- 239000003981 vehicle Substances 0.000 claims 1
- 0 *c1cc(*C2NNC3=C2C=C(*)C=C*3)nc(-c2c(C(F)(F)F)cccc2)n1 Chemical compound *c1cc(*C2NNC3=C2C=C(*)C=C*3)nc(-c2c(C(F)(F)F)cccc2)n1 0.000 description 4
- 230000004770 neurodegeneration Effects 0.000 description 3
- 230000000926 neurological effect Effects 0.000 description 3
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 description 2
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 description 2
- 102000002254 Glycogen Synthase Kinase 3 Human genes 0.000 description 2
- 108010014905 Glycogen Synthase Kinase 3 Proteins 0.000 description 2
- 208000034799 Tauopathies Diseases 0.000 description 2
- 230000033115 angiogenesis Effects 0.000 description 2
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 description 2
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- 208000033808 peripheral neuropathy Diseases 0.000 description 2
- FLZGOKYWHQKDDA-UHFFFAOYSA-N CN(C)CCCc1cc(Nc2n[nH]c3c2C=CCN3C)nc(-c2ccccc2C(F)(F)F)n1 Chemical compound CN(C)CCCc1cc(Nc2n[nH]c3c2C=CCN3C)nc(-c2ccccc2C(F)(F)F)n1 FLZGOKYWHQKDDA-UHFFFAOYSA-N 0.000 description 1
- GOXYECCEIJZLDT-UHFFFAOYSA-N CN(C)CCNCCCc1cc(Nc2n[nH]c3c2cccn3)nc(-c2ccccc2C(F)(F)F)n1 Chemical compound CN(C)CCNCCCc1cc(Nc2n[nH]c3c2cccn3)nc(-c2ccccc2C(F)(F)F)n1 GOXYECCEIJZLDT-UHFFFAOYSA-N 0.000 description 1
- AQHAJNPKECDVLW-UHFFFAOYSA-N CN(CCCc1cc(Nc2n[nH]c3ncccc23)nc(-c2ccccc2C(F)(F)F)n1)CCN1CCOCC1 Chemical compound CN(CCCc1cc(Nc2n[nH]c3ncccc23)nc(-c2ccccc2C(F)(F)F)n1)CCN1CCOCC1 AQHAJNPKECDVLW-UHFFFAOYSA-N 0.000 description 1
- VXUZPNCRQMAOSN-UHFFFAOYSA-N CNCCCc1cc(Nc2n[nH]c3ncccc23)nc(-c2ccccc2C(F)(F)F)n1 Chemical compound CNCCCc1cc(Nc2n[nH]c3ncccc23)nc(-c2ccccc2C(F)(F)F)n1 VXUZPNCRQMAOSN-UHFFFAOYSA-N 0.000 description 1
- WRVWHILNJVMKCM-UHFFFAOYSA-N Cc1cc(Nc(c2c3)n[nH]c2ccc3F)nc(-c2ccccc2C(F)(F)F)n1 Chemical compound Cc1cc(Nc(c2c3)n[nH]c2ccc3F)nc(-c2ccccc2C(F)(F)F)n1 WRVWHILNJVMKCM-UHFFFAOYSA-N 0.000 description 1
- 206010010904 Convulsion Diseases 0.000 description 1
- AIVIDAHSSPJVRI-UHFFFAOYSA-N FC(c(cccc1)c1-c1nc(C2CC2)cc(NC2=NNC3N=CC=CC23)n1)(F)F Chemical compound FC(c(cccc1)c1-c1nc(C2CC2)cc(NC2=NNC3N=CC=CC23)n1)(F)F AIVIDAHSSPJVRI-UHFFFAOYSA-N 0.000 description 1
- 206010020880 Hypertrophy Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- KIAZTGTVDUSYMD-UHFFFAOYSA-N OCCNCCCc1cc(Nc2n[nH]c3ncccc23)nc(-c2ccccc2C(F)(F)F)n1 Chemical compound OCCNCCCc1cc(Nc2n[nH]c3ncccc23)nc(-c2ccccc2C(F)(F)F)n1 KIAZTGTVDUSYMD-UHFFFAOYSA-N 0.000 description 1
- 102000001253 Protein Kinase Human genes 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 description 1
- 208000028683 bipolar I disease Diseases 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 210000004413 cardiac myocyte Anatomy 0.000 description 1
- 230000036755 cellular response Effects 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 201000001119 neuropathy Diseases 0.000 description 1
- 230000007823 neuropathy Effects 0.000 description 1
- 108060006633 protein kinase Proteins 0.000 description 1
- 239000003909 protein kinase inhibitor Substances 0.000 description 1
- 210000003625 skull Anatomy 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40096702P | 2002-08-02 | 2002-08-02 | |
| US60/400,967 | 2002-08-02 | ||
| PCT/US2003/023950 WO2004013140A1 (en) | 2002-08-02 | 2003-07-31 | Pyrazole compositions useful as inhibitors of gsk-3 |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006188629A Division JP2006273872A (ja) | 2002-08-02 | 2006-07-07 | Gsk−3のインヒビターとして有用なピラゾール組成物 |
| JP2010211448A Division JP2010280729A (ja) | 2002-08-02 | 2010-09-21 | Gsk−3のインヒビターとして有用なピラゾール組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005539012A JP2005539012A (ja) | 2005-12-22 |
| JP2005539012A5 true JP2005539012A5 (https=) | 2006-08-24 |
| JP4733388B2 JP4733388B2 (ja) | 2011-07-27 |
Family
ID=31495907
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004526255A Expired - Fee Related JP4733388B2 (ja) | 2002-08-02 | 2003-07-31 | Gsk−3のインヒビターとして有用なピラゾール組成物 |
| JP2006188629A Withdrawn JP2006273872A (ja) | 2002-08-02 | 2006-07-07 | Gsk−3のインヒビターとして有用なピラゾール組成物 |
| JP2010211448A Pending JP2010280729A (ja) | 2002-08-02 | 2010-09-21 | Gsk−3のインヒビターとして有用なピラゾール組成物 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006188629A Withdrawn JP2006273872A (ja) | 2002-08-02 | 2006-07-07 | Gsk−3のインヒビターとして有用なピラゾール組成物 |
| JP2010211448A Pending JP2010280729A (ja) | 2002-08-02 | 2010-09-21 | Gsk−3のインヒビターとして有用なピラゾール組成物 |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US7491730B2 (https=) |
| EP (1) | EP1532145B1 (https=) |
| JP (3) | JP4733388B2 (https=) |
| KR (1) | KR20050032105A (https=) |
| CN (2) | CN1319968C (https=) |
| AR (1) | AR040773A1 (https=) |
| AT (1) | ATE339419T1 (https=) |
| AU (2) | AU2003257078B2 (https=) |
| BR (1) | BR0313176A (https=) |
| CA (1) | CA2494100C (https=) |
| CO (1) | CO5700772A2 (https=) |
| DE (1) | DE60308387T2 (https=) |
| DK (1) | DK1532145T3 (https=) |
| EA (1) | EA200500299A1 (https=) |
| EC (1) | ECSP055640A (https=) |
| ES (1) | ES2273043T3 (https=) |
| IL (1) | IL166620A (https=) |
| MX (1) | MXPA05001367A (https=) |
| NO (1) | NO20051100L (https=) |
| NZ (2) | NZ550883A (https=) |
| PL (1) | PL374967A1 (https=) |
| PT (1) | PT1532145E (https=) |
| TW (1) | TWI324157B (https=) |
| WO (1) | WO2004013140A1 (https=) |
| ZA (1) | ZA200501124B (https=) |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6660731B2 (en) | 2000-09-15 | 2003-12-09 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| EP1317450B1 (en) | 2000-09-15 | 2006-11-22 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US7473691B2 (en) | 2000-09-15 | 2009-01-06 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| NZ526472A (en) | 2000-12-21 | 2004-04-30 | Vertex Pharma | Pyrazole compounds useful as protein kinase inhibitors |
| AU2003218215A1 (en) | 2002-03-15 | 2003-09-29 | Vertex Pharmaceuticals, Inc. | Azolylaminoazines as inhibitors of protein kinases |
| MY141867A (en) | 2002-06-20 | 2010-07-16 | Vertex Pharma | Substituted pyrimidines useful as protein kinase inhibitors |
| DK1532145T3 (da) | 2002-08-02 | 2007-01-15 | Vertex Pharma | Pyrazolpræparater der er anvendelige som inhibitorer af GSK-3 |
| WO2004072029A2 (en) | 2003-02-06 | 2004-08-26 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridazines useful as inhibitors of protein kinases |
| WO2006007864A1 (en) * | 2004-07-17 | 2006-01-26 | Max Planck Geselllschaft Zur Förderung Der Wissenschaft | Treating neurodegenerative conditions |
| EP1789413A1 (en) | 2004-09-13 | 2007-05-30 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| WO2006034207A2 (en) * | 2004-09-17 | 2006-03-30 | Vanderbilt University | Use of gsk3 inhibitors in combination with radiation therapies |
| AU2006279376B2 (en) | 2005-08-18 | 2011-04-14 | Vertex Pharmaceuticals Incoporated | Pyrazine kinase inhibitors |
| EP1928437A2 (en) | 2005-08-26 | 2008-06-11 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
| EP2258358A3 (en) | 2005-08-26 | 2011-09-07 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
| EP1940389A2 (en) | 2005-10-21 | 2008-07-09 | Braincells, Inc. | Modulation of neurogenesis by pde inhibition |
| US20070112017A1 (en) | 2005-10-31 | 2007-05-17 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
| EP1954277B1 (en) | 2005-11-03 | 2017-01-18 | Vertex Pharmaceuticals Incorporated | Aminopyrimidines useful as kinase inhibitors |
| CN102532133A (zh) | 2006-01-17 | 2012-07-04 | 沃泰克斯药物股份有限公司 | 适用作詹纳斯激酶抑制剂的吖吲哚类 |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| AU2007249399A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| SI2089367T1 (sl) | 2006-10-31 | 2012-02-29 | Pfizer Prod Inc | Spojine pirazolina kot antagonisti mineralokortikoidnih receptorjev |
| MX2009004807A (es) * | 2006-11-02 | 2009-06-15 | Vertex Pharma | Aminopiridinas y aminopirimidinas utiles como inhibidores de proteina cinasa. |
| NZ577768A (en) | 2006-12-19 | 2012-01-12 | Vertex Pharma | Aminopyrimidines useful as inhibitors of protein kinases |
| AU2007338754A1 (en) | 2006-12-21 | 2008-07-03 | Vertex Pharmaceuticals Incorporated | 5-cyan0-4- (pyrrolo [2, 3B] pyridine-3-yl) -pyrimidine derivatives useful as protein kinase inhibitors |
| US8802638B1 (en) | 2007-01-25 | 2014-08-12 | University Of South Florida | Flavonoid treatment of glycogen synthase kinase-based disease |
| AU2008210455A1 (en) * | 2007-01-31 | 2008-08-07 | Vertex Pharmaceuticals Incorporated | 2-aminopyridine derivatives useful as kinase inhibitors |
| MX2009009590A (es) * | 2007-03-09 | 2009-11-10 | Vertex Pharma | Aminopirimidinas utiles como inhibidores de proteinas cinasas. |
| MX2009009592A (es) | 2007-03-09 | 2009-11-10 | Vertex Pharma | Aminopiridinas utiles como inhibidores de proteinas cinasas. |
| ATE526328T1 (de) | 2007-03-09 | 2011-10-15 | Vertex Pharma | Als inhibitoren von proteinkinasen geeignete aminopyrimidine |
| AU2008240313A1 (en) | 2007-04-13 | 2008-10-23 | Aj Park | Aminopyrimidines useful as kinase inhibitors |
| AU2008247592A1 (en) | 2007-05-02 | 2008-11-13 | Vertex Pharmaceuticals Incorporated | Thiazoles and pyrazoles useful as kinase inhibitors |
| JP5389786B2 (ja) | 2007-05-02 | 2014-01-15 | バーテックス ファーマシューティカルズ インコーポレイテッド | キナーゼ阻害として有用なアミノピリミジン |
| JP5451602B2 (ja) * | 2007-06-08 | 2014-03-26 | アッヴィ・インコーポレイテッド | キナーゼ阻害薬としての5−ヘテロアリール置換インダゾール類 |
| US8648069B2 (en) | 2007-06-08 | 2014-02-11 | Abbvie Inc. | 5-substituted indazoles as kinase inhibitors |
| CN101790532B (zh) * | 2007-07-31 | 2013-11-20 | 沃泰克斯药物股份有限公司 | 5-氟-1H-吡唑并[3,4-b]吡啶-3-胺及其衍生物的制备方法 |
| KR20090031122A (ko) * | 2007-09-21 | 2009-03-25 | 주식회사 중외제약 | 인다졸 골격을 함유하는 화합물, 이의 제조방법 및 상기화합물을 함유하는 약제학적 조성물 |
| NZ586662A (en) | 2007-12-19 | 2012-08-31 | Vertex Pharma | PYRAZOLO[1,5-a]PYRIMIDINES USEFUL AS JANUS KINASE 2 INHIBITORS |
| WO2009145814A2 (en) * | 2008-03-10 | 2009-12-03 | Vertex Pharmaceuticals Incorporated | Pyrimidines and pyridines useful as inhibitors of protein kinases |
| WO2009154697A2 (en) | 2008-05-28 | 2009-12-23 | Massachusetts Institute Of Technology | Disc-1 pathway activators in the control of neurogenesis |
| WO2010099217A1 (en) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
| WO2010098888A1 (en) * | 2009-02-27 | 2010-09-02 | Massachusetts Institute Of Technology | Uses of chemicals to modulate gsk-3 signaling for treatment of bipolar disorder and other brain disorders |
| WO2010104307A2 (ko) * | 2009-03-07 | 2010-09-16 | 주식회사 메디젠텍 | 세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물 |
| RS57869B1 (sr) | 2009-06-17 | 2018-12-31 | Vertex Pharma | Inhibitori replikacije virusa gripa |
| WO2011059388A1 (en) * | 2009-11-13 | 2011-05-19 | Astrazeneca Ab | Oxazolo[4,5-c]pyridine substituted pyrazine |
| US8592485B2 (en) * | 2010-06-17 | 2013-11-26 | Healthpartners Research Foundation | Methods and pharmaceutical compositions for treating the animal central nervous system for psychiatric disorders |
| KR20120063283A (ko) * | 2010-12-07 | 2012-06-15 | 제일약품주식회사 | 신규한 피라졸로 피리딘 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 포함하는 약학적 조성물 |
| AU2011343642A1 (en) | 2010-12-16 | 2013-05-02 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
| UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
| EP2671885A1 (en) * | 2012-06-05 | 2013-12-11 | Ares Trading S.A. | Imidazo-oxadiazole and Imidazo-thiadiazole derivatives |
| US8992951B2 (en) | 2013-01-09 | 2015-03-31 | Sapna Life Sciences Corporation | Formulations, procedures, methods and combinations thereof for reducing or preventing the development, or the risk of development, of neuropathology as a result of trauma |
| LT2970890T (lt) | 2013-03-14 | 2020-07-10 | The Brigham And Women`S Hospital, Inc. | Kompozicijos ir būdai, skirti epitelinių kamieninių ląstelių padauginimui ir kultivavimui |
| HRP20181272T1 (hr) | 2013-11-13 | 2018-10-05 | Vertex Pharmaceuticals Incorporated | Postupci priprave inhibitora replikacije virusa influence |
| RS59144B1 (sr) | 2013-11-13 | 2019-09-30 | Vertex Pharma | Inhibitori replikacije virusa influence |
| US20170165230A1 (en) | 2014-04-09 | 2017-06-15 | Christopher Rudd | Use of gsk-3 inhibitors or activators which modulate pd-1 or t-bet expression to modulate t cell immunity |
| KR101731624B1 (ko) | 2014-07-01 | 2017-05-04 | 광주과학기술원 | 세포 리프로그래밍 유도용 조성물 |
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-
2003
- 2003-07-31 DK DK03767010T patent/DK1532145T3/da active
- 2003-07-31 KR KR1020057001908A patent/KR20050032105A/ko not_active Abandoned
- 2003-07-31 WO PCT/US2003/023950 patent/WO2004013140A1/en not_active Ceased
- 2003-07-31 AT AT03767010T patent/ATE339419T1/de active
- 2003-07-31 CA CA2494100A patent/CA2494100C/en not_active Expired - Fee Related
- 2003-07-31 ES ES03767010T patent/ES2273043T3/es not_active Expired - Lifetime
- 2003-07-31 NZ NZ550883A patent/NZ550883A/en unknown
- 2003-07-31 EP EP03767010A patent/EP1532145B1/en not_active Expired - Lifetime
- 2003-07-31 EA EA200500299A patent/EA200500299A1/ru unknown
- 2003-07-31 JP JP2004526255A patent/JP4733388B2/ja not_active Expired - Fee Related
- 2003-07-31 CN CNB038219859A patent/CN1319968C/zh not_active Expired - Fee Related
- 2003-07-31 AU AU2003257078A patent/AU2003257078B2/en not_active Ceased
- 2003-07-31 BR BR0313176-9A patent/BR0313176A/pt not_active IP Right Cessation
- 2003-07-31 CN CNA2007100961579A patent/CN101037438A/zh active Pending
- 2003-07-31 DE DE60308387T patent/DE60308387T2/de not_active Expired - Lifetime
- 2003-07-31 NZ NZ538426A patent/NZ538426A/en not_active IP Right Cessation
- 2003-07-31 PT PT03767010T patent/PT1532145E/pt unknown
- 2003-07-31 ZA ZA200501124A patent/ZA200501124B/en unknown
- 2003-07-31 PL PL03374967A patent/PL374967A1/xx not_active Application Discontinuation
- 2003-07-31 MX MXPA05001367A patent/MXPA05001367A/es active IP Right Grant
- 2003-08-01 AR AR20030102785A patent/AR040773A1/es unknown
- 2003-08-01 US US10/632,340 patent/US7491730B2/en not_active Expired - Fee Related
- 2003-08-01 TW TW092121162A patent/TWI324157B/zh not_active IP Right Cessation
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- 2005-02-01 IL IL166620A patent/IL166620A/en not_active IP Right Cessation
- 2005-02-25 CO CO05017965A patent/CO5700772A2/es not_active Application Discontinuation
- 2005-03-01 NO NO20051100A patent/NO20051100L/no not_active Application Discontinuation
- 2005-03-02 EC EC2005005640A patent/ECSP055640A/es unknown
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- 2006-07-07 JP JP2006188629A patent/JP2006273872A/ja not_active Withdrawn
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- 2008-12-18 US US12/338,129 patent/US7872129B2/en not_active Expired - Fee Related
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- 2010-09-21 JP JP2010211448A patent/JP2010280729A/ja active Pending
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