JP2002533335A5 - - Google Patents

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Publication number
JP2002533335A5
JP2002533335A5 JP2000589530A JP2000589530A JP2002533335A5 JP 2002533335 A5 JP2002533335 A5 JP 2002533335A5 JP 2000589530 A JP2000589530 A JP 2000589530A JP 2000589530 A JP2000589530 A JP 2000589530A JP 2002533335 A5 JP2002533335 A5 JP 2002533335A5
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JP
Japan
Prior art keywords
alkyl
tumor cells
aryl
ring
compound
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
JP2000589530A
Other languages
English (en)
Japanese (ja)
Other versions
JP2002533335A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US1999/027938 external-priority patent/WO2000037458A1/en
Publication of JP2002533335A publication Critical patent/JP2002533335A/ja
Publication of JP2002533335A5 publication Critical patent/JP2002533335A5/ja
Pending legal-status Critical Current

Links

JP2000589530A 1998-12-18 1999-12-16 ファルネシルタンパク質トランスフェラーゼインヒビター Pending JP2002533335A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US21656098A 1998-12-18 1998-12-18
US09/216,560 1998-12-18
PCT/US1999/027938 WO2000037458A1 (en) 1998-12-18 1999-12-16 Farnesyl protein transferase inhibitors

Publications (2)

Publication Number Publication Date
JP2002533335A JP2002533335A (ja) 2002-10-08
JP2002533335A5 true JP2002533335A5 (cg-RX-API-DMAC7.html) 2007-02-08

Family

ID=22807539

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000589530A Pending JP2002533335A (ja) 1998-12-18 1999-12-16 ファルネシルタンパク質トランスフェラーゼインヒビター

Country Status (23)

Country Link
EP (1) EP1140904B1 (cg-RX-API-DMAC7.html)
JP (1) JP2002533335A (cg-RX-API-DMAC7.html)
KR (1) KR20010081115A (cg-RX-API-DMAC7.html)
CN (1) CN1285588C (cg-RX-API-DMAC7.html)
AR (1) AR021716A1 (cg-RX-API-DMAC7.html)
AT (1) ATE293622T1 (cg-RX-API-DMAC7.html)
AU (1) AU2347900A (cg-RX-API-DMAC7.html)
BR (1) BR9916328A (cg-RX-API-DMAC7.html)
CA (1) CA2354774C (cg-RX-API-DMAC7.html)
CO (1) CO5160344A1 (cg-RX-API-DMAC7.html)
CZ (1) CZ20011900A3 (cg-RX-API-DMAC7.html)
DE (1) DE69924876T2 (cg-RX-API-DMAC7.html)
ES (1) ES2237963T3 (cg-RX-API-DMAC7.html)
HU (1) HUP0203054A3 (cg-RX-API-DMAC7.html)
ID (1) ID29065A (cg-RX-API-DMAC7.html)
IL (1) IL143409A0 (cg-RX-API-DMAC7.html)
NO (1) NO20012960L (cg-RX-API-DMAC7.html)
PE (1) PE20001516A1 (cg-RX-API-DMAC7.html)
PL (1) PL348294A1 (cg-RX-API-DMAC7.html)
SK (1) SK7582001A3 (cg-RX-API-DMAC7.html)
TR (1) TR200101754T2 (cg-RX-API-DMAC7.html)
WO (1) WO2000037458A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA200104236B (cg-RX-API-DMAC7.html)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1263726B1 (en) * 1999-11-10 2007-09-26 Sanofi-Aventis Deutschland GmbH N-acylpyrrolidin-2-ylalkylbenzamidine derivatives as inhibitors of factor xa
US7361663B2 (en) 1999-11-10 2008-04-22 Aventis Pharmaceuticals Inc. N-acylpyrrolidin-2-ylalkylbenzamidine derivatives as inhibitors of factor Xa
US6589978B2 (en) 2000-06-30 2003-07-08 Hoffman-La Roche Inc. 1-sulfonyl pyrrolidine derivatives
US7342016B2 (en) 2000-08-30 2008-03-11 Schering Corporation Farnesyl protein transferase inhibitors as antitumor agents
AR033680A1 (es) * 2000-08-30 2004-01-07 Schering Corp Compuestos triciclicos utiles como inhibidores de la farnesil proteino transferasa y su uso para la manufactura de medicamentos como agentes antitumorales
US6809093B2 (en) 2000-10-17 2004-10-26 H. Lee Moffitt Cancer & Research Institute, Inc. 2-substituted heterocyclic compounds
US6376514B1 (en) 2000-10-17 2002-04-23 The Procter & Gamble Co. Substituted six-membered heterocyclic compounds useful for treating multidrug resistance and compositions and methods thereof
US6693099B2 (en) 2000-10-17 2004-02-17 The Procter & Gamble Company Substituted piperazine compounds optionally containing a quinolyl moiety for treating multidrug resistance
US6645966B2 (en) 2001-01-22 2003-11-11 Schering Corporation Treatment of malaria with farnesyl protein transferase inhibitors
EP1362039B1 (en) 2001-02-16 2005-12-21 Aventis Pharmaceuticals Inc. Heterocyclic substituted carbonyl derivatives and their use as dopamine d3 receptor ligands
WO2002080895A2 (en) * 2001-04-06 2002-10-17 Schering Corporation Treatment of malaria with farsenyl protein transferase inhibitors
FR2825705B1 (fr) * 2001-06-08 2005-05-20 Aventis Pharma Sa Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens
GB0115862D0 (en) 2001-06-28 2001-08-22 Smithkline Beecham Plc Compounds
US6740757B2 (en) * 2001-08-29 2004-05-25 Pfizer Inc Enantiomers of 6-[(4-chloro-phenyl)-hydroxy-(3-methyl-3h-imidazol-4-yl)-methyl]-4-[3-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-1-methyl-1h-quinolin-2-one and salts thereof, useful in the treatment of cancer
FR2835186B1 (fr) 2002-01-28 2006-10-20 Aventis Pharma Sa Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
FR2844273B1 (fr) 2002-09-05 2008-04-04 Aventis Pharma Sa Nouveaux composes heterocycliques, procede et intermediaires de preparation et utilisation comme medicament, notamment comme inhibiteurs de beta-lactamases et anti-bacteriens.
WO2004060488A1 (en) * 2002-12-17 2004-07-22 Schering Corporation 17 beta-hydroxysteroid dehydrogenase type 3 inhibitors for the treatment of androgen dependent diseases
JP2008523104A (ja) * 2004-12-13 2008-07-03 シェーリング コーポレイション 癌を治療するための新規なファルネシルタンパク質トランスフェラーゼ阻害剤およびその使用
CA2591123A1 (en) * 2004-12-14 2006-06-22 Schering Corporation Farnesyl protein transferase inhibitors and methods for treating proliferative diseases
EP1973882A1 (en) * 2006-01-19 2008-10-01 Schering Corporation Piperazine derivatives as farnesyl protein transferase inhibitors
US8674093B2 (en) * 2008-05-22 2014-03-18 Merck Canada Inc. Process for the preparation of an orexin receptor antagonist
HU231150B1 (hu) 2017-03-13 2021-03-29 Richter Gedeon Nyrt Eljárás racém 3-alkilpiperidin-3-karbonsav-etil-észterek optikai izomerjeinek elválasztására
CA3140170A1 (en) 2019-06-04 2020-12-10 Belew Mekonnen Imidazolo derivatives, compositions and methods as orexin antagonists
CN120590392A (zh) 2020-08-05 2025-09-05 吉瑞工厂 药理学活性的杂环取代的吡唑并[1,5-a]嘧啶衍生物
CN114349711B (zh) * 2022-02-28 2023-08-15 四川依维欣医药科技有限公司 一种(R)-1-Boc-3-羟甲基哌嗪的合成方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL111235A (en) * 1993-10-15 2001-03-19 Schering Plough Corp Medicinal preparations for inhibiting protein G activity and for the treatment of malignant diseases, containing tricyclic compounds, some such new compounds and a process for the preparation of some of them
GB9420172D0 (en) * 1994-10-06 1994-11-23 Boots Co Plc Therapeutic agents
IL117798A (en) * 1995-04-07 2001-11-25 Schering Plough Corp Tricyclic compounds useful for inhibiting the function of protein - G and for the treatment of malignant diseases, and pharmaceutical preparations containing them
AU753658B2 (en) * 1997-06-17 2002-10-24 Pharmacopeia, Inc. Benzpyrido cycloheptane compounds useful for inhibition of farnesyl protein transferase

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