PE20011318A1 - Compuestos fenilo sustituidos inhibidores de la farnesiltransferasa - Google Patents

Compuestos fenilo sustituidos inhibidores de la farnesiltransferasa

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Publication number
PE20011318A1
PE20011318A1 PE2001000384A PE2001000384A PE20011318A1 PE 20011318 A1 PE20011318 A1 PE 20011318A1 PE 2001000384 A PE2001000384 A PE 2001000384A PE 2001000384 A PE2001000384 A PE 2001000384A PE 20011318 A1 PE20011318 A1 PE 20011318A1
Authority
PE
Peru
Prior art keywords
methyl
alkylene
cycloalkyl
alkyl
inhibitors
Prior art date
Application number
PE2001000384A
Other languages
English (en)
Inventor
W Hutchins Charles
T Wang Gary
M Sullivan Gerard
L Sham Hing
A Hasvold Lisa
Taka Jennings Nelson Lissa
Wang Xilu
Lin Nan-Horng
Li Qun
A Fakhoury Stephen
J O Connor Stephen
L Gwaltney Ii Stephen
Wang Wei-Bo
L Curtin Michael
Original Assignee
Abbott Lab
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 Abbott Lab filed Critical Abbott Lab
Publication of PE20011318A1 publication Critical patent/PE20011318A1/es

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30Oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
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    • 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
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • 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
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    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
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    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
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  • Life Sciences & Earth Sciences (AREA)
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  • Engineering & Computer Science (AREA)
  • Ophthalmology & Optometry (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Transplantation (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS FENILO SUSTITUIDOS DE FORMULA I DONDE A1 ES L1-M1-L2, ALQUILENO, DONDE EL ALQUILENO PUEDE ESTAR SUSTITUIDOS CON OH, OXO, Q1-Q2-R3, CON LA CONDICION QUE CUANDO A1 ES METILENO, EL METILENO ESTA SUSTITUIDO; L1 Y L2 SON ALQUILENO CON ALQUILO, CICLOALQUILO, CICLOALQUILALQUILO, ENTRE OTROS; M1 ES O, N(R4), N(R5)SO2, SO2N(R5), N(R5)C(O), ENTRE OTROS; Q1 ES O, N(R4), N(R5)C(O), N(R5)SO2, ENTRE OTROS; Q2 ES ALQUILENO, ALQUENILENO, ALQUINILENO; R1 ES HALO, CICLOALQUILO, ARILO, HETEROARILO; R2 ES HETEROARILO TAL COMO IMIDAZOLILO, PIRAZOLILO, PIRROLILO, ENTRE OTROS; R3 ES ALQUILO, CICLOALQUILO, ARILO, ENTRE OTROS; R4 ES H, ALQUILO, ALQUENILO, ALQUINILO, ALCANOILO, ENTRE OTROS; R5 ES H, ALQUILO, ARILO, ARILALQUILO, CICLOALQUILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS CLORHIDRATO DE 5-(BENCILOXI)(6-FLUORO-2'METIL(1,1'-BIFENIL)-3-IL)METIL)-1-METIL-1H-IMIDAZOL,CLORHIDRATO DE 2'-METIL(1,1'-BIFENIL)-3-IL)(-1-METIL-1H-IMIDAZOL-5-IL)METILETER BENCILICO,CLORHIDRATO DE 5-(BENCILOXI)(6-CLORO-2'METIL(1,1'-BIFENIL)-3-IL)METIL)-1-METIL-1H-IMIDAZOL, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO PARA LA PREPARACION Y A COMPOSICIONES FARMACEUTICAS. LOS COMPUESTOS FENILO SUSTITUIDOS SON INHIBIDORES DE LA FARNESIL TRANSFERASA UTILES PARA EL TRATAMIENTO DE CANCER
PE2001000384A 2000-04-27 2001-04-27 Compuestos fenilo sustituidos inhibidores de la farnesiltransferasa PE20011318A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US56325600A 2000-04-27 2000-04-27
US82220501A 2001-04-02 2001-04-02

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PE2001000384A PE20011318A1 (es) 2000-04-27 2001-04-27 Compuestos fenilo sustituidos inhibidores de la farnesiltransferasa

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EP (1) EP1276726A2 (es)
JP (1) JP2004509064A (es)
AU (1) AU2001259218A1 (es)
CA (1) CA2407093A1 (es)
HK (1) HK1053833A1 (es)
MX (1) MXPA02010608A (es)
PE (1) PE20011318A1 (es)
WO (1) WO2001081316A2 (es)

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US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
DE60231646D1 (de) * 2001-12-19 2009-04-30 Janssen Pharmaceutica Nv Durch c-verbundene imidazole substituierte 1,8-annellierten chinolon-derivate als farnesyl transferase inhibitoren
TW200413320A (en) 2002-10-21 2004-08-01 Chiron Corp Carbocycle based inhibitors of glycogen synthase kinase 3
PL1651612T3 (pl) 2003-07-22 2012-09-28 Astex Therapeutics Ltd Związki 3,4-pochodne 1h-pirazolu i ich zastosowanie jako kinazy zależne od cyklin (cdk) i modulatory kinazy syntazy glikogenu-3 (gsk-3)
AU2005230846A1 (en) 2004-03-31 2005-10-20 Lexicon Pharmaceuticals, Inc. 2-aminomethylthiazole-5-carboxamides as protein kinase modulators
US7309709B2 (en) * 2004-04-01 2007-12-18 Pfizer Inc. Thiazole sulfonamide compounds for the treatment of neurodegenerative disorders
AR054425A1 (es) 2005-01-21 2007-06-27 Astex Therapeutics Ltd Sales de adicion de piperidin 4-il- amida de acido 4-(2,6-dicloro-benzoilamino) 1h-pirazol-3-carboxilico.
US8404718B2 (en) 2005-01-21 2013-03-26 Astex Therapeutics Limited Combinations of pyrazole kinase inhibitors
TW200806284A (en) * 2006-03-31 2008-02-01 Alcon Mfg Ltd Prenyltransferase inhibitors for ocular hypertension control and the treatment of glaucoma
CN101678007B (zh) 2007-04-06 2013-07-03 纽罗克里生物科学有限公司 促性腺激素释放激素受体拮抗剂及其制药用途
CA2839703A1 (en) 2011-06-24 2012-12-27 Amgen Inc. Trpm8 antagonists and their use in treatments
MY157429A (en) 2011-06-24 2016-06-15 Amgen Inc Trpm8 antagonists and their use in treatments
US8952009B2 (en) 2012-08-06 2015-02-10 Amgen Inc. Chroman derivatives as TRPM8 inhibitors
MA49623A (fr) 2017-07-21 2021-03-17 Antabio Sas Composés chimiques
US20210261540A1 (en) * 2018-06-07 2021-08-26 Disarm Therapeutics, Inc. Inhibitors of sarm1

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AU8961382A (en) * 1981-11-06 1983-05-12 Imperial Chemical Industries Plc Amide derivatives
JP2868883B2 (ja) * 1990-10-15 1999-03-10 株式会社トクヤマ ジオキソラン誘導体
US5733666A (en) * 1995-08-23 1998-03-31 Wayne Pigment Corp. Aqueous sealer composition for wood surfaces and process
US6297239B1 (en) * 1997-10-08 2001-10-02 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
US6358985B1 (en) * 1998-07-02 2002-03-19 Merck & Co., Inc. Inhibitors of prenyl-protein transferase

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MXPA02010608A (es) 2003-05-14
CA2407093A1 (en) 2001-11-01
HK1053833A1 (zh) 2003-11-07
WO2001081316A3 (en) 2002-05-23
WO2001081316A2 (en) 2001-11-01
JP2004509064A (ja) 2004-03-25
EP1276726A2 (en) 2003-01-22

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