US4709016A
(en)
|
1982-02-01 |
1987-11-24 |
Northeastern University |
Molecular analytical release tags and their use in chemical analysis
|
US5516931A
(en)
|
1982-02-01 |
1996-05-14 |
Northeastern University |
Release tag compounds producing ketone signal groups
|
US4650750A
(en)
|
1982-02-01 |
1987-03-17 |
Giese Roger W |
Method of chemical analysis employing molecular release tag compounds
|
US5650270A
(en)
|
1982-02-01 |
1997-07-22 |
Northeastern University |
Molecular analytical release tags and their use in chemical analysis
|
US5360811A
(en)
|
1990-03-13 |
1994-11-01 |
Hoechst-Roussel Pharmaceuticals Incorporated |
1-alkyl-, 1-alkenyl-, and 1-alkynylaryl-2-amino-1,3-propanediols and related compounds as anti-inflammatory agents
|
JP3545461B2
(ja)
|
1993-09-10 |
2004-07-21 |
エーザイ株式会社 |
二環式ヘテロ環含有スルホンアミド誘導体
|
US6281230B1
(en)
|
1996-07-24 |
2001-08-28 |
Celgene Corporation |
Isoindolines, method of use, and pharmaceutical compositions
|
US6306663B1
(en)
|
1999-02-12 |
2001-10-23 |
Proteinex, Inc. |
Controlling protein levels in eucaryotic organisms
|
ATE380031T1
(de)
|
1999-12-10 |
2007-12-15 |
Pfizer Prod Inc |
Pyrrolo 2,3-d pyrimidinderivate enthaltende zusammensetzungen
|
DE10002509A1
(de)
|
2000-01-21 |
2001-07-26 |
Gruenenthal Gmbh |
Substituierte Glutarimide
|
EP1259514B9
(en)
|
2000-02-28 |
2005-11-09 |
Sugen, Inc. |
3-(pyrolyllactone)-2-indolinone compounds as kinase inhibitors
|
PE20020354A1
(es)
|
2000-09-01 |
2002-06-12 |
Novartis Ag |
Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
|
WO2002020740A2
(en)
|
2000-09-08 |
2002-03-14 |
California Institute Of Technology |
Proteolysis targeting chimeric pharmaceutical
|
US7208157B2
(en)
|
2000-09-08 |
2007-04-24 |
California Institute Of Technology |
Proteolysis targeting chimeric pharmaceutical
|
EP1389617B1
(en)
|
2001-04-27 |
2007-01-03 |
Zenyaku Kogyo Kabushiki Kaisha |
Heterocyclic compound and antitumor agent containing the same as active ingredient
|
TWI329105B
(en)
|
2002-02-01 |
2010-08-21 |
Rigel Pharmaceuticals Inc |
2,4-pyrimidinediamine compounds and their uses
|
WO2004019973A1
(en)
|
2002-08-14 |
2004-03-11 |
Atugen Ag |
Use of protein kinase n beta
|
CN1826331A
(zh)
|
2003-04-03 |
2006-08-30 |
塞马福尔药业公司 |
Pi-3激酶抑制剂前药
|
AU2004242928B2
(en)
|
2003-05-30 |
2011-03-10 |
Gemin X Pharmaceuticals Canada Inc. |
Triheterocyclic compounds, compositions, and methods for treating cancer or viral diseases
|
EP2371835A1
(en)
|
2003-07-03 |
2011-10-05 |
The Trustees Of The University Of Pennsylvania |
Inhibition of syk kinase expression
|
JP4398263B2
(ja)
|
2004-01-13 |
2010-01-13 |
富士通株式会社 |
経路設計方法
|
SI3153514T1
(sl)
|
2004-05-13 |
2022-02-28 |
Icos Corporation |
Kinazolinoni kot zaviralci človeške fosfatidilinozitol 3-kinaze delta
|
TWI309240B
(en)
|
2004-09-17 |
2009-05-01 |
Hoffmann La Roche |
Anti-ox40l antibodies
|
CN101115761B
(zh)
|
2005-01-19 |
2012-07-18 |
里格尔药品股份有限公司 |
2,4-嘧啶二胺化合物的前药及其应用
|
WO2006105021A2
(en)
|
2005-03-25 |
2006-10-05 |
Tolerrx, Inc. |
Gitr binding molecules and uses therefor
|
ES2493466T3
(es)
|
2005-05-12 |
2014-09-11 |
Abbvie Bahamas Ltd. |
Promotores de la apoptosis
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
EP2982379A1
(en)
|
2005-07-01 |
2016-02-10 |
E. R. Squibb & Sons, L.L.C. |
Human monoclonal antibodies to programmed death ligand 1 (pd-l1)
|
US7402325B2
(en)
|
2005-07-28 |
2008-07-22 |
Phoenix Biotechnology, Inc. |
Supercritical carbon dioxide extract of pharmacologically active components from Nerium oleander
|
AU2006302179C1
(en)
|
2005-10-07 |
2013-06-20 |
Exelixis, Inc. |
N- (3-amino-quinoxalin-2-yl) -sulfonamide derivatives and their use as phosphatidylinositol 3-kinase inhibitors
|
JP5191391B2
(ja)
|
2005-11-01 |
2013-05-08 |
ターゲジェン インコーポレーティッド |
キナーゼのビ−アリールメタ−ピリミジン阻害剤
|
LT2426129T
(lt)
|
2005-12-13 |
2017-02-10 |
Incyte Holdings Corporation |
Heteroarilu pakeisti pirolo[2,3-b]piridinai ir pirolo[2,3-b]pirimidinai kaip janus kinazės inhibitoriai
|
RU2494095C2
(ru)
|
2005-12-23 |
2013-09-27 |
Вайет |
Модифицированные миметики лизина
|
JO2660B1
(en)
|
2006-01-20 |
2012-06-17 |
نوفارتيس ايه جي |
Pi-3 inhibitors and methods of use
|
JP5148597B2
(ja)
|
2006-04-26 |
2013-02-20 |
エフ.ホフマン−ラ ロシュ アーゲー |
医薬化合物
|
KR101464424B1
(ko)
|
2006-09-22 |
2014-11-27 |
파마시클릭스, 인코포레이티드 |
브루톤 티로신 키나제 억제제
|
US20100279316A1
(en)
|
2007-01-19 |
2010-11-04 |
Leonid Gorelik |
Antibodies to Phosphorylated IRAK4
|
WO2008109943A1
(en)
|
2007-03-12 |
2008-09-18 |
Cytopia Research Pty Ltd |
Phenyl amino pyrimidine compounds and uses thereof
|
WO2008118802A1
(en)
|
2007-03-23 |
2008-10-02 |
Regents Of The University Of Minnesota |
Therapeutic compounds
|
EP1987839A1
(en)
|
2007-04-30 |
2008-11-05 |
I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale |
Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease
|
PE20090717A1
(es)
|
2007-05-18 |
2009-07-18 |
Smithkline Beecham Corp |
Derivados de quinolina como inhibidores de la pi3 quinasa
|
CA2693677C
(en)
|
2007-07-12 |
2018-02-13 |
Tolerx, Inc. |
Combination therapies employing gitr binding molecules
|
EP2044949A1
(en)
|
2007-10-05 |
2009-04-08 |
Immutep |
Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response
|
CA2960659C
(en)
|
2007-11-09 |
2021-07-13 |
The Salk Institute For Biological Studies |
Use of tam receptor inhibitors as immunoenhancers and tam activators as immunosuppressors
|
JP5583592B2
(ja)
|
2007-11-30 |
2014-09-03 |
ニューリンク ジェネティクス コーポレイション |
Ido阻害剤
|
JP5275371B2
(ja)
|
2008-03-11 |
2013-08-28 |
インサイト・コーポレイション |
Jak阻害剤としてのアゼチジン誘導体およびシクロブタン誘導体
|
CN102083429B
(zh)
|
2008-04-24 |
2014-05-28 |
新联基因公司 |
Ido抑制剂
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
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
|
PT2376535T
(pt)
|
2008-12-09 |
2017-06-23 |
Hoffmann La Roche |
Anticorpos anti-pd-l1 e a sua utilização para a melhoria do funcionamento das células t
|
US8921037B2
(en)
|
2008-12-16 |
2014-12-30 |
Bo Han |
PF4-depleted platelet rich plasma preparations and methods for hard and soft tissue repair
|
US8709424B2
(en)
|
2009-09-03 |
2014-04-29 |
Merck Sharp & Dohme Corp. |
Anti-GITR antibodies
|
JP2012254939A
(ja)
|
2009-10-07 |
2012-12-27 |
Astellas Pharma Inc |
オキサゾール化合物
|
EP2493862B1
(en)
|
2009-10-28 |
2016-10-05 |
Newlink Genetics Corporation |
Imidazole derivatives as ido inhibitors
|
PL2510010T3
(pl)
|
2009-12-10 |
2016-05-31 |
Hoffmann La Roche |
Przeciwciała wiążące zewnątrzkomórkową domenę 4 ludzkiego CSF1R i ich zastosowanie
|
MX2012009237A
(es)
*
|
2010-02-11 |
2012-08-23 |
Celgene Corp |
Derivados de arilmetoxi isoindolina y composiciones que los comprenden y metodos para utilizar los mismos.
|
MA34062B1
(fr)
|
2010-03-04 |
2013-03-05 |
Macrogenics Inc |
Anticorps réagissant avec b7-h3, fragments immunologiquement actifs associés et utilisations associées
|
RU2617966C2
(ru)
|
2010-03-05 |
2017-04-28 |
Ф.Хоффманн-Ля Рош Аг |
Антитела против csf-1r человека и их применение
|
CN102918060B
(zh)
|
2010-03-05 |
2016-04-06 |
霍夫曼-拉罗奇有限公司 |
抗人csf-1r抗体及其用途
|
US8114621B2
(en)
|
2010-03-12 |
2012-02-14 |
Saladax Biomedical Inc. |
Lenalidomide and thalidomide immunoassays
|
EP3943154A1
(en)
|
2010-05-04 |
2022-01-26 |
Five Prime Therapeutics, Inc. |
Antibodies that bind csf1r
|
AU2011272860A1
(en)
|
2010-06-30 |
2013-02-07 |
Brandeis University |
Small-molecule-targeted protein degradation
|
JP5985473B2
(ja)
|
2010-07-13 |
2016-09-06 |
エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft |
IRAK4モジュレーターとしてのピラゾロ[1,5a]ピリミジン及びチエノ[3,2b]ピリミジン誘導体
|
KR101527300B1
(ko)
|
2010-09-09 |
2015-06-09 |
화이자 인코포레이티드 |
4-1bb 결합 분자
|
RU2017135541A
(ru)
|
2010-11-19 |
2019-02-08 |
Лиганд Фармасьютикалс Инкорпорейтед |
Гетероциклические амины и их применения
|
EP2649099A4
(en)
|
2010-12-07 |
2016-10-19 |
Univ Yale |
SMALL MOLECULAR HYDROPHOBIC LABELING OF FUSION PROTEINS AND INDUCED REMOVAL FROM THIS
|
PH12013501201A1
(en)
|
2010-12-09 |
2013-07-29 |
Univ Pennsylvania |
Use of chimeric antigen receptor-modified t cells to treat cancer
|
US9073892B2
(en)
|
2010-12-20 |
2015-07-07 |
Merck Serono S.A. |
Indazolyl triazol derivatives
|
US8703941B2
(en)
|
2011-01-10 |
2014-04-22 |
Nimbus Iris, Inc. |
IRAK inhibitors and uses thereof
|
WO2012129258A1
(en)
|
2011-03-22 |
2012-09-27 |
Merck Sharp & Dohme Corp. |
Amidopyrazole inhibitors of interleukin receptor-associated kinases
|
NO2694640T3
(pt)
|
2011-04-15 |
2018-03-17 |
|
|
RS57324B1
(sr)
|
2011-04-20 |
2018-08-31 |
Medimmune Llc |
Antitela i drugi molekuli koji vezuju b7-h1 i pd-1
|
WO2013042137A1
(en)
|
2011-09-19 |
2013-03-28 |
Aurigene Discovery Technologies Limited |
Bicyclic heterocycles as irak4 inhibitors
|
US9221809B2
(en)
|
2011-10-31 |
2015-12-29 |
Merck Sharp & Dohme Corp. |
Aminopyrimidinones as interleukin receptor-associated kinase inhibitors
|
HUE051954T2
(hu)
|
2011-11-28 |
2021-03-29 |
Merck Patent Gmbh |
ANTI-PD-L1 ellenanyagok és alkalmazásaik
|
JP6242804B2
(ja)
|
2011-12-15 |
2017-12-06 |
エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト |
ヒトcsf−1rに対する抗体及びその使用
|
AU2013207972B2
(en)
|
2012-01-10 |
2017-06-15 |
Nimbus Iris, Inc. |
IRAK inhibitors and uses thereof
|
WO2013106646A2
(en)
|
2012-01-12 |
2013-07-18 |
Yale University |
Compounds and methods for the inhibition of vcb e3 ubiquitin ligase
|
JP2015508414A
(ja)
|
2012-01-12 |
2015-03-19 |
イエール ユニバーシティ |
E3ユビキチンリガーゼによる標的タンパク質および他のポリペプチドの分解増強のための化合物および方法
|
US8987311B2
(en)
|
2012-01-13 |
2015-03-24 |
Bristol-Myers Squibb Company |
Triazolyl-substituted pyridyl compounds useful as kinase inhibitors
|
US9242975B2
(en)
|
2012-01-13 |
2016-01-26 |
Bristol-Myers Squibb Company |
Heterocyclic-substituted pyridyl compounds useful as kinase inhibitors
|
JP6096219B2
(ja)
|
2012-01-13 |
2017-03-15 |
ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company |
キナーゼ阻害剤として有用なトリアゾリルまたはトリアジアゾリル置換されたピリジル化合物
|
KR20140127855A
(ko)
|
2012-02-06 |
2014-11-04 |
제넨테크, 인크. |
Csf1r 억제제를 사용하는 조성물 및 방법
|
AR090263A1
(es)
|
2012-03-08 |
2014-10-29 |
Hoffmann La Roche |
Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma
|
JP2015517490A
(ja)
|
2012-05-11 |
2015-06-22 |
ファイブ プライム セラピューティックス インコーポレイテッド |
コロニー刺激因子1受容体(csf1r)を結合させる抗体を用いて状態を治療する方法
|
UY34887A
(es)
|
2012-07-02 |
2013-12-31 |
Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware |
Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos
|
DK2872501T3
(en)
|
2012-07-10 |
2016-08-29 |
Ares Trading Sa |
PYRIMIDINE PYRAZOLYL DERIVATIVES
|
US20140018361A1
(en)
|
2012-07-11 |
2014-01-16 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
US9085586B2
(en)
|
2012-07-11 |
2015-07-21 |
Nimbus Iris, Inc. |
IRAK inhibitors and uses thereof
|
AU2013290080A1
(en)
|
2012-07-11 |
2015-01-29 |
Nimbus Iris, Inc. |
IRAK inhibitors and uses thereof
|
US20140079699A1
(en)
|
2012-08-31 |
2014-03-20 |
Five Prime Therapeutics, Inc. |
Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r)
|
EP2897972B1
(en)
|
2012-09-19 |
2016-11-30 |
F. Hoffmann-La Roche AG |
2-oxo-2,3,4,5-tetrahydro-1h-benzo[b]diazepines and their use in the treatment of cancer
|
WO2014058685A1
(en)
|
2012-10-08 |
2014-04-17 |
Merck Sharp & Dohme Corp. |
Inhibitors of irak4 activity
|
EP2903613B1
(en)
|
2012-10-08 |
2017-11-22 |
Merck Sharp & Dohme Corp. |
Pyrazole derivatives useful as inhibitors of irak4 activity
|
WO2014063061A1
(en)
|
2012-10-19 |
2014-04-24 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged small molecules as inducers of protein degradation
|
MX2015005562A
(es)
|
2012-11-08 |
2015-07-23 |
Squibb Bristol Myers Co |
Compuestos de piridilo sustituidos con heteroarilo utiles como moduladores de cinasa.
|
GB201311910D0
(en)
|
2013-07-03 |
2013-08-14 |
Glaxosmithkline Ip Dev Ltd |
Novel Compounds
|
PL2953944T3
(pl)
|
2013-02-07 |
2017-09-29 |
Merck Patent Gmbh |
Pochodne pirydazynonowe-amidowe
|
PT2953952T
(pt)
|
2013-02-07 |
2017-09-11 |
Merck Patent Gmbh |
Derivados de piridazinona macrocíclicos
|
US9617282B2
(en)
|
2013-03-15 |
2017-04-11 |
Biogen Ma Inc. |
Macrocyclic compounds as IRAK4 inhibitors for the treatment of inflammatory diseases
|
BR112016006319A2
(pt)
|
2013-09-27 |
2017-08-01 |
Nimbus Iris Inc |
inibidores de irak e usos dos mesmos
|
US9359365B2
(en)
|
2013-10-04 |
2016-06-07 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
JP6412148B2
(ja)
|
2013-11-08 |
2018-10-24 |
武田薬品工業株式会社 |
自己免疫疾患治療のためのピラゾール
|
MX2016006432A
(es)
|
2013-11-18 |
2016-07-19 |
Hoffmann La Roche |
Tetrahidro-benzodiazepinonas.
|
KR102398473B1
(ko)
|
2013-11-27 |
2022-05-16 |
시그널켐 라이프사이언시즈 코포레이션 |
Tam 패밀리 키나제 억제제로서의 아미노피리딘 유도체
|
TWI667233B
(zh)
|
2013-12-19 |
2019-08-01 |
德商拜耳製藥公司 |
新穎吲唑羧醯胺,其製備方法、含彼等之醫藥製劑及其製造醫藥之用途
|
TW201609693A
(zh)
|
2014-01-03 |
2016-03-16 |
必治妥美雅史谷比公司 |
雜芳基取代之菸鹼醯胺化合物
|
AU2015205348A1
(en)
|
2014-01-10 |
2016-07-28 |
Aurigene Discovery Technologies Limited |
Indazole compounds as IRAK4 inhibitors
|
AU2015205374B2
(en)
|
2014-01-13 |
2018-08-23 |
Aurigene Oncology Limited |
Bicyclic heterocyclyl derivatives as IRAK4 inhibitors
|
MX2016011992A
(es)
|
2014-03-17 |
2016-12-05 |
Hoffmann La Roche |
Derivados de piperidina-diona.
|
AU2015233654B2
(en)
|
2014-03-19 |
2018-12-06 |
Boehringer Ingelheim International Gmbh |
Heteroaryl Syk inhibitors
|
SI3126330T1
(sl)
|
2014-04-04 |
2019-05-31 |
Pfizer Inc. |
Biciklične kondenzirane heteroarilne ali arilne sestavine in njihova uporaba kot zaviralci IRAK-4
|
US20160058872A1
(en)
|
2014-04-14 |
2016-03-03 |
Arvinas, Inc. |
Imide-based modulators of proteolysis and associated methods of use
|
US20180228907A1
(en)
|
2014-04-14 |
2018-08-16 |
Arvinas, Inc. |
Cereblon ligands and bifunctional compounds comprising the same
|
KR20240038809A
(ko)
|
2014-04-14 |
2024-03-25 |
아비나스 오퍼레이션스, 인코포레이티드 |
단백질분해의 이미드-기초된 조절인자 및 연관된 이용 방법
|
EP3134091A4
(en)
|
2014-04-22 |
2017-08-30 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
WO2015193846A1
(en)
|
2014-06-20 |
2015-12-23 |
Aurigene Discovery Technologies Limited |
Substituted indazole compounds as irak4 inhibitors
|
EP3160486B1
(en)
|
2014-06-27 |
2020-11-18 |
Celgene Corporation |
Compositions and methods for inducing conformational changes in cereblon other e3 ubiquitin ligases
|
AR101229A1
(es)
|
2014-07-18 |
2016-11-30 |
Biogen Ma Inc |
Agentes inhibidores de irak4
|
US20160022642A1
(en)
|
2014-07-25 |
2016-01-28 |
Yale University |
Compounds Useful for Promoting Protein Degradation and Methods Using Same
|
US10071164B2
(en)
|
2014-08-11 |
2018-09-11 |
Yale University |
Estrogen-related receptor alpha based protac compounds and associated methods of use
|
US9969749B2
(en)
|
2014-09-30 |
2018-05-15 |
Merck Sharp & Dohme Corp. |
Inhibitors of IRAK4 activity
|
US9926330B2
(en)
|
2014-09-30 |
2018-03-27 |
Merck Sharp & Dohme Corp. |
Inhibitors of IRAK4 activity
|
EP3200790B1
(en)
|
2014-09-30 |
2020-08-26 |
Merck Sharp & Dohme Corp. |
Inhibitors of irak4 activity
|
WO2016053772A1
(en)
|
2014-09-30 |
2016-04-07 |
Merck Sharp & Dohme Corp. |
Inhibitors of irak4 activity
|
JP6787892B2
(ja)
|
2014-11-20 |
2020-11-18 |
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 |
Irakインヒビターとしてのヘテロアリール化合物及びその使用
|
CN107257800B
(zh)
|
2014-12-23 |
2020-06-30 |
达纳-法伯癌症研究所股份有限公司 |
通过双功能分子诱导靶蛋白降解的方法
|
US9694084B2
(en)
|
2014-12-23 |
2017-07-04 |
Dana-Farber Cancer Institute, Inc. |
Methods to induce targeted protein degradation through bifunctional molecules
|
US20170327469A1
(en)
|
2015-01-20 |
2017-11-16 |
Arvinas, Inc. |
Compounds and methods for the targeted degradation of androgen receptor
|
WO2016118666A1
(en)
|
2015-01-20 |
2016-07-28 |
Arvinas, Inc. |
Compounds and methods for the targeted degradation of the androgen receptor
|
WO2016144849A1
(en)
|
2015-03-12 |
2016-09-15 |
Merck Sharp & Dohme Corp. |
Thienopyrazine inhibitors of irak4 activity
|
WO2016144848A1
(en)
|
2015-03-12 |
2016-09-15 |
Merck Sharp & Dohme Corp. |
Pyrrolotriazine inhibitors of irak4 activity
|
US10329294B2
(en)
|
2015-03-12 |
2019-06-25 |
Merck Sharp & Dohme Corp. |
Pyrazolopyrimidine inhibitors of IRAK4 activity
|
US10155765B2
(en)
|
2015-03-12 |
2018-12-18 |
Merck Sharp & Dohme Corp. |
Carboxamide inhibitors of IRAK4 activity
|
US10040798B2
(en)
|
2015-03-12 |
2018-08-07 |
Merck Sharp & Dohme Corp. |
Pyrrolopyridazine inhibitors of IRAK4 activity
|
KR20230175343A
(ko)
|
2015-03-18 |
2023-12-29 |
아비나스 오퍼레이션스, 인코포레이티드 |
타겟화된 단백질들의 향상된 분해를 위한 화합물들 및 방법들
|
GB201504763D0
(en)
|
2015-03-20 |
2015-05-06 |
Mironid Ltd |
Compounds and uses
|
DK3286181T3
(da)
|
2015-04-22 |
2021-04-06 |
Rigel Pharmaceuticals Inc |
Pyrazolforbindelser og fremgangsmåde til fremstilling og anvendelse af forbindelserne
|
GB201506871D0
(en)
|
2015-04-22 |
2015-06-03 |
Glaxosmithkline Ip Dev Ltd |
Novel compounds
|
UY36660A
(es)
|
2015-04-30 |
2016-11-30 |
Bayer Pharma AG |
Combinaciones de inhibidores de irak4
|
WO2016197032A1
(en)
|
2015-06-04 |
2016-12-08 |
Arvinas, Inc. |
Imide-based modulators of proteolysis and associated methods of use
|
EP3302482A4
(en)
|
2015-06-05 |
2018-12-19 |
Arvinas, Inc. |
Tank-binding kinase-1 protacs and associated methods of use
|
EP3307728A4
(en)
|
2015-06-12 |
2019-07-17 |
Dana Farber Cancer Institute, Inc. |
ASSOCIATION THERAPY USING TRANSCRIPTION INHIBITORS AND KINASE INHIBITORS
|
JP6843775B2
(ja)
|
2015-06-24 |
2021-03-17 |
ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company |
ヘテロアリール置換のアミノピリジン化合物
|
CN105085620B
(zh)
|
2015-06-25 |
2018-05-08 |
中山大学附属第一医院 |
一种靶向泛素化降解Smad3的化合物
|
WO2017004133A1
(en)
|
2015-06-29 |
2017-01-05 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
WO2017004134A1
(en)
|
2015-06-29 |
2017-01-05 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
WO2017007612A1
(en)
|
2015-07-07 |
2017-01-12 |
Dana-Farber Cancer Institute, Inc. |
Methods to induce targeted protein degradation through bifunctional molecules
|
AU2016291578C1
(en)
|
2015-07-10 |
2021-07-15 |
Arvinas Operations, Inc. |
MDM2-based modulators of proteolysis and associated methods of use
|
EP3322986A4
(en)
|
2015-07-13 |
2018-09-05 |
Arvinas, Inc. |
Alanine-based modulators of proteolysis and associated methods of use
|
JP6802251B2
(ja)
|
2015-07-14 |
2020-12-16 |
ミッション セラピューティクス リミティド |
癌の処置のためのdub阻害剤としてのシアノピロリジン
|
CN108024971A
(zh)
|
2015-07-15 |
2018-05-11 |
奥列基因发现技术有限公司 |
作为irak-4抑制剂的取代的氮杂化合物
|
MX2018000512A
(es)
|
2015-07-15 |
2018-04-13 |
Aurigene Discovery Tech Ltd |
Compuestos de indazaol y azaindazol como inhibidores de la cinasa 4 asociada al receptor de interlucina 1 (irak-4).
|
EP3337476A4
(en)
|
2015-08-19 |
2019-09-04 |
Arvinas, Inc. |
Compounds and methods for the targeted degradation of bromodomain-containing proteins
|
RU2684324C1
(ru)
|
2015-08-27 |
2019-04-08 |
Пфайзер Инк. |
Бициклические конденсированные гетероарильные или арильные соединения в качестве модуляторов IRAK4
|
ES2911888T3
(es)
|
2015-09-18 |
2022-05-23 |
Merck Patent Gmbh |
Compuestos de heteroarilo como inhibidores de IRAK y usos de los mismos
|
CA2996316C
(en)
|
2015-09-18 |
2023-10-17 |
Merck Patent Gmbh |
Heteroaryl compounds as irak inhibitors and uses thereof
|
EP3355922A2
(en)
|
2015-10-02 |
2018-08-08 |
Dana Farber Cancer Institute, Inc. |
Combination therapy of bromodomain inhibitors and checkpoint blockade
|
US10526309B2
(en)
|
2015-10-02 |
2020-01-07 |
The University Of North Carolina At Chapel Hill |
Pan-TAM inhibitors and Mer/Axl dual inhibitors
|
CA3002709A1
(en)
|
2015-11-02 |
2017-05-11 |
Yale University |
Proteolysis targeting chimera compounds and methods of preparing and using same
|
CN108473498B
(zh)
|
2015-12-22 |
2021-11-02 |
豪夫迈·罗氏有限公司 |
作为IRAK4调节剂的吡唑并[1,5a]嘧啶衍生物
|
US20200216454A1
(en)
|
2015-12-30 |
2020-07-09 |
Dana-Farber Cancer Institute, Inc. |
Bifunctional molecules for her3 degradation and methods of use
|
US20190016703A1
(en)
|
2015-12-30 |
2019-01-17 |
Dana-Farber Cancer Institute, Inc. |
Bifunctional compounds for her3 degradation and methods of use
|
US11427561B2
(en)
|
2016-01-20 |
2022-08-30 |
Biogen Ma Inc. |
IRAK4 inhibiting agents
|
BR112018068906A2
(pt)
|
2016-03-16 |
2019-01-22 |
H. Lee Moffitt Cancer Center And Research Institute, Inc. |
composição, método, método de redução de risco, prevenção ou tratamento de um indivíduo que tem uma doença ou distúrbio autoimune, método de indução de degradação de uma proteína-alvo numa célula, método para reduzir o risco, prevenir ou tratar um estado da doença ou afecção num paciente em que a atividade proteica desregulada é responsável pelo referido estado da doença ou afecção, método para reduzir o risco, prevenir ou tratar câncer num indivíduo e método de tratamento de uma doença ou distúrbio genético num indivíduo
|
US20170281784A1
(en)
|
2016-04-05 |
2017-10-05 |
Arvinas, Inc. |
Protein-protein interaction inducing technology
|
JP7001614B2
(ja)
|
2016-04-06 |
2022-02-03 |
ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン |
リガンド依存性の標的タンパク質分解のための単官能性中間体
|
US11192898B2
(en)
|
2016-04-06 |
2021-12-07 |
The Regents Of The University Of Michigan |
MDM2 protein degraders
|
WO2017197051A1
(en)
|
2016-05-10 |
2017-11-16 |
C4 Therapeutics, Inc. |
Amine-linked c3-glutarimide degronimers for target protein degradation
|
CN109562107A
(zh)
|
2016-05-10 |
2019-04-02 |
C4医药公司 |
用于靶蛋白降解的杂环降解决定子体
|
EP4483875A2
(en)
|
2016-05-10 |
2025-01-01 |
C4 Therapeutics, Inc. |
Spirocyclic degronimers for target protein degradation
|
WO2017197056A1
(en)
|
2016-05-10 |
2017-11-16 |
C4 Therapeutics, Inc. |
Bromodomain targeting degronimers for target protein degradation
|
WO2017197046A1
(en)
|
2016-05-10 |
2017-11-16 |
C4 Therapeutics, Inc. |
C3-carbon linked glutarimide degronimers for target protein degradation
|
WO2017201069A1
(en)
|
2016-05-18 |
2017-11-23 |
Biotheryx, Inc. |
Oxoindoline derivatives as protein function modulators
|
EP3458101B1
(en)
|
2016-05-20 |
2020-12-30 |
H. Hoffnabb-La Roche Ag |
Protac antibody conjugates and methods of use
|
WO2017205766A1
(en)
|
2016-05-27 |
2017-11-30 |
Pharmacyclics Llc |
Inhibitors of interleukin-1 receptor-associated kinase
|
WO2017205762A1
(en)
|
2016-05-27 |
2017-11-30 |
Pharmacyclics Llc |
Inhibitors of interleukin-1 receptor-associated kinase
|
WO2017207385A1
(de)
|
2016-05-31 |
2017-12-07 |
Bayer Pharma Aktiengesellschaft |
Substituierte 3-methylindazole, verfahren zu ihrer herstellung, pharmazeutische präparate, die diese enthalten, sowie deren verwendung zur herstellung von arzneimitteln
|
GB201610147D0
(en)
|
2016-06-10 |
2016-07-27 |
Glaxosmithkline Ip Dev Ltd |
Novel compounds
|
WO2018005356A1
(en)
|
2016-06-27 |
2018-01-04 |
Rigel Pharmaceuticals, Inc. |
2,4-diamino-pyrimidine compounds and method for making and using the compounds
|
US10646488B2
(en)
|
2016-07-13 |
2020-05-12 |
Araxes Pharma Llc |
Conjugates of cereblon binding compounds and G12C mutant KRAS, HRAS or NRAS protein modulating compounds and methods of use thereof
|
JP2019196309A
(ja)
|
2016-09-15 |
2019-11-14 |
武田薬品工業株式会社 |
複素環化合物
|
WO2018089736A1
(en)
|
2016-11-10 |
2018-05-17 |
Dana-Farber Cancer Institute, Inc. |
Degradation of protein kinases by conjugation of protein kinase inhibitors with e3 ligase ligand and methods of use
|
US10975055B2
(en)
|
2016-11-22 |
2021-04-13 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of interleukin-1 receptor-associated kinases and uses thereof
|
EP3559002A4
(en)
|
2016-12-23 |
2021-02-17 |
Arvinas Operations, Inc. |
CHEMERICAL MOLECULES TARGETING EGFR PROTEOLYSIS AND RELATED METHODS OF USE
|
KR102747905B1
(ko)
|
2017-01-31 |
2024-12-31 |
아비나스 오퍼레이션스, 인코포레이티드 |
세레블론 리간드 및 이를 포함하는 이작용성 화합물
|
JOP20180011A1
(ar)
|
2017-02-16 |
2019-01-30 |
Gilead Sciences Inc |
مشتقات بيرولو [1، 2-b]بيريدازين
|
KR102604900B1
(ko)
|
2017-05-11 |
2023-11-21 |
브리스톨-마이어스 스큅 컴퍼니 |
Irak4 억제제로서 유용한 티에노피리딘 및 벤조티오펜
|
CN110769822A
(zh)
|
2017-06-20 |
2020-02-07 |
C4医药公司 |
用于蛋白降解的n/o-连接的降解决定子和降解决定子体
|
CN111278815B
(zh)
|
2017-09-04 |
2024-03-08 |
C4医药公司 |
戊二酰亚胺
|
IL273432B
(en)
|
2017-09-22 |
2022-09-01 |
Kymera Therapeutics Inc |
Protein degraders and uses thereof
|
EP3684366A4
(en)
|
2017-09-22 |
2021-09-08 |
Kymera Therapeutics, Inc. |
CRBN LIGANDS AND USES OF THE LATEST
|
EP3700901A1
(en)
|
2017-10-24 |
2020-09-02 |
Genentech, Inc. |
(4-hydroxypyrrolidin-2-yl)-heterocyclic compounds and methods of use thereof
|
WO2019084030A1
(en)
|
2017-10-24 |
2019-05-02 |
Genentech, Inc. |
(4-HYDROXYPYRROLIDIN-2-YL) -HYDROXAMATE COMPOUNDS AND METHODS OF USE
|
WO2019099868A2
(en)
|
2017-11-16 |
2019-05-23 |
C4 Therapeutics, Inc. |
Degraders and degrons for targeted protein degradation
|
WO2019099926A1
(en)
|
2017-11-17 |
2019-05-23 |
Arvinas, Inc. |
Compounds and methods for the targeted degradation of interleukin-1 receptor-associated kinase 4 polypeptides
|
IL315310A
(en)
*
|
2017-12-26 |
2024-10-01 |
Kymera Therapeutics Inc |
Irak degraders and uses thereof
|
WO2019140380A1
(en)
|
2018-01-12 |
2019-07-18 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
EP3737675A4
(en)
|
2018-01-12 |
2022-01-05 |
Kymera Therapeutics, Inc. |
Crbn ligands and uses thereof
|
AU2019220632B2
(en)
|
2018-02-14 |
2024-02-22 |
Dana-Farber Cancer Institute, Inc. |
IRAK degraders and uses thereof
|
JP7472026B2
(ja)
|
2018-02-23 |
2024-04-22 |
デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド |
選択的なタンパク質分解を誘導するための低分子およびその使用法
|
EP3578561A1
(en)
|
2018-06-04 |
2019-12-11 |
F. Hoffmann-La Roche AG |
Spiro compounds
|
US20220356185A1
(en)
|
2018-07-06 |
2022-11-10 |
Kymera Therapeutics, Inc. |
Mertk degraders and uses thereof
|
US11292792B2
(en)
|
2018-07-06 |
2022-04-05 |
Kymera Therapeutics, Inc. |
Tricyclic CRBN ligands and uses thereof
|
WO2020010227A1
(en)
|
2018-07-06 |
2020-01-09 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
CA3102996A1
(en)
|
2018-07-20 |
2020-01-23 |
Dana-Farber Cancer Institute, Inc. |
Degraders that target proteins via keap1
|
JP7623943B2
(ja)
|
2018-11-30 |
2025-01-29 |
カイメラ セラピューティクス, インコーポレイテッド |
Irak分解剤およびそれらの使用
|
US20220324880A1
(en)
|
2019-06-10 |
2022-10-13 |
Kymara Therapeutics, Inc. |
Smarca inhibitors and uses thereof
|
US20230149549A1
(en)
|
2019-06-10 |
2023-05-18 |
Kymera Therapeutics, Inc |
Smarca degraders and uses thereof
|
US20230087825A1
(en)
|
2019-06-10 |
2023-03-23 |
Kymera Therapeutics, Inc. |
Smarca degraders and uses thereof
|
WO2020251971A1
(en)
|
2019-06-10 |
2020-12-17 |
Kymera Therapeutics, Inc. |
Smarca degraders and uses thereof
|
US20230069104A1
(en)
*
|
2019-06-28 |
2023-03-02 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
WO2020264490A1
(en)
|
2019-06-28 |
2020-12-30 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
US20230093080A1
(en)
|
2019-07-15 |
2023-03-23 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
US20220281831A1
(en)
|
2019-07-15 |
2022-09-08 |
Kymera Therapeutics, Inc. |
Fused-glutarimide crbn ligands and uses thereof
|
US20230132715A1
(en)
|
2019-07-17 |
2023-05-04 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
WO2021011871A1
(en)
|
2019-07-17 |
2021-01-21 |
Kymera Therapeutics, Inc. |
Mertk degraders and uses thereof
|
CN114401960A
(zh)
|
2019-09-16 |
2022-04-26 |
诺华股份有限公司 |
胶降解剂及其使用方法
|
WO2021127278A1
(en)
|
2019-12-17 |
2021-06-24 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
EP4076524A4
(en)
|
2019-12-17 |
2023-11-29 |
Kymera Therapeutics, Inc. |
IRAQ DEGRADERS AND USES THEREOF
|
KR20220145325A
(ko)
|
2019-12-17 |
2022-10-28 |
카이메라 쎄라퓨틱스 인코포레이티드 |
Irak 분해제 및 이의 용도
|