TNSN05105A1 - Novel bicyclic inhibitors of hormone sensitive lipase - Google Patents

Novel bicyclic inhibitors of hormone sensitive lipase

Info

Publication number
TNSN05105A1
TNSN05105A1 TNP2005000105A TNSN05105A TNSN05105A1 TN SN05105 A1 TNSN05105 A1 TN SN05105A1 TN P2005000105 A TNP2005000105 A TN P2005000105A TN SN05105 A TNSN05105 A TN SN05105A TN SN05105 A1 TNSN05105 A1 TN SN05105A1
Authority
TN
Tunisia
Prior art keywords
sensitive lipase
hormone sensitive
novel bicyclic
bicyclic inhibitors
inhibitors
Prior art date
Application number
TNP2005000105A
Inventor
Stefan Petry
Karl-Heinz Baringhaus
Norbert Tennagels
Guenter Mueller
Hubert Heuer
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
Application filed by Aventis Pharma Deutschland Gmbh filed Critical Aventis Pharma Deutschland Gmbh
Publication of TNSN05105A1 publication Critical patent/TNSN05105A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/16Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • C07D249/18Benzotriazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/06Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10Spiro-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

THE INVENTION RELATES TO BENZOTRIAZOLES OF GENERAL FORMULA (I), WHEREIN R1 - R8 HAVE THE ABOVE MENTIONED MEANINGS. THE INVENTION ALSO RELATES TO A METHOD FOR THE PRODUCTION THEREOF. SAID COMPOUNDS HAVE AN INHIBITING EFFECT ON THE HORMONE SENSITIVE LIPASE.
TNP2005000105A 2002-10-12 2005-04-11 Novel bicyclic inhibitors of hormone sensitive lipase TNSN05105A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10247680A DE10247680B4 (en) 2002-10-12 2002-10-12 New bicyclic inhibitors of the hormone sensitive lipase
PCT/EP2003/010765 WO2004035550A1 (en) 2002-10-12 2003-09-27 Novel bicyclic inhibitors of hormone sensitive lipase

Publications (1)

Publication Number Publication Date
TNSN05105A1 true TNSN05105A1 (en) 2007-05-14

Family

ID=32038583

Family Applications (1)

Application Number Title Priority Date Filing Date
TNP2005000105A TNSN05105A1 (en) 2002-10-12 2005-04-11 Novel bicyclic inhibitors of hormone sensitive lipase

Country Status (39)

Country Link
EP (1) EP1554259B1 (en)
JP (2) JP4658607B2 (en)
KR (1) KR20050059254A (en)
CN (1) CN100366616C (en)
AR (1) AR041565A1 (en)
AT (1) ATE349433T1 (en)
AU (1) AU2003275997B8 (en)
BR (1) BR0315257A (en)
CA (1) CA2501734C (en)
CR (1) CR7717A (en)
CY (1) CY1106358T1 (en)
DE (2) DE10247680B4 (en)
DK (1) DK1554259T3 (en)
EC (1) ECSP055729A (en)
ES (1) ES2277152T3 (en)
GT (1) GT200300214A (en)
HK (1) HK1080473A1 (en)
HN (1) HN2003000316A (en)
HR (1) HRP20050325A2 (en)
IL (1) IL167907A (en)
JO (1) JO2497B1 (en)
MA (1) MA27404A1 (en)
MX (1) MXPA05003359A (en)
MY (1) MY138057A (en)
NO (1) NO20052291L (en)
OA (1) OA12941A (en)
PA (1) PA8585101A1 (en)
PE (1) PE20040776A1 (en)
PL (1) PL374605A1 (en)
PT (1) PT1554259E (en)
RS (1) RS51543B (en)
RU (1) RU2325385C2 (en)
SV (1) SV2004001633A (en)
TN (1) TNSN05105A1 (en)
TW (1) TWI313265B (en)
UA (1) UA79994C2 (en)
UY (1) UY28015A1 (en)
WO (1) WO2004035550A1 (en)
ZA (1) ZA200501757B (en)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102005002130A1 (en) 2005-01-17 2006-07-27 Sanofi-Aventis Deutschland Gmbh New substituted aminomethylene sulfonamides useful as hormone sensitive lipase inhibitors in medicaments for treatment and/or prevention of non-insulin dependent diabetes mellitus, diabetic syndrome or obesity
DE102005026808A1 (en) 2005-06-09 2006-12-14 Sanofi-Aventis Deutschland Gmbh Benzooxazol-2-one derivatives as inhibitors of lipases and phospholipases
DE102005026809A1 (en) * 2005-06-09 2006-12-14 Sanofi-Aventis Deutschland Gmbh Benzothiazol-2-one derivatives as inhibitors of lipases and phospholipases
DE102005026762A1 (en) 2005-06-09 2006-12-21 Sanofi-Aventis Deutschland Gmbh Azolopyridin-2-one derivatives as inhibitors of lipases and phospholipases
DE102005048897A1 (en) * 2005-10-12 2007-04-19 Sanofi-Aventis Deutschland Gmbh Diacylindazole derivatives as inhibitors of lipases and phospholipases
DE102005049953A1 (en) 2005-10-19 2007-04-26 Sanofi-Aventis Deutschland Gmbh Carbamoylbenzotriazole derivatives as inhibitors of lipases and phospholipases
DE102005049954A1 (en) 2005-10-19 2007-05-31 Sanofi-Aventis Deutschland Gmbh Triazolopyridine derivatives as inhibitors of lipases and phospholipases
FR2915199B1 (en) * 2007-04-18 2010-01-22 Sanofi Aventis TRIAZOLOPYRIDINE-CARBOXAMIDE AND TRIAZOLOPYRIMIDINE-CARBOXAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE.
FR2915198B1 (en) 2007-04-18 2009-12-18 Sanofi Aventis TRIAZOLOPYRIDINE CARBOXAMIDE AND TRIAZOLOPYRIDINE -CARBOXAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE.
FR2915197B1 (en) * 2007-04-18 2009-06-12 Sanofi Aventis Sa TRIAZOLOPYRIDINE CARBOXAMIDE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF.
AR072707A1 (en) 2008-07-09 2010-09-15 Sanofi Aventis HETEROCICLIC COMPOUNDS, PROCESSES FOR THEIR PREPARATION, DRUGS THAT UNDERSTAND THESE COMPOUNDS AND THE USE OF THEM
TWI469979B (en) * 2008-12-24 2015-01-21 Bial Portela & Ca Sa Faah inhibitor, and pharmaceutical composition and use thereof
US8329904B2 (en) * 2009-05-12 2012-12-11 Hoffmann-La Roche Inc. Azacyclic derivatives
US8440710B2 (en) * 2009-10-15 2013-05-14 Hoffmann-La Roche Inc. HSL inhibitors useful in the treatment of diabetes
US8097634B2 (en) 2010-04-15 2012-01-17 Hoffmann-La Roche Inc. Azacyclic derivatives
WO2011140296A1 (en) * 2010-05-05 2011-11-10 Infinity Pharmaceuticals Triazoles as inhibitors of fatty acid synthase
US8722721B2 (en) * 2011-03-16 2014-05-13 Hoffmann-La Roche Inc. SEC-hydroxycyclohexyl derivatives
US8703807B2 (en) * 2011-03-17 2014-04-22 Hoffmann-La Roche Inc. Azaspirodecanone compounds
US8809384B2 (en) 2011-03-25 2014-08-19 Hoffmann-La Roche Inc. Azaspirodecanone compounds
UA119247C2 (en) 2013-09-06 2019-05-27 РОЙВЕНТ САЙЕНСИЗ ҐмбГ Spirocyclic compounds as tryptophan hydroxylase inhibitors
GB201321740D0 (en) * 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
WO2015089137A1 (en) 2013-12-11 2015-06-18 Karos Pharmaceuticals, Inc. Acylguanidines as tryptophan hydroxylase inhibitors
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
CN113227093A (en) 2018-11-14 2021-08-06 阿尔塔万特科学公司 Crystalline spiro compounds, dosage forms comprising the compounds, methods for treatment of disease, and methods of recrystallization

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1124716A (en) * 1978-10-20 1982-06-01 Michael J. Simons Blocked benzotriazole compounds as development restrainer precursors
DE19942354A1 (en) * 1999-09-04 2001-03-08 Aventis Pharma Gmbh Substituted 3-phenyl-5-alkoxi-1,3,4-oxdiazol-2-one, their manufacture and use in medicinal products
AR033306A1 (en) * 2001-05-05 2003-12-10 Smithkline Beecham Plc COMPOUNDS
KR20040068240A (en) * 2001-12-14 2004-07-30 노보 노르디스크 에이/에스 Compounds and uses thereof for decreasing activity of hormone-sensitive lipase

Also Published As

Publication number Publication date
CN1688555A (en) 2005-10-26
IL167907A (en) 2010-12-30
ZA200501757B (en) 2005-09-07
JP2011026342A (en) 2011-02-10
BR0315257A (en) 2005-08-23
OA12941A (en) 2006-10-13
CA2501734C (en) 2011-05-31
UY28015A1 (en) 2004-04-30
ATE349433T1 (en) 2007-01-15
CR7717A (en) 2007-09-14
RU2005114394A (en) 2006-01-20
CA2501734A1 (en) 2004-04-29
AU2003275997B2 (en) 2010-03-25
JP2006509734A (en) 2006-03-23
MXPA05003359A (en) 2005-06-22
PL374605A1 (en) 2005-10-31
AU2003275997B8 (en) 2010-09-30
DE10247680B4 (en) 2005-09-01
CN100366616C (en) 2008-02-06
NO20052291D0 (en) 2005-05-10
WO2004035550A1 (en) 2004-04-29
JO2497B1 (en) 2009-10-05
RS51543B (en) 2011-06-30
EP1554259B1 (en) 2006-12-27
KR20050059254A (en) 2005-06-17
NO20052291L (en) 2005-05-10
DK1554259T3 (en) 2007-05-07
ES2277152T3 (en) 2007-07-01
DE10247680A1 (en) 2004-04-22
RU2325385C2 (en) 2008-05-27
HRP20050325A2 (en) 2005-06-30
MY138057A (en) 2009-04-30
HN2003000316A (en) 2006-06-12
DE50306134D1 (en) 2007-02-08
PA8585101A1 (en) 2004-09-16
AU2003275997A1 (en) 2004-05-04
MA27404A1 (en) 2005-06-01
TWI313265B (en) 2009-08-11
ECSP055729A (en) 2005-07-06
JP4658607B2 (en) 2011-03-23
TW200413335A (en) 2004-08-01
AR041565A1 (en) 2005-05-18
RS20050207A (en) 2007-08-03
EP1554259A1 (en) 2005-07-20
PE20040776A1 (en) 2004-12-24
CY1106358T1 (en) 2011-10-12
SV2004001633A (en) 2004-03-19
PT1554259E (en) 2007-02-28
HK1080473A1 (en) 2006-04-28
UA79994C2 (en) 2007-08-10
GT200300214A (en) 2007-02-05

Similar Documents

Publication Publication Date Title
TNSN05105A1 (en) Novel bicyclic inhibitors of hormone sensitive lipase
MXPA04008613A (en) New compounds.
PL372799A1 (en) New compounds
SG152239A1 (en) Compounds for proteasome enzyme inhibition
TW200512191A (en) Methods and compounds producing dipeptidyl peptidase iv inhibitors and intermediates thereof
YU5503A (en) Non-steroidal inflammation inhibitors
HK1099235A1 (en) Phosphonate analogs of hiv integrase inhibitor compounds hiv
TW200604184A (en) Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors
TW200616646A (en) Synthesis of boronic ester and acid compounds
MXPA04007396A (en) Process for the manufacture of hmg-coa reductase inhibitors.
MX341849B (en) Spirocyclic nitriles as protease inhibitors.
MY138618A (en) process for the manufacture of valsartan
TW200619205A (en) A method for preparing irbesartan and intermediates thereof
ZA200404752B (en) 6-aminomorphinane derivatives method for the production and use thereof
RS20060297A (en) Rearranged pentanols, a method for the production thereof, and their use as antiphlogistics
YU61103A (en) Processes for the production of substituted 2- (2-pyridylmethyl)sulfinyl-1h-benzimidazoles
GB0401201D0 (en) Cell culture method for obtaining prostate-like acini
WO2004032908A3 (en) Method of inhibiting angiogenesis
WO2004030664A3 (en) New compounds for the inhibition of undesired cell proliferation and use thereof
GB0327323D0 (en) Novel pharmaceuticals
GB0215392D0 (en) Chemical compounds
AU2003221867A1 (en) Method for inhibiting corrosion by post-dip of coated parts
RS20050563A (en) Acylaminothiazole derivatives, preparation method thereof and use of same as beta-amyloid peptide production inhibitors
IL168110A0 (en) Process for production of an acetylenic compound
MXPA05004262A (en) Process for making pyrazole compounds.