HK1160116A1 - Pyrrolo[2,3-d]pyrimidine compounds [23-d] - Google Patents
Pyrrolo[2,3-d]pyrimidine compounds [23-d]Info
- Publication number
- HK1160116A1 HK1160116A1 HK12100393.9A HK12100393A HK1160116A1 HK 1160116 A1 HK1160116 A1 HK 1160116A1 HK 12100393 A HK12100393 A HK 12100393A HK 1160116 A1 HK1160116 A1 HK 1160116A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- pyrrolo
- pyrimidine compounds
- pyrimidine
- compounds
- Prior art date
Links
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
- A61K31/495—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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (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)
- Epidemiology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9037108P | 2008-08-20 | 2008-08-20 | |
PCT/IB2009/053514 WO2010020905A1 (fr) | 2008-08-20 | 2009-08-10 | Composés pyrrolo[2,3-d]pyrimidines |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1160116A1 true HK1160116A1 (en) | 2012-08-10 |
Family
ID=41259411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK12100393.9A HK1160116A1 (en) | 2008-08-20 | 2012-01-13 | Pyrrolo[2,3-d]pyrimidine compounds [23-d] |
Country Status (27)
Country | Link |
---|---|
US (4) | US8133899B2 (fr) |
EP (1) | EP2384326B1 (fr) |
JP (1) | JP4884570B2 (fr) |
KR (1) | KR101335843B1 (fr) |
CN (1) | CN102131812B (fr) |
AR (2) | AR073073A1 (fr) |
AU (1) | AU2009283844B2 (fr) |
BR (1) | BRPI0917459B1 (fr) |
CA (1) | CA2733359C (fr) |
CL (1) | CL2011000353A1 (fr) |
CO (1) | CO6331437A2 (fr) |
DK (1) | DK2384326T3 (fr) |
EC (1) | ECSP11010904A (fr) |
ES (1) | ES2467109T3 (fr) |
HK (1) | HK1160116A1 (fr) |
HR (1) | HRP20140395T1 (fr) |
ME (1) | ME01269B (fr) |
MX (1) | MX2011001904A (fr) |
NZ (1) | NZ605292A (fr) |
PL (1) | PL2384326T3 (fr) |
PT (1) | PT2384326E (fr) |
RS (1) | RS53382B (fr) |
RU (1) | RU2493157C2 (fr) |
SI (1) | SI2384326T1 (fr) |
UY (1) | UY32059A (fr) |
WO (1) | WO2010020905A1 (fr) |
ZA (1) | ZA201101701B (fr) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LT2474545T (lt) | 2005-12-13 | 2017-02-27 | Incyte Holdings Corporation | Heteroarilu pakeisti pirolo[2,3-b]piridinai ir pirolo[2,3-b]pirimidinai kaip janus kinazės inhibitoriai |
WO2008063888A2 (fr) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Composés modulant l'activité de c-fms et/ou de c-kit et utilisations associées |
CA2689663C (fr) | 2007-06-13 | 2016-08-09 | Incyte Corporation | Sels de l'inhibiteur (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl)-3-cyclopentylpropanenitrile de la janus kinase |
MX349923B (es) | 2009-04-03 | 2017-08-21 | Hoffmann La Roche | Composiciones del ácido propano-1-sulfónico {3-[5-(4-cloro-fenil)- 1h-pirrolo [2,3-b]-piridina-3-carbonil]-2,4-difluoro-fenil]-amida y el uso de las mismas. |
DK2432472T3 (da) | 2009-05-22 | 2019-11-18 | Incyte Holdings Corp | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octan- eller heptan-nitril som jak-inhibitorer |
BRPI1012159B1 (pt) | 2009-05-22 | 2022-01-25 | Incyte Holdings Corporation | Compostos derivados de n-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2,3-d] pirimidinas e pirrol-3-il-pirrolo[2,3-d] pirimidinas como inibidores de janus cinase, composições farmacêuticas compreendendo os referidos compostos e usos dos mesmos |
TW201113285A (en) | 2009-09-01 | 2011-04-16 | Incyte Corp | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
WO2011045702A1 (fr) * | 2009-10-15 | 2011-04-21 | Pfizer Inc. | Composés pyrrolo[2,3-d]pyrimidine |
ES2633317T3 (es) | 2009-11-06 | 2017-09-20 | Plexxikon, Inc. | Compuestos y métodos para la modulación de quinasas, e indicaciones para ello |
CA2782720A1 (fr) * | 2009-12-18 | 2011-06-23 | Pfizer Inc. | Composes pyrrolo[2,3-d]pyrimidines |
AU2011219452B2 (en) * | 2010-02-24 | 2014-05-29 | Zoetis Llc | Veterinary compositions |
KR20220015492A (ko) | 2010-03-10 | 2022-02-08 | 인사이트 홀딩스 코포레이션 | Jak1 저해제로서의 피페리딘4일 아제티딘 유도체 |
TWI510487B (zh) | 2010-04-21 | 2015-12-01 | Plexxikon Inc | 用於激酶調節的化合物和方法及其適應症 |
PL2574168T3 (pl) | 2010-05-21 | 2016-10-31 | Preparaty inhibitora kinazy janusowej do stosowania miejscowego | |
ES2536415T3 (es) | 2010-11-19 | 2015-05-25 | Incyte Corporation | Pirrolopiridinas y pirrolopirimidinas sustituidas heterocíclicas como inhibidores de JAK |
CA2818542A1 (fr) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Derives pyrrolopyridine et pyrrolopyrimidine a substitution cyclobutyle utilises comme inhibiteurs des jak |
PT2672967T (pt) | 2011-02-07 | 2018-12-07 | Plexxikon Inc | Compostos e métodos de modulação da quinase e suas indicações |
US8637038B2 (en) | 2011-04-12 | 2014-01-28 | Rigel Pharmaceuticals, Inc. | Methods for inhibiting allograft rejection |
EP2721028B1 (fr) | 2011-06-20 | 2015-11-04 | Incyte Corporation | Dérivés d'azétidinyl-phényl-, de pyridyl- ou de pyrazinyl-carboxamide en tant qu'inhibiteurs des jak |
US8790651B2 (en) | 2011-07-21 | 2014-07-29 | Zoetis Llc | Interleukin-31 monoclonal antibody |
TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為jak抑制劑之環己基氮雜環丁烷衍生物 |
UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
WO2013173720A1 (fr) | 2012-05-18 | 2013-11-21 | Incyte Corporation | Dérivés de pyrrolopyridine et de pyrrolopyrimidine substitués par un pipéridinylcyclobutyle à titre d'inhibiteurs jak |
US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
MX349943B (es) * | 2012-07-17 | 2017-08-21 | Glaxosmithkline Ip No 2 Ltd | Indolcarbonitrilos como moduladores selectivos del receptor de androgeno. |
EP2874630B1 (fr) * | 2012-07-20 | 2018-12-05 | Zoetis Services LLC | Régime posologique destiné à des inhibiteurs de la janus kinase (jak) |
PE20200175A1 (es) | 2012-11-15 | 2020-01-24 | Incyte Holdings Corp | Formas de dosificacion de ruxolitinib de liberacion sostenida |
CN103896946B (zh) * | 2012-12-28 | 2018-04-03 | 浙江导明医药科技有限公司 | 用于预防及治疗多种自身免疫疾病的新化合物 |
WO2014118388A1 (fr) | 2013-02-04 | 2014-08-07 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Méthodes d'analyse de l'activité jak2 dans des globules rouges sanguins et leurs utilisations |
NZ710411A (en) | 2013-02-22 | 2017-11-24 | Pfizer | Pyrrolo [2, 3 -d]pyrimidine derivatives as inhibitors of janus- related kinases (jak) |
UA120162C2 (uk) | 2013-03-06 | 2019-10-25 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки при отриманні інгібітора jak |
US20140343034A1 (en) * | 2013-04-25 | 2014-11-20 | Japan Tobacco Inc. | Skin barrier function improving agent |
CA3155500A1 (fr) | 2013-08-07 | 2015-02-12 | Incyte Corporation | Formes galeniques a liberation prolongee pour un inhibiteur jak1 |
EP2924026A1 (fr) | 2014-03-28 | 2015-09-30 | Novartis Tiergesundheit AG | Aminosulfonylméthylcyclohexanes comme inhibiteurs de JAK |
US9498467B2 (en) | 2014-05-30 | 2016-11-22 | Incyte Corporation | Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1 |
EP3180344B1 (fr) | 2014-08-12 | 2019-09-18 | Pfizer Inc | Dérivés de pyrrolo[2,3-d]pyrimidine utiles pour inhiber la janus kinase |
EP3248980B1 (fr) * | 2015-01-20 | 2023-09-06 | Wuxi Fortune Pharmaceutical Co., Ltd | Inhibiteur de jak |
EP3290418B1 (fr) | 2015-04-29 | 2019-05-15 | Wuxi Fortune Pharmaceutical Co., Ltd | Inhibiteurs de janus kinase (jak) |
KR102081272B1 (ko) | 2015-05-29 | 2020-02-25 | 우시 포춘 파마슈티컬 컴퍼니 리미티드 | Janus 키나아제 억제제 |
WO2017013270A1 (fr) | 2015-07-23 | 2017-01-26 | Universite De Strasbourg | Utilisation d'un inhibiteur de la signalisation de la leptine pour la protection des reins de patients atteints de ciliopathie |
CN108602758B (zh) * | 2016-02-05 | 2021-01-26 | 斯福瑞股份公司 | 制备反式-4-氨基-1-环己烷基羧酸及其衍生物的方法 |
AU2017221193B2 (en) * | 2016-02-16 | 2019-03-14 | Zoetis Services Llc | Process for preparing 7H-pyrrolo (2, 3-d) pyrimidine compounds |
CN107365312B (zh) * | 2016-05-13 | 2021-10-01 | 瑞博(杭州)医药科技有限公司 | 一种制备Oclacitinib的新方法 |
US10875847B2 (en) | 2016-12-14 | 2020-12-29 | Intervet Inc. | Aminopyrazoles as selective janus kinase inhibitors |
US10093731B2 (en) | 2017-02-24 | 2018-10-09 | Kindred Biosciences, Inc. | Anti-IL31 antibodies for veterinary use |
WO2018167283A1 (fr) | 2017-03-17 | 2018-09-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés pour le diagnostic et le traitement d'un remodelage neuronal associé à un adénocarcinome canalaire pancréatique |
WO2018189335A1 (fr) | 2017-04-13 | 2018-10-18 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés de diagnostic et de traitement d'un adénocarcinome canalaire pancréatique |
CN110662747A (zh) | 2017-05-23 | 2020-01-07 | 施万生物制药研发Ip有限责任公司 | Janus激酶抑制剂的葡糖苷酸前药 |
US10596161B2 (en) | 2017-12-08 | 2020-03-24 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
CN112105608B (zh) | 2018-01-30 | 2023-07-14 | 因赛特公司 | 制备(1-(3-氟-2-(三氟甲基)异烟碱基)哌啶-4-酮)的方法 |
MA52011A (fr) | 2018-03-16 | 2021-01-20 | Zoetis Services Llc | Vaccins peptidiques contre l'interleukine-31 |
CA3093539A1 (fr) | 2018-03-16 | 2019-09-19 | Zoetis Services Llc | Anticorps monoclonaux anti-interleukine-31 a usage veterinaire |
MX2020010322A (es) | 2018-03-30 | 2022-11-30 | Incyte Corp | Tratamiento de la hidradenitis supurativa mediante el uso de inhibidores de actividad de la cinasa janus (jak). |
WO2020092015A1 (fr) | 2018-11-02 | 2020-05-07 | University Of Rochester | Atténuation thérapeutique d'une infection épithéliale |
CN113272306A (zh) * | 2018-11-05 | 2021-08-17 | 爱维斯塔制药解决方案有限公司 | 化学化合物 |
NL2022471B1 (en) | 2019-01-29 | 2020-08-18 | Vationpharma B V | Solid state forms of oclacitinib |
CN111499641B (zh) * | 2019-01-30 | 2021-06-04 | 格格巫(珠海)生物科技有限公司 | 一种jak抑制剂及其制备方法 |
US11992490B2 (en) | 2019-10-16 | 2024-05-28 | Incyte Corporation | Use of JAK1 inhibitors for the treatment of cutaneous lupus erythematosus and Lichen planus (LP) |
EP4077380A1 (fr) | 2019-12-20 | 2022-10-26 | Intervet International B.V. | Anticorps bispécifiques caninisés et partenaires de liaison bispécifiques pour le traitement de la dermatite atopique |
US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
CN112279854B (zh) * | 2020-08-25 | 2022-04-05 | 常州齐晖药业有限公司 | 一种7H-吡咯并[2,3-d]嘧啶化合物的制备方法 |
JP2023545182A (ja) | 2020-10-15 | 2023-10-26 | インターベット インターナショナル ベー. フェー. | イヌインターロイキン-31受容体アルファに対するイヌ化ラット抗体 |
JP2023554665A (ja) | 2020-12-18 | 2023-12-28 | ベーリンガー インゲルハイム アニマル ヘルス ユーエスエイ インコーポレイテッド | ホウ素含有ピラゾール化合物、それらを含む組成物、それらの方法及び使用 |
EP4294462A1 (fr) | 2021-02-22 | 2023-12-27 | Zoetis Services LLC | Modèle de prurit induit par l'il-31 équine |
AU2022331810A1 (en) | 2021-08-20 | 2024-02-29 | Intervet International B.V. | Fusion proteins for treating atopic dermatitis |
CA3239826A1 (fr) | 2021-12-16 | 2023-06-22 | Mohamad Morsey | Anticorps caninises contre le recepteur alpha ii de l'interleukine-31 canine |
AU2022418280A1 (en) | 2021-12-24 | 2024-06-13 | Intervet International B.V. | Use of aminopyrazole compounds |
CN114605420B (zh) * | 2022-04-25 | 2024-07-12 | 江苏慧聚药业股份有限公司 | 马来酸奥拉替尼的合成方法 |
CN118255769A (zh) * | 2022-12-28 | 2024-06-28 | 格格巫(珠海)生物科技有限公司 | 一种立体异构体的制备方法及中间体 |
Family Cites Families (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3037980A (en) * | 1955-08-18 | 1962-06-05 | Burroughs Wellcome Co | Pyrrolopyrimidine vasodilators and method of making them |
GB915303A (en) | 1958-03-13 | 1963-01-09 | Wellcome Found | Pyrrolo[2,3-d]pyrimidine derivatives and the manufacture thereof |
US3670079A (en) * | 1970-10-06 | 1972-06-13 | Merck & Co Inc | Anabolic agents |
US4997936A (en) * | 1977-10-19 | 1991-03-05 | Merck & Co., Inc. | 2-carbamimidoyl-6-substituted-1-carbadethiapen-2-em-3-carboxylic acids |
US4456464A (en) * | 1982-05-19 | 1984-06-26 | Zoecon Corporation | Phenoxy- and pyridyloxy-phenoxyalkyl phosphinates and related sulfur compounds for weed control |
US4526608A (en) * | 1982-07-14 | 1985-07-02 | Zoecon Corporation | Certain 2-pyridyloxyphenyl-oximino-ether-carboxylates, herbicidal compositions containing same and their herbicidal method of use |
US4590282A (en) * | 1984-09-24 | 1986-05-20 | Sandoz Ltd. | Pest control agents |
US4933339A (en) * | 1985-08-21 | 1990-06-12 | Rohm And Haas Company | (2-cyano-2-arylethyl)pyridine compounds useful in controlling fungicidal activity |
CA1328333C (fr) * | 1988-03-04 | 1994-04-05 | Quirico Branca | Derives d'acide amine |
NO169490C (no) | 1988-03-24 | 1992-07-01 | Takeda Chemical Industries Ltd | Analogifremgangsmaate for fremstilling av terapeutisk aktive pyrrolopyrimidinderivater |
US4879309A (en) * | 1988-09-27 | 1989-11-07 | Schering Corporation | Mercapto-acylamino acids as antihypertensives |
JP2983254B2 (ja) * | 1989-06-14 | 1999-11-29 | 武田薬品工業株式会社 | ピロロ〔2,3―d〕ピリミジン誘導体の製造法およびその中間体 |
US5356903A (en) * | 1993-04-22 | 1994-10-18 | Sterling Winthrop Inc. | 1-cyclopropyl-4-pyridyl-quinolines |
US6136595A (en) * | 1993-07-29 | 2000-10-24 | St. Jude Children's Research Hospital | Jak kinases and regulations of cytokine signal transduction |
US5389509A (en) * | 1993-10-04 | 1995-02-14 | Eastman Kodak Company | Ultrathin high chloride tabular grain emulsions |
IL112249A (en) | 1994-01-25 | 2001-11-25 | Warner Lambert Co | Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds |
EP0682027B1 (fr) | 1994-05-03 | 1997-10-15 | Novartis AG | Dérivés de la pyrrolopyrimidine avec une activité anti-proliférative |
JP3290666B2 (ja) | 1995-06-07 | 2002-06-10 | ファイザー・インコーポレーテッド | 複素環式の縮合環ピリミジン誘導体 |
KR19990028709A (ko) | 1995-07-05 | 1999-04-15 | 미리암 디. 메코너헤이 | 살진균 피리미디논 |
CZ1598A3 (cs) | 1995-07-06 | 1998-04-15 | Novartis Ag | Pyrrolopyrimidiny a způsoby jejich přípravy |
AR004010A1 (es) | 1995-10-11 | 1998-09-30 | Glaxo Group Ltd | Compuestos heterociclicos |
CN1168138A (zh) | 1995-11-14 | 1997-12-17 | 法玛西雅厄普约翰公司 | 芳基和杂芳基嘌呤化合物 |
EP0888349B1 (fr) | 1996-01-23 | 2002-05-22 | Novartis AG | Pyrrolopyrimidines et leurs procedes de preparation |
CH690773A5 (de) | 1996-02-01 | 2001-01-15 | Novartis Ag | Pyrrolo(2,3-d)pyrimide und ihre Verwendung. |
GB9604361D0 (en) | 1996-02-29 | 1996-05-01 | Pharmacia Spa | 4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors |
AU1794697A (en) | 1996-03-06 | 1997-09-22 | Novartis Ag | 7-alkyl-pyrrolo{2,3-d}pyrimidines |
AU3176297A (en) | 1996-06-25 | 1998-01-14 | Novartis Ag | Substituted 7-amino-pyrrolo{3,2-d}pyrimidines and the use thereof |
HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
EA199900021A1 (ru) | 1996-07-13 | 1999-08-26 | Глаксо, Груп Лимитед | Бициклические гетероароматические соединения в качестве ингибиторов протеинтирозинкиназы |
DK0938486T3 (da) * | 1996-08-23 | 2008-07-07 | Novartis Ag | Substituerede pyrrolopyrimidiner og fremgangsmåder til deres fremstilling |
EP0946554A1 (fr) | 1996-11-27 | 1999-10-06 | Pfizer Inc. | Derives de pyrimidines bicycliques fusionnes |
WO1998033798A2 (fr) | 1997-02-05 | 1998-08-06 | Warner Lambert Company | Pyrido[2,3d]pyrimidines et 4-aminopyrimidines en tant qu'inhibiteurs de la proliferation cellulaire |
AU6568398A (en) * | 1997-03-24 | 1998-10-20 | Pharmacia & Upjohn Company | Method for identifying inhibitors of jak2/cytokine receptor binding |
EP1068206A1 (fr) | 1998-04-02 | 2001-01-17 | Neurogen Corporation | Derives aminoalkyle substitues de pyrrolo 2,3-b]pyridine et pyrrolo 2,3-d]pyrimidine: modulateurs de recepteurs de crf1 |
AU4317399A (en) | 1998-05-28 | 1999-12-13 | Parker Hughes Institute | Quinazolines for treating brain tumor |
AU3951899A (en) * | 1998-06-19 | 2000-01-05 | Pfizer Products Inc. | Pyrrolo(2,3-d)pyrimidine compounds |
PA8474101A1 (es) | 1998-06-19 | 2000-09-29 | Pfizer Prod Inc | Compuestos de pirrolo [2,3-d] pirimidina |
AU4851599A (en) | 1998-06-30 | 2000-01-17 | Parker Hughes Institute | Method for inhibiting c-jun expression using jak-3 inhibitors |
MXPA01001893A (es) | 1998-08-21 | 2002-04-24 | Parker Hughes Inst | Derivados de quinazolina. |
JP2002526500A (ja) | 1998-09-18 | 2002-08-20 | ビーエーエスエフ アクチェンゲゼルシャフト | プロテインキナーゼ阻害剤としてのピロロピリミジン |
CZ27399A3 (cs) * | 1999-01-26 | 2000-08-16 | Ústav Experimentální Botaniky Av Čr | Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv |
US6080747A (en) * | 1999-03-05 | 2000-06-27 | Hughes Institute | JAK-3 inhibitors for treating allergic disorders |
CA2379640C (fr) * | 1999-09-30 | 2006-11-28 | Neurogen Corporation | Heterocycles a substitution alkylene-diamine |
AP1905A (en) * | 1999-12-10 | 2008-10-20 | Pfizer Prod Inc | Pyrrolo[2,3-d] Pyrimidine Compounds. |
UA74370C2 (uk) * | 2000-06-26 | 2005-12-15 | Пфайзер Продактс Інк. | Піроло(2,3-d)піримідинові сполуки як імуносупресори |
HU230302B1 (hu) * | 2000-10-20 | 2015-12-28 | Eisai R&D Management Co., Ltd. | Nitrogéntartalmú aromás származékok és ezeket tartalmazó gyógyászati készítmények |
US7301023B2 (en) * | 2001-05-31 | 2007-11-27 | Pfizer Inc. | Chiral salt resolution |
GB0119249D0 (en) * | 2001-08-07 | 2001-10-03 | Novartis Ag | Organic compounds |
GT200200234A (es) * | 2001-12-06 | 2003-06-27 | Compuestos cristalinos novedosos | |
BR0316487A (pt) * | 2002-11-26 | 2005-10-11 | Pfizer Prod Inc | Método todo de tratamento da rejeição de transplantes |
US7253166B2 (en) * | 2003-04-22 | 2007-08-07 | Irm Llc | 6-phenyl-7H-pyrrolo[2,3-d]pyrimidine compounds that induce neuronal differentiation in embryonic stem cells |
WO2005020921A2 (fr) * | 2003-08-29 | 2005-03-10 | Exelixis, Inc. | Modulateurs c-kit et leurs procedes d'utilisation |
EP1734967A2 (fr) * | 2003-12-17 | 2006-12-27 | Pfizer Products Incorporated | Methode pour traiter le rejet de greffe(en) pyrrolo [2,3-d] pyrimidine compounds for treating transplant rejection |
EP1715871A1 (fr) * | 2003-12-22 | 2006-11-02 | Gilead Sciences, Inc. | Conjugues de phosphonate inhibiteurs de kinase |
CA2553724A1 (fr) * | 2004-02-03 | 2005-08-18 | Abbott Laboratories | Utilisation d'aminobenzoxazoles comme agents therapeutiques |
CA2572331A1 (fr) * | 2004-07-02 | 2006-02-09 | Exelixis, Inc. | Modulateurs de c-met et leur methode d'utilisation |
JP2008508358A (ja) * | 2004-08-02 | 2008-03-21 | オーエスアイ・ファーマスーティカルズ・インコーポレーテッド | アリール−アミノ置換ピロロピリミジンマルチキナーゼ阻害化合物 |
AR054416A1 (es) | 2004-12-22 | 2007-06-27 | Incyte Corp | Pirrolo [2,3-b]piridin-4-il-aminas y pirrolo [2,3-b]pirimidin-4-il-aminas como inhibidores de las quinasas janus. composiciones farmaceuticas. |
JO2787B1 (en) | 2005-04-27 | 2014-03-15 | امجين إنك, | Alternative amide derivatives and methods of use |
WO2008089307A2 (fr) | 2007-01-18 | 2008-07-24 | Lexicon Pharmaceuticals, Inc. | Méthodes et compositions utilisés dans le traitement de la douleur, de l'inflammation et du cancer |
WO2008089310A2 (fr) | 2007-01-18 | 2008-07-24 | Lexicon Pharmaceuticals, Inc. | Méthodes et compositions utilisées dans le traitement de troubles corporels |
-
2009
- 2009-08-10 PT PT97868822T patent/PT2384326E/pt unknown
- 2009-08-10 NZ NZ605292A patent/NZ605292A/en unknown
- 2009-08-10 ES ES09786882.2T patent/ES2467109T3/es active Active
- 2009-08-10 KR KR1020117003834A patent/KR101335843B1/ko active Protection Beyond IP Right Term
- 2009-08-10 PL PL09786882T patent/PL2384326T3/pl unknown
- 2009-08-10 DK DK09786882.2T patent/DK2384326T3/da active
- 2009-08-10 ME MEP-2011-22A patent/ME01269B/me unknown
- 2009-08-10 CA CA2733359A patent/CA2733359C/fr active Active
- 2009-08-10 MX MX2011001904A patent/MX2011001904A/es active IP Right Grant
- 2009-08-10 BR BRPI0917459-1A patent/BRPI0917459B1/pt active IP Right Grant
- 2009-08-10 RU RU2011106331/04A patent/RU2493157C2/ru not_active Application Discontinuation
- 2009-08-10 CN CN200980132519.2A patent/CN102131812B/zh active Active
- 2009-08-10 AU AU2009283844A patent/AU2009283844B2/en active Active
- 2009-08-10 SI SI200930918T patent/SI2384326T1/sl unknown
- 2009-08-10 JP JP2011523467A patent/JP4884570B2/ja active Active
- 2009-08-10 WO PCT/IB2009/053514 patent/WO2010020905A1/fr active Application Filing
- 2009-08-10 EP EP09786882.2A patent/EP2384326B1/fr active Active
- 2009-08-10 RS RS20140332A patent/RS53382B/en unknown
- 2009-08-17 US US12/542,451 patent/US8133899B2/en active Active
- 2009-08-18 AR ARP090103164A patent/AR073073A1/es not_active Application Discontinuation
- 2009-08-19 UY UY0001032059A patent/UY32059A/es active IP Right Grant
-
2011
- 2011-02-18 CL CL2011000353A patent/CL2011000353A1/es unknown
- 2011-02-18 CO CO11019992A patent/CO6331437A2/es active IP Right Grant
- 2011-03-04 ZA ZA2011/01701A patent/ZA201101701B/en unknown
- 2011-03-21 EC EC2011010904A patent/ECSP11010904A/es unknown
-
2012
- 2012-01-13 HK HK12100393.9A patent/HK1160116A1/xx unknown
- 2012-01-30 US US13/360,963 patent/US8987283B2/en active Active
-
2014
- 2014-04-30 HR HRP20140395AT patent/HRP20140395T1/hr unknown
-
2015
- 2015-02-11 US US14/619,195 patent/US9161939B2/en active Active
- 2015-09-15 US US14/854,632 patent/US9271981B2/en active Active
-
2016
- 2016-10-04 AR ARP160103034A patent/AR106252A2/es not_active Application Discontinuation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HK1160116A1 (en) | Pyrrolo[2,3-d]pyrimidine compounds [23-d] | |
ZA201202718B (en) | Pyrrolo[2,3-d]pyrimidine compounds | |
IL257410A (en) | Pyrazolo [1, 5 – a ] pyrimidines as antiviral agents | |
IL278119B (en) | Disubstituted pyrazolo[5.1–a]pyrimidine compounds as trk kinase inhibitors | |
HK1143154A1 (en) | Pyrrolo [2, 3 -d] pyrimidin derivatives as protein kinase b inhibitors b[23-d] | |
ZA201004368B (en) | Pyrazolo [1,5-a] pyrimidines useful as jak2 inhibitors | |
ZA201104853B (en) | 2,5-diamino-substituted pyrido[4,3-d]pyrimidines as autotaxin inhibitors against cancer | |
ZA201200982B (en) | Substituted pyrazolo[1,5-a]pyrimidine compounds as trk kinase inhibitors | |
EP2608669A4 (fr) | Nouveaux dérivés de pyrazolo[1,5-a]pyrimidine utilisés comme inhibiteurs de mtor | |
ZA201004823B (en) | Novel pyrazolo [3,4-d]pyrimidine derivatives as anti-cancer agents | |
EP2525659A4 (fr) | Composés pyrazolo[1,5-a]pyrimidines en tant qu'inhibiteurs de mtor | |
BRPI0822239A2 (pt) | Composto de pirazolo[1,5-a] pirimidina | |
ZA201101550B (en) | 4-amino-3-(imidazolyl)-pyrazolo[3,4-d]pyrimidines | |
SI2167470T1 (sl) | Triazolo(1,5-a)kinolini kot adenozin A3 receptorski ligandi | |
EP2523552A4 (fr) | Pyrazolo[1,5-a]pyrimidines comme inhibiteurs de mark | |
EP2511276A4 (fr) | Dérivé de pyrrolo[2,3-d]pyrimidine | |
IL206666A0 (en) | N-PHENYLIMIDAZO[1,2-a]PYRIDINE-2- | |
IL206668A0 (en) | N-PHENYLIMIDAZO[1,2-a]PYRIDINE-2- |