JPH08510455A - 17,20―リアーゼ阻害活性を有するカルバゾール誘導体 - Google Patents

17,20―リアーゼ阻害活性を有するカルバゾール誘導体

Info

Publication number
JPH08510455A
JPH08510455A JP7500181A JP50018195A JPH08510455A JP H08510455 A JPH08510455 A JP H08510455A JP 7500181 A JP7500181 A JP 7500181A JP 50018195 A JP50018195 A JP 50018195A JP H08510455 A JPH08510455 A JP H08510455A
Authority
JP
Japan
Prior art keywords
formula
compound
group
carbazole
ylmethyl
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP7500181A
Other languages
English (en)
Japanese (ja)
Inventor
クライブ チェリー,ピーター
デリック クッカー,ジョン
デビッド サール,アンドリュウ
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Glaxo Group Ltd
Original Assignee
Glaxo Group Ltd
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 Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of JPH08510455A publication Critical patent/JPH08510455A/ja
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • 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
    • C07D401/06Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
JP7500181A 1993-05-21 1994-05-19 17,20―リアーゼ阻害活性を有するカルバゾール誘導体 Pending JPH08510455A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB939310635A GB9310635D0 (en) 1993-05-21 1993-05-21 Chemical compounds
GB9310635.9 1993-05-21
PCT/EP1994/001613 WO1994027989A1 (en) 1993-05-21 1994-05-19 Carbazole derivatives with 17,20-lyase-inhibiting activity

Publications (1)

Publication Number Publication Date
JPH08510455A true JPH08510455A (ja) 1996-11-05

Family

ID=10736007

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7500181A Pending JPH08510455A (ja) 1993-05-21 1994-05-19 17,20―リアーゼ阻害活性を有するカルバゾール誘導体

Country Status (19)

Country Link
EP (1) EP0699196A1 (fi)
JP (1) JPH08510455A (fi)
CN (1) CN1126473A (fi)
AU (1) AU6928794A (fi)
BG (1) BG100154A (fi)
CA (1) CA2162921A1 (fi)
CZ (1) CZ305195A3 (fi)
FI (1) FI955587A0 (fi)
GB (1) GB9310635D0 (fi)
HU (1) HUT73790A (fi)
IL (1) IL109703A0 (fi)
NO (1) NO954681D0 (fi)
OA (1) OA10195A (fi)
PE (1) PE31195A1 (fi)
PL (1) PL311702A1 (fi)
SK (1) SK142495A3 (fi)
TW (1) TW279866B (fi)
WO (1) WO1994027989A1 (fi)
ZA (1) ZA943494B (fi)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016515098A (ja) * 2013-02-27 2016-05-26 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company ブロモドメイン阻害剤として有用なカルバゾール化合物

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5807880A (en) * 1993-09-30 1998-09-15 Yamanouchi Pharmaceutical Co., Ltd. Azole derivative and pharmaceutical composition thereof
AU3846395A (en) * 1994-11-07 1996-05-31 Janssen Pharmaceutica N.V. Compositions comprising carbazoles and cyclodextrins
EP0820989A4 (en) * 1995-03-01 1998-05-06 Yamanouchi Pharma Co Ltd IMIDAZOLE DERIVATIVES AND MEDICINAL COMPOSITION BASED ON SAID DERIVATIVES
EP0974584B1 (en) * 1997-02-21 2003-01-15 Takeda Chemical Industries, Ltd. Fused ring compounds, process for producing the same and use thereof
TWI306099B (en) 2000-11-17 2009-02-11 Takeda Chemical Industries Ltd Novel imidazole derivatives, production method thereof and use thereof
CA2429437A1 (en) 2000-11-20 2002-05-23 Takeda Chemical Industries, Ltd. Imidazole derivatives, process for their preparation and their use
WO2002046186A1 (fr) 2000-12-08 2002-06-13 Takeda Chemical Industries, Ltd. Dérivés thiazole substitués porteurs de groupes 3-pyridyl, procédé d'élaboration et leur utilisation
CA2612723A1 (en) * 2005-06-24 2007-01-04 Eli Lilly And Company Tetrahydrocarbazole derivatives useful as androgen receptor modulators
US8093279B2 (en) 2005-12-13 2012-01-10 Gillian Reed, legal representative Compound
GB0525323D0 (en) * 2005-12-13 2006-01-18 Sterix Ltd Compound
CN100586932C (zh) * 2007-01-26 2010-02-03 中国医学科学院医药生物技术研究所 抗肿瘤化合物及其制备方法
GEP20156250B (en) 2009-06-26 2015-02-25 Novartis Ag 1,3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17
BR112012019551A2 (pt) * 2010-02-04 2016-08-09 Radius Health Inc moduladores seletivos do receptor de androgênio.
CA2799183A1 (en) 2010-05-12 2011-11-17 Radius Health, Inc. Therapeutic regimens
JP5998137B2 (ja) 2010-08-04 2016-09-28 ペルフィキュア ファーマシューティカルズ,インコーポレイテッド 前立腺癌を処置するための併用療法
WO2012035078A1 (en) 2010-09-16 2012-03-22 Novartis Ag 17α-HYDROXYLASE/C17,20-LYASE INHIBITORS
JP5965909B2 (ja) 2010-09-28 2016-08-10 ラジウス ヘルス,インコーポレイテッド 選択的アンドロゲン受容体モジュレーター
EA023064B1 (ru) 2011-04-28 2016-04-29 Новартис Аг ИНГИБИТОРЫ 17α-ГИДРОКСИЛАЗЫ/C-ЛИАЗЫ
WO2014158875A1 (en) 2013-03-14 2014-10-02 Pellficure Pharmaceuticals Inc. Novel therapy for prostate carcinoma
US9421264B2 (en) 2014-03-28 2016-08-23 Duke University Method of treating cancer using selective estrogen receptor modulators
HUE061499T2 (hu) 2014-03-28 2023-07-28 Univ Duke Mellrák kezelése szelektív ösztrogénreceptor-módosítók alkalmazásával
EP3191087A1 (en) 2014-09-12 2017-07-19 Pellficure Pharmaceuticals, Inc. Compositions and methods for treatment of prostate carcinoma
AU2017281038B2 (en) 2016-06-22 2021-09-09 Ellipses Pharma Ltd AR+ breast cancer treatment methods
EP3528799A1 (en) 2016-10-24 2019-08-28 Pellficure Pharmaceuticals, Inc. Pharmaceutical compositions of 5-hydroxy-2-methylnaphthalene-1, 4-dione
KR20230109795A (ko) 2017-01-05 2023-07-20 래디어스 파마슈티컬스, 인코포레이티드 Rad1901-2hcl의 다형 형태

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CS229934B2 (en) * 1981-07-07 1984-07-16 Pfizer Production method subst.indolylacryte acid derivative
GB8518743D0 (en) * 1985-07-24 1985-08-29 Glaxo Group Ltd Heterocyclic compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016515098A (ja) * 2013-02-27 2016-05-26 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company ブロモドメイン阻害剤として有用なカルバゾール化合物

Also Published As

Publication number Publication date
BG100154A (en) 1996-07-31
GB9310635D0 (en) 1993-07-07
TW279866B (fi) 1996-07-01
PL311702A1 (en) 1996-03-04
HUT73790A (en) 1996-09-30
CA2162921A1 (en) 1994-12-08
EP0699196A1 (en) 1996-03-06
CZ305195A3 (en) 1996-06-12
IL109703A0 (en) 1994-08-26
FI955587A (fi) 1995-11-20
OA10195A (en) 1996-12-18
SK142495A3 (en) 1996-06-05
PE31195A1 (es) 1995-10-18
ZA943494B (en) 1995-01-23
CN1126473A (zh) 1996-07-10
HU9503321D0 (en) 1996-01-29
FI955587A0 (fi) 1995-11-20
WO1994027989A1 (en) 1994-12-08
NO954681L (no) 1995-11-20
AU6928794A (en) 1994-12-20
NO954681D0 (no) 1995-11-20

Similar Documents

Publication Publication Date Title
JPH08510455A (ja) 17,20―リアーゼ阻害活性を有するカルバゾール誘導体
SU1574178A3 (ru) Способ получени производных 4-замещенного андростендиона, или их фармацевтически приемлемых солей
AU780989B2 (en) 3alpha-hydroxy-3beta methoxymethyl-21-heterocycle substituted steroids with anesthetic activity
JPS6383095A (ja) 4−置換6−アルキリデンアンドロステン−3,17−ジオン誘導体およびその製造方法
US5578630A (en) Heterocyclic compounds which inhibit aromatase
NO300497B1 (no) Analogifremgangsmåte for fremstilling av terapeutisk aktive benzazepin-forbindelser
WO1997026242A1 (fr) Derives de 3-(bis-phenylmethylene substitue) oxindole
JP4909889B2 (ja) 2h−又は3h−ベンゾ[e]インダゾール1−イルカルバメート誘導体、これらの調製及び治療的使用
US6689798B2 (en) Benzofuran derivatives
EP0812322A1 (en) PYRIMIDO 4,5-b]INDOLES
JPH0291074A (ja) 置換された5,6,7,8‐テトラヒドロイミダゾ[1,5‐a]ピリジン及びその製造方法
NO132201B (fi)
NO174928B (no) Analogifremgangsmåte for fremstilling av terapeutisk aktive enoletere av 6-klor-4-hydroksy-2-metyl-N-(2-pyridyl)-2H-tieno(2,3-e)-1,2-tiazin-3-karboksylsyreamid-1,1-dioksyd
JPS63101397A (ja) 1,2β−メチレン−4−置換アンドロステン−3,17−ジオン誘導体およびその製造方法
JP3252189B2 (ja) ピラゾロ〔1,5−a〕ピリミジン誘導体
US5726196A (en) Aromatase-inhibiting composition containing azole derivative
EP0574992A1 (en) 5-(1,2,4-Triazol-1-ylmethyl)-3H-isobenzofuran-1-one derivatives, their preparation and use as aromatase inhibitors
WO1991011434A1 (fr) Derive de bicyclolactame
HRP940940A2 (en) Chemical compounds
NO115111B (fi)
JPH01121274A (ja) 2−置換シクロヘプトイミダゾール誘導体、抗潰瘍剤並びにその製法
JPH0278681A (ja) 新規アルカロイドおよび該アルカロイドを有効成分とする降圧剤
JPS58146568A (ja) 新規なジベンズアゼピン−2−酢酸誘導体
JPS6061568A (ja) 新規な1位置換アミン誘導体
JPH10120632A (ja) N−シクロアルキル−〔ω−(3,4−ジヒドロ−2−ナフタレニル)アルキル〕アミン誘導体及びそれを含有する医薬組成物