AR107428A1 - COMPUESTOS DE ISOXAZOL DE ÁCIDO HIDROXÁMICO COMO INHIBIDORES DE LpxC - Google Patents

COMPUESTOS DE ISOXAZOL DE ÁCIDO HIDROXÁMICO COMO INHIBIDORES DE LpxC

Info

Publication number
AR107428A1
AR107428A1 ARP150104119A ARP150104119A AR107428A1 AR 107428 A1 AR107428 A1 AR 107428A1 AR P150104119 A ARP150104119 A AR P150104119A AR P150104119 A ARP150104119 A AR P150104119A AR 107428 A1 AR107428 A1 AR 107428A1
Authority
AR
Argentina
Prior art keywords
alkyl
optionally substituted
halo
alkoxy
hydroxy
Prior art date
Application number
ARP150104119A
Other languages
English (en)
Inventor
Zachary Kevin Sweeney
Ann Marie Madera
Guillaume Lapointe
Subramanian Karur
Xianming Jin
Jiping Fu
Original Assignee
Novartis Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of AR107428A1 publication Critical patent/AR107428A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/42Oxazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Reivindicación 1: Un compuesto de fórmula (1), o una sal farmacéuticamente aceptable del mismo, donde: X es -NH-, y R¹ es -CH(OH)-Y; o X es -CH₂-, y R¹ es -CH(OH)-Y o -SO₂R² donde R² es C₁₋₃ alquilo; R³ es H o halo; Y se selecciona de un anillo heteroarilo de 5 miembros que contiene 1 - 3 heteroátomos seleccionados de entre N, O y S como miembros del anillo, fenilo y alquilo C₁₋₃ y cada Y está opcionalmente sustituido con uno a tres R⁴; cada R⁴ se selecciona independientemente de halo, alquilo C₁₋₃ y cicloalquilo C₃₋₆, donde el alquilo C₁₋₃ Y el cicloalquilo C₃₋₆ están cada uno opcionalmente sustituido con hasta tres grupos seleccionados de entre halo, CN y -OH; L es -CºC- o -CR⁵=CR⁵-; R⁵ se selecciona independientemente en cada caso entre H, halo y metilo; y Z se selecciona de entre alquilo C₁₋₆, cicloalquilo C₃₋₆. piridinilo y fenilo, cada uno de los cuales está opcionalmente sustituido con hasta tres grupos seleccionados de entre halógeno, hidroxi, alcoxi C₁₋₄, haloalcoxi C₁₋₄ CN y alquilo C₁₋₄, que está opcionalmente sustituido con uno a tres grupos seleccionados de entre halógeno, hidroxi, amino, CN y alcoxi C₁₋₃; o, cuando L es -CR⁵=CR⁵-, Z junto con uno de los grupos R⁵ y cualesquiera átomos que conectan Z con el grupo R⁵ pueden formar un grupo cicloalquilo o cicloalquenilo de 3 a 7 miembros, que está opcionalmente sustituido con hasta tres grupos seleccionados de entre halógeno, hidroxi, alcoxi C₁₋₄, haloalcoxi C₁₋₄, CN y alquilo C₁₋₄ que está opcionalmente sustituido con uno a tres grupos seleccionados de entre halógeno, hidroxi, amino, CN y alcoxi C₁₋₃.
ARP150104119A 2014-12-16 2015-12-16 COMPUESTOS DE ISOXAZOL DE ÁCIDO HIDROXÁMICO COMO INHIBIDORES DE LpxC AR107428A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201462092402P 2014-12-16 2014-12-16

Publications (1)

Publication Number Publication Date
AR107428A1 true AR107428A1 (es) 2018-05-02

Family

ID=55025302

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP150104119A AR107428A1 (es) 2014-12-16 2015-12-16 COMPUESTOS DE ISOXAZOL DE ÁCIDO HIDROXÁMICO COMO INHIBIDORES DE LpxC

Country Status (41)

Country Link
US (3) US9549916B2 (es)
EP (1) EP3233843B1 (es)
JP (1) JP6697466B2 (es)
KR (1) KR20170094214A (es)
CN (1) CN107001295B (es)
AR (1) AR107428A1 (es)
AU (1) AU2015365455B2 (es)
BR (1) BR112017011422A2 (es)
CA (1) CA2969803A1 (es)
CL (1) CL2017001460A1 (es)
CO (1) CO2017005870A2 (es)
CR (1) CR20170260A (es)
CU (1) CU24443B1 (es)
CY (1) CY1122305T1 (es)
DK (1) DK3233843T3 (es)
EA (1) EA032138B1 (es)
EC (1) ECSP17045737A (es)
ES (1) ES2756300T3 (es)
GT (1) GT201700132A (es)
HR (1) HRP20192009T1 (es)
HU (1) HUE047225T2 (es)
IL (1) IL252373B (es)
JO (1) JO3818B1 (es)
LT (1) LT3233843T (es)
MA (1) MA41185B1 (es)
ME (1) ME03546B (es)
MX (1) MX2017007980A (es)
MY (1) MY195743A (es)
PE (1) PE20171044A1 (es)
PH (1) PH12017501019A1 (es)
PL (1) PL3233843T3 (es)
PT (1) PT3233843T (es)
RS (1) RS59507B1 (es)
SG (1) SG11201704053WA (es)
SI (1) SI3233843T1 (es)
SV (1) SV2017005462A (es)
TN (1) TN2017000207A1 (es)
TW (1) TWI693215B (es)
UA (1) UA121225C2 (es)
UY (1) UY36448A (es)
WO (1) WO2016097995A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112015028501B8 (pt) 2013-05-17 2023-01-24 Incyte Corp Compostos derivados de bipirazol, seus sais, composição compreendendo o composto ou o sal, método de inibição in vitro de uma atividade de jak1, e processo de preparação de sal de ácido fosfórico
AU2017283768B2 (en) * 2016-06-14 2019-05-23 Novartis Ag Crystalline form of (R)-4-(5-(cyclopropylethynyl)isoxazol-3-yl)-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide as an antibacterial agent
CN107434766A (zh) * 2017-08-09 2017-12-05 凯莱英医药集团(天津)股份有限公司 烷烃羟胺类化合物的合成装置及连续合成方法
MA51829A (fr) 2018-02-16 2020-12-23 Incyte Corp Inhibiteurs de la voie jak1 pour le traitement de troubles liés aux cytokines
US20220002279A1 (en) * 2018-11-21 2022-01-06 Taisho Pharmaceutical Co., Ltd. Novel imidazole derivative
IL298118A (en) 2020-06-02 2023-01-01 Incyte Corp Processes for making jak1 inhibitor
MX2023006542A (es) 2020-12-08 2023-08-25 Incyte Corp Inhibidores de la vía cinasa jano 1 (jak1) para el tratamiento del vitiligo.
CN112603936B (zh) * 2020-12-28 2022-08-02 仲恺农业工程学院 一种抑制气单胞菌属的组合物及其制备方法与应用
AR124841A1 (es) * 2021-02-11 2023-05-10 Forge Therapeutics Inc Compuestos antibacterianos
TW202245756A (zh) * 2021-02-11 2022-12-01 美商福吉醫療公司 抗菌化合物
TW202322818A (zh) * 2021-09-28 2023-06-16 美商福吉醫療公司 Lpxc抑制劑及其用途
WO2024067813A1 (zh) * 2022-09-28 2024-04-04 浙江海正药业股份有限公司 芳香乙炔类衍生物及其制备方法和其医药上的用途
WO2024067812A1 (zh) * 2022-09-28 2024-04-04 浙江海正药业股份有限公司 芳香乙炔类衍生物及其制备方法和用途

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0090505B1 (en) 1982-03-03 1990-08-08 Genentech, Inc. Human antithrombin iii, dna sequences therefor, expression vehicles and cloning vectors containing such sequences and cell cultures transformed thereby, a process for expressing human antithrombin iii, and pharmaceutical compositions comprising it
EP0418667B1 (de) 1989-09-22 1995-08-16 BASF Aktiengesellschaft Carbonsäureamide
AU4055697A (en) 1996-08-16 1998-03-06 Schering Corporation Mammalian cell surface antigens; related reagents
US6111090A (en) 1996-08-16 2000-08-29 Schering Corporation Mammalian cell surface antigens; related reagents
US6509173B1 (en) 1997-10-21 2003-01-21 Human Genome Sciences, Inc. Human tumor necrosis factor receptor-like proteins TR11, TR11SV1, and TR11SV2
AU2591599A (en) 1998-02-09 1999-08-23 Genentech Inc. Novel tumor necrosis factor receptor homolog and nucleic acids encoding the same
DE60036945T2 (de) 1999-07-12 2008-08-21 Genentech, Inc., South San Francisco Stimulierung oder hemmung von angiogenese und herzvaskularisierung mit tumor nekrose faktor ligand/rezeptor homologen
CA2508660C (en) 2002-12-23 2013-08-20 Wyeth Antibodies against pd-1 and uses therefor
CA2512582C (en) 2003-01-08 2014-07-08 University Of Washington Antibacterial agents
EP1631260A2 (en) 2003-02-28 2006-03-08 Transform Pharmaceuticals, Inc. Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
CA2525717A1 (en) 2003-05-23 2004-12-09 Wyeth Gitr ligand and gitr ligand-related molecules and antibodies and uses thereof
EP1660126A1 (en) 2003-07-11 2006-05-31 Schering Corporation Agonists or antagonists of the clucocorticoid-induced tumour necrosis factor receptor (gitr) or its ligand for the treatment of immune disorders, infections and cancer
EP1692318A4 (en) 2003-12-02 2008-04-02 Genzyme Corp COMPOSITIONS AND METHODS FOR DIAGNOSIS AND TREATMENT OF LUNG CANCER
GB0409799D0 (en) 2004-04-30 2004-06-09 Isis Innovation Method of generating improved immune response
WO2006083289A2 (en) 2004-06-04 2006-08-10 Duke University Methods and compositions for enhancement of immunity by in vivo depletion of immunosuppressive cell activity
GB0502418D0 (en) 2005-02-05 2005-03-16 Astrazeneca Ab Compounds
US7812135B2 (en) 2005-03-25 2010-10-12 Tolerrx, Inc. GITR-binding antibodies
NZ563193A (en) 2005-05-09 2010-05-28 Ono Pharmaceutical Co Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics
SI1907424T1 (sl) 2005-07-01 2015-12-31 E. R. Squibb & Sons, L.L.C. Humana monoklonska protitelesa proti programiranem smrtnem ligandu 1 (PD-L1)
WO2007133822A1 (en) 2006-01-19 2007-11-22 Genzyme Corporation Gitr antibodies for the treatment of cancer
ES2437327T3 (es) 2007-06-18 2014-01-10 Merck Sharp & Dohme B.V. Anticuerpos para el receptor PD-1 humano de muerte programada
EP3124046B1 (en) 2007-07-12 2019-12-25 GITR, Inc. Combination therapies employing gitr binding molecules
JP2011512332A (ja) 2008-02-11 2011-04-21 キュアー テック リミテッド 腫瘍治療のためのモノクローナル抗体
EP2262837A4 (en) 2008-03-12 2011-04-06 Merck Sharp & Dohme PD-1 BINDING PROTEINS
NZ590667A (en) 2008-07-02 2013-01-25 Emergent Product Dev Seattle Tgf-b antagonist multi-target binding proteins
AR072999A1 (es) 2008-08-11 2010-10-06 Medarex Inc Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos
AU2009288730B2 (en) 2008-08-25 2013-06-20 Amplimmune, Inc. Compositions of PD-1 antagonists and methods of use
US20110159023A1 (en) 2008-08-25 2011-06-30 Solomon Langermann Pd-1 antagonists and methods for treating infectious disease
CN102149820B (zh) 2008-09-12 2014-07-23 国立大学法人三重大学 能够表达外源gitr配体的细胞
CA2735929C (en) * 2008-09-19 2013-12-17 Pfizer Inc. Hydroxamic acid derivatives useful as antibacterial agents
CN114835812A (zh) 2008-12-09 2022-08-02 霍夫曼-拉罗奇有限公司 抗-pd-l1抗体及它们用于增强t细胞功能的用途
EP2393835B1 (en) 2009-02-09 2017-04-05 Université d'Aix-Marseille Pd-1 antibodies and pd-l1 antibodies and uses thereof
RU2595409C2 (ru) 2009-09-03 2016-08-27 Мерк Шарп И Доум Корп., Анти-gitr-антитела
WO2011045703A2 (en) * 2009-10-13 2011-04-21 Pfizer Inc. C-linked hydroxamic acid derivatives useful as antibacterial agents
GB0919054D0 (en) 2009-10-30 2009-12-16 Isis Innovation Treatment of obesity
JP2013512251A (ja) 2009-11-24 2013-04-11 アンプリミューン、インコーポレーテッド Pd−l1/pd−l2の同時阻害
SI2512474T1 (sl) * 2009-12-16 2014-12-31 Pfizer Inc. N-vezani derivati hidroksamske kisline, uporabni kot protibakterijska sredstva
JP5856073B2 (ja) 2009-12-29 2016-02-09 エマージェント プロダクト デベロップメント シアトル, エルエルシー Ron結合構築体およびその使用方法
US8877754B2 (en) 2010-09-06 2014-11-04 Boehringer Ingelheim International Gmbh Compounds, pharmaceutical compositions and uses thereof
EA201390626A1 (ru) 2010-11-10 2013-12-30 Эйкеоджен, Инк. Производные гидроксамовой кислоты и применение указанных производных в лечении бактериальных инфекций
MX341977B (es) 2011-03-07 2016-09-07 Pfizer Derivados de fluoro-piridinona utiles como agentes antibacterianos.
US8748466B2 (en) * 2011-04-08 2014-06-10 Pfizer Inc. Isoxazole derivatives useful as antibacterial agents
CA2830866A1 (en) * 2011-04-08 2012-10-11 Pfizer Inc. Imidazole, pyrazole, and triazole derivatives useful as antibacterial agents
WO2013039954A1 (en) 2011-09-14 2013-03-21 Sanofi Anti-gitr antibodies
EA036814B9 (ru) 2011-11-28 2021-12-27 Мерк Патент Гмбх Антитело против pd-l1 (варианты), композиция, содержащая это антитело, и их применение
UY34887A (es) 2012-07-02 2013-12-31 Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos
WO2014160649A1 (en) 2013-03-29 2014-10-02 Novartis Ag Hydroxamic acid derivatives as lpxc inhibitors for the treatment of bacterial infections

Also Published As

Publication number Publication date
LT3233843T (lt) 2019-12-10
CY1122305T1 (el) 2021-01-27
JP6697466B2 (ja) 2020-05-20
PL3233843T3 (pl) 2020-04-30
HRP20192009T1 (hr) 2020-02-07
US20180030004A1 (en) 2018-02-01
WO2016097995A1 (en) 2016-06-23
MX2017007980A (es) 2017-09-29
CN107001295A (zh) 2017-08-01
GT201700132A (es) 2019-10-10
JO3818B1 (ar) 2021-01-31
TWI693215B (zh) 2020-05-11
UY36448A (es) 2016-07-29
CA2969803A1 (en) 2016-06-23
JP2018500333A (ja) 2018-01-11
SV2017005462A (es) 2018-04-04
BR112017011422A2 (pt) 2018-04-03
CR20170260A (es) 2017-08-21
CO2017005870A2 (es) 2017-10-20
ME03546B (me) 2020-07-20
CU24443B1 (es) 2019-10-04
AU2015365455B2 (en) 2019-01-17
ES2756300T3 (es) 2020-04-27
EA032138B1 (ru) 2019-04-30
SG11201704053WA (en) 2017-06-29
EP3233843A1 (en) 2017-10-25
EP3233843B1 (en) 2019-10-16
IL252373A0 (en) 2017-07-31
US20170088525A1 (en) 2017-03-30
PH12017501019B1 (en) 2017-12-04
EA201791353A1 (ru) 2017-10-31
US20160166548A1 (en) 2016-06-16
AU2015365455A1 (en) 2017-06-08
ECSP17045737A (es) 2019-02-28
IL252373B (en) 2019-11-28
US9815804B2 (en) 2017-11-14
CL2017001460A1 (es) 2017-12-22
PH12017501019A1 (en) 2017-12-04
TW201629024A (zh) 2016-08-16
TN2017000207A1 (en) 2018-10-19
US9549916B2 (en) 2017-01-24
HUE047225T2 (hu) 2020-04-28
PE20171044A1 (es) 2017-07-19
UA121225C2 (uk) 2020-04-27
DK3233843T3 (da) 2019-11-18
SI3233843T1 (sl) 2019-12-31
CN107001295B (zh) 2021-02-02
PT3233843T (pt) 2019-11-26
MY195743A (en) 2023-02-08
CU20170084A7 (es) 2017-11-07
MA41185B1 (fr) 2019-12-31
RS59507B1 (sr) 2019-12-31
US10029994B2 (en) 2018-07-24
KR20170094214A (ko) 2017-08-17

Similar Documents

Publication Publication Date Title
AR107428A1 (es) COMPUESTOS DE ISOXAZOL DE ÁCIDO HIDROXÁMICO COMO INHIBIDORES DE LpxC
AR101815A1 (es) Compuestos y composiciones como inhibidores de quinasa
NI201700020A (es) Compuestos de aminopirimidinilo como inhibidores de jak
CY1120703T1 (el) Ετεροκυκλικες ενωσεις και χρησεις αυτων
CR20160564A (es) Dinucleótidos cíclicos como moduladores de sting
AR102204A1 (es) Compuestos derivados de amino-alquilbenzotiazepinas
TW201613911A (en) Heterocyclic compounds and uses thereof
BR112017006251A2 (pt) novos compostos
AR089671A1 (es) 1,4-dihidropirimidinas 4,4-disustituidas y su uso como medicamentos para el tratamiento de la hepatitis b
AR097082A1 (es) Compuestos terapéuticamente activos y sus métodos de uso
AR101558A1 (es) Difluoropirrolidinas como moduladores del receptor de orexina
AR100191A1 (es) Método para tratar adenocarcinoma de pulmón
RS54730B1 (sr) Inhibitori beta sekretaze
AR091519A1 (es) Inhibidores pirrolopirazona de tanquirasa
AR094812A1 (es) Derivado de piridina monocíclico como inhibidor del fgfr
AR098522A1 (es) Compuesto de triazolo-piridina
AR095523A1 (es) Derivados piridin-4-ilo
AR089814A1 (es) Compuestos que modulan la actividad de los proteasomas
AR097253A1 (es) Derivado de pirazolilpirazol sustituido y el uso del mismo como herbicida
AR101798A1 (es) Quinolinas herbicidas
AR105821A1 (es) COMPUESTOS ÚTILES PARA INHIBIR ROR-g-T
MY180006A (en) Azetidinyloxyphenylpyrrolidine compounds
AR091773A1 (es) Inhibidores de la histona desacetilasa y composiciones y sus metodos de uso
CO2019005165A2 (es) Compuesto de piridona como inhibidor de c-met
ES2571577T3 (es) Derivados novedosos de morfolinilo útiles como inhibidores de MOGAT-2

Legal Events

Date Code Title Description
FB Suspension of granting procedure