PE104798A1 - Compuestos utiles para la inhibicion de la enzima farnesilo transferasa - Google Patents

Compuestos utiles para la inhibicion de la enzima farnesilo transferasa

Info

Publication number
PE104798A1
PE104798A1 PE1998000505A PE00050598A PE104798A1 PE 104798 A1 PE104798 A1 PE 104798A1 PE 1998000505 A PE1998000505 A PE 1998000505A PE 00050598 A PE00050598 A PE 00050598A PE 104798 A1 PE104798 A1 PE 104798A1
Authority
PE
Peru
Prior art keywords
alkyl
aryl
formula
tumor cells
farnesilo
Prior art date
Application number
PE1998000505A
Other languages
English (en)
Inventor
B Cooper Alan
Ganguly Ashit
Huang Chia-Yu
M Girijavallabhan Viyyoor
J Baldwin John
J Doll Ronald
C Reader John
Original Assignee
Pharmacopeia Inc
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 Pharmacopeia Inc, Schering Corp filed Critical Pharmacopeia Inc
Publication of PE104798A1 publication Critical patent/PE104798A1/es

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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • 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
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

SE REFIERE A UN COMPUESTO BENZOCICLOHEPTANO PIRIDINA DE FORMULA (1.0), O SOLVATO, DONDE a ES N o NO; NO MAS DE DOS DE Ra, Rb, Rc Y Rd SON H Y EL RESTO SON HALO, ALQUILO, ALCOXI Y NO MAS DE 2 SON H; R ES H, -S(O)2R1, -S(O)2NR1R2, ENTRE OTROS, R1 Y R2 SON H, ALQUILO, ARILO, ENTRE OTROS; Re Y Rf SON H, ALQUILO, ALQUILOXIALQUILO, ENTRE OTROS; o Re ES H, ALQUILO o ARILO Y Rf ES -(CH2)n-R15, n ES 0-8; R15 ES -C(O)NH2, -SO2NH2, ARILO o -C(=A)-B; B ES OH o NH2 Y A ES NH, O, NOH o NCN o Re Y Rf JUNTO A N FORMAN UN ANILLO HETEROCICLOALQUILO DE 5-6 MIEMBROS OPCIONALMENTE SUSTITUIDO CON OH, NH2, NHR16, ENTRE OTROS; Rh ES H o =O, SI Rh ES H Y Rb Y Rd SON H, GRUPO DE FORMULA (a, b); o Re ES H Y Rf ES UN GRUPO DE FORMULA (c, d, e). EL COMPUESTO I PUEDE SER UTIL PARA INHIBIR EL DESARROLLO ANORMAL DE CELULAS TUMORALES QUE EXPRESAN EL ONCOGEN RAS ACTIVADO, PUDIENDO SER LAS CELULAS TUMORALES PANCREATICAS, CELULAS DE CANCER DE PULMON, CELULAS DE TUMOR DE LEUCEMIA MIELOIDE, CELULAS DE TUMORES FOLICULARES DE TIROIDES
PE1998000505A 1997-06-17 1998-06-15 Compuestos utiles para la inhibicion de la enzima farnesilo transferasa PE104798A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US87774197A 1997-06-17 1997-06-17

Publications (1)

Publication Number Publication Date
PE104798A1 true PE104798A1 (es) 1999-11-06

Family

ID=25370618

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1998000505A PE104798A1 (es) 1997-06-17 1998-06-15 Compuestos utiles para la inhibicion de la enzima farnesilo transferasa

Country Status (18)

Country Link
EP (1) EP0989983B1 (es)
JP (1) JP2002504144A (es)
KR (1) KR100640672B1 (es)
CN (1) CN1266433A (es)
AR (1) AR012991A1 (es)
AT (1) ATE273299T1 (es)
AU (1) AU753658B2 (es)
CA (1) CA2293714C (es)
DE (1) DE69825589T2 (es)
ES (1) ES2224408T3 (es)
HU (1) HUP0003138A3 (es)
IL (2) IL133386A0 (es)
MY (1) MY143570A (es)
NZ (1) NZ501376A (es)
PE (1) PE104798A1 (es)
TW (1) TW587935B (es)
WO (1) WO1998057960A1 (es)
ZA (1) ZA985203B (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002533335A (ja) * 1998-12-18 2002-10-08 シェーリング コーポレイション 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
US6372747B1 (en) 1998-12-18 2002-04-16 Schering Corporation Farnesyl protein transferase inhibitors
US6362188B1 (en) 1998-12-18 2002-03-26 Schering Corporation Farnesyl protein transferase inhibitors
US6800636B2 (en) 1998-12-18 2004-10-05 Schering Corporation Farnesyl protein transferase inhibitors
JP2002533336A (ja) 1998-12-18 2002-10-08 シェーリング コーポレイション 三環式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
US6432959B1 (en) * 1998-12-23 2002-08-13 Schering Corporation Inhibitors of farnesyl-protein transferase
US7342016B2 (en) 2000-08-30 2008-03-11 Schering Corporation Farnesyl protein transferase inhibitors as antitumor agents
AU2002236813A1 (en) * 2001-01-22 2002-07-30 Schering Corporation Treatment of malaria with farnesyl protein transferase inhibitors
AU2002257114A1 (en) * 2001-04-06 2002-10-21 Schering Corporation Treatment of malaria with farsenyl protein transferase inhibitors
CA2499732A1 (en) * 2002-09-20 2004-04-15 Applied Research Systems Ars Holding N.V. Piperazine derivatives and methods of use
MX2007007074A (es) 2004-12-13 2007-09-04 Schering Corp Inhibidores novedosos de proteina transferasa de farnesilo y su uso para tratar cancer.
JP2008523148A (ja) 2004-12-14 2008-07-03 シェーリング コーポレイション 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および増殖性疾患を処置するための方法
EP2807153B1 (en) * 2012-01-25 2020-03-25 Novartis AG Heterocyclic compounds and methods for their use
WO2018093695A1 (en) 2016-11-18 2018-05-24 Merck Sharp & Dohme Corp. FACTOR XIIa INHIBITORS

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW308594B (es) * 1993-10-15 1997-06-21 Schering Corp
IL111235A (en) * 1993-10-15 2001-03-19 Schering Plough Corp Medicinal preparations for inhibiting protein G activity and for the treatment of malignant diseases, containing tricyclic compounds, some such new compounds and a process for the preparation of some of them
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
US5712280A (en) * 1995-04-07 1998-01-27 Schering Corporation Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases

Also Published As

Publication number Publication date
EP0989983A1 (en) 2000-04-05
EP0989983B1 (en) 2004-08-11
CA2293714C (en) 2009-09-08
HUP0003138A2 (hu) 2001-06-28
KR20010013822A (ko) 2001-02-26
AU8058098A (en) 1999-01-04
IL133386A0 (en) 2001-04-30
CA2293714A1 (en) 1998-12-23
IL133386A (en) 2006-12-10
AR012991A1 (es) 2000-11-22
ZA985203B (en) 1999-01-05
CN1266433A (zh) 2000-09-13
DE69825589T2 (de) 2005-09-08
KR100640672B1 (ko) 2006-11-02
ES2224408T3 (es) 2005-03-01
ATE273299T1 (de) 2004-08-15
AU753658B2 (en) 2002-10-24
HUP0003138A3 (en) 2002-11-28
TW587935B (en) 2004-05-21
JP2002504144A (ja) 2002-02-05
WO1998057960A1 (en) 1998-12-23
NZ501376A (en) 2002-03-28
DE69825589D1 (de) 2004-09-16
MY143570A (en) 2011-05-31

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FG Grant, registration
FD Application declared void or lapsed