MA33803B1 - Inhibiteur de bromodomaine de benzodiazépine - Google Patents
Inhibiteur de bromodomaine de benzodiazépineInfo
- Publication number
- MA33803B1 MA33803B1 MA34934A MA34934A MA33803B1 MA 33803 B1 MA33803 B1 MA 33803B1 MA 34934 A MA34934 A MA 34934A MA 34934 A MA34934 A MA 34934A MA 33803 B1 MA33803 B1 MA 33803B1
- Authority
- MA
- Morocco
- Prior art keywords
- benzodiazepine
- bromodomaine
- inhibitor
- compound
- formula
- Prior art date
Links
Classifications
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- 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
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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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (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)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne un composé benzodiazépine de formule (I), des procédés pour sa préparation, des compositions pharmaceutiques contenant un tel composé et son utilisation en thérapie.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0919433A GB0919433D0 (en) | 2009-11-05 | 2009-11-05 | Novel compounds |
GBGB1010509.6A GB201010509D0 (en) | 2010-06-22 | 2010-06-22 | Novel compounds |
PCT/EP2010/061518 WO2011054553A1 (fr) | 2009-11-05 | 2010-08-06 | Inhibiteur de bromodomaine de benzodiazépine |
Publications (1)
Publication Number | Publication Date |
---|---|
MA33803B1 true MA33803B1 (fr) | 2012-12-03 |
Family
ID=42667965
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA34934A MA33803B1 (fr) | 2009-11-05 | 2012-06-04 | Inhibiteur de bromodomaine de benzodiazépine |
Country Status (32)
Country | Link |
---|---|
US (3) | US9023842B2 (fr) |
EP (3) | EP2496580B1 (fr) |
JP (1) | JP5524343B2 (fr) |
KR (1) | KR101424989B1 (fr) |
CN (1) | CN102762569B (fr) |
AU (1) | AU2010314395B2 (fr) |
BR (1) | BR112012010706A2 (fr) |
CA (1) | CA2779355C (fr) |
CL (1) | CL2012001178A1 (fr) |
CO (1) | CO6540003A2 (fr) |
CR (1) | CR20120283A (fr) |
CY (2) | CY1114988T1 (fr) |
DK (2) | DK2496580T3 (fr) |
DO (1) | DOP2012000114A (fr) |
EA (1) | EA020390B1 (fr) |
ES (3) | ES2446647T3 (fr) |
HK (3) | HK1191012A1 (fr) |
HR (2) | HRP20140107T1 (fr) |
HU (1) | HUE026421T2 (fr) |
IL (2) | IL219090A0 (fr) |
MA (1) | MA33803B1 (fr) |
ME (1) | ME02360B (fr) |
MX (1) | MX2012005295A (fr) |
MY (1) | MY160456A (fr) |
NZ (1) | NZ599258A (fr) |
PE (1) | PE20121181A1 (fr) |
PL (2) | PL2722334T3 (fr) |
PT (2) | PT2496580E (fr) |
RS (2) | RS54592B1 (fr) |
SI (2) | SI2722334T1 (fr) |
SM (2) | SMT201400024B (fr) |
WO (1) | WO2011054553A1 (fr) |
Families Citing this family (95)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0919432D0 (en) * | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Use |
MX341212B (es) * | 2009-11-05 | 2016-08-11 | Glaxosmithkline Llc * | Inhibidor de bromodominio de benzodiazepina. |
AU2011252799B2 (en) | 2010-05-14 | 2015-05-14 | Cold Spring Harbor Laboratory | Compositions and methods for treating leukemia |
JP6022442B2 (ja) | 2010-05-14 | 2016-11-09 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | 男性用避妊組成物および使用方法 |
BR122014024883A2 (pt) | 2010-05-14 | 2019-08-20 | Dana-Farber Cancer Institute, Inc. | Compostos no tratamento de neoplasia |
AR084070A1 (es) | 2010-12-02 | 2013-04-17 | Constellation Pharmaceuticals Inc | Inhibidores del bromodominio y usos de los mismos |
US9249161B2 (en) | 2010-12-02 | 2016-02-02 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
US9422292B2 (en) | 2011-05-04 | 2016-08-23 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
EP2721031B1 (fr) | 2011-06-17 | 2016-01-20 | Constellation Pharmaceuticals, Inc. | Inhibiteurs à bromodomaine et leurs utilisations |
WO2013027168A1 (fr) | 2011-08-22 | 2013-02-28 | Pfizer Inc. | Nouveaux composés hétérocycliques utilisés en tant qu'inhibiteurs de bromodomaine |
DE102011082013A1 (de) | 2011-09-01 | 2013-03-07 | Bayer Pharma AG | 6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine |
WO2013097052A1 (fr) | 2011-12-30 | 2013-07-04 | Abbott Laboratories | Inhibiteurs de bromodomaine |
CA2870931A1 (fr) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Derives d'iso-indolone |
US9624244B2 (en) | 2012-06-06 | 2017-04-18 | Constellation Pharmaceuticals, Inc. | Benzo [B] isoxazoloazepine bromodomain inhibitors and uses thereof |
TWI602820B (zh) | 2012-06-06 | 2017-10-21 | 星宿藥物公司 | 溴域抑制劑及其用途 |
KR20150023722A (ko) | 2012-06-12 | 2015-03-05 | 애브비 인코포레이티드 | 피리디논 및 피리다지논 유도체 |
EP2884983B1 (fr) | 2012-08-16 | 2017-10-04 | GlaxoSmithKline LLC | Benzodiazepines pour traiter le carcinome pulmonaire à petites cellules |
US9890147B2 (en) | 2012-08-16 | 2018-02-13 | Bayer Pharma Aktiengesellshaft | 2,3-benzodiazepines |
WO2014048945A1 (fr) | 2012-09-28 | 2014-04-03 | Bayer Pharma Aktiengesellschaft | 5-aryl-triazolo-azepines inhibant la protéine bet |
US9422290B2 (en) | 2012-11-13 | 2016-08-23 | Boehringer Ingelheim International Gmbh | Triazolopyridazine |
US9266891B2 (en) * | 2012-11-16 | 2016-02-23 | Boehringer Ingelheim International Gmbh | Substituted [1,2,4]triazolo[4,3-A]pyrazines that are BRD4 inhibitors |
US9765039B2 (en) | 2012-11-21 | 2017-09-19 | Zenith Epigenetics Ltd. | Biaryl derivatives as bromodomain inhibitors |
WO2014080290A2 (fr) | 2012-11-21 | 2014-05-30 | Rvx Therapeutics Inc. | Amines cycliques servant d'inhibiteurs de bromodomaines |
EP2935253B1 (fr) | 2012-12-21 | 2018-08-01 | Zenith Epigenetics Ltd. | Nouveaux composés hétérocycliques en tant qu'inhibiteurs de bromodomaine |
US9492460B2 (en) * | 2013-02-27 | 2016-11-15 | Bristol-Myers Squibb Company | Carbazole compounds useful as bromodomain inhibitors |
CA2902225A1 (fr) * | 2013-02-28 | 2014-09-04 | Washington University | Methodes de traitement de maladies et d'infections par le cytomegalovirus humain au moyen d'inhibiteurs de bromodomaines |
EP2970262A1 (fr) | 2013-03-11 | 2016-01-20 | AbbVie Inc. | Inhibiteurs de bromodomaine |
CA2904049A1 (fr) | 2013-03-11 | 2014-10-09 | Abbvie Inc. | Inhibiteurs de bromodomaines tetracycliques de fusion |
WO2014159392A1 (fr) | 2013-03-14 | 2014-10-02 | Dana-Farber Cancer Institute, Inc. | Réactifs de liaison à des bromodomaines et leurs utilisations |
US9695179B2 (en) * | 2013-03-14 | 2017-07-04 | Convergene Llc | Methods and compositions for inhibition of bromodomain-containing proteins |
CN105189515B (zh) * | 2013-03-14 | 2018-07-03 | 葛兰素史克知识产权第二有限公司 | 作为溴结构域抑制剂的呋喃并吡啶类 |
SG11201506924YA (en) | 2013-03-15 | 2015-09-29 | Incyte Corp | Tricyclic heterocycles as bet protein inhibitors |
EP2792355A1 (fr) | 2013-04-17 | 2014-10-22 | Albert-Ludwigs-Universität Freiburg | Composés destinés à être utilisés comme inhibiteurs de bromodomaine |
AU2014256750B2 (en) | 2013-04-26 | 2018-08-23 | Beigene, Ltd. | Substituted5-(3,5-dimethylisoxazol-4-yl)indoline-2-ones |
CN105492439B (zh) | 2013-06-21 | 2019-11-22 | 齐尼思表观遗传学有限公司 | 作为溴结构域抑制剂的取代的双环化合物 |
KR102307566B1 (ko) | 2013-06-21 | 2021-10-05 | 제니쓰 에피제네틱스 리미티드 | 신규한 바이사이클릭 브로모도메인 억제제 |
AR096758A1 (es) * | 2013-06-28 | 2016-02-03 | Abbvie Inc | Inhibidores cristalinos de bromodominios |
JP2016523964A (ja) | 2013-07-08 | 2016-08-12 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Betタンパク質阻害剤としての三環式複素環 |
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EP3027604B1 (fr) | 2013-07-31 | 2019-02-20 | Zenith Epigenetics Ltd. | Nouvelles quinazolones en tant qu'inhibiteurs de bromodomaine |
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JP6637884B2 (ja) | 2013-11-08 | 2020-01-29 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | ブロモドメインおよびエクストラターミナル(bet)タンパク質インヒビターを使用するがんのための併用療法 |
WO2015081203A1 (fr) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Hétérocycles bicycliques servant d'inhibiteurs des protéines bet |
WO2015081189A1 (fr) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Hétérocycles bicycliques servant d'inhibiteurs des protéines bet |
GB201320994D0 (en) * | 2013-11-28 | 2014-01-15 | Univ Dundee | Enzyme function probes |
US9309246B2 (en) | 2013-12-19 | 2016-04-12 | Incyte Corporation | Tricyclic heterocycles as BET protein inhibitors |
RU2016134941A (ru) | 2014-01-31 | 2018-03-01 | Дана-Фарбер Кансер Институт, Инк. | Производные диазепана и их применения |
EP3099677A4 (fr) | 2014-01-31 | 2017-07-26 | Dana-Farber Cancer Institute, Inc. | Dérivés de diaminopyrimidine benzènesulfone et leurs utilisations |
WO2015117087A1 (fr) | 2014-01-31 | 2015-08-06 | Dana-Farber Cancer Institute, Inc. | Utilisations des dérivés de diazépane |
WO2015120476A1 (fr) * | 2014-02-10 | 2015-08-13 | Salk Institute For Biological Studies | Augmentation du stockage de vitamine a, de vitamine d et/ou de lipides |
CN106459056A (zh) | 2014-02-10 | 2017-02-22 | 康塞特医药品公司 | 经取代的三唑苯二氮卓 |
WO2015121230A1 (fr) * | 2014-02-14 | 2015-08-20 | Bayer Pharma Aktiengesellschaft | 2,3-benzodiazépines substituées en position 9 |
RU2722179C2 (ru) | 2014-02-28 | 2020-05-28 | Тэнша Терапеутикс, Инк. | Лечение состояний, ассоциированных с гиперинсулинемией |
ES2751642T3 (es) | 2014-04-09 | 2020-04-01 | Kainos Medicine Inc | Compuestos inhibidores de bromodominios y composición farmacéutica que los comprende para prevenir o tratar un cáncer |
EA039678B1 (ru) | 2014-04-23 | 2022-02-24 | Инсайт Корпорейшн | 1H-ПИРРОЛО[2,3-c]ПИРИДИН-7(6H)-ОНЫ И ПИРАЗОЛО[3,4-c]ПИРИДИН-7(6H)-ОНЫ В КАЧЕСТВЕ ИНГИБИТОРОВ БЕЛКОВ BET |
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NO2719005T3 (fr) | 2014-07-28 | 2018-01-20 | ||
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WO2016087942A1 (fr) | 2014-12-01 | 2016-06-09 | Zenith Epigenetics Corp. | Pyridines substituées comme inhibiteurs de bromodomaine |
WO2016090219A1 (fr) * | 2014-12-05 | 2016-06-09 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Inhibiteur de bromodomaines comme adjuvant en immunothérapie anticancéreuse |
EP3230277B1 (fr) | 2014-12-11 | 2019-09-18 | Zenith Epigenetics Ltd. | Hétérocycles substitués à titre d'inhibiteurs de bromodomaines |
EP3233846A4 (fr) | 2014-12-17 | 2018-07-18 | Zenith Epigenetics Ltd. | Inhibiteurs de bromodomaines |
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WO2020191326A1 (fr) | 2019-03-20 | 2020-09-24 | Sumitomo Dainippon Pharma Oncology, Inc. | Traitement de la leucémie myéloïde aiguë (aml) après échec du vénétoclax |
GB201905721D0 (en) | 2019-04-24 | 2019-06-05 | Univ Dundee | Compounds |
WO2021175432A1 (fr) | 2020-03-04 | 2021-09-10 | Boehringer Ingelheim International Gmbh | Procédé d'administration d'un agent anticancéreux |
US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
MX2022016454A (es) | 2020-06-23 | 2023-03-06 | Genentech Inc | Compuestos macrociclicos y metodos de uso de los mismos. |
GB202016977D0 (en) | 2020-10-26 | 2020-12-09 | In4Derm Ltd | Compounds |
WO2022116968A1 (fr) | 2020-12-01 | 2022-06-09 | 成都苑东生物制药股份有限公司 | Nouvel inhibiteur de bromodomaine bet n-hétérocyclique, procédé de préparation s'y rapportant et utilisation médicale associée |
JP2024523491A (ja) | 2021-06-29 | 2024-06-28 | タイ セラピューティクス リミテッド | がんの治療に有用なピロロピリドン誘導体 |
WO2023205251A1 (fr) | 2022-04-19 | 2023-10-26 | Nuevolution A/S | Composés actifs vis-à-vis de bromodomaines |
WO2024018423A1 (fr) | 2022-07-21 | 2024-01-25 | Tay Therapeutics Limited | Pyrroles et imidazoles utilisés comme inhibiteurs de protéines bet |
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DE3610848A1 (de) * | 1986-04-01 | 1987-10-15 | Boehringer Ingelheim Kg | Neue 1,4-diazepine |
GB9004781D0 (en) | 1990-03-02 | 1990-04-25 | Glaxo Group Ltd | Device |
EP0638560A4 (fr) | 1991-10-11 | 1995-03-29 | Yoshitomi Pharmaceutical | Medicament utilise pour traiter l'osteoporose et compose de diazepine. |
JPH06128257A (ja) | 1992-10-13 | 1994-05-10 | Yoshitomi Pharmaceut Ind Ltd | ピリドジアゼピン化合物 |
AU686715B2 (en) | 1993-11-22 | 1998-02-12 | Merck & Co., Inc. | Tricyclic benzodiazepinyl amide derivatives as amtiarrhythmics |
IT1285567B1 (it) | 1996-02-21 | 1998-06-18 | Alfa Chem Ital | Nuovo processo per la sintesi del nabumetone |
BR9710453A (pt) * | 1996-06-12 | 1999-08-17 | Japan Tobacco Inc | Inhibidor de produ-Æo de citocina composto de triazepina e intermedi rio para o mesmo |
KR100338144B1 (ko) | 1996-09-13 | 2002-05-24 | 가마쿠라 아키오 | 티에노트리아졸로디아제핀 화합물 및 그의 약제학적 용도 |
JPH11228576A (ja) * | 1997-12-10 | 1999-08-24 | Japan Tobacco Inc | アポトーシス抑制剤 |
CN1901958B (zh) | 2003-11-03 | 2011-03-09 | 葛兰素集团有限公司 | 流体分配装置 |
US7223733B2 (en) | 2004-03-31 | 2007-05-29 | National University Of Singapore | Modulation of TRIP-Br function and method of treating proliferative disorders |
GB0420970D0 (en) | 2004-09-21 | 2004-10-20 | Smithkline Beecham Corp | Novel triazoloquinoline compounds |
JP5159305B2 (ja) | 2005-05-30 | 2013-03-06 | 田辺三菱製薬株式会社 | チエノトリアゾロジアゼピン化合物及びその医薬としての用途 |
JP2008156311A (ja) | 2006-12-26 | 2008-07-10 | Institute Of Physical & Chemical Research | Brd2ブロモドメイン結合剤 |
EP2239264A4 (fr) | 2007-12-28 | 2012-01-11 | Mitsubishi Tanabe Pharma Corp | Agent antitumoral |
GB0919431D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
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