WO2005002572A3 - Use of [3.2.0] heterocyclic compounds and analogs thereof for the treatment of cancer, inflammation and infectious diseases - Google Patents

Use of [3.2.0] heterocyclic compounds and analogs thereof for the treatment of cancer, inflammation and infectious diseases Download PDF

Info

Publication number
WO2005002572A3
WO2005002572A3 PCT/US2004/019543 US2004019543W WO2005002572A3 WO 2005002572 A3 WO2005002572 A3 WO 2005002572A3 US 2004019543 W US2004019543 W US 2004019543W WO 2005002572 A3 WO2005002572 A3 WO 2005002572A3
Authority
WO
WIPO (PCT)
Prior art keywords
cancer
analogs
inflammation
treatment
infectious diseases
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.)
Ceased
Application number
PCT/US2004/019543
Other languages
French (fr)
Other versions
WO2005002572A2 (en
Inventor
Michael Palladino
Saskia Theodora Corn Neuteboom
Venkata Rami Reddy Macherla
Barbara Christine Potts
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.)
Nereus Pharmaceuticals Inc
Original Assignee
Nereus Pharmaceuticals Inc
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 to DE602004031614T priority Critical patent/DE602004031614D1/en
Priority to AU2004253478A priority patent/AU2004253478A1/en
Priority to AT04776757T priority patent/ATE499934T1/en
Priority to BRPI0411677-1A priority patent/BRPI0411677A/en
Priority to NZ544588A priority patent/NZ544588A/en
Priority to JP2006517404A priority patent/JP2007523862A/en
Priority to EP04776757A priority patent/EP1638552B1/en
Priority to MXPA05013982A priority patent/MXPA05013982A/en
Application filed by Nereus Pharmaceuticals Inc filed Critical Nereus Pharmaceuticals Inc
Priority to CA2532066A priority patent/CA2532066C/en
Publication of WO2005002572A2 publication Critical patent/WO2005002572A2/en
Publication of WO2005002572A3 publication Critical patent/WO2005002572A3/en
Priority to IL172705A priority patent/IL172705A/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • A61P25/28Drugs 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
    • 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
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • A61P33/02Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • A61P33/02Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06Antimalarials
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pulmonology (AREA)
  • Rheumatology (AREA)
  • Hospice & Palliative Care (AREA)
  • Dermatology (AREA)
  • Psychiatry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Disclosed are methods of treating cancer, inflammatory conditions, and/or infectious disease in an animal comprising: administering to the animal, a therapeutically effective amount of a [3.2.0] heterocyclic compound, Preferably a 6-oxa-2-azabicyclo [3.2.0] heptane-3, 7-dione, such as salinosporamide A. The animal is a mammal, preferably a human or a rodent.
PCT/US2004/019543 2003-06-20 2004-06-18 Use of [3.2.0] heterocyclic compounds and analogs thereof for the treatment of cancer, inflammation and infectious diseases Ceased WO2005002572A2 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
EP04776757A EP1638552B1 (en) 2003-06-20 2004-06-18 Use of (3.2.0) heterocyclic compounds and analogs thereof for the treatment of cancer
AT04776757T ATE499934T1 (en) 2003-06-20 2004-06-18 USE OF (3.2.0) HETEROCYCLIC COMPOUNDS AND THEIR ANALOGUES FOR THE TREATMENT OF CANCER
BRPI0411677-1A BRPI0411677A (en) 2003-06-20 2004-06-18 methods of using heterocyclic compounds [3.2.0] and their analogues
NZ544588A NZ544588A (en) 2003-06-20 2004-06-18 Use of salinosporamide A and analogs thereof for the treatment of cancer, inflammation and infectious diseases
JP2006517404A JP2007523862A (en) 2003-06-20 2004-06-18 Use of [3.2.0] heterocyclic compounds and their analogs for the treatment of cancer, inflammation and infectious diseases
DE602004031614T DE602004031614D1 (en) 2003-06-20 2004-06-18 USE OF (3.2.0) HETEROCYCLIC COMPOUNDS AND ITS ANALOGUE FOR THE TREATMENT OF CANCER
AU2004253478A AU2004253478A1 (en) 2003-06-20 2004-06-18 Use of [3.2.0] heterocyclic compounds and analogs thereof for the treatment of cancer, inflammation and infectious diseases
MXPA05013982A MXPA05013982A (en) 2003-06-20 2004-06-18 Use of [3.2.0] heterocyclic compounds and analogs thereof for the treatment of cancer, inflammation and infectious diseases.
CA2532066A CA2532066C (en) 2003-06-20 2004-06-18 Methods of using [3.2.0] heterocyclic compounds and analogs thereof
IL172705A IL172705A (en) 2003-06-20 2005-12-20 Use of 4-(2-chloroethyl)-1-((2-cyclohexen-1-yl)hydroxymethyl)-5-methyl-6-oxa-2-azabicyclo[3.2.0]heptane-3,7-dione and its esters in the manufacture of medicaments

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US48027003P 2003-06-20 2003-06-20
US60/480,270 2003-06-20
US56695204P 2004-04-30 2004-04-30
US60/566,952 2004-04-30

Publications (2)

Publication Number Publication Date
WO2005002572A2 WO2005002572A2 (en) 2005-01-13
WO2005002572A3 true WO2005002572A3 (en) 2005-05-12

Family

ID=33567612

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2004/019543 Ceased WO2005002572A2 (en) 2003-06-20 2004-06-18 Use of [3.2.0] heterocyclic compounds and analogs thereof for the treatment of cancer, inflammation and infectious diseases

Country Status (14)

Country Link
US (2) US20050049294A1 (en)
EP (1) EP1638552B1 (en)
JP (2) JP2007523862A (en)
KR (1) KR20060026052A (en)
CN (1) CN102151261A (en)
AT (1) ATE499934T1 (en)
AU (1) AU2004253478A1 (en)
BR (1) BRPI0411677A (en)
CA (1) CA2532066C (en)
DE (1) DE602004031614D1 (en)
IL (1) IL172705A (en)
MX (1) MXPA05013982A (en)
NZ (1) NZ544588A (en)
WO (1) WO2005002572A2 (en)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4395549B2 (en) * 2000-11-16 2010-01-13 ザ レジェンツ オブ ザ ユニヴァースティ オブ カリフォルニア Marine actinomycete taxa for the discovery of drugs and fermentation products
US7176232B2 (en) 2002-06-24 2007-02-13 The Regents Of The University Of California Salinosporamides and methods for use thereof
US7179834B2 (en) * 2002-06-24 2007-02-20 The Regents Of The University Of California Salinosporamides and methods for use thereof
KR20060026052A (en) 2003-06-20 2006-03-22 니리어스 파마슈티컬즈, 인코퍼레이션 How to use [3.2.0] heterocyclic compounds and their analogs for the treatment of cancer, inflammatory and infectious diseases
EP2441767B1 (en) * 2003-06-20 2015-06-10 The Regents of The University of California Salinosporamides and methods for use thereof
JP4691041B2 (en) 2003-11-20 2011-06-01 チルドレンズ ホスピタル メディカル センター GTPase inhibitors and methods of use
WO2005099687A2 (en) * 2004-04-09 2005-10-27 President And Fellows Of Harvard College Analogs of salinosporamide a
US7579371B2 (en) 2004-04-30 2009-08-25 Nereus Pharmaceuticals, Inc. Methods of using [3.2.0] heterocyclic compounds and analogs thereof
BRPI0509824A (en) * 2004-04-30 2007-10-09 Nereus Pharmaceuticals Inc heterocyclic compounds [3.2.0] and methods of use thereof
MX2007000392A (en) * 2004-07-12 2007-06-15 Bayer Cropscience Ag Substituted 2-pyrrolidone derivatives as fungicides and insecticides.
CA2590334A1 (en) * 2004-12-03 2006-06-08 Nereus Pharmaceuticals, Inc. Methods of using [3.2.0] heterocyclic compounds and analogs thereof
SG157365A1 (en) * 2004-12-03 2009-12-29 Dana Farber Cancer Inst Inc Compositions and methods for treating neoplastic diseases
US7826982B2 (en) 2005-07-29 2010-11-02 Children's Hospital Medical Center Method of identifying inhibitors using a 3-D structure of RAC-1 GTPASE
US7691896B2 (en) 2005-08-10 2010-04-06 President And Fellows Of Harvard College Analogs of salinosporamide A
WO2007021897A1 (en) * 2005-08-10 2007-02-22 President And Fellows Of Harvard College Analogs of salinosporamide a
US7572606B1 (en) * 2005-09-09 2009-08-11 Nereus Pharmaceuticals, Inc. Biosyntheses of salinosporamide A and its analogs and related methods of making salinosporamide A and its analogs
US7465720B2 (en) 2005-09-12 2008-12-16 President And Fellows Of Harvard College Proteasome inhibiting β-lactam compounds
BRPI0618198A2 (en) * 2005-11-04 2018-06-26 Nereus Pharmaceuticals Inc cancer and lymphoma treatment, prevention or inhibition methods, composition, kit, and therapy resistant cancer treatment method
NZ572026A (en) 2006-04-06 2011-12-22 Nereus Pharmaceuticals Inc Total synthesis of salinosporamide a and analogs thereof
US20090280130A1 (en) * 2006-06-14 2009-11-12 Children's Medical Center Corporation Method for the treatment of anthrax toxicity
US8986971B2 (en) 2006-09-22 2015-03-24 Triphase Research And Development I Corp. Salt formulations for the fermentation of marine microorganisms
WO2008095195A2 (en) 2007-02-02 2008-08-07 Nereus Pharmaceuticals, Inc. Lyophilized formulations of salinosporamide a
WO2008137780A2 (en) * 2007-05-04 2008-11-13 Nereus Pharmaceuticals, Inc. Use of [3.2.0] heterocyclic compounds and analogs thereof for treating infectious diseases
US8394816B2 (en) * 2007-12-07 2013-03-12 Irene Ghobrial Methods of using [3.2.0] heterocyclic compounds and analogs thereof in treating Waldenstrom's Macroglobulinemia
EP2088205A1 (en) 2008-02-11 2009-08-12 Institut National De La Sante Et De La Recherche Medicale (Inserm) PSMB10: A diagnosis marker and therapeutic target of chronic rejection.
JP2011514352A (en) 2008-03-07 2011-05-06 ネレアス ファーマシューティカルズ インコーポレイテッド Total synthesis of salinosporamide A and its analogs
US20090285836A1 (en) * 2008-04-14 2009-11-19 Nereus Pharmaceuticals, Inc. Use of salinosporamide a to inhibit metastasis
CN102089312A (en) * 2008-05-12 2011-06-08 尼瑞斯药品公司 Salinosporamide derivatives as proteasome inhibitors
US20110111417A1 (en) 2008-05-14 2011-05-12 Millennium Pharmaceuticals, Inc. Methods and kits for monitoring the effects of immunomodulators on adaptive immunity
US8073633B2 (en) * 2008-12-30 2011-12-06 The Invention Science Fund I, Llc Computational methods and systems for suggesting modulators of CYP450 as treatment options
US8321151B2 (en) 2008-12-30 2012-11-27 The Invention Science Fund I, Llc Computational methods and systems for treatment in relation to modulation of CYP450 enzyme activity
US8315815B2 (en) 2008-12-30 2012-11-20 The Invention Science Fund I, Llc Computational methods and systems for suggesting modulators of CYP450 as treatment options
WO2010096574A1 (en) 2009-02-20 2010-08-26 Lisanti Michael P A method of diagnosis or prognosis of a neoplasm comprising determining the level of expression of a protein in stromal cells adjacent to the neoplasm
US9126997B1 (en) 2010-09-07 2015-09-08 Northwestern University Synergistic effect of glucocorticoid receptor agonists in combination with proteosome inhibitors for treating leukemia and myeloma
US9272014B2 (en) 2011-03-29 2016-03-01 Texas Tech University System Galectin-3C combination therapy for human cancer
JP6238900B2 (en) 2011-10-28 2017-11-29 ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. Biomarkers of response to NAE inhibitors
CN104126017A (en) 2011-11-11 2014-10-29 米伦纽姆医药公司 Biomarkers of response to proteasome inhibitors
CA2862492A1 (en) 2012-01-24 2013-08-01 Millennium Pharmaceuticals, Inc. Methods of treatment of cancer
WO2013112881A1 (en) 2012-01-27 2013-08-01 Thomas Jefferson University Mct protein inhibitor-related prognostic and therapeutic methods
EP2904115B1 (en) 2012-10-01 2018-08-08 Millennium Pharmaceuticals, Inc. Biomarkers and methods to predict response to inhibitors and uses thereof
EA201590916A1 (en) 2012-11-09 2016-02-29 Корнэлл Юниверсити LOW MOLECULAR INHIBITORS MALT1
US10022372B2 (en) 2013-04-19 2018-07-17 Thomas Jefferson University Caveolin-1 related methods for treating glioblastoma with temozolomide
US10028503B2 (en) 2014-06-18 2018-07-24 Children's Hospital Medical Center Platelet storage methods and compositions for same
JP7171550B2 (en) 2016-06-01 2022-11-15 セルジュヌ アンテルナシオナル ドゥジエム ソシエテ ア レスポンサビリテ リミティー Use of marizomib for treatment of central nervous system (CNS) cancer
US10703760B2 (en) 2016-08-19 2020-07-07 Celgene International Ii Sàrl Morphic forms of marizomib and uses thereof
KR101953671B1 (en) * 2017-08-21 2019-03-04 충남대학교산학협력단 Composition for preventing, improving or treating atopic dermatitis containing proteasome inhibitor as effective component
EP3546447A1 (en) * 2018-03-29 2019-10-02 Heidelberg Pharma GmbH Synthesis of (2s,3r,4r)-4,5-dihydroxyisoleucine and derivatives
CN115006532A (en) * 2021-03-05 2022-09-06 广州医科大学 Use of proteasome inhibitors

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996032105A1 (en) * 1995-04-12 1996-10-17 President And Fellows Of Harvard College Lactacystin analogs
WO2000023614A1 (en) * 1998-10-20 2000-04-27 Millennium Pharmaceuticals, Inc. Method for monitoring proteasome inhibitor drug action
US20010002391A1 (en) * 1997-02-15 2001-05-31 Stephen Brand Treatment of infarcts
US20010051654A1 (en) * 1997-09-25 2001-12-13 Elliott Peter J. Treatment of inflammatory and autoimmune diseases
WO2002047610A2 (en) * 2000-11-16 2002-06-20 The Regents Of The University Of California Marine actinomycete taxon for drug and fermentation product dicovery
US20040138196A1 (en) * 2002-06-24 2004-07-15 William Fenical Salinosporamides and methods for use thereof
WO2004071382A2 (en) * 2003-02-14 2004-08-26 Bayer Healthcare Ag Substituted heterocycles
WO2005003137A1 (en) * 2003-06-20 2005-01-13 The Regents Of The University Of California Salinosporamides and methods for use thereof

Family Cites Families (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5133974A (en) * 1989-05-05 1992-07-28 Kv Pharmaceutical Company Extended release pharmaceutical formulations
US5276182A (en) * 1990-07-09 1994-01-04 The Dow Chemical Company Process for preparing polyurea oligomers
DE4039602A1 (en) * 1990-12-12 1992-06-17 Bauer Kurt Heinz Prof Dr PHARMACEUTICAL FORMULATIONS
KR100221695B1 (en) * 1991-08-12 1999-09-15 그린 마틴, 브라이언 쥐 테슬리 Pharmaceutical Formulation Formulations
US5653962A (en) * 1991-12-12 1997-08-05 Glaxo Group Limited Aerosol formulations containing P134a and particulate medicaments
AU5612694A (en) * 1992-11-27 1994-06-22 Napro Biotherapeutics, Inc. Injectable composition
JPH08507754A (en) 1993-02-10 1996-08-20 ザ・プレジデント・アンド・フェローズ・オブ・ハーバード・カレッジ Role of ATP-ubiquitin-dependent proteolysis in MHC-1-restricted antigen presentation and its inhibitor
US5654286A (en) * 1993-05-12 1997-08-05 Hostetler; Karl Y. Nucleotides for topical treatment of psoriasis, and methods for using same
EP1475091A1 (en) * 1993-10-01 2004-11-10 Roche Palo Alto LLC Mycophenolate mofetil - high dose oral suspensions
US5707641A (en) * 1994-10-13 1998-01-13 Pharmaderm Research & Development Ltd. Formulations comprising therapeutically-active proteins or polypeptides
IE80468B1 (en) * 1995-04-04 1998-07-29 Elan Corp Plc Controlled release biodegradable nanoparticles containing insulin
US6838477B2 (en) * 1995-04-12 2005-01-04 President And Fellows Of Harvard College Lactacystin analogs
US5653987A (en) * 1995-05-16 1997-08-05 Modi; Pankaj Liquid formulations for proteinic pharmaceuticals
US5726181A (en) * 1995-06-05 1998-03-10 Bionumerik Pharmaceuticals, Inc. Formulations and compositions of poorly water soluble camptothecin derivatives
US5667809A (en) * 1995-06-07 1997-09-16 Alliance Pharmaceutical Corp. Continuous fluorochemical microdispersions for the delivery of lipophilic pharmaceutical agents
US5874443A (en) * 1995-10-19 1999-02-23 Trega Biosciences, Inc. Isoquinoline derivatives and isoquinoline combinatorial libraries
US5886210A (en) * 1996-08-22 1999-03-23 Rohm And Haas Company Method for preparing aromatic compounds
CA2283636A1 (en) 1997-03-20 1998-09-24 Variagenics, Inc. Target genes for allele-specific drugs
US5922683A (en) * 1997-05-29 1999-07-13 Abbott Laboratories Multicyclic erythromycin derivatives
US6333358B1 (en) * 1997-08-04 2001-12-25 Taisho Pharmaceutical Co., Ltd. Aryloxyaniline derivatives
BR9811304A (en) 1997-08-15 2001-11-13 Francois Soucy Synthesis of clasto-lactacistin "beta" -lactone and its analogues
US6133308A (en) * 1997-08-15 2000-10-17 Millennium Pharmaceuticals, Inc. Synthesis of clasto-lactacystin beta-lactone and analogs thereof
WO1999015183A1 (en) 1997-09-25 1999-04-01 Proscript Inc. PROTEASOME INHIBITORS, UBIQUITIN PATHWAY INHIBITORS OR AGENTS THAT INTERFERE WITH THE ACTIVATION OF NF-λB VIA THE UBIQUITIN PROTEASOME PATHWAY TO TREAT INFLAMMATORY AND AUTOIMMUNE DISEASES
CA2219867A1 (en) 1997-10-31 1999-04-30 Jiangping Wu The use of proteasome inhibitors for treating cancer, inflammation, autoimmune disease, graft rejection and septic shock
EP1032377B1 (en) * 1997-11-21 2010-11-17 Purdue Neuroscience Company Substituted 2-aminoacetamides and the use thereof
US6617171B2 (en) * 1998-02-27 2003-09-09 The General Hospital Corporation Methods for diagnosing and treating autoimmune disease
BR9909146A (en) * 1998-03-26 2000-12-05 Shionogi & Co Indole derivatives showing antiviral activity
US6509331B1 (en) * 1998-06-22 2003-01-21 Elan Pharmaceuticals, Inc. Deoxyamino acid compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
FR2784988B1 (en) * 1998-10-23 2002-09-20 Adir NOVEL DIHYDRO AND TETRAHYDROQUINOLEINIC COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
WO2000033654A1 (en) 1998-12-04 2000-06-15 University Of Maryland Biotechnology Institute Use of protease inhibitors to modulate cellular pathways, immunity and therapies associated therewith
US20020049157A1 (en) * 1999-08-25 2002-04-25 Jiangping Wu Use of proteasome inhibitors for treating cancer, inflammation, autoimmune disease, graft rejection and septic shock
ES2272558T3 (en) * 2000-10-12 2007-05-01 Viromics Gmbh PROTEASOME INHIBITORS FOR THE TREATMENT OF INFECTIONS CAUSED BY HEPATITIS VIRUSES.
DE10316735A1 (en) * 2002-04-05 2003-11-20 Viromics Gmbh Inhibiting release, maturation and replication of Flaviviridae family viruses, e.g. for the treatment of hepatitis C virus infections, using proteasome inhibitor such as lactacystine or epoxomicin
AU2003249930A1 (en) 2002-07-03 2004-01-23 Charite - Universitatsmedizin Berlin Proteaseome inhibitors for the treatment of herpesviridae infected individuals
EP1565193B1 (en) 2002-11-06 2013-04-24 Dana-Farber Cancer Institute, Inc. Compositions for treating cancer using proteasome inhibitor PS-341
EP2441767B1 (en) * 2003-06-20 2015-06-10 The Regents of The University of California Salinosporamides and methods for use thereof
KR20060026052A (en) * 2003-06-20 2006-03-22 니리어스 파마슈티컬즈, 인코퍼레이션 How to use [3.2.0] heterocyclic compounds and their analogs for the treatment of cancer, inflammatory and infectious diseases
US7371875B2 (en) * 2004-03-12 2008-05-13 Miikana Therapeutics, Inc. Cytotoxic agents and methods of use
US7183417B2 (en) * 2004-04-09 2007-02-27 President And Fellows Of Harvard College Simple stereocontrolled synthesis of salinosporamide A
WO2005099687A2 (en) * 2004-04-09 2005-10-27 President And Fellows Of Harvard College Analogs of salinosporamide a
BRPI0509824A (en) 2004-04-30 2007-10-09 Nereus Pharmaceuticals Inc heterocyclic compounds [3.2.0] and methods of use thereof
US20060264495A1 (en) * 2004-04-30 2006-11-23 Michael Palladino Methods of using [3.2.0] heterocyclic compounds and analogs thereof
US7579371B2 (en) * 2004-04-30 2009-08-25 Nereus Pharmaceuticals, Inc. Methods of using [3.2.0] heterocyclic compounds and analogs thereof
SG157365A1 (en) * 2004-12-03 2009-12-29 Dana Farber Cancer Inst Inc Compositions and methods for treating neoplastic diseases
WO2006124902A2 (en) * 2005-05-16 2006-11-23 Sloan-Kettering Institute For Cancer Research Synthesis of salinosporamide a and analogues thereof
US7572606B1 (en) * 2005-09-09 2009-08-11 Nereus Pharmaceuticals, Inc. Biosyntheses of salinosporamide A and its analogs and related methods of making salinosporamide A and its analogs
DE102005046344A1 (en) * 2005-09-28 2007-03-29 Saltigo Gmbh Process for the coupling of benzylamines with haloaromatics
BRPI0618198A2 (en) * 2005-11-04 2018-06-26 Nereus Pharmaceuticals Inc cancer and lymphoma treatment, prevention or inhibition methods, composition, kit, and therapy resistant cancer treatment method
GB0605217D0 (en) * 2006-03-15 2006-04-26 Novartis Ag Method and compositions for assessing acute rejection
NZ572026A (en) 2006-04-06 2011-12-22 Nereus Pharmaceuticals Inc Total synthesis of salinosporamide a and analogs thereof
US8088923B2 (en) * 2006-07-07 2012-01-03 The Texas A&M University System Cyclic-fused beta-lactones and their synthesis
WO2008137780A2 (en) * 2007-05-04 2008-11-13 Nereus Pharmaceuticals, Inc. Use of [3.2.0] heterocyclic compounds and analogs thereof for treating infectious diseases
US8394816B2 (en) * 2007-12-07 2013-03-12 Irene Ghobrial Methods of using [3.2.0] heterocyclic compounds and analogs thereof in treating Waldenstrom's Macroglobulinemia
EP2088205A1 (en) 2008-02-11 2009-08-12 Institut National De La Sante Et De La Recherche Medicale (Inserm) PSMB10: A diagnosis marker and therapeutic target of chronic rejection.
JP2011514352A (en) 2008-03-07 2011-05-06 ネレアス ファーマシューティカルズ インコーポレイテッド Total synthesis of salinosporamide A and its analogs
CN102089312A (en) * 2008-05-12 2011-06-08 尼瑞斯药品公司 Salinosporamide derivatives as proteasome inhibitors

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996032105A1 (en) * 1995-04-12 1996-10-17 President And Fellows Of Harvard College Lactacystin analogs
US20010002391A1 (en) * 1997-02-15 2001-05-31 Stephen Brand Treatment of infarcts
US20010051654A1 (en) * 1997-09-25 2001-12-13 Elliott Peter J. Treatment of inflammatory and autoimmune diseases
WO2000023614A1 (en) * 1998-10-20 2000-04-27 Millennium Pharmaceuticals, Inc. Method for monitoring proteasome inhibitor drug action
WO2002047610A2 (en) * 2000-11-16 2002-06-20 The Regents Of The University Of California Marine actinomycete taxon for drug and fermentation product dicovery
US20040138196A1 (en) * 2002-06-24 2004-07-15 William Fenical Salinosporamides and methods for use thereof
WO2004071382A2 (en) * 2003-02-14 2004-08-26 Bayer Healthcare Ag Substituted heterocycles
WO2005003137A1 (en) * 2003-06-20 2005-01-13 The Regents Of The University Of California Salinosporamides and methods for use thereof

Non-Patent Citations (11)

* Cited by examiner, † Cited by third party
Title
BEERS M., BERKOW R.: "The Merck Manual of Diagnosis and Therapy, seventeenth edition", 1999, MERCK RESEARCH LABORATORIES, WHITEHOUSE STATION N.J., XP002318189 *
CRANE, SHELDON N. ET AL: "A Novel Enantioselective Synthetic Route to Omuralide Analogues with the Potential for Species Selectivity in Proteasome Inhibition", ORGANIC LETTERS , 3(9), 1395-1397 CODEN: ORLEF7; ISSN: 1523-7060, 2001, XP008038134 *
ELLIOTT, PETER J. ET AL: "The proteasome : A new target for novel drug therapies", AMERICAN JOURNAL OF CLINICAL PATHOLOGY , 116(5), 637-646 CODEN: AJCPAI; ISSN: 0002-9173, 2001, XP008007324 *
FELING ROBERT H ET AL: "Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora.", ANGEWANDTE CHEMIE (INTERNATIONAL ED. IN ENGLISH), (2003 JAN 20) 42 (3) 355-7. JOURNAL CODE: 0370543. ISSN: 0570-0833., 20 January 2003 (2003-01-20), XP002304842 *
FENICAL W. ET AL: "Marine microorganisms as a developing resource for drug discovery.", PHARMACEUTICAL NEWS, 9/6 (489-494). REFS: 14 ISSN: 1071-894X CODEN: PHNEEP, 2002, XP008038137 *
GANTT, SOREN M. ET AL: "Proteasome inhibitors block development of Plasmodium spp.", ANTIMICROBIAL AGENTS AND CHEMOTHERAPY , 42(10), 2731-2738 CODEN: AMACCQ; ISSN: 0066-4804, 1998, XP008038135 *
GOLDBERG, ALFRED L. ET AL: "Not just research tools- proteasome inhibitors offer therapeutic promise", NATURE MEDICINE (NEW YORK, NY, UNITED STATES) , 8(4), 338-340 CODEN: NAMEFI; ISSN: 1078-8956, 2002, XP008038140 *
NICOLAUS B J R: "Symbiotic Approach to Drug Design", DECISION MAKING IN DRUG RESEARCH, XX, XX, 1983, pages 173 - 186, XP002197412 *
REDDY, LELETI RAJENDER ET AL: "A Simple Stereocontrolled Synthesis of Salinosporamide A", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY , 126(20), 6230-6231 CODEN: JACSAT; ISSN: 0002-7863, 22 April 2004 (2004-04-22), XP008038141 *
TANG GUANGQING ET AL: "Proteasome activity is required for anthrax lethal toxin to kill macrophages", INFECTION AND IMMUNITY, vol. 67, no. 6, June 1999 (1999-06-01), pages 3055 - 3060, XP008038136, ISSN: 0019-9567 *
XP002304843, Retrieved from the Internet <URL:http://www.newton.rcs.it/PrimoPiano/News/2003/02_Febbraio/03/Antobiotico.shtml> [retrieved on 20030202] *

Also Published As

Publication number Publication date
CA2532066C (en) 2015-07-28
US8168803B2 (en) 2012-05-01
MXPA05013982A (en) 2006-05-25
JP2007523862A (en) 2007-08-23
BRPI0411677A (en) 2006-08-29
CA2532066A1 (en) 2005-01-13
NZ544588A (en) 2010-06-25
EP1638552A2 (en) 2006-03-29
EP1638552B1 (en) 2011-03-02
IL172705A0 (en) 2006-04-10
JP2012031198A (en) 2012-02-16
IL172705A (en) 2017-06-29
AU2004253478A1 (en) 2005-01-13
CN102151261A (en) 2011-08-17
US20090182027A1 (en) 2009-07-16
US20050049294A1 (en) 2005-03-03
ATE499934T1 (en) 2011-03-15
WO2005002572A2 (en) 2005-01-13
KR20060026052A (en) 2006-03-22
DE602004031614D1 (en) 2011-04-14

Similar Documents

Publication Publication Date Title
WO2005002572A3 (en) Use of [3.2.0] heterocyclic compounds and analogs thereof for the treatment of cancer, inflammation and infectious diseases
WO2006060809A3 (en) Methods of using [3.2.0] heterocyclic compounds and analogs thereof
CY1118651T1 (en) Azacyclic Compounds for Use in Therapeutic Treatment of Serotonin-Related Diseases
PT1326613E (en) USE OF IMIDAZO [1,2-A] PYRIDIN-, IMIDAZO [1,2-A] PYRIMIDIN- AND IMIDAZO [1,2-A] PYRAZIN-3-IL-AMINE DERIVATIVES FOR THE MANUFACTURE OF MEDICINES FOR INHIBITION OF WE
DK0893998T3 (en) Delivery of nicotine into the large intestine for the treatment of inflammatory bowel diseases
WO2007044085A3 (en) Heteroaryl compounds and their uses as therapeutic agents
EA200401355A1 (en) APPLICATION OF CYCLOPAMINE IN THE TREATMENT OF PSORIASIS AND OTHER SKIN DISEASES
WO2008137780A3 (en) Use of [3.2.0] heterocyclic compounds and analogs thereof for treating infectious diseases
PT950057E (en) 3-PYRIDYL ENANTIOMERS AND THEIR USE AS ANALGESICS
WO2004045593A3 (en) Combination cancer therapy with a gst-activated anticancer compound and another anticancer therapy
WO2002085861A8 (en) Imidazolidine compounds and their use as cxcr3 antagonists
WO2007046868A3 (en) Thiazolidine derivatives and their uses as therapeutic agents
WO2007046867A3 (en) Piperidine derivatives and their uses as therapeutic agents
ATE366107T1 (en) USE OF SULFODEHYDROABIETIC ACID TO TREAT INFLAMMATORY BOWEL DISEASE
WO2006081431A3 (en) Compounds for treating inflammatory and demyelinating diseases
WO2000037063A3 (en) Triazineone compounds for treating diseases due to sarcosystis, neospora and toxoplasma
WO2006125178A3 (en) Tricyclic pyridazine compounds and their uses as therapeutic agents
WO2006118973A3 (en) Methods of using heterobyclic compounds for treatment of rectal cancer
EP1050303A3 (en) Methods and compositions for treating age-related behavioral disorders in companion animals
SI1596879T1 (en) Use of kahalalide compounds for the manufacture of a medicament for the treatment of psoriasis
ATE320797T1 (en) USE OF 6-DIMETHYLAMINOMETHYL-1-PHENYL-CYCLOHEXANE COMPOUNDS FOR THE THERAPY OF URINARY INCONTINENCE
WO2002076400A3 (en) Inosine compounds and their use for treating or preventing an inflamation or a reperfusion disease
WO2001007029A3 (en) Substituted guanidines and the use thereof
EP2266566A3 (en) Nicotinamide derivatives and their use as therapeutic agents
PL374696A1 (en) Use of 4-pyridylmethyl-phthalazine derivatives for the manufacture of a medicament for the treatment of myelodysplastic syndromes

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200480023710.0

Country of ref document: CN

AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: PA/a/2005/013982

Country of ref document: MX

Ref document number: 172705

Country of ref document: IL

Ref document number: 2006517404

Country of ref document: JP

Ref document number: 1020057024503

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 2004253478

Country of ref document: AU

ENP Entry into the national phase

Ref document number: 2532066

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 544588

Country of ref document: NZ

WWE Wipo information: entry into national phase

Ref document number: 2004776757

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2006/00536

Country of ref document: ZA

Ref document number: 200600536

Country of ref document: ZA

ENP Entry into the national phase

Ref document number: 2004253478

Country of ref document: AU

Date of ref document: 20040618

Kind code of ref document: A

WWP Wipo information: published in national office

Ref document number: 1020057024503

Country of ref document: KR

WWP Wipo information: published in national office

Ref document number: 2004776757

Country of ref document: EP

ENP Entry into the national phase

Ref document number: PI0411677

Country of ref document: BR