JP2012502111A5 - - Google Patents

Download PDF

Info

Publication number
JP2012502111A5
JP2012502111A5 JP2011526999A JP2011526999A JP2012502111A5 JP 2012502111 A5 JP2012502111 A5 JP 2012502111A5 JP 2011526999 A JP2011526999 A JP 2011526999A JP 2011526999 A JP2011526999 A JP 2011526999A JP 2012502111 A5 JP2012502111 A5 JP 2012502111A5
Authority
JP
Japan
Prior art keywords
compound
alkyl
occurrence
haloalkyl
halogen
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.)
Granted
Application number
JP2011526999A
Other languages
English (en)
Other versions
JP2012502111A (ja
JP5567573B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2009/056675 external-priority patent/WO2010030891A2/en
Publication of JP2012502111A publication Critical patent/JP2012502111A/ja
Publication of JP2012502111A5 publication Critical patent/JP2012502111A5/ja
Application granted granted Critical
Publication of JP5567573B2 publication Critical patent/JP5567573B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (23)

  1. 下記式Iで表される化合物であって:
    Figure 2012502111
    その塩、エステルおよびプロドラッグを含み、式中、
    は、
    Figure 2012502111
    であり;
    は−N(R)−、Oまたは−C(R−であり;
    は−N(H)−、−N(アルキル)−、−N(ヒドロキシアルキル)−、O、Sまたは−C(R−であり;
    は−N(R)−、−C(R−または−C(RC(R−であり;
    およびRは出現するごとに独立に水素または(C〜C)アルキルを表し;
    は、
    Figure 2012502111
    であり;
    は出現するごとに独立に水素、ハロゲン、アルキル、ハロアルキル、−NOまたは−CNを表し;
    は出現するごとに独立に水素またはアルキルを表し;
    は出現するごとに独立にハロゲン、アルキル、ハロアルキルまたはアルコキシを表し;
    は出現するごとに独立に水素、ハロゲン、アルキル、ハロアルキルまたはアルコキシを表し;
    nは0、1、2、3または4であり;
    mは出現するごとに独立に1または2を表し;
    式Iで表される化合物の立体中心の立体配置はR、Sまたはこれらの混合物である、
    化合物。
  2. は、
    Figure 2012502111
    である、請求項1に記載の化合物。
  3. は、
    Figure 2012502111
    である、請求項1に記載の化合物。
  4. は、
    Figure 2012502111
    である、請求項1に記載の化合物。
  5. は、
    Figure 2012502111
    である、請求項1に記載の化合物。
  6. は−N(R)−であり、Xは−N(H)−、−N(アルキル)−または−N(ヒドロキシアルキル)−である、請求項5に記載の化合物。
  7. は−N(R)−であり、XはOである、請求項5に記載の化合物。
  8. は−N(R)−であり、Xは−C(H)(アルキル)−である、請求項5に記載の化合物。
  9. およびRは水素である、請求項1〜8のいずれか1項に記載の化合物。
  10. は、
    Figure 2012502111
    である、請求項1〜9のいずれか1項に記載の化合物。
  11. はアルキルまたはハロアルキルである、請求項1〜10のいずれか1項に記載の化合物。
  12. は水素、ハロゲンまたはアルキルである、請求項1〜11のいずれか1項に記載の化合物。
  13. mは1である、請求項1〜12のいずれか1項に記載の化合物。
  14. はハロゲンである、請求項1〜13のいずれか1項に記載の化合物。
  15. nは0、1または2である、請求項1〜14のいずれか1項に記載の化合物。
  16. は、
    Figure 2012502111
    であり;Xは−N(R)−であり;Rはハロゲンであり;Rはアルキルまたはハロアルキルであり;Rは水素であり、mは1であり;nは0、1または2である、請求項1に記載の化合物。
  17. 下記式IIで表される化合物であって:
    Figure 2012502111
    その塩、エステルおよびプロドラッグを含み、式中、
    、RおよびRは出現するごとに独立に水素または(C〜C)アルキルを表し;
    は、
    Figure 2012502111
    であり;
    は出現するごとに独立に水素、ハロゲン、アルキルまたはハロアルキルを表し;
    は出現するごとに独立に(C〜C)アルキルまたはハロアルキルを表し;
    は出現するごとに独立に水素、ハロゲン、アルキルまたはハロアルキルを表し;
    nは0、1、2、3または4であり;
    mは出現するごとに独立に1または2を表し;
    式IIで表される化合物の立体中心の立体配置はR、Sまたはこれらの混合物であり、ただしRがハロゲンである場合、Rはハロアルキルではない、
    化合物。
  18. は、
    Figure 2012502111
    である、請求項17に記載の化合物。
  19. 前記化合物は表I〜Vに記載した化合物の1つである、請求項1または17に記載の化合物。
  20. 請求項1〜19のいずれか1項に記載の化合物および薬学的に許容されるキャリアを含む、医薬組成物。
  21. ループス、関節リウマチ、乾癬、移植片対宿主病、クローン病、炎症性腸疾患、多発性硬化症、循環器疾患、骨髄腫、リンパ腫、癌および細菌感染症からなる群から選択される障害を処置するための、請求項20に記載の医薬組成物。
  22. 前記障害はクローン病、炎症性腸疾患、多発性硬化症、移植片対宿主病、ループス、関節リウマチまたは乾癬である、請求項21に記載の医薬組成物
  23. −ATPアーゼを阻害するための、請求項20に記載の医薬組成物
JP2011526999A 2008-09-11 2009-09-11 アリールグアニジンf1f0−atpアーゼ阻害剤およびそれと関連する方法 Expired - Fee Related JP5567573B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US9618408P 2008-09-11 2008-09-11
US61/096,184 2008-09-11
PCT/US2009/056675 WO2010030891A2 (en) 2008-09-11 2009-09-11 Aryl guanidine f1f0-atpase inhibitors and related methods

Publications (3)

Publication Number Publication Date
JP2012502111A JP2012502111A (ja) 2012-01-26
JP2012502111A5 true JP2012502111A5 (ja) 2012-10-25
JP5567573B2 JP5567573B2 (ja) 2014-08-06

Family

ID=42005765

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011526999A Expired - Fee Related JP5567573B2 (ja) 2008-09-11 2009-09-11 アリールグアニジンf1f0−atpアーゼ阻害剤およびそれと関連する方法

Country Status (5)

Country Link
US (1) US8497307B2 (ja)
EP (1) EP2352724B1 (ja)
JP (1) JP5567573B2 (ja)
AU (1) AU2009291632B2 (ja)
WO (1) WO2010030891A2 (ja)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2639439T3 (es) * 2010-12-08 2017-10-26 Lycera Corporation Inhibidores de F1F0-ATPasas de tipo pirazolilguanidina y sus usos terapéuticos de éstos
WO2012078869A1 (en) 2010-12-08 2012-06-14 Lycera Corporation Pyridonyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
US9169199B2 (en) 2010-12-08 2015-10-27 Lycera Corporation Cycloalkyl guanidine F1F0-ATPase inhibitors and therapeutic uses thereof
US9920012B2 (en) 2012-06-08 2018-03-20 Lycera Corporation Indazole guanidine F1F0-ATPase inhibitors and therapeutic uses thereof
US9580391B2 (en) 2012-06-08 2017-02-28 Lycera Corporation Saturated acyl guanidine for inhibition of F1F0-ATPase
US9221814B2 (en) 2012-06-08 2015-12-29 Lycera Corporation Heterocyclic guanidine F1F0-atpase inhibitors and therapeutic uses thereof
EP2874997A4 (en) 2012-07-19 2016-01-06 Univ Drexel NEW SIGMA RECEPTOR LIGANDS AND METHOD FOR REGULATING CELLULAR PROTEIN HOMEOSTASIS THEREWITH
CN103396349B (zh) * 2013-07-19 2014-12-17 浙江工业大学 一种含1-甲基环己基的酰基硫脲类化合物、制备方法及其应用
CN103351360B (zh) * 2013-07-19 2015-03-25 浙江工业大学 一种含1,3,4-噻二唑基团的酰基硫脲类化合物、制备方法及其应用
CA2931850A1 (en) 2013-12-10 2015-06-18 Lycera Corporation Alkylpyrazolyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
JP6486364B2 (ja) 2013-12-10 2019-03-20 リセラ・コーポレイションLycera Corporation トリフルオロメチルピラゾリルグアニジンf1f0−atpアーゼ阻害剤及びその治療用途
CA2931792A1 (en) 2013-12-10 2015-06-18 Lycera Corporation N-substituted pyrazolyl guanidine f1f0-atpase inhibitors and therapeutic uses thereof
WO2019089902A1 (en) 2017-11-01 2019-05-09 Drexel University Compounds, compositions, and methods for treating diseases

Family Cites Families (104)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2457405A (en) 1945-09-25 1948-12-28 Monsanto Chemicals Halo nitroparaffin modified aminoplasts
US3374264A (en) 1962-10-04 1968-03-19 Hoffmann La Roche N-haloacetyl-anthranilic acids and esters
US3261828A (en) 1962-10-04 1966-07-19 Hoffmann La Roche 3h-1,4-benzodiazepine-2,5(1h,4h)-dione compounds
US3384635A (en) 1966-09-28 1968-05-21 Sterling Drug Inc 1, 4-benzodiazepine derivatives
US3415814A (en) 1966-09-28 1968-12-10 Sterling Drug Inc 4-(cyclopropylmethyl)-3h-1,4-benzodiazepine-2,5(1h,4h)-dione
AT280290B (de) 1967-11-24 1970-04-10 Boehringer Sohn Ingelheim Verfahren zur Herstellung von neuen 1-Phenyl-4-alkyl-3H-1,4-benzodiazepin-2,5-[1H,4H]-dionen
USRE30293E (en) 1969-03-18 1980-06-03 Knoll A.G. Process for preparing 1,5-benzodiazepine-2-ones
US4108852A (en) 1969-03-18 1978-08-22 Knoll Ag. Process for preparing 1,5-benzodiazepine-2-ones
GB1363735A (en) 1970-10-23 1974-08-14 Hoechst Ag Process for the manufacture of benzimidazolones
GB1324469A (en) 1970-10-28 1973-07-25 Knoll Ag Derivatives of benzodiazepines
ZA7467B (en) 1973-01-16 1974-11-27 J Voorhees Compositions and treatment of proliferative skin diseases with b2 agonists
IE38931B1 (en) 1973-03-09 1978-07-05 Lipha Triazolobenzodiazepines
US4076823A (en) 1977-08-18 1978-02-28 E. R. Squibb & Sons, Inc. Triazolo-2,4-benzodiazepines
JPS59112984A (ja) 1982-12-21 1984-06-29 Shionogi & Co Ltd 1,4−ベンゾジアゼピン誘導体
US4495101A (en) 1983-04-28 1985-01-22 American Home Products Corporation Antiinflammatory 5H-tetrazolo (5,1-c)(1,4)benzodiazepine derivatives
US4551480A (en) 1983-06-21 1985-11-05 Stiefel Laboratories, Inc. Compositions for the treatment of psoriasis
US4894366A (en) 1984-12-03 1990-01-16 Fujisawa Pharmaceutical Company, Ltd. Tricyclo compounds, a process for their production and a pharmaceutical composition containing the same
US4820834A (en) 1984-06-26 1989-04-11 Merck & Co., Inc. Benzodiazepine analogs
US5004741A (en) 1984-06-26 1991-04-02 Merck & Co., Inc. Methods of antagonizing CCK or gastrin with benzodiazepine analogs
DE3435974A1 (de) 1984-10-01 1986-04-10 Boehringer Ingelheim KG, 6507 Ingelheim Diazepine enthaltende pharmazeutische zusammensetzungen mit paf-antagonistischer wirkung
FR2591596B1 (fr) 1985-12-13 1988-09-09 Roussel Uclaf Nouvelles 4h-triazolo(4,3-a)(1,4)benzodiazepines, leur procede de preparation, leur application comme medicaments et les compositions les renfermant
GB8608080D0 (en) 1986-04-02 1986-05-08 Fujisawa Pharmaceutical Co Solid dispersion composition
US4946778A (en) 1987-09-21 1990-08-07 Genex Corporation Single polypeptide chain binding molecules
US4751223A (en) 1986-10-14 1988-06-14 Hoechst-Roussel Pharmaceuticals, Inc. Antiinflammatory and analgesic aminoalkyl tetracyclic benzodiazepines
US4898861A (en) 1987-03-26 1990-02-06 Hoffmann-La Roche Inc. Method for inhibiting the proliferation of tumor cells
US5147872A (en) 1987-06-09 1992-09-15 Golwyn Daniel H Treatment of immunologically based disorders, specifically psoriasis
US4970207A (en) 1988-07-07 1990-11-13 Fujisawa Pharmaceutical Company, Ltd. Benzodiazepine derivatives
US5258510A (en) 1989-10-20 1993-11-02 Otsuka Pharma Co Ltd Benzoheterocyclic compounds
US5041438A (en) 1989-10-30 1991-08-20 Hoffmann-La Roche Inc. Method for treating retroviral infections with benzodiazepine compounds
US5324726A (en) 1989-12-18 1994-06-28 Merck & Co., Inc. Benzodiazepine analogs
EP0465254B1 (en) 1990-07-06 1996-11-13 Yoshitomi Pharmaceutical Industries, Ltd. Fused thiophene compounds and uses thereof
BR9200951A (pt) 1991-03-21 1992-11-17 Hoffmann La Roche Compostos, processo para sua producao,preparacoes farmaceuticas e uso
US5597915A (en) 1992-03-16 1997-01-28 Merck Sharp & Dohme Ltd. Benzodiazepine derivatives, compositions containing them and their use in therapy
US5599352A (en) 1992-03-19 1997-02-04 Medtronic, Inc. Method of making a drug eluting stent
US5288514A (en) 1992-09-14 1994-02-22 The Regents Of The University Of California Solid phase and combinatorial synthesis of benzodiazepine compounds on a solid support
GB9307527D0 (en) 1993-04-13 1993-06-02 Fujisawa Pharmaceutical Co New venzamide derivatives,processes for the preparation thereof and pharmaceutical composition comprising the same
US5391566A (en) 1993-07-20 1995-02-21 Merck & Co., Inc. Benzimidazolinones substituted with phenoxyphenylacetic acid derivatives
WO1996005827A1 (en) 1994-08-18 1996-02-29 Merck & Co., Inc. N-2,3-dihydro-1-(2-propyl)-2-oxo-5-phenyl-1h-1,4-benzodiazepines
US6524832B1 (en) 1994-02-04 2003-02-25 Arch Development Corporation DNA damaging agents in combination with tyrosine kinase inhibitors
US5444092A (en) 1994-07-20 1995-08-22 Collins; Jerry Method and composition for treating psoriasis
CA2196062A1 (en) 1994-07-29 1996-02-15 Yoshinari Sato Benzodiazepine derivatives
US5618792A (en) 1994-11-21 1997-04-08 Cortech, Inc. Substituted heterocyclic compounds useful as inhibitors of (serine proteases) human neutrophil elastase
WO1996036361A1 (en) 1995-05-18 1996-11-21 The Regents Of The University Of Michigan Dna binding antibodies
US5677282A (en) 1995-06-07 1997-10-14 Proscript, Inc. Amino acid amides of 1,3,4-thiadiazoles as matrix metalloproteinase
US5962337A (en) 1995-06-29 1999-10-05 Pharmacopeia, Inc. Combinatorial 1,4-benzodiazepin-2,5-dione library
RU2096044C1 (ru) 1995-07-19 1997-11-20 Малое предприятие "Ветта" Ветеринарный имплантируемый препарат для регулирования биологического ритма животных
US5776946A (en) 1995-08-28 1998-07-07 Mcgeer; Patrick L. Peripheral benzodiazepine receptor ligands as antiinflammatory agents
EP0861092A4 (en) 1995-08-30 2002-04-10 Univ California THERAPY FOR CELL ACCUMULATION IN CHRONIC INFLAMMATORY DISEASES
CA2233012A1 (en) 1995-09-21 1997-03-27 Koichi Shudo Compounds enhancing the activity of retinoids
US6579854B1 (en) 1996-08-14 2003-06-17 Vanderbilt University Diagnosis and management of infection caused by chlamydia
US7351421B2 (en) 1996-11-05 2008-04-01 Hsing-Wen Sung Drug-eluting stent having collagen drug carrier chemically treated with genipin
ES2206754T3 (es) 1996-12-10 2004-05-16 Zeria Pharmaceutical Co., Ltd. Derivados de 1,5 - benzodiazepina.
US6074859A (en) 1997-07-08 2000-06-13 Kikkoman Corporation Mutant-type bioluminescent protein, and process for producing the mutant-type bioluminescent protein
JP4261049B2 (ja) 1997-10-08 2009-04-30 アイソテクニカ インコーポレイテッド 重水素化シクロスポリンアナログおよび免疫調節剤としてのそれらの使用
US6100254A (en) 1997-10-10 2000-08-08 Board Of Regents, The University Of Texas System Inhibitors of protein tyrosine kinases
US6206914B1 (en) 1998-04-30 2001-03-27 Medtronic, Inc. Implantable system with drug-eluting cells for on-demand local drug delivery
FR2779963A1 (fr) 1998-06-22 1999-12-24 Centre Nat Rech Scient Utilisation d'un compose possedant une affinite pour le recepteur mitochondrial des benzodiazepines en therapie du cancer
US6277844B1 (en) 1998-09-14 2001-08-21 Sydney Spector Compound for selective treatment of malignant cells by inhibiting cell cycle progression, decreasing Bcl2, and increasing apoptosis
US20030044776A1 (en) 1998-09-25 2003-03-06 James A. Dykens Compositions and methods for identifying agents that alter mitochondrial permeability transition pores
FR2785803B1 (fr) 1998-11-17 2005-03-25 Sanofi Sa Utilisation d'une substance se liant au recepteur peripherique des benzodiazepines dans le traitement des stress cutanes
AU760174B2 (en) * 1999-02-09 2003-05-08 Bristol-Myers Squibb Company Lactam inhibitors of FXa and method
US7175953B2 (en) 1999-04-09 2007-02-13 Institute Fuer Diagnostik Forschung Short-warp peptide-dye conjugate as contrast agent for optical diagnostic
US20030119029A1 (en) 1999-04-30 2003-06-26 Regents Of The University Of Michigan Compositions and methods relating to novel benzodiazepine compounds and targets thereof
US20040176358A1 (en) 1999-04-30 2004-09-09 The Regents Of The University Of Michigan Compositions and methods relating to novel compounds and targets thereof
US20050113460A1 (en) 1999-04-30 2005-05-26 The Regents Of The University Of Michigan Compositions and methods relating to novel compounds and targets thereof
US20060025388A1 (en) 1999-04-30 2006-02-02 Glick Gary D Compositions and methods relating to novel compounds and targets thereof
ES2214273T3 (es) 1999-04-30 2004-09-16 The Regents Of The University Of Michigan Utilizacion de benzodiazepinas para el tratamiento de enfermedades autoinmunes inducidas por apoptosis.
US7572788B2 (en) 1999-04-30 2009-08-11 The Regents Of The University Of Michigan Compositions and methods relating to novel compounds and targets thereof
US7276348B2 (en) 1999-04-30 2007-10-02 Regents Of The University Of Michigan Compositions and methods relating to F1F0-ATPase inhibitors and targets thereof
WO2001004103A1 (en) 1999-07-13 2001-01-18 F. Hoffmann-La Roche Ag Benzazepinones and quinazolines
KR20020033777A (ko) * 1999-08-27 2002-05-07 추후보정 치환된 α-히드록시 산 카스파제 억제제 및 이의 용도
US6524623B1 (en) 1999-11-12 2003-02-25 Milton Hodosh Therapeutic compositions and methods of use thereof
AU2001255709A1 (en) 2000-05-11 2001-11-20 Eastman Chemical Company Acylated cyclodextrin guest inclusion complexes
US6511973B2 (en) * 2000-08-02 2003-01-28 Bristol-Myers Squibb Co. Lactam inhibitors of FXa and method
US20020048566A1 (en) 2000-09-14 2002-04-25 El-Deiry Wafik S. Modulation of cellular apoptosis and methods for treating cancer
US20020128208A1 (en) 2000-12-15 2002-09-12 Snyder James P. Nonpeptide agonists and antagonists of vasopressin receptors
WO2002098865A2 (fr) 2001-06-07 2002-12-12 Neuro3D Inhibiteurs des phosphodiesterases des nucleotides cycliques, preparation et utilisations de ces inhibiteurs
EP1423122A4 (en) 2001-08-15 2008-12-10 Univ Michigan COMPOSITIONS AND METHODS RELATED TO NEW BENZODIAZEPINE COMPOUNDS AND THEIR OBJECTIVES
WO2003050261A2 (en) * 2001-12-10 2003-06-19 Bristol-Myers Squibb Company (1-phenyl-2-heteroaryl)ethyl-guanidine compounds as inhibitors of mitochondrial f1f0 atp hydrolase
AU2003276648A1 (en) * 2002-06-17 2003-12-31 Bristol-Myers Squibb Company Benzodiazepine inhibitors of mitochondial f¿1?f¿0? atp hydrolase and methods of inhibiting f¿1?f¿0? atp hydrolase
US7150433B2 (en) 2002-08-16 2006-12-19 Toyota Motor Sales, U.S.A., Inc. Aircraft bolster trays
AU2003295402A1 (en) 2002-11-06 2004-06-03 Bristol-Myers Squibb Company Acyl guanidine compounds and use thereof
US20040087489A1 (en) 2002-11-06 2004-05-06 Antonio Ruiz Compositions and methods for the treatment of mycobacterial infections
US7745431B2 (en) 2002-12-03 2010-06-29 Vela Acquisition Corporation Pharmaceutical composition of 1-(3,4-dimethoxyphenyl)-4-methyl-5-ethyl-7-methoxy-8-hydroxy-5H-2,3-benzodiazepine and uses thereof
JP2006509014A (ja) * 2002-12-04 2006-03-16 ジーン ロジック インコーポレイテッド メラノコルチンレセプターの調節因子
WO2005004988A2 (en) 2003-05-01 2005-01-20 The Regents Of The University Of Michigan Compositions and methods relating to novel compounds and targets thereof
US7351241B2 (en) 2003-06-02 2008-04-01 Carl Zeiss Meditec Ag Method and apparatus for precision working of material
US20090275099A1 (en) 2004-04-27 2009-11-05 Regents Of The University Of Michigan Methods and compositions for treating diseases and conditions associated with mitochondrial function
US20050272723A1 (en) * 2004-04-27 2005-12-08 The Regents Of The University Of Michigan Methods and compositions for treating diseases and conditions associated with mitochondrial function
US7872005B2 (en) 2004-07-01 2011-01-18 Synta Pharmaceuticals Corporation 2-substituted heteroaryl compounds
US20060052369A1 (en) 2004-09-07 2006-03-09 The Regents Of The University Of Michigan Compositions and methods relating to novel compounds and targets thereof
US20080314334A1 (en) 2004-11-10 2008-12-25 Garden Guardian, Inc. Device and Method for Controlling Animal Behavior
JP2008528448A (ja) 2005-01-03 2008-07-31 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン 新規化合物に関連する組成物および方法、ならびにその標的
JP2008545757A (ja) 2005-06-01 2008-12-18 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン 溶媒和されていないベンゾジアゼピン組成物および方法
EP1742460A1 (en) 2005-06-18 2007-01-10 TTE Germany GmbH Raster distortion correction circuit
US20070105844A1 (en) 2005-10-26 2007-05-10 Regents Of The University Of Michigan Therapeutic compositions and methods
JP2009513644A (ja) 2005-10-26 2009-04-02 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン 治療組成物および方法
JP5241501B2 (ja) 2005-11-01 2013-07-17 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン 治療特性を有する新規の1,4−ベンゾジアゼピン−2,5−ジオン
US7759338B2 (en) 2006-04-27 2010-07-20 The Regents Of The University Of Michigan Soluble 1,4 benzodiazepine compounds and stable salts thereof
EP2037741B1 (en) 2006-06-09 2013-11-27 The Regents Of The University Of Michigan Benzodiazepine derivatives for use in the treatment of immune, inflammatory and proliferative disorders
GB0615068D0 (en) 2006-07-28 2006-09-06 Ttp Communications Ltd Digital radio systems
EP2139331B1 (en) 2007-03-09 2013-02-20 The Regents of the University of Michigan Compositions and methods relating to novel compounds and targets thereof
CN101855203B (zh) * 2007-09-14 2014-03-19 密执安州立大学董事会 F1f0-atp合成酶抑制剂以及相关的方法
CA2703005A1 (en) 2007-11-06 2009-05-14 The Regents Of The University Of Michigan Benzodiazepinone compounds useful in the treatment of skin conditions

Similar Documents

Publication Publication Date Title
JP2012502111A5 (ja)
JP2010518090A5 (ja)
JP2013537203A5 (ja)
JP2014508811A5 (ja)
JP2013505929A5 (ja)
JP2018519329A5 (ja)
JP2019519587A5 (ja)
JP2010530897A5 (ja)
JP2014051526A5 (ja)
JP2016500661A5 (ja)
JP2015509535A5 (ja)
JP2014521625A5 (ja)
JP2010536766A5 (ja)
JP2016501246A5 (ja)
JP2012121931A5 (ja)
JP2012092103A5 (ja)
JP2013540755A5 (ja)
JP2020500916A5 (ja)
JP2012504133A5 (ja)
JP2011530521A5 (ja)
JP2013542261A5 (ja)
JP2016518317A5 (ja)
JP2019501927A5 (ja)
JP2009543795A5 (ja)
JP2018500287A5 (ja)