AU2001294515A1 - Use of stat-6 inhibitors as therapeutic agents - Google Patents

Use of stat-6 inhibitors as therapeutic agents

Info

Publication number
AU2001294515A1
AU2001294515A1 AU2001294515A AU9451501A AU2001294515A1 AU 2001294515 A1 AU2001294515 A1 AU 2001294515A1 AU 2001294515 A AU2001294515 A AU 2001294515A AU 9451501 A AU9451501 A AU 9451501A AU 2001294515 A1 AU2001294515 A1 AU 2001294515A1
Authority
AU
Australia
Prior art keywords
stat
inhibitors
therapeutic agents
therapeutic
agents
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.)
Abandoned
Application number
AU2001294515A
Inventor
Sylvie Barchechath
Dennis A. Carson
Howard B Cottam
Lorenzo M. Leoni
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.)
University of California
Original Assignee
University of California
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
Priority claimed from US09/637,531 external-priority patent/US6696441B1/en
Application filed by University of California filed Critical University of California
Publication of AU2001294515A1 publication Critical patent/AU2001294515A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
AU2001294515A 2000-08-11 2001-08-10 Use of stat-6 inhibitors as therapeutic agents Abandoned AU2001294515A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US09/637,531 2000-08-11
US09/637,531 US6696441B1 (en) 2000-08-11 2000-08-11 Inhibition of p53-induced stress response
US30134001P 2001-06-26 2001-06-26
US60/301,340 2001-06-26
PCT/US2001/025175 WO2002014321A1 (en) 2000-08-11 2001-08-10 Use of stat-6 inhibitors as therapeutic agents

Publications (1)

Publication Number Publication Date
AU2001294515A1 true AU2001294515A1 (en) 2002-02-25

Family

ID=26972310

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2001294515A Abandoned AU2001294515A1 (en) 2000-08-11 2001-08-10 Use of stat-6 inhibitors as therapeutic agents

Country Status (2)

Country Link
AU (1) AU2001294515A1 (en)
WO (1) WO2002014321A1 (en)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
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WO2002076439A2 (en) * 2001-03-23 2002-10-03 The Board Of Trustees Of The University Of Illinois Compounds capable of modulating the activity of multidrug transporters and therapeutic use of the same
WO2002088107A1 (en) * 2001-04-26 2002-11-07 Eisai Co., Ltd. Nitrogenous fused-ring compound having pyrazolyl group as substituent and medicinal composition thereof
AU2003299651A1 (en) 2002-12-11 2004-06-30 Merck And Co., Inc. Tyrosine kinase inhibitors
US7157460B2 (en) 2003-02-20 2007-01-02 Sugen Inc. Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
US7186832B2 (en) 2003-02-20 2007-03-06 Sugen Inc. Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
US7671058B2 (en) 2006-06-21 2010-03-02 Institute Of Medicinal Molecular Design, Inc. N-(3,4-disubstituted phenyl) salicylamide derivatives
FR2910895B1 (en) * 2006-12-29 2010-08-27 Biopharmed "IMINO-TETRAHYDROBENZOTRIAZOLES DERIVATIVES HAVING ANTI-MIGRATORY PROPERTIES OF DEPENDENT METASTASES"
WO2008155441A1 (en) * 2007-06-20 2008-12-24 Marikki Laiho Activators and therapeutic applications thereof
US8188083B2 (en) 2007-06-28 2012-05-29 Abbott Laboratories Triazolopyridazines
EP2218464A1 (en) * 2009-02-11 2010-08-18 Technische Universität München Compounds for non-invasive measurement of aggregates of amyloid peptides
US8569002B2 (en) 2010-10-20 2013-10-29 The Board Of Regents Of The University Of Texas System Multiplexed luciferase reporter assay systems
WO2015027431A1 (en) * 2013-08-29 2015-03-05 Merck Sharp & Dohme Corp. 2,2-difluorodioxolo a2a receptor antagonists
TWI648282B (en) * 2014-03-27 2019-01-21 印度商托仁特生技有限公司 New fusion imidazole benzothiazole compound
US20170107216A1 (en) 2015-10-19 2017-04-20 Incyte Corporation Heterocyclic compounds as immunomodulators
PL3377488T3 (en) 2015-11-19 2022-12-19 Incyte Corporation Heterocyclic compounds as immunomodulators
MD3394033T2 (en) 2015-12-22 2021-04-30 Incyte Corp Heterocyclic compounds as immunomodulators
US20170320875A1 (en) 2016-05-06 2017-11-09 Incyte Corporation Heterocyclic compounds as immunomodulators
WO2017205464A1 (en) 2016-05-26 2017-11-30 Incyte Corporation Heterocyclic compounds as immunomodulators
MY197280A (en) 2016-06-20 2023-06-09 Incyte Corp Heterocyclic compounds as immunomodulators
EP3484866B1 (en) 2016-07-14 2022-09-07 Incyte Corporation Heterocyclic compounds as immunomodulators
WO2018044783A1 (en) 2016-08-29 2018-03-08 Incyte Corporation Heterocyclic compounds as immunomodulators
ES2899402T3 (en) 2016-12-22 2022-03-11 Incyte Corp Pyridine derivatives as immunomodulators
MD3558990T2 (en) 2016-12-22 2023-02-28 Incyte Corp Tetrahydro imidazo[4,5-c]pyridine derivatives as PD-L1 internalization inducers
KR20190111025A (en) 2016-12-22 2019-10-01 인사이트 코포레이션 Benzoxazole Derivatives As Immunomodulators
WO2018119236A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Triazolo[1,5-a]pyridine derivatives as immunomodulators
PE20211911A1 (en) 2018-03-30 2021-09-28 Incyte Corp HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS
JOP20200288A1 (en) 2018-05-11 2020-11-11 Incyte Corp Tetrahydro-imidazo[4,5-c]pyridine derivatives as pd-l1 immunomodulators
AR119624A1 (en) 2019-08-09 2021-12-29 Incyte Corp SALTS OF A PD-1/PD-L1 INHIBITOR
EP4037773A1 (en) 2019-09-30 2022-08-10 Incyte Corporation Pyrido[3,2-d]pyrimidine compounds as immunomodulators
KR20220101664A (en) 2019-11-11 2022-07-19 인사이트 코포레이션 Salts and crystalline forms of PD-1/PD-L1 inhibitors
PE20231438A1 (en) 2020-11-06 2023-09-14 Incyte Corp PROCESS FOR MAKING A PD-1/PD-L1 INHIBITOR AND SALTS AND CRYSTALLINE FORMS THEREOF
WO2022099075A1 (en) 2020-11-06 2022-05-12 Incyte Corporation Crystalline form of a pd-1/pd-l1 inhibitor
US11780836B2 (en) 2020-11-06 2023-10-10 Incyte Corporation Process of preparing a PD-1/PD-L1 inhibitor

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5185446A (en) * 1990-09-04 1993-02-09 Neurogen Corporation Certain cycloalkyl imidazopyrimidines; a new class of gaba brainreceptor ligands
JPH11106340A (en) * 1997-10-02 1999-04-20 Sumitomo Pharmaceut Co Ltd Stat6 activation inhibitor
EP1143943B1 (en) * 1999-01-29 2007-12-12 The Board Of Trustees Of The University Of Illinois USE OF p53 INHIBITORS FOR THE TREATMENT OF SIDE EFFECTS OF CANCER THERAPY

Also Published As

Publication number Publication date
WO2002014321A9 (en) 2003-03-27
WO2002014321A1 (en) 2002-02-21

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