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WO2002003992A3 - Therapie pour degenerescence osseuse en rapport avec une prothese - Google Patents

Therapie pour degenerescence osseuse en rapport avec une prothese Download PDF

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Publication number
WO2002003992A3
WO2002003992A3 PCT/US2001/021084 US0121084W WO0203992A3 WO 2002003992 A3 WO2002003992 A3 WO 2002003992A3 US 0121084 W US0121084 W US 0121084W WO 0203992 A3 WO0203992 A3 WO 0203992A3
Authority
WO
WIPO (PCT)
Prior art keywords
treating
alkyl
prosthesis
formulae
substituted indole
Prior art date
Application number
PCT/US2001/021084
Other languages
English (en)
Other versions
WO2002003992A2 (fr
Inventor
Simon Nicholas Jenkins
Barry Samuel Komm
Christopher Paul Miller
Original Assignee
Wyeth 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 Wyeth Corp filed Critical Wyeth Corp
Priority to AU2001271784A priority Critical patent/AU2001271784A1/en
Publication of WO2002003992A2 publication Critical patent/WO2002003992A2/fr
Publication of WO2002003992A3 publication Critical patent/WO2002003992A3/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/439—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease

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

Abstract

Cette invention concerne des méthodes de traitement d'une dégénérescence osseuse en rapport avec une prothèse. Ces méthodes consistent à administrer un composé représenté par la formule (I) ou (II), ou un sel acceptable de ce composé, ou, éventuellement, un oestrogène. Dans la formule (I) ou (II), Z est une fraction prise dans le groupe de formules (a, b ou c) dans lequel: R1 est pris dans H, OH ou les esters en C1-C12 ou des alkyl éthers en C1-C12, ou des halogènes ; ou des éthers halogénés en C1-C4 comprenant un trifluorométhyl éther et un trichlorométhyl éther; R2, R3, R4, R5, et R6 sont H, OH ou des esters en C1-C12 ou des alkyl éthers en C1-C12, des halogènes, ou des éthers halogénés en C1-C4, cyano, alkyle en C1-C6, ou trifluorométhyle, à condition que, quand R1 est H, R2 N'est pas OH; Y est la fraction de la formule (d), R7 et R8 sont un alkyle ou sont concaténés pour former un noyau renfermant de l'azote éventuellement substitué.
PCT/US2001/021084 2000-07-06 2001-06-29 Therapie pour degenerescence osseuse en rapport avec une prothese WO2002003992A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2001271784A AU2001271784A1 (en) 2000-07-06 2001-06-29 Therapy for prosthesis-related bone degeneration

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US21640700P 2000-07-06 2000-07-06
US21640600P 2000-07-06 2000-07-06
US60/216,406 2000-07-06
US60/216,407 2000-07-06

Publications (2)

Publication Number Publication Date
WO2002003992A2 WO2002003992A2 (fr) 2002-01-17
WO2002003992A3 true WO2002003992A3 (fr) 2002-06-27

Family

ID=26910981

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2001/021084 WO2002003992A2 (fr) 2000-07-06 2001-06-29 Therapie pour degenerescence osseuse en rapport avec une prothese

Country Status (2)

Country Link
AU (1) AU2001271784A1 (fr)
WO (1) WO2002003992A2 (fr)

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SG162615A1 (en) * 2002-06-13 2010-07-29 Wyeth Corp Bazedoxifene treatment regimens
WO2004009035A2 (fr) 2002-07-24 2004-01-29 Children's Hospital Medical Center Compositions et produits contenant de l'equol enantiomere, et procedes de fabrication
US8668914B2 (en) 2002-07-24 2014-03-11 Brigham Young University Use of equol for treating skin diseases
US8580846B2 (en) 2002-10-29 2013-11-12 Brigham Young University Use of equol for ameliorating or preventing neuropsychiatric and neurodegenerative diseases or disorders
JP4889944B2 (ja) 2002-10-29 2012-03-07 コロラド ステート ユニバーシティー リサーチ ファウンデーション アンドロゲンによって仲介される疾患を治療するためのエクオールの使用
US7781478B2 (en) 2004-07-14 2010-08-24 Ptc Therapeutics, Inc. Methods for treating hepatitis C
JO3112B1 (ar) 2010-03-29 2017-09-20 Ferring Bv تركيبة دوائية سريعة التحلل
WO2011120904A2 (fr) 2010-03-29 2011-10-06 Ferring B.V. Composition pharmaceutique à dissolution rapide
AU2016331065B2 (en) 2015-10-01 2021-04-29 Olema Pharmaceuticals, Inc. Tetrahydro-1H-pyrido(3,4-b)indole anti-estrogenic drugs
MX373946B (es) 2015-12-09 2020-07-13 Univ Illinois Reguladores a la baja del receptor de estrogeno selectivo de benzotiofeno.
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
CN109562113A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的螺环降解决定子体
EP3454856B1 (fr) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Dégronimères hétérocycliques pour la dégradation de protéines cibles
WO2017197051A1 (fr) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Dégronimères de c3-glutarimide liés à une amine pour la dégradation de protéines cibles
AU2017290748A1 (en) 2016-07-01 2019-01-17 G1 Therapeutics, Inc. Pyrimidine-based antiproliferative agents
WO2018081168A2 (fr) 2016-10-24 2018-05-03 The Board Of Trustees Of The University Of Illinois Répresseurs du récepteur oestrogénique sélectifs mixtes à base de benzothiophène
AR110728A1 (es) 2017-01-06 2019-04-24 G1 Therapeutics Inc Terapia combinada para el tratamiento del cáncer
TW201835064A (zh) 2017-02-10 2018-10-01 美商G1治療公司 苯并噻吩雌激素受體調節劑
EP3641762A4 (fr) 2017-06-20 2021-03-10 C4 Therapeutics, Inc. Dégrons et dégronimères à liaison n/o pour la dégradation de protéines
AU2018291026B2 (en) 2017-06-29 2022-09-01 Pharmacosmos Holding A/S Morphic forms of GIT38 and methods of manufacture thereof
WO2020132561A1 (fr) 2018-12-20 2020-06-25 C4 Therapeutics, Inc. Dégradation ciblée de protéines
CA3144791A1 (fr) 2019-07-07 2021-01-14 Olema Pharmaceuticals, Inc. Regimes d'antagonistes du recepteur des oestrogenes
MX2022007659A (es) 2019-12-20 2022-07-19 C4 Therapeutics Inc Compuestos de isoindolinona e indazol para la degradacion del receptor del factor de crecimiento epidermico (egfr).
CN115279370B (zh) 2020-03-05 2025-01-10 C4医药公司 用于brd9的靶向降解的化合物
CA3188313A1 (fr) 2020-08-05 2022-02-10 C4 Therapeutics, Inc. Composes pour la degradation ciblee de ret
WO2024030968A1 (fr) 2022-08-03 2024-02-08 Brystol-Myers Squibb Company Composés pour moduler la protéine ret
KR20250116017A (ko) 2022-11-04 2025-07-31 브리스톨-마이어스 스큅 컴퍼니 Ret-ldd 단백질 억제제
CN120569388A (zh) 2022-11-04 2025-08-29 百时美施贵宝公司 Ret-ldd蛋白降解剂
WO2025006753A2 (fr) 2023-06-30 2025-01-02 Merck Patent Gmbh Composés hétérobifonctionnels pour la dégradation de la protéine kras

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996005824A1 (fr) * 1994-08-22 1996-02-29 Eli Lilly And Company Procedes enrayant la degenerescence des protheses osseuses
EP0802184A1 (fr) * 1996-04-19 1997-10-22 American Home Products Corporation N-Benzyl-2-phénylindoles comme agents estrogènes
EP0802183A1 (fr) * 1996-04-19 1997-10-22 American Home Products Corporation Composés oestrogènes
US5880137A (en) * 1996-04-19 1999-03-09 American Home Products Corporation 2-phenyl-1- 4-(amino-1-yl-alk-1-ynyl)-benzyl!-1H-indol-5-ols as estrogenic agents
WO1999059969A1 (fr) * 1998-05-15 1999-11-25 American Home Products Corporation Compositions comprenant des composes a base de 2-phenyl-indole et de formulations d'oestrogenes
WO1999059581A1 (fr) * 1998-05-15 1999-11-25 American Home Products Corporation 2-phenyl-1-[4-(2-aminoethoxy)-benzyl]-indole en combinaison avec des oestrogenes
EP1123717A2 (fr) * 2000-01-26 2001-08-16 Pfizer Products Inc. Compositions contenant des agoniste-antagonistes d' oestrogène et une statine pour le traitement de l'ostéoporose et pour diminuer la valeur du choléstérol dans le sang

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996005824A1 (fr) * 1994-08-22 1996-02-29 Eli Lilly And Company Procedes enrayant la degenerescence des protheses osseuses
EP0802184A1 (fr) * 1996-04-19 1997-10-22 American Home Products Corporation N-Benzyl-2-phénylindoles comme agents estrogènes
EP0802183A1 (fr) * 1996-04-19 1997-10-22 American Home Products Corporation Composés oestrogènes
US5880137A (en) * 1996-04-19 1999-03-09 American Home Products Corporation 2-phenyl-1- 4-(amino-1-yl-alk-1-ynyl)-benzyl!-1H-indol-5-ols as estrogenic agents
WO1999059969A1 (fr) * 1998-05-15 1999-11-25 American Home Products Corporation Compositions comprenant des composes a base de 2-phenyl-indole et de formulations d'oestrogenes
WO1999059581A1 (fr) * 1998-05-15 1999-11-25 American Home Products Corporation 2-phenyl-1-[4-(2-aminoethoxy)-benzyl]-indole en combinaison avec des oestrogenes
EP1123717A2 (fr) * 2000-01-26 2001-08-16 Pfizer Products Inc. Compositions contenant des agoniste-antagonistes d' oestrogène et une statine pour le traitement de l'ostéoporose et pour diminuer la valeur du choléstérol dans le sang

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE DRUGNL [online] "TSE 424", XP002195073, retrieved from STN Database accession no. 2000:1286 *
R&D FOCUS DRUG NEWS, 17 April 2000 (2000-04-17) *

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Publication number Publication date
WO2002003992A2 (fr) 2002-01-17
AU2001271784A1 (en) 2002-01-21

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