NO20004281L - 6,9-disubstituerte 2-[trans-(4-aminocykloheksyl)amino]puriner, farmasoytisk preparat inneholdende disse, og anvendelse derav for fremstilling av et medikament - Google Patents

6,9-disubstituerte 2-[trans-(4-aminocykloheksyl)amino]puriner, farmasoytisk preparat inneholdende disse, og anvendelse derav for fremstilling av et medikament

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Publication number
NO20004281L
NO20004281L NO20004281A NO20004281A NO20004281L NO 20004281 L NO20004281 L NO 20004281L NO 20004281 A NO20004281 A NO 20004281A NO 20004281 A NO20004281 A NO 20004281A NO 20004281 L NO20004281 L NO 20004281L
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NO
Norway
Prior art keywords
present
provides
group
alkyl
formula
Prior art date
Application number
NO20004281A
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English (en)
Other versions
NO20004281D0 (no
Inventor
Jennifer Ann Dumont
Alan Joseph Bitonti
David Roger Borcherding
Harry Randall Munson
Patrick Wai-Kwok Shum
Norton Paul Peet
Original Assignee
Aventis Holdings Inc
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.)
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Publication date
Application filed by Aventis Holdings Inc filed Critical Aventis Holdings Inc
Publication of NO20004281D0 publication Critical patent/NO20004281D0/no
Publication of NO20004281L publication Critical patent/NO20004281L/no

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/16Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Foreliggende oppfinnelse tilveiebringer nye forbindelser av formel (I). hvori R er valgt fra gruppen bestående av R, RNH-, eller HN-R- hvori Rer valgt fra gruppen bestående av C^-C,-alkyl og formel (II). hvori Z er valgt fra gruppen bestående av fenyl, heterosyklus og sykloalkyl, hver Rer uavhengig hydrogen eller C-C-alkyl, og n er et helt tall på 1-8;. hvori hver C-C-alkyl og Z eventuelt er substituert med 1 til 3 substituenter som kan være like eller forskjellige, valgt fra gruppen bestående av Hal, OH og Cj-C-alkyl; Rer q-C-alkylen; og R,, er valgt fra gruppen bestående av syklopentyl og isopropyl, og farmasøyt-isk akseptable salter, optiske isbmerer • og hydrater derav. I tillegg tilveiebringer foreliggende oppfinnelse en metode for inhibering av cellesyklus-progresjon. Mer spesifikt tilveiebringer foreliggende oppfinnelse en metode for inhibering av syklinav-hengige kinaser, i særdeleshet cdk-2. Foreliggende oppfinnelse tilveiebringer også en metode for forhindring av apoptose i neuronalceller og en metode for inhibering av utviklingen a-v neo-plasmer. I tillegg tilveiebringer foreliggende oppfinnelse et preparat, omfattende en målbar mengde av efor-. bindelse av formel (I) i blanding eller på annen måte i assosiasjon med en inert bærer. Foreliggende oppfinnelse tilveiebringer også et farmasøytisk preparat omfattende en effektiv inhi-berende mengde av en forbindelse av formel (I), i blanding eller på annen måte i assosiasjon med én eller flére farmasøytisk akseptable bærere eller eksipienser.
NO20004281A 1998-02-26 2000-08-25 6,9-disubstituerte 2-[trans-(4-aminocykloheksyl)amino]puriner, farmasoytisk preparat inneholdende disse, og anvendelse derav for fremstilling av et medikament NO20004281L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US3238198A 1998-02-26 1998-02-26
PCT/US1999/003451 WO1999043676A2 (en) 1998-02-26 1999-02-18 6,9-disubstituted 2-[trans-(4- aminocyclohexyl) amino]purines

Publications (2)

Publication Number Publication Date
NO20004281D0 NO20004281D0 (no) 2000-08-25
NO20004281L true NO20004281L (no) 2000-10-18

Family

ID=21864658

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20004281A NO20004281L (no) 1998-02-26 2000-08-25 6,9-disubstituerte 2-[trans-(4-aminocykloheksyl)amino]puriner, farmasoytisk preparat inneholdende disse, og anvendelse derav for fremstilling av et medikament

Country Status (30)

Country Link
EP (1) EP1056745B1 (no)
JP (1) JP2002504553A (no)
KR (1) KR100568658B1 (no)
CN (1) CN1128149C (no)
AP (1) AP1258A (no)
AR (1) AR019822A1 (no)
AT (1) ATE269332T1 (no)
AU (1) AU748178B2 (no)
BR (1) BR9908325A (no)
CA (1) CA2320448C (no)
CZ (1) CZ291604B6 (no)
DE (1) DE69918062T2 (no)
DK (1) DK1056745T3 (no)
EE (1) EE04315B1 (no)
ES (1) ES2219038T3 (no)
HU (1) HUP0100931A3 (no)
IL (2) IL138044A0 (no)
NO (1) NO20004281L (no)
NZ (1) NZ506234A (no)
OA (1) OA11480A (no)
PL (1) PL344021A1 (no)
PT (1) PT1056745E (no)
RU (1) RU2191777C2 (no)
SI (1) SI1056745T1 (no)
SK (1) SK12912000A3 (no)
TR (1) TR200002482T2 (no)
TW (1) TW541308B (no)
UA (1) UA62996C2 (no)
WO (1) WO1999043676A2 (no)
ZA (1) ZA991548B (no)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6969720B2 (en) 1999-03-17 2005-11-29 Amr Technology, Inc. Biaryl substituted purine derivatives as potent antiproliferative agents
US6627633B2 (en) * 1999-03-17 2003-09-30 Albany Molecular Research, Inc. 6-substituted biaryl purine derivatives as potent cyclin/CDK inhibitors and antiproliferative agents
US20030187261A1 (en) * 2000-01-07 2003-10-02 Libor Havlicek Purine derivatives, process for their preparation and use thereof
YU54202A (sh) 2000-01-18 2006-01-16 Agouron Pharmaceuticals Inc. Jedinjenja indazola, farmaceutske smeše i postupci za stimulisanje i inhibiranje ćelijske proliferacije
HN2001000008A (es) 2000-01-21 2003-12-11 Inc Agouron Pharmaceuticals Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo
FR2806626B1 (fr) * 2000-03-22 2003-11-28 Centre Nat Rech Scient Utilisation de substances modulatrices de l'expression ou de la fonction d'une proteine impliquee dans le cycle cellulaire pour le traitement ou la prevention des lesions neurales aigues
JP2004501083A (ja) 2000-04-18 2004-01-15 アゴーロン・ファーマシューティカルズ・インコーポレイテッド プロテインキナーゼを阻害するためのピラゾール
JP2004505983A (ja) 2000-08-09 2004-02-26 アグーロン ファーマシューティカルズ,インコーポレイテッド ピラゾール−チアゾール化合物、これらを含む医薬組成物、およびサイクリン依存性キナーゼの阻害のためのこれらの使用方法
CA2411924A1 (en) 2000-08-18 2002-02-28 Agouron Pharmaceuticals, Inc. Heterocyclic-hydroxyimino-fluorenes and their use for inhibiting proteinkinases
ATE426603T1 (de) * 2000-10-31 2009-04-15 Aventis Pharma Inc Acyl- und sulfonylderivative 6,9- disubstitutierter 2-(trans-1,4-diaminocyclohexyl)-purine und ihre verwendung als antiproliferative mittel
GB0117075D0 (en) * 2000-10-31 2001-09-05 Aventis Pharm Prod Inc Acyl and sulfonyl derivatives of 6, 9-distributed 2-(trans-1, 4-diaminocyclohexyl)-purines and their use as antiproliferative agents
US6756374B2 (en) 2001-01-22 2004-06-29 Hoffmann-La Roche Inc. Diaminothiazoles having antiproliferative activity
WO2003002565A1 (en) * 2001-06-27 2003-01-09 Cyclacel Limited 2,6,9-substituted purine derivatives and their use n the treatment of proliferative disorders
US6667311B2 (en) 2001-09-11 2003-12-23 Albany Molecular Research, Inc. Nitrogen substituted biaryl purine derivatives as potent antiproliferative agents
US6812232B2 (en) 2001-09-11 2004-11-02 Amr Technology, Inc. Heterocycle substituted purine derivatives as potent antiproliferative agents
GB0219052D0 (en) 2002-08-15 2002-09-25 Cyclacel Ltd New puring derivatives
GB0219054D0 (en) 2002-08-15 2002-09-25 Cyclacel Ltd New purine derivatives
EP1591112A4 (en) * 2003-02-04 2006-06-14 Yakult Honsha Kk BREAST CANCER RESISTANT PROTEIN INHIBITOR
US7211576B2 (en) 2004-04-20 2007-05-01 Hoffmann-La Roche Inc. Diaminothiazoles
RU2462246C2 (ru) * 2006-03-30 2012-09-27 ПиТиСи ТЕРАПЬЮТИКС, ИНК. Способы получения функционального белка из днк, имеющей нонсенс-мутацию, и лечения нарушений, ассоциированных с ней
CN104119336B (zh) * 2007-10-05 2016-08-24 维拉斯通股份有限公司 嘧啶取代的嘌呤衍生物
CN102241646B (zh) * 2010-05-14 2014-04-09 中国人民解放军军事医学科学院毒物药物研究所 己烯酮类化合物及其医药用途
WO2013130461A1 (en) 2012-02-29 2013-09-06 The Scripps Research Institute Wee1 degradation inhibitors
WO2015005491A1 (ja) * 2013-07-12 2015-01-15 国立大学法人京都大学 疾病の発症又は進行の一因となる異常スプライシングを抑制できる物質のスクリーニング方法
PL3244891T3 (pl) 2015-01-16 2022-12-27 The General Hospital Corporation Związki poprawiające splicing mRNA
CN107903274A (zh) * 2017-12-28 2018-04-13 窦玉玲 一种胺类化合物及其在抗肿瘤药物中的应用
WO2021016263A1 (en) * 2019-07-21 2021-01-28 University Of Virginia Patent Foundation Cysteine binding compositions and methods of use thereof
WO2024105159A1 (en) * 2022-11-16 2024-05-23 University Of Zurich Ligands of the m6a-rna readers

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9301000D0 (en) * 1993-01-20 1993-03-10 Glaxo Group Ltd Chemical compounds
GB9414208D0 (en) * 1994-07-14 1994-08-31 Glaxo Group Ltd Compounds
DE69627195T2 (de) * 1995-11-01 2004-01-29 Novartis Ag Purinderivate und verfahren zu ihrer herstellung
FR2741881B1 (fr) * 1995-12-01 1999-07-30 Centre Nat Rech Scient Nouveaux derives de purine possedant notamment des prorietes anti-proliferatives et leurs applications biologiques

Also Published As

Publication number Publication date
OA11480A (en) 2004-05-05
ES2219038T3 (es) 2004-11-16
EP1056745B1 (en) 2004-06-16
CZ20003106A3 (cs) 2000-12-13
DK1056745T3 (da) 2004-10-25
CN1128149C (zh) 2003-11-19
AU748178B2 (en) 2002-05-30
SK12912000A3 (sk) 2001-08-06
WO1999043676A2 (en) 1999-09-02
CA2320448C (en) 2005-02-01
AP2000001923A0 (en) 2000-09-30
AP1258A (en) 2004-03-15
IL138044A (en) 2006-04-10
WO1999043676A3 (en) 1999-10-21
PT1056745E (pt) 2004-09-30
AR019822A1 (es) 2002-03-20
CN1291983A (zh) 2001-04-18
PL344021A1 (en) 2001-09-24
KR100568658B1 (ko) 2006-04-07
HUP0100931A3 (en) 2002-08-28
NO20004281D0 (no) 2000-08-25
AU3299099A (en) 1999-09-15
CZ291604B6 (cs) 2003-04-16
EP1056745A2 (en) 2000-12-06
TR200002482T2 (tr) 2002-10-21
JP2002504553A (ja) 2002-02-12
HUP0100931A2 (hu) 2002-04-29
IL138044A0 (en) 2001-10-31
DE69918062T2 (de) 2005-06-02
BR9908325A (pt) 2000-11-07
DE69918062D1 (de) 2004-07-22
SI1056745T1 (en) 2004-12-31
EE200000501A (et) 2002-02-15
HK1030948A1 (en) 2001-05-25
KR20010041315A (ko) 2001-05-15
ZA991548B (en) 1999-08-26
EE04315B1 (et) 2004-06-15
CA2320448A1 (en) 1999-09-02
RU2191777C2 (ru) 2002-10-27
NZ506234A (en) 2003-05-30
ATE269332T1 (de) 2004-07-15
UA62996C2 (en) 2004-01-15
TW541308B (en) 2003-07-11

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