AR087328A1 - Derivados de imidazo[1,2-b]piridazina e imidazo[4,5-b]piridina como inhibidores de jak - Google Patents
Derivados de imidazo[1,2-b]piridazina e imidazo[4,5-b]piridina como inhibidores de jakInfo
- Publication number
- AR087328A1 AR087328A1 ARP110104376A AR087328A1 AR 087328 A1 AR087328 A1 AR 087328A1 AR P110104376 A ARP110104376 A AR P110104376A AR 087328 A1 AR087328 A1 AR 087328A1
- Authority
- AR
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- Prior art keywords
- group
- hydroxyalkyl
- haloalkyl
- cycloalkyl
- linear
- Prior art date
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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
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- 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
- A61K31/437—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 five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
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- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
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- 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
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- 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
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- 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
- A61P11/02—Nasal agents, e.g. decongestants
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- 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
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- 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
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- 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
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- 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
- A61P17/06—Antipsoriatics
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- 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
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- 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
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- 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
- A61P27/04—Artificial tears; Irrigation solutions
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- 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
- A61P27/14—Decongestants or antiallergics
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- 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]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- 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
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- 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
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- 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
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- 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
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- 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
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- 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
Abstract
Los compuestos son útiles para terapia de enfermedades de tipo inmune e inflamatoria.Reivindicación 1: Un compuesto de fórmula (1), o una sal farmacéuticamente aceptable, o solvato, o N-óxido, o estereoisómero o derivado deuterado o tautómero del mismo, donde, m es 0 o un número entero de 1 a 3; cada uno de X e Y independientemente representa un átomo de nitrógeno o un grupo -CR7, en donde al menos uno de X e Y representa un grupo -CR7; uno de G1 y G2 representa un átomo de nitrógeno y el otro representa un átomo de carbono; cada uno de R1 y R2 independientemente representa un átomo de hidrógeno, un átomo de halógeno, un grupo hidroxi, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-10, un grupo cicloalquenilo C3-10, un grupo arilo monocíclico o policíclico C5-14, un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, un grupo heterocíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos alquilo, haloalquilo, hidroxialquilo, cicloalquilo, cicloalquenilo, arilo, heteroarilo, y heterocíclico están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo alquilsulfonilo C1-4, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; o cada uno de R1 y R2 independientemente representa un grupo -(CH2)0-2OR9, un grupo -O-(CH2)1-2OR9, o un grupo -NR8R9; R3 representa un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-10, un grupo cicloalquenilo C3-10, un grupo arilo monocíclico o policíclico C5-14, un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, un grupo heterocíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos alquilo, haloalquilo, hidroxialquilo, cicloalquilo, cicloalquenilo, arilo, heteroarilo, y heterocíclico están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo, un grupo piperidilo, un grupo -(CH2)nOR9, un grupo -NR8R9, un grupo -C(O)-(CH2)n-R8, un grupo -C(O)-(CH2)n-NR8R9, un grupo -S(O)2(CH2)nR9 o un grupo -S(O)2(CH2)nNR8R9; en donde cada n es 0, 1 ó 2; R4 representa un átomo de hidrógeno, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo C1-6 lineal o ramificado, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; cada uno de R5 y R6 independientemente representa un átomo de hidrógeno, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo lineal o ramificado C1-6, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; R7 representa un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un grupo cicloalquilo C3-10, un grupo cicloalquenilo C3-10, un grupo arilo monocíclico o policíclico C5-14, un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, un grupo heterocíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos alquilo, haloalquilo, hidroxialquilo, cicloalquilo, cicloalquenilo, arilo, heteroarilo, y heterocíclico están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo ciano, un grupo alquilo lineal o ramificado C1-6, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4, un cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; R8 representa un átomo de hidrógeno, un grupo ciano, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo lineal o ramificado C1-6, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo; R9 representa un átomo de hidrógeno, un grupo haloalquilo C1-4, un grupo hidroxialquilo C1-4 o un grupo alquilo lineal o ramificado C1-6, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo ciano, un grupo cicloalquilo C3-7, un grupo fenilo, un grupo piridilo, un grupo pirimidinilo o un grupo piperidilo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP20100382318 EP2463289A1 (en) | 2010-11-26 | 2010-11-26 | Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors |
Publications (1)
Publication Number | Publication Date |
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AR087328A1 true AR087328A1 (es) | 2014-03-19 |
Family
ID=43585650
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP110104376 AR087328A1 (es) | 2010-11-26 | 2011-11-24 | Derivados de imidazo[1,2-b]piridazina e imidazo[4,5-b]piridina como inhibidores de jak |
Country Status (22)
Country | Link |
---|---|
US (1) | US9133200B2 (es) |
EP (2) | EP2463289A1 (es) |
JP (1) | JP5809704B2 (es) |
KR (1) | KR20140004637A (es) |
CN (1) | CN103228654A (es) |
AR (1) | AR087328A1 (es) |
AU (1) | AU2011334146A1 (es) |
BR (1) | BR112013012965A2 (es) |
CA (1) | CA2815029A1 (es) |
CL (1) | CL2013001464A1 (es) |
CO (1) | CO6781467A2 (es) |
CR (1) | CR20130210A (es) |
EA (1) | EA201300620A1 (es) |
GT (1) | GT201300137A (es) |
IL (1) | IL225232A0 (es) |
MX (1) | MX2013005257A (es) |
NZ (1) | NZ608718A (es) |
PE (1) | PE20140390A1 (es) |
SG (1) | SG190042A1 (es) |
TW (1) | TW201236683A (es) |
UY (1) | UY33752A (es) |
WO (1) | WO2012069202A1 (es) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20140070676A (ko) | 2002-09-06 | 2014-06-10 | 인설트 테라페틱스, 인코퍼레이티드 | 공유결합된 치료제 전달을 위한 사이클로덱스트린-기초 중합체 |
US20080176958A1 (en) | 2007-01-24 | 2008-07-24 | Insert Therapeutics, Inc. | Cyclodextrin-based polymers for therapeutics delivery |
UY33213A (es) | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
EP2463289A1 (en) | 2010-11-26 | 2012-06-13 | Almirall, S.A. | Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors |
EP2554544A1 (en) * | 2011-08-01 | 2013-02-06 | Almirall, S.A. | Pyridin-2(1h)-one derivatives as jak inhibitors |
WO2014055493A1 (en) | 2012-10-02 | 2014-04-10 | Cerulean Pharma Inc. | Methods and systems for polymer precipitation and generation of particles |
EP2916915A4 (en) * | 2012-11-07 | 2016-06-22 | Teva Pharma | LAQUINIMOD AMINE SALTS |
CN103845726A (zh) * | 2012-12-07 | 2014-06-11 | 天津市汉康医药生物技术有限公司 | 克拉屈滨和乙酸格拉默的组合用于治疗多发性硬化的用途 |
EP2964230A4 (en) | 2013-03-07 | 2016-10-26 | Califia Bio Inc | KINASEHEMMER WITH MIXED ABSTRACT AND TREATMENT PROCESS THEREWITH |
TW201519892A (zh) | 2013-03-14 | 2015-06-01 | Teva Pharma | 拉喹莫德鈉之結晶及其製造之改良方法 |
AU2014273983A1 (en) * | 2013-05-31 | 2015-12-17 | Cerulean Pharma Inc. | Cyclodextrin-based polymers for the therapeutic delivery |
GB201321734D0 (en) * | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic Agents |
WO2017013270A1 (en) | 2015-07-23 | 2017-01-26 | Universite De Strasbourg | Use of leptin signaling inhibitor for protecting kidneys from patients having ciliopathy |
WO2017096262A1 (en) | 2015-12-04 | 2017-06-08 | Jomoco, Corp. | Compositions and methods to mitigate or prevent an immune response to an immunogenic therapeutic molecule in non-human primates |
US11629124B2 (en) * | 2017-03-09 | 2023-04-18 | Novartis Ag | Solid forms comprising an oxime ether compound, compositions and methods of use thereof |
JP2021008407A (ja) * | 2017-10-02 | 2021-01-28 | 武田薬品工業株式会社 | 複素環化合物 |
WO2020092015A1 (en) | 2018-11-02 | 2020-05-07 | University Of Rochester | Therapeutic mitigation of epithelial infection |
CA3157394A1 (en) | 2019-12-19 | 2021-06-24 | Helena ERIKSSON | Compounds for treatment of eye diseases associated with excessive vascularisation |
CA3184811A1 (en) | 2020-06-12 | 2021-12-16 | Incyte Corporation | Imidazopyridazine compounds with activity as alk2 inhibitors |
WO2022194779A1 (en) * | 2021-03-15 | 2022-09-22 | Chiesi Farmaceutici S.P.A. | Heterocyclic derivatives as janus kinase inhibitors |
CA3211584A1 (en) * | 2021-03-15 | 2022-09-22 | Chiesi Farmaceutici S.P.A. | Heterocyclic derivatives as janus kinase inhibitors |
CN117157294A (zh) * | 2021-03-16 | 2023-12-01 | 怡诺安有限公司 | 作为蛋白激酶抑制剂的杂环化合物的结晶形式 |
BR112023018672A2 (pt) * | 2021-03-16 | 2023-10-03 | Hk Inno N Corp | Sal de ácido orgânico, composição e uso |
WO2023133201A1 (en) * | 2022-01-05 | 2023-07-13 | K36 Therapeutics, Inc. | Deuterium-enriched piperidinyl-methyl-purine amines and related compounds and their use in treating diseases and conditions |
WO2024052513A1 (en) * | 2022-09-09 | 2024-03-14 | Chiesi Farmaceutici S.P.A. | Heterocyclic derivatives as janus kinase inhibitors |
WO2024052512A1 (en) * | 2022-09-09 | 2024-03-14 | Chiesi Farmaceutici S.P.A. | Heterocyclic derivatives as janus kinase inhibitors |
Family Cites Families (80)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54128591A (en) | 1978-03-25 | 1979-10-05 | Kyowa Hakko Kogyo Co Ltd | Cephalosporin analog |
IT7920688V0 (it) | 1979-02-05 | 1979-02-05 | Chiesi Paolo Parma | Inalatore per sostanze medicamentose pulverulente, con combinata funzione di dosatore. |
ATE23272T1 (de) | 1981-07-08 | 1986-11-15 | Draco Ab | Pulverinhalator. |
US4570630A (en) | 1983-08-03 | 1986-02-18 | Miles Laboratories, Inc. | Medicament inhalation device |
FI69963C (fi) | 1984-10-04 | 1986-09-12 | Orion Yhtymae Oy | Doseringsanordning |
DE3927170A1 (de) | 1989-08-17 | 1991-02-21 | Boehringer Ingelheim Kg | Inhalator |
IT1237118B (it) | 1989-10-27 | 1993-05-18 | Miat Spa | Inalatore multidose per farmaci in polvere. |
US5201308A (en) | 1990-02-14 | 1993-04-13 | Newhouse Michael T | Powder inhaler |
GB9004781D0 (en) | 1990-03-02 | 1990-04-25 | Glaxo Group Ltd | Device |
SG45171A1 (en) | 1990-03-21 | 1998-01-16 | Boehringer Ingelheim Int | Atomising devices and methods |
GB9015522D0 (en) | 1990-07-13 | 1990-08-29 | Braithwaite Philip W | Inhaler |
WO1992003175A1 (en) | 1990-08-11 | 1992-03-05 | Fisons Plc | Inhalation device |
DE4027391A1 (de) | 1990-08-30 | 1992-03-12 | Boehringer Ingelheim Kg | Treibgasfreies inhalationsgeraet |
DK0503031T3 (da) | 1990-09-26 | 1999-01-04 | Pharmachemie Bv | Inhalator med et reservoir til flere doser af et materiale, der skal inhaleres |
GB9026025D0 (en) | 1990-11-29 | 1991-01-16 | Boehringer Ingelheim Kg | Inhalation device |
AU650953B2 (en) | 1991-03-21 | 1994-07-07 | Novartis Ag | Inhaler |
DE4239402A1 (de) | 1992-11-24 | 1994-05-26 | Bayer Ag | Pulverinhalator |
CA2152088C (en) | 1992-12-18 | 1999-12-07 | Thomas J. Ambrosio | Inhaler for powdered medications |
ES2206572T3 (es) | 1995-04-14 | 2004-05-16 | Smithkline Beecham Corporation | Inhalador de dosis medida para salmeterol. |
DK0837710T3 (da) | 1995-06-21 | 2002-04-02 | Sofotec Gmbh & Co Kg | Lægemiddelpulverpatron med integreret doseringsindretning og inhalator for lægemidler på pulverform |
GB9518953D0 (en) | 1995-09-15 | 1995-11-15 | Pfizer Ltd | Pharmaceutical formulations |
DE19536902A1 (de) | 1995-10-04 | 1997-04-10 | Boehringer Ingelheim Int | Vorrichtung zur Hochdruckerzeugung in einem Fluid in Miniaturausführung |
WO2000035298A1 (en) | 1996-11-27 | 2000-06-22 | Wm. Wrigley Jr. Company | Chewing gum containing medicament active agents |
GB9919778D0 (en) | 1999-08-21 | 1999-10-27 | Zeneca Ltd | Chemical compounds |
PE20020506A1 (es) | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | Derivados de pirazol fusionados como inhibidores de la proteina cinasa |
ATE402164T1 (de) | 2001-04-26 | 2008-08-15 | Eisai R&D Man Co Ltd | Stickstoffhaltige verbindung mit kondensiertem ring und pyrazolylgruppe als substituent und medizinische zusammensetzung davon |
DE10129703A1 (de) | 2001-06-22 | 2003-01-02 | Sofotec Gmbh & Co Kg | Zerstäubungssystem für eine Pulvermischung und Verfahren für Trockenpulverinhalatoren |
WO2003000682A1 (en) | 2001-06-25 | 2003-01-03 | Merck & Co., Inc. | (pyrimidyl)(phenyl)substituted fused heteroaryl p38 inhibiting and pkg kinase inhibiting compounds |
GB0206723D0 (en) * | 2002-03-21 | 2002-05-01 | Glaxo Group Ltd | Novel compounds |
WO2003092595A2 (en) | 2002-05-02 | 2003-11-13 | Merck & Co., Inc | Tyrosine kinase inhibitors |
ES2195785B1 (es) | 2002-05-16 | 2005-03-16 | Almirall Prodesfarma, S.A. | Nuevos derivados de piridazin-3(2h)-ona. |
ES2211344B1 (es) | 2002-12-26 | 2005-10-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de piridazin-3(2h)-ona. |
ES2232306B1 (es) | 2003-11-10 | 2006-08-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de piridazin-3(2h)-ona. |
AR048454A1 (es) | 2004-03-30 | 2006-04-26 | Vertex Pharma | Azaindoles utiles como inhibidores de las proteinas quinasas jak u otras proteinas quinasas |
EP1598348A1 (en) * | 2004-05-18 | 2005-11-23 | Aventis Pharma Deutschland GmbH | Novel pyridazinone derivatives as inhibitors of CDK2 |
ES2251866B1 (es) | 2004-06-18 | 2007-06-16 | Laboratorios Almirall S.A. | Nuevos derivados de piridazin-3(2h)-ona. |
ES2251867B1 (es) | 2004-06-21 | 2007-06-16 | Laboratorios Almirall S.A. | Nuevos derivados de piridazin-3(2h)-ona. |
DK1616592T3 (da) | 2004-07-16 | 2011-01-10 | Almirall Sa | Inhalator til administration af lægemidler i pulverform og en pulverpatron til anvendelse sammen med denne inhalator |
WO2006038001A1 (en) | 2004-10-06 | 2006-04-13 | Celltech R & D Limited | Aminopyrimidine derivatives as jnk inhibitors |
EP1828185B1 (en) | 2004-12-21 | 2009-05-06 | SmithKline Beecham Corporation | 2-pyrimidinyl pyrazolopyridine erbb kinase inhibitors |
ATE530545T1 (de) | 2005-02-04 | 2011-11-15 | Astrazeneca Ab | Als kinaseinhibitoren geeignete pyrazolylaminopyridinderivate |
ES2265276B1 (es) | 2005-05-20 | 2008-02-01 | Laboratorios Almirall S.A. | Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico. |
WO2007025090A2 (en) * | 2005-08-25 | 2007-03-01 | Kalypsys, Inc. | Heterobicyclic and - tricyclic inhibitors of mapk/erk kinase |
ES2296516B1 (es) | 2006-04-27 | 2009-04-01 | Laboratorios Almirall S.A. | Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico. |
EP2038279A2 (en) | 2006-06-06 | 2009-03-25 | Avigen, Inc. | Substituted pyrazolo [1,5- alpha] pyridine compounds and their methods of use |
EP1900739A1 (en) * | 2006-08-30 | 2008-03-19 | Cellzome Ag | Diazolodiazine derivatives as kinase inhibitors |
US20110021513A1 (en) * | 2006-09-07 | 2011-01-27 | Biogen Idec Ma Inc. | Modulators of interleukin-1 receptor-associated kinase |
US7919490B2 (en) | 2006-10-04 | 2011-04-05 | Wyeth Llc | 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression |
AU2007307031B2 (en) | 2006-10-11 | 2011-11-24 | Amgen Inc. | Imidazo- and triazolo-pyridine compounds and methods of use therof |
ES2302447B1 (es) | 2006-10-20 | 2009-06-12 | Laboratorios Almirall S.A. | Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico. |
BRPI0718266A2 (pt) * | 2006-10-30 | 2014-01-07 | Novartis Ag | Compostos heterocíclicos como agentes anti-inflamatórios. |
ES2319596B1 (es) | 2006-12-22 | 2010-02-08 | Laboratorios Almirall S.A. | Nuevos derivados de los acidos amino-nicotinico y amino-isonicotinico. |
EP2121687B1 (en) | 2006-12-22 | 2015-10-14 | Astex Therapeutics Limited | Tricyclic amine derivatives as protein tyrosine kinase inhibitors |
US7977336B2 (en) | 2006-12-28 | 2011-07-12 | Banyu Pharmaceutical Co. Ltd | Aminopyrimidine derivatives as PLK1 inhibitors |
ES2306595B1 (es) | 2007-02-09 | 2009-09-11 | Laboratorios Almirall S.A. | Sal de napadisilato de 5-(2-((6-(2,2-difluoro-2-feniletoxi)hexil)amino)-1-hidroxietil)-8-hidroxiquinolin-2(1h)-ona como agonista del receptor adrenergico beta2. |
US7834024B2 (en) | 2007-03-26 | 2010-11-16 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the JAK pathway |
UY31272A1 (es) | 2007-08-10 | 2009-01-30 | Almirall Lab | Nuevos derivados de ácido azabifenilaminobenzoico |
CL2008002397A1 (es) | 2007-08-14 | 2009-09-25 | Bayer Schering Pharma Ag | Compuestos derivados de imidazoles biciclicos fusionados; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar neoplasia benigna o maligna. |
AU2008289101A1 (en) | 2007-08-17 | 2009-02-26 | Icagen, Inc. | Heterocycles as potassium channel modulators |
MX2010004244A (es) | 2007-10-17 | 2010-04-30 | Novartis Ag | Derivados de imidazo [i,2-a]-piridina utiles como inhibidores de cinasa tipo activina (alk). |
JP2011500806A (ja) | 2007-10-25 | 2011-01-06 | メルク・シャープ・エンド・ドーム・コーポレイション | 治療用化合物 |
WO2009058298A1 (en) | 2007-10-31 | 2009-05-07 | Merck & Co., Inc. | P2x3, receptor antagonists for treatment of pain |
ES2320961B1 (es) | 2007-11-28 | 2010-03-17 | Laboratorios Almirall, S.A. | Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor adrenergico beta2. |
JP5587206B2 (ja) | 2007-12-19 | 2014-09-10 | 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 | JAK2阻害剤として有用なピラゾロ[1,5−a]ピリミジン |
EP2231660A1 (en) | 2007-12-21 | 2010-09-29 | Wyeth LLC | Imidazo [1,2-a] pyridine compounds |
WO2009093012A1 (en) * | 2008-01-22 | 2009-07-30 | Vernalis (R & D) Ltd | Indolyl- pyridone derivatives having checkpoint kinase 1 inhibitory activity |
WO2009106442A1 (en) | 2008-02-25 | 2009-09-03 | F. Hoffmann-La Roche Ag | Pyrrolopyrazine kinase inhibitors |
KR101324804B1 (ko) * | 2008-05-13 | 2013-11-01 | 아이알엠 엘엘씨 | 키나제 억제제로서의 질소 함유 융합 헤테로사이클 및 그의 조성물 |
ATE542813T1 (de) | 2008-08-06 | 2012-02-15 | Pfizer | 6-substituierte 2- heterocyclylaminopyrazinverbindungen als chk-1- inhibitoren |
EP2196465A1 (en) | 2008-12-15 | 2010-06-16 | Almirall, S.A. | (3-oxo)pyridazin-4-ylurea derivatives as PDE4 inhibitors |
UY32297A (es) | 2008-12-22 | 2010-05-31 | Almirall Sa | Sal mesilato de 5-(2-{[6-(2,2-difluoro-2-fenilitoxi) hexil]amino}-1-hidroxietil)-8-hidroxiquinolin-2( 1h)-ona como agonista del receptor b(beta)2 acrenérgico |
AR074870A1 (es) | 2008-12-24 | 2011-02-16 | Palau Pharma Sa | Derivados de pirazolo (1,5-a ) piridina |
WO2010094645A1 (en) | 2009-02-17 | 2010-08-26 | Neurosearch A/S | Substituted pyridine derivatives and their medical use |
BR112012010186B8 (pt) | 2009-10-29 | 2021-05-25 | Palau Pharma Sa | derivados de heteroarila contendo n como inibidores de quinase jak3 e composição farmacêutica compreendendo os mesmos |
EP2338888A1 (en) | 2009-12-24 | 2011-06-29 | Almirall, S.A. | Imidazopyridine derivatives as JAK inhibitors |
UY33213A (es) | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
EP2397482A1 (en) | 2010-06-15 | 2011-12-21 | Almirall, S.A. | Heteroaryl imidazolone derivatives as jak inhibitors |
EP2463289A1 (en) | 2010-11-26 | 2012-06-13 | Almirall, S.A. | Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors |
EP2527344A1 (en) | 2011-05-25 | 2012-11-28 | Almirall, S.A. | Pyridin-2(1H)-one derivatives useful as medicaments for the treatment of myeloproliferative disorders, transplant rejection, immune-mediated and inflammatory diseases |
EP2554544A1 (en) | 2011-08-01 | 2013-02-06 | Almirall, S.A. | Pyridin-2(1h)-one derivatives as jak inhibitors |
-
2010
- 2010-11-26 EP EP20100382318 patent/EP2463289A1/en not_active Withdrawn
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2011
- 2011-11-18 TW TW100142217A patent/TW201236683A/zh unknown
- 2011-11-24 SG SG2013032453A patent/SG190042A1/en unknown
- 2011-11-24 PE PE2013000970A patent/PE20140390A1/es not_active Application Discontinuation
- 2011-11-24 AR ARP110104376 patent/AR087328A1/es unknown
- 2011-11-24 JP JP2013540267A patent/JP5809704B2/ja not_active Expired - Fee Related
- 2011-11-24 UY UY33752A patent/UY33752A/es unknown
- 2011-11-24 EP EP11788775.2A patent/EP2643321A1/en not_active Withdrawn
- 2011-11-24 MX MX2013005257A patent/MX2013005257A/es not_active Application Discontinuation
- 2011-11-24 AU AU2011334146A patent/AU2011334146A1/en not_active Abandoned
- 2011-11-24 WO PCT/EP2011/005929 patent/WO2012069202A1/en active Application Filing
- 2011-11-24 CA CA2815029A patent/CA2815029A1/en active Pending
- 2011-11-24 NZ NZ60871811A patent/NZ608718A/en not_active IP Right Cessation
- 2011-11-24 BR BR112013012965A patent/BR112013012965A2/pt not_active IP Right Cessation
- 2011-11-24 EA EA201300620A patent/EA201300620A1/ru unknown
- 2011-11-24 CN CN2011800569943A patent/CN103228654A/zh active Pending
- 2011-11-24 KR KR1020137010392A patent/KR20140004637A/ko not_active Application Discontinuation
- 2011-11-24 US US13/988,798 patent/US9133200B2/en not_active Expired - Fee Related
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- 2013-03-14 IL IL225232A patent/IL225232A0/en unknown
- 2013-05-10 CO CO13117486A patent/CO6781467A2/es active IP Right Grant
- 2013-05-10 CR CR20130210A patent/CR20130210A/es unknown
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Also Published As
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MX2013005257A (es) | 2014-02-06 |
US9133200B2 (en) | 2015-09-15 |
NZ608718A (en) | 2015-04-24 |
AU2011334146A1 (en) | 2013-04-04 |
GT201300137A (es) | 2014-04-03 |
JP2014501724A (ja) | 2014-01-23 |
IL225232A0 (en) | 2013-06-27 |
PE20140390A1 (es) | 2014-03-29 |
CR20130210A (es) | 2013-08-09 |
JP5809704B2 (ja) | 2015-11-11 |
US20130309200A1 (en) | 2013-11-21 |
EA201300620A1 (ru) | 2013-12-30 |
TW201236683A (en) | 2012-09-16 |
EP2643321A1 (en) | 2013-10-02 |
SG190042A1 (en) | 2013-06-28 |
CO6781467A2 (es) | 2013-10-31 |
EP2463289A1 (en) | 2012-06-13 |
CA2815029A1 (en) | 2012-05-31 |
CL2013001464A1 (es) | 2013-09-06 |
CN103228654A (zh) | 2013-07-31 |
UY33752A (es) | 2012-05-31 |
BR112013012965A2 (pt) | 2016-08-23 |
WO2012069202A1 (en) | 2012-05-31 |
KR20140004637A (ko) | 2014-01-13 |
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