MA35601B1 - Pyrrolotriazines substituées par hydroxyméthylaryle utilisées comme inhibiteurs d'alk1 - Google Patents
Pyrrolotriazines substituées par hydroxyméthylaryle utilisées comme inhibiteurs d'alk1Info
- Publication number
- MA35601B1 MA35601B1 MA36620A MA36620A MA35601B1 MA 35601 B1 MA35601 B1 MA 35601B1 MA 36620 A MA36620 A MA 36620A MA 36620 A MA36620 A MA 36620A MA 35601 B1 MA35601 B1 MA 35601B1
- Authority
- MA
- Morocco
- Prior art keywords
- hydroxymethyl substituted
- compounds
- pyrrolotriazines
- alk1 inhibitors
- alk1
- Prior art date
Links
- 101100490437 Mus musculus Acvrl1 gene Proteins 0.000 title 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000003921 pyrrolotriazines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 230000033115 angiogenesis Effects 0.000 abstract 2
- -1 aryl pyrrolo [2,1-f] [1,2,4] triazin-4-amines Chemical class 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000030533 eye disease Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Cette invention porte sur de nouvelles pyrrolo[2,1-f][1,2,4]triazin-4-amines 5-substituées par (hydroxyméthyl)aryle représentées par la formule (i), sur des procédés pour la préparation de tels composés, sur des compositions pharmaceutiques contenant de tels composés et sur l'utilisation de tels composés ou de telles compositions pour le traitement de troubles liés à l'angiogenèse, en particulier de troubles oculaires liés à l'angiogenèse.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12161547 | 2012-03-27 | ||
| PCT/EP2012/062366 WO2013004551A1 (fr) | 2011-07-01 | 2012-06-26 | Pyrrolotriazines substituées par hydroxyméthylaryle utilisées comme inhibiteurs d'alk1 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA35601B1 true MA35601B1 (fr) | 2014-11-01 |
Family
ID=47436537
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA36620A MA35601B1 (fr) | 2012-03-27 | 2013-12-27 | Pyrrolotriazines substituées par hydroxyméthylaryle utilisées comme inhibiteurs d'alk1 |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US9040691B2 (fr) |
| EP (1) | EP2726482B1 (fr) |
| JP (1) | JP5955953B2 (fr) |
| KR (1) | KR20140036269A (fr) |
| CN (1) | CN103764657B (fr) |
| AP (1) | AP3529A (fr) |
| AR (1) | AR087017A1 (fr) |
| AU (1) | AU2012280508A1 (fr) |
| BR (1) | BR112014000049A2 (fr) |
| CA (1) | CA2840518A1 (fr) |
| CO (1) | CO6870031A2 (fr) |
| CU (1) | CU20130170A7 (fr) |
| DO (1) | DOP2013000300A (fr) |
| EA (1) | EA023775B1 (fr) |
| EC (1) | ECSP13013120A (fr) |
| ES (1) | ES2598027T3 (fr) |
| GT (1) | GT201300313A (fr) |
| IL (1) | IL229533A0 (fr) |
| MA (1) | MA35601B1 (fr) |
| MX (1) | MX2013014315A (fr) |
| PE (1) | PE20140570A1 (fr) |
| PH (1) | PH12013502695A1 (fr) |
| SG (1) | SG195100A1 (fr) |
| UY (1) | UY34167A (fr) |
| WO (1) | WO2013004551A1 (fr) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2834164A1 (fr) | 2011-05-10 | 2012-11-15 | Gilead Sciences, Inc. | Benzoxazinones fusionnees comme modulateurs de canal ionique |
| NO3175985T3 (fr) | 2011-07-01 | 2018-04-28 | ||
| TW201837023A (zh) | 2011-07-01 | 2018-10-16 | 美商基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
| AU2012294342B2 (en) | 2011-08-10 | 2017-07-27 | Lankenau Institute For Medical Research | Methods and compositions for the treatment of autoimmune and inflammatory diseases |
| JP5985658B2 (ja) * | 2012-01-31 | 2016-09-06 | ナンジン アルゲン ファルマ カンパニー リミテッドNanjing Allgen Pharma Co. Ltd. | ブルトンチロシンキナーゼ阻害薬としての環状分子 |
| WO2015157644A1 (fr) | 2014-04-10 | 2015-10-15 | Lankenau Institute For Medical Research | Méthodes et compositions pour le traitement de maladies et de troubles oculaires |
| WO2015181097A1 (fr) | 2014-05-28 | 2015-12-03 | Bayer Cropscience Ag | Procédé de préparation de dérivés de thiazole |
| US10214537B2 (en) | 2014-10-22 | 2019-02-26 | Bristol-Myers Squibb Company | Bicyclic heteroaryl amine compounds |
| US10023576B2 (en) | 2014-10-22 | 2018-07-17 | Bristol-Myers Squibb Company | Heteroaryl substituted pyrrolotriazine amine compounds as PI3K inhibitors |
| JP2017535573A (ja) | 2014-11-25 | 2017-11-30 | バイエル ファーマ アクチエンゲゼルシャフト | 置換されたピリドベンゾジアゼピノン誘導体およびそれの使用 |
| CN107531697A (zh) | 2015-04-16 | 2018-01-02 | 默克专利股份公司 | 3‑(1h‑苯并咪唑‑2‑基)‑1h‑吡啶‑2‑酮衍生物 |
| US10053465B2 (en) | 2015-08-26 | 2018-08-21 | Incyte Corporation | Pyrrolopyrimidine derivatives as TAM inhibitors |
| MD3436461T2 (ro) | 2016-03-28 | 2024-05-31 | Incyte Corp | Compuși pirolotriazină ca inhibitori TAM |
| CN109111447A (zh) | 2017-06-23 | 2019-01-01 | 中国科学院上海药物研究所 | 7-位取代吡咯并三嗪类化合物或其药学上可用的盐,及其制备方法和用途 |
| SI3687996T1 (sl) | 2017-09-27 | 2022-04-29 | Incyte Corporation | Soli pirolotriazinskih derivatov, ki so uporabne kot zaviralci TAM |
| MD3813800T2 (ro) | 2018-06-29 | 2025-10-31 | Incyte Corp | Formulări de inhibitor al AXL/MER |
| US10829493B2 (en) | 2019-04-12 | 2020-11-10 | Blueprint Medicines Corporation | Compositions and methods for treating KIT- and PDGFRA-mediated diseases |
| EP4114401A1 (fr) | 2020-03-06 | 2023-01-11 | Incyte Corporation | Polythérapie comprenant des inhibiteurs d'axl/mer et de pd-1/pd-l1 |
| CN120530116A (zh) | 2022-11-04 | 2025-08-22 | 百时美施贵宝公司 | Ret-ldd蛋白抑制剂 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60026297T2 (de) * | 1999-05-21 | 2006-11-02 | Bristol-Myers Squibb Co. | Pyrrolotriazin kinasehemmer |
| PL213095B1 (pl) | 2002-08-08 | 2013-01-31 | Kissei Pharmaceutical | Pochodna pirazolu, kompozycja farmaceutyczna, srodek do leczenia lub hamowania choroby i zastosowanie pochodnej pirazolu |
| US7148226B2 (en) | 2003-02-21 | 2006-12-12 | Agouron Pharmaceuticals, Inc. | Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same |
| UY28931A1 (es) | 2004-06-03 | 2005-12-30 | Bayer Pharmaceuticals Corp | Derivados de pirrolotriazina utiles para tratar trastornos hiper-proliferativos y enfermedades asociadas con angiogenesis |
| DE102005042742A1 (de) * | 2005-09-02 | 2007-03-08 | Schering Ag | Substituierte Imidazo[1,2b]pyridazine als Kinase-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
| CA2627839C (fr) | 2005-11-02 | 2014-08-19 | Bayer Healthcare Ag | Derives pyrrolo-[2,1-f]-[1,2,4]-triazin-4-ylamines inhibiteurs de la igf-1r kinase pour le traitement des cancers et autres maladies hyperproliferatives |
| US7514435B2 (en) * | 2005-11-18 | 2009-04-07 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
| PE20070855A1 (es) | 2005-12-02 | 2007-10-14 | Bayer Pharmaceuticals Corp | Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas |
| KR101461680B1 (ko) | 2005-12-02 | 2014-11-19 | 바이엘 헬스케어 엘엘씨 | 과다-증식성 장애 및 맥관형성과 관련된 질환의 치료에유용한 치환된 4-아미노-피롤로트리아진 유도체 |
| TW200801008A (en) | 2005-12-29 | 2008-01-01 | Abbott Lab | Protein kinase inhibitors |
| EP1873157A1 (fr) * | 2006-06-21 | 2008-01-02 | Bayer Schering Pharma Aktiengesellschaft | Pyrazolopyrimidines et sels de ceux-ci, compositions pharmaceutiques contenant ces composes, procedes de preparation associes, et leur utilisation |
| CN101522682A (zh) * | 2006-10-30 | 2009-09-02 | 诺瓦提斯公司 | 作为抗炎剂的杂环化合物 |
| SI2114980T1 (sl) | 2007-01-12 | 2012-11-30 | Biocryst Pharm Inc | Protivirusni nukleozidni analogi |
| US8124759B2 (en) | 2007-05-09 | 2012-02-28 | Abbott Laboratories | Inhibitors of protein kinases |
| ES2375425T3 (es) * | 2007-07-26 | 2012-02-29 | Novartis Ag | Compuestos org�?nicos. |
| BRPI0817434A2 (pt) * | 2007-10-17 | 2015-06-16 | Novartis Ag | Composto orgânicos |
| WO2009140128A2 (fr) * | 2008-05-13 | 2009-11-19 | Irm Llc | Composés et compositions servant d'inhibiteurs de kinases |
| EP2424368B1 (fr) | 2009-04-29 | 2014-12-31 | Locus Pharmaceuticals, Inc. | Composés de pyrrolotriazine |
-
2012
- 2012-06-26 PE PE2013002774A patent/PE20140570A1/es not_active Application Discontinuation
- 2012-06-26 KR KR1020137034741A patent/KR20140036269A/ko not_active Withdrawn
- 2012-06-26 AP AP2014007378A patent/AP3529A/xx active
- 2012-06-26 WO PCT/EP2012/062366 patent/WO2013004551A1/fr not_active Ceased
- 2012-06-26 EA EA201490103A patent/EA023775B1/ru not_active IP Right Cessation
- 2012-06-26 SG SG2013086426A patent/SG195100A1/en unknown
- 2012-06-26 EP EP12730515.9A patent/EP2726482B1/fr active Active
- 2012-06-26 AU AU2012280508A patent/AU2012280508A1/en not_active Abandoned
- 2012-06-26 MX MX2013014315A patent/MX2013014315A/es unknown
- 2012-06-26 BR BR112014000049A patent/BR112014000049A2/pt not_active IP Right Cessation
- 2012-06-26 CA CA2840518A patent/CA2840518A1/fr not_active Abandoned
- 2012-06-26 US US14/130,586 patent/US9040691B2/en not_active Expired - Fee Related
- 2012-06-26 ES ES12730515.9T patent/ES2598027T3/es active Active
- 2012-06-26 JP JP2014517662A patent/JP5955953B2/ja not_active Expired - Fee Related
- 2012-06-26 CN CN201280042804.7A patent/CN103764657B/zh not_active Expired - Fee Related
- 2012-06-26 PH PH1/2013/502695A patent/PH12013502695A1/en unknown
- 2012-06-27 UY UY0001034167A patent/UY34167A/es not_active Application Discontinuation
- 2012-06-29 AR ARP120102378A patent/AR087017A1/es unknown
-
2013
- 2013-11-21 IL IL229533A patent/IL229533A0/en unknown
- 2013-12-05 CO CO13285797A patent/CO6870031A2/es active IP Right Grant
- 2013-12-11 DO DO2013000300A patent/DOP2013000300A/es unknown
- 2013-12-19 GT GT201300313A patent/GT201300313A/es unknown
- 2013-12-27 EC ECSP13013120 patent/ECSP13013120A/es unknown
- 2013-12-27 MA MA36620A patent/MA35601B1/fr unknown
- 2013-12-30 CU CUP2013000170A patent/CU20130170A7/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| AP2014007378A0 (en) | 2014-01-31 |
| PH12013502695A1 (en) | 2019-06-14 |
| US20140256718A1 (en) | 2014-09-11 |
| AP3529A (en) | 2016-01-11 |
| EP2726482B1 (fr) | 2016-07-20 |
| NZ619453A (en) | 2016-01-29 |
| DOP2013000300A (es) | 2014-02-28 |
| KR20140036269A (ko) | 2014-03-25 |
| PE20140570A1 (es) | 2014-04-28 |
| IL229533A0 (en) | 2014-01-30 |
| MX2013014315A (es) | 2014-01-31 |
| EA201490103A1 (ru) | 2014-06-30 |
| ECSP13013120A (es) | 2014-02-28 |
| ES2598027T3 (es) | 2017-01-24 |
| CU20130170A7 (es) | 2014-04-24 |
| CA2840518A1 (fr) | 2013-01-10 |
| AR087017A1 (es) | 2014-02-05 |
| US9040691B2 (en) | 2015-05-26 |
| SG195100A1 (en) | 2013-12-30 |
| EP2726482A1 (fr) | 2014-05-07 |
| UY34167A (es) | 2013-01-31 |
| BR112014000049A2 (pt) | 2017-02-07 |
| CN103764657B (zh) | 2016-05-25 |
| WO2013004551A1 (fr) | 2013-01-10 |
| JP2014525902A (ja) | 2014-10-02 |
| AU2012280508A1 (en) | 2013-12-12 |
| JP5955953B2 (ja) | 2016-07-20 |
| EA023775B1 (ru) | 2016-07-29 |
| CN103764657A (zh) | 2014-04-30 |
| CU24146B1 (fr) | 2016-02-29 |
| CO6870031A2 (es) | 2014-02-20 |
| GT201300313A (es) | 2014-11-13 |
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| MA41185B1 (fr) | Composés d'acide isoxazole hydroxamique comme inhibiteurs de lpxc | |
| MA34308B1 (fr) | Triazolopyridines substituées | |
| CA2878796C (fr) | Derives de pyridinone comme inhibiteurs de la transglutaminase tissulaire | |
| MA46229B1 (fr) | Composés d'hétéroaryle carboxamide en tant qu'inhibiteurs de ripk2 | |
| MA49127B1 (fr) | Dérivés d'indole n-substitués | |
| MA31863B1 (fr) | Dérivés de pyrazole comme inhibiteurs de 5-lo | |
| MA43913B1 (fr) | Modulateurs allostériques positifs du récepteur m1 muscarinique | |
| MA39229A1 (fr) | Pyrrolidines, térahydrofuranes et cyclopentanes substitués utiles en tant qu'antagonistes des récepteurs des orexines | |
| MA52375A1 (fr) | Inhibiteurs de cdk8/19 |