SG11201607465UA - Chromene and 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones as gamma-secretase modulators - Google Patents
Chromene and 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones as gamma-secretase modulatorsInfo
- Publication number
- SG11201607465UA SG11201607465UA SG11201607465UA SG11201607465UA SG11201607465UA SG 11201607465U A SG11201607465U A SG 11201607465UA SG 11201607465U A SG11201607465U A SG 11201607465UA SG 11201607465U A SG11201607465U A SG 11201607465UA SG 11201607465U A SG11201607465U A SG 11201607465UA
- Authority
- SG
- Singapore
- Prior art keywords
- chromene
- pyridopyrazinediones
- tetrahydrocyclopropa
- gamma
- secretase modulators
- Prior art date
Links
- VHNYOQKVZQVBLC-RTCGXNAVSA-N (4r,7e,9as)-7-[[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]methylidene]-4-(3,4,5-trifluorophenyl)-1,3,4,8,9,9a-hexahydropyrido[2,1-c][1,4]oxazin-6-one Chemical compound C1([C@@H]2COC[C@@H]3CC\C(C(N32)=O)=C/C=2C=C(C(=CC=2)N2C=C(C)N=C2)OC)=CC(F)=C(F)C(F)=C1 VHNYOQKVZQVBLC-RTCGXNAVSA-N 0.000 title 1
- -1 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones Chemical class 0.000 title 1
- QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical compound C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 title 1
- 229940124648 γ-Secretase Modulator Drugs 0.000 title 1
Classifications
-
- 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
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461973436P | 2014-04-01 | 2014-04-01 | |
| PCT/IB2015/051988 WO2015150957A1 (fr) | 2014-04-01 | 2015-03-18 | Chromène et 1,1a,2,7b-tétrahydrocyclopropa[c]chromène pyridopyrazinediones comme modulateurs de gamma-sécrétase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG11201607465UA true SG11201607465UA (en) | 2016-10-28 |
Family
ID=52815058
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11201607465UA SG11201607465UA (en) | 2014-04-01 | 2015-03-18 | Chromene and 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones as gamma-secretase modulators |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US20150274721A1 (fr) |
| EP (1) | EP3126361B1 (fr) |
| JP (1) | JP6643247B2 (fr) |
| KR (1) | KR101886945B1 (fr) |
| CN (1) | CN106211770B (fr) |
| AP (1) | AP2016009465A0 (fr) |
| AR (1) | AR099874A1 (fr) |
| AU (1) | AU2015242330B2 (fr) |
| BR (1) | BR112016022519A8 (fr) |
| CA (1) | CA2944308A1 (fr) |
| CL (1) | CL2016002422A1 (fr) |
| CR (1) | CR20160454A (fr) |
| CU (1) | CU20160140A7 (fr) |
| DK (1) | DK3126361T3 (fr) |
| DO (1) | DOP2016000266A (fr) |
| EA (1) | EA031419B1 (fr) |
| EC (1) | ECSP16078289A (fr) |
| ES (1) | ES2759277T3 (fr) |
| IL (1) | IL248154B (fr) |
| MD (1) | MD20160102A2 (fr) |
| MX (1) | MX369074B (fr) |
| NI (1) | NI201600149A (fr) |
| PE (1) | PE20161364A1 (fr) |
| PH (1) | PH12016501864A1 (fr) |
| SG (1) | SG11201607465UA (fr) |
| TW (1) | TWI568733B (fr) |
| UY (1) | UY36054A (fr) |
| WO (1) | WO2015150957A1 (fr) |
| ZA (1) | ZA201606252B (fr) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
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| UA110688C2 (uk) | 2012-09-21 | 2016-01-25 | Пфайзер Інк. | Біциклічні піридинони |
| EP3253755B1 (fr) * | 2015-02-03 | 2020-08-26 | Pfizer Inc | Nouveaux pyridopyrazinediones cyclopropabenzofuranyl |
| CN106580997B (zh) * | 2016-12-09 | 2018-01-19 | 张田 | 一种治疗先兆流产的药物组合物 |
| CA3047096A1 (fr) | 2016-12-16 | 2018-06-21 | Pipeline Therapeutics, Inc. | Methodes de traitement de la synaptopathie cochleaire |
| WO2020053654A1 (fr) * | 2018-09-12 | 2020-03-19 | Novartis Ag | Composés antiviraux de pyridopyrazinedione |
| CN110907542A (zh) * | 2018-09-17 | 2020-03-24 | 复旦大学 | 一种液质联用检测唾液中司来吉兰及其代谢物的方法 |
| WO2020087031A1 (fr) | 2018-10-26 | 2020-04-30 | The Research Foundation For The State University Of New York | Combinaison d'un inhibiteur de réabsorption spécifique de la sérotonine et d'un agoniste partiel du récepteur de la sérotonine 1a pour réduire la dyskinésie induite par l-dopa |
| CN113543852A (zh) | 2019-03-06 | 2021-10-22 | 第一三共株式会社 | 吡咯并吡唑衍生物 |
| CA3155287A1 (fr) | 2019-09-26 | 2021-04-01 | Novartis Ag | Composes antiviraux de pyrazolopyridinone |
| IL319392A (en) | 2022-10-18 | 2025-05-01 | Pfizer | Pectin-like phospholipase domain-containing protein 3 (PNPLA3) modification preparations |
| EP4604955A1 (fr) | 2022-10-18 | 2025-08-27 | Pfizer Inc. | Utilisation de composés de protéine 3 contenant un domaine phospholipase de type patatine |
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| ATE239797T1 (de) | 1993-01-25 | 2003-05-15 | Takeda Chemical Industries Ltd | Antikörper gegen beta-amyloid oder derivative davon und seine verwendung |
| DE19709877A1 (de) | 1997-03-11 | 1998-09-17 | Bayer Ag | 1,5-Dihydro-pyrazolo[3,4-d]-pyrimidinon-derivate |
| US8173127B2 (en) | 1997-04-09 | 2012-05-08 | Intellect Neurosciences, Inc. | Specific antibodies to amyloid beta peptide, pharmaceutical compositions and methods of use thereof |
| WO1998044955A1 (fr) | 1997-04-09 | 1998-10-15 | Mindset Ltd. | Anticorps recombines specifiques contre les terminaisons beta-amyloide, codage par molecule d'adn, et leurs procedes d'utilisation |
| GB9722520D0 (en) | 1997-10-24 | 1997-12-24 | Pfizer Ltd | Compounds |
| TWI239847B (en) | 1997-12-02 | 2005-09-21 | Elan Pharm Inc | N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease |
| US6743427B1 (en) | 1997-12-02 | 2004-06-01 | Neuralab Limited | Prevention and treatment of amyloidogenic disease |
| WO2001062801A2 (fr) | 2000-02-24 | 2001-08-30 | Washington University | Anticorps humanises sequestrant un peptide a$g(b) |
| DE10045112A1 (de) | 2000-09-11 | 2002-03-21 | Merck Patent Gmbh | Verwendung von Indolderivaten zur Behandlung von Erkrankungen des zentralen Nervensystems |
| AU3976402A (en) | 2000-11-03 | 2002-06-03 | Proteotech Inc | Methods of isolating amyloid-inhibiting compounds and use of compounds isolated from uncaria tomentosa and related plants |
| EP1432444A4 (fr) | 2001-08-17 | 2005-11-02 | Lilly Co Eli | Anticorps anti-a beta |
| US20030195205A1 (en) | 2001-11-02 | 2003-10-16 | Pfizer Inc. | PDE9 inhibitors for treating cardiovascular disorders |
| DK1480983T3 (da) * | 2002-02-28 | 2006-03-27 | Sanofi Aventis | Heteroarylsubstituerede 2-pyridinyl- og 2-pyrimidinyl- 6,7,8,9-tetrahydropyrimido[1,2a]pyrimidin-4-onderivater |
| DE10238723A1 (de) | 2002-08-23 | 2004-03-11 | Bayer Ag | Phenyl-substituierte Pyrazolyprimidine |
| DE10238724A1 (de) | 2002-08-23 | 2004-03-04 | Bayer Ag | Alkyl-substituierte Pyrazolpyrimidine |
| CA2501945A1 (fr) | 2002-10-09 | 2004-04-22 | Rinat Neuroscience Corp. | Methodes de traitement de la maladie d'alzheimer au moyen d'anticorps diriges contre le peptide beta-amyloide et compositions les comprenant |
| US20040220186A1 (en) | 2003-04-30 | 2004-11-04 | Pfizer Inc. | PDE9 inhibitors for treating type 2 diabetes,metabolic syndrome, and cardiovascular disease |
| WO2004110996A1 (fr) | 2003-06-19 | 2004-12-23 | Pfizer Products Inc. | Antagoniste de nk1 |
| WO2005025616A1 (fr) | 2003-09-09 | 2005-03-24 | Takeda Pharmaceutical Company Limited | Utilisation d'un anticorps |
| GB0327319D0 (en) | 2003-11-24 | 2003-12-24 | Pfizer Ltd | Novel pharmaceuticals |
| EP1720847A1 (fr) | 2004-02-02 | 2006-11-15 | Pfizer Products Incorporated | Modulateurs du recepteur de l'histamine-3 |
| US7456164B2 (en) | 2004-05-07 | 2008-11-25 | Pfizer, Inc | 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands |
| EP1595881A1 (fr) | 2004-05-12 | 2005-11-16 | Pfizer Limited | Dérivés de tetrahydronaphthyridine en tant que ligands de récepteur H3 d'histamine |
| CA2575663C (fr) | 2004-07-30 | 2013-04-23 | Rinat Neuroscience Corp. | Anticorps anti peptide amyloide beta, et leurs procedes d'utilisation |
| GB0423356D0 (en) | 2004-10-21 | 2004-11-24 | Merck Sharp & Dohme | Therapeutic agents |
| WO2006069081A2 (fr) | 2004-12-22 | 2006-06-29 | Washington University In St. Louis | Utilisation d'anticorps anti-a$g(b) pour le traitement d'un traumatisme cerebral |
| UY29504A1 (es) | 2005-04-29 | 2006-10-31 | Rinat Neuroscience Corp | Anticuerpos dirigidos contra el péptido amiloide beta y métodos que utilizan los mismos. |
| NZ564187A (en) | 2005-05-12 | 2010-03-26 | Pfizer | Anhydrous crystalline forms of N-[1-(2-ethoxyethyl)-5-(N-ethyl-N-methylamino)-7-(4-methylpyridin-2-yl-amino)-1H-pyrazolo[4,3-d]pyrimidine-3-carbonyl]methanesulfonamide |
| CA2603830A1 (fr) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Co Llc | Pyridine [2,3-b] pyrazinones |
| WO2006126083A1 (fr) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Company Llc | Composes de pyridine [3 , 4-b] pyrazinones utilises comme inhibiteurs de pde-5 |
| WO2006126082A2 (fr) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Company Llc | Pyridine [3,4-b] pyrazinones |
| EP1899296B1 (fr) | 2005-06-22 | 2010-11-17 | Pfizer Products Inc. | Antagonistes du recepteur 3 de l'histamine |
| US8158673B2 (en) | 2005-10-27 | 2012-04-17 | Pfizer Inc. | Histamine-3 receptor antagonists |
| JP2009514846A (ja) | 2005-11-04 | 2009-04-09 | ファイザー・リミテッド | テトラヒドロナフチリジン誘導体 |
| WO2007063385A2 (fr) | 2005-12-01 | 2007-06-07 | Pfizer Products Inc. | Antagonistes des recepteurs de l'histamine 3 pour des amines spirocycliques |
| WO2007069053A1 (fr) | 2005-12-14 | 2007-06-21 | Pfizer Products Inc. | Antagonistes benzimidazoliques du récepteur h-3 |
| WO2007088450A2 (fr) | 2006-02-01 | 2007-08-09 | Pfizer Products Inc. | Chromane antagoniste du récepteur h-3 |
| WO2007088462A1 (fr) | 2006-02-01 | 2007-08-09 | Pfizer Products Inc. | Antagonistes du récepteur du h-3 à base de spirochromane |
| WO2007099423A1 (fr) | 2006-03-02 | 2007-09-07 | Pfizer Products Inc. | Dérivés de 1-pyrrolidine indane en tant qu'antagonistes du récepteur d'histamine 3 |
| JP2009539762A (ja) | 2006-03-13 | 2009-11-19 | ファイザー・プロダクツ・インク | H3受容体のテトラリン拮抗薬 |
| HRP20110539T1 (hr) | 2006-04-21 | 2011-08-31 | Pfizer Products Inc. | PIRIDINO[3,4-b]PIRAZINONI |
| WO2007138431A2 (fr) | 2006-05-30 | 2007-12-06 | Pfizer Products Inc. | Antagonistes de l'éther histamine-3 azabicyclique |
| BRPI0806473A2 (pt) | 2007-01-22 | 2011-09-27 | Pfizer Prod Inc | sal de tosilato de um composto terapêutico e composições farmacêuticas do mesmo |
| AU2009307892A1 (en) * | 2008-10-23 | 2010-04-29 | Merck Sharp & Dohme Corp. | Fused heterocyclic M1 receptor positive allosteric modulators |
| WO2012131539A1 (fr) | 2011-03-31 | 2012-10-04 | Pfizer Inc. | Nouvelles pyridones bicycliques |
| SG11201407051XA (en) * | 2012-05-16 | 2014-11-27 | Janssen Pharmaceuticals Inc | Substituted 3, 4 - dihydro - 2h - pyrido [1, 2 -a] pyrazine - 1, 6 - dione derivatives useful for the treatment of (inter alia) alzheimer's disease |
| UA110688C2 (uk) * | 2012-09-21 | 2016-01-25 | Пфайзер Інк. | Біциклічні піридинони |
| EP2945944B1 (fr) * | 2013-01-17 | 2016-11-09 | Janssen Pharmaceutica, N.V. | Nouveaux dérivés de pyrido-pipérazinone substitués en tant que modulateurs de la gamma sécrétase |
| WO2015049616A1 (fr) * | 2013-10-04 | 2015-04-09 | Pfizer Inc. | Nouvelles pyridinones bicycliques utilisées comme modulateurs de gamma-sécrétase |
-
2015
- 2015-03-18 AP AP2016009465A patent/AP2016009465A0/en unknown
- 2015-03-18 CN CN201580018466.7A patent/CN106211770B/zh not_active Expired - Fee Related
- 2015-03-18 SG SG11201607465UA patent/SG11201607465UA/en unknown
- 2015-03-18 JP JP2016559879A patent/JP6643247B2/ja not_active Expired - Fee Related
- 2015-03-18 MX MX2016012904A patent/MX369074B/es active IP Right Grant
- 2015-03-18 EA EA201600619A patent/EA031419B1/ru not_active IP Right Cessation
- 2015-03-18 AU AU2015242330A patent/AU2015242330B2/en not_active Ceased
- 2015-03-18 WO PCT/IB2015/051988 patent/WO2015150957A1/fr not_active Ceased
- 2015-03-18 ES ES15714951T patent/ES2759277T3/es active Active
- 2015-03-18 CR CR20160454A patent/CR20160454A/es unknown
- 2015-03-18 DK DK15714951.9T patent/DK3126361T3/da active
- 2015-03-18 EP EP15714951.9A patent/EP3126361B1/fr active Active
- 2015-03-18 KR KR1020167030135A patent/KR101886945B1/ko not_active Expired - Fee Related
- 2015-03-18 MD MDA20160102A patent/MD20160102A2/ro not_active Application Discontinuation
- 2015-03-18 BR BR112016022519A patent/BR112016022519A8/pt not_active IP Right Cessation
- 2015-03-18 CA CA2944308A patent/CA2944308A1/fr not_active Withdrawn
- 2015-03-18 PE PE2016001895A patent/PE20161364A1/es not_active Application Discontinuation
- 2015-03-27 UY UY0001036054A patent/UY36054A/es not_active Application Discontinuation
- 2015-03-27 AR ARP150100922A patent/AR099874A1/es unknown
- 2015-03-27 US US14/670,746 patent/US20150274721A1/en not_active Abandoned
- 2015-03-31 TW TW104110551A patent/TWI568733B/zh not_active IP Right Cessation
-
2016
- 2016-09-09 ZA ZA2016/06252A patent/ZA201606252B/en unknown
- 2016-09-22 PH PH12016501864A patent/PH12016501864A1/en unknown
- 2016-09-22 CU CUP2016000140A patent/CU20160140A7/es unknown
- 2016-09-27 CL CL2016002422A patent/CL2016002422A1/es unknown
- 2016-09-29 NI NI201600149A patent/NI201600149A/es unknown
- 2016-09-29 DO DO2016000266A patent/DOP2016000266A/es unknown
- 2016-09-29 IL IL248154A patent/IL248154B/en active IP Right Grant
- 2016-09-30 EC ECIEPI201678289A patent/ECSP16078289A/es unknown
-
2017
- 2017-02-24 US US15/441,882 patent/US20170166566A1/en not_active Abandoned
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