CN108558871B - 作为抗癌剂的三环化合物 - Google Patents

作为抗癌剂的三环化合物 Download PDF

Info

Publication number
CN108558871B
CN108558871B CN201810460901.7A CN201810460901A CN108558871B CN 108558871 B CN108558871 B CN 108558871B CN 201810460901 A CN201810460901 A CN 201810460901A CN 108558871 B CN108558871 B CN 108558871B
Authority
CN
China
Prior art keywords
optionally substituted
alkyl
hydrogen
methyl
pyrido
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201810460901.7A
Other languages
English (en)
Chinese (zh)
Other versions
CN108558871A (zh
Inventor
D·J·诺里斯
G·V·德卢卡
A·V·加瓦伊
C·A·奎内勒
P·吉尔
D·奥马利
W·瓦卡罗
F·Y·李
M·V·德贝内代托
A·P·德格南
方海权
M·D·希尔
黄红
W·D·施米茨
小约翰·E·斯塔雷特
韩文景
J·S·托卡尔斯基
S·K·曼达勒
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bristol Myers Squibb Co
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of CN108558871A publication Critical patent/CN108558871A/zh
Application granted granted Critical
Publication of CN108558871B publication Critical patent/CN108558871B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Peptides Or Proteins (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Steroid Compounds (AREA)
CN201810460901.7A 2013-12-24 2014-12-23 作为抗癌剂的三环化合物 Active CN108558871B (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361920500P 2013-12-24 2013-12-24
US61/920,500 2013-12-24
CN201480076189.0A CN106029663B (zh) 2013-12-24 2014-12-23 作为抗癌剂的新颖三环化合物

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CN201480076189.0A Division CN106029663B (zh) 2013-12-24 2014-12-23 作为抗癌剂的新颖三环化合物

Publications (2)

Publication Number Publication Date
CN108558871A CN108558871A (zh) 2018-09-21
CN108558871B true CN108558871B (zh) 2022-02-18

Family

ID=52293305

Family Applications (2)

Application Number Title Priority Date Filing Date
CN201810460901.7A Active CN108558871B (zh) 2013-12-24 2014-12-23 作为抗癌剂的三环化合物
CN201480076189.0A Active CN106029663B (zh) 2013-12-24 2014-12-23 作为抗癌剂的新颖三环化合物

Family Applications After (1)

Application Number Title Priority Date Filing Date
CN201480076189.0A Active CN106029663B (zh) 2013-12-24 2014-12-23 作为抗癌剂的新颖三环化合物

Country Status (34)

Country Link
US (1) US20160318928A1 (enExample)
EP (2) EP3087071B1 (enExample)
JP (2) JP6466456B2 (enExample)
KR (1) KR102457145B1 (enExample)
CN (2) CN108558871B (enExample)
AR (2) AR099379A1 (enExample)
AU (1) AU2014369982B2 (enExample)
BR (1) BR112016013744B1 (enExample)
CA (1) CA2934953C (enExample)
CL (1) CL2016001629A1 (enExample)
CY (2) CY1121076T1 (enExample)
DK (2) DK3087071T3 (enExample)
EA (2) EA201990240A1 (enExample)
ES (2) ES2857848T3 (enExample)
HR (2) HRP20181849T1 (enExample)
HU (2) HUE054183T2 (enExample)
IL (1) IL246359B (enExample)
LT (2) LT3087071T (enExample)
MA (1) MA39211B1 (enExample)
MX (1) MX369491B (enExample)
MY (1) MY176489A (enExample)
NZ (1) NZ722326A (enExample)
PE (1) PE20160844A1 (enExample)
PH (1) PH12016500953A1 (enExample)
PL (2) PL3087071T3 (enExample)
PT (2) PT3087071T (enExample)
RS (2) RS61479B1 (enExample)
SG (1) SG11201605097SA (enExample)
SI (2) SI3087071T1 (enExample)
SM (2) SMT202100165T1 (enExample)
TN (1) TN2016000238A1 (enExample)
TW (2) TWI726544B (enExample)
UY (1) UY35916A (enExample)
WO (1) WO2015100282A1 (enExample)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105189488B (zh) 2013-02-27 2018-07-24 百时美施贵宝公司 用作溴区结构域抑制剂的咔唑化合物
RU2016122654A (ru) 2013-11-08 2017-12-14 Дана-Фарбер Кэнсер Инститьют, Инк. Комбинированная терапия злокачественной опухоли с использованием ингибиторов бромодоменового и экстратерминального (вет) белка
MA39211B1 (fr) * 2013-12-24 2019-01-31 Bristol Myers Squibb Co Composés tricycliques comme agents anti-cancers
US9458156B2 (en) 2014-12-23 2016-10-04 Bristol-Myers Squibb Company Tricyclic compounds as anticancer agents
WO2015131005A1 (en) * 2014-02-28 2015-09-03 The Regents Of The University Of Michigan 9h-pyrimido[4,5-b]indoles and related analogs as bet bromodomain inhibitors
US9725449B2 (en) 2015-05-12 2017-08-08 Bristol-Myers Squibb Company Tricyclic compounds as anticancer agents
ES2770349T3 (es) 2015-05-12 2020-07-01 Bristol Myers Squibb Co Compuestos de 5H-pirido[3,2-b]indol como agentes antineoplásicos
HK1248115A1 (zh) 2015-07-16 2018-10-12 Bioxcel Therapeutics, Inc. 一种使用免疫调节治疗癌症的新颖方法
KR20180081507A (ko) * 2015-10-02 2018-07-16 다나-파버 캔서 인스티튜트 인크. 브로모도메인 저해제와 관문 차단의 조합 요법
WO2017124936A1 (zh) * 2016-01-20 2017-07-27 宁波文达医药科技有限公司 作为布罗莫区结构域抑制剂的咔啉衍生物
WO2017124934A1 (zh) * 2016-01-20 2017-07-27 宁波文达医药科技有限公司 作为布罗莫区结构域抑制剂的含膦咔啉衍生物
EP3412669A4 (en) * 2016-02-05 2019-09-04 Chia Tai Tianqing Pharmaceutical Group Co.,Ltd TRICYCLIC COMPOUND FOR PROTEIN INHIBITOR CONTAINING BROMODOMAINE AND PREPARATION, PHARMACEUTICAL COMPOSITION AND USE THEREOF
KR102845317B1 (ko) 2016-03-01 2025-08-13 코어셉트 쎄라퓨틱스 인코포레이티드 체크포인트 억제제를 강화시키기 위한 글루코코르티코이드 수용체 조정제의 용도
US10150754B2 (en) * 2016-04-19 2018-12-11 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
RU2019117356A (ru) 2016-11-10 2020-12-10 Лосинь Фармасьютикал (Шанхай) Ко., Лтд. Азотсодержащее макроциклическое соединение, способ его получения, фармацевтическая композиция и применение
CN106905347B (zh) * 2017-04-18 2019-04-16 四川大学 Brd4抑制剂及其在肿瘤治疗药物中的应用
CN111356695B (zh) * 2017-10-27 2022-12-30 北京加科思新药研发有限公司 新的三环化合物
EP3814352A4 (en) 2018-06-25 2022-03-30 Jacobio Pharmaceuticals Co., Ltd. TRICYCLIC COMPOUNDS
CN108840868B (zh) * 2018-08-01 2019-10-18 上海山的实业有限公司 具有抗肿瘤活性的吲哚并吡啶酮类化合物的制备方法及应用
US11234971B2 (en) 2018-12-19 2022-02-01 Corcept Therapeutics Incorporated Methods of treating cancer comprising administration of a glucocorticoid receptor modulator and a cancer chemotherapy agent
WO2020132046A1 (en) 2018-12-19 2020-06-25 Corcept Therapeutics Incorporated Methods of treating cancer comprising administration of a glucocorticoid receptor modulator and a cancer chemotherapy agent
CN113544129B (zh) * 2019-04-04 2024-07-23 上海华汇拓医药科技有限公司 三环类化合物制备方法及其在医药领域的应用
CN110003204B (zh) * 2019-04-30 2020-08-11 上海勋和医药科技有限公司 一种bet蛋白抑制剂、其制备方法及用途
US10947253B2 (en) 2019-08-05 2021-03-16 Ankh Life Sciences Limited Fused polycyclic dimers
AU2020360170A1 (en) 2019-09-30 2022-05-19 Kyowa Kirin Co., Ltd. Bet degrader
US12129265B2 (en) 2020-07-21 2024-10-29 Ankh Life Sciences Limited Therapeutic agents and uses thereof
JP2024506260A (ja) * 2021-01-22 2024-02-13 ジンルイ バイオファーマ カンパニー リミテッド 抗がん剤としての三環式化合物
EP4297750A1 (en) * 2021-02-25 2024-01-03 Impact Biomedicines, Inc. Use of a bet inhibitor alone or in combination with fedratinib or ruxolitinib for treating a hematological malignancy such as myelofibrosis
JP2024517608A (ja) * 2021-05-06 2024-04-23 ラジエル セラピューティクス エルティーディー. 結晶性カルバゾール誘導体
WO2024099441A1 (en) * 2022-11-11 2024-05-16 Jingrui Biopharma (Shandong) Co., Ltd. Bromodomain and extra-terminal (bet) protein degrader

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102917590A (zh) * 2010-03-29 2013-02-06 肿瘤疗法科学股份有限公司 三环化合物及含有所述化合物的pbk抑制剂
CN103313989A (zh) * 2010-12-16 2013-09-18 霍夫曼-拉罗奇有限公司 三环pi3k抑制剂化合物和使用方法
WO2014086739A1 (de) * 2012-12-06 2014-06-12 Bayer Pharma Aktiengesellschaft Neuartige benzimidazolderivate als ep4-antagonisten
WO2014134267A1 (en) * 2013-02-27 2014-09-04 Bristol-Myers Squibb Company Carbazole compounds useful as bromodomain inhibitors
WO2014134232A1 (en) * 2013-02-27 2014-09-04 Bristol-Myers Squibb Company Carbazole compounds useful as bromodomain inhibitors
WO2014164596A1 (en) * 2013-03-11 2014-10-09 The Regents Of The University Of Michigan Bet bromodomain inhibitors and therapeutic methods using the same

Family Cites Families (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993014080A1 (en) * 1992-01-15 1993-07-22 E.I. Du Pont De Nemours And Company Bridged heterocyclic fungicides
CA2542682A1 (en) 2003-10-18 2005-05-06 Bayer Healthcare Ag 5-substituted 2-(phenylmethyl) thio-4-phenyl-4h-1,2,4-triazole derivatives and related compounds as gaba-agonists for the treatment of urinary incontinence and related diseases
WO2005051318A2 (en) * 2003-11-24 2005-06-09 Viropharma Incorporated Compounds, compositions and methods for treatment and prophylaxis of hepatitis c viral infections and associated diseases
TWI380996B (zh) 2004-09-17 2013-01-01 Hoffmann La Roche 抗ox40l抗體
ES2657443T3 (es) 2005-03-25 2018-03-05 Gitr, Inc. Anticuerpos anti-GITR y usos de los mismos
GB0507298D0 (en) 2005-04-11 2005-05-18 Novartis Ag Organic compounds
AU2006244068B9 (en) 2005-05-10 2012-10-25 Incyte Holdings Corporation Modulators of indoleamine 2,3-dioxygenase and methods of using the same
KR101411165B1 (ko) 2005-07-01 2014-06-25 메다렉스, 엘.엘.시. 예정 사멸 리간드 1 (피디-엘1)에 대한 인간 모노클로날항체
CA2634198C (en) 2005-12-20 2014-06-03 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
US7696166B2 (en) 2006-03-28 2010-04-13 Albany Molecular Research, Inc. Use of cyclosporin alkyne/alkene analogues for preventing or treating viral-induced disorders
CL2007002650A1 (es) 2006-09-19 2008-02-08 Incyte Corp Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras.
JP5319532B2 (ja) 2006-09-19 2013-10-16 インサイト・コーポレイション インドールアミン2,3−ジオキシゲナーゼのモジュレーターとしてのn−ヒドロキシアミジノヘテロサイクル
UY30892A1 (es) 2007-02-07 2008-09-02 Smithkline Beckman Corp Inhibidores de la actividad akt
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
US8591886B2 (en) 2007-07-12 2013-11-26 Gitr, 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
CA2932121A1 (en) 2007-11-30 2009-06-11 Newlink Genetics Corporation Ido inhibitors
FR2927330B1 (fr) 2008-02-07 2010-02-19 Sanofi Aventis Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii
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
WO2010077634A1 (en) 2008-12-09 2010-07-08 Genentech, Inc. Anti-pd-l1 antibodies and their use to enhance t-cell function
JP5557849B2 (ja) * 2008-12-19 2014-07-23 ブリストル−マイヤーズ スクイブ カンパニー カルバゾールおよびカルボリンキナーゼ阻害剤
CA2772613C (en) 2009-09-03 2020-03-10 Schering Corporation Anti-gitr antibodies
US8722720B2 (en) 2009-10-28 2014-05-13 Newlink Genetics Corporation Imidazole derivatives as IDO inhibitors
PL2949670T3 (pl) 2009-12-10 2019-07-31 F. Hoffmann-La Roche Ag Przeciwciała wiążące się preferencyjnie z zewnątrzkomórkową domeną 4 ludzkiego CSF-1R i ich zastosowanie
EA201201191A1 (ru) 2010-02-26 2013-04-30 Бёрингер Ингельхайм Интернациональ Гмбх 4-[циклоалкилокси(гетеро)ариламино]тиено[2,3-d]пиримидины, обладающие ингибирующей активностью по отношению к mnkl/mnk2, предназначенные для фармацевтических композиций
US9150656B2 (en) 2010-03-04 2015-10-06 Macrogenics, Inc. Antibodies reactive with B7-H3, immunologically active fragments thereof and uses thereof
US9221910B2 (en) 2010-03-05 2015-12-29 Hoffmann-La Roche Inc. Antibodies against human CSF-1R
US9169323B2 (en) 2010-03-05 2015-10-27 Hoffmann-La Roche Inc. Antibodies against human CSF-1R
AU2011248083B2 (en) 2010-05-04 2015-09-10 Five Prime Therapeutics, Inc. Antibodies that bind CSF1R
EP2582698B1 (en) 2010-06-16 2016-09-14 Vitae Pharmaceuticals, Inc. Substituted 5-,6- and 7-membered heterocycles, medicaments containing such compounds, and their use
MX337040B (es) 2010-09-09 2016-02-09 Pfizer Moleculas de union a 4-1bb.
US8580399B2 (en) * 2011-04-08 2013-11-12 Universal Display Corporation Substituted oligoazacarbazoles for light emitting diodes
NO2694640T3 (enExample) 2011-04-15 2018-03-17
PL2699264T3 (pl) 2011-04-20 2018-08-31 Medimmune, Llc Przeciwciała i inne cząsteczki wiążące B7-H1 i PD-1
US9991447B2 (en) * 2011-09-28 2018-06-05 Idemitsu Korea Co., Ltd. Material for organic electroluminescent element, and organic electroluminescent element produced using same
EP2785375B1 (en) 2011-11-28 2020-07-22 Merck Patent GmbH Anti-pd-l1 antibodies and uses thereof
CA2853889A1 (en) 2011-12-15 2013-06-20 F. Hoffmann-La Roche Ag Antibodies against human csf-1r and uses thereof
BR112014018961A8 (pt) 2012-02-06 2017-07-11 Genentech Inc Anticorpo isolado, anticorpo biespecífico, fragmento, ácido nucleico isolado, vetor, célula hospedeira, método de produção de anticorpos, composição farmacêutica, uso do anticorpo, método de tratamento, método de inibição e artigo industrializado
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
HK1208233A1 (en) 2012-05-11 2016-02-26 戊瑞治疗有限公司 Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r)
AR091649A1 (es) 2012-07-02 2015-02-18 Bristol Myers Squibb Co Optimizacion de anticuerpos que se fijan al gen de activacion de linfocitos 3 (lag-3) y sus usos
EP2890398A4 (en) 2012-08-31 2016-03-09 Five Prime Therapeutics Inc METHODS OF TREATING DISEASES WITH ANTIBODIES THAT BIND COLONY STIMULATING FACTOR RECEIVER 1 (CSF1R)
MA39211B1 (fr) * 2013-12-24 2019-01-31 Bristol Myers Squibb Co Composés tricycliques comme agents anti-cancers

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102917590A (zh) * 2010-03-29 2013-02-06 肿瘤疗法科学股份有限公司 三环化合物及含有所述化合物的pbk抑制剂
CN103313989A (zh) * 2010-12-16 2013-09-18 霍夫曼-拉罗奇有限公司 三环pi3k抑制剂化合物和使用方法
WO2014086739A1 (de) * 2012-12-06 2014-06-12 Bayer Pharma Aktiengesellschaft Neuartige benzimidazolderivate als ep4-antagonisten
WO2014134267A1 (en) * 2013-02-27 2014-09-04 Bristol-Myers Squibb Company Carbazole compounds useful as bromodomain inhibitors
WO2014134232A1 (en) * 2013-02-27 2014-09-04 Bristol-Myers Squibb Company Carbazole compounds useful as bromodomain inhibitors
WO2014164596A1 (en) * 2013-03-11 2014-10-09 The Regents Of The University Of Michigan Bet bromodomain inhibitors and therapeutic methods using the same

Also Published As

Publication number Publication date
TW202028203A (zh) 2020-08-01
ES2698998T3 (es) 2019-02-06
MA39211B1 (fr) 2019-01-31
HRP20210212T8 (hr) 2021-08-20
ES2857848T3 (es) 2021-09-29
CN106029663A (zh) 2016-10-12
EP3466949A1 (en) 2019-04-10
LT3466949T (lt) 2021-03-25
CY1124061T1 (el) 2022-05-27
BR112016013744B1 (pt) 2022-08-30
WO2015100282A1 (en) 2015-07-02
CN108558871A (zh) 2018-09-21
CY1121076T1 (el) 2019-12-11
KR20160095168A (ko) 2016-08-10
EP3087071A1 (en) 2016-11-02
RS58014B1 (sr) 2019-02-28
PL3087071T3 (pl) 2019-03-29
EP3466949B1 (en) 2020-12-23
DK3087071T3 (da) 2019-01-02
RS61479B1 (sr) 2021-03-31
TWI726544B (zh) 2021-05-01
JP2017505762A (ja) 2017-02-23
HRP20210212T1 (hr) 2021-07-09
MX369491B (es) 2019-11-11
MX2016007928A (es) 2016-08-03
EA032469B1 (ru) 2019-05-31
JP6675501B2 (ja) 2020-04-01
PH12016500953A1 (en) 2016-06-27
AU2014369982A1 (en) 2016-08-04
SMT202100165T1 (it) 2021-05-07
AR099379A1 (es) 2016-07-20
SMT201800643T1 (it) 2019-01-11
TN2016000238A1 (en) 2017-10-06
SG11201605097SA (en) 2016-07-28
KR102457145B1 (ko) 2022-10-19
SI3087071T1 (sl) 2018-11-30
CA2934953A1 (en) 2015-07-02
LT3087071T (lt) 2018-11-12
MA39211A1 (fr) 2018-08-31
HRP20181849T1 (hr) 2018-12-28
EA201990240A1 (ru) 2019-06-28
NZ722326A (en) 2019-09-27
HUE041719T2 (hu) 2019-05-28
CA2934953C (en) 2022-09-20
SI3466949T1 (sl) 2021-03-31
TW201609725A (zh) 2016-03-16
JP6466456B2 (ja) 2019-02-06
BR112016013744A2 (enExample) 2017-10-03
PE20160844A1 (es) 2016-09-03
PL3466949T3 (pl) 2021-05-31
CN106029663B (zh) 2018-06-01
MY176489A (en) 2020-08-12
UY35916A (es) 2015-06-30
JP2019070014A (ja) 2019-05-09
AR123996A2 (es) 2023-02-01
AU2014369982B2 (en) 2019-04-18
PT3087071T (pt) 2018-11-29
IL246359A0 (en) 2016-08-31
CL2016001629A1 (es) 2017-02-17
DK3466949T3 (da) 2021-03-15
EP3087071B1 (en) 2018-09-05
TWI736517B (zh) 2021-08-21
US20160318928A1 (en) 2016-11-03
PT3466949T (pt) 2021-02-25
HUE054183T2 (hu) 2021-08-30
EA201691070A1 (ru) 2016-11-30
IL246359B (en) 2020-04-30

Similar Documents

Publication Publication Date Title
CN108558871B (zh) 作为抗癌剂的三环化合物
US10112941B2 (en) Tricyclic compounds as anticancer agents
CN107709322B (zh) 作为抗癌剂的三环化合物
CN110167935B (zh) 作为αV整合素抑制剂的3-经取代的丙酸
CN105008352B (zh) 用作溴区结构域抑制剂的咔唑化合物
CN112204036A (zh) 作为mcl-1抑制剂的大环稠合的吡唑
TWI845638B (zh) Eed及prc2調節劑之巨環唑并吡啶衍生物
CN110845520A (zh) 作为mcl-1抑制剂的大环吲哚
CN106817900A (zh) 新颖的萘啶和异喹啉及其作为cdk8/19抑制剂的用途
CN107257798A (zh) TGFβR拮抗剂
TW201444828A (zh) 可作爲溴區結構域蛋白抑制劑之咔唑化合物
HK1243417B (zh) 吡啶酮和氮杂吡啶酮化合物及使用方法
HK1248678A1 (zh) 核受體調節劑
HK1225023B (en) Tricyclic compounds as anticancer agents
HK1225023A1 (en) Tricyclic compounds as anticancer agents
HK1248678B (zh) 核受体调节剂

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant