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BE2015C029I2 - - Google Patents

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Publication number
BE2015C029I2
BE2015C029I2 BE2015C029C BE2015C029C BE2015C029I2 BE 2015C029 I2 BE2015C029 I2 BE 2015C029I2 BE 2015C029 C BE2015C029 C BE 2015C029C BE 2015C029 C BE2015C029 C BE 2015C029C BE 2015C029 I2 BE2015C029 I2 BE 2015C029I2
Authority
BE
Belgium
Prior art keywords
disclosed
synthesis
novel
ceramide
udp
Prior art date
Application number
BE2015C029C
Other languages
French (fr)
Original Assignee
Univ Michigan Regents
Genzyme Corp
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=23182463&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=BE2015C029(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Univ Michigan Regents, Genzyme Corp filed Critical Univ Michigan Regents
Publication of BE2015C029I2 publication Critical patent/BE2015C029I2/fr

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/4025Heterocyclic 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 not condensed and containing further heterocyclic rings, e.g. cromakalim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • 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
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • 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
    • 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/185Radicals derived from carboxylic acids from aliphatic carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/101,4-Dioxanes; Hydrogenated 1,4-dioxanes
    • C07D319/141,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
    • C07D319/161,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D319/18Ethylenedioxybenzenes, not substituted on the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Neurology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Dermatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Obesity (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pyrrole Compounds (AREA)
  • Cosmetics (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Disclosed is a novel enantiomeric synthesis of ceramide-like inhibitors of UDP-glucose: N -acylsphingosine glucosyltransferase. Also disclosed are novel intermediates formed during the synthesis.
BE2015C029C 2001-07-16 2015-05-12 BE2015C029I2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US30581401P 2001-07-16 2001-07-16
PCT/US2002/022659 WO2003008399A1 (en) 2001-07-16 2002-07-16 Synthesis of udp-glucose: n-acylsphingosine glucosyltransferase inhibitors

Publications (1)

Publication Number Publication Date
BE2015C029I2 true BE2015C029I2 (en) 2021-07-19

Family

ID=23182463

Family Applications (1)

Application Number Title Priority Date Filing Date
BE2015C029C BE2015C029I2 (en) 2001-07-16 2015-05-12

Country Status (15)

Country Link
US (11) US6855830B2 (en)
EP (3) EP2067775B1 (en)
JP (6) JP5038582B2 (en)
AT (2) ATE554082T1 (en)
BE (1) BE2015C029I2 (en)
BR (3) BR122015016313B8 (en)
CA (1) CA2453978C (en)
CY (1) CY2015028I2 (en)
DK (3) DK2067775T3 (en)
ES (3) ES2395122T3 (en)
FR (1) FR15C0036I2 (en)
IL (3) IL159905A0 (en)
LU (1) LU92717I2 (en)
PT (3) PT2266968E (en)
WO (1) WO2003008399A1 (en)

Families Citing this family (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6890949B1 (en) * 1999-07-09 2005-05-10 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
MY164523A (en) * 2000-05-23 2017-12-29 Univ Degli Studi Cagliari Methods and compositions for treating hepatitis c virus
CA2434028C (en) 2001-01-10 2010-11-09 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
US7723296B2 (en) 2001-01-18 2010-05-25 Genzyme Corporation Methods for introducing mannose-6-phosphate and other oligosaccharides onto glycoproteins and its application thereof
EP2067775B1 (en) * 2001-07-16 2012-04-25 Genzyme Corporation A N-Acylsphingosine glucosyltransferase inhibitor
US6835831B2 (en) * 2001-11-26 2004-12-28 Genzyme Corporation Diastereoselective synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors
US20060217560A1 (en) * 2002-04-29 2006-09-28 Shayman James A Amino ceramide-like compounds and therapeutic methods of use
US6916802B2 (en) * 2002-04-29 2005-07-12 Genzyme Corporation Amino ceramide-like compounds and therapeutic methods of use
JP4195411B2 (en) * 2004-04-12 2008-12-10 セイコーエプソン株式会社 Method for manufacturing organic electroluminescence device
JP2008519840A (en) * 2004-11-10 2008-06-12 ジェンザイム・コーポレイション How to treat diabetes
ATE549020T1 (en) 2005-01-26 2012-03-15 Allergan Inc PHARMACEUTICAL COMPOSITIONS CONTAINING 1-BENZYL-1-HYDROXY-2,3-DIAMINO-PROPYLAMINE, 3-BENZYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS AS ANALGESICS
ES2546181T3 (en) 2006-05-09 2015-09-21 Genzyme Corporation Methods of treating fatty liver disease by inhibiting the synthesis of glycosphingolipids
PL2457920T3 (en) 2007-01-18 2018-03-30 Genzyme Corporation Oligosaccharides comprising an aminooxy group and conjugates thereof
US20140179925A1 (en) 2009-09-04 2014-06-26 Allergan, Inc. Methods for treating cognitive disorders using 3-aryl-3-hydroxy-2-amino-propionic acid amides, 3-heteroaryl-3-hydroxy-2-amino-propionic acid amides and related compounds
WO2008109285A1 (en) 2007-03-06 2008-09-12 Allergan, Inc. Methods for treating cognitive disorders
US9314466B2 (en) 2007-03-06 2016-04-19 Allergan, Inc. Methods for treating cognitive disorders using 1-benzyl-1-hydroxy-2,3-diamino-propyl amines, 3-benzyl-3-hydroxy-2-amino-propionic acid amides and related compounds
EP2131837B1 (en) * 2007-03-06 2012-05-16 Allergan, Inc. Specific 3-heteroaryl-3-hydroxy-2-amino-propionic acid amide derivative for use in the treatment of certain cognitive disorders
WO2008150486A2 (en) 2007-05-31 2008-12-11 Genzyme Corporation 2-acylaminopropoanol-type glucosylceramide synthase inhibitors
BRPI0823522A2 (en) 2007-10-05 2014-01-07 Genzyme Corp USE OF CERAMIDE DERIVATIVE COMPOUND
US8168631B2 (en) 2008-02-05 2012-05-01 Allergan, Inc. 3-(4-fluorophenyl)-3-hydroxy-2-amino-propionic acid amides and related compounds having analgesic activity
CA2731685A1 (en) 2008-07-28 2010-02-04 Genzyme Corporation Glucosylceramide synthase inhibition for the treatment of collapsing glomerulopathy and other glomerular disease
US8309593B2 (en) 2008-10-03 2012-11-13 Genzyme Corporation 2-acylaminopropoanol-type glucosylceramide synthase inhibitors
MX2011006347A (en) 2008-12-16 2011-09-06 Genzyme Corp Oligosaccharide-protein conjugates.
CN102712629B (en) * 2009-11-27 2016-10-12 基酶有限公司 Amorphous and crystalline forms of Genz 112638 hemitartrate as an inhibitor of glucosylceramide synthase
KR20130012953A (en) 2010-04-16 2013-02-05 교세라 가부시키가이샤 Wireless communication system, high-power base station, low-power base station, and communication control method
WO2012145644A1 (en) 2011-04-22 2012-10-26 Genzyme Corporation Modified acid alpha glucosidase with accelerated processing
WO2013059119A1 (en) 2011-10-17 2013-04-25 The Regents Of The University Of Michigan Glucosylceramide synthase inhibitors and therapeutic methods using the same
EP2968268B1 (en) 2013-03-15 2020-07-29 Concert Pharmaceuticals Inc. Inhibitors of the enzyme udp-glucose: n-acyl-sphingosine glucosyltransferase
JP6537500B2 (en) 2013-09-20 2019-07-03 ビオマリン プハルマセウトイカル インコーポレイテッド Glucosylceramide synthase inhibitors for the treatment of diseases
WO2015059679A1 (en) * 2013-10-25 2015-04-30 Dr. Reddy's Laboratories Limited Improved process for the preparation of eliglustat
CA2927798C (en) 2013-10-29 2022-03-15 Biomarin Pharmaceutical Inc. N-(1-hydroxy-3-(pyrrolidinyl)propan-2-yl)pyrrolidine-3-carboxamide derivatives as glucosylceramide synthase inhibitors
JP6749923B2 (en) 2015-02-02 2020-09-02 ザ リージェンツ オブ ザ ユニバーシティー オブ ミシガン Glucosylceramide synthase inhibitor and treatment method using the same
CN104557851B (en) * 2015-02-10 2017-04-05 苏州明锐医药科技有限公司 The preparation method of Yi Lusita
EP3283483B1 (en) 2015-04-14 2018-12-19 Sandoz AG Crystalline eliglustat hydrochloride
WO2017068496A1 (en) * 2015-10-20 2017-04-27 Dr. Reddy' S Laboratories Limited Improved process for the preparation of eliglustat and its salts
CN105646442A (en) * 2015-10-27 2016-06-08 北京凯莱天成医药科技有限公司 Preparation method of eliglustat
WO2017178499A1 (en) 2016-04-11 2017-10-19 Spedding Research Solutions Inhibitors of glucosylceramide degradation in the treatment of diseases of the motor units
CN106349210A (en) * 2016-08-24 2017-01-25 北京阳光诺和药物研究有限公司 Method for preparing tartrate EGS
CN106967042B (en) * 2017-03-21 2020-08-14 浙江奥翔药业股份有限公司 Synthesis method of eligerlat and intermediate compound thereof
CN108822072B (en) * 2017-04-11 2021-01-12 中国医学科学院药物研究所 Method for preparing Elligusurgitol
WO2018193090A2 (en) 2017-04-21 2018-10-25 Amneal Pharmaceuticals Company Gmbh Process for preparation of eliglustat hemitartrate and intermediates thereof
WO2018225085A1 (en) 2017-06-05 2018-12-13 Cipla Limited Stable solid dispersions of eliglustat hemitartrate
KR102791275B1 (en) 2017-12-15 2025-04-08 젠자임 코포레이션 Treatment of Gaucher's disease
WO2019123476A1 (en) 2017-12-20 2019-06-27 Sarudbhava Formulations Private Limited Stable amorphous eliglustat premix and process for the preparation thereof
CN111217791B (en) * 2018-11-27 2024-02-02 广东东阳光药业股份有限公司 Ibrutin intermediate and preparation method thereof
WO2020194138A1 (en) * 2019-03-22 2020-10-01 Piramal Enterprises Limited An improved process for the preparation of eliglustat and its intermediate
WO2020193746A1 (en) 2019-03-28 2020-10-01 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for predicting the survival of patients suffering from melanoma
WO2021081141A1 (en) 2019-10-23 2021-04-29 The Regents Of The University Of Michigan Glucosylceramide synthase inhibitors and therapeutic methods using the same
WO2021214771A1 (en) 2020-04-23 2021-10-28 The Israel Institute of Biological Research (IIBR) Glucosylceramide synthase inhibitors for prevention and treatment of viral diseases
WO2021221953A1 (en) 2020-04-28 2021-11-04 The Regents Of The University Of Michigan Pyridine inhibitors of glucosylceramide synthase and therapeutic methods using the same
CN116120274A (en) 2021-11-12 2023-05-16 曙方(上海)医药科技有限公司 Pharmaceutically acceptable salts of irinotecan and crystalline forms thereof
EP4201403A1 (en) 2021-12-21 2023-06-28 Som Innovation Biotech, S.L. Compounds tirapazamine and quazinone for use in the treatment of gm2 gangliosidoses
WO2026006099A1 (en) 2024-06-24 2026-01-02 Genzyme Corporation Eliglustat for the treatment of gaucher disease

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8311286D0 (en) 1983-04-26 1983-06-02 Searle & Co Carboxyalkyl peptide derivatives
DE3522475A1 (en) 1985-06-22 1987-01-02 Kali Chemie Pharma Gmbh NEW AROMATIC COMPOUNDS, THEIR PRODUCTION AND USE
JPH0416856A (en) 1990-05-10 1992-01-21 Canon Inc Positively charged non-magnetic toner
ZA929008B (en) 1991-12-13 1993-05-21 Bristol Myers Squibb Co Piperazinyl- and piperidinyl-cyclohexanols.
JP3778926B2 (en) * 1993-08-13 2006-05-24 生化学工業株式会社 Neurological treatment
ATE195944T1 (en) * 1994-02-02 2000-09-15 Liposome Co Inc PHARMACEUTICALLY ACTIVE COMPOUNDS AND LIPOSOMES AND METHOD FOR THE PRODUCTION THEREOF
DE69524592T2 (en) * 1994-06-10 2002-07-18 Seikagaku Corp., Tokio/Tokyo 2-acylaminopropanol compound and its pharmaceutical composition
FR2734819B1 (en) 1995-05-31 1997-07-04 Adir NOVEL COMPOUNDS OF PIPERAZINE, PIPERIDINE AND 1,2,5,6-TETRAHYDROPYRIDINE, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
US20030073680A1 (en) * 1995-09-20 2003-04-17 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
WO2001004108A1 (en) 1999-07-09 2001-01-18 Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
US6255336B1 (en) * 1995-09-20 2001-07-03 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
WO1997010817A1 (en) 1995-09-20 1997-03-27 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
US6890949B1 (en) 1999-07-09 2005-05-10 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
NO965193L (en) * 1995-12-08 1997-06-09 Seikagaku Kogyo Kk Seikagaku C Aminal alcohol derivative and process for its preparation
JP3993908B2 (en) * 1995-12-08 2007-10-17 生化学工業株式会社 Amino alcohol derivative and method for producing the derivative
JP4140984B2 (en) 1995-12-20 2008-08-27 生化学工業株式会社 Drug with differentiation-inducing action
US5916802A (en) * 1997-02-19 1999-06-29 Fritz Berthold Device for measuring ATP
US5972928A (en) 1997-05-21 1999-10-26 Johns Hopkins University Methods for treatment of conditions associated with lactosylceramide
JP4036500B2 (en) 1997-05-23 2008-01-23 生化学工業株式会社 Amino alcohol derivatives and pharmaceuticals containing the same
JP4176170B2 (en) 1997-06-06 2008-11-05 生化学工業株式会社 Medicine containing amino alcohol derivative and therapeutic agent for abnormal proliferative disease
ES2285852T3 (en) * 1998-07-27 2007-11-16 Johns Hopkins University DIAMINO-PROPANOL COMPOUNDS FOR THE TREATMENT OF ISCHEMIA.
US20040260099A1 (en) 2001-01-10 2004-12-23 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
CA2434028C (en) 2001-01-10 2010-11-09 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
US20020198240A1 (en) * 2001-01-10 2002-12-26 Shayman James A. Amino ceramide - like compounds and therapeutic methods of use
US7148251B2 (en) * 2001-01-10 2006-12-12 The Regents Of The University Of Michigan Amino ceramide-like compounds and therapeutic methods of use
EP2067775B1 (en) * 2001-07-16 2012-04-25 Genzyme Corporation A N-Acylsphingosine glucosyltransferase inhibitor
US20060217560A1 (en) 2002-04-29 2006-09-28 Shayman James A Amino ceramide-like compounds and therapeutic methods of use
US6916802B2 (en) * 2002-04-29 2005-07-12 Genzyme Corporation Amino ceramide-like compounds and therapeutic methods of use
ES2546181T3 (en) * 2006-05-09 2015-09-21 Genzyme Corporation Methods of treating fatty liver disease by inhibiting the synthesis of glycosphingolipids

Also Published As

Publication number Publication date
EP2067775A1 (en) 2009-06-10
EP2067775B1 (en) 2012-04-25
JP4708073B2 (en) 2011-06-22
BR122015016313B1 (en) 2019-04-16
HK1153733A1 (en) 2012-04-05
CY2015028I1 (en) 2016-07-27
BRPI0211379B8 (en) 2021-05-25
US20050222244A1 (en) 2005-10-06
DK2067775T3 (en) 2012-07-16
EP2266968A3 (en) 2011-05-18
CY2015028I2 (en) 2016-07-27
JP2017075151A (en) 2017-04-20
PT1409467E (en) 2012-10-24
BR122015016314B1 (en) 2019-04-16
US9546161B2 (en) 2017-01-17
BRPI0211379B1 (en) 2018-02-14
FR15C0036I1 (en) 2015-06-26
ES2395122T3 (en) 2013-02-08
PT2266968E (en) 2013-02-25
WO2003008399A1 (en) 2003-01-30
HK1132267A1 (en) 2010-02-19
US7615573B2 (en) 2009-11-10
US8138353B2 (en) 2012-03-20
EP2266968B1 (en) 2013-01-09
EP1409467B1 (en) 2012-04-18
PT2067775E (en) 2012-07-16
US20110003987A1 (en) 2011-01-06
US20030050299A1 (en) 2003-03-13
JP2013136618A (en) 2013-07-11
US20070203223A1 (en) 2007-08-30
US20170334888A1 (en) 2017-11-23
JP6182254B2 (en) 2017-08-16
IL159905A (en) 2009-05-04
EP1409467A1 (en) 2004-04-21
JP5227348B2 (en) 2013-07-03
JP2010095546A (en) 2010-04-30
ATE555102T1 (en) 2012-05-15
JP2005502635A (en) 2005-01-27
IL159905A0 (en) 2004-06-20
US20080058514A1 (en) 2008-03-06
ES2395463T3 (en) 2013-02-15
US8779163B2 (en) 2014-07-15
US20050009872A1 (en) 2005-01-13
IL193244A0 (en) 2009-02-11
US20120296088A1 (en) 2012-11-22
US6855830B2 (en) 2005-02-15
ATE554082T1 (en) 2012-05-15
ES2395463T4 (en) 2013-02-12
CA2453978A1 (en) 2003-01-30
DK1409467T3 (en) 2012-07-16
US20190322649A1 (en) 2019-10-24
LU92717I2 (en) 2015-11-24
US7763738B2 (en) 2010-07-27
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ES2399323T3 (en) 2013-03-27
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US7196205B2 (en) 2007-03-27
DK2266968T3 (en) 2013-04-08
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US7265228B2 (en) 2007-09-04
US20210171507A1 (en) 2021-06-10
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