[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

SG10201805844QA - 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase - Google Patents

1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase

Info

Publication number
SG10201805844QA
SG10201805844QA SG10201805844QA SG10201805844QA SG10201805844QA SG 10201805844Q A SG10201805844Q A SG 10201805844QA SG 10201805844Q A SG10201805844Q A SG 10201805844QA SG 10201805844Q A SG10201805844Q A SG 10201805844QA SG 10201805844Q A SG10201805844Q A SG 10201805844QA
Authority
SG
Singapore
Prior art keywords
indoleamine
dioxygenase
inhibitors
oxadiazoles
oxadiazole derivatives
Prior art date
Application number
SG10201805844QA
Inventor
Andrew Combs
Eddy Yue
Richard Sparks
Wenyu Zhu
Jiacheng Zhou
Qiyan Lin
Lingkai Weng
Tai-Yuen Yue
Pingli Liu
Original Assignee
Incyte Holdings Corp
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41128289&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG10201805844Q(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Incyte Holdings Corp filed Critical Incyte Holdings Corp
Publication of SG10201805844QA publication Critical patent/SG10201805844QA/en

Links

Classifications

    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4245Oxadiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/12Ophthalmic agents for cataracts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/081,2,5-Oxadiazoles; Hydrogenated 1,2,5-oxadiazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • Psychiatry (AREA)
  • Communicable Diseases (AREA)
  • Pain & Pain Management (AREA)
  • Ophthalmology & Optometry (AREA)
  • Dermatology (AREA)
  • Mycology (AREA)
  • Microbiology (AREA)
  • Endocrinology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • AIDS & HIV (AREA)
  • Pulmonology (AREA)
  • Transplantation (AREA)
  • Hospice & Palliative Care (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

1,2,5-OXADIAZOLES AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE The present invention is directed to 1,2,5-oxadiazole derivatives, and compositions of the same, which are inhibitors of indoleamine 2,3-dioxygenase and are useful in the treatment of cancer and other disorders, and to the processes and intermediates for making such 1,2,5- oxadiazole derivatives. Figure 1 accompanies the abstract
SG10201805844QA 2008-07-08 2009-07-07 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase SG10201805844QA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US7887608P 2008-07-08 2008-07-08
US15087309P 2009-02-09 2009-02-09

Publications (1)

Publication Number Publication Date
SG10201805844QA true SG10201805844QA (en) 2018-08-30

Family

ID=41128289

Family Applications (2)

Application Number Title Priority Date Filing Date
SG2013052485A SG192485A1 (en) 2008-07-08 2009-07-07 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
SG10201805844QA SG10201805844QA (en) 2008-07-08 2009-07-07 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase

Family Applications Before (1)

Application Number Title Priority Date Filing Date
SG2013052485A SG192485A1 (en) 2008-07-08 2009-07-07 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase

Country Status (37)

Country Link
US (12) US8088803B2 (en)
EP (3) EP2824100B1 (en)
JP (2) JP5465720B2 (en)
KR (5) KR101927291B1 (en)
CN (2) CN102164902B (en)
AR (1) AR072490A1 (en)
AU (6) AU2009268739B2 (en)
BR (2) BRPI0915692B8 (en)
CA (2) CA2743975C (en)
CL (2) CL2009001554A1 (en)
CO (1) CO6341622A2 (en)
CR (1) CR11871A (en)
CY (1) CY1120617T1 (en)
DK (2) DK2315756T5 (en)
EA (2) EA022669B1 (en)
EC (1) ECSP11010798A (en)
ES (2) ES2524266T3 (en)
HK (2) HK1157692A1 (en)
HR (2) HRP20141094T1 (en)
HU (1) HUE036813T2 (en)
IL (2) IL210402A (en)
LT (1) LT2824100T (en)
ME (1) ME03065B (en)
MX (1) MX2011000235A (en)
MY (3) MY192633A (en)
NO (1) NO2824100T3 (en)
NZ (1) NZ590268A (en)
PE (1) PE20110308A1 (en)
PH (1) PH12014500947B1 (en)
PL (2) PL2315756T3 (en)
PT (2) PT2315756E (en)
RS (2) RS57132B1 (en)
SG (2) SG192485A1 (en)
SI (2) SI2315756T1 (en)
SM (1) SMT201400179B (en)
TW (1) TWI453204B (en)
WO (1) WO2010005958A2 (en)

Families Citing this family (169)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL1879573T3 (en) 2005-05-10 2013-05-31 Incyte Holdings Corp Modulators of indoleamine 2,3-dioxygenase and methods of using the same
ES2540561T3 (en) * 2005-12-20 2015-07-10 Incyte Corporation N-hydroxyamidinoheterocycles as indolamine 2,3-dioxygenase modulators
CL2007002650A1 (en) 2006-09-19 2008-02-08 Incyte Corp COMPOUNDS DERIVED FROM HETEROCICLO N-HIDROXIAMINO; PHARMACEUTICAL COMPOSITION, USEFUL TO TREAT CANCER, VIRAL INFECTIONS AND NEURODEGENERATIVE DISORDERS BETWEEN OTHERS.
EP2064207B1 (en) * 2006-09-19 2013-11-06 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
EP2824100B1 (en) 2008-07-08 2018-02-21 Incyte Holdings Corporation 1,2,5-Oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
GB0919757D0 (en) * 2009-11-12 2009-12-30 Johnson Matthey Plc Polymorphs of bromfenac sodium and methods for preparing bromfenac sodium polymorphs
US8299295B2 (en) 2009-10-15 2012-10-30 Johnson Matthey Public Limited Company Polymorphs of bromfenac sodium and methods for preparing bromfenac sodium polymorphs
NO2694640T3 (en) 2011-04-15 2018-03-17
EP2781517B1 (en) 2011-11-09 2017-10-11 Kyowa Hakko Kirin Co., Ltd. Nitrogen-containing heterocyclic compound
GB201120860D0 (en) 2011-12-05 2012-01-18 Cambridge Entpr Ltd Cancer immunotherapy
CN104797267A (en) 2012-06-26 2015-07-22 德玛医药 Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or ahi1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof
US10034939B2 (en) 2012-10-26 2018-07-31 The University Of Chicago Synergistic combination of immunologic inhibitors for the treatment of cancer
JP2016519684A (en) 2013-04-08 2016-07-07 デニス エム ブラウン Methods and compositions for improving the efficacy of suboptimally administered medication and / or reducing side effects
AR098343A1 (en) * 2013-11-08 2016-05-26 Incyte Holdings Corp PROCESS FOR THE SYNTHESIS OF AN INDOLAMINE 2,3-DIOXYGENASE INHIBITOR
MX2016010080A (en) * 2014-02-04 2016-10-07 Incyte Corp Combination of a pd-1 antagonist and an ido1 inhibitor for treating cancer.
SG11201608106PA (en) 2014-03-31 2016-10-28 Genentech Inc Combination therapy comprising anti-angiogenesis agents and ox40 binding agonists
DK3126394T3 (en) 2014-03-31 2020-01-13 Hoffmann La Roche Anti-OX40 antibodies and methods of use
CN115925946A (en) 2014-05-28 2023-04-07 阿吉纳斯公司 Anti-GITR antibodies and methods of use thereof
RU2016149812A (en) 2014-06-06 2018-07-17 Флексус Байосайенсиз, Инк. IMMUNO REGULATORY MEANS
EP3169684B1 (en) * 2014-07-17 2019-06-26 CHDI Foundation, Inc. Combination of kmo inhibitor 6-(3-chloro-4-cyclopropoxyphenyl)pyrimidine-4-carboxylic acid with antiviral agent for treating hiv related neurological disorders
CN105481789B (en) * 2014-09-15 2020-05-19 中国科学院上海有机化学研究所 Indoleamine-2,3-dioxygenase inhibitor and preparation method thereof
US11242319B2 (en) 2014-11-05 2022-02-08 Flexus Biosciences, Inc. Immunoregulatory agents
UY36390A (en) 2014-11-05 2016-06-01 Flexus Biosciences Inc MODULATING COMPOUNDS OF INDOLAMINE ENZYME 2,3-DIOXYGENASE (IDO), ITS SYNTHESIS METHODS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
AR102537A1 (en) 2014-11-05 2017-03-08 Flexus Biosciences Inc IMMUNOMODULATING AGENTS
WO2016100851A1 (en) 2014-12-18 2016-06-23 Lankenau Institute For Medical Research Methods and compositions for the treatment of retinopathy and other ocular diseases
LT3097102T (en) 2015-03-04 2018-01-25 Gilead Sciences, Inc. Toll-like receptor modulating 4,6-diamino-pyrido[3,2-d]pyrimidine compounds
BR112017019699A2 (en) * 2015-03-17 2018-09-04 Pfizer Inc. 3-indole substituted derivatives, pharmaceutical compositions and methods for use
WO2016155545A1 (en) * 2015-03-31 2016-10-06 江苏恒瑞医药股份有限公司 Sulfamyl-containing 1,2,5-oxadiazole derivative, preparation method therefor and use thereof in pharmaceuticals
AU2016246695A1 (en) 2015-04-07 2017-10-26 Genentech, Inc. Antigen binding complex having agonistic activity and methods of use
JP6801159B2 (en) 2015-04-21 2020-12-16 ジエンス ヘンルイ メデイシンカンパニー リミテッドJiangsu Hengrui Medicine Co.,Ltd. Imidazoisoindole derivative, its manufacturing method and its pharmaceutical use
SI3303394T1 (en) 2015-05-29 2020-10-30 Agenus Inc. Anti-ctla-4 antibodies and methods of use thereof
US9891882B2 (en) * 2015-06-01 2018-02-13 Nagravision S.A. Methods and systems for conveying encrypted data to a communication device
CN107810011A (en) 2015-06-08 2018-03-16 豪夫迈·罗氏有限公司 Methods of treating cancer using anti-OX 40 antibodies
KR20180025888A (en) 2015-06-08 2018-03-09 제넨테크, 인크. Methods for treating cancer using anti-OX40 antibodies and PD-1 axis-binding antagonists
JP6654208B2 (en) * 2015-07-02 2020-02-26 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited Indoleamine 2,3-dioxygenase inhibitor
WO2017010106A1 (en) * 2015-07-14 2017-01-19 Kyowa Hakko Kirin Co., Ltd. A therapeutic agent for a tumor comprising an ido inhibitor administered in combination with an antibody
MX2017016844A (en) 2015-07-16 2018-08-15 Biokine Therapeutics Ltd Compositions and methods for treating cancer.
US9732035B2 (en) 2015-07-24 2017-08-15 Newlink Genetics Corporation Salts and prodrugs of 1-methyl-D-tryptophan
WO2017024996A1 (en) * 2015-08-07 2017-02-16 江苏恒瑞医药股份有限公司 Hydroxy amidine derivative, preparation method and use in medicine thereof
MA42684A (en) 2015-08-26 2018-07-04 Gilead Sciences Inc TOLL RECEIVER DEUTERATED MODULATORS
SG10201913276WA (en) 2015-09-01 2020-02-27 Agenus Inc Anti-pd-1 antibodies and methods of use thereof
CN105120571B (en) 2015-09-14 2018-05-01 昂宝电子(上海)有限公司 System and method for the current regulation in LED illumination system
CN106565696B (en) * 2015-10-09 2020-07-28 江苏恒瑞医药股份有限公司 Oxadiazole derivative, preparation method and medical application thereof
MA43172A (en) * 2015-11-04 2018-09-12 Incyte Corp PHARMACEUTICAL COMPOSITIONS AND METHODS OF INHIBITION OF INDOLAMINE 2,3-DIOXYGENASE AND THEIR INDICATIONS
WO2017080934A1 (en) 2015-11-09 2017-05-18 F. Hoffmann-La Roche Ag Screening assay to identify id01 and/or tdo modulators
EP3383430A4 (en) 2015-12-02 2019-12-18 Agenus Inc. Antibodies and methods of use thereof
EP3389783B1 (en) * 2015-12-15 2024-07-03 Merck Sharp & Dohme LLC Novel compounds as indoleamine 2,3-dioxygenase inhibitors
CN106883193B (en) * 2015-12-15 2021-10-15 上海翰森生物医药科技有限公司 Indoleamine 2,3-dioxygenase inhibitor as well as preparation method and application thereof
CA2954892A1 (en) 2016-01-19 2017-07-19 Pfizer Inc. Immunogens derived from tumor-associated antigens or nucleic acid molecules encoding the immunogens
US9624185B1 (en) * 2016-01-20 2017-04-18 Yong Xu Method for preparing IDO inhibitor epacadostat
CN105646389B (en) * 2016-01-28 2019-06-28 中国科学院上海有机化学研究所 A kind of sulfamic acid rouge and its preparation method and application as indoles amine -2,3- dioxygenase inhibitor
JP7066186B2 (en) 2016-02-19 2022-05-13 アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル Methods and pharmaceutical compositions for the treatment of obesity
EP3398942B1 (en) * 2016-02-25 2021-01-27 Shenzhen TargetRx, Inc. Substituted oxadiazole chemical compound and composition containing said chemical compound and use thereof
CN107176933B (en) * 2016-03-09 2020-10-09 中国科学院上海有机化学研究所 Indoleamine-2,3-dioxygenase inhibitor containing nitrogen alkylated and arylated sulfoximine
WO2017181849A1 (en) * 2016-04-20 2017-10-26 江苏豪森药业集团有限公司 Indoleamine 2,3-dioxygenase inhibitor, preparation method therefor, and application
CN107304191B (en) * 2016-04-20 2023-09-29 上海翰森生物医药科技有限公司 Indolylamine 2,3-dioxygenase inhibitor and preparation method and application thereof
BR112018071602B1 (en) * 2016-04-29 2024-02-27 Iomet Pharma Ltd. SUBSTITUTED IMIDAZOPYRIDINE COMPOUNDS, THEIR COMPOSITION AND THEIR USE AS INHIBITORS OF INDOLAMINE 2,3-DIOXYGENASE AND/OR TRYPTOPHAN-2,3-DIOXYGENASE
WO2017192811A1 (en) 2016-05-04 2017-11-09 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
EP3463469B1 (en) 2016-05-27 2023-12-13 Gilead Sciences, Inc. Combination of ledipasvir and sofosbuvir for use in the treatment of hepatitis b virus infections in humans
BR102017010009A2 (en) 2016-05-27 2017-12-12 Gilead Sciences, Inc. COMPOUNDS FOR THE TREATMENT OF HEPATITIS B VIRUS INFECTION
CN118359722A (en) 2016-05-27 2024-07-19 艾吉纳斯公司 Anti-TIM-3 antibodies and methods of use thereof
JOP20170131B1 (en) 2016-06-10 2021-08-17 Lilly Co Eli 1-trahydropyranylcarbonyl-2,3-dihydro-1h-indole compounds for treating cancer
CN106109472A (en) * 2016-06-13 2016-11-16 中山大学 Chlordiazepoxide is as the purposes of indole amine 2,3-dioxygenase-1 inhibitor
JP2019527699A (en) * 2016-08-02 2019-10-03 シャンドン ルイ ファーマシューティカル カンパニー リミテッド IDO1 inhibitor and its production method and application
JP2019530434A (en) 2016-08-05 2019-10-24 ジェネンテック, インコーポレイテッド Multivalent and multi-epitope antibodies with agonist activity and methods of use
US20190185439A1 (en) * 2016-08-24 2019-06-20 H. Lee Moffitt Cancer Center & Research Institute, Inc. Radiofluorinated carboximidamides as ido targeting pet tracer for cancer imaging
EP3503916A1 (en) * 2016-08-26 2019-07-03 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
JOP20190024A1 (en) 2016-08-26 2019-02-19 Gilead Sciences Inc Substituted pyrrolizine compounds and uses thereof
US10640499B2 (en) 2016-09-02 2020-05-05 Gilead Sciences, Inc. Toll like receptor modulator compounds
US10370342B2 (en) 2016-09-02 2019-08-06 Gilead Sciences, Inc. Toll like receptor modulator compounds
JP7358236B2 (en) 2016-09-19 2023-10-10 ユニヴァーシティ オブ サウス フロリダ How to target oncolytic viruses to tumors
MX2019003683A (en) 2016-10-11 2019-08-22 Agenus Inc Anti-lag-3 antibodies and methods of use thereof.
MA50839A (en) 2016-10-13 2019-08-21 Juno Therapeutics Inc METHODS AND COMPOSITIONS OF IMMUNOTHERAPY INVOLVING MODULATORS OF THE TRYPTOPHAN METABOLIC PATHWAY
CN110023495A (en) 2016-10-14 2019-07-16 精密生物科学公司 To the engineering meganuclease of the identification sequence-specific in Hepatitis B virus-DNA
WO2018072697A1 (en) * 2016-10-17 2018-04-26 上海医药集团股份有限公司 Oxadiazole ring-containing compound, preparation method therefor, and intermediate, composite, and application thereof
WO2018081648A2 (en) 2016-10-29 2018-05-03 Genentech, Inc. Anti-mic antibidies and methods of use
UY37466A (en) 2016-11-03 2018-01-31 Phenex Discovery Verwaltungs Gmbh N-HYDROXIAMIDINHETEROCICLES SUBSTITUTED AS MODULATORS OF INDOLAMINE 2,3-DIOXYGENASE
AU2017359467A1 (en) 2016-11-09 2019-05-02 Agenus Inc. Anti-OX40 antibodies, anti-GITR antibodies, and methods of use thereof
EP3544965A4 (en) * 2016-11-28 2020-05-20 Shanghai Fochon Pharmaceutical Co., Ltd. Sulfoximine, sulfonimidamide, sulfondiimine and diimidosulfonamide compounds as inhibitors of indoleamine 2, 3-dioxygenase
MX2019006340A (en) 2016-12-07 2019-11-07 Agenus Inc Anti-ctla-4 antibodies and methods of use thereof.
AU2017373945A1 (en) 2016-12-07 2019-06-20 Agenus Inc. Antibodies and methods of use thereof
CN108218807A (en) * 2016-12-22 2018-06-29 上海长森药业有限公司 A kind of sulfone amidine as indoles amine -2,3- dioxygenase inhibitors and its preparation method and application
CN110382508B (en) 2016-12-22 2022-08-02 卡里塞拉生物科学股份公司 Compositions and methods for inhibiting arginase activity
JP2020503883A (en) 2017-01-13 2020-02-06 アジェナス インコーポレイテッド T-cell receptor binding to NY-ESO-1 and method of using same
CA3047002A1 (en) 2017-01-17 2018-07-26 Board Of Regents, The University Of Texas System Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
AR110768A1 (en) 2017-01-31 2019-05-02 Gilead Sciences Inc CRYSTAL FORMS OF TENOFOVIR ALAFENAMIDA
JOP20180008A1 (en) 2017-02-02 2019-01-30 Gilead Sciences Inc Compounds for the treatment of hepatitis b virus infection
MX2019011558A (en) * 2017-03-29 2019-11-28 Merck Sharp & Dohme Novel substituted n'-hydroxycarbamimidoyl-1,2,5-oxadiazole compounds as indoleamine 2,3-dioxygenase (ido) inhibitors.
US11439623B2 (en) 2017-04-04 2022-09-13 Case Western Reserve University Method of modulating ribonucleotide reductase
CN108689958B (en) * 2017-04-05 2021-09-17 南京华威医药科技集团有限公司 Indoleamine 2,3-dioxygenase inhibitor containing hydrazino
CN106967005B (en) * 2017-04-07 2019-07-16 上海肇钰医药科技有限公司 A kind of compound that can inhibit IDO, Its Preparation Method And Use
EP3609921A2 (en) 2017-04-13 2020-02-19 Agenus Inc. Anti-cd137 antibodies and methods of use thereof
JOP20180040A1 (en) 2017-04-20 2019-01-30 Gilead Sciences Inc Pd-1/pd-l1 inhibitors
CN114920710B (en) * 2017-04-27 2024-09-20 鲁南制药集团股份有限公司 Imido urea derivatives
PL3618863T3 (en) 2017-05-01 2023-11-06 Agenus Inc. Anti-tigit antibodies and methods of use thereof
CN109081818B (en) * 2017-06-14 2022-04-22 南京华威医药科技集团有限公司 Novel indoleamine 2, 3-bis-oxidase inhibitors
CN109111438B (en) * 2017-06-26 2021-11-02 正大天晴药业集团股份有限公司 Amidine compounds for IDO inhibitors
CN111065408A (en) 2017-07-11 2020-04-24 辉瑞公司 Immunogenic compositions
CA3072989A1 (en) 2017-08-17 2019-02-21 Idorsia Pharmaceuticals Ltd Inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan 2,3-dioxygenase
CN107311956A (en) * 2017-08-22 2017-11-03 合肥圣迪利克医药科技有限公司 One kind Chinese mugwort card, which is stamped, takes charge of his synthetic method
EP3679062A1 (en) 2017-09-04 2020-07-15 Agenus Inc. T cell receptors that bind to mixed lineage leukemia (mll)-specific phosphopeptides and methods of use thereof
CN108863976B (en) * 2017-09-11 2022-09-16 郑州泰基鸿诺医药股份有限公司 Compounds useful as IDO modulators and uses thereof
JP2020533283A (en) 2017-09-11 2020-11-19 アトッサ セラピューティクス,インク. How to make and use endoxyphen
EP4176876A1 (en) 2017-09-14 2023-05-10 Lankenau Institute for Medical Research Methods and compositions for the treatment of cancer
WO2019057104A1 (en) * 2017-09-20 2019-03-28 上海翰森生物医药科技有限公司 Salt of dioxygenase inhibitor and preparation method therefor and use thereof
CN109897011B (en) * 2017-12-08 2023-10-31 上海华汇拓医药科技有限公司 IDO inhibitor and application thereof
CN109928922A (en) * 2017-12-18 2019-06-25 成都华健未来科技有限公司 A kind of cyclohexanes compound
EP3728283B1 (en) 2017-12-20 2023-11-22 Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. 3'3' cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
EP3728282B1 (en) 2017-12-20 2023-11-22 Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. 2'3' cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
CN109942565B (en) 2017-12-20 2021-03-26 海创药业股份有限公司 Indoleamine-2, 3-dioxygenase inhibitor and preparation method and application thereof
AU2019205904A1 (en) 2018-01-05 2020-06-18 Dicerna Pharmaceuticals, Inc. Reducing beta-catenin and IDO expression to potentiate immunotherapy
CN111601810A (en) 2018-01-15 2020-08-28 爱杜西亚药品有限公司 Inhibitors of indoleamine 2, 3-dioxygenase and/or tryptophan 2, 3-dioxygenase
CN108586378B (en) 2018-01-22 2020-06-19 南京华威医药科技集团有限公司 Indoleamine 2, 3-bis-oxidase inhibitor and preparation method and application thereof
CN110066253B (en) * 2018-01-24 2023-06-23 江苏柯菲平医药股份有限公司 1,2, 5-oxadiazole derivative, preparation method thereof and application thereof in medicines
US11369589B2 (en) 2018-01-24 2022-06-28 Nanjing Carephar Shenghui Pharmaceutical Co., Ltd. Modulator of indoleamine 2,3-dioxygenase, preparation method and use thereof
CN110577501A (en) * 2018-06-07 2019-12-17 江苏柯菲平医药股份有限公司 indoleamine 2, 3-dioxygenase modulators, method for the production and use thereof
WO2019149255A1 (en) * 2018-02-02 2019-08-08 成都海创药业有限公司 Indoleamine-2,3-dioxygenase inhibitor, preparation method therefor and use thereof
CN108101899B (en) * 2018-02-11 2021-01-26 中国药科大学 Preparation method of intermediate of IDO1 inhibitor Epacadostat
TWI796596B (en) 2018-02-13 2023-03-21 美商基利科學股份有限公司 Pd-1/pd-l1 inhibitors
AU2019223182B2 (en) 2018-02-26 2021-08-19 Gilead Sciences, Inc. Substituted pyrrolizine compounds as HBV replication inhibitors
US10870691B2 (en) 2018-04-05 2020-12-22 Gilead Sciences, Inc. Antibodies and fragments thereof that bind hepatitis B virus protein X
TWI833744B (en) 2018-04-06 2024-03-01 捷克科學院有機化學與生物化學研究所 3'3'-cyclic dinucleotides
TW202005654A (en) 2018-04-06 2020-02-01 捷克科學院有機化學與生物化學研究所 2'2'-cyclic dinucleotides
TWI818007B (en) 2018-04-06 2023-10-11 捷克科學院有機化學與生物化學研究所 2'3'-cyclic dinucleotides
US11142750B2 (en) 2018-04-12 2021-10-12 Precision Biosciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the Hepatitis B virus genome
US20190314324A1 (en) 2018-04-13 2019-10-17 The University Of Chicago Combination of micheliolide derivatives or nanoparticles with ionizing radiation and checkpoint inhibitors for cancer therapy
EP3781556A1 (en) 2018-04-19 2021-02-24 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2019210055A2 (en) 2018-04-26 2019-10-31 Agenus Inc. Heat shock protein-binding peptide compositions and methods of use thereof
CN110407765B (en) * 2018-04-28 2022-12-06 上海挚盟医药科技有限公司 1,2,5-oxadiazole derivative, preparation method and medical application thereof
TW202014193A (en) 2018-05-03 2020-04-16 捷克科學院有機化學與生物化學研究所 2’3’-cyclic dinucleotides comprising carbocyclic nucleotide
GB201809050D0 (en) 2018-06-01 2018-07-18 E Therapeutics Plc Modulators of tryptophan catabolism
SG11202012425QA (en) 2018-07-13 2021-01-28 Gilead Sciences Inc Pd-1/pd-l1 inhibitors
EP3823604A4 (en) 2018-07-17 2022-03-16 Board of Regents, The University of Texas System Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
WO2020028097A1 (en) 2018-08-01 2020-02-06 Gilead Sciences, Inc. Solid forms of (r)-11-(methoxymethyl)-12-(3-methoxypropoxy)-3,3-dimethyl-8-0x0-2,3,8,13b-tetrahydro-1h-pyrido[2,1-a]pyrrolo[1,2-c] phthalazine-7-c arboxylic acid
CN109180603A (en) * 2018-10-10 2019-01-11 中国药科大学 The preparation method of Epacadostat key intermediate
EP3870566A1 (en) 2018-10-24 2021-09-01 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
JP7273172B2 (en) 2018-10-31 2023-05-12 ギリアード サイエンシーズ, インコーポレイテッド Substituted 6-azabenzimidazole compounds with HPK1 inhibitory activity
CA3117556A1 (en) 2018-10-31 2020-05-07 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds as hpk1 inhibitors
CN111617078B (en) * 2019-02-28 2023-02-03 四川科伦博泰生物医药股份有限公司 Pharmaceutical compositions, methods and uses thereof for the treatment and/or prevention of disease
EP3935065A1 (en) 2019-03-07 2022-01-12 Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. 3'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator
WO2020178769A1 (en) 2019-03-07 2020-09-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotides and prodrugs thereof
CA3129011C (en) 2019-03-07 2023-12-19 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotides and prodrugs thereof
TW202210480A (en) 2019-04-17 2022-03-16 美商基利科學股份有限公司 Solid forms of a toll-like receptor modulator
TW202212339A (en) 2019-04-17 2022-04-01 美商基利科學股份有限公司 Solid forms of a toll-like receptor modulator
EP3972695A1 (en) 2019-05-23 2022-03-30 Gilead Sciences, Inc. Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors
WO2020255038A1 (en) 2019-06-18 2020-12-24 Janssen Sciences Ireland Unlimited Company Combination of hepatitis b virus (hbv) vaccines and pyridopyrimidine derivatives
AU2020301161B2 (en) 2019-06-25 2023-10-26 Gilead Sciences, Inc. FLT3L-Fc fusion proteins and methods of use
CN110204537B (en) * 2019-07-10 2021-10-08 盛世泰科生物医药技术(苏州)有限公司 1,2, 5-oxadiazole derivatives as inhibitors of indoleamine 2, 3-dioxygenase
WO2021005222A1 (en) 2019-07-11 2021-01-14 Idorsia Pharmaceuticals Ltd Inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan 2,3-dioxygenase
WO2021011891A1 (en) 2019-07-18 2021-01-21 Gilead Sciences, Inc. Long-acting formulations of tenofovir alafenamide
MX2022001133A (en) 2019-08-01 2022-04-25 Incyte Corp A dosing regimen for an ido inhibitor.
WO2021034804A1 (en) 2019-08-19 2021-02-25 Gilead Sciences, Inc. Pharmaceutical formulations of tenofovir alafenamide
JP2022545741A (en) 2019-08-30 2022-10-28 アジェナス インコーポレイテッド ANTI-CD96 ANTIBODY AND METHODS OF USE THEREOF
TWI755055B (en) * 2019-09-18 2022-02-11 台灣神隆股份有限公司 Process for preparing elagolix sodium and intermediates thereof
BR112022005687A2 (en) 2019-09-30 2022-06-21 Gilead Sciences Inc Vaccines against hbv and methods to treat hbv
EP4069729A1 (en) 2019-12-06 2022-10-12 Precision BioSciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the hepatitis b virus genome
CN113045655A (en) 2019-12-27 2021-06-29 高诚生物医药(香港)有限公司 anti-OX 40 antibodies and uses thereof
AR121620A1 (en) 2020-03-20 2022-06-22 Gilead Sciences Inc 4-C-SUBSTITUTED-2-HALO-2-DEOXIADENOSINE NUCLEOSIDE PRODRUGS AND METHODS OF PREPARATION AND USE THEREOF
US20230303599A1 (en) 2020-08-07 2023-09-28 Gilead Sciences, Inc. Prodrugs of phosphonamide nucleotide analogues and their pharmaceutical use
WO2022064526A1 (en) * 2020-09-25 2022-03-31 Msn Laboratories Private Limited, R&D Center Solid state forms of epacadostat and their processes for preparation thereof
TW202406932A (en) 2020-10-22 2024-02-16 美商基利科學股份有限公司 Interleukin-2-fc fusion proteins and methods of use
BR112023017582A2 (en) 2021-03-05 2023-12-05 Univ Basel COMPOSITIONS FOR THE TREATMENT OF DISEASES OR CONDITIONS ASSOCIATED WITH EBV
EP4052705A1 (en) 2021-03-05 2022-09-07 Universität Basel Vizerektorat Forschung Compositions for the treatment of ebv associated diseases or conditions
WO2022241134A1 (en) 2021-05-13 2022-11-17 Gilead Sciences, Inc. COMBINATION OF A TLR8 MODULATING COMPOUND AND ANTI-HBV siRNA THERAPEUTICS
JP2024522594A (en) 2021-06-23 2024-06-21 ギリアード サイエンシーズ, インコーポレイテッド Diacylglycerol kinase modulating compounds
AU2022299051A1 (en) 2021-06-23 2023-12-07 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
AU2022297373A1 (en) 2021-06-23 2024-01-04 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271659A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
GB202303250D0 (en) 2023-03-06 2023-04-19 King S College London Method and compounds

Family Cites Families (126)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236855A (en) 1964-01-17 1966-02-22 Merck & Co Inc Certain n-phenyl(thiazole-hydroxamidine) compounds and their preparation
US3354174A (en) 1964-02-19 1967-11-21 Sterling Drug Inc 1-and 2-benzimidazolyl-lower-alkylamidoximes, amidines-, and guanidines
US3553228A (en) 1967-09-26 1971-01-05 Colgate Palmolive Co 3-substituted-4h(1)benzopyrano(3,4-d) isoxazoles
DE2040628A1 (en) 1970-08-17 1972-02-24 Fahlberg List Veb Substd hydroxyguanidines prepn
US3948928A (en) 1972-03-17 1976-04-06 Dainippon Pharmaceutical Co., Ltd. 3-Substituted-1,2-benzisoxazoles and pharmaceutically acceptable acid addition salts thereof
JPS5621033B2 (en) 1973-09-05 1981-05-16
FR2323683A1 (en) 1975-09-11 1977-04-08 Philagro Sa Phytohormonal and herbicidal amidoxime derivs. - prepd. by treatment of an imino ether with an O-amino oxy-acetate
DD128918A5 (en) 1975-09-11 1977-12-21 Philagro Sa PHYTHOHORMONAL AND HERBICIDAL COMPOSITIONS
US4399216A (en) 1980-02-25 1983-08-16 The Trustees Of Columbia University Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials
US5179017A (en) 1980-02-25 1993-01-12 The Trustees Of Columbia University In The City Of New York Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials
US4634665A (en) 1980-02-25 1987-01-06 The Trustees Of Columbia University In The City Of New York Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials
US4323681A (en) 1980-09-29 1982-04-06 American Home Products Corporation 4-Amino-2-substituted-5-pyrimidinecarboxamidoximes and carbothioamides
US5156840A (en) 1982-03-09 1992-10-20 Cytogen Corporation Amine-containing porphyrin derivatives
JPS58208275A (en) 1982-05-20 1983-12-03 Lion Corp 5-amino-pyrazole derivative and antitumor agent containing it
DE3462259D1 (en) 1983-07-22 1987-03-05 Bayer Ag SUBSTITUTED FURAZANS
US4507485A (en) 1984-01-23 1985-03-26 Bristol-Myers Company 3,4-Disubstituted-1,2,5-oxadiazoles having histamine H2 -receptor antagonist activity
JPS60193968A (en) 1984-03-13 1985-10-02 Toyo Jozo Co Ltd Imidazoleamidoxime having cyclopentene ring and its preparation
JPS6259283A (en) 1985-09-10 1987-03-14 Kaken Pharmaceut Co Ltd Cephalosporin compound
US5057313A (en) 1986-02-25 1991-10-15 The Center For Molecular Medicine And Immunology Diagnostic and therapeutic antibody conjugates
JPS6320710A (en) 1986-07-11 1988-01-28 Matsushita Electric Ind Co Ltd Production of thin film magnetic head
WO1988007089A1 (en) 1987-03-18 1988-09-22 Medical Research Council Altered antibodies
JP2696342B2 (en) 1988-06-27 1998-01-14 日本曹達株式会社 Amidine derivative, method for producing the same, acaricide and agricultural / horticultural fungicide
ES2051986T3 (en) 1988-07-05 1994-07-01 Akzo Nv COMPOUNDS WITH BRONCHODILATING ACTIVITY.
US5530101A (en) 1988-12-28 1996-06-25 Protein Design Labs, Inc. Humanized immunoglobulins
IL162181A (en) 1988-12-28 2006-04-10 Pdl Biopharma Inc A method of producing humanized immunoglubulin, and polynucleotides encoding the same
DE3920358A1 (en) 1989-06-22 1991-01-17 Behringwerke Ag BISPECIFIC AND OLIGO-SPECIFIC, MONO- AND OLIGOVALENT ANTI-BODY CONSTRUCTS, THEIR PRODUCTION AND USE
US5859205A (en) 1989-12-21 1999-01-12 Celltech Limited Humanised antibodies
JPH04297449A (en) 1991-03-27 1992-10-21 Hokko Chem Ind Co Ltd N-hydroxybenzylguanidine derivative and germicide for agriculture and horticulture
JPH05186458A (en) 1991-04-26 1993-07-27 Japan Tobacco Inc New benzopyran derivative
FR2677019B1 (en) 1991-05-27 1994-11-25 Pf Medicament NOVEL PIPERIDINES DISUBSTITUEES-1,4, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION.
EP0940468A1 (en) 1991-06-14 1999-09-08 Genentech, Inc. Humanized antibody variable domain
EP0617706B1 (en) 1991-11-25 2001-10-17 Enzon, Inc. Multivalent antigen-binding proteins
US5714350A (en) 1992-03-09 1998-02-03 Protein Design Labs, Inc. Increasing antibody affinity by altering glycosylation in the immunoglobulin variable region
US5521184A (en) 1992-04-03 1996-05-28 Ciba-Geigy Corporation Pyrimidine derivatives and processes for the preparation thereof
JP2709677B2 (en) 1992-06-19 1998-02-04 株式会社大塚製薬工場 Phosphonic acid diester derivatives
SI9200344B (en) 1992-11-26 1998-06-30 Lek, New process for preparing benzensulfonate salts
US5827690A (en) 1993-12-20 1998-10-27 Genzyme Transgenics Corporatiion Transgenic production of antibodies in milk
FR2720396B1 (en) 1994-05-27 1996-06-28 Adir New N-pyridyl carboxamides and derivatives, their preparation process and the pharmaceutical compositions containing them.
US5731168A (en) 1995-03-01 1998-03-24 Genentech, Inc. Method for making heteromultimeric polypeptides
US5869046A (en) 1995-04-14 1999-02-09 Genentech, Inc. Altered polypeptides with increased half-life
US5731315A (en) 1995-06-07 1998-03-24 Rhone-Poulenc Rorer Pharmaceuticals Inc. Substituted sulfonic acid n- (aminoiminomethyl)phenylalkyl!-azaheterocyclamide compounds
WO1997008320A1 (en) 1995-08-18 1997-03-06 Morphosys Gesellschaft Für Proteinoptimierung Mbh Protein/(poly)peptide libraries
US5883102A (en) 1995-10-17 1999-03-16 Astra Pharmaceuticals Limited Pharmaceutically active compounds
WO1997030047A1 (en) 1996-02-17 1997-08-21 Agrevo Uk Limited Fungicidal 1,2,4-oxadiazoles and analogues
US5955495A (en) 1996-05-03 1999-09-21 Hoffmann-La Roche Inc. Method of treating diseases of the CNS
JPH11171702A (en) 1997-09-24 1999-06-29 Takeda Chem Ind Ltd Pest controlling method
US6395876B1 (en) 1997-12-05 2002-05-28 Medical College Of Georgia Research Institute, Inc. High-affinity tryptophan transporter
NZ505002A (en) 1997-12-10 2001-11-30 Dainippon Ink & Chemicals 1,2,5-oxadiazolyl, 1,2,5-thiadiazolyl or 1,2,3-thiadiazolyl oxime derivatives substituted by another heterocyclic group useful as agricultural chemicals
CN1131863C (en) 1998-06-02 2003-12-24 住化武田农药株式会社 Oxadiazoline derivatives and their use as insecticides
BR9912938B1 (en) 1998-08-11 2011-06-28 isoquinoline derivatives, composition comprising them, process for preparation and use thereof.
FR2784678B1 (en) 1998-09-23 2002-11-29 Sod Conseils Rech Applic NOVEL N- (IMINOMETHYL) AMINE DERIVATIVES, THEIR PREPARATION, THEIR USE AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
US6133031A (en) 1999-08-19 2000-10-17 Isis Pharmaceuticals Inc. Antisense inhibition of focal adhesion kinase expression
EP1075469B1 (en) 1999-03-03 2004-05-26 Samjin Pharmaceutical Co., Ltd. Piperazine derivatives and process for the preparation thereof
GB9905075D0 (en) 1999-03-06 1999-04-28 Zeneca Ltd Chemical compounds
EP1165601A2 (en) 1999-04-09 2002-01-02 Basf Aktiengesellschaft Prodrugs of thrombin inhibitors
ES2244438T3 (en) 1999-05-24 2005-12-16 Mitsubishi Pharma Corporation PHENOXYPROPYLAMINE COMPOUNDS.
JP2001158785A (en) 1999-11-30 2001-06-12 Takeda Chem Ind Ltd Agrochemical composition
JP2001158786A (en) 1999-11-30 2001-06-12 Takeda Chem Ind Ltd Controller against mammalian ectoparasite
JP2003519676A (en) 2000-01-13 2003-06-24 トゥラリック インコーポレイテッド Antibacterial agent
JP2001233861A (en) 2000-02-22 2001-08-28 Ube Ind Ltd Pyrazole oxime compound, method for producing the same and use of the same
GB0004890D0 (en) 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
ES2225624T3 (en) 2000-06-28 2005-03-16 Smithkline Beecham Plc GRINDING PROCEDURE BY WET.
GB0108102D0 (en) 2001-03-30 2001-05-23 Pfizer Ltd Compounds
RS99503A (en) 2001-06-18 2006-12-15 Applied Research Systems Ars Holding N.V. Pyrrolidine oxadiazole- and thiadiazole derivatives
MXPA04002243A (en) 2001-09-19 2004-06-29 Aventis Pharma Sa Chemical compounds.
DE60213842T2 (en) 2001-10-30 2007-09-06 Novartis Ag STAUROSPORINE DERIVATIVES AS INHIBITORS OF THE FLT3 RECEPTOR TYROSINE KINASE EFFECT
KR20060111716A (en) 2002-01-22 2006-10-27 워너-램버트 캄파니 엘엘씨 2-(pyridin-2-ylamino)-pyrido[2,3-d]pyrimidin-7-ones
JP2005529850A (en) 2002-02-19 2005-10-06 ファルマシア・イタリア・エス・ピー・エー Tricyclic pyrazole derivatives, their preparation and their use as antitumor agents
GB0208224D0 (en) 2002-04-10 2002-05-22 Celltech R&D Ltd Chemical compounds
WO2003087347A1 (en) 2002-04-12 2003-10-23 Medical College Of Georgia Research Institute, Inc. Antigen-presenting cell populations and their use as reagents for enhancing or reducing immune tolerance
EP1549632A4 (en) 2002-05-28 2005-11-09 Dimensional Pharm Inc Novel thiophene amidines, compositions thereof, and methods of treating complement-mediated diseases and conditions
TW200406374A (en) 2002-05-29 2004-05-01 Novartis Ag Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases
GB0215676D0 (en) 2002-07-05 2002-08-14 Novartis Ag Organic compounds
US7157462B2 (en) 2002-09-24 2007-01-02 Euro-Celtique S.A. Therapeutic agents useful for treating pain
US7015321B2 (en) 2002-10-12 2006-03-21 The Scripps Research Institute Synthesis of non-symmetrical sulfamides using burgess-type reagents
CL2003002353A1 (en) 2002-11-15 2005-02-04 Vertex Pharma COMPOUNDS DERIVED FROM DIAMINOTRIAZOLS, INHIBITORS D ELA PROTEINA QUINASA; PHARMACEUTICAL COMPOSITION; PREPARATION PROCEDURE; AND ITS USE OF THE COMPOUND IN THE TREATMENT OF DISEASES OF ALLERGIC DISORDERS, PROLIFERATION, AUTOIMMUNES, CONDIC
UA80767C2 (en) 2002-12-20 2007-10-25 Pfizer Prod Inc Pyrimidine derivatives for the treatment of abnormal cell growth
WO2004063351A2 (en) 2003-01-09 2004-07-29 Macrogenics, Inc. IDENTIFICATION AND ENGINEERING OF ANTIBODIES WITH VARIANT Fc REGIONS AND METHODS OF USING SAME
AU2004205631A1 (en) 2003-01-16 2004-08-05 Genentech, Inc. Synthetic antibody phage libraries
WO2004072266A2 (en) 2003-02-13 2004-08-26 Kalobios Inc. Antibody affinity engineering by serial epitope-guided complementarity replacement
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
CA2520172C (en) 2003-03-27 2012-10-02 Lankenau Institute For Medical Research Novel methods for the treatment of cancer with an indoleamine 2, 3-dioxygenase inhibitor
US7598287B2 (en) 2003-04-01 2009-10-06 Medical College Of Georgia Research Institute, Inc. Use of inhibitors of indoleamine-2,3-dioxygenase in combination with other therapeutic modalities
KR20120090094A (en) 2003-06-13 2012-08-16 바이오겐 아이덱 엠에이 인코포레이티드 Aglycosyl anti-cd154(cd-40 ligand) antibodies and uses thereof
AU2004267094A1 (en) 2003-08-20 2005-03-03 Vertex Pharmaceuticals Incorporated (4 -amino -1,2, 5-oxadiazol-4-yl) -hetxiroaromatic compounds useful as protein kinase inhibitors
JP2007503206A (en) 2003-08-22 2007-02-22 バイオジェン・アイデック・エムエイ・インコーポレイテッド Improved antibody with altered effector function and method for producing the antibody
PE20050952A1 (en) 2003-09-24 2005-12-19 Novartis Ag DERIVATIVES OF ISOQUINOLINE AS INHIBITORS OF B-RAF
DE10348023A1 (en) 2003-10-15 2005-05-19 Imtm Gmbh New alanyl aminopeptidase inhibitors for the functional manipulation of different cells and for the treatment of immunological, inflammatory, neuronal and other diseases
DE10348022A1 (en) 2003-10-15 2005-05-25 Imtm Gmbh New dipeptidyl peptidase IV inhibitors for the functional influence of different cells and for the treatment of immunological, inflammatory, neuronal and other diseases
ES2396135T3 (en) 2004-06-10 2013-02-19 Irm Llc Compounds and compositions as protein kinase inhibitors
CN101014580B (en) 2004-09-08 2011-05-04 田边三菱制药株式会社 Morpholine compound
JP2008520612A (en) 2004-11-24 2008-06-19 ノバルティス アクチエンゲゼルシャフト Combination of JAK inhibitor and at least one of Bcr-Abl, Flt-3, FAK or RAF kinase inhibitor
WO2006067532A1 (en) 2004-12-24 2006-06-29 Prosidion Ltd G-protein coupled receptor agonists
US7429667B2 (en) 2005-01-20 2008-09-30 Ardea Biosciences, Inc. Phenylamino isothiazole carboxamidines as MEK inhibitors
EP2161336B2 (en) * 2005-05-09 2017-03-29 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
PL1879573T3 (en) 2005-05-10 2013-05-31 Incyte Holdings Corp Modulators of indoleamine 2,3-dioxygenase and methods of using the same
WO2006133417A1 (en) 2005-06-07 2006-12-14 Valeant Pharmaceuticals International Phenylamino isothiazole carboxamidines as mek inhibitors
WO2007005807A2 (en) 2005-06-30 2007-01-11 Anthrogenesis Corporation Repair of tympanic membrane using placenta derived collagen biofabric
DE102005060466A1 (en) 2005-12-17 2007-06-28 Bayer Cropscience Ag carboxamides
ES2540561T3 (en) 2005-12-20 2015-07-10 Incyte Corporation N-hydroxyamidinoheterocycles as indolamine 2,3-dioxygenase modulators
US20070203140A1 (en) 2006-02-09 2007-08-30 Combs Andrew P N-hydroxyguanidines as modulators of indoleamine 2,3-dioxygenase
JP4297449B2 (en) 2006-05-12 2009-07-15 株式会社サクラクレパス India ink
CL2007002650A1 (en) 2006-09-19 2008-02-08 Incyte Corp COMPOUNDS DERIVED FROM HETEROCICLO N-HIDROXIAMINO; PHARMACEUTICAL COMPOSITION, USEFUL TO TREAT CANCER, VIRAL INFECTIONS AND NEURODEGENERATIVE DISORDERS BETWEEN OTHERS.
EP2064207B1 (en) 2006-09-19 2013-11-06 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
US20080146624A1 (en) 2006-09-19 2008-06-19 Incyte Corporation Amidines as modulators of indoleamine 2,3-dioxygenase
WO2008036643A2 (en) 2006-09-19 2008-03-27 Incyte Corporation Amidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
US20080182882A1 (en) 2006-11-08 2008-07-31 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
AU2007333194A1 (en) 2006-12-08 2008-06-19 Exelixis, Inc. LXR and FXR modulators
CL2008000066A1 (en) 2007-01-12 2008-08-01 Smithkline Beecham Corp COMPOUNDS DERIVED FROM (5-HYDROXY-3-OXO-2,3-DIHYDROPIRIDAZINE-4-CARBONYL) GLYCINE, HIFROXYLASE HYDROXYLASE HIF INHIBITORS; PREPARATION PROCEDURE; PHARMACEUTICAL COMPOSITION THAT INCLUDES SUCH COMPOUNDS; AND ITS USE IN THE TREATMENT OF THE ANEM
EA201001030A1 (en) 2007-12-19 2011-02-28 Амген Инк. Condensed Compounds of Pyridine, Pyrimidine, and Triazine as Cellular Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Cycle Capsule inhibitors
CA2709784A1 (en) 2007-12-21 2009-07-09 University Of Rochester Method for altering the lifespan of eukaryotic organisms
EP2824100B1 (en) * 2008-07-08 2018-02-21 Incyte Holdings Corporation 1,2,5-Oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
PA8852901A1 (en) 2008-12-22 2010-07-27 Lilly Co Eli PROTEIN CINASE INHIBITORS
UY33227A (en) 2010-02-19 2011-09-30 Novartis Ag PIRROLOPIRIMIDINE COMPOUNDS AS INHIBITORS OF THE CDK4 / 6
PT2632467T (en) 2010-10-25 2016-08-29 G1 Therapeutics Inc Cdk inhibitors
MX2013010871A (en) 2011-03-23 2014-01-31 Amgen Inc Fused tricyclic dual inhibitors of cdk 4/6 and flt3.
US10034939B2 (en) 2012-10-26 2018-07-31 The University Of Chicago Synergistic combination of immunologic inhibitors for the treatment of cancer
AR098343A1 (en) 2013-11-08 2016-05-26 Incyte Holdings Corp PROCESS FOR THE SYNTHESIS OF AN INDOLAMINE 2,3-DIOXYGENASE INHIBITOR
MX2016010080A (en) 2014-02-04 2016-10-07 Incyte Corp Combination of a pd-1 antagonist and an ido1 inhibitor for treating cancer.
WO2016054555A2 (en) 2014-10-03 2016-04-07 Novartis Ag Combination therapies
CN107847574B (en) 2015-07-30 2023-05-23 宏观基因有限公司 PD-1 binding molecules and methods of use thereof
CN109562137A (en) 2015-09-01 2019-04-02 第波生物公司 For treating the method and composition for reacting the related patient's condition with abnormal inflammatory
MA43172A (en) 2015-11-04 2018-09-12 Incyte Corp PHARMACEUTICAL COMPOSITIONS AND METHODS OF INHIBITION OF INDOLAMINE 2,3-DIOXYGENASE AND THEIR INDICATIONS
JP2018020710A (en) 2016-08-05 2018-02-08 三井造船株式会社 Rudder for craft, and craft
AU2019205904A1 (en) 2018-01-05 2020-06-18 Dicerna Pharmaceuticals, Inc. Reducing beta-catenin and IDO expression to potentiate immunotherapy
MX2022001133A (en) 2019-08-01 2022-04-25 Incyte Corp A dosing regimen for an ido inhibitor.

Also Published As

Publication number Publication date
KR101847107B1 (en) 2018-04-10
IL235870A0 (en) 2015-01-29
RS53688B9 (en) 2020-01-31
DK2315756T3 (en) 2014-10-13
HUE036813T2 (en) 2018-07-30
TW201006827A (en) 2010-02-16
CA3012229A1 (en) 2010-01-14
US8088803B2 (en) 2012-01-03
IL235870A (en) 2016-05-31
SG192485A1 (en) 2013-08-30
DK2315756T5 (en) 2015-08-03
BR122019015876B1 (en) 2020-03-10
KR101783004B1 (en) 2017-09-28
US20140023663A1 (en) 2014-01-23
CO6341622A2 (en) 2011-11-21
KR101927291B1 (en) 2018-12-10
AU2018267589A1 (en) 2018-12-06
CA2743975A1 (en) 2010-01-14
JP2011527686A (en) 2011-11-04
US10034864B2 (en) 2018-07-31
JP5465720B2 (en) 2014-04-09
ME03065B (en) 2019-01-20
IL210402A (en) 2015-02-26
HK1206029A1 (en) 2015-12-31
RS53688B1 (en) 2015-04-30
KR20160110969A (en) 2016-09-23
US10369137B2 (en) 2019-08-06
AU2020239772A1 (en) 2020-10-22
AR072490A1 (en) 2010-09-01
HRP20141094T1 (en) 2015-01-16
US20100015178A1 (en) 2010-01-21
BRPI0915692B1 (en) 2019-12-03
PL2315756T3 (en) 2015-02-27
US9789094B2 (en) 2017-10-17
CA3012229C (en) 2020-11-10
CA2743975C (en) 2018-09-11
EP2824100B1 (en) 2018-02-21
PH12014500947A1 (en) 2015-03-30
KR102031538B1 (en) 2019-11-08
AU2009268739B2 (en) 2014-05-08
SI2315756T1 (en) 2014-12-31
MY192633A (en) 2022-08-29
EA022669B1 (en) 2016-02-29
EP2824100A1 (en) 2015-01-14
US20180177769A1 (en) 2018-06-28
AU2016204914A1 (en) 2016-08-04
CN102164902B (en) 2014-07-23
ES2524266T3 (en) 2014-12-04
US9320732B2 (en) 2016-04-26
ES2665419T3 (en) 2018-04-25
MY177058A (en) 2020-09-03
CL2009001554A1 (en) 2009-10-30
US20190298700A1 (en) 2019-10-03
HRP20180662T1 (en) 2018-06-01
CN104042611B (en) 2019-05-14
US20140315962A1 (en) 2014-10-23
CR11871A (en) 2011-03-30
US20220331296A1 (en) 2022-10-20
PL2824100T3 (en) 2018-07-31
US8822511B2 (en) 2014-09-02
WO2010005958A3 (en) 2010-06-24
US20240173303A1 (en) 2024-05-30
AU2018200457A1 (en) 2018-02-08
SMT201400179B (en) 2015-01-15
MY171866A (en) 2019-11-05
PT2315756E (en) 2014-12-16
JP5819451B2 (en) 2015-11-24
US20150190378A1 (en) 2015-07-09
KR20110031971A (en) 2011-03-29
TWI453204B (en) 2014-09-21
KR20180133538A (en) 2018-12-14
US8993605B2 (en) 2015-03-31
RS57132B1 (en) 2018-07-31
KR101649548B1 (en) 2016-08-19
NZ590268A (en) 2012-11-30
LT2824100T (en) 2018-05-10
AU2014210662A1 (en) 2014-08-28
US20170348289A1 (en) 2017-12-07
ECSP11010798A (en) 2011-03-31
EP2315756B9 (en) 2015-07-22
CN104042611A (en) 2014-09-17
CN102164902A (en) 2011-08-24
US20160220543A1 (en) 2016-08-04
EP3360873A1 (en) 2018-08-15
US10653677B2 (en) 2020-05-19
MX2011000235A (en) 2011-02-23
AU2020239772B2 (en) 2022-09-15
EP2315756B1 (en) 2014-09-03
JP2014114299A (en) 2014-06-26
PH12014500947B1 (en) 2015-03-30
EA201500530A1 (en) 2015-08-31
EA201170161A1 (en) 2011-08-30
WO2010005958A2 (en) 2010-01-14
NO2824100T3 (en) 2018-07-21
BRPI0915692B8 (en) 2021-05-25
IL210402A0 (en) 2011-03-31
KR20170113707A (en) 2017-10-12
PE20110308A1 (en) 2011-06-10
BR122019015876B8 (en) 2021-07-27
HK1157692A1 (en) 2012-07-06
PT2824100T (en) 2018-05-10
KR20180037325A (en) 2018-04-11
CL2014000363A1 (en) 2014-08-01
US20210030722A1 (en) 2021-02-04
EA029781B1 (en) 2018-05-31
US8796319B2 (en) 2014-08-05
CY1120617T1 (en) 2019-12-11
AU2018267589B2 (en) 2020-06-25
SI2824100T1 (en) 2018-06-29
EP2315756A2 (en) 2011-05-04
DK2824100T3 (en) 2018-04-16
AU2009268739A1 (en) 2010-01-14
ES2524266T9 (en) 2015-10-05
US20120058079A1 (en) 2012-03-08
US11207302B2 (en) 2021-12-28

Similar Documents

Publication Publication Date Title
SG10201805844QA (en) 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
NZ730134A (en) Substituted tricyclic compounds as fgfr inhibitors
EP2170337A4 (en) Novel triazolopyridazines
NZ700928A (en) Dna-pk inhibitors
GEP20135785B (en) Pyrrolopyrimidine compounds as cdk inhibitors
EA201101650A1 (en) NEW PYRIMIDINE DERIVATIVES AND THEIR APPLICATION IN THE TREATMENT OF MALIGNANT NONFORMS AND THE FOLLOWING DISEASES
UA101493C2 (en) Azetidine and cyclobutane derivatives as jak inhibitors
UA108743C2 (en) HINAZOLINE-4 (3H) -ONE DERIVATIVES FOR APPLICATION AS RI-KINASE INHIBITORS
CA2818187C (en) Bromodomain inhibitors and uses thereof
EA201001143A1 (en) ACTIVATORS OF THE PERFORMERS "EXECUTORS" 3, 6 And 7
MX2011006006A (en) Compounds, pharmaceutical composition and methods for use in treating metabolic disorders.
EA201291099A1 (en) NEW IMMUNODULATOR AND ANTI-INFLAMMATORY CONNECTIONS
MX2011013032A (en) Inhibitors of phosphatidylinositol 3-kinase.
AU2009319796A8 (en) Substituted octahydrocyclopnta (c) pyrrol-4 -amines as calcium channel blockers
MX2012000178A (en) 2-carboxamide cycloamino ureas useful as pi3k inhibitors.
MX2011008645A (en) Tetrahydrothiazolopyridine inhibitors of phosphatidylinositol 3-kinase.
MX2011012524A (en) Inhibitors of c-met protein kinase.
MX2011012522A (en) Substituted pyrazole inhibitors of c-met protein kinase.
MX2011013324A (en) Use of substituted oxindole derivatives for the treatment and prophylaxis of pain.
WO2009126335A3 (en) Ant2 inhibitor compounds and methods of use thereof
WO2009151495A3 (en) Oxazole compounds, compositions and methods of use
UA105010C2 (en) 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
EA201890183A1 (en) 1,2,5-OXADIAZOLES AS INDOLAMIN-2,3-DIOXYGENASE INHIBITORS
CY1115799T1 (en) 1,2,5-oxadiazoles as inhibitors of 2,3-indoleamine dioxygenation
PH12016502133A1 (en) Substituted tricycle compounds as fgfr inhibitors