JP2002501054A5 - - Google Patents

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Publication number
JP2002501054A5
JP2002501054A5 JP2000528545A JP2000528545A JP2002501054A5 JP 2002501054 A5 JP2002501054 A5 JP 2002501054A5 JP 2000528545 A JP2000528545 A JP 2000528545A JP 2000528545 A JP2000528545 A JP 2000528545A JP 2002501054 A5 JP2002501054 A5 JP 2002501054A5
Authority
JP
Japan
Prior art keywords
alkyl
aryl
heteroaryl
group
formula
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.)
Abandoned
Application number
JP2000528545A
Other languages
English (en)
Japanese (ja)
Other versions
JP2002501054A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP1999/000242 external-priority patent/WO1999037621A1/en
Publication of JP2002501054A publication Critical patent/JP2002501054A/ja
Publication of JP2002501054A5 publication Critical patent/JP2002501054A5/ja
Abandoned legal-status Critical Current

Links

JP2000528545A 1998-01-23 1999-01-16 骨吸収の阻害剤として及び細胞接着の阻害剤としての新規のスルホンアミド誘導体 Abandoned JP2002501054A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US1248998A 1998-01-23 1998-01-23
US09/012,489 1998-01-23
PCT/EP1999/000242 WO1999037621A1 (en) 1998-01-23 1999-01-16 Novel sulfonamide derivatives as inhibitors of bone resorption and as inhibitors of cell adhesion

Publications (2)

Publication Number Publication Date
JP2002501054A JP2002501054A (ja) 2002-01-15
JP2002501054A5 true JP2002501054A5 (enExample) 2006-03-02

Family

ID=21755208

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000528545A Abandoned JP2002501054A (ja) 1998-01-23 1999-01-16 骨吸収の阻害剤として及び細胞接着の阻害剤としての新規のスルホンアミド誘導体

Country Status (25)

Country Link
EP (1) EP1049677A1 (enExample)
JP (1) JP2002501054A (enExample)
KR (1) KR20010034319A (enExample)
CN (1) CN1177832C (enExample)
AP (1) AP1269A (enExample)
AR (1) AR014456A1 (enExample)
AU (1) AU752882B2 (enExample)
BG (1) BG104630A (enExample)
BR (1) BR9907735A (enExample)
CA (1) CA2318221A1 (enExample)
EA (1) EA003102B1 (enExample)
HR (1) HRP20000493A2 (enExample)
HU (1) HUP0100520A3 (enExample)
ID (1) ID26219A (enExample)
IL (1) IL137423A0 (enExample)
NO (1) NO318795B1 (enExample)
NZ (1) NZ505613A (enExample)
PL (1) PL341871A1 (enExample)
SK (1) SK10632000A3 (enExample)
TR (1) TR200002160T2 (enExample)
TW (1) TWI247742B (enExample)
UA (1) UA63990C2 (enExample)
WO (1) WO1999037621A1 (enExample)
YU (1) YU47200A (enExample)
ZA (1) ZA99476B (enExample)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000006169A1 (en) * 1998-07-29 2000-02-10 Merck & Co., Inc. Integrin receptor antagonists
EP1028114A1 (en) 1999-02-13 2000-08-16 Aventis Pharma Deutschland GmbH Novel guanidine derivatives as inhibitors of cell adhesion
EP1065208A1 (en) * 1999-07-02 2001-01-03 Aventis Pharma Deutschland GmbH Substituted purine derivatives as inhibitors of cell adhesion
EP1065207A1 (en) * 1999-07-02 2001-01-03 Aventis Pharma Deutschland GmbH Naphthyridine derivatives, processes for their preparation, their use, and pharmaceutical compositions comprising them
EP1070707A1 (en) * 1999-07-21 2001-01-24 Aventis Pharma Deutschland GmbH 1,4,5,6-tetrahydropyrimidine derivative as a vitronectin inhibitor
US6849639B2 (en) 1999-12-14 2005-02-01 Amgen Inc. Integrin inhibitors and their methods of use
EP1108721A1 (en) 1999-12-15 2001-06-20 Aventis Pharma Deutschland GmbH Thienylalanine derivatives as inhibitors of cell adhesion
WO2001047874A1 (en) * 1999-12-24 2001-07-05 Smithkline Beecham P.L.C. (hetero)bicyclymethanesulfonylamino-substituted hydroxamic acid derivatives
FR2808798A1 (fr) * 2000-05-09 2001-11-16 Hoechst Marion Roussel Inc Nouveaux derives antagonistes du recepteur de la vitronectine
FR2847254B1 (fr) 2002-11-19 2005-01-28 Aventis Pharma Sa Nouveaux derives antagonistes du recepteur de la vitronectine, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les refermant
AU2005223356B2 (en) * 2004-03-24 2012-05-17 Takeda Pharmaceutical Company Limited New compounds for the inhibition of angiogenesis and use of thereof
FR2870541B1 (fr) 2004-05-18 2006-07-14 Proskelia Sas Derives de pyrimidines antigonistes du recepteur de la vitronectine
GB0412553D0 (en) * 2004-06-04 2004-07-07 Univ Aberdeen Therapeutic agents for the treatment of bone conditions
UA87854C2 (en) 2004-06-07 2009-08-25 Мерк Энд Ко., Инк. N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators
FR2873585B1 (fr) * 2004-07-27 2006-11-17 Aventis Pharma Sa Nouvelles formulations galeniques de principes actifs
GB0705400D0 (en) 2007-03-21 2007-05-02 Univ Aberdeen Therapeutic compounds andm their use
GB0817207D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd therapeutic apsac compounds and their use
GB0817208D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd Therapeutic apsap compounds and their use
GB201311361D0 (en) 2013-06-26 2013-08-14 Pimco 2664 Ltd Compounds and their therapeutic use
JP6649902B2 (ja) 2014-05-30 2020-02-19 ファイザー・インク 選択的アンドロゲン受容体モジュレーターとしてのカルボニトリル誘導体
ES2899852T3 (es) 2014-12-17 2022-03-15 Pimco 2664 Ltd Compuestos de N-(4-hidroxi-4-metil-ciclohexil)-4-fenil-bencenosulfonamida y N-(-4-hidroxi-4-metil-ciclohexil)-4-(2-piridil)-bencenosulfonamida y su uso terapéutico
WO2023275715A1 (en) 2021-06-30 2023-01-05 Pfizer Inc. Metabolites of selective androgen receptor modulators

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10501222A (ja) * 1994-05-27 1998-02-03 メルク エンド カンパニー インコーポレーテッド 破骨細胞仲介骨吸収を抑制するための化合物
JP3895792B2 (ja) * 1995-12-08 2007-03-22 プロスケリア・エス・ア・エス 骨形成促進剤

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