GB0214147D0
(en)
*
|
2002-06-19 |
2002-07-31 |
Glaxo Group Ltd |
Formulations
|
PL375557A1
(en)
*
|
2002-08-23 |
2005-11-28 |
Pharmacia Corporation |
Crystalline solid form of (2s-5z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid
|
TWI328009B
(en)
|
2003-05-21 |
2010-08-01 |
Glaxo Group Ltd |
Quinoline derivatives as phosphodiesterase inhibitors
|
GB0316290D0
(en)
|
2003-07-11 |
2003-08-13 |
Glaxo Group Ltd |
Novel compounds
|
AR049384A1
(en)
|
2004-05-24 |
2006-07-26 |
Glaxo Group Ltd |
PURINA DERIVATIVES
|
TWI307630B
(en)
|
2004-07-01 |
2009-03-21 |
Glaxo Group Ltd |
Immunoglobulins
|
GB0418045D0
(en)
|
2004-08-12 |
2004-09-15 |
Glaxo Group Ltd |
Compounds
|
ATE517908T1
(en)
|
2005-01-10 |
2011-08-15 |
Glaxo Group Ltd |
ANDROSTAN-17-ALPHA-CARBONATE DERIVATIVES FOR USE IN THE TREATMENT OF ALLERGIC AND INFLAMMATORY CONDITIONS
|
UY29440A1
(en)
|
2005-03-25 |
2006-10-02 |
Glaxo Group Ltd |
NEW COMPOUNDS
|
PE20061193A1
(en)
|
2005-03-25 |
2006-12-02 |
Glaxo Group Ltd |
DERIVATIVES OF 3,4-DIHYDROPYRIMIDO [4,5-d] PYRIMIDIN-2- [1H] -0NA AS KINASE INHIBITORS p38
|
GB0514809D0
(en)
|
2005-07-19 |
2005-08-24 |
Glaxo Group Ltd |
Compounds
|
TW200730498A
(en)
|
2005-12-20 |
2007-08-16 |
Glaxo Group Ltd |
Compounds
|
BRPI0710240A2
(en)
|
2006-04-20 |
2011-08-09 |
Glaxo Group Ltd |
compound, use of a compound, method for treating a human or animal patient with a condition or disease, pharmaceutical composition, combination, and process for preparing a compound
|
GB0611587D0
(en)
|
2006-06-12 |
2006-07-19 |
Glaxo Group Ltd |
Novel compounds
|
DK2046787T3
(en)
|
2006-08-01 |
2011-07-18 |
Glaxo Group Ltd |
Pyrazolo [3,4-B] pyridine compounds, and their use as PDE4 inhibitors
|
WO2008147445A2
(en)
*
|
2006-11-09 |
2008-12-04 |
University Of Maryland, Baltimore |
Use of 5,6-dimethylxanthenone-4-acetic acid as an antimicrobial agent
|
AR065804A1
(en)
|
2007-03-23 |
2009-07-01 |
Smithkline Beecham Corp |
COMPOSITE OF INDOL CARBOXAMIDE, PHARMACEUTICAL COMPOSITION THAT UNDERSTANDS IT AND USE OF THIS COMPOUND TO PREPARE A MEDICINAL PRODUCT
|
KR20160129109A
(en)
|
2008-05-23 |
2016-11-08 |
아미라 파마슈티칼스 인코포레이티드 |
5-lipoxygenase-activating protein inhibitor
|
WO2009147187A1
(en)
|
2008-06-05 |
2009-12-10 |
Glaxo Group Limited |
4-carboxamide indazole derivatives useful as inhibitors of p13-kinases
|
JP5502077B2
(en)
|
2008-06-05 |
2014-05-28 |
グラクソ グループ リミテッド |
New compounds
|
WO2010094643A1
(en)
|
2009-02-17 |
2010-08-26 |
Glaxo Group Limited |
Quinoline derivatives and their uses for rhinitis and urticaria
|
EP2406255B1
(en)
|
2009-03-09 |
2015-04-29 |
Glaxo Group Limited |
4-oxadiazol-2-yl-indazoles as inhibitors of pi3 kinases
|
JP2012520257A
(en)
|
2009-03-10 |
2012-09-06 |
グラクソ グループ リミテッド |
Indole derivatives as IKK2 inhibitors
|
EP2408769A1
(en)
|
2009-03-17 |
2012-01-25 |
Glaxo Group Limited |
Pyrimidine derivatives used as itk inhibitors
|
WO2010107957A2
(en)
|
2009-03-19 |
2010-09-23 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF GATA BINDING PROTEIN 3 (GATA3) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
JP2012520683A
(en)
|
2009-03-19 |
2012-09-10 |
メルク・シャープ・エンド・ドーム・コーポレイション |
RNA interference-mediated inhibition of connective tissue growth factor (CTGF) gene expression using small interfering nucleic acids (siNA)
|
JP2012520686A
(en)
|
2009-03-19 |
2012-09-10 |
メルク・シャープ・エンド・ドーム・コーポレイション |
RNA interference-mediated inhibition of signal transduction transcription factor 6 (STAT6) gene expression using small interfering nucleic acids (siNA)
|
CN102439151A
(en)
|
2009-03-19 |
2012-05-02 |
默沙东公司 |
Rna interference mediated inhibition of btb and cnc homology 1, basic leucine zipper transcription factor 1 (bach 1) gene expression using short interfering nucleic acid (sina) sequence listing
|
JP2012521764A
(en)
|
2009-03-27 |
2012-09-20 |
メルク・シャープ・エンド・ドーム・コーポレイション |
RNA interference-mediated inhibition of thymic stromal lymphocyte formation factor (TSLP) gene expression using small interfering nucleic acids (siNA)
|
WO2010111464A1
(en)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF APOPTOSIS SIGNAL-REGULATING KINASE 1 (ASK1) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
EP2411018A2
(en)
|
2009-03-27 |
2012-02-01 |
Merck Sharp&Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF THE NERVE GROWTH FACTOR BETA CHAIN (NGFß) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (SINA)
|
SG174581A1
(en)
|
2009-03-27 |
2011-10-28 |
Merck Sharp & Dohme |
RNA INTERFERENCE MEDIATED INHIBITION OF THE INTERCELLULAR ADHESION MOLECULE 1 (ICAM-1)GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
WO2010111471A2
(en)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1 (STAT1) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
JP2012524754A
(en)
|
2009-04-24 |
2012-10-18 |
グラクソ グループ リミテッド |
Pyrazole and triazolcarboxamides as CRAC channel inhibitors
|
US8399436B2
(en)
|
2009-04-24 |
2013-03-19 |
Glaxo Group Limited |
N-pyrazolyl carboxamides as CRAC channel inhibitors
|
JO3025B1
(en)
|
2009-04-30 |
2016-09-05 |
Glaxo Group Ltd |
Oxazole substituted indazoles as pi3 - kinase inhibitors
|
EP2507226A1
(en)
|
2009-12-03 |
2012-10-10 |
Glaxo Group Limited |
Novel compounds
|
JP2013512880A
(en)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
Indazole derivatives as PI3-kinase inhibitors
|
JP2013512879A
(en)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
Benzpyrazole derivatives as inhibitors of PI3 kinase
|
WO2011084316A2
(en)
|
2009-12-16 |
2011-07-14 |
3M Innovative Properties Company |
Formulations and methods for controlling mdi particle size delivery
|
TWI375671B
(en)
*
|
2010-03-01 |
2012-11-01 |
Univ China Medical |
Pharmaceutical compositions containing brazilin for inhibiting expression of cytokines of t helper cell type ii and/or inhibiting expression of chemokines and uses of the same
|
WO2011110575A1
(en)
|
2010-03-11 |
2011-09-15 |
Glaxo Group Limited |
Derivatives of 2-[2-(benzo- or pyrido-) thiazolylamino]-6-aminopyridine, useful in the treatment of respiratoric, allergic or inflammatory diseases
|
GB201007203D0
(en)
|
2010-04-29 |
2010-06-16 |
Glaxo Group Ltd |
Novel compounds
|
DK2614058T3
(en)
|
2010-09-08 |
2015-09-28 |
Glaxosmithkline Ip Dev Ltd |
Polymorphs, and the salts of N- [5- [4- (5 - {[(2R, 6S) -2,6-dimethyl-4-morpholinyl] methyl} -1,3-oxazol-2-yl) -1H-indazole -6-yl] -2- (methyloxy) -3-pyridinyl] methanesulfonamide.
|
ES2602972T3
(en)
|
2010-09-08 |
2017-02-23 |
Glaxosmithkline Intellectual Property Development Limited |
Indazole derivatives for use in the treatment of influenza virus infection
|
WO2012035055A1
(en)
|
2010-09-17 |
2012-03-22 |
Glaxo Group Limited |
Novel compounds
|
JP5795643B2
(en)
|
2010-10-21 |
2015-10-14 |
グラクソ グループ リミテッドGlaxo Group Limited |
Pyrazole compounds acting on allergic, immune and inflammatory conditions
|
US9149462B2
(en)
|
2010-10-21 |
2015-10-06 |
Glaxo Group Limited |
Pyrazole compounds acting against allergic, inflammatory and immune disorders
|
GB201018124D0
(en)
|
2010-10-27 |
2010-12-08 |
Glaxo Group Ltd |
Polymorphs and salts
|
JP2012140390A
(en)
*
|
2011-01-06 |
2012-07-26 |
Sumitomo Chemical Co Ltd |
METHOD FOR PRODUCING α-AMINO-γ-BUTYROLACTONE
|
GB201104153D0
(en)
|
2011-03-11 |
2011-04-27 |
Glaxo Group Ltd |
Novel compounds
|
EP2683716A1
(en)
|
2011-03-11 |
2014-01-15 |
Glaxo Group Limited |
Pyrido[3,4-b]pyrazine derivatives as syk inhibitors
|
CN102344397B
(en)
*
|
2011-08-23 |
2013-09-04 |
浙江升华拜克生物股份有限公司 |
Method for purifying valnemulin hydrochloride
|
BR112016003229A8
(en)
|
2013-09-22 |
2020-02-04 |
Calitor Sciences Llc |
compound, pharmaceutical composition, and, use of a compound or pharmaceutical composition
|
WO2015148867A1
(en)
|
2014-03-28 |
2015-10-01 |
Calitor Sciences, Llc |
Substituted heteroaryl compounds and methods of use
|
CN107072976A
(en)
|
2014-05-12 |
2017-08-18 |
葛兰素史克知识产权第二有限公司 |
The pharmaceutical composition for including Danirixin for treating communicable disease
|
WO2017044434A1
(en)
|
2015-09-11 |
2017-03-16 |
Sunshine Lake Pharma Co., Ltd. |
Substituted heteroaryl compounds and methods of use
|
WO2017214159A1
(en)
*
|
2016-06-06 |
2017-12-14 |
The Regents Of The University Of California |
A host cell modified to produce lactams
|
JP7254076B2
(en)
|
2017-11-19 |
2023-04-07 |
サンシャイン・レイク・ファーマ・カンパニー・リミテッド |
Substituted heteroaryl compounds and methods of use
|
WO2019143874A1
(en)
|
2018-01-20 |
2019-07-25 |
Sunshine Lake Pharma Co., Ltd. |
Substituted aminopyrimidine compounds and methods of use
|
CN109369432B
(en)
*
|
2018-11-02 |
2021-06-25 |
永农生物科学有限公司 |
Preparation method of (S) -4-chloro-2-aminobutyrate
|
EP4125919A1
(en)
|
2020-03-26 |
2023-02-08 |
GlaxoSmithKline Intellectual Property Development Limited |
Cathepsin inhibitors for preventing or treating viral infections
|