WO2009014150A1 - ベンズイミダゾール誘導体 - Google Patents

ベンズイミダゾール誘導体 Download PDF

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Publication number
WO2009014150A1
WO2009014150A1 PCT/JP2008/063212 JP2008063212W WO2009014150A1 WO 2009014150 A1 WO2009014150 A1 WO 2009014150A1 JP 2008063212 W JP2008063212 W JP 2008063212W WO 2009014150 A1 WO2009014150 A1 WO 2009014150A1
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WIPO (PCT)
Prior art keywords
indole
benzimidazole derivative
17βhsd type
prostatomegaly
phenyl group
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PCT/JP2008/063212
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English (en)
French (fr)
Inventor
Akio Kakefuda
Yutaka Kondoh
Masaaki Hirano
Akio Kamikawa
Kentaro Enjo
Takashi Furutani
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Astellas Pharma Inc.
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Publication date
Application filed by Astellas Pharma Inc. filed Critical Astellas Pharma Inc.
Priority to EP08791469A priority Critical patent/EP2172454A4/en
Priority to JP2009524500A priority patent/JP5251876B2/ja
Priority to CN200880100054A priority patent/CN101835747A/zh
Priority to CA2694216A priority patent/CA2694216A1/en
Priority to US12/670,384 priority patent/US20100190826A1/en
Priority to MX2010000918A priority patent/MX2010000918A/es
Publication of WO2009014150A1 publication Critical patent/WO2009014150A1/ja

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    • C07ORGANIC CHEMISTRY
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    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/08Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • 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
    • A61K31/40Heterocyclic 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
    • A61K31/403Heterocyclic 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
    • A61K31/404Indoles, e.g. pindolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P17/00Drugs for dermatological disorders
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/08Antiseborrheics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/10Anti-acne agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/28Antiandrogens
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/38Drugs for disorders of the endocrine system of the suprarenal hormones
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
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    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
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    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
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    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Endocrinology (AREA)
  • Dermatology (AREA)
  • Diabetes (AREA)
  • Urology & Nephrology (AREA)
  • Reproductive Health (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

 17βHSDtype5の選択的阻害作用に基づく前立腺肥大症や前立腺癌等の新規かつ優れた治療及び/又は予防方法を提供する。COOHが置換したフェニル基がインドール環又はベンズイミダゾール環の窒素原子に置換したインドール又はベンズイミダゾール誘導体が、強力な17βHSDtype5選択的阻害活性を有すること、及び、テストステロン減少による副作用を伴わない前立腺肥大症や前立腺癌等の17βHSDtype5の関与する疾患の治療剤及び/又は予防剤となりうることを知見して本発明を完成した。
PCT/JP2008/063212 2007-07-24 2008-07-23 ベンズイミダゾール誘導体 WO2009014150A1 (ja)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP08791469A EP2172454A4 (en) 2007-07-24 2008-07-23 benzimidazole derivative
JP2009524500A JP5251876B2 (ja) 2007-07-24 2008-07-23 ベンズイミダゾール誘導体
CN200880100054A CN101835747A (zh) 2007-07-24 2008-07-23 苯并咪唑衍生物
CA2694216A CA2694216A1 (en) 2007-07-24 2008-07-23 Benzimidazole derivative
US12/670,384 US20100190826A1 (en) 2007-07-24 2008-07-23 Benzimidazole derivative
MX2010000918A MX2010000918A (es) 2007-07-24 2008-07-23 Derivado de bencimidazol.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007192242 2007-07-24
JP2007-192242 2007-07-24

Publications (1)

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WO2009014150A1 true WO2009014150A1 (ja) 2009-01-29

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PCT/JP2008/063212 WO2009014150A1 (ja) 2007-07-24 2008-07-23 ベンズイミダゾール誘導体

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US (1) US20100190826A1 (ja)
EP (1) EP2172454A4 (ja)
JP (1) JP5251876B2 (ja)
KR (1) KR20100046107A (ja)
CN (1) CN101835747A (ja)
CA (1) CA2694216A1 (ja)
MX (1) MX2010000918A (ja)
WO (1) WO2009014150A1 (ja)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010101128A1 (ja) * 2009-03-03 2010-09-10 アステラス製薬株式会社 アミド化合物
US9346803B2 (en) 2011-10-17 2016-05-24 Vanderbilt University Indomethacin analogs for the treatment of castrate-resistant prostate cancer

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Publication number Priority date Publication date Assignee Title
BR112015000443A2 (pt) 2012-07-10 2017-06-27 Bayer Pharma AG derivados de estra-1,3,5(10),16-tetraeno 3-substituídos, processo para a sua produção, preparações farmacêuticas que contêm os mesmos, bem como seu uso para a produção de medicamentos
AP3826A (en) 2013-02-21 2016-09-30 Bayer Pharma Aktiengellschaft Estra-1,3,5(10),16-tetraene-3-carboxamides for inhibition of 17.beta.-hydroxysteroid dehydrogenase (akr1 c3)
WO2018151810A1 (en) * 2017-02-17 2018-08-23 The Scripps Research Institute Defining rna-small molecule affinity landscapes enables design of a small molecular inhibitor of an oncogenic non-coding rna
EP3421483A1 (en) 2017-06-29 2019-01-02 Bayer Pharma Aktiengesellschaft Novel steroidal 17-beta heteroaryl compounds as inhibitors of akr1c3

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US9346803B2 (en) 2011-10-17 2016-05-24 Vanderbilt University Indomethacin analogs for the treatment of castrate-resistant prostate cancer
EP3078374A1 (en) 2011-10-17 2016-10-12 Vanderbilt University Indomethacin analogs for the treatment of castrate-resistant prostate cancer
US9895351B2 (en) 2011-10-17 2018-02-20 Vanderbilt University Indomethacin analogs for the treatment of castrate-resistant prostate cancer
US10398678B2 (en) 2011-10-17 2019-09-03 Vanderbilt University Indomethacin analogs for the treatment of castrate-resistant prostate cancer
US11738004B2 (en) 2011-10-17 2023-08-29 Vanderbilt University Indomethacin analogs for the treatment of castrate-resistant prostate cancer

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JPWO2009014150A1 (ja) 2010-10-07
MX2010000918A (es) 2010-03-15
EP2172454A1 (en) 2010-04-07
CN101835747A (zh) 2010-09-15
CA2694216A1 (en) 2009-01-29
US20100190826A1 (en) 2010-07-29
EP2172454A4 (en) 2010-12-08
KR20100046107A (ko) 2010-05-06
JP5251876B2 (ja) 2013-07-31

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