HK1257100A1 - 使用新型苯丙胺酸小分子有機化合物來直接調節pcsk9的蛋白活性的組合物和方法 - Google Patents
使用新型苯丙胺酸小分子有機化合物來直接調節pcsk9的蛋白活性的組合物和方法Info
- Publication number
- HK1257100A1 HK1257100A1 HK18116351.9A HK18116351A HK1257100A1 HK 1257100 A1 HK1257100 A1 HK 1257100A1 HK 18116351 A HK18116351 A HK 18116351A HK 1257100 A1 HK1257100 A1 HK 1257100A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- composition
- methods
- organic compounds
- small organic
- protein activity
- 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
- A61K31/495—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
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4409—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 4, e.g. isoniazid, iproniazid
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/20—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Obesity (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201562208054P | 2015-08-21 | 2015-08-21 | |
US201662298852P | 2016-02-23 | 2016-02-23 | |
PCT/US2016/047810 WO2017034994A1 (en) | 2015-08-21 | 2016-08-19 | Composition and methods of use of novel phenylalanine small organic compounds to directly modulate pcsk9 protein activity |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1257100A1 true HK1257100A1 (zh) | 2019-10-11 |
Family
ID=58101008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK18116351.9A HK1257100A1 (zh) | 2015-08-21 | 2018-12-20 | 使用新型苯丙胺酸小分子有機化合物來直接調節pcsk9的蛋白活性的組合物和方法 |
Country Status (4)
Country | Link |
---|---|
US (2) | US10821106B2 (zh) |
EP (1) | EP3337497B1 (zh) |
HK (1) | HK1257100A1 (zh) |
WO (1) | WO2017034994A1 (zh) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017034994A1 (en) | 2015-08-21 | 2017-03-02 | Portola Pharmaceuticals, Inc. | Composition and methods of use of novel phenylalanine small organic compounds to directly modulate pcsk9 protein activity |
WO2017034990A1 (en) | 2015-08-21 | 2017-03-02 | Portola Pharmaceuticals, Inc. | Composition and methods of use of tetrahydroisoquinoline small molecules to bind and modulate pcsk9 protein activity |
EP3337788A4 (en) | 2015-08-21 | 2019-03-27 | Portola Pharmaceuticals, Inc. | PHENYLPIPERAZINE PROPROTEIN CONVERTASE SUBTILISIN / -KEXIN TYPE 9 P (CSK9) MODULATORS AND THEIR USE |
CN105214087B (zh) | 2015-10-29 | 2017-12-26 | 陈敏 | Pcsk9单克隆抗体在制备治疗炎症免疫性疾病药物中的应用 |
US20190119236A1 (en) | 2016-02-23 | 2019-04-25 | Portola Pharmaceuticals, Inc. | Compounds for binding proprotein convertase subtilisin/kexin type 9 (pcsk9) |
Family Cites Families (64)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US769101A (en) * | 1903-12-30 | 1904-08-30 | Melvin Mitchell | Attachment for grain-drills. |
YU163075A (en) | 1975-07-21 | 1982-05-31 | Science Union & Cie | Process for preparing new phenoxy derivatives |
JP2969359B2 (ja) | 1989-01-13 | 1999-11-02 | 武田薬品工業株式会社 | 環状アミン化合物 |
IE912760A1 (en) | 1990-08-06 | 1992-02-12 | Smith Kline French Lab | Compounds |
DK0641320T3 (da) | 1991-04-17 | 2001-08-20 | Upjohn Co | Substituerede (S)-3-phenylpiperidinderivater, deres fremstilling og deres anvendelse som dopaminautoreceptorantagonister |
US5236934A (en) | 1992-08-26 | 1993-08-17 | E. I. Du Pont De Nemours And Company | 1,2,3,4-tetrahydroisoquinolines useful in the treatment of CNS disorders |
JPH11501281A (ja) * | 1993-06-18 | 1999-02-02 | ユニバーシティ オブ シンシナティ | 神経ペプチドyアンタゴニスト及びアゴニスト |
US5863903A (en) | 1994-03-09 | 1999-01-26 | Novo Nordisk A/S | Use of hydroxy alkyl piperidine and pyrrolidine compounds to treat diabetes |
CA2187257A1 (en) | 1995-10-12 | 1997-04-13 | Enrique Luis Michelotti | Aryl-substituted cycloalkanes and cycloalkenes and herbicidal use thereof |
US5977134A (en) | 1996-12-05 | 1999-11-02 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
BR9810991A (pt) | 1997-07-11 | 2000-08-08 | Smithkline Beecham Plc | Novos compostos |
US6381025B1 (en) | 1999-08-19 | 2002-04-30 | Texas Tech University | Interferometric detection system and method |
EP1295873A4 (en) | 2000-06-14 | 2004-05-19 | METHODS OF PRODUCING RACEMIC PIPERIDINE DERIVATIVE AND PRODUCING OPTICALLY ACTIVE PIPERIDINE DERIVATIVE | |
US7148197B2 (en) * | 2000-08-24 | 2006-12-12 | The Regents Of The University Of California | Orally administered small peptides synergize statin activity |
AR031152A1 (es) | 2000-10-31 | 2003-09-10 | Upjohn Co | Tratamientos nuevos para el sindrome de piernas inquietas |
WO2003072558A2 (en) | 2002-02-22 | 2003-09-04 | Pharmacia & Upjohn Company | Arylsulfone derivatives |
US20040082641A1 (en) | 2002-10-28 | 2004-04-29 | Rytved Klaus Asger | Use of glycogen phosphorylase inhibitors for treatment of cardiovascular diseases |
WO2004043929A1 (en) | 2002-11-12 | 2004-05-27 | Pfizer Products Inc. | Quinoline derivatives |
SE0300010D0 (sv) | 2003-01-07 | 2003-01-07 | Astrazeneca Ab | Novel Compounds |
US20040192728A1 (en) | 2003-02-03 | 2004-09-30 | Ellen Codd | Quinoline-derived amide modulators of vanilloid VR1 receptor |
US20060293298A1 (en) | 2003-04-10 | 2006-12-28 | Bamford Mark J | Compounds |
WO2005000309A2 (en) | 2003-06-27 | 2005-01-06 | Ionix Pharmaceuticals Limited | Chemical compounds |
US7268232B2 (en) | 2004-05-17 | 2007-09-11 | Acadia Pharmaceuticals Inc. | Androgen receptor modulators and method of treating disease using the same |
WO2006049597A1 (en) * | 2004-10-27 | 2006-05-11 | Avanir Pharmaceuticals | Amino acid-derived compounds as modulators of the reverse cholesterol transport |
CA2613236A1 (en) | 2005-06-30 | 2007-01-11 | Prosidion Limited | G-protein coupled receptor agonists |
GB0514812D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
DE102005044817A1 (de) | 2005-09-20 | 2007-03-22 | Sanofi-Aventis Deutschland Gmbh | Substituierte 4-Phenyltetrahydroisochinoline, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament, sowie sie enthaltendes Medikament |
AU2006333522A1 (en) | 2005-12-21 | 2007-07-12 | Decode Genetics, Ehf. | Biaryl nitrogen heterocycle inhibitors of LTA4H for treating inflammation |
US20090042857A1 (en) | 2006-02-20 | 2009-02-12 | Masuo Yamaoka | Novel Pharmaceutical |
US7834178B2 (en) | 2006-03-01 | 2010-11-16 | Bristol-Myers Squibb Company | Triazine 11-beta hydroxysteroid dehydrogenase type 1 inhibitors |
US9187485B2 (en) | 2007-02-02 | 2015-11-17 | Baylor College Of Medicine | Methods and compositions for the treatment of cancer and related hyperproliferative disorders |
EP2170866B1 (en) | 2007-06-25 | 2014-08-13 | Amgen Inc. | Phthalazine compounds, compositions and methods of use |
US8445217B2 (en) | 2007-09-20 | 2013-05-21 | Vanderbilt University | Free solution measurement of molecular interactions by backscattering interferometry |
WO2009076372A2 (en) | 2007-12-10 | 2009-06-18 | Molecular Sensing, Inc. | Temperature-stable interferometer |
US8673850B2 (en) | 2008-05-30 | 2014-03-18 | Institut De Recherches Cliniques De Montreal | PCSK9 inhibitors and methods of use thereof |
US8324385B2 (en) | 2008-10-30 | 2012-12-04 | Madrigal Pharmaceuticals, Inc. | Diacylglycerol acyltransferase inhibitors |
EP2483266B1 (en) | 2009-10-01 | 2015-02-25 | Cadila Healthcare Limited | Compounds for the treatment of dyslipidemia and related diseases |
WO2012039660A1 (en) | 2010-09-20 | 2012-03-29 | A. Carlsson Research Ab | Phenylpiperidine compounds for the treatment of neurological and psychiatric disorders |
JP5934787B2 (ja) | 2011-05-10 | 2016-06-15 | ギリアード サイエンシーズ, インコーポレイテッド | イオンチャネルモジュレーターとしての縮合複素環式化合物 |
JOP20200043A1 (ar) | 2011-05-10 | 2017-06-16 | Amgen Inc | طرق معالجة أو منع الاضطرابات المختصة بالكوليسترول |
US20150057949A1 (en) | 2012-04-19 | 2015-02-26 | Molecular Sensing, Inc. | Event Detection For Back-Scattering Interferometry |
AU2013266087A1 (en) | 2012-05-25 | 2014-12-04 | Catabasis Pharmaceuticals, Inc. | Methods of lowering proprotein convertase subtilisin/kexin type 9 (PCSK9) |
WO2014002105A1 (en) | 2012-06-25 | 2014-01-03 | Cadila Healthcare Limited | Compounds for the treatment of dyslipidemia and other diseases |
WO2014101120A1 (en) | 2012-12-28 | 2014-07-03 | Merck Sharp & Dohme Corp. | Heterobicyclo-substituted-7-methoxy-[1,2,4]triazolo[1,5-c]quinazolin-5-amine compounds with a2a antagonist properties |
US10287317B2 (en) | 2013-02-15 | 2019-05-14 | Srx Cardio, Llc | Proprotein convertase subtilisin kexin type 9 (PCSK9) allosteric binding ligands to modulate serum low density lipoprotein (LDL) levels |
JP2016508722A (ja) | 2013-02-15 | 2016-03-24 | エスアールエックス カーディオ,エル エル シー | 血清低密度リポタンパク質(ldl)レベルを調節するためのpcsk9(プロタンパク質転換酵素サブチリシン/ケキシン9型)アロステリック結合リガンド |
ES2489815B1 (es) | 2013-02-21 | 2015-08-10 | Centro De Investigación Príncipe Felipe | Nuevos p-terfenilos hexakis-sustituidos con grupos bilaterales para el tratamiento de la infección por el virus de la inmunodeficiencia humana tipo 1 (VIH-1) y otras enfermedades |
CN105473141A (zh) | 2013-03-15 | 2016-04-06 | 实发生物医学公司 | 治疗和/或预防心血管疾病的抗pcsk9化合物和方法 |
WO2014150983A2 (en) * | 2013-03-15 | 2014-09-25 | Amgen Inc. | Human antigen binding proteins that bind to proprotein convertase subtilisin kexin type 9 |
WO2015024016A2 (en) | 2013-08-16 | 2015-02-19 | Duke University | 2-piperidinyl substituted n,3-dihydroxybutanamides |
WO2015058129A1 (en) | 2013-10-17 | 2015-04-23 | Blueprint Medicines Corporation | Compositions useful for treating disorders related to kit |
US10034892B2 (en) | 2014-08-21 | 2018-07-31 | Srx Cardio, Llc | Composition and methods of use of small molecules as binding ligands for the modulation of proprotein convertase subtilisin/kexin type 9(PCSK9) protein activity |
US20170267689A1 (en) | 2014-08-25 | 2017-09-21 | The Governors Of The University Of Alberta | Stimuli-switchable moieties, monomers and polymers incorporating stimuli-switchable moieties, and methods of making and using same |
WO2016107602A1 (zh) | 2015-01-01 | 2016-07-07 | 成都贝斯凯瑞生物科技有限公司 | 一类取代氮杂环衍生物及其应用 |
WO2016107603A1 (zh) | 2015-01-01 | 2016-07-07 | 成都贝斯凯瑞生物科技有限公司 | 取代氮杂环衍生物及其应用 |
WO2017034990A1 (en) | 2015-08-21 | 2017-03-02 | Portola Pharmaceuticals, Inc. | Composition and methods of use of tetrahydroisoquinoline small molecules to bind and modulate pcsk9 protein activity |
WO2017034994A1 (en) | 2015-08-21 | 2017-03-02 | Portola Pharmaceuticals, Inc. | Composition and methods of use of novel phenylalanine small organic compounds to directly modulate pcsk9 protein activity |
EP3337788A4 (en) | 2015-08-21 | 2019-03-27 | Portola Pharmaceuticals, Inc. | PHENYLPIPERAZINE PROPROTEIN CONVERTASE SUBTILISIN / -KEXIN TYPE 9 P (CSK9) MODULATORS AND THEIR USE |
DK3386511T3 (da) | 2015-12-10 | 2021-07-05 | Ptc Therapeutics Inc | Fremgangsmåder til behandling af huntingtons sygdom |
US20190119236A1 (en) | 2016-02-23 | 2019-04-25 | Portola Pharmaceuticals, Inc. | Compounds for binding proprotein convertase subtilisin/kexin type 9 (pcsk9) |
WO2018026866A1 (en) * | 2016-08-03 | 2018-02-08 | Neuropore Therapies, Inc. | Lipid-substituted amino 1,2-and 1,3-diol compounds as modulators of tlr2 dimerization |
EP3609882B1 (en) | 2017-03-17 | 2022-07-13 | Cardio Therapeutics Pty Ltd | Heterocyclic inhibitors of pcsk9 |
AU2020291468A1 (en) | 2019-06-14 | 2022-01-06 | Srx Cardio, Llc | Compounds for the modulation of proprotein convertase subtilisin/kexin type 9 (PCSK9) |
US20220193058A1 (en) | 2020-12-16 | 2022-06-23 | Srx Cardio, Llc | Compounds for the modulation of proprotein convertase subtilisin/kexin type 9 (pcsk9) |
-
2016
- 2016-08-19 WO PCT/US2016/047810 patent/WO2017034994A1/en active Application Filing
- 2016-08-19 US US15/753,768 patent/US10821106B2/en active Active
- 2016-08-19 EP EP16839890.7A patent/EP3337497B1/en active Active
-
2018
- 2018-12-20 HK HK18116351.9A patent/HK1257100A1/zh unknown
-
2020
- 2020-09-14 US US17/020,276 patent/US11944619B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
WO2017034994A1 (en) | 2017-03-02 |
EP3337497A1 (en) | 2018-06-27 |
EP3337497B1 (en) | 2023-07-12 |
US20180237381A1 (en) | 2018-08-23 |
US20210236481A1 (en) | 2021-08-05 |
US10821106B2 (en) | 2020-11-03 |
EP3337497A4 (en) | 2019-04-17 |
US11944619B2 (en) | 2024-04-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HK1257100A1 (zh) | 使用新型苯丙胺酸小分子有機化合物來直接調節pcsk9的蛋白活性的組合物和方法 | |
IL267090A (en) | Amine-disubstituted heterocyclic compounds as ehmt2 inhibitors and methods of using them | |
EP3268006A4 (en) | Pyrrolotriazine inhibitors of irak4 activity | |
EP3080100A4 (en) | Inhibitors of lysine specific demethylase-1 | |
HK1211471A1 (zh) | 通過抑制含布羅莫結構域蛋白 治療 介導的疾病 | |
CL2015000261A1 (es) | Alimento para peces de piscifactoría y método para promover el crecimiento de peces de piscifactoría usando el mismo. | |
EP3558303A4 (en) | AMINO ACID COMPOUNDS AND METHOD FOR USE | |
HK1213471A1 (zh) | 作為蛋白脫乙酰基酶抑制劑的嘧啶羥基酰胺化合物及其使用方法 | |
HK1222864A1 (zh) | 的小分子調節劑和其使用方法 | |
EP3407916A4 (en) | PHOSPHONATE LINKERS AND THEIR USE TO FACILITATE THE CELLULAR RETENTION OF COMPOUNDS | |
IL251111B (en) | An antibody capable of neutralizing a substance with alternative activity to coagulation factor viii (fviii) | |
EP3142652A4 (en) | Heterocyclic hydroxamic acids as protein deacetylase inhibitors and dual protein deacetylase-protein kinase inhibitors and methods of use thereof | |
EP3228626A4 (en) | Peptide having activity to improve skin condition and use thereof | |
EP2968244A4 (en) | COMPOSITIONS AND METHODS FOR USING ALIGAL COMPOUNDS | |
HK1260897A1 (zh) | 使用四氫異喹啉小分子來結合並調節pcsk9的蛋白活性的組合物和方法 | |
EP3313865A4 (en) | SYNTHETIC PEPTIDE COMPOUNDS AND METHODS OF USE | |
EP3191116A4 (en) | METHODS OF IDENTIFYING MODULATORS OF SESTRIN-GATOR2 INTERACTION AND USE OF SAME TO MODULATE mTORC1 | |
EP3092244A4 (en) | Dipeptides as inhibitors of human immunoproteasomes | |
EP3219324A4 (en) | Application of dipeptide as ace enzyme activity inhibitor | |
EP3198038A4 (en) | Compositions and methods to modulate cell activity | |
IL248567A0 (en) | Using compounds known as d-amino acid oxidase inhibitors | |
EP3445170A4 (en) | CHINOLINE COMPOUNDS AS RAGE ACTIVITY MODULATORS AND USES THEREOF | |
EP3193904A4 (en) | Dipeptidomimetics as inhibitors of human immunoproteasomes | |
EP3036219A4 (en) | Novel beta lactams as modulators of glutamate uptake and methods for use thereof | |
EP2994461A4 (en) | Methods of treating skin conditions using cyclolignan compounds |