MA38493A1 - Composés tricycliques utilisés en tant qu'inhibiteurs de l'immunosuppression dont la médiation est assurée par la métabolisation du tryptophane - Google Patents
Composés tricycliques utilisés en tant qu'inhibiteurs de l'immunosuppression dont la médiation est assurée par la métabolisation du tryptophaneInfo
- Publication number
- MA38493A1 MA38493A1 MA38493A MA38493A MA38493A1 MA 38493 A1 MA38493 A1 MA 38493A1 MA 38493 A MA38493 A MA 38493A MA 38493 A MA38493 A MA 38493A MA 38493 A1 MA38493 A1 MA 38493A1
- Authority
- MA
- Morocco
- Prior art keywords
- tryptophan
- treat
- immunosuppression
- inhibitors
- metabolism
- Prior art date
Links
- 206010062016 Immunosuppression Diseases 0.000 title abstract 4
- 230000001506 immunosuppresive effect Effects 0.000 title abstract 4
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 title abstract 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title 1
- 230000001404 mediated effect Effects 0.000 title 1
- 230000004060 metabolic process Effects 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 208000035473 Communicable disease Diseases 0.000 abstract 1
- 101710136122 Tryptophan 2,3-dioxygenase Proteins 0.000 abstract 1
- 102000057288 Tryptophan 2,3-dioxygenases Human genes 0.000 abstract 1
- 238000011394 anticancer treatment Methods 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 102000006639 indoleamine 2,3-dioxygenase Human genes 0.000 abstract 1
- 108020004201 indoleamine 2,3-dioxygenase Proteins 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
-
- 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
- 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
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Enzymes And Modification Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La présente invention concerne des inhibiteurs d'ido et de tdo et des compositions pharmaceutiques les comprenant, qui peuvent être utilisés pour moduler une activité de l'indoleamine 2,3-dioxygénase et de la tryptophane 2,3 dioxygénase ; traiter l'immunosuppression ; traiter des états pathologiques qui sont améliorés par inhibition de la dégradation du tryptophane ; augmenter l'efficacité d'un traitement anticancéreux qui consiste à administrer un agent anticancéreux ; traiter l'immunosuppression spécifique d'une tumeur associée à un cancer ; et traiter l'immunosuppression associée à une maladie infectieuse.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361784089P | 2013-03-14 | 2013-03-14 | |
| PCT/US2014/022680 WO2014159248A1 (fr) | 2013-03-14 | 2014-03-10 | Composés tricycliques utilisés en tant qu'inhibiteurs de l'immunosuppression dont la médiation est assurée par la métabolisation du tryptophane |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA38493A1 true MA38493A1 (fr) | 2017-02-28 |
| MA38493B1 MA38493B1 (fr) | 2017-10-31 |
Family
ID=50686105
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA38493A MA38493B1 (fr) | 2013-03-14 | 2014-03-10 | Composés tricycliques utilisés en tant qu'inhibiteurs de l'immunosuppression dont la médiation est assurée par la métabolisation du tryptophane |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US9617272B2 (fr) |
| EP (2) | EP2976332B1 (fr) |
| JP (2) | JP6093903B2 (fr) |
| KR (1) | KR20150126623A (fr) |
| CN (1) | CN105189466A (fr) |
| AU (2) | AU2014241079C1 (fr) |
| BR (1) | BR112015022588A2 (fr) |
| CA (1) | CA2902174A1 (fr) |
| CL (2) | CL2015002649A1 (fr) |
| CR (1) | CR20150485A (fr) |
| IL (1) | IL241027A0 (fr) |
| MA (1) | MA38493B1 (fr) |
| MX (1) | MX361375B (fr) |
| PE (1) | PE20151593A1 (fr) |
| PH (1) | PH12015501866A1 (fr) |
| RU (1) | RU2667509C2 (fr) |
| SA (1) | SA515361127B1 (fr) |
| SG (2) | SG10201707545XA (fr) |
| UA (1) | UA118103C2 (fr) |
| WO (1) | WO2014159248A1 (fr) |
| ZA (1) | ZA201607948B (fr) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO2694640T3 (fr) | 2011-04-15 | 2018-03-17 | ||
| TWI599567B (zh) | 2013-03-14 | 2017-09-21 | 健生藥品公司 | P2x7調節劑 |
| US10053463B2 (en) | 2013-03-14 | 2018-08-21 | Janssen Pharmaceutica Nv | Substituted [1,2,4]triazolo[4,3-a]pyrazines as P2X7 modulators |
| JP6294953B2 (ja) | 2013-03-14 | 2018-03-14 | ヤンセン ファーマシューティカ エヌ.ベー. | P2x7調節物質 |
| TWI627174B (zh) | 2013-03-14 | 2018-06-21 | 比利時商健生藥品公司 | P2x7調控劑 |
| AU2014230814B2 (en) | 2013-03-14 | 2017-12-21 | Boehringer Ingelheim International Gmbh | Substituted 2-Aza-bicyclo[2.2.1]heptane-3-carboxylic acid (benzyl-cyano-methyl)-amides inhibitors of Cathepsin C |
| CN103570727B (zh) | 2013-11-12 | 2015-08-19 | 复旦大学 | 一种n-苄基色胺酮衍生物及其制备方法和应用 |
| CA2956465A1 (fr) | 2014-09-05 | 2016-03-10 | Merck Patent Gmbh | Composes diaza- et triaza- tricycliques a cyclohexyl-ethyle substitue comme antagonistes de l'indoleamine 2,3-dioxygenase (ido) pour le traitement du cancer |
| AP2017009733A0 (en) | 2014-09-12 | 2017-02-28 | Boehringer Ingelheim Int | Spirocyclic inhibitors of cathepsin c |
| EA034015B1 (ru) | 2014-09-12 | 2019-12-19 | Янссен Фармацевтика Нв | Модуляторы р2х7 |
| WO2016039983A1 (fr) | 2014-09-12 | 2016-03-17 | Janssen Pharmaceutica Nv | N-acyl-triazolopyrazines modulant le p2x7 |
| GB201417369D0 (en) * | 2014-10-01 | 2014-11-12 | Redx Pharma Ltd | Compounds |
| US20160145344A1 (en) * | 2014-10-20 | 2016-05-26 | University Of Southern California | Murine and human innate lymphoid cells and lung inflammation |
| KR102602947B1 (ko) * | 2014-11-03 | 2023-11-16 | 아이오메트 파마 엘티디 | 제약 화합물 |
| US10525035B2 (en) | 2014-12-18 | 2020-01-07 | Lankenau Institute For Medical Research | Methods and compositions for the treatment of retinopathy and other ocular diseases |
| CN105884828A (zh) * | 2015-02-16 | 2016-08-24 | 上海迪诺医药科技有限公司 | 多环化合物、其药物组合物及应用 |
| CN110872289A (zh) | 2015-04-10 | 2020-03-10 | 百济神州(北京)生物科技有限公司 | 作为IDO1和/或TDO抑制剂的新颖的8-取代的咪唑并[1,5-a]吡啶 |
| EP3283488A4 (fr) | 2015-04-12 | 2018-10-24 | Hangzhou Innogate Pharma Co., Ltd. | Hétérocycles utiles comme inhibiteurs d'ido et de tdo |
| US9951065B2 (en) | 2015-05-15 | 2018-04-24 | Gilead Sciences, Inc. | Benzimidazole and imadazopyridine carboximidamide compounds |
| GB2548542A (en) * | 2015-06-16 | 2017-09-27 | Redx Pharma Plc | Compounds |
| CN105037371A (zh) * | 2015-06-30 | 2015-11-11 | 西华大学 | 一种氘代的吲哚胺-2,3-双加氧酶抑制剂 |
| WO2017019175A1 (fr) | 2015-07-24 | 2017-02-02 | Newlink Genetics Corporation | Sels et promédicaments de 1-méthyl-d-tryptophane |
| JP7227005B2 (ja) | 2015-12-24 | 2023-02-21 | ジェネンテック, インコーポレイテッド | Tdo2阻害剤 |
| CN107056785B (zh) * | 2016-01-02 | 2021-06-22 | 杭州英创医药科技有限公司 | 作为ido和tdo抑制剂的杂环化合物 |
| AU2017215424A1 (en) | 2016-02-02 | 2018-08-09 | Emcure Pharmaceuticals Limited | Derivatives of pyrroloimidazole or analogues thereof which are useful for the treatment of inter alia cancer |
| TWI743088B (zh) * | 2016-02-19 | 2021-10-21 | 大陸商正大天晴藥業集團股份有限公司 | 作爲免疫調節劑的三並環化合物 |
| WO2017140272A1 (fr) * | 2016-02-19 | 2017-08-24 | 正大天晴药业集团股份有限公司 | Composé tricyclique servant d'immunomodulateur |
| WO2017149469A1 (fr) | 2016-03-03 | 2017-09-08 | Emcure Pharmaceuticals Limited | Composés hétérocycliques utiles en tant que modulateurs de l'ido et/ou de la tdo |
| BR112018071602B1 (pt) * | 2016-04-29 | 2024-02-27 | Iomet Pharma Ltd. | Compostos de imidazopiridina substituídos, sua composição e seus usos como inibidores da indolamina 2,3-dioxigenase e/ou triptofano-2,3- dioxigenase |
| CN107383012B (zh) * | 2016-05-16 | 2021-09-28 | 鲁南制药集团股份有限公司 | 含二环的咪唑醇衍生物 |
| WO2017198159A1 (fr) * | 2016-05-16 | 2017-11-23 | 鲁南制药集团股份有限公司 | Dérivé d'imidazole contenant un cycle de liaison |
| CN107663159A (zh) * | 2016-07-29 | 2018-02-06 | 上海迪诺医药科技有限公司 | 多环化合物、其药物组合物及应用 |
| EP4268838A3 (fr) | 2016-09-19 | 2023-12-27 | University Of South Florida | Procédé de ciblage de virus oncolytiques aux tumeurs |
| TW201815766A (zh) | 2016-09-22 | 2018-05-01 | 美商普雷辛肯公司 | 用於ido及tdo調節之化合物及方法以及其適應症 |
| EP3515914A4 (fr) | 2016-09-24 | 2020-04-15 | BeiGene, Ltd. | Nouvelles imidazo[1,5-a]pyridines substituées en position 5 ou 8 en tant qu'indoleamine et/ou tryptophane 2,3-dioxygénases |
| WO2018071873A2 (fr) | 2016-10-13 | 2018-04-19 | Juno Therapeutics, Inc. | Méthodes et compositions d'immunothérapie impliquant des modulateurs de la voie métabolique du tryptophane |
| TW201815793A (zh) * | 2016-10-21 | 2018-05-01 | 江蘇恆瑞醫藥股份有限公司 | 一種咪唑並異吲哚類衍生物的遊離鹼的結晶形式及其製備方法 |
| CN108203438B (zh) * | 2016-12-20 | 2021-09-28 | 深圳微芯生物科技股份有限公司 | 具有吲哚胺2,3-双加氧酶抑制活性的稠合咪唑化合物 |
| MX378460B (es) | 2016-12-22 | 2025-03-10 | Calithera Biosciences Inc | Composiciones y métodos para inhibir la actividad de la arginasa. |
| CN110191709A (zh) | 2017-01-17 | 2019-08-30 | 德州大学系统董事会 | 可用作吲哚胺2,3-双加氧酶和/或色氨酸双加氧酶抑制剂的化合物 |
| US11603373B2 (en) | 2017-06-28 | 2023-03-14 | Genentech, Inc. | TDO2 and IDO1 inhibitors |
| WO2019006047A1 (fr) | 2017-06-28 | 2019-01-03 | Genentech, Inc. | Inhibiteurs de tdo2 et ido1 |
| CN109384791B (zh) * | 2017-08-09 | 2020-09-11 | 江苏恒瑞医药股份有限公司 | 一种咪唑并异吲哚类衍生物游离碱的晶型及其制备方法 |
| KR102891807B1 (ko) * | 2017-08-22 | 2025-12-01 | 길리애드 사이언시즈, 인코포레이티드 | 치료 헤테로시클릭 화합물 |
| KR102403289B1 (ko) * | 2017-09-15 | 2022-05-30 | 다이호야쿠힌고교 가부시키가이샤 | Ido 의 발현이 관여하는 질환의 예방 및/또는 치료제 |
| WO2019078246A1 (fr) * | 2017-10-19 | 2019-04-25 | 一般社団法人ファルマバレープロジェクト支援機構 | Inhibiteur de ido/tdo |
| WO2019101188A1 (fr) | 2017-11-25 | 2019-05-31 | Beigene, Ltd. | Nouveaux benzoimidazoles en tant qu'inhibiteurs sélectifs de l'indoléamine 2, 3-dioxygénases |
| WO2019136157A2 (fr) | 2018-01-05 | 2019-07-11 | Dicerna Pharmaceuticals, Inc. | Diminution de l'expression de la bêta-caténine et de ido pour potentialiser une immunothérapie |
| WO2019183145A1 (fr) | 2018-03-20 | 2019-09-26 | Plexxikon Inc. | Composés et procédés de modulation d'ido et de tdo, et indications pour ceux-ci |
| EP3823604A4 (fr) | 2018-07-17 | 2022-03-16 | Board of Regents, The University of Texas System | Composés utiles en tant qu'inhibiteurs de l'indoléamine 2,3-dioxygénase et/ou de la tryptophane dioxygénase |
| CN110950842B (zh) * | 2018-09-27 | 2023-06-20 | 深圳微芯生物科技股份有限公司 | 具有吲哚胺-2,3-双加氧酶抑制活性的喹啉衍生物 |
| MY205440A (en) | 2018-09-28 | 2024-10-21 | Janssen Pharmaceutica Nv | Monoacylglycerol lipase modulators |
| MX2021003661A (es) | 2018-09-28 | 2021-08-19 | Janssen Pharmaceutica Nv | Moduladores de la monoacilglicerol lipasa. |
| EP4038070B1 (fr) | 2019-09-30 | 2025-07-09 | Janssen Pharmaceutica NV | Ligands mgl pet radiomarqués |
| CA3176946A1 (fr) | 2020-03-26 | 2021-09-30 | Janssen Pharmaceutica Nv | Modulateurs de la monoacylglycerol lipase |
| US11839659B2 (en) | 2020-07-02 | 2023-12-12 | Northwestern University | Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein |
| KR20230152715A (ko) | 2021-03-05 | 2023-11-03 | 유니버시타트 바셀 | Ebv 관련 질환 또는 질병의 치료용 조성물 |
| EP4052705A1 (fr) | 2021-03-05 | 2022-09-07 | Universität Basel Vizerektorat Forschung | Compositions pour le traitement des maladies ou des pathologies associées à l'ebv |
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| DE102007020493A1 (de) | 2007-04-30 | 2008-11-06 | Grünenthal GmbH | Substituierte Amid-Derivate |
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| WO2009132238A2 (fr) | 2008-04-24 | 2009-10-29 | Newlink Genetics | Inhibiteurs de l’ido |
| US8541595B2 (en) * | 2008-11-13 | 2013-09-24 | Merch Sharp & Dohme Corp. | Imidazoisoindole neuropeptide S receptor antagonists |
| WO2011056652A1 (fr) | 2009-10-28 | 2011-05-12 | Newlink Genetics | Dérivés imidazole comme inhibiteurs de l'ido |
| JP2012037986A (ja) | 2010-08-04 | 2012-02-23 | Canon Inc | 画像形成装置及びその制御方法と画像形成システム |
| NO2694640T3 (fr) | 2011-04-15 | 2018-03-17 |
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2014
- 2014-03-10 EP EP14722814.2A patent/EP2976332B1/fr not_active Not-in-force
- 2014-03-10 JP JP2016501035A patent/JP6093903B2/ja not_active Expired - Fee Related
- 2014-03-10 AU AU2014241079A patent/AU2014241079C1/en not_active Ceased
- 2014-03-10 MA MA38493A patent/MA38493B1/fr unknown
- 2014-03-10 EP EP18152869.6A patent/EP3366678A1/fr not_active Withdrawn
- 2014-03-10 CN CN201480015368.3A patent/CN105189466A/zh active Pending
- 2014-03-10 US US14/774,450 patent/US9617272B2/en not_active Expired - Fee Related
- 2014-03-10 MX MX2015011385A patent/MX361375B/es active IP Right Grant
- 2014-03-10 WO PCT/US2014/022680 patent/WO2014159248A1/fr not_active Ceased
- 2014-03-10 RU RU2015143990A patent/RU2667509C2/ru not_active IP Right Cessation
- 2014-03-10 KR KR1020157025259A patent/KR20150126623A/ko not_active Withdrawn
- 2014-03-10 BR BR112015022588A patent/BR112015022588A2/pt not_active Application Discontinuation
- 2014-03-10 SG SG10201707545XA patent/SG10201707545XA/en unknown
- 2014-03-10 PE PE2015001907A patent/PE20151593A1/es not_active Application Discontinuation
- 2014-03-10 SG SG11201507255QA patent/SG11201507255QA/en unknown
- 2014-03-10 CA CA2902174A patent/CA2902174A1/fr not_active Abandoned
- 2014-10-03 UA UAA201510014A patent/UA118103C2/uk unknown
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2015
- 2015-08-25 PH PH12015501866A patent/PH12015501866A1/en unknown
- 2015-09-01 IL IL241027A patent/IL241027A0/en unknown
- 2015-09-11 CL CL2015002649A patent/CL2015002649A1/es unknown
- 2015-09-14 CR CR20150485A patent/CR20150485A/es unknown
- 2015-09-14 SA SA515361127A patent/SA515361127B1/ar unknown
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2016
- 2016-08-01 CL CL2016001940A patent/CL2016001940A1/es unknown
- 2016-11-14 JP JP2016221202A patent/JP6352368B2/ja not_active Expired - Fee Related
- 2016-11-17 ZA ZA2016/07948A patent/ZA201607948B/en unknown
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2017
- 2017-02-16 US US15/434,414 patent/US9981973B2/en not_active Expired - Fee Related
- 2017-03-13 AU AU2017201693A patent/AU2017201693A1/en not_active Abandoned
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