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YU19099A - Supstituisani tricikli - Google Patents

Supstituisani tricikli

Info

Publication number
YU19099A
YU19099A YU19099A YU19099A YU19099A YU 19099 A YU19099 A YU 19099A YU 19099 A YU19099 A YU 19099A YU 19099 A YU19099 A YU 19099A YU 19099 A YU19099 A YU 19099A
Authority
YU
Yugoslavia
Prior art keywords
group
nitrogen
sulfur
hydrogen
carbon
Prior art date
Application number
YU19099A
Other languages
English (en)
Inventor
Nicholas James Bach
Jolie Anne Bastian
Douglas Wade Beight
Michael John Martinelli
Edward David Mihelich
John Michael Morin
Daniel Jon Sall
Jason Scott Sawyer
Edward C.R. Smith
Tulio Suarez
Qiuping Wang
Thomas Michael Wilson
Michael Dean Kinnick
Original Assignee
Eli Lilly And Company
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 Eli Lilly And Company filed Critical Eli Lilly And Company
Publication of YU19099A publication Critical patent/YU19099A/sh

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56Ring systems containing three or more rings
    • C07D209/58[b]- or [c]-condensed
    • C07D209/70[b]- or [c]-condensed containing carbocyclic rings other than six-membered
    • 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic 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
    • C07D513/02Heterocyclic 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
    • C07D513/04Ortho-condensed systems

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)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Hematology (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Ovaj pronalazak se odnosi na nova supstituisana triciklicna jedinjenja koja su pogodna za inhibiranje sPLA2 posredno oslobodjenog iz masnih kiselina u uslovima kao sto je septicni sok, i koja se mogu predstaviti opstom formulom I: A je fenil ili piridin, gde je azot u polozaju 5-, 6-, 7- ili 8; jedan od B ili D je azot i drugi je ugljenik; Z-cikloheksenil ili fenil, piridil, pri cemu azot je u polozaju 1-, 2- ili 3-, ili 6-clani heterociklicni prsten sa jednim heteroatomom izabranim iz grupe koju cine sumpor ili kiseonik u polozaju 1-, 2-, ili 3- i azot u polozaju 1-, 2-, 3-, ili 4-; ---- je dvostruka ili jednostruka veza; R20 se bira iz grupa (a), (b) i (c) gde je: (a) -(C5-C20) alkil, -(C5-C20) alkenil, -(C5-C20) alkinil, karbociklicni radikali, ili heterociklicni radikali, ili (b) clan od (a) supstituisan sa jednim ili vise nezavisno izabranih ne-interreagujucih substituenata; ili (c) je grupa -(L)-R80; gde, (L)-je dvovalentna vezujuca grupa od 1 ili 12 atoma izabranih od ugljenika, vodonika, kiseonika, azota, ili sumpora; gde je kombinacija atoma u -(L) izabrana iz grupe koja se sastoji od (i) ugljenika i vodonika jedino, (ii) samo jednog sumpora, (iii) samo jednog kiseonika, (iv) jedino od jednog ili dva azota i vodonika, (v) samo od ugljenika, vodonika, i jednog sumpora, i (vi) samo od ugljenika, vodonika i kiseonika; i gde je R80 je grupa izabrana iz (a) ili (b); R21 je ne-interreagujucih substituenata gde je f od 1-3; R1 je -NHNH2, -NH2, ili -CONH2; R2 se bira iz grupa koje sadrze -OH, i -O(CH2)tR5 gde R5 je H, -CH, -NH2, -CONH2, -CONR9R10 - NHSO2R15, -CONHSO2R15 gde R15 cini -(C1-C6) alkil ili -CF3; fenil ili fenil supstituisan sa -CO2H ili -CO2(C1-C4) alkil; i-(La)-kisela grupa, gde je -(La)- je kiseli veznik koji ima duzinu kiselog veznog dela od 1 do 7 i t je 1-5. R3 se bira od ne-interagujucih substituenata, karbociklicnih radikala, i heterociklicnih radikala substituisanih sa ne-interagujucim substituentima; ili farmaceutski prihvatljivih racemata, solvata, tautomera, optickih izomera, prolekovitih derivata ili njihovih soli; pod uslovom da jedan od A ili Z je heterociklicni prsten i kada D je azot, hetero atom u Z se bira iz grupe koju cine sumpor ili kiseonik u polozaju 1-, 2-, ili 3-, i azot u polozaju 1-, 2-, 3-, ili 4-.
YU19099A 1998-04-17 1999-04-16 Supstituisani tricikli YU19099A (sh)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US6216598A 1998-04-17 1998-04-17

Publications (1)

Publication Number Publication Date
YU19099A true YU19099A (sh) 2001-09-28

Family

ID=22040624

Family Applications (1)

Application Number Title Priority Date Filing Date
YU19099A YU19099A (sh) 1998-04-17 1999-04-16 Supstituisani tricikli

Country Status (27)

Country Link
EP (2) EP0950661B1 (sh)
JP (1) JP4435325B2 (sh)
KR (1) KR19990083234A (sh)
CN (1) CN1235968A (sh)
AR (1) AR018185A1 (sh)
AT (2) ATE259818T1 (sh)
AU (1) AU757454B2 (sh)
BR (1) BR9901275A (sh)
CA (1) CA2269256A1 (sh)
CO (1) CO5080728A1 (sh)
CZ (1) CZ137199A3 (sh)
DE (2) DE69914951T2 (sh)
EA (1) EA003129B1 (sh)
ES (2) ES2213668T3 (sh)
HU (1) HUP9901219A1 (sh)
ID (1) ID23219A (sh)
IL (1) IL129484A0 (sh)
NO (1) NO991823L (sh)
NZ (1) NZ335252A (sh)
PE (1) PE20000472A1 (sh)
PL (1) PL332564A1 (sh)
SG (1) SG106035A1 (sh)
SV (1) SV1999000052A (sh)
TR (1) TR199900842A2 (sh)
TW (1) TW555760B (sh)
YU (1) YU19099A (sh)
ZA (1) ZA992773B (sh)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6610728B2 (en) * 1997-08-28 2003-08-26 Eli Lilly And Company Method for treatment of non-rheumatoid arthritis
AU2001244635A1 (en) * 2000-03-30 2001-10-15 Yamanouchi Pharmaceutical Co..Ltd. Hydrazide derivatives
CA2413582A1 (en) * 2000-07-14 2002-01-24 Eli Lilly And Company Use of a spla2 inhibitor for the treatment of sepsis
AU2002239264A1 (en) * 2000-12-18 2002-07-01 Eli Lilly And Company Tetracyclic derivatives as spla2 inhibitors
ATE353876T1 (de) * 2001-03-28 2007-03-15 Lilly Co Eli Substituierte carbazole als inhibitoren von spla2
ATE312817T1 (de) * 2001-08-09 2005-12-15 Lilly Co Eli Cyclohept'bö indolderivate als spla2-inhibitoren
JP2005527464A (ja) 2001-08-09 2005-09-15 イーライ・リリー・アンド・カンパニー sPLA2インヒビターとしてのシクロヘプタBインドール誘導体
US6992100B2 (en) 2001-12-06 2006-01-31 Eli Lilly And Company sPLA2 inhibitors
EP1807427A2 (en) 2004-11-01 2007-07-18 Wyeth Substituted indolizines and derivatives as cns agents
BRPI0907122B8 (pt) 2008-01-11 2021-05-25 Albany Molecular Res Inc compostos de piridoindóis (1-azinona) substituídos, composição farmacêutica compreendendo os referidos compostos, e usos dos mesmos
WO2011003021A1 (en) 2009-07-01 2011-01-06 Albany Molecular Research, Inc. Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof
US8993765B2 (en) 2010-12-21 2015-03-31 Albany Molecular Research, Inc. Tetrahydro-azacarboline MCH-1 antagonists, methods of making, and uses thereof
SG193902A1 (en) * 2011-04-14 2013-11-29 Actelion Pharmaceuticals Ltd 7-(heteroaryl-amino)-6,7,8,9-tetrahydropyrido[1,2-a]indol acetic acid derivatives and their use as prostaglandin d2 receptor modulators
EA026431B1 (ru) 2012-03-16 2017-04-28 Вайтаи Фармасьютиклз, Инк. Модуляторы x рецепторов печени
JP6114814B2 (ja) 2012-03-16 2017-04-12 ヴァイティー ファーマシューティカルズ,インコーポレイテッド 肝臓xレセプターモジュレーター

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3979391A (en) * 1972-11-22 1976-09-07 Sterling Drug Inc. 1,2,3,4-Tetrahydrocarbazoles
PT95692A (pt) * 1989-10-27 1991-09-13 American Home Prod Processo para a preparacao de derivados de acidos indole-,indeno-,piranoindole- e tetra-hidrocarbazole-alcanoicos, ou quais sao uteis como inibidores de pla2 e da lipoxigenase
IL109309A (en) * 1993-04-16 2000-06-29 Lilly Co Eli 1-H-indole-3-acetic acid hydrazide SPLA2 inhibitors and pharmaceutical compositions containing them
IL109311A0 (en) * 1993-04-16 1994-07-31 Lilly Co Eli 1H-indole-3-acetamide sPla2 inhibitors
BR9508298A (pt) * 1994-07-21 1998-11-03 Shionogi & Co Inibidores de indolizina de spla2
ES2159347T3 (es) * 1995-12-13 2001-10-01 Lilly Co Eli Naftil-acetamidas como inhibidores de spla2.
BR9713261A (pt) * 1996-10-30 2000-03-28 Lilly Co Eli Tricìclicos substituìdos
EP1007056A1 (en) * 1997-09-26 2000-06-14 Eli Lilly And Company Method for the treatment of cystic fibrosis
EP1043991A4 (en) * 1997-11-14 2005-02-02 Lilly Co Eli TREATMENT OF ALZHEIMER DISEASE

Also Published As

Publication number Publication date
IL129484A0 (en) 2000-02-29
DE69912670D1 (de) 2003-12-18
CA2269256A1 (en) 1999-10-17
CN1235968A (zh) 1999-11-24
DE69912670T2 (de) 2004-08-12
EP1156050A3 (en) 2001-11-28
CZ137199A3 (cs) 1999-11-17
SV1999000052A (es) 2000-03-14
PL332564A1 (en) 1999-10-25
AU2381899A (en) 1999-10-28
EA199900304A3 (ru) 2000-04-24
ES2210979T3 (es) 2004-07-01
NZ335252A (en) 2000-11-24
DE69914951D1 (de) 2004-03-25
HU9901219D0 (en) 1999-06-28
EA199900304A2 (ru) 1999-10-28
NO991823L (no) 1999-10-18
EP0950661B1 (en) 2003-11-12
HUP9901219A1 (hu) 2000-08-28
AR018185A1 (es) 2001-10-31
ID23219A (id) 2000-03-30
PE20000472A1 (es) 2000-06-02
ZA992773B (en) 2002-07-16
BR9901275A (pt) 2000-05-02
ATE254128T1 (de) 2003-11-15
NO991823D0 (no) 1999-04-16
EA003129B1 (ru) 2003-02-27
CO5080728A1 (es) 2001-09-25
JPH11322745A (ja) 1999-11-24
EP1156050B1 (en) 2004-02-18
SG106035A1 (en) 2004-09-30
ES2213668T3 (es) 2004-09-01
ATE259818T1 (de) 2004-03-15
TW555760B (en) 2003-10-01
EP0950661A1 (en) 1999-10-20
AU757454B2 (en) 2003-02-20
JP4435325B2 (ja) 2010-03-17
EP1156050A2 (en) 2001-11-21
DE69914951T2 (de) 2004-12-23
KR19990083234A (ko) 1999-11-25
TR199900842A2 (xx) 2000-09-21

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