YU57802A - Substituisani 3-fenil-5-alkoksi-1,3,4-oksidiazol-2-oni i njihova primena za inhibiranje hormon-senzitivne lipaze - Google Patents

Substituisani 3-fenil-5-alkoksi-1,3,4-oksidiazol-2-oni i njihova primena za inhibiranje hormon-senzitivne lipaze

Info

Publication number
YU57802A
YU57802A YU57802A YUP57802A YU57802A YU 57802 A YU57802 A YU 57802A YU 57802 A YU57802 A YU 57802A YU P57802 A YUP57802 A YU P57802A YU 57802 A YU57802 A YU 57802A
Authority
YU
Yugoslavia
Prior art keywords
substituted
alkyl
aryl
cycloalkyl
hydrogen
Prior art date
Application number
YU57802A
Other languages
English (en)
Inventor
Karl Schoenafinger
Stefan Petry
Guenter Mueller
Karl-Heinz Baringhaus
Original Assignee
Aventis Pharma Deutschland Gmbh.
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
Priority claimed from DE2000110968 external-priority patent/DE10010968A1/de
Priority claimed from DE2001102265 external-priority patent/DE10102265C1/de
Application filed by Aventis Pharma Deutschland Gmbh. filed Critical Aventis Pharma Deutschland Gmbh.
Publication of YU57802A publication Critical patent/YU57802A/sh

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/101,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
    • C07D271/1131,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • 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
    • A61P1/18Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/10Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

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)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Enzymes And Modification Thereof (AREA)

Abstract

Pronalazak se odnosi na supstituisane 3-fenil-5-alkoksi-1,3,4-oksidiazol-2-one Formule 1, pri tome R1 oznacava supstituisani C1-C6alkil i C3-C9-cikloalkil, R2 R3, R4 i R5 oznacavaju vodonik, halogen, nitro,. C1-C4alkil, C1-C9alkoksi, supstituisani C6-C10aril- C1-C4-alkoksi, C6-C10ariloksi, C6-C10aril, C3-C8cikloalkil ili O-C3-C9-cikloalkil, ili 2-oks-pirolidin-1-il, 2,5-dimetilpirol-1-il ili NR6-A-R7, sa izuzetkom da R2, R3, R4 i R5 ne mogu istovremeno da oznacavaju vodonik i da najmanje jedan od ostataka R2, R3, R4 ili R5 stoje umesto ostatka 2-okso-pirolidin-1-il, 2,5-dimetilpirol-1-il ili NR6-A-R7, sa R6 = vodonik, C1-C4-alkil, ili supstituisani C8-C10-aril-C1-C4-alkil, A=jedna obicna veza, COn, SOn li CONH, N = 1 ili 2, R7 = vodonik, supstituisani C1-C18-alkenil, C2-C18-alkenil, C8-C10-aril-C1-C4-alkil, C5-C8-cikloalkil-C1-C4-alkil, C5-C8-cikloalkil, C6-C10-aril-C2-C6alkenil, C6-C10-aril, difenil, difenil-C1C4-alkil, indanil, ili grupa het.(CH2)r-, sa r=0, 1, 2 ili 3 i het = zasiceni ili nezasiceni 5-7 clani heterocikl, koji moze da bude spojen sa benzolom i da bude supstituisan, isto tako na postupak za njihovu proizvodnju. Ova jedinjenja pokazuju inhibirajuce dejstvo na hormon-senzitivnu lipazu, HSL.
YU57802A 2000-03-07 2001-02-20 Substituisani 3-fenil-5-alkoksi-1,3,4-oksidiazol-2-oni i njihova primena za inhibiranje hormon-senzitivne lipaze YU57802A (sh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2000110968 DE10010968A1 (de) 2000-03-07 2000-03-07 Substituierte 3-Phenyl-5-alkoxi-1,3,4-oxdiazol-2-one, ihre Herstellung und Verwendung in Arzneistoffen
DE2001102265 DE10102265C1 (de) 2001-01-18 2001-01-18 Substituierte 3-Phenyl-5-alkoxi-1,3,4-oxdiazol-2-one, ihre Herstellung und Verwendung in Arzneistoffen

Publications (1)

Publication Number Publication Date
YU57802A true YU57802A (sh) 2005-07-19

Family

ID=26004720

Family Applications (1)

Application Number Title Priority Date Filing Date
YU57802A YU57802A (sh) 2000-03-07 2001-02-20 Substituisani 3-fenil-5-alkoksi-1,3,4-oksidiazol-2-oni i njihova primena za inhibiranje hormon-senzitivne lipaze

Country Status (28)

Country Link
US (1) US6369088B2 (sh)
EP (1) EP1263745B1 (sh)
JP (1) JP2003525931A (sh)
KR (1) KR100790763B1 (sh)
CN (1) CN1261419C (sh)
AR (1) AR027611A1 (sh)
AT (1) ATE267184T1 (sh)
AU (1) AU784827B2 (sh)
BR (1) BR0108974A (sh)
CA (1) CA2401953A1 (sh)
DE (1) DE50102325D1 (sh)
DK (1) DK1263745T3 (sh)
EE (1) EE04877B1 (sh)
ES (1) ES2218383T3 (sh)
HK (1) HK1054036B (sh)
HR (1) HRP20020732A2 (sh)
HU (1) HUP0302772A3 (sh)
IL (1) IL151518A (sh)
MX (1) MXPA02008038A (sh)
NO (1) NO323483B1 (sh)
NZ (1) NZ521207A (sh)
PL (1) PL359702A1 (sh)
PT (1) PT1263745E (sh)
RU (1) RU2281283C2 (sh)
SK (1) SK12752002A3 (sh)
TR (1) TR200401217T4 (sh)
WO (1) WO2001066531A1 (sh)
YU (1) YU57802A (sh)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
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US6087350A (en) * 1997-08-29 2000-07-11 University Of Pittsburgh Of The Commonwealth System Of Higher Education Use of pretreatment chemicals to enhance efficacy of cytotoxic agents
US6900233B2 (en) 2002-02-28 2005-05-31 Aventis Pharma Deutschland Gmbh Substituted 3-phenyl-5-alkoxy-3H-(1,3,4)-oxadiazol-2-ones, pharmaceutical composition and method for treating obesity thereof
DE10208987A1 (de) * 2002-02-28 2003-09-11 Aventis Pharma Gmbh Substituierte 3-Phenyl-5-alkoxi-1,3,4-oxidiazol-2-one, ihre Herstellung und Verwendung in Arzneistoffen
DE10208986A1 (de) * 2002-02-28 2003-09-11 Aventis Pharma Gmbh Verwendung substituierter 3-Phenyl-5-alkoxi-1,3,4-oxdiazol-2-one zur Herstellung von Arzneimitteln mit hemmender Wirkung an der pankreatischen Lipase
US20030236288A1 (en) * 2002-02-28 2003-12-25 Karl Schoenafinger Use of substituted 3-phenyl-5-alkoxy-3H-(1,3,4)-oxadizol-2-ones for inhibiting pancreatic lipase
SE0203753D0 (sv) * 2002-12-17 2002-12-17 Astrazeneca Ab New compounds
SE0203754D0 (sv) * 2002-12-17 2002-12-17 Astrazeneca Ab New compounds
US20090082435A1 (en) * 2005-04-28 2009-03-26 The Regents Of The University Of California Methods, Compositions, And Compounds For Modulation Of Monoacylglycerol Lipase, Pain, And Stress-Related Disorders
CN101225085B (zh) * 2007-01-17 2011-09-21 天津天士力集团有限公司 苯基呋咱氮类一氧化氮供体型2-苯胺嘧啶衍生物、其制备方法、含有该化合物的组合物及其用途
TW201033163A (en) * 2008-10-20 2010-09-16 Sumitomo Chemical Co Method for manufacturing oxadiazolinone compound and intermediate thereof
TW201028406A (en) 2008-12-23 2010-08-01 Bial Portela & Ca Sa 5-O-substituted 3-N-aryl-1,3,4-oxadiazolones for medical use
WO2011108724A1 (ja) 2010-03-04 2011-09-09 味の素株式会社 糖尿病又は肥満症の予防又は治療剤
US8501768B2 (en) * 2011-05-17 2013-08-06 Hoffmann-La Roche Inc. Hexahydrocyclopentapyrrolone, hexahydropyrrolopyrrolone, octahydropyrrolopyridinone and octahydropyridinone compounds
JP6007417B2 (ja) * 2011-05-31 2016-10-12 レセプトス エルエルシー 新規glp−1受容体安定剤および調節剤
AU2012352349B2 (en) 2011-12-12 2017-08-17 Receptos Llc Carboxylic acid derivatives comprising four cycles acting as GLP-1 receptor modulators for therapy of diseases such as diabetes
KR102271179B1 (ko) 2013-06-11 2021-07-01 셀진 인터내셔널 Ii 에스에이알엘 신규의 glp-1 수용체 조절제
UA119247C2 (uk) 2013-09-06 2019-05-27 РОЙВЕНТ САЙЕНСИЗ ҐмбГ Спіроциклічні сполуки як інгібітори триптофангідроксилази
WO2015089137A1 (en) 2013-12-11 2015-06-18 Karos Pharmaceuticals, Inc. Acylguanidines as tryptophan hydroxylase inhibitors
MX2017000972A (es) 2014-07-25 2017-07-27 Celgene Int Ii Sarl Nuevos moduladores del receptor de peptido similar a glucagon 1 (glp-1).
WO2016094729A1 (en) 2014-12-10 2016-06-16 Celgene International Ii Sarl Glp-1 receptor modulators
WO2016109501A1 (en) 2014-12-30 2016-07-07 Karos Pharmaceuticals, Inc. Amide compounds as tryptophan hydroxylase inhibitors
US9611201B2 (en) 2015-03-05 2017-04-04 Karos Pharmaceuticals, Inc. Processes for preparing (R)-1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanol and 1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanone
CN108863774A (zh) * 2018-06-09 2018-11-23 石家庄市绿丰化工有限公司 一种2,4-二氯苯乙酰氯合成的方法
CN113227093A (zh) 2018-11-14 2021-08-06 阿尔塔万特科学公司 结晶螺环化合物、包含该化合物的剂型、用于疾病治疗的方法和再结晶方法

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FR2299328A1 (fr) 1975-02-03 1976-08-27 Rhone Poulenc Ind Derives de l'alcoyloxy-5 phenyl-3 oxyde azo
US4076824A (en) 1975-02-03 1978-02-28 Rhone-Poulenc Industries Anthelmintic oxadiazolinone derivatives
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US5641796A (en) * 1994-11-01 1997-06-24 Eli Lilly And Company Oral hypoglycemic agents

Also Published As

Publication number Publication date
PT1263745E (pt) 2004-09-30
NO20024201D0 (no) 2002-09-03
MXPA02008038A (es) 2004-04-05
WO2001066531A1 (de) 2001-09-13
TR200401217T4 (tr) 2004-06-21
CN1416424A (zh) 2003-05-07
RU2281283C2 (ru) 2006-08-10
JP2003525931A (ja) 2003-09-02
AU784827B2 (en) 2006-06-29
BR0108974A (pt) 2003-06-03
ATE267184T1 (de) 2004-06-15
KR100790763B1 (ko) 2008-01-03
CN1261419C (zh) 2006-06-28
AR027611A1 (es) 2003-04-02
AU3378701A (en) 2001-09-17
EP1263745B1 (de) 2004-05-19
IL151518A0 (en) 2003-04-10
DE50102325D1 (de) 2004-06-24
NO20024201L (no) 2002-09-03
US20010031772A1 (en) 2001-10-18
HUP0302772A2 (hu) 2003-11-28
SK12752002A3 (sk) 2003-04-01
PL359702A1 (en) 2004-09-06
IL151518A (en) 2008-06-05
EP1263745A1 (de) 2002-12-11
US6369088B2 (en) 2002-04-09
NZ521207A (en) 2005-04-29
KR20020079986A (ko) 2002-10-21
HK1054036A1 (en) 2003-11-14
NO323483B1 (no) 2007-05-21
WO2001066531A8 (de) 2002-07-25
ES2218383T3 (es) 2004-11-16
HRP20020732A2 (en) 2004-12-31
EE04877B1 (et) 2007-08-15
CA2401953A1 (en) 2001-09-13
EE200200498A (et) 2004-02-16
HUP0302772A3 (en) 2007-03-28
HK1054036B (zh) 2006-11-17
DK1263745T3 (da) 2004-08-16

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