JP2008074862A5 - - Google Patents

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Publication number
JP2008074862A5
JP2008074862A5 JP2007279663A JP2007279663A JP2008074862A5 JP 2008074862 A5 JP2008074862 A5 JP 2008074862A5 JP 2007279663 A JP2007279663 A JP 2007279663A JP 2007279663 A JP2007279663 A JP 2007279663A JP 2008074862 A5 JP2008074862 A5 JP 2008074862A5
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JP
Japan
Prior art keywords
alkyl
aryl
group
cycloalkyl
heteroaryl
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.)
Withdrawn
Application number
JP2007279663A
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English (en)
Japanese (ja)
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JP2008074862A (ja
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Publication date
Application filed filed Critical
Publication of JP2008074862A publication Critical patent/JP2008074862A/ja
Publication of JP2008074862A5 publication Critical patent/JP2008074862A5/ja
Withdrawn legal-status Critical Current

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JP2007279663A 2001-03-29 2007-10-26 Aidsの処置に有用なccr5アンタゴニスト Withdrawn JP2008074862A (ja)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US27993801P 2001-03-29 2001-03-29

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2002577819A Division JP4248251B2 (ja) 2001-03-29 2002-03-27 Aidsの処置に有用なccr5アンタゴニスト

Publications (2)

Publication Number Publication Date
JP2008074862A JP2008074862A (ja) 2008-04-03
JP2008074862A5 true JP2008074862A5 (https=) 2009-01-15

Family

ID=23070981

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2002577819A Expired - Fee Related JP4248251B2 (ja) 2001-03-29 2002-03-27 Aidsの処置に有用なccr5アンタゴニスト
JP2007279663A Withdrawn JP2008074862A (ja) 2001-03-29 2007-10-26 Aidsの処置に有用なccr5アンタゴニスト

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2002577819A Expired - Fee Related JP4248251B2 (ja) 2001-03-29 2002-03-27 Aidsの処置に有用なccr5アンタゴニスト

Country Status (29)

Country Link
US (5) US6720325B2 (https=)
EP (2) EP1373256B1 (https=)
JP (2) JP4248251B2 (https=)
KR (1) KR100613528B1 (https=)
CN (1) CN100519554C (https=)
AR (1) AR033452A1 (https=)
AT (2) ATE299139T1 (https=)
AU (1) AU2002255947B8 (https=)
BR (1) BR0208398A (https=)
CA (1) CA2442227C (https=)
CZ (1) CZ20032636A3 (https=)
DE (2) DE60204951T2 (https=)
DK (1) DK1373256T3 (https=)
ES (2) ES2242856T3 (https=)
HU (1) HUP0400349A3 (https=)
IL (1) IL157551A0 (https=)
MX (1) MXPA03008853A (https=)
MY (1) MY128609A (https=)
NO (1) NO326349B1 (https=)
NZ (1) NZ527768A (https=)
PE (1) PE20020996A1 (https=)
PL (1) PL364560A1 (https=)
PT (1) PT1373256E (https=)
RU (1) RU2316553C2 (https=)
SI (1) SI1373256T1 (https=)
SK (1) SK287521B6 (https=)
TW (1) TWI237638B (https=)
WO (1) WO2002079194A1 (https=)
ZA (1) ZA200307474B (https=)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR033452A1 (es) * 2001-03-29 2003-12-17 Schering Corp Antagonistas de ccr5 utiles para el tratamiento del sida
ATE319703T1 (de) 2001-07-02 2006-03-15 Piperidinverbindungen, die sich als modulatoren der chemokinrezeptoraktivität eignen
SE0200843D0 (sv) 2002-03-19 2002-03-19 Astrazeneca Ab Chemical compounds
SE0200844D0 (sv) 2002-03-19 2002-03-19 Astrazeneca Ab Chemical compounds
TW200504033A (en) 2002-10-23 2005-02-01 Procter & Gamble Melanocortin receptor ligands
AU2003300911A1 (en) * 2002-12-13 2004-07-09 Smithkline Beecham Corporation Heterocyclic compounds as ccr5 antagonists
PE20040769A1 (es) * 2002-12-18 2004-11-06 Schering Corp Derivados de piperidina utiles como antagonisas ccr5
SE0300957D0 (sv) 2003-04-01 2003-04-01 Astrazeneca Ab Chemical compounds
KR20060100409A (ko) * 2003-11-03 2006-09-20 쉐링 코포레이션 케모킨 수용체 억제제로서 유용한 비피페리디닐 유도체
CA2554465A1 (en) * 2004-02-05 2005-08-25 Schering Corporation Piperidine derivatives useful as ccr3 antagonists
SE0400925D0 (sv) * 2004-04-06 2004-04-06 Astrazeneca Ab Chemical compounds
EA015517B1 (ru) * 2004-04-13 2011-08-30 Инсайт Корпорейшн Производные пиперазинилпиперидина в качестве антагонистов хемокинового рецептора
US8143404B2 (en) * 2004-09-13 2012-03-27 Ono Pharmaceutical Co., Ltd Nitrogenous heterocylic derivative and medicine containing the same as an active ingredient
WO2006071958A1 (en) 2004-12-29 2006-07-06 Millennium Pharmaceuticals, Inc. Compounds useful as chemokine receptor antagonists
WO2006071875A1 (en) * 2004-12-29 2006-07-06 Millennium Pharmaceuticals, Inc. Compounds useful as chemokine receptor antagonists
SG158861A1 (en) * 2005-01-06 2010-02-26 Schering Corp Synthesis of ccr5 receptor antagonists
JP2008526862A (ja) * 2005-01-06 2008-07-24 シェーリング コーポレイション ピペラジン化合物の薬学的な塩の調製
JP4822367B2 (ja) * 2005-02-23 2011-11-24 シェーリング コーポレイション ケモカイン受容体のインヒビターとして有用なピペリジニルピペリジン誘導体
EP1858887A1 (en) * 2005-02-23 2007-11-28 Schering Corporation Piperidinyl piperazine derivatives useful as inhibitors of chemokine receptors
JP2009501793A (ja) 2005-07-21 2009-01-22 アストラゼネカ・アクチエボラーグ 新規ピペリジン誘導体
US7462485B2 (en) * 2005-10-07 2008-12-09 Glaser Lawrence F Modified erythrocytes and uses thereof
TW200745087A (en) * 2006-02-24 2007-12-16 Schering Corp CCR5 antagonists useful for treating HIV
WO2008030853A2 (en) * 2006-09-06 2008-03-13 Incyte Corporation Combination therapy for human immunodeficiency virus infection
CA2673233A1 (en) * 2006-12-22 2008-07-03 Schering Corporation Process for preparing ccr-5 receptor antagonists utilizing 4-substituted 1-cyclopropane-sulfonyl-piperidinyl compounds
CA2716838C (en) * 2008-02-29 2014-01-07 Schering Corporation Ccr5 antagonists as prophylactics for preventing hiv infection and methods of inhibiting transmission of same
US11629196B2 (en) 2020-04-27 2023-04-18 Incelldx, Inc. Method of treating SARS-CoV-2-associated hypercytokinemia by administering a human monoclonal antibody (PRO-140) that inhibits CCR5/CCL5 binding interactions

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5368854A (en) 1992-08-20 1994-11-29 Schering Corporation Use of IL-10 to treat inflammatory bowel disease
WO1994018192A1 (en) 1993-02-12 1994-08-18 Merck & Co., Inc. Piperazine derivatives as hiv protease inhibitors
IL117149A0 (en) 1995-02-23 1996-06-18 Schering Corp Muscarinic antagonists
US5889006A (en) 1995-02-23 1999-03-30 Schering Corporation Muscarinic antagonists
EP1103276B1 (en) 1995-06-07 2003-09-10 Kimberly-Clark Worldwide, Inc. Inhibition of exoprotein in absorbent article
NZ321575A (en) 1995-10-30 1999-05-28 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4- substituted piperazine derivatives
TW531537B (en) 1995-12-27 2003-05-11 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4-substituted piperidine derivatives
US5952349A (en) 1996-07-10 1999-09-14 Schering Corporation Muscarinic antagonists for treating memory loss
US5977138A (en) 1996-08-15 1999-11-02 Schering Corporation Ether muscarinic antagonists
CA2296314A1 (en) 1997-07-25 1999-02-04 Merck & Co., Inc. Cyclic amine modulators of chemokine receptor activity
US6066636A (en) 1998-06-30 2000-05-23 Schering Corporation Muscarinic antagonists
EP1013276A1 (en) * 1998-12-23 2000-06-28 Pfizer Inc. Aminoazacycloalkanes as CCR5 modulators
KR100439357B1 (ko) * 1999-05-04 2004-07-07 쉐링 코포레이션 Ccr5 길항제로서 유용한 피페리딘 유도체
SK287418B6 (sk) 1999-05-04 2010-09-07 Schering Corporation Farmaceutický prípravok s obsahom CCR5 antagonistov a súprava s obsahom tohto prípravku
AR033452A1 (es) * 2001-03-29 2003-12-17 Schering Corp Antagonistas de ccr5 utiles para el tratamiento del sida

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