KR20030034161A - 파르네실 단백질 트랜스퍼라제 억제제인 트리사이클릭항종양 화합물 - Google Patents

파르네실 단백질 트랜스퍼라제 억제제인 트리사이클릭항종양 화합물 Download PDF

Info

Publication number
KR20030034161A
KR20030034161A KR10-2003-7003012A KR20037003012A KR20030034161A KR 20030034161 A KR20030034161 A KR 20030034161A KR 20037003012 A KR20037003012 A KR 20037003012A KR 20030034161 A KR20030034161 A KR 20030034161A
Authority
KR
South Korea
Prior art keywords
compound
substituted
alkyl
mmol
preparation
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.)
Ceased
Application number
KR10-2003-7003012A
Other languages
English (en)
Korean (ko)
Inventor
은조로게에프.죠지
비불반반카
쿠퍼알랜비.
구지티모씨
레인디나나쓰에프.
마이너케이쓰피.
돌로날드제이.
기리자발라반비요르무필
산타남바마
핀토패트릭에이.
주휴와이.
키르티카르카르틱엠.
알바레즈카르멘에스.
볼드윈죤제이.
리게
후앙치아-유
제임스레이에이.
비숍로버트더블유.
왕제임스
데사이재그디쉬에이.
Original Assignee
쉐링 코포레이션
파마코페이아, 인크.
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 쉐링 코포레이션, 파마코페이아, 인크. filed Critical 쉐링 코포레이션
Publication of KR20030034161A publication Critical patent/KR20030034161A/ko
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • 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
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • 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
    • 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
KR10-2003-7003012A 2000-08-30 2001-08-28 파르네실 단백질 트랜스퍼라제 억제제인 트리사이클릭항종양 화합물 Ceased KR20030034161A (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22918300P 2000-08-30 2000-08-30
US60/229,183 2000-08-30
PCT/US2001/026792 WO2002018368A1 (en) 2000-08-30 2001-08-28 Tricyclic antitumor compounds being farnesyl protein transferase inhibitors

Publications (1)

Publication Number Publication Date
KR20030034161A true KR20030034161A (ko) 2003-05-01

Family

ID=22860141

Family Applications (1)

Application Number Title Priority Date Filing Date
KR10-2003-7003012A Ceased KR20030034161A (ko) 2000-08-30 2001-08-28 파르네실 단백질 트랜스퍼라제 억제제인 트리사이클릭항종양 화합물

Country Status (27)

Country Link
US (1) US20020198216A1 (https=)
EP (1) EP1313725B1 (https=)
JP (1) JP2004513885A (https=)
KR (1) KR20030034161A (https=)
CN (1) CN100384837C (https=)
AR (1) AR033680A1 (https=)
AT (1) ATE359281T1 (https=)
AU (2) AU2001288451C1 (https=)
BR (1) BR0113675A (https=)
CA (1) CA2420673A1 (https=)
CO (1) CO5640109A2 (https=)
DE (1) DE60127846T2 (https=)
EC (1) ECSP034494A (https=)
ES (1) ES2284686T3 (https=)
HK (1) HK1054548B (https=)
HU (1) HUP0302942A3 (https=)
IL (1) IL154528A0 (https=)
MX (1) MXPA03001849A (https=)
NO (1) NO20030918L (https=)
NZ (1) NZ524246A (https=)
PE (1) PE20020486A1 (https=)
PL (1) PL361103A1 (https=)
RU (1) RU2293734C9 (https=)
SK (1) SK2292003A3 (https=)
TW (1) TWI268280B (https=)
WO (1) WO2002018368A1 (https=)
ZA (1) ZA200301545B (https=)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7342016B2 (en) 2000-08-30 2008-03-11 Schering Corporation Farnesyl protein transferase inhibitors as antitumor agents
WO2002072085A1 (en) 2001-03-14 2002-09-19 Bristol-Myers Squibb Company Combination of epothilone analogs and chemotherapeutic agents for the treatment of proliferative diseases
WO2003030908A2 (en) * 2001-10-09 2003-04-17 The University Of Cincinnati Inhibitors of the egf receptor for the treatment of thyroid cancer
WO2003047697A2 (en) * 2001-11-30 2003-06-12 Schering Corporation Use of an farsenyl protein tranferase inhibitor in combination with other antineoplastic agents for the manufacture of a medicament against cancer
AU2002346644A1 (en) * 2001-12-03 2003-06-17 Schering Corporation Use of fpt inhibitors and at least two antineoplastic agents in the treatment of cancer
US20030195192A1 (en) * 2002-04-05 2003-10-16 Fortuna Haviv Nicotinamides having antiangiogenic activity
US20040014744A1 (en) * 2002-04-05 2004-01-22 Fortuna Haviv Substituted pyridines having antiangiogenic activity
WO2004094409A1 (en) 2003-03-27 2004-11-04 Lankenau Institute For Medical Research Novel ido inhibitors and methods of use
CA2525987A1 (en) * 2003-06-05 2005-01-06 Charles Achkar Methods of treating hyperproliferative cell disorders
CN1972712A (zh) * 2003-06-09 2007-05-30 塞缪尔·瓦克萨尔 用胞外拮抗物和胞内拮抗物抑制受体酪氨酸激酶的方法
ES2235611B2 (es) * 2003-07-25 2006-07-16 Universidade De Santiago De Compostela Metodo cuantitativo para la deteccion de yesotoxinas en productos pesqueros basado en la activacion que producen en las fosfodiesterasas.
ES2317047T3 (es) 2003-08-07 2009-04-16 Schering Corporation Nuevos inhibidores de la farnesil proteina transferasa como agentes antitumorales.
US7592466B2 (en) 2003-10-09 2009-09-22 Abbott Laboratories Ureas having antiangiogenic activity
MX2007007611A (es) * 2004-12-21 2007-09-04 Schering Corp Nuevos inhibidores de la farnesil protein-transferasa como agentes antitumorales.
RU2361587C1 (ru) * 2008-02-14 2009-07-20 Михаил Владимирович Кутушов Лекарственное средство для лечения онкологических заболеваний
WO2010006432A1 (en) * 2008-07-14 2010-01-21 Queen's University At Kingston Pharmaceutical compositions comprising ret inhibitors and methods for the treatment of cancer
US20220257540A1 (en) * 2019-06-28 2022-08-18 Anhui Ronghang Biotech Development Co., Ltd. Compositions and methods for treatment of hepatitis b virus infection

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5089496A (en) * 1986-10-31 1992-02-18 Schering Corporation Benzo[5,6]cycloheptapyridine compounds, compositions and method of treating allergies
IE68935B1 (en) * 1990-06-22 1996-07-24 Schering Corp Bis-benzo or benzopyrido cyclohepta piperidene piperidylidene and piperazine compounds compositions and methods of use
US5719148A (en) * 1993-10-15 1998-02-17 Schering Corporation Tricyclic amide and urea compounds useful for inhibition of g-protein function and for treatment of proliferative diseases
PE92098A1 (es) * 1996-07-31 1998-12-31 Schering Corp N-cianoiminas triciclicas utiles como inhibidores de transferasa de proteina farnesilo
US6071907A (en) * 1996-09-13 2000-06-06 Schering Corporation Tricyclic compounds useful as FPT inhibitors
US5925648A (en) * 1997-07-29 1999-07-20 Schering Corporation Tricyclic N-cyanoimines useful as inhibitors of a farnesyl-protein transferase
TR200101754T2 (tr) * 1998-12-18 2002-05-21 Schering Corporation Farnezil protein transferaz inhibitörleri

Also Published As

Publication number Publication date
ATE359281T1 (de) 2007-05-15
TWI268280B (en) 2006-12-11
EP1313725B1 (en) 2007-04-11
AU2001288451C1 (en) 2008-03-06
HK1054548A1 (en) 2003-12-05
RU2293734C2 (ru) 2007-02-20
JP2004513885A (ja) 2004-05-13
DE60127846D1 (en) 2007-05-24
AR033680A1 (es) 2004-01-07
HUP0302942A3 (en) 2007-02-28
PE20020486A1 (es) 2002-06-14
ES2284686T3 (es) 2007-11-16
NZ524246A (en) 2004-11-26
WO2002018368A1 (en) 2002-03-07
DE60127846T2 (de) 2008-03-06
AU2001288451B2 (en) 2007-05-24
SK2292003A3 (en) 2003-08-05
NO20030918D0 (no) 2003-02-27
CN100384837C (zh) 2008-04-30
CO5640109A2 (es) 2006-05-31
MXPA03001849A (es) 2003-06-04
CN1471524A (zh) 2004-01-28
HUP0302942A2 (hu) 2003-12-29
CA2420673A1 (en) 2002-03-07
NO20030918L (no) 2003-04-29
EP1313725A1 (en) 2003-05-28
ZA200301545B (en) 2004-06-22
IL154528A0 (en) 2003-09-17
ECSP034494A (es) 2003-04-25
BR0113675A (pt) 2003-06-24
RU2293734C9 (ru) 2007-10-10
US20020198216A1 (en) 2002-12-26
AU8845101A (en) 2002-03-13
HK1054548B (en) 2007-10-18
PL361103A1 (en) 2004-09-20

Similar Documents

Publication Publication Date Title
KR20030034161A (ko) 파르네실 단백질 트랜스퍼라제 억제제인 트리사이클릭항종양 화합물
US20030229099A1 (en) Novel farnesyl protein transferase inhibitors as antitumor agents
US20040006087A1 (en) Method of treating cancer using FPT inhibitors and antineoplastic agents
JP2002503249A (ja) 癌の治療方法
CN105189456A (zh) Kras g12c的共价抑制剂
US7342016B2 (en) Farnesyl protein transferase inhibitors as antitumor agents
AU2001288451A1 (en) Tricyclic antitumor compounds being farnesyl protein transferase inhibitors
CN107454898A (zh) 生长素释放肽o‑酰基转移酶抑制剂
TW200536539A (en) Organic compounds
JP2005525356A5 (https=)
AU753658B2 (en) Benzpyrido cycloheptane compounds useful for inhibition of farnesyl protein transferase
CN1326850C (zh) 三环类法尼基蛋白转移酶抑制剂
KR20010013829A (ko) 파르네실 단백질 전이효소 억제제로서의벤조(5,6)사이클로헵타(1,2-b)피리딘 유도체
AU2007202115A1 (en) Tricyclic antitumor compounds being farnesyl protein transferase inhibitors
CN121399117A (zh) 一类羧酸类化合物及其制备方法和应用
CN121913973A (zh) 一种吲哚类化合物、合成方法及其用途
MXPA01006241A (en) Tricyclic farnesyl protein transferase inhibitors

Legal Events

Date Code Title Description
PA0105 International application

Patent event date: 20030228

Patent event code: PA01051R01D

Comment text: International Patent Application

PG1501 Laying open of application
N231 Notification of change of applicant
PN2301 Change of applicant

Patent event date: 20050202

Comment text: Notification of Change of Applicant

Patent event code: PN23011R01D

A201 Request for examination
PA0201 Request for examination

Patent event code: PA02012R01D

Patent event date: 20060822

Comment text: Request for Examination of Application

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

Comment text: Notification of reason for refusal

Patent event date: 20070928

Patent event code: PE09021S01D

E601 Decision to refuse application
PE0601 Decision on rejection of patent

Patent event date: 20090219

Comment text: Decision to Refuse Application

Patent event code: PE06012S01D

Patent event date: 20070928

Comment text: Notification of reason for refusal

Patent event code: PE06011S01I