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SG169236A1 - Novel compunds, pharmaceutical compositions containing same, and methods of use for same - Google Patents

Novel compunds, pharmaceutical compositions containing same, and methods of use for same

Info

Publication number
SG169236A1
SG169236A1 SG200806632-6A SG2008066326A SG169236A1 SG 169236 A1 SG169236 A1 SG 169236A1 SG 2008066326 A SG2008066326 A SG 2008066326A SG 169236 A1 SG169236 A1 SG 169236A1
Authority
SG
Singapore
Prior art keywords
same
alkylaryl
arylalkyl
cycloalkyl
alkenyl
Prior art date
Application number
SG200806632-6A
Other languages
English (en)
Inventor
Francis P Kuhajda
Susan M Medghalchi
Jill M Mcfadden
Jagan Thupari
Craig A Townsend
Original Assignee
Fasgen Inc
Univ Johns Hopkins
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 Fasgen Inc, Univ Johns Hopkins filed Critical Fasgen Inc
Publication of SG169236A1 publication Critical patent/SG169236A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30—Hetero atoms other than halogen
    • C07D333/32—Oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Diabetes (AREA)
  • Communicable Diseases (AREA)
  • Obesity (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
SG200806632-6A 2002-07-09 2003-07-09 Novel compunds, pharmaceutical compositions containing same, and methods of use for same SG169236A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US39458502P 2002-07-09 2002-07-09

Publications (1)

Publication Number Publication Date
SG169236A1 true SG169236A1 (en) 2011-03-30

Family

ID=30115739

Family Applications (1)

Application Number Title Priority Date Filing Date
SG200806632-6A SG169236A1 (en) 2002-07-09 2003-07-09 Novel compunds, pharmaceutical compositions containing same, and methods of use for same

Country Status (13)

Country Link
US (2) US7649012B2 (fr)
EP (3) EP1539730A4 (fr)
JP (3) JP2005533835A (fr)
KR (1) KR101087559B1 (fr)
CN (2) CN100513404C (fr)
AU (1) AU2003265267B2 (fr)
BR (1) BRPI0312649A2 (fr)
CA (2) CA2767092C (fr)
EA (1) EA013371B1 (fr)
IL (2) IL166108A0 (fr)
MX (1) MXPA05000365A (fr)
SG (1) SG169236A1 (fr)
WO (1) WO2004005277A1 (fr)

Families Citing this family (32)

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AU2003215111A1 (en) 2002-02-08 2003-09-02 The Johns Hopkins University School Of Medicine Stimulation of cpt-1 as a means to reduce weight
SG149701A1 (en) * 2002-07-09 2009-02-27 Fasgen Llc Methods of treating microbial infections in humans and animals
EP1539730A4 (fr) * 2002-07-09 2007-03-28 Fasgen Inc Nouveaux composes, compositions pharmaceutiques les contenant et methodes d'utilisation desdits composes
KR20070095754A (ko) * 2004-05-26 2007-10-01 파스젠, 엘엘씨. 신규 화합물, 그것을 함유하는 약학 조성물, 및 그것을사용하는 방법
EP2061767B1 (fr) 2006-08-08 2014-12-17 Sanofi Imidazolidin-2,4-diones arylaminoaryl-alkyl-substituées, procédé de fabrication, médicaments les contenant et leur utilisation
WO2008057585A1 (fr) * 2006-11-08 2008-05-15 Fasgen Llc Nouveaux composés, leurs compositions pharmaceutiques et procédés d'application
WO2008059214A1 (fr) * 2006-11-13 2008-05-22 Astrazeneca Ab Dérivés de bisamide et utilisation de ceux-ci en tant qu'inhibiteurs de l'acide gras synthase
WO2009149066A1 (fr) * 2008-06-02 2009-12-10 Fasgen, Inc. Nouveaux composés, compositions pharmaceutiques contenant ceux-ci, et procédés d'utilisation de ceux-ci
US8470841B2 (en) 2008-07-09 2013-06-25 Sanofi Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof
WO2010068601A1 (fr) 2008-12-08 2010-06-17 Sanofi-Aventis Hydrate de fluoroglycoside hétéroaromatique cristallin, ses procédés de fabrication, ses procédés d'utilisation et compositions pharmaceutiques le contenant
US8729239B2 (en) 2009-04-09 2014-05-20 Nuclea Biotechnologies, Inc. Antibodies against fatty acid synthase
WO2011019498A1 (fr) * 2009-07-27 2011-02-17 The Trustees Of Princeton University Inhibition de glycérol-3-phosphate acyltransférase (gpat) et enzymes associées pour le traitement d'infections virales
CN102482312A (zh) 2009-08-26 2012-05-30 赛诺菲 新颖的杂芳族氟代糖苷结晶水合物、含有这些化合物的药物和它们的用途
US8450350B2 (en) 2010-05-05 2013-05-28 Infinity Pharmaceuticals, Inc. Triazoles as inhibitors of fatty acid synthase
EP3159331A1 (fr) 2010-05-05 2017-04-26 Infinity Pharmaceuticals, Inc. Tretrazolones utilisées comme inhibiteurs de synthase d'acide gras
EP2683705B1 (fr) 2011-03-08 2015-04-22 Sanofi Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation
EP2683702B1 (fr) 2011-03-08 2014-12-24 Sanofi Nouveaux dérivés de phényle-oxathiazine substitués, leur procédé de fabrication, médicament contenant ces liaisons et son utilisation
US8846666B2 (en) 2011-03-08 2014-09-30 Sanofi Oxathiazine derivatives which are substituted with benzyl or heteromethylene groups, method for producing them, their use as medicine and drug containing said derivatives and the use thereof
US8901114B2 (en) 2011-03-08 2014-12-02 Sanofi Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof
WO2012120056A1 (fr) 2011-03-08 2012-09-13 Sanofi Dérivés oxathiazine tétra-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation
WO2012120053A1 (fr) 2011-03-08 2012-09-13 Sanofi Dérivés oxathiazine ramifiés, procédé pour leur préparation, utilisation en tant que médicament, agents pharmaceutiques contenant ces dérivés et leur utilisation
WO2012120051A1 (fr) 2011-03-08 2012-09-13 Sanofi Dérivés benzyl-oxathiazine substitués avec adamantane ou noradamantane, médicaments contenant ces composés et leur utilisation
EP2683699B1 (fr) 2011-03-08 2015-06-24 Sanofi Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation
EP2683703B1 (fr) 2011-03-08 2015-05-27 Sanofi Nouveaux dérivés phényl-oxathiazine substitués, procédé pour leur préparation, agent pharmaceutique contenant ces composés et leur utilisation
WO2012135027A2 (fr) * 2011-03-25 2012-10-04 The Research Foundation Of State University Of New York Antibiotiques de thiolactone
EP2567959B1 (fr) 2011-09-12 2014-04-16 Sanofi Dérivés d'amide d'acide 6-(4-hydroxy-phényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase
JP6228198B2 (ja) * 2012-06-25 2017-11-08 トーマス・ジェファーソン・ユニバーシティＴｈｏｍａｓ Ｊｅｆｆｅｒｓｏｎ Ｕｎｉｖｅｒｓｉｔｙ 異常な脂質生合成シグナル伝達を有するがんを処置するための組成物および方法
US20150099730A1 (en) * 2012-09-07 2015-04-09 Janssen Pharmaceutica, Nv Imidazolin-5-one derivative useful as fasn inhibitors for the treatment of cancer
KR102194745B1 (ko) 2013-03-13 2020-12-24 포르마 세라퓨틱스 인크. Ｆａｓｎ 억제용 신규 화합물 및 조성물
EP3220901B1 (fr) 2014-11-20 2020-02-19 VIB vzw Compositions et méthodes pour le traitement de la maladie de parkinson précoce
EP3873214A4 (fr) 2018-10-29 2022-07-13 Forma Therapeutics, Inc. Formes solides de (4-(2-fluoro-4-(1-méthyl-1h-benzo[d]imidazol-5-yl)benzoyl)pipérazin-1-yl)(1-hydroxycyclopropyl)méthanone
CN114480521B (zh) * 2020-11-13 2024-07-26 中国科学院青岛生物能源与过程研究所 一种三氮菌素c的制备方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996035664A1 (fr) * 1995-05-09 1996-11-14 Bayer Aktiengesellschaft Enols cetoniques substitues par des phenyles dihalogenes d'alkyle servant de pesticides et herbicides
WO2001049278A2 (fr) * 2000-01-06 2001-07-12 University College Cardiff Consultants Limited Composes et compositions utilises pour inhiber la biosynthese d'acides gras d'endoparasites

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US3496187A (en) * 1967-03-20 1970-02-17 American Home Prod N-(heterocyclyl)aconamides
US3472878A (en) * 1969-01-27 1969-10-14 American Home Prod N-(hydroxyaryl)aconamides
JPS5859920A (ja) * 1981-10-05 1983-04-09 Chugai Pharmaceut Co Ltd 生体防禦能賦活剤
US4565699A (en) * 1983-07-18 1986-01-21 The Upjohn Company Composition of matter and process
US4720503A (en) * 1985-08-02 1988-01-19 Merck & Co., Inc. N-substituted fused-heterocyclic carboxamide derivatives as dual cyclooxygenase and lipoxygenase inhibitors
CH667655A5 (de) * 1986-09-24 1988-10-31 Lonza Ag Verfahren zur herstellung von 4-alkoxy-2(5h)-thiophenonen.
US4753871A (en) * 1986-12-12 1988-06-28 Eastman Kodak Company Cyan dye-forming couplers and photographic materials containing same
WO1988004652A1 (fr) * 1986-12-17 1988-06-30 Nippon Soda Co., Ltd. Composes heterocycliques possedant un squelette triketo
US5759837A (en) 1989-01-17 1998-06-02 John Hopkins University Chemotherapy for cancer by inhibiting the fatty acid biosynthetic pathway
US5665874A (en) * 1989-01-17 1997-09-09 John Hopkins University Cancer related antigen
US5759791A (en) * 1989-01-17 1998-06-02 The Johns Hopkins University Cancer related antigen
US5679801A (en) * 1991-04-12 1997-10-21 American Home Products Corporation Tetronic and thiotetronic acid derivatives as phospholipase A2 inhibitors
US5614551A (en) 1994-01-24 1997-03-25 The Johns Hopkins University Inhibitors of fatty acid synthesis as antimicrobial agents
US5981575A (en) 1996-11-15 1999-11-09 Johns Hopkins University, The Inhibition of fatty acid synthase as a means to reduce adipocyte mass
JPH10212284A (ja) * 1996-11-27 1998-08-11 Sagami Chem Res Center テトロン酸−３−カルボン酸誘導体、その製造方法、製造中間体、抗がん剤、及び蛋白脱リン酸化酵素阻害剤
US6391912B1 (en) * 1996-12-12 2002-05-21 Bayer Aktiengesellschaft Substituted phenylketoenols
CO4970714A1 (es) * 1997-09-05 2000-11-07 Boehringer Mannheim Gmbh Derivados ureido y tioureido de 4-amino-2(5h)-furanonas y 4-amino-2(5h) tiofenonas como agentes antitumorales
HN2000000051A (es) * 1999-05-19 2001-02-02 Pfizer Prod Inc Derivados heterociclicos utiles como agentes anticancerosos
IT1315267B1 (it) * 1999-12-23 2003-02-03 Novuspharma Spa Derivati di 2-(1h-indol-3-il)-2-oxo-acetammidi ad attivita'antitumorale
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EP1383493A4 (fr) * 2001-05-02 2005-09-21 Univ New York Inhibition de la pigmentation par l'inhibition de l'acide gras synthase
AU2003215111A1 (en) * 2002-02-08 2003-09-02 The Johns Hopkins University School Of Medicine Stimulation of cpt-1 as a means to reduce weight
EP1539730A4 (fr) * 2002-07-09 2007-03-28 Fasgen Inc Nouveaux composes, compositions pharmaceutiques les contenant et methodes d'utilisation desdits composes
SG149701A1 (en) * 2002-07-09 2009-02-27 Fasgen Llc Methods of treating microbial infections in humans and animals
US9690894B1 (en) 2015-11-02 2017-06-27 Altera Corporation Safety features for high level design

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996035664A1 (fr) * 1995-05-09 1996-11-14 Bayer Aktiengesellschaft Enols cetoniques substitues par des phenyles dihalogenes d'alkyle servant de pesticides et herbicides
WO2001049278A2 (fr) * 2000-01-06 2001-07-12 University College Cardiff Consultants Limited Composes et compositions utilises pour inhiber la biosynthese d'acides gras d'endoparasites

Also Published As

Publication number Publication date
EA200500178A1 (ru) 2006-02-24
JP2011037881A (ja) 2011-02-24
CA2491802A1 (fr) 2004-01-15
BRPI0312649A2 (pt) 2017-05-16
CA2491802C (fr) 2012-04-10
CN100513404C (zh) 2009-07-15
AU2003265267A1 (en) 2004-01-23
CN101602756B (zh) 2014-11-12
KR20060002007A (ko) 2006-01-06
JP2005533835A (ja) 2005-11-10
CA2767092C (fr) 2013-10-15
CA2767092A1 (fr) 2004-01-15
AU2003265267B2 (en) 2010-03-11
EA013371B1 (ru) 2010-04-30
WO2004005277A1 (fr) 2004-01-15
CN101602756A (zh) 2009-12-16
CN1675192A (zh) 2005-09-28
US20060247302A1 (en) 2006-11-02
EP2386550A1 (fr) 2011-11-16
MXPA05000365A (es) 2005-09-20
EP1539730A4 (fr) 2007-03-28
HK1083835A1 (zh) 2006-07-14
KR101087559B1 (ko) 2011-11-29
JP2013189464A (ja) 2013-09-26
US7649012B2 (en) 2010-01-19
EP2386551A1 (fr) 2011-11-16
IL190218A0 (en) 2008-11-03
US20100120901A1 (en) 2010-05-13
IL166108A0 (en) 2006-01-15
EP1539730A1 (fr) 2005-06-15

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