CO4940447A1 - TRICYCLIC COMPOUNDS USEFUL AS INHIBITORS OF THE TRANSFER RASA OF PROTEIN TO FARNESILO - Google Patents

TRICYCLIC COMPOUNDS USEFUL AS INHIBITORS OF THE TRANSFER RASA OF PROTEIN TO FARNESILO

Info

Publication number
CO4940447A1
CO4940447A1 CO98034143A CO98034143A CO4940447A1 CO 4940447 A1 CO4940447 A1 CO 4940447A1 CO 98034143 A CO98034143 A CO 98034143A CO 98034143 A CO98034143 A CO 98034143A CO 4940447 A1 CO4940447 A1 CO 4940447A1
Authority
CO
Colombia
Prior art keywords
protein
farnesilo
rasa
inhibitors
transfer
Prior art date
Application number
CO98034143A
Other languages
Spanish (es)
Inventor
Alan B Cooper
A Desai Jagdish
K Sansena Anil
James J-S Wang
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 CO4940447A1 publication Critical patent/CO4940447A1/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
    • C07D401/14Heterocyclic 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
    • 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
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Se describen nuevos compuestos de fórmulaAsí mismo se describe un método para inhibir la función transferasa de proteína al farnesilo y porlo tanto para inhibir el desarrollo anormal de las células. El método comprende administrar uncompuesto de la precedente fórmula a un sistema biológico. En particular, el método inhibe eldesarrollo anormal de las células en un mamífero tal como un ser humano. También se describe unmétodo para provocar una respuesta antialérgica mediante la administración de estos compuestos.Novel compounds of formula are described. A method is also described to inhibit the protein transferase function to farnesyl and therefore to inhibit abnormal cell development. The method comprises administering a compound of the preceding formula to a biological system. In particular, the method inhibits abnormal cell development in a mammal such as a human. Also described is a method of eliciting an allergy response by administering these compounds.

CO98034143A 1997-06-17 1998-06-16 TRICYCLIC COMPOUNDS USEFUL AS INHIBITORS OF THE TRANSFER RASA OF PROTEIN TO FARNESILO CO4940447A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US87774397A 1997-06-17 1997-06-17

Publications (1)

Publication Number Publication Date
CO4940447A1 true CO4940447A1 (en) 2000-07-24

Family

ID=25370623

Family Applications (1)

Application Number Title Priority Date Filing Date
CO98034143A CO4940447A1 (en) 1997-06-17 1998-06-16 TRICYCLIC COMPOUNDS USEFUL AS INHIBITORS OF THE TRANSFER RASA OF PROTEIN TO FARNESILO

Country Status (13)

Country Link
EP (1) EP0989984A1 (en)
JP (1) JP2002504145A (en)
KR (1) KR20010013825A (en)
CN (1) CN1266432A (en)
AR (1) AR015122A1 (en)
AU (1) AU744153B2 (en)
CA (1) CA2293713C (en)
CO (1) CO4940447A1 (en)
HU (1) HUP0004274A3 (en)
IL (1) IL133388A0 (en)
NZ (1) NZ501418A (en)
WO (1) WO1998057961A1 (en)
ZA (1) ZA985214B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102548986A (en) 2009-06-05 2012-07-04 链接医药公司 Aminopyrrolidinone derivatives and uses thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL111235A (en) * 1993-10-15 2001-03-19 Schering Plough Corp Pharmaceutical compositions for inhibition of g-protein function and for treatment of proliferative diseases containing tricyclic compounds some such compounds and process for preparing part of them
DK0723538T3 (en) * 1993-10-15 2002-03-18 Schering Corp Tricyclic carbamate compounds useful for inhibition of G protein function and for the treatment of proliferative diseases
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
EP1380581A1 (en) * 1995-12-22 2004-01-14 Schering Corporation Tricyclic amides useful for inhibition of G-protein function and for treatment of proliferative diseases

Also Published As

Publication number Publication date
AU8058198A (en) 1999-01-04
AU744153B2 (en) 2002-02-14
CA2293713A1 (en) 1998-12-23
EP0989984A1 (en) 2000-04-05
KR20010013825A (en) 2001-02-26
WO1998057961A1 (en) 1998-12-23
IL133388A0 (en) 2001-04-30
ZA985214B (en) 1999-01-07
NZ501418A (en) 2001-04-27
HUP0004274A2 (en) 2001-08-28
CA2293713C (en) 2006-12-05
CN1266432A (en) 2000-09-13
AR015122A1 (en) 2001-04-18
HUP0004274A3 (en) 2002-03-28
JP2002504145A (en) 2002-02-05

Similar Documents

Publication Publication Date Title
ES2133807T3 (en) PEPTIDYL COMPOUNDS AND THEIR THERAPEUTIC USE AS METALOPROTEASE INHIBITORS.
EA199800563A1 (en) ANTAGONISTS OF HORMONE, GROWING GONADOTROPIN
ES2168737T3 (en) INHIBITORS OF NITRICO SINTASA OXIDE.
DK1017692T3 (en) 4-Heteroberl tetrahydroquinolines and their use as inhibitors of cholesterol ester transfer proteins
ES2182234T3 (en) METALOPROTEASE INHIBITORS.
AR026410A1 (en) '' 2-ARIL-3- (HETEROARIL) -IMIDAZO [1,2-A] SUBSTITUTED PYRIMIDINS, AND RELATED PHARMACEUTICAL COMPOSITIONS AND METHODS
SE8602723D0 (en) THIAZOLES, THEIR PRODUCTION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
GT199900029A (en) HETERO-CYCLE COMPOUNDS AS INHIBITORS OF ROTAMASAS ENZYMES.
BR9916894A (en) sulfohydroxamic acids and sulfohydroxamates and their use as mek inhibitors
EA199700087A1 (en) METHOD OF INHIBITING KATEPSIN K
ATE286038T1 (en) COMPOUNDS WITH SULFONIC ACID AMIDE GROUP
NO973017L (en) New trienoic retinoid compounds and methods
ES2134924T3 (en) SULFONILALCANOYLAMINO-HYDROXYETHYLAMINE-SULPHAMIC ACIDS USEFUL AS RETROVIRAL PROTEASE INHIBITORS.
GT200200095A (en) NEW DERIVATIVES OF SULFONIC ACID
ES2187738T3 (en) DERIVATIVES OF FLAVONAS, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOUNDS THAT CONTAIN THEM.
ES2060818T3 (en) DERIVATIVES OF INDOL, BENZOFURANO AND BENZOTIOFENO SUBSTITUTED AS INHIBITORS OF 5-LIPOOXIGENASA.
CO5011061A1 (en) INHIBITION OF MATRIX METALOPROTESES BY REPLACED BIARILOXOBUTIRIC ACIDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
EE03745B1 (en) Substituted 4-Biphenyl-4-hydroxybutanoic Acid Derivatives as Inhibitors of Metalloprotease Matrix
NO20012817L (en) Phenethyl-5-bromopyridylthiourea (PBT) and dihydroalkoxybenzyloxopyrimidine (DABO) derivatives as overspermicidal activity
CO4940447A1 (en) TRICYCLIC COMPOUNDS USEFUL AS INHIBITORS OF THE TRANSFER RASA OF PROTEIN TO FARNESILO
ATE320422T1 (en) METALLOPROTEINASE INHIBITORS
ES2141978T3 (en) TRICYCLIC RETINOIDS, METHODS FOR THEIR PRODUCTION AND USE.
EA200200663A1 (en) NEW COMPOUNDS OF OCTAGIDRO-2H-PYRIDO [1,2-α] PYRAZINE, METHOD OF THEIR PRODUCTION AND PHARMACEUTICAL PREPARATIONS, THEIR CONTAINING
ES2171743T3 (en) DERIVATIVES OF AMIDINES AND ISOTIOURES AS INHIBITORS OF THE SYNTHETIC ENZYME OF NITRIC OXIDE.
AR014738A1 (en) NEW PROCEDURE FOR PREPARATION OF FEXOFENADINE AND INTERMEDIARY COMPOUNDS