SG11201704053WA - Isoxazole hydroxamic acid compounds as lpxc inhibitors - Google Patents

Isoxazole hydroxamic acid compounds as lpxc inhibitors

Info

Publication number
SG11201704053WA
SG11201704053WA SG11201704053WA SG11201704053WA SG11201704053WA SG 11201704053W A SG11201704053W A SG 11201704053WA SG 11201704053W A SG11201704053W A SG 11201704053WA SG 11201704053W A SG11201704053W A SG 11201704053WA SG 11201704053W A SG11201704053W A SG 11201704053WA
Authority
SG
Singapore
Prior art keywords
acid compounds
hydroxamic acid
lpxc inhibitors
isoxazole
isoxazole hydroxamic
Prior art date
Application number
SG11201704053WA
Other languages
English (en)
Inventor
Jiping Fu
Xianming Jin
Subramanian Karur
Guillaume Lapointe
Ann Marie Madera
Zachary Kevin Sweeney
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 SG11201704053WA publication Critical patent/SG11201704053WA/en

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)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (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)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pulmonology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (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)
SG11201704053WA 2014-12-16 2015-12-15 Isoxazole hydroxamic acid compounds as lpxc inhibitors SG11201704053WA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201462092402P 2014-12-16 2014-12-16
PCT/IB2015/059631 WO2016097995A1 (fr) 2014-12-16 2015-12-15 Composés d'acides d'isoxazole en tant qu'inhibiteurs de lpxc

Publications (1)

Publication Number Publication Date
SG11201704053WA true SG11201704053WA (en) 2017-06-29

Family

ID=55025302

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201704053WA SG11201704053WA (en) 2014-12-16 2015-12-15 Isoxazole hydroxamic acid compounds as lpxc inhibitors

Country Status (41)

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

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20160126A1 (es) 2013-05-17 2016-02-24 Incyte Corp Derivados del bipirazol como inhibidores jak
HUE050796T2 (hu) * 2016-06-14 2021-01-28 Novartis Ag (R)-4-(5-(ciklopropiletinil)izoxazol-3-il)-N-hidroxi-2-metil-2-(metilszulfonil)butánamid kristályos formája baktériumellenes szerként
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
IL311485A (en) 2018-02-16 2024-05-01 Incyte Corp JAK1 pathway inhibitors for the treatment of cytokine-related disorders
BR112021009536A2 (pt) * 2018-11-21 2021-08-17 Taisho Pharmaceutical Co., Ltd. derivado de imidazol
PE20231102A1 (es) 2020-06-02 2023-07-19 Incyte Corp Procesos para preparar un inhibidor de jak1
KR20230118118A (ko) 2020-12-08 2023-08-10 인사이트 코포레이션 백반증의 치료를 위한 jak1 경로 저해제
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
JP2024507140A (ja) * 2021-02-11 2024-02-16 ブラックスミス メディシンズ,インク. 抗菌性化合物
CN117279897A (zh) * 2021-02-11 2023-12-22 布莱克史密斯医药公司 抗菌化合物
CA3233328A1 (fr) * 2021-09-28 2023-04-06 Min Teng Inhibiteurs de lpxc et leurs utilisations
WO2024067812A1 (fr) * 2022-09-28 2024-04-04 浙江海正药业股份有限公司 Dérivé d'acétylène aromatique, son procédé de préparation et son utilisation
WO2024067813A1 (fr) * 2022-09-28 2024-04-04 浙江海正药业股份有限公司 Dérivé d'acétylène aromatique, son procédé de préparation et son utilisation pharmaceutique

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3381783D1 (de) 1982-03-03 1990-09-13 Genentech Inc Menschliches antithrombin iii, dns sequenzen dafuer, expressions- und klonierungsvektoren die solche sequenzen enthalten und damit transformierte zellkulturen, verfahren zur expression von menschlichem antithrombin iii und diese enthaltende pharmazeutische zusammensetzungen.
DE59009528D1 (de) 1989-09-22 1995-09-21 Basf Ag Carbonsäureamide.
US6111090A (en) 1996-08-16 2000-08-29 Schering Corporation Mammalian cell surface antigens; related reagents
DK0920505T3 (da) 1996-08-16 2008-09-08 Schering Corp Pattedyrcelleoverfladeantigener og tilhörende reagenser
CA2308114A1 (fr) 1997-10-21 1999-04-29 Human Genome Sciences, Inc. Proteines tr11, tr11sv1 et tr11sv2 de type recepteur du facteur de necrose tumorale humain
CA2319236A1 (fr) 1998-02-09 1999-08-12 Genentech, Inc. Nouveaux homologues recepteurs du facteur necrosant des tumeurs et acides nucleiques codant ceux-ci
DK1196186T3 (da) 1999-07-12 2008-03-03 Genentech Inc Stimulering eller inhibering af angiogenese og kardiovaskularisation med tumornekrosefaktorligand/receptorhomologer
ATE514713T1 (de) 2002-12-23 2011-07-15 Wyeth Llc Antikörper gegen pd-1 und ihre verwendung
EA011808B1 (ru) 2003-01-08 2009-06-30 Новартис Вэксинес Энд Дайэгностикс, Инк. Антибактериальные агенты
CA2514733A1 (fr) 2003-02-28 2004-09-16 Transform Pharmaceuticals, Inc. Compositions pharmaceutiques a base d'un co-cristal
EP1631588A2 (fr) 2003-05-23 2006-03-08 Wyeth Ligand du gitr et molecules et anticorps lies au ligand du gitr et leurs utilisations
WO2005007190A1 (fr) 2003-07-11 2005-01-27 Schering Corporation Agonistes ou antagonistes du recepteur du facteur de necrose tumorale induit par les glucocorticoides (gitr) ou de son ligand utilises dans le traitement des troubles immuns, des infections et du cancer
EP1692318A4 (fr) 2003-12-02 2008-04-02 Genzyme Corp Compositions et methodes pour le diagnostic et le traitement du cancer du poumon
GB0409799D0 (en) 2004-04-30 2004-06-09 Isis Innovation Method of generating improved immune response
US20060002932A1 (en) 2004-06-04 2006-01-05 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
WO2006105021A2 (fr) 2005-03-25 2006-10-05 Tolerrx, Inc. Molecules de liaison gitr et leurs utilisations
EP2439273B1 (fr) 2005-05-09 2019-02-27 Ono Pharmaceutical Co., Ltd. Anticorps monoclonaux humains pour mort programmée 1 (PD-1) et procédés de traitement du cancer à l'aide d'anticorps anti-PD-1 seuls ou combinés à d'autres formulations immunothérapeutiques
ES2546333T3 (es) 2005-07-01 2015-09-22 E. R. Squibb & Sons, L.L.C. Anticuerpos monoclonales humanos para ligandos 1 (PD-L1) de muerte programada
US20110212086A1 (en) 2006-01-19 2011-09-01 Genzyme Corporation GITR Antibodies For The Treatment of Cancer
BRPI0812913B8 (pt) 2007-06-18 2021-05-25 Merck Sharp & Dohme anticorpos monoclonais ou fragmento de anticorpo para o receptor de morte programada humano pd-1, polinucleotideo, método para produzir os referidos anticorpos ou fragmentos de anticorpos, composição que os compreende e uso dos mesmos
ES2591281T3 (es) 2007-07-12 2016-11-25 Gitr, Inc. Terapias de combinación que emplean moléculas de enlazamiento a GITR
MX2010008786A (es) 2008-02-11 2010-12-01 Curetech Ltd Anticuerpos monoclonales para tratamiento de tumores.
EP2262837A4 (fr) 2008-03-12 2011-04-06 Merck Sharp & Dohme Protéines de liaison avec pd-1
EP2310508A1 (fr) 2008-07-02 2011-04-20 Emergent Product Development Seattle, LLC Protéines de liaison multi-cibles antagonistes du tgf-b
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
JP2012500855A (ja) 2008-08-25 2012-01-12 アンプリミューン、インコーポレーテッド Pd−1アンタゴニストおよび感染性疾患を処置するための方法
PL2350129T3 (pl) 2008-08-25 2015-12-31 Amplimmune Inc Kompozycje antagonistów PD-1 i sposoby stosowania
US8586023B2 (en) 2008-09-12 2013-11-19 Mie University Cell capable of expressing exogenous GITR ligand
JP5524215B2 (ja) 2008-09-19 2014-06-18 ファイザー・インク 抗菌剤として有用なヒドロキサム酸誘導体
KR20190069615A (ko) 2008-12-09 2019-06-19 제넨테크, 인크. 항-pd-l1 항체 및 t 세포 기능을 향상시키기 위한 그의 용도
EP2393835B1 (fr) 2009-02-09 2017-04-05 Université d'Aix-Marseille Anticorps contre pd-1 et anticorps contre pd-l1 et leurs utilisations
ES2788869T3 (es) 2009-09-03 2020-10-23 Merck Sharp & Dohme Anticuerpos anti-GITR
CA2774250C (fr) * 2009-10-13 2013-12-17 Pfizer Inc. Derives d'acide hydroxamique a liaison c utiles comme agents antibacteriens
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
WO2011073845A1 (fr) * 2009-12-16 2011-06-23 Pfizer Inc. Dérivés d'acide hydroxamique à liaison n, utiles comme agents antibactériens
US20130089554A1 (en) 2009-12-29 2013-04-11 Emergent Product Development Seattle, Llc RON Binding Constructs and Methods of Use Thereof
US8877754B2 (en) 2010-09-06 2014-11-04 Boehringer Ingelheim International Gmbh Compounds, pharmaceutical compositions and uses thereof
MX2013005200A (es) 2010-11-10 2013-06-28 Achaogen Inc Derivados de acido hidroxamico y su so en el tratamiento de infecciones bacterianas.
BR112013022536B1 (pt) 2011-03-07 2020-05-26 Pfizer, Inc. Derivados flúor-piridinona, suas composições farmacêuticas e usos como agentes antibacterianos
EP2694481B1 (fr) * 2011-04-08 2015-12-30 Pfizer Inc Dérivés d'imidazole, de pyrazole et de triazole, utiles en tant qu'agents antibactériens
SG193367A1 (en) 2011-04-08 2013-10-30 Pfizer Isoxazole derivatives useful as antibacterial agents
WO2013039954A1 (fr) 2011-09-14 2013-03-21 Sanofi Anticorps anti-gitr
JP6138813B2 (ja) 2011-11-28 2017-05-31 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung 抗pd−l1抗体及びその使用
AR091649A1 (es) 2012-07-02 2015-02-18 Bristol Myers Squibb Co Optimizacion de anticuerpos que se fijan al gen de activacion de linfocitos 3 (lag-3) y sus usos
WO2014160649A1 (fr) 2013-03-29 2014-10-02 Novartis Ag Dérivés d'acide hydroxamique utilisés comme inhibiteurs de lpxc pour le traitement d'infections bactériennes

Also Published As

Publication number Publication date
JO3818B1 (ar) 2021-01-31
US20180030004A1 (en) 2018-02-01
CR20170260A (es) 2017-08-21
DK3233843T3 (da) 2019-11-18
CA2969803A1 (fr) 2016-06-23
SI3233843T1 (sl) 2019-12-31
ME03546B (fr) 2020-07-20
CN107001295A (zh) 2017-08-01
HRP20192009T1 (hr) 2020-02-07
SV2017005462A (es) 2018-04-04
AR107428A1 (es) 2018-05-02
LT3233843T (lt) 2019-12-10
EA032138B1 (ru) 2019-04-30
ES2756300T3 (es) 2020-04-27
TW201629024A (zh) 2016-08-16
US20160166548A1 (en) 2016-06-16
EP3233843B1 (fr) 2019-10-16
US10029994B2 (en) 2018-07-24
JP2018500333A (ja) 2018-01-11
JP6697466B2 (ja) 2020-05-20
RS59507B1 (sr) 2019-12-31
WO2016097995A1 (fr) 2016-06-23
MY195743A (en) 2023-02-08
TN2017000207A1 (en) 2018-10-19
AU2015365455B2 (en) 2019-01-17
US9549916B2 (en) 2017-01-24
TWI693215B (zh) 2020-05-11
PL3233843T3 (pl) 2020-04-30
PH12017501019B1 (en) 2017-12-04
CY1122305T1 (el) 2021-01-27
EP3233843A1 (fr) 2017-10-25
CU24443B1 (es) 2019-10-04
MA41185B1 (fr) 2019-12-31
IL252373B (en) 2019-11-28
HUE047225T2 (hu) 2020-04-28
BR112017011422A2 (pt) 2018-04-03
US9815804B2 (en) 2017-11-14
CO2017005870A2 (es) 2017-10-20
CN107001295B (zh) 2021-02-02
CL2017001460A1 (es) 2017-12-22
MX2017007980A (es) 2017-09-29
GT201700132A (es) 2019-10-10
UA121225C2 (uk) 2020-04-27
AU2015365455A1 (en) 2017-06-08
US20170088525A1 (en) 2017-03-30
KR20170094214A (ko) 2017-08-17
PE20171044A1 (es) 2017-07-19
ECSP17045737A (es) 2019-02-28
UY36448A (es) 2016-07-29
PH12017501019A1 (en) 2017-12-04
CU20170084A7 (es) 2017-11-07
EA201791353A1 (ru) 2017-10-31
IL252373A0 (en) 2017-07-31
PT3233843T (pt) 2019-11-26

Similar Documents

Publication Publication Date Title
IL252373A0 (en) Hydrobromic acid isoxazole compounds as lpxc inhibitors
HK1245266A1 (zh) 作為usp30抑制劑的1-氰基吡咯烷化合物
IL248505B (en) Inhibitors of specific lysine demethylase-1
IL250876A0 (en) Inhibitors of specific lysine demethylase-1
IL249733A0 (en) Inhibitors of specific lysine demethylase-1
IL249881B (en) Inhibitors of specific lysine demethylase-1
AP2016009496A0 (en) Substituted spirocydic inhibitors of autotaxin
ZA202001074B (en) Inhibitors of a-amino-b-carboxymuconic acid semialdehyde decarboxylase
IL249876B (en) Inhibitors of specific lysine demethylase-1
IL251780A0 (en) New compounds as nik inhibitors
GB2540917B (en) Solid acid scale inhibitors
EP3494971C0 (fr) Sels de inhibiteurs de erk
GB201403536D0 (en) Inhibitor compounds
ZA201700022B (en) A novel formulation of meloxicam