US5521184A
(en)
|
1992-04-03 |
1996-05-28 |
Ciba-Geigy Corporation |
Pyrimidine derivatives and processes for the preparation thereof
|
DE69309670T2
(de)
|
1992-12-28 |
1997-11-20 |
Eisai Co Ltd |
Heterocyclische carbonsäure-derivate, die an rar rezeptoren binden können
|
AU5620299A
(en)
|
1998-08-11 |
2000-03-06 |
Novartis Ag |
Isoquinoline derivatives with angiogenesis inhibiting activity
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
GB9905075D0
(en)
|
1999-03-06 |
1999-04-28 |
Zeneca Ltd |
Chemical compounds
|
TWI271406B
(en)
|
1999-12-13 |
2007-01-21 |
Eisai Co Ltd |
Tricyclic condensed heterocyclic compounds, preparation method of the same and pharmaceuticals comprising the same
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
MXPA03000051A
(es)
|
2000-06-28 |
2003-08-19 |
Smithkline Beecham Plc |
Procedimiento de molido en humedo.
|
PL369530A1
(en)
|
2001-09-19 |
2005-05-02 |
Aventis Pharma S.A. |
Chemical compounds
|
CN1582150B
(zh)
|
2001-10-30 |
2011-09-07 |
诺瓦提斯公司 |
作为flt3受体酪氨酸激酶活性抑制剂的星形孢菌素衍生物
|
EP1456652A4
(en)
|
2001-11-13 |
2005-11-02 |
Dana Farber Cancer Inst Inc |
IMMUNOCELL ACTIVATION MODULATING SUBSTANCES AND USE METHOD THEREFOR
|
AP1767A
(en)
|
2002-01-22 |
2007-08-13 |
Warner Lambert Co |
2-(pyridin-2-ylamino)-pyrido[2,3-d]pyrimidin-7-ones.
|
AR037647A1
(es)
|
2002-05-29 |
2004-12-01 |
Novartis Ag |
Derivados de diarilurea utiles para el tratamiento de enfermedades dependientes de la cinasa de proteina
|
GB0215676D0
(en)
|
2002-07-05 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
CL2003002353A1
(es)
|
2002-11-15 |
2005-02-04 |
Vertex Pharma |
Compuestos derivados de diaminotriazoles, inhibidores d ela proteina quinasa; composicion farmaceutica; procedimiento de preparacion; y su uso del compuesto en el tratamiento de enfermedades de desordenes alergicos, proliferacion, autoinmunes, condic
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
ATE514713T1
(de)
|
2002-12-23 |
2011-07-15 |
Wyeth Llc |
Antikörper gegen pd-1 und ihre verwendung
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
BRPI0414045A
(pt)
|
2003-09-05 |
2006-10-24 |
Anadys Pharmaceuticals Inc |
administração de ligantes de tlr7 e pró-medicamentos dos mesmos para tratamento de infecção por vìrus de hepatite c
|
PE20050952A1
(es)
|
2003-09-24 |
2005-12-19 |
Novartis Ag |
Derivados de isoquinolina como inhibidores de b-raf
|
ZA200609261B
(en)
|
2004-04-28 |
2008-08-27 |
Takeda Pharmaceutical |
Fused quinoline derivative and use thereof
|
WO2006038923A2
(en)
|
2004-06-18 |
2006-04-13 |
3M Innovative Properties Company |
Aryl substituted imidazonaphthyridines
|
AU2005282523A1
(en)
|
2004-09-02 |
2006-03-16 |
3M Innovative Properties Company |
2-amino 1H imidazo ring systems and methods
|
WO2006056399A2
(en)
|
2004-11-24 |
2006-06-01 |
Novartis Ag |
Combinations of jak inhibitors and at least one of bcr-abl, flt-3, fak or raf kinase inhibitors
|
US8658666B2
(en)
|
2005-02-11 |
2014-02-25 |
3M Innovative Properties Company |
Substituted imidazoquinolines and imidazonaphthyridines
|
AU2006216686A1
(en)
|
2005-02-23 |
2006-08-31 |
Coley Pharmaceutical Group, Inc. |
Method of preferentially inducing the biosynthesis of interferon
|
CA2598656A1
(en)
|
2005-02-23 |
2006-08-31 |
Coley Pharmaceutical Group, Inc. |
Hydroxyalkyl substituted imidazoquinoline compounds and methods
|
EP2439273B1
(en)
|
2005-05-09 |
2019-02-27 |
Ono Pharmaceutical Co., Ltd. |
Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics
|
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
|
GB0522715D0
(en)
|
2005-11-08 |
2005-12-14 |
Helperby Therapeutics Ltd |
New use
|
GB0709513D0
(en)
|
2007-05-17 |
2007-06-27 |
Helperby Therapeutics Ltd |
Topical formulations
|
EP1972629A1
(en)
|
2007-03-23 |
2008-09-24 |
Mutabilis SA |
New imidazolo-heteroaryl derivatives with antibacterial properties
|
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
|
JP5537439B2
(ja)
|
2007-12-19 |
2014-07-02 |
アムジエン・インコーポレーテツド |
細胞周期阻害剤としての縮合ピリジン、ピリミジンおよびトリアジン化合物
|
EP2262837A4
(en)
|
2008-03-12 |
2011-04-06 |
Merck Sharp & Dohme |
PD-1 BINDING PROTEINS
|
US8436005B2
(en)
|
2008-04-03 |
2013-05-07 |
Abbott Laboratories |
Macrocyclic pyrimidine derivatives
|
WO2010030785A2
(en)
|
2008-09-10 |
2010-03-18 |
Kalypsys Inc. |
Heterocyclic inhibitors of histamine receptors for the treatment of disease
|
KR102197527B1
(ko)
|
2008-09-26 |
2020-12-31 |
다나-파버 캔서 인스티튜트 인크. |
인간 항-pd-1, pd-l1, 및 pd-l2 항체 및 그의 용도
|
WO2010049366A1
(en)
|
2008-10-27 |
2010-05-06 |
Glaxo Group Limited |
Tricyclic compounds as glutamate receptor modulators
|
KR20190069615A
(ko)
|
2008-12-09 |
2019-06-19 |
제넨테크, 인크. |
항-pd-l1 항체 및 t 세포 기능을 향상시키기 위한 그의 용도
|
JO2885B1
(en)
|
2008-12-22 |
2015-03-15 |
ايلي ليلي اند كومباني |
Protein kinase inhibitors
|
EP2393835B1
(en)
|
2009-02-09 |
2017-04-05 |
Université d'Aix-Marseille |
Pd-1 antibodies and pd-l1 antibodies and uses thereof
|
US20100298302A1
(en)
|
2009-05-20 |
2010-11-25 |
Fabrice Pierre |
Novel protein kinase modulators
|
WO2011001212A1
(en)
|
2009-06-30 |
2011-01-06 |
Piramal Life Sciences Limited |
Imidazo [4,5-c]quinoline derivatives and their use in the treatment of tumors and/or inflammation
|
MX339584B
(es)
|
2009-09-09 |
2016-06-01 |
Avila Therapeutics Inc |
Inhibidores de pi3 cinasa y usos de los mismos.
|
GB0919423D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Novel compounds
|
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
|
WO2011082400A2
(en)
|
2010-01-04 |
2011-07-07 |
President And Fellows Of Harvard College |
Modulators of immunoinhibitory receptor pd-1, and methods of use thereof
|
UY33227A
(es)
|
2010-02-19 |
2011-09-30 |
Novartis Ag |
Compuestos de pirrolopirimidina como inhibidores de la cdk4/6
|
EP2571877B1
(en)
|
2010-05-17 |
2018-08-15 |
Boehringer Ingelheim International GmbH |
1h-imidazo[4,5-c]quinolines
|
CA2802344C
(en)
|
2010-06-18 |
2023-06-13 |
The Brigham And Women's Hospital, Inc. |
Bi-specific antibodies against tim-3 and pd-1 for immunotherapy in chronic immune conditions
|
US8907053B2
(en)
|
2010-06-25 |
2014-12-09 |
Aurigene Discovery Technologies Limited |
Immunosuppression modulating compounds
|
WO2012007926A1
(en)
|
2010-07-16 |
2012-01-19 |
Piramal Life Sciences Limited |
Substituted imidazoquinoline derivatives as kinase inhibitors
|
KR101432247B1
(ko)
|
2010-07-23 |
2014-08-22 |
고려대학교 산학협력단 |
염료감응 태양전지용 준고체 고분자 전해질, 그에 포함되는 정공수송물질, 및 그 전해질을 포함하는 염료감응 태양전지
|
CN102399218A
(zh)
|
2010-09-16 |
2012-04-04 |
和记黄埔医药(上海)有限公司 |
一类并合三杂环及其作为pi3k抑制剂的用途
|
KR102186969B1
(ko)
|
2010-10-25 |
2020-12-04 |
쥐원 쎄라퓨틱스, 인크. |
Cdk 억제제
|
CN102655637A
(zh)
|
2011-03-01 |
2012-09-05 |
中兴通讯股份有限公司 |
一种移动通信系统和组网方法
|
ES2620521T3
(es)
|
2011-03-23 |
2017-06-28 |
Amgen Inc. |
Inhibidores duales tricíclicos condensados de CDK 4/6 y FLT3
|
WO2012154731A1
(en)
|
2011-05-08 |
2012-11-15 |
Vanderbilt University |
Substituted 1h-pyrrolo[3,2-c]quinolin-4(5h)-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m4
|
WO2013033270A2
(en)
|
2011-08-29 |
2013-03-07 |
Coferon, Inc. |
Bromodomain ligands capable of dimerizing in an aqueous solution, and methods of using same
|
US9169246B2
(en)
|
2011-09-26 |
2015-10-27 |
Sanofi |
Pyrazoloquinolinone derivatives, preparation thereof and therapeutic use thereof
|
CN103012397B
(zh)
|
2011-09-26 |
2017-03-01 |
赛诺菲 |
吡唑并喹啉酮衍生物、其制备方法及其治疗用途
|
EP2573073B1
(en)
|
2011-09-26 |
2014-10-22 |
Sanofi |
Pyrazoloquinolinone derivatives, preparation thereof and therapeutic use thereof
|
AU2012318694B2
(en)
|
2011-10-04 |
2016-12-22 |
Janus Biotherapeutics, Inc. |
Novel imidazole quinoline-based immune system modulators
|
CN103930423B
(zh)
|
2011-10-07 |
2015-09-16 |
卫材Rd管理有限公司 |
吡唑并喹啉衍生物
|
AU2012325971B2
(en)
|
2011-10-21 |
2016-03-31 |
Glaxosmithkline Llc |
Compounds and methods for enhancing innate immune responses
|
EP2968285A4
(en)
|
2013-03-13 |
2016-12-21 |
Flatley Discovery Lab |
COMPOUNDS AND METHODS FOR THE TREATMENT OF CYSTIC FIBROSIS
|
CA2904820C
(en)
|
2013-04-05 |
2021-05-18 |
Eisai R&D Management Co., Ltd. |
Pyridinylpyrazoloquinoline compound
|
RU2655171C2
(ru)
|
2013-04-05 |
2018-05-24 |
Эйсай Ар Энд Ди Менеджмент Ко., Лтд. |
Соль производного пиразолохинолина и ее кристалл
|
KR20140142088A
(ko)
|
2013-06-03 |
2014-12-11 |
삼성디스플레이 주식회사 |
아릴 아민계 화합물 및 이를 포함한 유기 발광 소자
|
US20160264570A1
(en)
|
2013-11-15 |
2016-09-15 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Serv |
Method of blocking transmission of malarial parasite
|
CA2975277A1
(en)
|
2015-03-04 |
2016-09-09 |
Dana-Farber Cancer Institute, Inc. |
Tricyclic kinase inhibitors of melk and methods of use
|
US10487078B2
(en)
|
2015-04-03 |
2019-11-26 |
Nantbio, Inc. |
Compositions and methods of targeting mutant K-RAS
|
US10428064B2
(en)
|
2015-04-15 |
2019-10-01 |
Araxes Pharma Llc |
Fused-tricyclic inhibitors of KRAS and methods of use thereof
|
WO2016199943A1
(en)
|
2015-06-11 |
2016-12-15 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compounds
|
CN108976300B
(zh)
|
2015-07-30 |
2023-04-14 |
宏观基因有限公司 |
Pd-1结合分子和其使用方法
|
JP6873980B2
(ja)
|
2015-09-14 |
2021-05-19 |
ファイザー・インク |
LRRK2阻害薬としての新規のイミダゾ[4,5−c]キノリンおよびイミダゾ[4,5−c][1,5]ナフチリジン誘導体
|
EP3356354A1
(en)
|
2015-09-28 |
2018-08-08 |
Araxes Pharma LLC |
Inhibitors of kras g12c mutant proteins
|
US20170107216A1
(en)
|
2015-10-19 |
2017-04-20 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
WO2017087528A1
(en)
|
2015-11-16 |
2017-05-26 |
Araxes Pharma Llc |
2-substituted quinazoline compounds comprising a substituted heterocyclic group and methods of use thereof
|
PL3377488T3
(pl)
|
2015-11-19 |
2022-12-19 |
Incyte Corporation |
Związki heterocykliczne jako immunomodulatory
|
CN106188138B
(zh)
|
2015-12-02 |
2018-07-24 |
深圳市塔吉瑞生物医药有限公司 |
一种二氨基嘧啶化合物及包含该化合物的组合物
|
MA44075A
(fr)
|
2015-12-17 |
2021-05-19 |
Incyte Corp |
Dérivés de n-phényl-pyridine-2-carboxamide et leur utilisation en tant que modulateurs des interactions protéine/protéine pd-1/pd-l1
|
ES2844374T3
(es)
|
2015-12-22 |
2021-07-22 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
US10730871B2
(en)
|
2016-01-28 |
2020-08-04 |
Regents Of The University Of Minnesota |
Immunomodulators and immunomodulator conjugates
|
KR102606277B1
(ko)
|
2016-04-06 |
2023-11-27 |
삼성디스플레이 주식회사 |
유기 발광 소자
|
TW201808950A
(zh)
|
2016-05-06 |
2018-03-16 |
英塞特公司 |
作為免疫調節劑之雜環化合物
|
EP3464279B1
(en)
|
2016-05-26 |
2021-11-24 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
IL263825B
(en)
|
2016-06-20 |
2022-08-01 |
Incyte Corp |
Heterocyclic compounds as immunomodulators
|
WO2018013789A1
(en)
|
2016-07-14 |
2018-01-18 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
MA46045A
(fr)
|
2016-08-29 |
2021-04-28 |
Incyte Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
CA3047986A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Benzooxazole derivatives as immunomodulators
|
ES2918974T3
(es)
|
2016-12-22 |
2022-07-21 |
Incyte Corp |
Compuestos heteroaromaticos biciclicos como inmunomoduladores
|
MY196830A
(en)
|
2016-12-22 |
2023-05-03 |
Amgen Inc |
Kras g12c inhibitors and methods of using the same
|
EP3558989B1
(en)
|
2016-12-22 |
2021-04-14 |
Incyte Corporation |
Triazolo[1,5-a]pyridine derivatives as immunomodulators
|
PE20200005A1
(es)
|
2016-12-22 |
2020-01-06 |
Incyte Corp |
Derivados de tetrahidro imidazo[4,5-c]piridina como inductores de internalizacion pd-l1
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
MA47120A
(fr)
|
2016-12-22 |
2021-04-28 |
Incyte Corp |
Dérivés pyridine utilisés en tant qu'immunomodulateurs
|
CN118515666A
(zh)
|
2017-04-27 |
2024-08-20 |
博笛生物科技有限公司 |
2-氨基-喹啉衍生物
|
JOP20190272A1
(ar)
|
2017-05-22 |
2019-11-21 |
Amgen Inc |
مثبطات kras g12c وطرق لاستخدامها
|
CN108003153B
(zh)
|
2017-11-24 |
2021-04-30 |
中国医学科学院肿瘤医院 |
含氮五元杂环并喹啉类化合物及其盐、制法、药物组合物和用途
|
TW201938561A
(zh)
|
2017-12-08 |
2019-10-01 |
瑞典商阿斯特捷利康公司 |
化學化合物
|
TW201942115A
(zh)
*
|
2018-02-01 |
2019-11-01 |
美商輝瑞股份有限公司 |
作為抗癌藥之經取代的喹唑啉和吡啶並嘧啶衍生物
|
WO2019177971A1
(en)
|
2018-03-12 |
2019-09-19 |
Mavupharma, Inc. |
Ectonucleotide pyrophosphatase-phosphodiesterase 1 (enpp-1) inhibitors and uses thereof
|
IL313101A
(en)
|
2018-03-30 |
2024-07-01 |
Incyte Corp |
Heterocyclic compounds as immunomodulators
|
WO2019201283A1
(en)
|
2018-04-20 |
2019-10-24 |
Xrad Therapeutics, Inc. |
Dual atm and dna-pk inhibitors for use in anti-tumor therapy
|
ES2971122T3
(es)
|
2018-04-25 |
2024-06-03 |
Innate Tumor Immunity Inc |
Moduladores de NLRP3
|
AU2019262589B2
(en)
|
2018-05-04 |
2022-07-07 |
Amgen Inc. |
KRAS G12C inhibitors and methods of using the same
|
FI3790877T3
(fi)
|
2018-05-11 |
2023-05-09 |
Incyte Corp |
Tetrahydroimidatso[4,5-c]pyridiinijohdannaisia pd-l1-immunomodulaattoreina
|
KR20210045430A
(ko)
|
2018-08-16 |
2021-04-26 |
인네이트 튜머 이뮤니티, 인코포레이티드 |
이미다조[4,5-c]퀴놀린 유래 NLRP3-조정제
|
CN113038989A
(zh)
|
2018-08-16 |
2021-06-25 |
先天肿瘤免疫公司 |
咪唑并[4,5-c]喹啉衍生的nlrp3调节剂
|
CA3111392A1
(en)
|
2018-09-04 |
2020-03-12 |
Magenta Therapeutics, Inc. |
Aryl hydrocarbon receptor antagonists and methods of use
|
CN112574224A
(zh)
*
|
2019-09-30 |
2021-03-30 |
上海迪诺医药科技有限公司 |
Kras g12c抑制剂及其应用
|
IL294526A
(en)
|
2020-01-10 |
2022-09-01 |
Incyte Corp |
Tricyclic compounds as kras inhibitors
|
WO2021150613A1
(en)
|
2020-01-20 |
2021-07-29 |
Incyte Corporation |
Spiro compounds as inhibitors of kras
|
PE20230825A1
(es)
*
|
2020-04-16 |
2023-05-19 |
Incyte Corp |
Inhibidores de kras triciclicos fusionados
|
WO2021231526A1
(en)
|
2020-05-13 |
2021-11-18 |
Incyte Corporation |
Fused pyrimidine compounds as kras inhibitors
|
WO2022037631A1
(zh)
|
2020-08-21 |
2022-02-24 |
浙江海正药业股份有限公司 |
杂环类衍生物及其制备方法和用途
|
WO2022047093A1
(en)
|
2020-08-28 |
2022-03-03 |
Incyte Corporation |
Vinyl imidazole compounds as inhibitors of kras
|
US11767320B2
(en)
|
2020-10-02 |
2023-09-26 |
Incyte Corporation |
Bicyclic dione compounds as inhibitors of KRAS
|
US12077539B2
(en)
|
2021-03-22 |
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