[go: up one dir, main page]

AR057661A1 - Un derivado de oxima y sus preparaciones - Google Patents

Un derivado de oxima y sus preparaciones

Info

Publication number
AR057661A1
AR057661A1 ARP060102967A ARP060102967A AR057661A1 AR 057661 A1 AR057661 A1 AR 057661A1 AR P060102967 A ARP060102967 A AR P060102967A AR P060102967 A ARP060102967 A AR P060102967A AR 057661 A1 AR057661 A1 AR 057661A1
Authority
AR
Argentina
Prior art keywords
substituted
unsubstituted
heteroaryl
hydrogen atom
halogen atom
Prior art date
Application number
ARP060102967A
Other languages
English (en)
Inventor
K Sugawara
T Matsudaira
H Sugama
M Nawano
R Ohashi
Original Assignee
Tanabe Seiyaku Co
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 Tanabe Seiyaku Co filed Critical Tanabe Seiyaku Co
Publication of AR057661A1 publication Critical patent/AR057661A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/02—Heterocyclic 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
    • C07D405/12—Heterocyclic 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 chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/433—Thidiazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • 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
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen 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
    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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
    • C07D241/20—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D277/38—Nitrogen atoms
    • C07D277/44—Acylated amino or imino radicals
    • C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01—Five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/14—Heterocyclic 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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Biomedical Technology (AREA)
  • Vascular Medicine (AREA)
  • Endocrinology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

El problema de la presente es proveer un compuesto util como un agente activador de glucoquinasa, que es el derivado de oxima de la formula (1), se divulgan derivados de oxima, un método para su preparacion e intermediarios. Estos compuestos ejercen un efecto de activacion de la glucoquinasa, siendo al parecer utiles para tratar la diabetes tipo II. Reivindicacion 1: Un activador de glucoquinasa caracterizado porque comprende un compuesto de la formula general (1), en donde el Anillo A es arilo o heteroarilo; Q es cicloalquilo, heterociclo, alquilo o alquenilo; Anillo T es heteroarilo o heterociclo; R1 es un átomo de hidrogeno, átomo de halogeno, cicloalquilsulfonilo, alquilsulfonilo, alquilsulfinilo, alquiltio, o tetrazolilo sustituido o no sustituido; R2 es un átomo de hidrogeno, átomo de halogeno, cicloalquilsulfonilo, alquilsulfonilo sustituido o no sustituido, alquiltio sustituido o no sustituido, nitro, amino sustituido o no sustituido, aminosulfonilo sustituido o no sustituido, heterociclil-tio sustituido o no sustituido, heterociclil-sulfonilo sustituido o no sustituido, heterociclil-sulfonilo sustituido o no sustituido, heteroarilsulfonilo sustituido o no sustituido, alqueniloxi, alcoxi sustituido o no sustituido, alquilsulfinilo sustituido o no sustituido, heteroarilo sustituido o no sustituido, heteroariltio sustituido o no sustituido; R3 y R4 son, de modo independientemente, un átomo de hidrogeno, alcoxi, heterociclo sustituido o no sustituido, heteroarilo sustituido o no sustituido, alcoxialcoxi, cicloalquilo sustituido o no sustituido, ciano, arilo sustituido o no sustituido, carbamoilo sustituido o no sustituido, hidroxi, alcanoilo, alquiltio, alcoxicarbonilo, ariloxi sustituido o no sustituido, átomo de halogeno, oxo, o arilcarboniloxi sustituido o no sustituido; R5 es átomo de hidrogeno, formilo, átomo de halogeno, oxo, alcoxi sustituido o no sustituido, aminosulfonilo sustituido o no sustituido, alquiltio sustituido o no sustituido, ciano, heterociclilsulfonilo sustituido o no sustituido, nitro, cicloalquilo sustituido o no sustituido, alcoxicarbonilo, alquenilo, alquilsulfonilo, carbamoilo sustituido o no sustituido, heteroariltio sustituido o no sustituido, amino sustituido o no sustituido, carboxilo, heteroarilo sustituido o no sustituido, alquinilo sustituido o no sustituido, heterociclil-carbonilo sustituido o no sustituido, heterociclil-oxi sustituido o no sustituido, heterociclo sustituido o no sustituido, heterocicliltio sustituido o no sustituido, cicloalquiloxi sustituido o no sustituido, alcanoilo, o alquilo sustituido o no sustituido; R6 es átomo de hidrogeno, alquilo sustituido o no sustituido, un átomo de halogeno, o carboxilo; o una de sus sales farmacéuticamente aceptable como un ingrediente activo.
ARP060102967A 2005-07-11 2006-07-10 Un derivado de oxima y sus preparaciones AR057661A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2005202014 2005-07-11
JP2006114243 2006-04-18

Publications (1)

Publication Number Publication Date
AR057661A1 true AR057661A1 (es) 2007-12-12

Family

ID=37388432

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060102967A AR057661A1 (es) 2005-07-11 2006-07-10 Un derivado de oxima y sus preparaciones

Country Status (16)

Country Link
US (2) US7514439B2 (es)
EP (1) EP1907387A1 (es)
JP (1) JP4033409B1 (es)
KR (1) KR100965040B1 (es)
CN (1) CN101218237B (es)
AR (1) AR057661A1 (es)
AU (1) AU2006267387B2 (es)
BR (1) BRPI0613451A2 (es)
CA (1) CA2613303C (es)
IL (1) IL188258A0 (es)
MX (1) MX2008000560A (es)
NO (1) NO20080717L (es)
NZ (1) NZ564743A (es)
RU (1) RU2420525C2 (es)
TW (1) TWI359149B (es)
WO (1) WO2007007886A1 (es)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007007886A1 (en) * 2005-07-11 2007-01-18 Mitsubishi Tanabe Pharma Corporation An oxime derivative and preparations thereof
PE20080251A1 (es) 2006-05-04 2008-04-25 Boehringer Ingelheim Int Usos de inhibidores de dpp iv
JP2009544648A (ja) 2006-07-24 2009-12-17 エフ．ホフマン−ラ ロシュ アーゲー グルコキナーゼ活性化剤としてのピラゾール類
EP2061767B1 (de) 2006-08-08 2014-12-17 Sanofi Arylaminoaryl-alkyl-substituierte Imidazolidin-2,4-dione, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Arzneimittel und ihre Verwendung
EP2066619A2 (en) * 2006-11-02 2009-06-10 Arete Therapeutics, INC. Soluble epoxide hydrolase inhibitors
US7902248B2 (en) 2006-12-14 2011-03-08 Hoffmann-La Roche Inc. Oxime glucokinase activators
WO2008084873A1 (ja) * 2007-01-10 2008-07-17 Mitsubishi Tanabe Pharma Corporation オキシム誘導体
WO2008084872A1 (ja) * 2007-01-10 2008-07-17 Mitsubishi Tanabe Pharma Corporation ヒドラゾン誘導体
US8563732B2 (en) 2007-05-31 2013-10-22 Shionogi & Co., Ltd. Oxyimino compounds and the use thereof
AR066845A1 (es) 2007-06-05 2009-09-16 Takeda Pharmaceutical Derivados de triazolopiridina e imidazopiridina una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento del cancer
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
EP2181987B9 (en) 2007-08-23 2014-09-03 Takeda Pharmaceutical Company Limited 2-Carbonylaminobenzothiazoles and their use for the prophylaxis and treatment of cancer
KR20100113518A (ko) 2008-01-18 2010-10-21 아스텔라스세이야쿠 가부시키가이샤 페닐아세트아미드 유도체
WO2009099080A1 (ja) * 2008-02-06 2009-08-13 Daiichi Sankyo Company, Limited 新規フェニルピロール誘導体
US7741327B2 (en) 2008-04-16 2010-06-22 Hoffmann-La Roche Inc. Pyrrolidinone glucokinase activators
US8258134B2 (en) 2008-04-16 2012-09-04 Hoffmann-La Roche Inc. Pyridazinone glucokinase activators
PL2275414T3 (pl) 2008-04-28 2016-01-29 Kyorin Seiyaku Kk Pochodne cyklopentyloakryloamidu
WO2009140624A2 (en) 2008-05-16 2009-11-19 Takeda San Diego, Inc. Glucokinase activators
ES2408159T3 (es) 2008-06-11 2013-06-18 Shionogi & Co., Ltd. Compuestos de oxicarbamoilo y su utilización
US8470841B2 (en) 2008-07-09 2013-06-25 Sanofi Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof
WO2010064611A1 (ja) 2008-12-01 2010-06-10 武田薬品工業株式会社 複素環化合物およびその用途
JO3101B1 (ar) 2008-12-02 2017-09-20 Takeda Pharmaceuticals Co مشتقات بنزوثيازول كعوامل مضادة للسرطان
WO2010068601A1 (en) 2008-12-08 2010-06-17 Sanofi-Aventis A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof
UA104742C2 (uk) 2008-12-19 2014-03-11 Эли Лилли Энд Компани Похідні арилциклопропілацетаміду, застосовні як активатори глюкокінази
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
US8222416B2 (en) 2009-12-14 2012-07-17 Hoffmann-La Roche Inc. Azaindole glucokinase activators
WO2011093423A1 (ja) * 2010-01-29 2011-08-04 田辺三菱製薬株式会社 （ｅ）－ヒドロキシイミノフェニル酢酸誘導体の製法
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
US8178689B2 (en) 2010-06-17 2012-05-15 Hoffman-La Roche Inc. Tricyclic compounds
EP2582709B1 (de) 2010-06-18 2018-01-24 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
MX2012014607A (es) 2010-06-22 2013-02-21 Bayer Ip Gmbh Proceso para preparacion de derivados de 1-alquiltetrazolil oxima 5-sustituidos.
EP2402327B1 (en) 2010-06-29 2018-03-07 Impetis Biosciences Ltd. Acetamide compounds as glucokinase activators, their process and medicinal applications
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
EP2683705B1 (de) 2011-03-08 2015-04-22 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
EP2683699B1 (de) 2011-03-08 2015-06-24 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2012120053A1 (de) 2011-03-08 2012-09-13 Sanofi Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2012120056A1 (de) 2011-03-08 2012-09-13 Sanofi Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
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
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
EP2760862B1 (en) 2011-09-27 2015-10-21 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013057944A1 (ja) 2011-10-19 2013-04-25 興和株式会社 新規なスピロインドリン化合物、及びそれを含有する医薬
CN119930479A (zh) * 2025-04-09 2025-05-06 安徽昊帆生物有限公司 牛磺酰胺盐酸盐的制备方法

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE783448A (fr) 1971-05-14 1972-11-13 Glaxo Lab Ltd Perfectionnements relatifs aux antibiotiques
GB1399089A (en) 1971-05-14 1975-06-25 Glaxo Lab Ltd Carboxylic acids and derivatives thereof
GB1445979A (en) 1972-10-25 1976-08-11 Glaxo Lab Ltd Cephalosporin derivatives
BE791214A (fr) 1972-05-08 1973-05-10 Glaxo Lab Ltd Procede de preparation d'isomeres de derives d'acide hydroxyiminoacetique etherifie purs
GB1446435A (en) * 1972-11-02 1976-08-18 Cooper Ltd Ethyl Lubricant additives
MX4573E (es) 1975-10-03 1982-06-18 Fujisawa Pharmaceutical Co Procedimiento microbiologico para la produccion de nocardicina c d e f y g
US4355172A (en) 1976-11-05 1982-10-19 Eli Lilly And Company Process for 4-(D-3-amino-3-carboxypropoxy)-phenylglyoxylic acid oxime derivatives
IT1110460B (it) 1977-03-02 1985-12-23 Ciba Geigy Ag Prodotti che favoriscono la crescita delle piante e prodotti che proteggono le piante a base di eteri di ossime e di esteri di ossime loro preparazione e loro impiego
CH632130A5 (en) 1977-03-02 1982-09-30 Ciba Geigy Ag Compositions on the basis of oxime ethers, oxime esters or oxime carbamates which are suitable in agriculture for crop protection
GR75487B (es) 1981-06-22 1984-07-23 Fujisawa Pharmaceutical Co
EP0137442A3 (de) 1983-10-08 1986-01-15 Hoechst Aktiengesellschaft Cephalosporinderivate und Verfahren zu ihrer Herstellung
GB2161476B (en) 1984-05-25 1988-01-27 Toyama Chemical Co Ltd 2-aminothiazolyl-2-methoxyimino acetamides and their use in preparing cephalosporins
EP0219923B1 (en) 1985-04-30 1992-09-02 Takeda Chemical Industries, Ltd. Antibiotic derivatives, their production and use
GB8617648D0 (en) 1986-07-18 1986-08-28 Ici Plc Fungicides
GB8905160D0 (en) 1989-03-07 1989-04-19 Beecham Group Plc Novel compounds
US5192770A (en) 1990-12-07 1993-03-09 Syntex (U.S.A.) Inc. Serotonergic alpha-oxoacetamides
FR2714059B1 (fr) * 1993-12-21 1996-03-08 Sanofi Elf Dérivés amino ramifiés du thiazole, leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent.
ES2099014B1 (es) 1994-03-22 1998-01-16 Univ Cordoba Nuevos eteres de oxima quirales derivados del limoneno, procedimiento para su preparacion y aplicaciones.
JPH10503171A (ja) * 1994-05-17 1998-03-24 ダウエランコ Ｎ−（５−イソチアゾリル）アミド有害生物防除剤
MX9705726A (es) * 1995-01-30 1997-11-29 Bayer Ag Amidas del acido alcoximinoacetico.
GB9602866D0 (en) * 1996-02-13 1996-04-10 Smithkline Beecham Plc Novel process
GB9823871D0 (en) * 1998-10-30 1998-12-23 Pharmacia & Upjohn Spa 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents
BR0013143A (pt) * 1999-08-12 2002-06-11 Pharmacia Italia Spa Derivados de 3 (5) amino pirazol, processo para sua preparação e uso dos mesmos como agentes antitumorais
ATE256102T1 (de) 1999-08-13 2003-12-15 Monsanto Technology Llc Oxim-amide und hydrazon-amide mit fungizider wirkung
WO2001025218A1 (en) 1999-10-01 2001-04-12 Japan Energy Corporation Novel quinazoline derivatives
EP1229026A4 (en) 1999-11-10 2003-09-24 Takeda Chemical Industries Ltd ALCOXYIMINOALKANOIC ACID DERIVATIVES
PE20010830A1 (es) * 2000-01-28 2001-09-06 Syngenta Ltd Derivados de azol insecticidas o fungicidas y composiciones que los comprenden
US6369232B1 (en) 2000-08-15 2002-04-09 Hoffmann-La Roche Inc. Tetrazolyl-phenyl acetamide glucokinase activators
WO2002059078A1 (en) 2001-01-23 2002-08-01 Sankyo Agro Company, Limited PROCESS FOR PRODUCING Z-α-ALKOXYIMINOPHENYLACETIC ACID DERIVATIVE
ES2197001B1 (es) * 2002-03-26 2004-11-16 Laboratorios Vita, S.A. Procedimiento de obtencion de un compuesto farmaceuticamente activo.
EA011297B1 (ru) 2002-04-26 2009-02-27 Ф. Хоффманн-Ля Рош Аг Замещённые фенилацетамиды и их применение в качестве активаторов глюкокиназы
WO2004058724A1 (ja) 2002-12-25 2004-07-15 Sumitomo Chemical Company, Limited フェニルピラゾール化合物及びそれを用いた植物病害の防除方法
EP1594863A1 (en) * 2003-02-11 2005-11-16 Prosidion Limited Tri(cyclo) substituted amide glucokinase activator compounds
PL378117A1 (pl) 2003-02-11 2006-03-06 Prosidion Limited Tricyklopodstawione związki amidowe
WO2004111044A1 (en) * 2003-06-17 2004-12-23 Glenmark Pharmaceuticals Ltd. Tricyclic compounds useful for the treatment of inflammatory and allergic disorders:process for their preparation
WO2005023761A2 (en) * 2003-09-11 2005-03-17 Kemia, Inc. Cytokine inhibitors
JP2007126358A (ja) 2004-01-20 2007-05-24 Fujiyakuhin Co Ltd フェニルアラニン誘導体
WO2007007886A1 (en) * 2005-07-11 2007-01-18 Mitsubishi Tanabe Pharma Corporation An oxime derivative and preparations thereof
US7902248B2 (en) 2006-12-14 2011-03-08 Hoffmann-La Roche Inc. Oxime glucokinase activators

Also Published As

Publication number Publication date
AU2006267387B2 (en) 2010-11-18
IL188258A0 (en) 2008-08-07
CN101218237A (zh) 2008-07-09
AU2006267387A1 (en) 2007-01-18
KR20080016736A (ko) 2008-02-21
EP1907387A1 (en) 2008-04-09
BRPI0613451A2 (pt) 2011-01-11
CA2613303C (en) 2012-06-19
US20080132479A1 (en) 2008-06-05
RU2420525C2 (ru) 2011-06-10
NO20080717L (no) 2008-04-09
WO2007007886A1 (en) 2007-01-18
KR100965040B1 (ko) 2010-06-21
JP4033409B1 (ja) 2008-01-16
MX2008000560A (es) 2008-03-10
RU2008104919A (ru) 2009-08-20
TW200732333A (en) 2007-09-01
JP2008510735A (ja) 2008-04-10
CA2613303A1 (en) 2007-01-18
NZ564743A (en) 2010-03-26
US8119626B2 (en) 2012-02-21
US20090291936A1 (en) 2009-11-26
TWI359149B (en) 2012-03-01
US7514439B2 (en) 2009-04-07
CN101218237B (zh) 2012-03-28

Similar Documents

Publication Publication Date Title
AR057661A1 (es) Un derivado de oxima y sus preparaciones
NO20080391L (no) Pyrazolbaserte LXR modulatorer
PE20071001A1 (es) Derivados de 1-(azolin-2-il)-amino-1-fenil-2-hetaril-etano con actividad pesticida
PE20091573A1 (es) Derivados heterociclicos de urea como inhibidores de adn girasa y/o topoisomerasa
PE20121127A1 (es) Derivados de piridina y pirazina como moduladores de cinasa de proteina
PE20090641A1 (es) Amidas heterociclicas
PE20120620A1 (es) Dihidropirazolonas sustituidas como inhibidores de hif-propil-4-hidroxilasas
PE20060691A1 (es) Serinamidas sustituidas por benzoilo
AR058587A1 (es) Compuestos de pirrolo-1,5-naftiridinona,su uso como agentes antibacterianos, composiciones farmaceuticas que los contienen y compuestos intermediarios para preparar dichos compuestos
NO20063599L (no) Ytterligere heterosykliske forbindelser og deres anvendelse som metabotrofiske glutamatreseptorantagonister
PE20091842A1 (es) Pirrolidinonas como activadores de glucoquinasa
AR080233A1 (es) Derivados de dihidrofurano como compuestos insecticidas
NO341631B1 (no) Hydroksybenzamidderivater og deres anvendelse, fremgangsmåte for fremstilling og farmasøytiske sammensetninger
PE20090601A1 (es) Derivados de piridin-il-oxi-piridinas como inhibidores de alk5
PE20070112A1 (es) Mimeticos de glucocorticoides, metodos para su fabricacion, composiciones farmaceuticas y usos de los mismos
AR064490A1 (es) Ciano-benzanilidas sustituidas, intermediarios para su preparacion, una composicion pesticida que las comprende y su utilizacion en un metodo para combatir plagas.
EA200701121A1 (ru) Потенциаторы рецепторов глутамата
NO20081001L (no) Derivater av karboksamid som antagonister for muskarinisk reseptor
PE20061106A1 (es) Derivados de 2-(4-oxo-4h-quinazolin-3-il)acetamida
IL195877A0 (en) Pest control agent containing novel pyridyl-methanamine derivative or salt thereof
AR068115A1 (es) Derivado del acido pirazolcarboxilico metodo de produccion del mismo y fungicida
PE20142282A1 (es) Nuevos derivados de aril-quinolina
PE20140968A1 (es) Derivados de benzamida sustituida
PE20051054A1 (es) Compuestos heterociclicos utiles como secretagogos de la hormona de crecimiento
PE20141000A1 (es) Ureas asimetricas y usos medicos de las mismas

Legal Events

Date Code Title Description
FA Abandonment or withdrawal