JP2002507192A - ファルネシルタンパク質トランスフェラーゼの新規三環式スルホンアミドインヒビター - Google Patents

ファルネシルタンパク質トランスフェラーゼの新規三環式スルホンアミドインヒビター

Info

Publication number
JP2002507192A
JP2002507192A JP54752198A JP54752198A JP2002507192A JP 2002507192 A JP2002507192 A JP 2002507192A JP 54752198 A JP54752198 A JP 54752198A JP 54752198 A JP54752198 A JP 54752198A JP 2002507192 A JP2002507192 A JP 2002507192A
Authority
JP
Japan
Prior art keywords
compound
alkyl
heteroaryl
hydrogen
aryl
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP54752198A
Other languages
English (en)
Japanese (ja)
Other versions
JP2002507192A5 (zh
Inventor
ニョロージ,エフ.ジョージ
ビブルバン,バンチャ
ジー. タベラス,アーサー
ジェイ. ドール,ロナルド
エム. ギリジャバラバン,ビヨール
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Sharp and Dohme Corp
Original Assignee
Schering 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
Application filed by Schering Corp filed Critical Schering Corp
Publication of JP2002507192A publication Critical patent/JP2002507192A/ja
Publication of JP2002507192A5 publication Critical patent/JP2002507192A5/ja
Pending legal-status Critical Current

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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/04Ortho- or peri-condensed ring systems
    • C07D221/06Ring systems of three rings
    • C07D221/16Ring systems of three rings containing carbocyclic rings other than six-membered
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero 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
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
JP54752198A 1997-06-17 1998-06-15 ファルネシルタンパク質トランスフェラーゼの新規三環式スルホンアミドインヒビター Pending JP2002507192A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US87705097A 1997-06-17 1997-06-17
US08/877,050 1997-06-17
PCT/US1998/011508 WO1998057949A1 (en) 1997-06-17 1998-06-15 Novel tricyclic sulfonamide inhibitors of farnesyl-protein transferase

Publications (2)

Publication Number Publication Date
JP2002507192A true JP2002507192A (ja) 2002-03-05
JP2002507192A5 JP2002507192A5 (zh) 2005-12-08

Family

ID=25369146

Family Applications (1)

Application Number Title Priority Date Filing Date
JP54752198A Pending JP2002507192A (ja) 1997-06-17 1998-06-15 ファルネシルタンパク質トランスフェラーゼの新規三環式スルホンアミドインヒビター

Country Status (14)

Country Link
EP (1) EP0989980A1 (zh)
JP (1) JP2002507192A (zh)
KR (1) KR20010013826A (zh)
CN (1) CN1267290A (zh)
AR (1) AR012989A1 (zh)
AU (1) AU8253698A (zh)
CA (1) CA2293358C (zh)
CO (1) CO4940475A1 (zh)
HU (1) HUP0004627A2 (zh)
IL (1) IL133393A0 (zh)
NZ (1) NZ501619A (zh)
PE (1) PE86199A1 (zh)
WO (1) WO1998057949A1 (zh)
ZA (1) ZA985218B (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016508521A (ja) * 2013-02-19 2016-03-22 アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai 抗腫瘍剤としての三環式複素環

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6689789B2 (en) 1997-06-17 2004-02-10 Schering Corporation Compounds useful for inhibition of farnesyl protein transferase
US7517884B2 (en) 1998-03-30 2009-04-14 Kalypsys Inc. Sulfonyl-substituted bicyclic compounds as modulators of PPAR
US7342016B2 (en) 2000-08-30 2008-03-11 Schering Corporation Farnesyl protein transferase inhibitors as antitumor agents
JP2004514717A (ja) * 2000-11-29 2004-05-20 シェーリング コーポレイション 新規ファルネシルプロテイントランスフェラーゼインヒビター
BRPI0516435B1 (pt) 2004-10-29 2021-09-21 Kalypsys , Inc Composto, e composição farmacêutica
EP1940815B1 (en) 2005-10-25 2018-08-15 Kalypsys, Inc. Salts of modulators of ppar and methods of treating metabolic disorders
WO2008091863A1 (en) 2007-01-23 2008-07-31 Kalypsys, Inc. Sulfonyl-substituted bicyclic compounds as ppar modulators for the treatment of non-alcoholic steatohepatitis

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08510445A (ja) * 1993-10-15 1996-11-05 シェーリング コーポレイション G−タンパク質機能の阻害および増殖性疾患の治療に有用な三環式スルホンアミド化合物

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL117798A (en) * 1995-04-07 2001-11-25 Schering Plough Corp Tricyclic compounds useful for inhibiting the function of protein - G and for the treatment of malignant diseases, and pharmaceutical preparations containing them
IL117797A0 (en) * 1995-04-07 1996-08-04 Pharmacopeia Inc Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08510445A (ja) * 1993-10-15 1996-11-05 シェーリング コーポレイション G−タンパク質機能の阻害および増殖性疾患の治療に有用な三環式スルホンアミド化合物

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016508521A (ja) * 2013-02-19 2016-03-22 アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai 抗腫瘍剤としての三環式複素環

Also Published As

Publication number Publication date
NZ501619A (en) 2002-02-01
PE86199A1 (es) 1999-09-24
ZA985218B (en) 1998-12-15
WO1998057949A1 (en) 1998-12-23
IL133393A0 (en) 2001-04-30
CN1267290A (zh) 2000-09-20
AU8253698A (en) 1999-01-04
CA2293358A1 (en) 1998-12-23
CO4940475A1 (es) 2000-07-24
EP0989980A1 (en) 2000-04-05
CA2293358C (en) 2008-08-05
HUP0004627A2 (hu) 2001-10-28
KR20010013826A (ko) 2001-02-26
AR012989A1 (es) 2000-11-22

Similar Documents

Publication Publication Date Title
JP2002506444A (ja) ファルネシルタンパク質トランスフェラーゼの新規n置換尿素インヒビター
AU711238B2 (en) Tricyclic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
KR100295224B1 (ko) G-단백질기능의억제및증식성질환의치료에유용한트리사이클릭아미드
AU2014294866B2 (en) Novel derivatives of indole and pyrrole, method for the production thereof and pharmaceutical compositions containing same
JP2002504149A (ja) G−タンパク質機能の阻害および増殖性疾患の処置のために有用なカルボキシピペリジルアセトアミド三環式化合物(ファルネシルタンパク質トランスフェラーゼインヒビター)
TW202342473A (zh) Parp1抑制劑及其用途
JP2002507192A (ja) ファルネシルタンパク質トランスフェラーゼの新規三環式スルホンアミドインヒビター
JP3269636B2 (ja) ファルネシルタンパク質トランスフェラーゼインヒビターとして有用な三環式ケトアミド誘導体
JP2002504144A (ja) ファルネシルタンパク質トランスフェラーゼの阻害に有用なベンズピリドシクロヘプタン化合物
JP2001500505A (ja) Fptインヒビターとして有用な三環式化合物
US6426352B1 (en) Sulfonamide inhibitors of farnesyl-protein transferase
US6071907A (en) Tricyclic compounds useful as FPT inhibitors
JP2000513034A (ja) ファルネシルタンパク質トランスフェラーゼインヒビターとして有用なベンゾ(5,6)シクロヘプタピリジン化合物
US6218401B1 (en) Phenyl-substituted tricyclic inhibitors of farnesyl-protein transferase
JP2000513033A (ja) ファルネシルタンパク質トランスフェラーゼインヒビターとして有用なベンゾ(5,6)シクロヘプタピリジン環状尿素およびラクタム
JP3153555B2 (ja) ファルネシルタンパク質トランスフェラーゼのインヒビターとして有用な新規三環式n―シアノイミン
JP2002504151A (ja) ファルネシルタンパク質トランスフェラーゼの新規アミノオキシアミド三環式インヒビター
JP2002504150A (ja) ファルネシルタンパク質トランスフェラーゼの新規フェニル置換三環式インヒビター
KR20010013828A (ko) 파르네실 단백질 트랜스퍼라제의 억제에 유용한벤조(5,6)사이클로헵타(1,2b)피리딘 유도체
MXPA99012084A (en) Novel tricyclic sulfonamide inhibitors of farnesyl-protein transferase
MXPA99012080A (en) Novel aminooxyamide tricyclic inhibitors of farnesylprotein transferase
CZ84499A3 (cs) Substituované deriváty benzocykloheptapyridinu použitelné pro inhibici farnesylprotein transferasy
MXPA99001110A (en) Novel tricyclic n-cyanoimines useful as inhibitors of farnesyl-protein transferase
MXPA99012079A (en) Novel phenyl-substituted tricyclic inhibitors of farnesyl-protein transferase
JP2002504146A (ja) ファルネシルタンパク質トランスフェラーゼの阻害に有用なベンゾ(5,6)シクロヘプタ(1,2−b)ピリジン誘導体

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20050614

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20050614

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20090120

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20090417

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20090601

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20090518

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20090629

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20090616

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20090727

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20090716

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20100511