PE20190973A1 - Compuestos de tetrahidropirazolopirimidina - Google Patents
Compuestos de tetrahidropirazolopirimidinaInfo
- Publication number
- PE20190973A1 PE20190973A1 PE2019000725A PE2019000725A PE20190973A1 PE 20190973 A1 PE20190973 A1 PE 20190973A1 PE 2019000725 A PE2019000725 A PE 2019000725A PE 2019000725 A PE2019000725 A PE 2019000725A PE 20190973 A1 PE20190973 A1 PE 20190973A1
- Authority
- PE
- Peru
- Prior art keywords
- compounds
- tetrahydropirazolopirimidine
- tetrahydropirazolo
- recruitors
- erythemate
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 206010025135 lupus erythematosus Diseases 0.000 abstract 1
- 230000009885 systemic effect Effects 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- 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
-
- 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
- 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
- C07D487/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Biomedical Technology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
SE REFIERE A UN METODO PARA EL TRATAMIENTO DE LUPUS ERITEMATOSO SISTEMICO QUE COMPRENDE ADMINISTRAR UNA CANTIDAD FARMACEUTICAMENTE EFICAZ DE UN COMPUESTO 4,5,6,7-TETRAHIDROPIRAZOLO[1,5-A]PIRIMIDINA DE FORMULA (I) DONDE R1 ES PIPERIDINILO OPCIONALMENTE SUSTITUIDO, PIRROLIDINILO OPCIONALMENTE SUSTITUIDO, 1,4-DIMETILTIAZOLILO, ENTRE OTROS; R7 ES -CF3 O -CHF2; R8 ES 1,2-DIMETOXIBENCENO O 1,3-DIMETIL-1H-PIRAZOL; R9 ES Br, Cl, F, I O H. DICHOS COMPUESTOS ACTUAN COMO ANTAGONISTAS O INIHIBIDORES DE LOS RECEPTORES SIMILARES A TOLL (TLR) 7 Y 8
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261654023P | 2012-05-31 | 2012-05-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20190973A1 true PE20190973A1 (es) | 2019-07-09 |
Family
ID=48626649
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2019000725A PE20190973A1 (es) | 2012-05-31 | 2013-05-31 | Compuestos de tetrahidropirazolopirimidina |
PE2014002228A PE20150220A1 (es) | 2012-05-31 | 2013-05-31 | Compuestos de tetrahidropirazolopirimidina |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2014002228A PE20150220A1 (es) | 2012-05-31 | 2013-05-31 | Compuestos de tetrahidropirazolopirimidina |
Country Status (34)
Country | Link |
---|---|
US (5) | US9126999B2 (es) |
EP (1) | EP2855476B1 (es) |
JP (2) | JP6285918B2 (es) |
KR (2) | KR102268155B1 (es) |
CN (2) | CN107344941B (es) |
AR (1) | AR091236A1 (es) |
AU (2) | AU2013267204B8 (es) |
BR (1) | BR112014030060B1 (es) |
CA (1) | CA2874445C (es) |
CL (1) | CL2014003278A1 (es) |
CY (1) | CY1122692T1 (es) |
DK (1) | DK2855476T3 (es) |
ES (1) | ES2709119T3 (es) |
HK (1) | HK1203498A1 (es) |
HR (1) | HRP20181889T1 (es) |
HU (1) | HUE040562T2 (es) |
IL (2) | IL268013B2 (es) |
JO (1) | JO3407B1 (es) |
LT (1) | LT2855476T (es) |
MX (1) | MX368455B (es) |
MY (1) | MY172926A (es) |
NZ (1) | NZ703459A (es) |
PE (2) | PE20190973A1 (es) |
PH (2) | PH12014502660A1 (es) |
PL (1) | PL2855476T3 (es) |
PT (1) | PT2855476T (es) |
RS (1) | RS57977B1 (es) |
RU (2) | RU2677291C2 (es) |
SG (1) | SG11201407890VA (es) |
SI (1) | SI2855476T1 (es) |
TW (1) | TWI572606B (es) |
UA (1) | UA113440C2 (es) |
WO (1) | WO2013181579A2 (es) |
ZA (1) | ZA201409273B (es) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JO3407B1 (ar) * | 2012-05-31 | 2019-10-20 | Eisai R&D Man Co Ltd | مركبات رباعي هيدرو بيرازولو بيريميدين |
TWI652014B (zh) * | 2013-09-13 | 2019-03-01 | 美商艾佛艾姆希公司 | 雜環取代之雙環唑殺蟲劑 |
CN106414432B (zh) | 2013-10-14 | 2019-06-14 | 卫材R&D管理有限公司 | 选择性取代的喹啉化合物 |
RU2671496C2 (ru) | 2013-10-14 | 2018-11-01 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Производные 5-пиперидин-8-цианохинолина |
JP2016540013A (ja) * | 2013-12-13 | 2016-12-22 | 武田薬品工業株式会社 | Tlr阻害剤としてのピロロ[3,2−c]ピリジン誘導体 |
KR102455518B1 (ko) * | 2014-03-27 | 2022-10-14 | 얀센 파마슈티카 엔.브이. | ROS1 저해제로서 치환된 4,5,6,7-테트라히드로피라졸로[1,5-a]피리미딘 유도체 및 2,3-디히드로-1H-이미다조[1,2-b]피라졸 유도체 |
ES2741831T3 (es) | 2014-07-31 | 2020-02-12 | Basf Se | Proceso para la preparación de pirazoles |
US9938100B2 (en) | 2014-12-30 | 2018-04-10 | Kodak Alaris Inc. | System and method for metallic object detection in a media transport system |
KR102585412B1 (ko) | 2015-05-11 | 2023-10-05 | 바스프 에스이 | 4-아미노-피리다진의 제조 방법 |
AU2015401326B2 (en) * | 2015-07-03 | 2018-07-26 | China Agricultural University | Benzylhydrazone compounds and preparation method and application thereof |
MX2018009453A (es) | 2016-02-02 | 2018-09-21 | Basf Se | Proceso de hidrogenacion catalitico para preparar pirazoles. |
CN107174585A (zh) * | 2016-03-10 | 2017-09-19 | 兰州大学 | 可用作雄激素受体拮抗剂的吡啶并咪唑类化合物的新用途 |
US10071079B2 (en) | 2016-06-29 | 2018-09-11 | Bristol-Myers Squibb Company | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
EP3490983B1 (en) * | 2016-07-30 | 2021-02-17 | Bristol-Myers Squibb Company | Dimethoxyphenyl substituted indole compounds as tlr7, tlr8 or tlr9 inhibitors |
EP3494107A1 (en) * | 2016-08-02 | 2019-06-12 | Solvay Sa | Manufacture of hydrazinyl compounds useful in the manufacture of pyrazole carboxylic acid and derivatives, hydrazinyl compounds and their use |
US10954233B2 (en) * | 2016-09-09 | 2021-03-23 | Novartis Ag | Compounds and compositions as inhibitors of endosomal toll-like receptors |
JP7028861B2 (ja) * | 2016-09-09 | 2022-03-02 | ブリストル-マイヤーズ スクイブ カンパニー | ピリジル置換のインドール化合物 |
EP3636646A4 (en) | 2017-05-18 | 2020-12-09 | Jiangsu Hengrui Medicine Co., Ltd. | HETEROARYL PYRAZOL DERIVATIVE AND MANUFACTURING METHOD FOR IT AND MEDICAL USES THEREOF |
WO2019028302A1 (en) | 2017-08-04 | 2019-02-07 | Bristol-Myers Squibb Company | SUBSTITUTED INDOLE COMPOUNDS USEFUL AS TLR7 / 8/9 INHIBITORS |
CN110997670B (zh) | 2017-08-04 | 2022-11-01 | 百时美施贵宝公司 | [1,2,4]三唑并[4,3-a]吡啶基取代的吲哚化合物 |
WO2019099336A1 (en) | 2017-11-14 | 2019-05-23 | Bristol-Myers Squibb Company | Substituted indole compounds |
KR102037494B1 (ko) | 2017-12-11 | 2019-10-28 | 씨제이헬스케어 주식회사 | 광학활성을 갖는 피페리딘 유도체의 중간체 및 이의 제조방법 |
KR20200100687A (ko) * | 2017-12-15 | 2020-08-26 | 브리스톨-마이어스 스큅 컴퍼니 | 치환된 인돌 에테르 화합물 |
AR113959A1 (es) * | 2017-12-18 | 2020-07-01 | Bristol Myers Squibb Co | Compuestos de 4-azaindol |
KR20200101398A (ko) * | 2017-12-19 | 2020-08-27 | 브리스톨-마이어스 스큅 컴퍼니 | Tlr 억제제로서 유용한 아미드 치환된 인돌 화합물 |
EA202091508A1 (ru) * | 2017-12-19 | 2020-09-14 | Бристол-Маерс Сквибб Компани | 6-азаиндольные соединения |
ES2932361T3 (es) * | 2017-12-19 | 2023-01-18 | Bristol Myers Squibb Co | Compuestos de indol sustituidos útiles como inhibidores de TLR |
CN111491918B (zh) | 2017-12-20 | 2023-10-24 | 百时美施贵宝公司 | 芳基和杂芳基取代的吲哚化合物 |
MX2020006014A (es) | 2017-12-20 | 2020-08-17 | Bristol Myers Squibb Co | Compuestos de diazaindol. |
CA3086431A1 (en) | 2017-12-20 | 2019-06-27 | Bristol-Myers Squibb Company | Amino indole compounds useful as tlr inhibitors |
WO2019123294A2 (en) | 2017-12-22 | 2019-06-27 | Novartis Ag | Novel uses of pyrazolo piperidine derivatives |
US20210171468A1 (en) * | 2017-12-22 | 2021-06-10 | Solvay Sa | Process for the manufacture of pyrazole carboxylic derivatives and precursors thereof |
US20210238136A1 (en) * | 2018-06-07 | 2021-08-05 | Daiichi Sankyo Company, Limited | Azetidine derivative, and prodrug thereof |
EP3847173B1 (en) * | 2018-09-06 | 2023-04-12 | F. Hoffmann-La Roche AG | Novel pyrazolopyridine compounds for the treatment of autoimmune disease |
CN112912382B (zh) | 2018-10-24 | 2024-07-02 | 百时美施贵宝公司 | 经取代的吲哚二聚体化合物 |
JP2022506790A (ja) * | 2018-11-09 | 2022-01-17 | エフ.ホフマン-ラ ロシュ アーゲー | 全身性エリテマトーデスを処置するためのTLR7~9アンタゴニストとしての、5-[6-[[3-(4,5,6,7-テトラヒドロピラゾロ[4,3-c]ピリジン-1-イル)アゼチジン-1-イル]メチル]モルホリン-4-イル]キノリン-8-カルボニトリル誘導体及び類似化合物 |
JP7564112B2 (ja) * | 2019-02-07 | 2024-10-08 | ベイジーン リミテッド | TLR7アゴニストとしてのイミダゾ[2,1-f][1,2,4]トリアジン-4-アミン誘導体 |
EP4008720A4 (en) * | 2019-08-02 | 2023-08-02 | BeiGene, Ltd. | IMIDAZO [2,1-F][1,2,4] TRIAZINE-4-AMINE DERIVATIVES AS A TLR8 AGONIST |
KR20190120112A (ko) | 2019-10-08 | 2019-10-23 | 씨제이헬스케어 주식회사 | 광학활성을 갖는 피페리딘 유도체의 중간체 및 이의 제조방법 |
WO2021112251A1 (ja) * | 2019-12-06 | 2021-06-10 | 第一三共株式会社 | アゼチジンスルホンアミド化合物 |
US11661431B2 (en) | 2021-04-16 | 2023-05-30 | Gilead Sciences, Inc. | Thienopyrrole compounds |
EP4398989A1 (en) | 2021-09-10 | 2024-07-17 | Gilead Sciences, Inc. | Thienopyrrole compounds |
Family Cites Families (118)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3116230B2 (ja) | 1989-02-15 | 2000-12-11 | 武田薬品工業株式会社 | 三環式縮合ピリミジン誘導体 |
JPH04133055A (ja) | 1990-09-25 | 1992-05-07 | Konica Corp | 色再現性の改良されたハロゲン化銀カラー写真感光材料 |
US5356897A (en) | 1991-09-09 | 1994-10-18 | Fujisawa Pharmaceutical Co., Ltd. | 3-(heteroaryl)-pyrazololi[1,5-a]pyrimidines |
FR2733749B1 (fr) | 1995-05-05 | 1997-06-13 | Oreal | Compositions pour la teinture des fibres keratiniques contenant des diamino pyrazoles, procede de teinture, nouveaux diamino pyrazoles et leur procede de preparation |
DE19709877A1 (de) | 1997-03-11 | 1998-09-17 | Bayer Ag | 1,5-Dihydro-pyrazolo[3,4-d]-pyrimidinon-derivate |
US6472416B1 (en) | 1999-08-27 | 2002-10-29 | Abbott Laboratories | Sulfonylphenylpyrazole compounds useful as COX-2 inhibitors |
UA72611C2 (uk) | 2000-05-17 | 2005-03-15 | Орто-Макнейл Фармацевтикал, Інк. | Похідні заміщеного піролопіридинону, корисні як інгібітори фосфодіестерази |
PL362320A1 (en) | 2000-12-06 | 2004-10-18 | Aventis Pharma Deutschland Gmbh | Guanidine and amidine derivatives as factor xa inhibitors |
PL364388A1 (en) * | 2001-03-14 | 2004-12-13 | Grünenthal GmbH | Substituted pyrazolopyrimidines and thiazolopyrimidines used as analgesics |
AU2003219410A1 (en) | 2002-04-26 | 2003-11-10 | Pfizer Products Inc. | Triaryl-oxy-aryl-spiro-pyrimidine-2, 4, 6-trione metalloproteinase inhibitors |
DE10221100C1 (de) | 2002-05-03 | 2003-06-05 | Neuhaus Elektronik Gmbh | Elektrisch leitfähige Dichtung sowie Verfahren und Vorrichtung zu deren Herstellung |
JP2003327860A (ja) | 2002-05-09 | 2003-11-19 | Konica Minolta Holdings Inc | 着色組成物、着色微粒子分散物、インクジェット用インク、インクジェット記録方法 |
DE60317684D1 (de) | 2002-06-19 | 2008-01-03 | Janssen Pharmaceutica Nv | SUBSTITUIERTE 2,4-DIHYDROPYRROLOc3,4BÜCHINOLIN-9-ONDERIVATE, DIE SICH ALS PHOSPHODIESTERASEINHIBITOREN EIGNEN |
JP4133055B2 (ja) | 2002-07-11 | 2008-08-13 | 株式会社イトーキ | 移載機構を備えた自動倉庫 |
ZA200500782B (en) * | 2002-08-26 | 2007-10-31 | Takeda Pharmaceutical | Calcium receptor modulating compound and use thereof |
EP1572113B1 (en) | 2002-08-26 | 2017-05-17 | Takeda Pharmaceutical Company Limited | Calcium receptor modulating compound and use thereof |
AU2003274652A1 (en) | 2002-10-23 | 2004-05-13 | Obetherapy Biotechnology | Compounds, compositions and methods for modulating fat metabolism |
SE0300120D0 (sv) | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
WO2004089415A2 (en) * | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | COMBINATIONS OF AN 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITOR AND A GLUCOCORTICOID RECEPTOR AGONIST |
EP1628970A2 (en) | 2003-04-30 | 2006-03-01 | The Institutes of Pharmaceutical Discovery, LLC | Heterocycle substituted carboxylic acids as inhibitors of protein tyrosine phosphatase-1b |
EP1618094B1 (en) | 2003-04-30 | 2007-09-05 | The Institutes for Pharmaceutical Discovery, LLC | Substituted heteroaryls as inhibitors of protein tyrosine phosphatases |
JP4580932B2 (ja) | 2003-06-12 | 2010-11-17 | メルク・シャープ・エンド・ドーム・コーポレイション | 有糸分裂キネシン阻害剤のプロドラッグ |
US20050096256A1 (en) | 2003-07-01 | 2005-05-05 | President And Fellows Of Harvard College | Compositions for manipulating the lifespan and stress response of cells and organisms |
US20060025337A1 (en) | 2003-07-01 | 2006-02-02 | President And Fellows Of Harvard College | Sirtuin related therapeutics and diagnostics for neurodegenerative diseases |
US20050085531A1 (en) | 2003-10-03 | 2005-04-21 | Hodge Carl N. | Thiophene-based compounds exhibiting ATP-utilizing enzyme inhibitory activity, and compositions, and uses thereof |
GB0324159D0 (en) | 2003-10-15 | 2003-11-19 | Glaxo Group Ltd | Novel compounds |
US8017634B2 (en) | 2003-12-29 | 2011-09-13 | President And Fellows Of Harvard College | Compositions for treating obesity and insulin resistance disorders |
FR2865208B1 (fr) | 2004-01-16 | 2009-01-16 | Sanofi Synthelabo | Derives de 1,4-diazabicyclo[3.2.1]octanecarboxmique, leur preparation et leur application en therapeutique |
US7279232B2 (en) | 2004-01-26 | 2007-10-09 | Universal Display Corporation | Electroluminescent stability |
US20080004263A1 (en) | 2004-03-04 | 2008-01-03 | Santora Vincent J | Ligands of Follicle Stimulating Hormone Receptor and Methods of Use Thereof |
US7825265B2 (en) | 2004-05-04 | 2010-11-02 | Acadia Pharmaceuticals Inc. | Compounds with activity at estrogen receptors |
RU2006142683A (ru) | 2004-05-04 | 2008-06-10 | Акэдиа Фармасьютикалз Инк. (Us) | Соединения с активностью эстрогенных рецепторов |
AU2005295902A1 (en) | 2004-10-12 | 2006-04-27 | Decode Genetics Ehf | Aryl sulfonamide peri-substituted bicyclics for occlusive artery disease |
US20060122222A1 (en) | 2004-11-18 | 2006-06-08 | The Institutes For Pharmaceutical Discovery, Llc | Heterocycle substituted carboxylic acids |
WO2006057448A1 (ja) | 2004-11-26 | 2006-06-01 | Takeda Pharmaceutical Company Limited | アリールアルカン酸誘導体 |
CA2595486A1 (en) | 2005-01-20 | 2006-07-27 | Sirtris Pharmaceuticals, Inc. | Use of sirtuin-activating compounds for treating flushing and drug induced weight gain |
CA2610854A1 (en) | 2005-03-30 | 2006-10-05 | Sirtris Pharmaceuticals, Inc. | Nicotinamide riboside and analogues thereof |
WO2006129587A1 (ja) | 2005-05-30 | 2006-12-07 | Genecare Research Institute Co., Ltd. | ピラゾロン誘導体を含有する医薬組成物 |
JPWO2006129583A1 (ja) | 2005-05-30 | 2009-01-08 | 株式会社ジーンケア研究所 | ピラゾロン誘導体 |
EP1888512A2 (en) | 2005-06-06 | 2008-02-20 | Smithkline Beecham Corporation | Chemical compounds |
WO2006138418A2 (en) | 2005-06-14 | 2006-12-28 | President And Fellows Of Harvard College | Improvement of cognitive performance with sirtuin activators |
GB0513886D0 (en) | 2005-07-06 | 2005-08-10 | Glaxo Group Ltd | Novel compounds |
US20070149466A1 (en) | 2005-07-07 | 2007-06-28 | Michael Milburn | Methods and related compositions for treating or preventing obesity, insulin resistance disorders, and mitochondrial-associated disorders |
WO2007008541A2 (en) | 2005-07-08 | 2007-01-18 | Kalypsys, Inc. | Cellular cholesterol absorption modifiers |
JP5066516B2 (ja) | 2005-09-01 | 2012-11-07 | アステラス製薬株式会社 | 疼痛の治療に用いられるピリダジノン誘導体 |
US20070203236A1 (en) | 2006-01-11 | 2007-08-30 | Smith Jeffrey W | Novel antagonists of the human fatty acid synthase thioesterase |
JP5498703B2 (ja) | 2006-01-23 | 2014-05-21 | 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 | プロテインキナーゼのインヒビターとして有用なチオフェン−カルボキサミド |
US20090304821A1 (en) | 2006-03-08 | 2009-12-10 | Takeda Pharmaceutical Company Limited | Pharmaceutical Combination |
JP2009534454A (ja) | 2006-04-25 | 2009-09-24 | アステックス、セラピューティックス、リミテッド | 医薬化合物 |
EP2439206A1 (en) | 2006-05-23 | 2012-04-11 | Vertex Pharmaceuticals Incorporated | Thiophene-carboxamides useful as inhibitors of protein kinases |
CA2653005A1 (en) | 2006-05-23 | 2007-12-06 | Vertex Pharmaceuticals Incorporated | Thiophene-carboxamides useful as inhibitors of protein kinases |
WO2007146838A2 (en) | 2006-06-09 | 2007-12-21 | Icos Corporation | Substituted phenyl acetic acids as dp-2 antagonists |
AR061974A1 (es) | 2006-07-14 | 2008-08-10 | Novartis Ag | Derivados de pirimidina como inhibidores de alk, composiciones farmaceuticas y procesos de obtencion |
AR063680A1 (es) * | 2006-08-04 | 2009-02-11 | Merz Pharma Gmbh & Co Kgaa | Derivados de pirazolo[1, 5-a]pirimidina, metodos e intermediario para su preparacion, composiciones farmaceuticas que los comprenden y su uso en la fabricacion de medicamentos para el tratamiento de enfermedades mediadas por la modulacion de mglur5. |
WO2008033894A2 (en) | 2006-09-14 | 2008-03-20 | Acadia Pharmaceuticals Inc. | Compounds with activity at estrogen receptors |
EP2099454A4 (en) | 2006-11-17 | 2010-11-10 | Abbott Lab | AMINOPYRROLIDINES AS CHEMOKINE RECEPTOR ANTAGONISTS |
PE20081581A1 (es) | 2006-12-21 | 2008-11-12 | Plexxikon Inc | COMPUESTOS PIRROLO[2,3-b]PIRIDINAS COMO MODULADORES DE QUINASA |
GB0625659D0 (en) | 2006-12-21 | 2007-01-31 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
AU2008210455A1 (en) | 2007-01-31 | 2008-08-07 | Vertex Pharmaceuticals Incorporated | 2-aminopyridine derivatives useful as kinase inhibitors |
AU2008214372A1 (en) | 2007-02-08 | 2008-08-14 | Merck Sharp & Dohme Corp. | Therapeutic agents |
EP2009002A1 (en) | 2007-06-21 | 2008-12-31 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | New process for the manufacture of 1H-imidazo [4,5-c]-quinoline ring systems |
WO2009005675A1 (en) | 2007-06-28 | 2009-01-08 | Abbott Laboratories | Novel triazolopyridazines |
US8022209B2 (en) | 2007-09-12 | 2011-09-20 | Janssen Pharmaceutica Nv | Substituted nitrogen-containing heteroaryl derivatives useful as modulators of the histamine H4 receptor |
GB0720390D0 (en) | 2007-10-18 | 2007-11-28 | Prosidion Ltd | G-Protein coupled receptor agonists |
KR20100088695A (ko) * | 2007-11-15 | 2010-08-10 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 거울상 이성질체가 강화된 이미다조아제피논 화합물 |
KR20100102646A (ko) * | 2007-12-11 | 2010-09-24 | 가부시키가이샤 사이토파스파인더 | 카르복스아미드 화합물 및 케모카인 수용체 길항제로서의 이의 용도 |
JP2011507910A (ja) | 2007-12-21 | 2011-03-10 | ユニバーシティー オブ ロチェスター | 真核生物の寿命を変更するための方法 |
PL2231642T3 (pl) | 2008-01-11 | 2014-04-30 | Novartis Ag | Pirymidyny jako inhibitory kinazy |
AR070127A1 (es) | 2008-01-11 | 2010-03-17 | Novartis Ag | Pirrolo - pirimidinas y pirrolo -piridinas |
US8338392B2 (en) | 2008-02-20 | 2012-12-25 | The Wistar Institute | MicroRNA modulators and method for identifying and using the same |
US20120010177A1 (en) | 2008-02-20 | 2012-01-12 | The Wistar Institute / North Carolina State University | MicroRNA Modulators and Method for Identifying And Using The Same |
US20110003849A1 (en) | 2008-03-04 | 2011-01-06 | Hong Shen | Soluble epoxide hydrolase inhibitors, compositions containing such compounds and methods of treatment |
US9066951B2 (en) | 2008-05-29 | 2015-06-30 | Wisconsin Alumni Research Foundation | Drugs to treat HPV infection |
JP2011523959A (ja) | 2008-06-11 | 2011-08-25 | メルク・シャープ・エンド・ドーム・コーポレイション | Faahの阻害剤として有用なイミダゾール誘導体 |
AU2009257795A1 (en) | 2008-06-11 | 2009-12-17 | Merck Sharp & Dohme Corp. | Pyrazole derivatives useful as inhibitors of FAAH |
JP2011524894A (ja) | 2008-06-18 | 2011-09-08 | ファイザー・リミテッド | ニコチンアミド誘導体 |
WO2009153720A1 (en) | 2008-06-18 | 2009-12-23 | Pfizer Limited | Nicotinamide derivatives |
US8242124B2 (en) | 2008-06-25 | 2012-08-14 | Bristol-Myers Squibb Company | Diketopiperidine derivatives as HIV attachment inhibitors |
CN102131810B (zh) | 2008-06-25 | 2014-02-26 | 百时美施贵宝公司 | 作为抗hiv剂的二酮稠合的吡咯并哌啶类和吡咯并哌嗪类 |
US8263642B2 (en) | 2008-06-25 | 2012-09-11 | Vanderbilt University | Antimicrobial compounds and methods of use thereof |
UY31952A (es) | 2008-07-02 | 2010-01-29 | Astrazeneca Ab | 5-metilideno-1,3-tiazolidina-2,4-dionas sustituidas como inhibidores de quinasa pim |
CA2731323A1 (en) | 2008-07-28 | 2010-02-04 | Gilead Sciences, Inc. | Cycloalkylidene and heterocycloalkylidene histone deacetylase inhibitor compounds |
AU2009279874B2 (en) | 2008-08-04 | 2015-02-12 | Merck Sharp & Dohme Corp. | Oxazole derivatives useful as inhibitors of FAAH |
WO2010019392A1 (en) | 2008-08-13 | 2010-02-18 | Merck Sharp & Dohme Corp. | Purine derivatives for treatment of alzheimer's disease |
CA2733533C (en) | 2008-08-25 | 2013-12-17 | Irm Llc | Hedgehog pathway modulators |
CN102223798A (zh) | 2008-09-24 | 2011-10-19 | 巴斯夫欧洲公司 | 用于防治无脊椎动物害虫的吡唑化合物 |
US8809344B2 (en) | 2008-10-29 | 2014-08-19 | Apath, Llc | Compounds, compositions, and methods for control of hepatitis C viral infections |
CA2741537A1 (en) | 2008-11-07 | 2010-05-14 | Wyeth Llc | Quinoxaline-based lxr modulators |
EP2380878B1 (en) | 2009-01-19 | 2013-08-14 | Daiichi Sankyo Company, Limited | Cyclic compound having hetero atom |
WO2010083199A1 (en) | 2009-01-19 | 2010-07-22 | Abbott Laboratories | Benzthiazole inhibitors of poly(adp-ribose)polymerase |
HUE047643T2 (hu) | 2009-03-02 | 2020-05-28 | Stemsynergy Therapeutics Inc | Módszerek és készítmények rák kezelésére és a WNT által közvetített hatások csökkentésére egy sejtben |
TW201041888A (en) | 2009-05-06 | 2010-12-01 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
WO2010141696A1 (en) | 2009-06-04 | 2010-12-09 | Dara Biosciences, Inc. | Methods of treating or preventing psoriasis, and/or alzheimer's disease using indane acetic acid derivatives |
US20110021531A1 (en) | 2009-07-27 | 2011-01-27 | Chobanian Harry | Oxazole derivatives useful as inhibitors of faah |
EP2470183B1 (en) | 2009-08-26 | 2015-09-16 | Merck Sharp & Dohme Corp. | Heterocyclic amide compounds as protein kinase inhibitors |
WO2011045415A2 (en) | 2009-10-15 | 2011-04-21 | Guerbet | New imaging agents and their use for the diagnostic in vivo of neurodegenerative diseases, notably alzheimer's disease and derivative diseases |
AR078887A1 (es) | 2009-11-06 | 2011-12-07 | Boehringer Ingelheim Int | Derivados arilo y heteroarilcarbonilo de hexahidroindenopiridina y octahidrobenzoquinolina y composiciones farmaceuticas que los contienen. |
JP2013032290A (ja) * | 2009-11-20 | 2013-02-14 | Dainippon Sumitomo Pharma Co Ltd | 新規縮合ピリミジン誘導体 |
WO2011072064A1 (en) | 2009-12-08 | 2011-06-16 | Array Biopharma Inc. | S piro [chroman - 4, 4 ' - imidazol] ones as beta - secretase inhibitors |
FR2953837B1 (fr) | 2009-12-10 | 2012-03-09 | Sanofi Aventis | Derives 9h-pyridino[3,4-b]indole disubstitues, leur preparation et leur utilisation therapeutique |
WO2011079000A1 (en) | 2009-12-22 | 2011-06-30 | Schering Corporation | DERIVATIVES OF 7,8-DIHYDRO-1H-IMIDAZO[2,1-b]PURIN-4(5H)-ONE AND METHODS OF USE THEREOF |
JP2013517281A (ja) | 2010-01-13 | 2013-05-16 | テンペロ、ファーマシューティカルズ、インコーポレイテッド | 化合物及び方法 |
CN102858338A (zh) | 2010-01-28 | 2013-01-02 | 默沙东公司 | 治疗疼痛及其它适应症的药物组合物 |
US20110190266A1 (en) | 2010-02-04 | 2011-08-04 | Daniel Chu | 5,6,6a,7,8,9-HEXAHYDRO-2H-PYRIDOPHTHALAZINONE INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE (PARP) |
EP2552905B1 (en) | 2010-03-26 | 2016-10-05 | Boehringer Ingelheim International GmbH | B-Raf kinase inhibitors |
US8865703B2 (en) | 2010-03-26 | 2014-10-21 | Boehringer Ingelheim International Gmbh | Pyridyltriazoles |
EP2371219A1 (en) | 2010-04-01 | 2011-10-05 | Basf Se | Herbicidal acylhydrazides |
CN103079558A (zh) | 2010-04-05 | 2013-05-01 | 满康德股份有限公司 | IRE-1α抑制剂 |
JP5856606B2 (ja) | 2010-04-22 | 2016-02-10 | メルク・シャープ・エンド・ドーム・コーポレイション | Faahの調節薬として有用なオキサゾール誘導体 |
CA2811989A1 (en) | 2010-04-23 | 2011-10-27 | Kineta, Inc. | Diarylpyridine anti-viral compounds |
EP2401915A1 (en) | 2010-06-29 | 2012-01-04 | Basf Se | Pyrazolopyridine compounds |
CN102048738A (zh) | 2010-12-08 | 2011-05-11 | 辽宁利锋科技开发有限公司 | 含有环嘧耐平药用复合物的药物组合物制剂 |
EA201490406A1 (ru) | 2011-07-29 | 2014-07-30 | Кариофарм Терапевтикс, Инк. | Модуляторы ядерного транспорта и их применение |
PL2736887T3 (pl) | 2011-07-29 | 2018-03-30 | Karyopharm Therapeutics, Inc. | Modulatory transportu jądrowego zawierające ugrupowanie hydrazydu i ich zastosowania |
JP2013159564A (ja) * | 2012-02-02 | 2013-08-19 | Kowa Co | ピラゾロピリミジン−7−アミン誘導体を有効成分とするtlr9阻害剤 |
RS55763B1 (sr) | 2012-02-13 | 2017-07-31 | Bristol Myers Squibb Co | Jedinjenja enedina, njihovi konjugati, primene i metode |
UA117913C2 (uk) | 2012-05-31 | 2018-10-25 | Фінекс Фармас'Ютікалс Аг | КАРБОКСАМІД- АБО СУЛЬФОНАМІДЗАМІЩЕНІ ТІАЗОЛИ ТА СПОРІДНЕНІ ПОХІДНІ ЯК МОДУЛЯТОРИ ОРФАНОВОГО ЯДЕРНОГО РЕЦЕПТОРА RORγ |
JO3407B1 (ar) * | 2012-05-31 | 2019-10-20 | Eisai R&D Man Co Ltd | مركبات رباعي هيدرو بيرازولو بيريميدين |
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