CN102171185A - 甲硫氨酸类似物及其使用方法 - Google Patents

甲硫氨酸类似物及其使用方法 Download PDF

Info

Publication number
CN102171185A
CN102171185A CN2009801390134A CN200980139013A CN102171185A CN 102171185 A CN102171185 A CN 102171185A CN 2009801390134 A CN2009801390134 A CN 2009801390134A CN 200980139013 A CN200980139013 A CN 200980139013A CN 102171185 A CN102171185 A CN 102171185A
Authority
CN
China
Prior art keywords
compound
alkyl
optionally substituted
cycloalkyl
moiety
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.)
Pending
Application number
CN2009801390134A
Other languages
English (en)
Chinese (zh)
Inventor
曼索尔.巴希里
阿夫萨内.拉希米-拉里贾尼
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.)
Bioxiness Pharmaceuticals Inc
Original Assignee
Bioxiness 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
Application filed by Bioxiness Pharmaceuticals Inc filed Critical Bioxiness Pharmaceuticals Inc
Publication of CN102171185A publication Critical patent/CN102171185A/zh
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/50Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
    • C07C323/51Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/60Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
    • 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
    • C07C259/04Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
    • C07C259/06Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/64Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
    • C07C323/66Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton containing sulfur atoms of sulfo, esterified sulfo or halosulfonyl groups, bound to the carbon skeleton

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Virology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
CN2009801390134A 2008-08-01 2009-07-31 甲硫氨酸类似物及其使用方法 Pending CN102171185A (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US8555608P 2008-08-01 2008-08-01
US61/085,556 2008-08-01
PCT/US2009/052474 WO2010014943A2 (en) 2008-08-01 2009-07-31 Methionine analogs and methods of using same

Publications (1)

Publication Number Publication Date
CN102171185A true CN102171185A (zh) 2011-08-31

Family

ID=41414372

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2009801390134A Pending CN102171185A (zh) 2008-08-01 2009-07-31 甲硫氨酸类似物及其使用方法

Country Status (8)

Country Link
US (5) US8580859B2 (https=)
EP (1) EP2326619B1 (https=)
JP (1) JP5650642B2 (https=)
CN (1) CN102171185A (https=)
AU (1) AU2009276343A1 (https=)
CA (1) CA2733390A1 (https=)
IL (1) IL210956A0 (https=)
WO (1) WO2010014943A2 (https=)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102171185A (zh) 2008-08-01 2011-08-31 拜奥西尼斯医药股份有限公司 甲硫氨酸类似物及其使用方法
US9200251B1 (en) 2011-03-31 2015-12-01 David Gordon Bermudes Bacterial methionine analogue and methionine synthesis inhibitor anticancer, antiinfective and coronary heart disease protective microcins and methods of treatment therewith
WO2019169029A1 (en) 2018-02-28 2019-09-06 Bioxiness Pharmaceuticals, Inc. Target specific chemotherapeutic agents

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0618221A2 (en) * 1993-04-02 1994-10-05 Bristol-Myers Squibb Company Heterocyclic inhibitors of farnesyl protein transferase
WO1999018074A1 (en) * 1997-10-03 1999-04-15 Britol-Myers Squibb Pharma Company Novel lactam metalloprotease inhibitors
WO2000000473A1 (fr) * 1998-06-30 2000-01-06 Adir Et Compagnie Composes acides carboxyliques et hydroxamiques inhibiteurs de metalloproteases, procede pour leur preparation et les compositions pharmaceutiques les contenant
WO2000059874A1 (en) * 1999-04-02 2000-10-12 Du Pont Pharmaceuticals Company NOVEL AMIDE DERIVATIVES AS INHIBITORS OF MATRIX METALLOPROTEINASES, TNF-α, AND AGGRECANASE
WO2000063197A1 (en) * 1999-04-19 2000-10-26 Sumitomo Pharmaceuticals Company, Limited Hydroxamic acid derivative
WO2002028829A2 (en) * 2000-09-25 2002-04-11 Questcor Pharmaceuticals, Inc. Peptide deformylase inhibitors
US6403632B1 (en) * 2000-03-01 2002-06-11 Bristol Myers Squibb Pharma Co Lactam metalloprotease inhibitors
WO2004062601A2 (en) * 2003-01-08 2004-07-29 Chiron Corporation Antibacterial agents
WO2007069020A2 (en) * 2005-12-15 2007-06-21 Vicuron Pharmaceuticals Inc. N-hydroxyamide derivatives possessing antibacterial activity

Family Cites Families (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR961832A (https=) 1943-03-20 1950-05-23
CH254537A (de) 1947-12-18 1948-05-15 Ag Sandoz Verfahren zur Herstellung eines neuen kapillaraktiven Stoffes.
DE1020144B (de) 1956-07-02 1957-11-28 Dehydag Gmbh Wasch- und Reinigungsmittel
FR1390191A (fr) 1963-07-19 1965-02-26 Dehydag Gmbh Procédé de préparation de sulfobétaïnes à bases hétérocycliques de type aromatique
US3519683A (en) 1967-03-31 1970-07-07 Meiji Seika Co Process for preparing 5-amino-5-deoxy-d-glucose-1-sulfonic acid
GB1580899A (en) 1976-07-27 1980-12-10 Fujisawa Pharmaceutical Co Hydroxyaminohydrocarbonphosphonic acid derivatives and production and use thereof
JPS5463024A (en) 1977-10-27 1979-05-21 Fujisawa Pharmaceut Co Ltd 3-(n-formyl-n-hydroxyamino)-2(r)-hydroxypropyl-phosphonic acid, its preparation, and its use
US4169950A (en) 1977-12-08 1979-10-02 Research Organics Amino-hydroxy-alkyl sulfonic acid zwitterions
IL61985A0 (en) 1980-02-01 1981-02-27 Sparamedica Ag Phosphinic and phosphonic acid derivatives,their manufacture and pharmaceutical compositions containing them
DE3273586D1 (en) 1981-11-02 1986-11-06 Ici Plc Substituted propyl phosphonic acid derivatives, their use as herbicides, herbicidal compositions containing them, and methods of preparing them
DE3245887A1 (de) 1982-12-11 1984-06-14 Degussa Ag, 6000 Frankfurt Verfahren zur herstellung substituierter phosphon und phosphinsaeuren
GB8308506D0 (en) 1983-03-28 1983-05-05 Ici Plc Heterocyclic compounds
GB8410989D0 (en) 1984-04-30 1984-06-06 Ici Plc Heterocyclic compounds
DE3435156A1 (de) 1984-09-25 1986-04-03 Boehringer Mannheim Gmbh, 6800 Mannheim Verfahren zur herstellung der stereoisomeren von 1-amino-alkylphosphonsaeuren oder 1-aminoalkylphosphinsaeuren
JPS62215597A (ja) 1986-03-14 1987-09-22 Mitsubishi Chem Ind Ltd β−メルカプト−α−アミノエチルホスホン酸誘導体
IT1211792B (it) 1987-09-21 1989-11-03 Sigma Tau Ind Farmaceuti O-alcanoil derivati dell'acido 3ammino-2-idrossipropansolfonico adattivita'anticonvulsivante e loro composizioni farmaceutiche per il trattamento terapeutico dell'epilessia
GB8727792D0 (en) 1987-11-27 1987-12-31 Merck Sharp & Dohme Therapeutic agents
SE8801729D0 (sv) 1988-05-06 1988-05-06 Astra Ab Purine derivatives for use in therapy
JP2733511B2 (ja) 1988-10-22 1998-03-30 日本臓器製薬株式会社 新規アミノアルカン誘導体
JP3174566B2 (ja) 1990-04-20 2001-06-11 日本臓器製薬株式会社 アミノアルカン誘導体
DE69125216T2 (de) * 1990-07-19 1997-09-25 Nippon Zoki Pharmaceutical Co Aminoalkanesulfonsäurederivate und pharmazeutische Zusammensetzungen davon zur Prävention oder Behandlung von Herzerkrankungen
JP2724906B2 (ja) 1990-07-19 1998-03-09 日本臓器製薬株式会社 新規フェニルアラニルアミノアルカン誘導体
DE4124004C2 (de) 1991-07-19 1995-01-26 Hell Ag Linotype Vorrichtung zum Auf- und Abspannen von Filmmaterial und Betriebsweise der Vorrichtung
GB9122859D0 (en) * 1991-10-28 1991-12-11 Smithkline Beecham Plc Novel compounds
JPH07116382B2 (ja) 1992-01-28 1995-12-13 株式会社同仁化学研究所 水溶性メチレンビスジアルキルアニリン誘導体及びその塩類並びにそれらを用いた過酸化物質定量用組成物
GB9202779D0 (en) 1992-02-10 1992-03-25 Ici Plc Novel compounds
US5760021A (en) 1992-05-29 1998-06-02 The Procter & Gamble Company Phosphonocarboxylate compounds pharmaceutical compositions, and methods for treating abnormal calcium and phosphate metabolism
JP3526575B2 (ja) * 1993-03-08 2004-05-17 エーザイ株式会社 ホスホン酸誘導体
WO1995001955A1 (en) 1993-07-09 1995-01-19 Kao Corporation 2-hydroxypropanediamine derivative and detergent composition containing the same
US5658749A (en) 1994-04-05 1997-08-19 Corning Clinical Laboratories, Inc. Method for processing mycobacteria
JPH09316474A (ja) 1996-05-24 1997-12-09 Hitachi Maxell Ltd 潤滑性物質およびこの潤滑性物質を用いた磁気記録媒体
WO1998015525A1 (en) 1996-10-07 1998-04-16 Sumitomo Pharmaceuticals Co., Ltd. Hydroxamic acids
CZ141399A3 (cs) 1996-10-24 1999-07-14 Novartis Ag Substituované aminoalkanfosfonové kyseliny, způsob jejich přípravy a farmaceutické prostředky, které je obsahují
US6172057B1 (en) * 1997-02-27 2001-01-09 American Cyanamid Company N-Hydroxy-2-(alkyl, aryl, or heteroaryl sulfanyl, sulfinyl or sulfonyl)-3-substituted alkyl, aryl or heteroarylamides as matrix metalloproteinase inhibitors
KR100352316B1 (ko) * 1997-07-31 2002-09-12 더 프록터 앤드 갬블 캄파니 메탈로프로테아제억제제로서사용되는술포닐아미노치환히드록삼산유도체
IT1299266B1 (it) * 1998-05-15 2000-02-29 Sigma Tau Ind Farmaceuti Inibitori reversibili della carnitina palmitoil trasferasi
KR20010080709A (ko) 1998-12-10 2001-08-22 프리돌린 클라우스너, 롤란드 비. 보레르 프로콜라겐 c-프로티나제 저해제
FR2788526B1 (fr) 1999-01-20 2002-07-05 Inst Nat Sante Rech Med Composes tripeptidiques utiles a titre d'hinhibiteurs selectifs de l'aminopeptidase a et compositions pharmaceutiques correspondantes
FR2791982B1 (fr) 1999-04-06 2002-12-27 Inst Nat Sante Rech Med Inhibiteurs de lta4 hydrolase et leurs applications therapeutiques.
AU5994900A (en) * 1999-07-09 2001-01-30 Isis Innovation Limited Compounds for inhibiting diseases and preparing cells for transplantation
JP4153647B2 (ja) 2000-04-05 2008-09-24 三菱重工業株式会社 フェントン反応抑制剤および一重項酸素産生抑制剤
WO2001093872A1 (de) 2000-06-08 2001-12-13 Jomaa Pharmaka Gmbh Verwendung von phosphororganischen hydroxamsäurederivaten zur herstellung von arzneimitteln
WO2002018395A1 (en) * 2000-08-31 2002-03-07 Merck & Co., Inc. Phosphate derivatives as immunoregulatory agents
EP1361872A4 (en) * 2000-10-03 2004-05-19 Univ Virginia NOVEL LYSOPHOSPHATIDIC ACID RECEPTOR AGONISTS AND ANTAGONISTS
FR2816837A1 (fr) 2000-11-17 2002-05-24 Oreal Utilisation d'au moins un derive amino sulfonique dans une composition destinee a favoriser la desquamation de la peau
FR2821621B1 (fr) 2001-03-05 2004-11-05 Oreal Polyurethannes anioniques a caractere elastique et leur utilisation dans des compositions cosmetiques
US20050070506A1 (en) 2002-01-18 2005-03-31 Doherty George A. Selective s1p1/edg1 receptor agonists
US7456157B2 (en) 2003-02-18 2008-11-25 Kyorin Pharmaceutical Co., Ltd. Aminophosphonic acid derivatives, addition salts thereof and S1P receptor modulators
JP5146714B2 (ja) 2003-06-23 2013-02-20 ビーエイチアイ リミテッド パートナーシップ アミロイド関連疾患を治療するための方法および組成物
FR2858617A1 (fr) 2003-08-06 2005-02-11 Inst Nat Sante Rech Med Derives de 4',4'-dithiobis-(3-aminobutane-1-sulfonate-1- sulfonates) nouveaux et compositions les contenant
WO2005020973A2 (en) 2003-08-29 2005-03-10 The University Of Houston System Compositions having antimycrobial activity including a hydroxamate or a hydroxamate and a hydroxylamine
US20050107447A1 (en) 2003-11-03 2005-05-19 Lynch Kevin R. Novel lysophosphatidic acid receptor agonists and antagonists
JP4182910B2 (ja) 2004-03-30 2008-11-19 ダイソー株式会社 スフィンゴミエリン類縁体とその製造法
US20060183800A1 (en) 2004-11-12 2006-08-17 Xianqi Kong Methods and fluorinated compositions for treating amyloid-related diseases
WO2006085149A2 (en) * 2004-12-22 2006-08-17 Neurochem (International) Limited Methods and compositions for treating amyloid-related diseases
DK2839830T3 (da) * 2005-01-14 2019-08-19 Urigen Inc Kits og sammensætninger til behandling af lidelser i de nedre urinveje
JP2006257069A (ja) 2005-02-17 2006-09-28 Kemikurea:Kk 蛍光標識化スフィンゴシン1−リン酸メチレン置換体およびリン酸アルケニル置換体
AU2008333929A1 (en) 2007-12-03 2009-06-11 Signum Biosciences, Inc. Acid mimic compounds for the inhibition of isoprenyl-S-cysteinyl methyltransferase
CN102171185A (zh) 2008-08-01 2011-08-31 拜奥西尼斯医药股份有限公司 甲硫氨酸类似物及其使用方法

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0618221A2 (en) * 1993-04-02 1994-10-05 Bristol-Myers Squibb Company Heterocyclic inhibitors of farnesyl protein transferase
WO1999018074A1 (en) * 1997-10-03 1999-04-15 Britol-Myers Squibb Pharma Company Novel lactam metalloprotease inhibitors
WO2000000473A1 (fr) * 1998-06-30 2000-01-06 Adir Et Compagnie Composes acides carboxyliques et hydroxamiques inhibiteurs de metalloproteases, procede pour leur preparation et les compositions pharmaceutiques les contenant
WO2000059874A1 (en) * 1999-04-02 2000-10-12 Du Pont Pharmaceuticals Company NOVEL AMIDE DERIVATIVES AS INHIBITORS OF MATRIX METALLOPROTEINASES, TNF-α, AND AGGRECANASE
WO2000063197A1 (en) * 1999-04-19 2000-10-26 Sumitomo Pharmaceuticals Company, Limited Hydroxamic acid derivative
US6403632B1 (en) * 2000-03-01 2002-06-11 Bristol Myers Squibb Pharma Co Lactam metalloprotease inhibitors
WO2002028829A2 (en) * 2000-09-25 2002-04-11 Questcor Pharmaceuticals, Inc. Peptide deformylase inhibitors
WO2004062601A2 (en) * 2003-01-08 2004-07-29 Chiron Corporation Antibacterial agents
WO2007069020A2 (en) * 2005-12-15 2007-06-21 Vicuron Pharmaceuticals Inc. N-hydroxyamide derivatives possessing antibacterial activity

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
ERIC N. CHAUVEL 等: "Differential Inhibition of Aminopeptidase A and Aminopeptidase N by New P-Amino Thiols", 《J. MED. CHEM.》 *
JEEWOO LEE 等: "Methionine Analogues as Inhibitors of Methionyl-tRNA Synthetase", 《BIOORGANIC & MEDICINAL CHEMISTRY LETTERS》 *
STEPHAN K. GRANT 等: "Inhibition and Structure–Activity Studies of Methionine Hydroxamic Acid Derivatives with Bacterial Peptide Deformylase", 《BIOORGANIC CHEMISTRY》 *

Also Published As

Publication number Publication date
US20110196014A1 (en) 2011-08-11
JP2011529921A (ja) 2011-12-15
EP2326619B1 (en) 2019-02-27
WO2010014943A2 (en) 2010-02-04
IL210956A0 (en) 2011-04-28
WO2010014943A3 (en) 2011-01-13
US20170267632A1 (en) 2017-09-21
US8580859B2 (en) 2013-11-12
US9695119B2 (en) 2017-07-04
US20140142189A1 (en) 2014-05-22
JP5650642B2 (ja) 2015-01-07
EP2326619A2 (en) 2011-06-01
US20170029369A1 (en) 2017-02-02
US20150329481A1 (en) 2015-11-19
AU2009276343A1 (en) 2010-02-04
CA2733390A1 (en) 2010-02-04

Similar Documents

Publication Publication Date Title
US11339136B2 (en) Compounds and compositions for treating conditions associated with NLRP activity
EP2120965B1 (en) N-halogenated amino compounds and derivatives
JP2002502815A (ja) 抗菌剤
CA3220889A1 (en) Heterocyclic aldehyde trapping compounds and uses thereof
ES2283589T3 (es) Compuestos biciclicos de pirrolidina.
KR20010034861A (ko) 항박테리아제로서의 히드록삼산 유도체
US7129374B2 (en) Catalytic antioxidants and methods of use
KR20170052613A (ko) 효모/곰팡이에 의해 유발되는 감염을 치료하기 위한 시스테아민의 사용
JP2005515263A6 (ja) 新規な置換アルカン化合物及びその使用法
US20170267632A1 (en) Methionine analogs and methods of using same
JP2005515263A (ja) 新規な置換アルカン化合物及びその使用法
CA3059192A1 (en) Compounds and methods for hematopoietic regeneration
JP2001509790A (ja) 金属タンパク質分解酵素阻害剤
WO1998023588A9 (en) Metalloproteinase inhibitors
US20070135353A1 (en) Crystalline n-formyl hydroxylamine compounds
WO2002041886A1 (en) Ydroxamic acid or n-formyl hydroxylamine derivatives as inhibitors of bakterial polypeptide deformylase for treating microbial infections

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20110831