ECSP088704A - Derivados de tieno-piridina como inhibidores de mek - Google Patents
Derivados de tieno-piridina como inhibidores de mekInfo
- Publication number
- ECSP088704A ECSP088704A EC2008008704A ECSP088704A ECSP088704A EC SP088704 A ECSP088704 A EC SP088704A EC 2008008704 A EC2008008704 A EC 2008008704A EC SP088704 A ECSP088704 A EC SP088704A EC SP088704 A ECSP088704 A EC SP088704A
- Authority
- EC
- Ecuador
- Prior art keywords
- pyridine derivatives
- tieno
- mek inhibitors
- substituted
- mapkk
- Prior art date
Links
- 239000002829 mitogen activated protein kinase inhibitor Substances 0.000 title 1
- 102000004232 Mitogen-Activated Protein Kinase Kinases Human genes 0.000 abstract 2
- 108090000744 Mitogen-Activated Protein Kinase Kinases Proteins 0.000 abstract 2
- 229940124639 Selective inhibitor Drugs 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 230000001363 autoimmune Effects 0.000 abstract 1
- 230000009286 beneficial effect Effects 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000002526 effect on cardiovascular system Effects 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 230000003040 nociceptive effect Effects 0.000 abstract 1
- 230000000771 oncological effect Effects 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- SMZMHUCIDGHERP-UHFFFAOYSA-N thieno[2,3-b]pyridine Chemical class C1=CN=C2SC=CC2=C1 SMZMHUCIDGHERP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- A61K31/4365—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 having sulfur as a ring hetero atom, e.g. ticlopidine
-
- 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
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Heart & Thoracic Surgery (AREA)
- Transplantation (AREA)
- Cardiology (AREA)
- Oncology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Una serie de derivados de tieno[2,3-b]piridina que están sustituidos en la posición 2 con un resto anilino sustituido, que son inhibidores selectivos de las enzimas MEK (MAPKK)humanas, son por consiguiente beneficiosos en medicina, por ejemplo en el tratamiento de afecciones inflamatorias, autoinmunes, cardiovasculares, proliferativas (con inclusión de las oncológicas) y nociceptivas
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0601962.4A GB0601962D0 (en) | 2006-01-31 | 2006-01-31 | Therapeutic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP088704A true ECSP088704A (es) | 2008-09-29 |
Family
ID=36100789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2008008704A ECSP088704A (es) | 2006-01-31 | 2008-08-28 | Derivados de tieno-piridina como inhibidores de mek |
Country Status (26)
| Country | Link |
|---|---|
| US (3) | US8283359B2 (es) |
| EP (1) | EP1981892B1 (es) |
| JP (1) | JP5249787B2 (es) |
| KR (1) | KR101446919B1 (es) |
| CN (1) | CN101379067B (es) |
| AU (1) | AU2007211377B2 (es) |
| BR (1) | BRPI0708016B1 (es) |
| CA (1) | CA2640594C (es) |
| CY (1) | CY1115404T1 (es) |
| DK (1) | DK1981892T3 (es) |
| EA (1) | EA016128B1 (es) |
| EC (1) | ECSP088704A (es) |
| ES (1) | ES2471970T3 (es) |
| GB (1) | GB0601962D0 (es) |
| HR (1) | HRP20140503T1 (es) |
| IL (1) | IL192603A (es) |
| MY (1) | MY146387A (es) |
| NO (1) | NO341064B1 (es) |
| NZ (1) | NZ569638A (es) |
| PL (1) | PL1981892T3 (es) |
| PT (1) | PT1981892E (es) |
| RS (1) | RS53342B (es) |
| SI (1) | SI1981892T1 (es) |
| UA (1) | UA95939C2 (es) |
| WO (1) | WO2007088345A1 (es) |
| ZA (1) | ZA200807447B (es) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
| GB0616214D0 (en) * | 2006-08-15 | 2006-09-27 | Ucb Sa | Therapeutic Agents |
| GB0714384D0 (en) | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
| NZ586575A (en) * | 2007-12-21 | 2012-03-30 | Genentech Inc | Azaindolizines and methods of use |
| EP2240494B1 (en) | 2008-01-21 | 2016-03-30 | UCB Biopharma SPRL | Thieno-pyridine derivatives as mek inhibitors |
| GB0811304D0 (en) | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
| JP5503930B2 (ja) * | 2009-09-18 | 2014-05-28 | 住友化学株式会社 | 3−アミノ−1−tert−ブトキシカルボニルピペリジンの精製方法およびそのクエン酸塩 |
| WO2012018638A2 (en) | 2010-07-26 | 2012-02-09 | Biomatrica, Inc. | Compositions for stabilizing dna, rna and proteins in blood and other biological samples during shipping and storage at ambient temperatures |
| EP2598661B1 (en) | 2010-07-26 | 2017-09-27 | Biomatrica, INC. | Compositions for stabilizing dna, rna and proteins in saliva and other biological samples during shipping and storage at ambient temperatures |
| EP2934572A4 (en) | 2012-12-20 | 2016-11-23 | Biomatrica Inc | FORMULATIONS AND METHODS FOR STABILIZING PCR REAGENTS |
| WO2014130932A2 (en) | 2013-02-25 | 2014-08-28 | Novartis Ag | Novel androgen receptor mutation |
| EP3008073B1 (en) | 2013-06-11 | 2020-01-01 | Latvian Institute Of Organic Synthesis | Thieno[2,3-b]pyridines as multidrug resistance modulators |
| EP3007556B1 (en) | 2013-06-13 | 2020-05-20 | Biomatrica, INC. | Cell stabilization |
| JP6661554B2 (ja) | 2014-06-10 | 2020-03-11 | バイオマトリカ,インク. | 周囲温度における血小板の安定化 |
| CN105384754B (zh) * | 2014-09-02 | 2018-04-20 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途 |
| WO2017033113A1 (en) | 2015-08-21 | 2017-03-02 | Acerta Pharma B.V. | Therapeutic combinations of a mek inhibitor and a btk inhibitor |
| JP6827048B2 (ja) | 2015-12-08 | 2021-02-10 | バイオマトリカ,インク. | 赤血球沈降速度の低下 |
| ES3030506T3 (en) | 2017-05-19 | 2025-06-30 | Nflection Therapeutics Inc | Pyrrolopyridine-aniline compounds for treatment of dermal disorders |
| EP3624795B1 (en) * | 2017-05-19 | 2022-04-20 | NFlection Therapeutics, Inc. | Fused heteroaromatic-aniline compounds for treatment of dermal disorders |
| CN109836434B (zh) * | 2017-11-27 | 2020-09-25 | 上海宇耀生物科技有限公司 | 噻吩并环类化合物及其合成方法和应用 |
| CA3120337A1 (en) | 2018-11-20 | 2020-05-28 | Nflection Therapeutics, Inc. | Naphthyridinone-aniline compounds for treatment of dermal disorders |
| MA55141A (fr) | 2018-11-20 | 2021-09-29 | Nflection Therapeutics Inc | Composés cyanoaryl-aniline pour le traitement d'affections de la peau |
| CA3120351A1 (en) * | 2018-11-20 | 2020-05-28 | Nflection Therapeutics, Inc. | Aryl-aniline and heteroaryl-aniline compounds for treatment of skin cancers |
| JP7546297B2 (ja) * | 2018-11-20 | 2024-09-06 | エヌフレクション セラピューティクス インコーポレイテッド | 皮膚障害の処置のためのチエニル-アニリン化合物 |
| BR112021018168B1 (pt) | 2019-03-21 | 2023-11-28 | Onxeo | Composição farmacêutica, combinação e kit compreendendo uma molécula dbait e um inibidor de quinase para o tratamento de câncer |
| CA3159348A1 (en) | 2019-11-08 | 2021-05-14 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
| CN111138449B (zh) * | 2020-01-15 | 2022-11-29 | 四川大学华西医院 | 双靶向erk1和erk5抑制剂的制备及其抗肿瘤应用 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| US12280055B2 (en) | 2021-05-27 | 2025-04-22 | Mirati Therapeutics, Inc. | Combination therapies |
| EP4436570A4 (en) | 2021-11-23 | 2025-10-22 | Nflection Therapeutics Inc | FORMULATIONS OF PYRROLOPYRIDINE-ANILINE COMPOUNDS |
| GB202205203D0 (en) | 2022-04-08 | 2022-05-25 | UCB Biopharma SRL | Combination with inhibitor |
| WO2025073765A1 (en) | 2023-10-03 | 2025-04-10 | Institut National de la Santé et de la Recherche Médicale | Methods of prognosis and treatment of patients suffering from melanoma |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ501277A (en) | 1997-07-01 | 2002-12-20 | Warner Lambert Co | -2(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as MEK inhibitors |
| US6232320B1 (en) | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| WO2000041505A2 (en) | 1999-01-13 | 2000-07-20 | Warner-Lambert Company | Anthranilic acid derivatives |
| HRP20010524A2 (en) | 1999-01-13 | 2002-08-31 | Warner Lambert Co | Benzoheterocycles and their use as mek inhibitors |
| CA2416685C (en) | 2000-07-19 | 2008-10-07 | Warner-Lambert Company | Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids |
| DE60330227D1 (de) | 2002-03-13 | 2010-01-07 | Array Biopharma Inc | N3-alkylierte benzimidazol-derivate als mek-hemmer |
| US7235537B2 (en) | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
| RU2300528C2 (ru) | 2002-03-13 | 2007-06-10 | Эррэй Биофарма, Инк. | N3-алкилированные бензимидазольные производные в качестве ингибиторов мек |
| US20030225273A1 (en) * | 2002-03-21 | 2003-12-04 | Michaelides Michael R. | Thiopyrimidine and isothiazolopyrimidine kinase inhibitors |
| GB0214268D0 (en) * | 2002-06-20 | 2002-07-31 | Celltech R&D Ltd | Chemical compounds |
| CL2003002287A1 (es) * | 2002-11-25 | 2005-01-14 | Wyeth Corp | COMPUESTOS DERIVADOS DE TIENO[3,2-b]-PIRIDINA-6-CARBONITRILOS Y TIENEO[2,3-b]-PIRIDINA-5-CARBONITRILOS, COMPOSICION FARMACEUTICA, PROCEDIMIENTO DE PREPARACION Y COMPUESTOS INTERMEDIARIOS, Y SU USO EN EL TRATAMIENTO DEL CANCER, APOPLEJIA, OSTEOPOROSIS |
| BR0317183A (pt) * | 2002-12-12 | 2005-11-01 | Pharmacia Corp | Método de usar compostos de aminocianopiridina como inibidores de proteìna quinase-2 ativada por proteìna quinase ativada por mitógeno |
| EP1641804A1 (en) | 2003-06-20 | 2006-04-05 | Celltech R & D Limited | Thienopyridone derivatives as kinase inhibitors |
| WO2004113348A1 (en) * | 2003-06-20 | 2004-12-29 | Celltech R & D Limited | Thienopyridone derivatives as kinase inhibitors |
| US20050049276A1 (en) | 2003-07-23 | 2005-03-03 | Warner-Lambert Company, Llc | Imidazopyridines and triazolopyridines |
| EP1651214B1 (en) | 2003-07-24 | 2009-09-16 | Warner-Lambert Company LLC | Benzimidazole derivatives as mek inhibitors |
| US7144907B2 (en) | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
| US20070275962A1 (en) * | 2003-09-10 | 2007-11-29 | Gpc Biotech Ag | Heterobicyclic Compounds as Pharmaceutically Active Agents |
| CN1905873A (zh) | 2003-11-19 | 2007-01-31 | 阵列生物制药公司 | Mek的杂环抑制剂及其使用方法 |
| US7217723B2 (en) | 2004-02-02 | 2007-05-15 | Eisai Co., Ltd. | Heterocyclic compound having oxime group |
| AU2006284751A1 (en) | 2005-09-01 | 2007-03-08 | Array Biopharma Inc. | Raf inhibitor compounds and methods of use thereof |
| DE602006021205D1 (de) | 2005-10-07 | 2011-05-19 | Exelixis Inc | Azetidine als mek-inhibitoren bei der behandlung proliferativer erkrankungen |
| GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
| TW200808769A (en) | 2006-04-18 | 2008-02-16 | Astrazeneca Ab | Therapeutic compounds |
| GB0616214D0 (en) | 2006-08-15 | 2006-09-27 | Ucb Sa | Therapeutic Agents |
| JP2010500994A (ja) | 2006-08-16 | 2010-01-14 | エグゼリクシス, インコーポレイテッド | Pi3kおよびmekモジュレーターを使用する方法 |
| JP5311673B2 (ja) | 2006-12-14 | 2013-10-09 | エグゼリクシス, インコーポレイテッド | Mek阻害剤の使用方法 |
| GB0714384D0 (en) | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
| EP2240494B1 (en) | 2008-01-21 | 2016-03-30 | UCB Biopharma SPRL | Thieno-pyridine derivatives as mek inhibitors |
| GB0811304D0 (en) | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
-
2006
- 2006-01-31 GB GBGB0601962.4A patent/GB0601962D0/en not_active Ceased
-
2007
- 2007-01-30 EP EP07705076.3A patent/EP1981892B1/en active Active
- 2007-01-30 DK DK07705076.3T patent/DK1981892T3/da active
- 2007-01-30 SI SI200731467T patent/SI1981892T1/sl unknown
- 2007-01-30 EA EA200801684A patent/EA016128B1/ru not_active IP Right Cessation
- 2007-01-30 KR KR1020087018972A patent/KR101446919B1/ko not_active Expired - Fee Related
- 2007-01-30 PT PT77050763T patent/PT1981892E/pt unknown
- 2007-01-30 CA CA2640594A patent/CA2640594C/en active Active
- 2007-01-30 ZA ZA200807447A patent/ZA200807447B/xx unknown
- 2007-01-30 CN CN2007800040774A patent/CN101379067B/zh not_active Expired - Fee Related
- 2007-01-30 RS RS20140304A patent/RS53342B/sr unknown
- 2007-01-30 ES ES07705076.3T patent/ES2471970T3/es active Active
- 2007-01-30 WO PCT/GB2007/000310 patent/WO2007088345A1/en not_active Ceased
- 2007-01-30 AU AU2007211377A patent/AU2007211377B2/en not_active Ceased
- 2007-01-30 NZ NZ569638A patent/NZ569638A/en not_active IP Right Cessation
- 2007-01-30 MY MYPI20082765A patent/MY146387A/en unknown
- 2007-01-30 UA UAA200809945A patent/UA95939C2/ru unknown
- 2007-01-30 HR HRP20140503TT patent/HRP20140503T1/hr unknown
- 2007-01-30 BR BRPI0708016-6A patent/BRPI0708016B1/pt not_active IP Right Cessation
- 2007-01-30 PL PL07705076T patent/PL1981892T3/pl unknown
- 2007-01-30 JP JP2008552878A patent/JP5249787B2/ja active Active
-
2008
- 2008-07-03 IL IL192603A patent/IL192603A/en active IP Right Grant
- 2008-07-30 US US12/182,931 patent/US8283359B2/en active Active
- 2008-08-28 EC EC2008008704A patent/ECSP088704A/es unknown
- 2008-08-29 NO NO20083739A patent/NO341064B1/no unknown
-
2012
- 2012-09-05 US US13/604,282 patent/US8394822B2/en active Active
-
2013
- 2013-02-06 US US13/760,788 patent/US8604051B2/en active Active
-
2014
- 2014-06-11 CY CY20141100415T patent/CY1115404T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ECSP088704A (es) | Derivados de tieno-piridina como inhibidores de mek | |
| NO20060279L (no) | Thienopyridonderivater som kinaseinhibitorer | |
| WO2008020206A3 (en) | Fused thiophene derivatives as mek inhibitors | |
| MX356086B (es) | Produccion de acidos grasos y derivados de los mismos. | |
| CR20110261A (es) | COMPUESTOS PIRAZOLO[1,5-a]PIRIMIDINA SUSTITUIDA COMO IHNIBIDORES DE TRK CINASA | |
| ECSP066927A (es) | Sintesis regioespecífica de los derivados de 42 - ester de rapamicina | |
| CY1114419T1 (el) | Παραγωγα συντηγμενου θειαζολιου ως αναστολεις κινασης | |
| CY1120304T1 (el) | Ενωσεις microrna και μεθοδοι για τη διαμορφωση της mir-21 δραστικοτητας | |
| MX2009009371A (es) | Produccion mejorada de derivados de acidos grasos. | |
| AR081515A1 (es) | Agente de sustentacion de un material vitroceramico | |
| DK2021577T3 (da) | Konfigurerbart borehulszoneisolationssystem og tilhørende fremgangsmåder | |
| SG196782A1 (en) | Compositions and methods for the increased production of isoprene and other products with 6 - phosphogluconolactonase (pgl) | |
| EP2508600A4 (en) | MUTANT ENZYM AND ITS APPLICATION | |
| MX2009004883A (es) | Piridil sulfoximinas multi-substituidas y su uso como insecticidas. | |
| DK2254996T3 (da) | Lipaser med høj specificitet for kortkædede fedtsyrer og anvendelser deraf | |
| SI2046797T1 (sl) | Derivati furo B pirol ona in njihova uporaba kot inhibitorji cisteinil proteinaze | |
| SMT201400013B (it) | Attivatori di ampk tieno[2,3-B] piridina dione e loro impieghi terapeutici | |
| BR112014001075A2 (pt) | sonda, seu uso, método in vitro para associar uma sonda com um alvo e kit | |
| CU24052B1 (es) | Derivados de anilina-pirimidina sustituidos con sulfoximina como inhibidores de quinasas dependientes de ciclina (cdk), y método de producción de los mismos | |
| IS8178A (is) | Oxazólidinon fúkalyf setin með sýklóprópýlhóp og afleiður þeirra | |
| CO6710901A2 (es) | Método de vitrificación de superficie con nitrógeno líquido | |
| BRPI0722074A2 (pt) | Problemas de perda de circulação em uma zona de um furo de poço, e dispositivo | |
| BRPI0816676A2 (pt) | Estrutura de furo de corrida para fornalha de fusão e método de reparo do mesmo. | |
| MX2014006088A (es) | Biomarcadores para canceres que responden a moduladores de la actividad de hec1. | |
| DK1689222T3 (da) | Solsikkeolie, solsikkefrø og solsikkeplanter med modificeret fedtsyrefordeling i triacylglycerolmolekylet |