US1044508A
(en)
*
|
1911-04-21 |
1912-11-19 |
Ajax Forge Company |
Railway-frog.
|
BE789948A
(en)
|
1971-10-13 |
1973-04-11 |
Sandoz Sa |
NEW DERIVATIVES OF PYRAZOLE, THEIR PREPARATION AND THEIR APPLICATION AS MEDICINAL PRODUCTS
|
JPS5113156B2
(en)
|
1972-10-21 |
1976-04-26 |
|
|
US4016037A
(en)
|
1975-10-15 |
1977-04-05 |
Ajinomoto Co., Inc. |
Method for producing L-amino acid
|
US4110536A
(en)
|
1977-04-18 |
1978-08-29 |
Miles Laboratories, Inc. |
Derivatives of 5-(indol-3-yl)hydantoin
|
DE2728523C2
(en)
|
1977-06-23 |
1986-02-27 |
Schering AG, 1000 Berlin und 4709 Bergkamen |
4-Methyl-1,2,3-thiadiazole-5-carboxylic acid (cyclohexylmethyl) amide, agents having a herbicidal and growth-regulating action, containing this compound and a process for its preparation
|
JPS55136279A
(en)
|
1979-04-09 |
1980-10-23 |
Ajinomoto Co Inc |
Preparation of tryptophan hydantoin
|
JPS5810074B2
(en)
|
1979-07-18 |
1983-02-24 |
味の素株式会社 |
new microorganisms
|
US4332952A
(en)
|
1980-07-28 |
1982-06-01 |
Pfizer Inc. |
Hypoglycemic 5-substituted oxazolidine-2,4-diones
|
SG56656G
(en)
|
1980-07-28 |
1987-03-27 |
Pfizer |
Hypoglycemic 5-substituted oxazolidine-2, 4-diones
|
DE3567460D1
(en)
|
1984-06-07 |
1989-02-16 |
Pfizer Ltd |
Dihydropyridines
|
JPS6122081A
(en)
|
1984-07-10 |
1986-01-30 |
Mitsui Toatsu Chem Inc |
Preparation of hydantoin compound
|
US4684735A
(en)
|
1985-07-01 |
1987-08-04 |
Stauffer Chemical Company |
Promotion of raney nickel hydrogenation catalyst
|
JPH0623148B2
(en)
|
1985-09-05 |
1994-03-30 |
三井東圧化学株式会社 |
Method for producing N-acetyl-DL-amino acid
|
CA1292840C
(en)
|
1985-09-26 |
1991-12-03 |
David Harry Hawke |
Sequencing of peptides
|
JPH0659227B2
(en)
|
1985-11-08 |
1994-08-10 |
三井東圧化学株式会社 |
Method for producing D-α-amino acid
|
JPS6225990A
(en)
|
1986-07-19 |
1987-02-03 |
Kanegafuchi Chem Ind Co Ltd |
Production of d-alpha-amino acid
|
US4705864A
(en)
|
1986-11-10 |
1987-11-10 |
The Standard Oil Company |
Aryl oxime derivatives of hydantoins
|
US4911931A
(en)
|
1987-08-03 |
1990-03-27 |
Baylink David J |
Pharmaceutical combination for treatment of bone-wasting diseases
|
JP2661111B2
(en)
|
1988-03-09 |
1997-10-08 |
三菱化学株式会社 |
Method for producing DN-carbamyl-α-amino acid
|
US4868061A
(en)
|
1988-05-19 |
1989-09-19 |
The Standard Oil Company |
Olefinic aryl oxime derivatives of hydantoins
|
IE940525L
(en)
|
1988-05-25 |
1989-11-25 |
Warner Lambert Co |
Known and selected novel arylmethylenyl derivatives of¹thiazolidinones, imidazolidinones and oxazolidinones useful¹as antiallergy agents and antiinflammatory agents
|
JPH0219363A
(en)
|
1988-07-06 |
1990-01-23 |
Fujisawa Pharmaceut Co Ltd |
Imidazolidine derivative
|
WO1990004183A1
(en)
|
1988-10-07 |
1990-04-19 |
Commonwealth Scientific And Industrial Research Organisation |
Method for preparation of thiohydantoins and for protein sequence analysis
|
DE58905691D1
(en)
|
1989-01-02 |
1993-10-28 |
Ruetgerswerke Ag |
Process for the production of L-alpha amino acids.
|
JPH054910A
(en)
|
1990-07-31 |
1993-01-14 |
Nikka Chem Co Ltd |
Cosmetic composition
|
CA2088195A1
(en)
|
1990-08-31 |
1992-03-01 |
David C. Horwell |
Cholecystokinin antagonists, their preparation and therapeutic use
|
JP2651755B2
(en)
|
1991-03-01 |
1997-09-10 |
富士写真フイルム株式会社 |
Silver halide color photographic materials
|
NZ242065A
(en)
|
1991-03-26 |
1996-06-25 |
Csl Ltd |
Delayed release implant having a degradable or rupturable polymeric coating
|
US5693643A
(en)
|
1991-09-16 |
1997-12-02 |
Merck & Co., Inc. |
Hydantoin and succinimide-substituted derivatives of spiroindanylcamphorsulfonyl oxytocin antagonists
|
DE69223573D1
(en)
|
1991-09-16 |
1998-01-29 |
Merck & Co Inc |
Hydantoin and succinimide substituted spiroindanylcamphorsulfonyl as oxytocin antagonists
|
EP0545478A1
(en)
|
1991-12-03 |
1993-06-09 |
MERCK SHARP & DOHME LTD. |
Heterocyclic compounds as tachykinin antagonists
|
JP3163361B2
(en)
|
1992-03-12 |
2001-05-08 |
味の素株式会社 |
Method for producing 5-alkylhydantoin derivative
|
US5574030A
(en)
|
1992-07-14 |
1996-11-12 |
Nippon Chemiphar Co., Ltd. |
N-aminoalkyl-substituted nitrogen-containing five membered heterocyclic compounds
|
PH31474A
(en)
|
1992-07-14 |
1998-11-03 |
Nippon Chemiphar Co |
N-aminoboalkyl-substituted nitrogen-containing five membered heterocyclic compounds.
|
US5830854A
(en)
|
1992-12-14 |
1998-11-03 |
Merck Sharp & Dohme, Limited |
Method of treating cystic fibrosis using a tachykinin receptor antagonist
|
US5338859A
(en)
|
1993-02-12 |
1994-08-16 |
Hoechst Celanese Corporation |
Process for the production of calcium salts of hydantoic acids
|
EP0640594A1
(en)
|
1993-08-23 |
1995-03-01 |
Fujirebio Inc. |
Hydantoin derivative as metalloprotease inhibitor
|
DE69513832T2
(en)
|
1994-09-08 |
2000-04-13 |
Lilly Co Eli |
EXCITATIVE AMINO ACID RECEPTOR ANTAGONISTS
|
AU4424496A
(en)
|
1995-03-27 |
1996-10-16 |
Warner-Lambert Company |
A method for the synthesis of mixtures of compounds
|
US6166054A
(en)
|
1995-03-31 |
2000-12-26 |
Nihon Nohyaku Co., Ltd. |
Agricultural and horticultural disease controller and a method for controlling the diseases
|
US5674734A
(en)
|
1995-05-18 |
1997-10-07 |
President And Fellows Of Harvard College |
Cell death protein
|
DE19519717C1
(en)
|
1995-05-30 |
1996-08-22 |
Degussa |
New microorganism DSM 9771 for prepn of L-alpha-amino acids
|
US6846839B1
(en)
|
1995-06-07 |
2005-01-25 |
Sugen, Inc. |
Methods for treating diseases and disorders related to unregulated angiogenesis and/or vasculogenesis
|
US5962478A
(en)
|
1995-09-19 |
1999-10-05 |
Margolin; Solomon B. |
Inhibition of tumor necrosis factor α
|
AU7457796A
(en)
|
1995-10-23 |
1997-05-15 |
Tularik Inc. |
Rip: novel human protein involved in tumor necrosis factor signal transduction, and screening assays
|
EP0907643B1
(en)
|
1996-04-24 |
2003-01-15 |
Novo Nordisk A/S |
Compounds with growth hormone releasing properties
|
EP0930305B1
(en)
|
1996-09-30 |
2003-05-14 |
Nihon Nohyaku Co., Ltd. |
1,2,3-thiadiazole derivatives and salts thereof, disease controlling agents for agricultural and horticultural use, and method for the use thereof
|
US5859190A
(en)
|
1997-02-04 |
1999-01-12 |
Trega Biosciences, Inc. |
Combinatorial libraries of hydantoin and thiohydantoin derivatives, methods of making the libraries and compounds therein
|
EP0966447B1
(en)
|
1997-03-03 |
2003-03-05 |
Boehringer Ingelheim Pharmaceuticals Inc. |
Small molecules useful in the treatment of inflammatory disease
|
IL126024A0
(en)
|
1998-03-19 |
1999-05-09 |
Yeda Res & Dev |
Modulators of the function of receptors of the tnf/ngf receptor family and other proteins
|
DE69907331T2
(en)
|
1998-07-30 |
2003-10-23 |
Nihon Nohyaku Co Ltd |
Fungicidal composition containing a 1,2,3-thiadiazole derivative and their use
|
DE59905623D1
(en)
|
1998-09-22 |
2003-06-26 |
Degussa |
Process for the preparation of imidazolidine-2,4-diones
|
US6020198A
(en)
|
1998-09-25 |
2000-02-01 |
Isis Pharmaceuticals Inc. |
Antisense modulation of RIP-1 expression
|
AU754989B2
(en)
|
1998-11-16 |
2002-11-28 |
Nippon Zoki Pharmaceutical Co., Ltd. |
A therapeutic agent for intractable vasculitis
|
WO2001007048A1
(en)
|
1999-07-21 |
2001-02-01 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Small molecules useful in the treatment of inflammatory disease
|
WO2001007044A1
(en)
|
1999-07-21 |
2001-02-01 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Small molecules useful in the treatment of inflammatory disease
|
US6756394B1
(en)
|
1999-10-15 |
2004-06-29 |
President And Fellow Of Harvard College |
Small molecule inhibitors of necrosis
|
WO2001028493A2
(en)
|
1999-10-15 |
2001-04-26 |
President And Fellows Of Harvard College |
Small molecule inhibitors of necrosis
|
US6706766B2
(en)
|
1999-12-13 |
2004-03-16 |
President And Fellows Of Harvard College |
Small molecules used to increase cell death
|
WO2001074807A1
(en)
|
2000-03-30 |
2001-10-11 |
Sagami Chemical Research Center |
Indolylpyrrole derivatives and cell death inhibitors
|
US20020155172A1
(en)
|
2000-04-07 |
2002-10-24 |
Junying Yuan |
Methods and compounds for decreasing cell toxicity or death
|
GB0011071D0
(en)
|
2000-05-08 |
2000-06-28 |
Novartis Ag |
Organic compounds
|
US6846643B2
(en)
|
2000-08-14 |
2005-01-25 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Methods and molecules useful for identifying molecules that bind LFA-1 and for determining receptor occupancy
|
US20020064736A1
(en)
|
2000-09-27 |
2002-05-30 |
Fuji Photo Film Co., Ltd. |
Dye-forming coupler, silver halide photographic light-sensitive material, and method for producing an azomethine dye
|
JP2002145192A
(en)
|
2000-11-07 |
2002-05-22 |
Yamaha Motor Co Ltd |
Fuel tank structure for surface vehicle
|
JP4529338B2
(en)
|
2001-03-08 |
2010-08-25 |
味の素株式会社 |
DNA encoding hydantoinase, DNA encoding N-carbamyl-L-amino acid hydrolase, recombinant DNA, transformed cell, protein production method and optically active amino acid production method
|
HUP0401492A3
(en)
|
2001-09-14 |
2008-05-28 |
Novo Nordisk As |
Novel ligands for the hisb10 zn2+ sites of r-state insulin hexa
|
AU2002363655A1
(en)
|
2001-11-14 |
2003-05-26 |
Novartis Ag |
Non-peptide somatostatin receptor ligands
|
JPWO2003043988A1
(en)
|
2001-11-22 |
2005-03-10 |
小野薬品工業株式会社 |
Piperidin-2-one derivative compound and drug containing the compound as an active ingredient
|
US6797708B2
(en)
|
2001-12-03 |
2004-09-28 |
Wyeth |
Inhibitors of cytosolic phospholipase A2
|
JP3659224B2
(en)
|
2001-12-26 |
2005-06-15 |
村田機械株式会社 |
Internet facsimile machine
|
US7189856B2
(en)
|
2001-12-28 |
2007-03-13 |
Gideon Shapiro |
Non-peptide somatostatin receptor ligands
|
WO2003068914A2
(en)
|
2002-02-11 |
2003-08-21 |
Wyeth |
Solution structure of rip dd and uses therof
|
WO2004023146A2
(en)
|
2002-09-06 |
2004-03-18 |
Mount Sinai Hospital |
Methods for assaying protein-protein interactions
|
WO2004050894A2
(en)
|
2002-11-27 |
2004-06-17 |
Artesian Therapeutics, Inc. |
Heart failure gene determination and therapeutic screening
|
WO2004056347A2
(en)
|
2002-12-20 |
2004-07-08 |
Novo Nordisk A/S |
Pharmaceutical compositions comprising insulin and legends of insulin hexamer
|
FR2850652B1
(en)
|
2003-01-31 |
2008-05-30 |
Aventis Pharma Sa |
NOVEL CYCLIC UREA DERIVATIVES, THEIR PREPARATION AND THEIR PHARMACEUTICAL USE AS INHIBITORS OF KINASES
|
GB0302671D0
(en)
|
2003-02-06 |
2003-03-12 |
Astrazeneca Ab |
Pharmaceutical formulations
|
US7320986B2
(en)
|
2003-03-07 |
2008-01-22 |
Abbott Labortories |
Fused tri and tetra-cyclic pyrazole kinase inhibitors
|
EP1610812A1
(en)
|
2003-03-11 |
2006-01-04 |
Novo Nordisk A/S |
Pharmaceutical preparations comprising acid-stabilised insulin
|
EP1605967A1
(en)
|
2003-03-13 |
2005-12-21 |
Novo Nordisk A/S |
Novel nph insulin preparations
|
SI2384753T1
(en)
*
|
2003-08-29 |
2016-06-30 |
The Brigham And Women's Hospital, Inc. |
Hydantoin derivatives as inhibitors of cellular necrosis
|
JP4452914B2
(en)
|
2003-09-08 |
2010-04-21 |
味の素株式会社 |
Novel transporter protein
|
DE10342839A1
(en)
|
2003-09-17 |
2005-04-28 |
Symrise Gmbh & Co Kg |
Use of hydantoin derivatives for cosmetic, dermatological or therapeutic lightening of the skin and hair, act by inhibiting tyrosinase or other processes involved in pigmentation
|
US20080019909A1
(en)
|
2003-09-17 |
2008-01-24 |
Francis Ka-Ming Chan |
Modulation of Programmed Necrosis
|
US6887993B1
(en)
|
2003-11-12 |
2005-05-03 |
Kosan Biosciences, Inc. |
11-O-methylgeldanamycin compounds
|
US8097629B2
(en)
|
2004-02-19 |
2012-01-17 |
Bayer Pharma Aktiengesellschaft |
Dihydropyridinone derivatives
|
US7935510B2
(en)
|
2004-04-30 |
2011-05-03 |
Intrexon Corporation |
Mutant receptors and their use in a nuclear receptor-based inducible gene expression system
|
GB0410379D0
(en)
|
2004-05-11 |
2004-06-16 |
Univ Leicester |
Treatment of cancer
|
KR101155288B1
(en)
|
2004-07-30 |
2012-07-02 |
엑셀리시스, 인코포레이티드 |
Pyrrole Derivatives as Pharmaceutical Agents
|
US7595337B2
(en)
|
2005-02-10 |
2009-09-29 |
Merck & Co. Inc. |
Mitotic kinesin inhibitors
|
WO2006103995A1
(en)
|
2005-03-25 |
2006-10-05 |
Kaneka Corporation |
PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE α-AMINO ACID DERIVATIVE
|
BRPI0615307A2
(en)
|
2005-08-25 |
2009-08-04 |
Schering Corp |
alpha2c adrenoreceptor agonists
|
BRPI0617271A2
(en)
|
2005-10-11 |
2011-07-19 |
Intermune Inc |
viral replication inhibitors
|
CA2628259A1
(en)
|
2005-11-01 |
2007-05-10 |
Janssen Pharmaceutica N.V. |
Dihydroisoindolones as allosteric modulators of glucokinase
|
EP1968583A4
(en)
|
2005-12-20 |
2010-09-15 |
Harvard College |
Compounds, screens, and methods of treatment
|
AR056882A1
(en)
|
2006-02-01 |
2007-10-31 |
Bayer Cropscience Sa |
DERIVATIVES OF THE FUNGICIDE N- CICLOALQUIL- BENCIL- AMIDA
|
US8007790B2
(en)
|
2006-04-03 |
2011-08-30 |
Stowers Institute For Medical Research |
Methods for treating polycystic kidney disease (PKD) or other cyst forming diseases
|
EP2041141A2
(en)
|
2006-07-13 |
2009-04-01 |
4Sc Ag |
Benzopyranopyrazoles
|
EP2076134A4
(en)
|
2006-10-10 |
2020-07-29 |
President and Fellows of Harvard College |
Compounds, screens, and methods of treatment
|
ATE551328T1
(en)
|
2007-06-06 |
2012-04-15 |
Dsm Sinochem Pharm Nl Bv |
NOVEL 5-SUBSTITUTED HYDANTOINS
|
EP3034494A1
(en)
|
2007-08-15 |
2016-06-22 |
President and Fellows of Harvard College |
Heterocyclic inhibitors of necroptosis
|
JP2011517313A
(en)
|
2007-12-11 |
2011-06-02 |
ビアメト ファーマシューティカルズ,インク. |
Metalloenzyme inhibitors that use a metal binding moiety in combination with a targeting moiety
|
EP2245182A1
(en)
|
2008-02-14 |
2010-11-03 |
F. Hoffmann-La Roche AG |
Prediction of bone marrow toxicity
|
US20120061324A1
(en)
*
|
2008-03-28 |
2012-03-15 |
Global Material Technologies, Inc. |
Element removal process and apparatus
|
US8304421B2
(en)
|
2008-09-30 |
2012-11-06 |
Vanderbilt University |
Indole compounds and their use as radiation sensitizing agents and chemotherapeutic agents
|
WO2010075290A1
(en)
|
2008-12-22 |
2010-07-01 |
President And Fellows Of Harvard College |
Unsaturated heterocyclic inhibitors of necroptosis
|
JP2012513481A
(en)
|
2008-12-23 |
2012-06-14 |
プレジデント アンド フェロウズ オブ ハーバード カレッジ |
Small molecule inhibitors of necrotosis
|
JP2010202575A
(en)
|
2009-03-03 |
2010-09-16 |
Takeda Chem Ind Ltd |
Heterocyclic compound
|
DE102009002044A1
(en)
|
2009-03-31 |
2010-10-07 |
Evonik Degussa Gmbh |
Dipeptides as feed additives
|
JP5332882B2
(en)
|
2009-04-30 |
2013-11-06 |
豊田合成株式会社 |
Semiconductor light emitting device
|
JP2010275229A
(en)
|
2009-05-28 |
2010-12-09 |
Ikutoku Gakuen |
Hydantoin derivative
|
EP2519517B1
(en)
|
2009-12-29 |
2015-03-25 |
Dana-Farber Cancer Institute, Inc. |
Type ii raf kinase inhibitors
|
AR080234A1
(en)
|
2010-02-25 |
2012-03-21 |
Marrone Bio Innovations Inc |
BACTERIAL CEPA ISOLATED FROM THE BURKHOLDERIA AND METABOLITES PESTICIDES OF THE SAME
|
KR20130006664A
(en)
|
2010-03-16 |
2013-01-17 |
다나-파버 캔서 인스티튜트 인크. |
Indazole compounds and their uses
|
WO2011123609A1
(en)
|
2010-03-31 |
2011-10-06 |
Glaxo Group Limited |
Imidazolyl-imidazoles as kinase inhibitors
|
US20130137642A1
(en)
|
2010-04-23 |
2013-05-30 |
Demetrios Vavvas |
Methods and compositions for preserving photoreceptor and retinal pigment epithelial cells
|
US20140024598A1
(en)
|
2010-11-01 |
2014-01-23 |
Demetrios Vavvas |
Methods and compositions for preserving retinal ganglion cells
|
JP2014509852A
(en)
|
2011-03-07 |
2014-04-24 |
ジ・オハイオ・ステート・ユニバーシティ |
Mutagenic activity induced by microRNA-155 (miR-155) links inflammation and cancer
|
WO2012154858A1
(en)
|
2011-05-09 |
2012-11-15 |
Whitehead Institute For Biomedical Research |
Chaperone interaction assays and uses thereof
|
CN102850252B
(en)
|
2011-06-30 |
2014-08-13 |
山东大学 |
Preparation method for 3,5,5'-trisubstituted hydantoin
|
WO2013013826A1
(en)
|
2011-07-27 |
2013-01-31 |
Friedrich-Alexander-Universität Erlangen-Nürnberg |
Necroptosis inhibitors for the treatment of inflammatory diseases of the gastrointestinal tract
|
US9314328B2
(en)
|
2011-08-16 |
2016-04-19 |
W. L. Gore & Associates, Inc. |
Branched stent graft device and deployment
|
AU2012301466B2
(en)
|
2011-08-27 |
2015-07-23 |
Marrone Bio Innovations, Inc. |
Isolated bacterial strain of the genus Burkholderia and pesticidal metabolites therefrom-formulations and uses
|
US20140357570A1
(en)
*
|
2011-10-21 |
2014-12-04 |
Massachusetts Eye And Ear Infirmary |
Compositions comprising necrosis inhibitors, such as necrostatins, alone or in combination, for promoting axon regeneration and nerve function, thereby treating cns disorders
|
US8492556B2
(en)
|
2011-11-10 |
2013-07-23 |
Allergan, Inc. |
2,5-Dioxoimidazolidin-1-yl-3-phenylurea derivatives as formyl peptide receptor like-1 (FPRL-1) receptor modulators
|
EP2844764B1
(en)
|
2012-05-04 |
2016-06-22 |
Novartis AG |
Biomarkers for iap inhibitor therapy
|
EP2864362A4
(en)
|
2012-06-26 |
2015-11-18 |
Biovalence Sdn Bhd |
Anticancer treatment
|
US20150185215A1
(en)
|
2012-07-02 |
2015-07-02 |
Cell Assay Innovations, Inc. |
Cell-Based Assays For Post-Translational Enzyme Activity
|
JPWO2014126127A1
(en)
|
2013-02-13 |
2017-02-02 |
国立大学法人北海道大学 |
Pharmaceutical composition for treatment of necroptosis-related diseases and method for screening active ingredients thereof
|
TWI637951B
(en)
|
2013-02-15 |
2018-10-11 |
英商葛蘭素史克智慧財產發展有限公司 |
Heterocyclic amides as kinase inhibitors
|
WO2014134351A2
(en)
|
2013-02-27 |
2014-09-04 |
The Broad Institute, Inc. |
T cell balance gene expression, compositions of matters and methods of use thereof
|
WO2014152182A1
(en)
*
|
2013-03-15 |
2014-09-25 |
President And Fellows Of Harvard College |
Deuterated heterocyclic inhibitors of necroptosis
|
WO2014145022A1
(en)
|
2013-03-15 |
2014-09-18 |
President And Fellows Of Harvard College |
Hybrid necroptosis inhibitors
|
HUE034308T2
(en)
|
2013-03-21 |
2018-02-28 |
Sanofi Aventis Deutschland |
Synthesis of hydantoin containing peptide products
|
US20160051629A1
(en)
|
2013-04-15 |
2016-02-25 |
Yeda Research And Development Co. Ltd. |
Inhibition of rip kinases for treating lysosomal storage diseases
|
GB201316651D0
(en)
|
2013-09-19 |
2013-11-06 |
Univ Southampton |
Asthma
|
WO2015039705A1
(en)
|
2013-09-23 |
2015-03-26 |
Carl Zeiss Smt Gmbh |
Multilayer mirror
|
EP2857839A1
(en)
|
2013-10-01 |
2015-04-08 |
AIT Austrian Institute of Technology GmbH |
Breast cancer diagnostic method and means
|
US20150147780A1
(en)
|
2013-11-22 |
2015-05-28 |
World Biotechnology LLC |
Method for harvesting organic compounds from genetically modified organisms
|
WO2015095449A1
(en)
|
2013-12-19 |
2015-06-25 |
Ptc Therapeutics, Inc. |
Methods for modulating the amount rna transcripts
|
EP3082820B1
(en)
|
2013-12-19 |
2022-07-20 |
PTC Therapeutics, Inc. |
Methods for modulating the amount of rna transcripts
|
US20150191511A1
(en)
|
2014-01-08 |
2015-07-09 |
World Biotechnology LLC |
Genetically Modified Organisms to Produce Organic Compounds
|
WO2015154197A1
(en)
|
2014-04-11 |
2015-10-15 |
Children's Hospital Of Eastern Ontario Research Institute Inc. |
Compositions and methods for glioblastoma treatment
|
US20170226514A1
(en)
|
2014-08-13 |
2017-08-10 |
MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. |
Prevention of tumour metastasis by inhibition of necroptosis
|
US20160045609A1
(en)
|
2014-08-14 |
2016-02-18 |
Mamoun M. Alhamadsheh |
Conjugation of pharmaceutically active agents with transthyretin ligands through adjustable linkers to increase serum half-life
|
WO2016044777A1
(en)
|
2014-09-18 |
2016-03-24 |
Abbvie Inc. |
Hat inhibitors and methods for their use
|
EP3017825A1
(en)
|
2014-11-06 |
2016-05-11 |
Ludwig-Maximilians-Universität München |
An inhibitor of the RIPK1-dependent necrosis pathway and a pharmaceutical composition comprising the same
|
EP3229807A4
(en)
|
2014-12-11 |
2018-10-17 |
President and Fellows of Harvard College |
Inhibitors of cellular necrosis and related methods
|
JP6772141B2
(en)
|
2014-12-24 |
2020-10-21 |
ナショナル・インスティチュート・オブ・バイオロジカル・サイエンシズ,ベイジン |
Necrosis inhibitor
|
AU2015371824B2
(en)
|
2014-12-24 |
2019-09-19 |
National Institute Of Biological Sciences, Beijing |
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|