SG11201704053WA - Isoxazole hydroxamic acid compounds as lpxc inhibitors - Google Patents
Isoxazole hydroxamic acid compounds as lpxc inhibitorsInfo
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/42—Oxazoles
-
- 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
- A61K31/41—Heterocyclic 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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic 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
- C07D261/08—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic 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
- C07D413/06—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic 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
- C07D413/12—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against 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)
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)
Families Citing this family (13)
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)
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 |
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2015
- 2015-12-15 CN CN201580066726.8A patent/CN107001295B/zh not_active Expired - Fee Related
- 2015-12-15 ES ES15816893T patent/ES2756300T3/es active Active
- 2015-12-15 KR KR1020177016102A patent/KR20170094214A/ko not_active Application Discontinuation
- 2015-12-15 AU AU2015365455A patent/AU2015365455B2/en not_active Ceased
- 2015-12-15 HU HUE15816893A patent/HUE047225T2/hu unknown
- 2015-12-15 CA CA2969803A patent/CA2969803A1/fr not_active Abandoned
- 2015-12-15 RS RS20191403A patent/RS59507B1/sr unknown
- 2015-12-15 PE PE2017001078A patent/PE20171044A1/es unknown
- 2015-12-15 SG SG11201704053WA patent/SG11201704053WA/en unknown
- 2015-12-15 UA UAA201705042A patent/UA121225C2/uk unknown
- 2015-12-15 LT LT15816893T patent/LT3233843T/lt unknown
- 2015-12-15 DK DK15816893T patent/DK3233843T3/da active
- 2015-12-15 MA MA41185A patent/MA41185B1/fr unknown
- 2015-12-15 US US14/969,930 patent/US9549916B2/en active Active
- 2015-12-15 TW TW104142164A patent/TWI693215B/zh not_active IP Right Cessation
- 2015-12-15 SI SI201530987T patent/SI3233843T1/sl unknown
- 2015-12-15 BR BR112017011422-4A patent/BR112017011422A2/pt not_active IP Right Cessation
- 2015-12-15 PL PL15816893T patent/PL3233843T3/pl unknown
- 2015-12-15 WO PCT/IB2015/059631 patent/WO2016097995A1/fr active Application Filing
- 2015-12-15 MY MYPI2017701741A patent/MY195743A/en unknown
- 2015-12-15 MX MX2017007980A patent/MX2017007980A/es active IP Right Grant
- 2015-12-15 JP JP2017532143A patent/JP6697466B2/ja not_active Expired - Fee Related
- 2015-12-15 CR CR20170260A patent/CR20170260A/es unknown
- 2015-12-15 TN TN2017000207A patent/TN2017000207A1/en unknown
- 2015-12-15 EA EA201791353A patent/EA032138B1/ru not_active IP Right Cessation
- 2015-12-15 CU CU2017000084A patent/CU24443B1/es unknown
- 2015-12-15 EP EP15816893.0A patent/EP3233843B1/fr active Active
- 2015-12-15 ME MEP-2019-305A patent/ME03546B/fr unknown
- 2015-12-15 PT PT158168930T patent/PT3233843T/pt unknown
- 2015-12-16 JO JOP/2015/0318A patent/JO3818B1/ar active
- 2015-12-16 UY UY0001036448A patent/UY36448A/es not_active Application Discontinuation
- 2015-12-16 AR ARP150104119A patent/AR107428A1/es unknown
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2016
- 2016-12-12 US US15/375,560 patent/US9815804B2/en active Active
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2017
- 2017-05-18 IL IL25237317A patent/IL252373B/en active IP Right Grant
- 2017-06-01 PH PH12017501019A patent/PH12017501019A1/en unknown
- 2017-06-08 CL CL2017001460A patent/CL2017001460A1/es unknown
- 2017-06-14 CO CONC2017/0005870A patent/CO2017005870A2/es unknown
- 2017-06-16 GT GT201700132A patent/GT201700132A/es unknown
- 2017-06-16 SV SV2017005462A patent/SV2017005462A/es unknown
- 2017-07-16 EC ECIEPI201745737A patent/ECSP17045737A/es unknown
- 2017-10-09 US US15/728,351 patent/US10029994B2/en active Active
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2019
- 2019-11-06 HR HRP20192009TT patent/HRP20192009T1/hr unknown
- 2019-11-11 CY CY20191101181T patent/CY1122305T1/el unknown
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