NO311083B1 - Nye cykloalkylderivater, fremgangsmåte for fremstilling derav, farmasöytiske preparater inneholdende forbindelsene samtanvendelse av forbindelsene - Google Patents

Nye cykloalkylderivater, fremgangsmåte for fremstilling derav, farmasöytiske preparater inneholdende forbindelsene samtanvendelse av forbindelsene Download PDF

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Publication number
NO311083B1
NO311083B1 NO19973399A NO973399A NO311083B1 NO 311083 B1 NO311083 B1 NO 311083B1 NO 19973399 A NO19973399 A NO 19973399A NO 973399 A NO973399 A NO 973399A NO 311083 B1 NO311083 B1 NO 311083B1
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NO
Norway
Prior art keywords
formula
cell
compound
prophylaxis
acceptable salts
Prior art date
Application number
NO19973399A
Other languages
English (en)
Norwegian (no)
Other versions
NO973399L (no
NO973399D0 (no
Inventor
Volkmar Wehner
Jochen Knolle
Hans Ulrich Stilz
Jean-Francois Gourvest
Denis Carniato
Thomas Richard Gadek
Robert Mcdowell
Robert Maurice Pitti
Sarah Catherine Bodary
Original Assignee
Genentech 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.)
Filing date
Publication date
Application filed by Genentech Inc filed Critical Genentech Inc
Publication of NO973399D0 publication Critical patent/NO973399D0/no
Publication of NO973399L publication Critical patent/NO973399L/no
Publication of NO311083B1 publication Critical patent/NO311083B1/no

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C277/00Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • C07C277/08Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups of substituted guanidines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C279/00Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • C07C279/20Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/44Nitrogen atoms not forming part of a nitro radical
    • C07D233/48Nitrogen atoms not forming part of a nitro radical with acyclic hydrocarbon or substituted acyclic hydrocarbon radicals, attached to said nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/06Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D239/08Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms directly attached in position 2
    • C07D239/12Nitrogen atoms not forming part of a nitro radical
    • C07D239/16Nitrogen atoms not forming part of a nitro radical acylated on said nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/56Ring systems containing bridged rings
    • C07C2603/58Ring systems containing bridged rings containing three rings
    • C07C2603/70Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74Adamantanes
NO19973399A 1996-07-24 1997-07-23 Nye cykloalkylderivater, fremgangsmåte for fremstilling derav, farmasöytiske preparater inneholdende forbindelsene samtanvendelse av forbindelsene NO311083B1 (no)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19629816A DE19629816A1 (de) 1996-07-24 1996-07-24 Neue Cycloalkyl-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten

Publications (3)

Publication Number Publication Date
NO973399D0 NO973399D0 (no) 1997-07-23
NO973399L NO973399L (no) 1998-01-26
NO311083B1 true NO311083B1 (no) 2001-10-08

Family

ID=7800671

Family Applications (1)

Application Number Title Priority Date Filing Date
NO19973399A NO311083B1 (no) 1996-07-24 1997-07-23 Nye cykloalkylderivater, fremgangsmåte for fremstilling derav, farmasöytiske preparater inneholdende forbindelsene samtanvendelse av forbindelsene

Country Status (24)

Country Link
US (3) US6399620B1 (fr)
EP (1) EP0820991B1 (fr)
JP (1) JP4077535B2 (fr)
KR (1) KR100541172B1 (fr)
CN (1) CN1064352C (fr)
AR (1) AR007961A1 (fr)
AT (1) ATE371650T1 (fr)
AU (1) AU726376B2 (fr)
BR (1) BR9704072A (fr)
CA (1) CA2211270C (fr)
CZ (1) CZ234397A3 (fr)
DE (2) DE19629816A1 (fr)
HK (1) HK1006779A1 (fr)
HR (1) HRP970404A2 (fr)
HU (1) HUP9701264A3 (fr)
ID (1) ID17615A (fr)
IL (1) IL121359A0 (fr)
NO (1) NO311083B1 (fr)
NZ (1) NZ328388A (fr)
PL (1) PL189189B1 (fr)
RU (1) RU2180331C2 (fr)
SK (1) SK100597A3 (fr)
TW (1) TW490461B (fr)
ZA (1) ZA976532B (fr)

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DE19629816A1 (de) 1996-07-24 1998-01-29 Hoechst Ag Neue Cycloalkyl-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten
US6482821B2 (en) 1996-12-20 2002-11-19 Hoechst Aktiengellschaft Vitronectin receptor antagonists, their preparation and their use
DE19653647A1 (de) * 1996-12-20 1998-06-25 Hoechst Ag Vitronectin - Rezeptorantagonisten, deren Herstellung sowie deren Verwendung
US6218387B1 (en) 1996-12-20 2001-04-17 Hoechst Aktiengesellschaft Vitronectin receptor anatagonists, their preparation and their use
DE19653645A1 (de) * 1996-12-20 1998-06-25 Hoechst Ag Vitronectin - Rezeptorantagonisten, deren Herstellung sowie deren Verwendung
US6313119B1 (en) 1998-01-23 2001-11-06 Adventis Pharma Deutschland Gmbh Sulfonamide derivatives as inhibitors of bone resorption and as inhibitors of cell adhesion
WO1999052872A1 (fr) 1998-04-09 1999-10-21 Meiji Seika Kaisha, Ltd. DERIVES D'AMINOPIPERIDINE COMME ANTAGONISTES D'INTEGRINE αvβ¿3?
US6689754B1 (en) 1998-04-10 2004-02-10 G. D. Searle & Co. Heterocyclic glycyl β-alanine derivatives
NZ507292A (en) * 1998-04-10 2003-12-19 G Heterocyclic glycyl beta-alanine derivatives useful as vitronectin antagonists
AU3561099A (en) * 1998-04-14 1999-11-01 American Home Products Corporation Acylresorcinol derivatives as selective vitronectin receptor inhibitors
EP0960882A1 (fr) * 1998-05-19 1999-12-01 Hoechst Marion Roussel Deutschland GmbH Acylguanidines de thienyl et leur utilisation comme inhibiteurs de la résorptionosseuse et comme antagonistes du récepteur de la vitronectine
DE19842415A1 (de) 1998-09-16 2000-03-23 Merck Patent Gmbh Pharmazeutische Zubereitung
FR2786184B1 (fr) * 1998-11-24 2002-09-20 Hoechst Marion Roussel Inc Nouveaux derives du benzofurane, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant
FR2786182B1 (fr) * 1998-11-24 2001-01-12 Hoechst Marion Roussel Inc Nouveaux derives d'acylguanidines, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant
AU2713600A (en) 1998-12-23 2000-07-31 G.D. Searle & Co. Use of a matrix metalloproteinase inhibitor and an integrin antagonist in the treatment of neoplasia
EP1028114A1 (fr) * 1999-02-13 2000-08-16 Aventis Pharma Deutschland GmbH Nouveaux dérivés de guanidine et leur utilisation comme inhibiteurs de l'adhésion des cellules
US6455734B1 (en) 2000-08-09 2002-09-24 Magnesium Diagnostics, Inc. Antagonists of the magnesium binding defect as therapeutic agents and methods for treatment of abnormal physiological states
JP2003505416A (ja) * 1999-07-21 2003-02-12 ワイス αvβ3インテグリンに対して選択的な二環式拮抗薬
AU777634B2 (en) * 1999-07-28 2004-10-28 Kazuhiro Aoki Methods of inhibiting osteoclastogenesis
EP1209152A4 (fr) 1999-08-05 2003-03-12 Meiji Seika Kaisha Derives d'acide omega-amino-alpha-hydroxycarboxylique possedant un antagonisme alpha v beta 3 d'integrine
EP1108721A1 (fr) * 1999-12-15 2001-06-20 Aventis Pharma Deutschland GmbH Dérivés de thiénylalanine comme inhibiteurs de l'adhésion cellulaire
FR2808798A1 (fr) * 2000-05-09 2001-11-16 Hoechst Marion Roussel Inc Nouveaux derives antagonistes du recepteur de la vitronectine
EP1197488A1 (fr) * 2000-10-10 2002-04-17 Aventis Pharma Deutschland GmbH Ester isopropylique de l' acide (2s)-2-(adamantyl1-méthoxycarbonylamino)-3-(4-(2-(1,4,5,6-tétrahydropyrimidin-2-ylcarbamoyl)éthyl)benzoylamino)propionique, sa préparation et son usage
KR20100054884A (ko) 2001-10-22 2010-05-25 더 스크립스 리서치 인스티튜트 항체 표적화 화합물
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
DK1730119T3 (da) * 2004-03-23 2008-08-11 Pfizer Prod Inc Imidazolforbindelser til behandling af neurodegenerative forstyrrelser
FR2870541B1 (fr) 2004-05-18 2006-07-14 Proskelia Sas Derives de pyrimidines antigonistes du recepteur de la vitronectine
UA87854C2 (en) 2004-06-07 2009-08-25 Мерк Энд Ко., Инк. N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators
AU2006293619A1 (en) * 2005-09-22 2007-03-29 Pfizer Products Inc. Imidazole compounds for the treatment of neurological disorders
JP2009512443A (ja) * 2005-10-20 2009-03-26 ザ スクリップス リサーチ インスチチュート 免疫染色及び免疫標的化のためのFc標識化
US8518927B2 (en) 2009-02-10 2013-08-27 The Scripps Research Institute Chemically programmed vaccination
RU2016146826A (ru) 2014-05-30 2018-07-04 Пфайзер Инк. Производные карбонитрилов как селективные модуляторы андрогенового рецептора
EP3509590A4 (fr) 2016-09-07 2020-12-02 Pliant Therapeutics, Inc. Composés d'acides aminés n-acyle et méthodes d'utilisation
WO2023275715A1 (fr) 2021-06-30 2023-01-05 Pfizer Inc. Métabolites de modulateurs sélectifs du récepteur des androgènes

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JPH04367367A (ja) 1991-06-11 1992-12-18 Nkk Corp ロータリノズル
US5217994A (en) * 1991-08-09 1993-06-08 Merck & Co., Inc. Method of inhibiting osteoclast-mediated bone resorption by administration of aminoalkyl-substituted phenyl derivatives
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CA2144762A1 (fr) * 1992-10-14 1994-04-28 George D. Hartman Antagonistes des recepteurs du fibrinogene
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CZ382496A3 (en) * 1994-06-29 1997-12-17 Smithkline Beecham Corp Compounds representing antagonists of vitronectin receptors, process of their preparation, intermediates of such process, pharmaceutical composition containing the compounds and their use
WO1996000574A1 (fr) * 1994-06-29 1996-01-11 Smithkline Beecham Corporation Antagonistes du recepteur de la vibronectine
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DE19629817A1 (de) * 1996-07-24 1998-01-29 Hoechst Ag Neue Imino-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten
DE19629816A1 (de) 1996-07-24 1998-01-29 Hoechst Ag Neue Cycloalkyl-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten
CA2277273C (fr) 1997-01-17 2008-03-25 Merck & Co., Inc. Antagonistes d'integrine
US6017925A (en) 1997-01-17 2000-01-25 Merck & Co., Inc. Integrin antagonists
US6313119B1 (en) * 1998-01-23 2001-11-06 Adventis Pharma Deutschland Gmbh Sulfonamide derivatives as inhibitors of bone resorption and as inhibitors of cell adhesion
FR2786182B1 (fr) * 1998-11-24 2001-01-12 Hoechst Marion Roussel Inc Nouveaux derives d'acylguanidines, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant
EP1028114A1 (fr) * 1999-02-13 2000-08-16 Aventis Pharma Deutschland GmbH Nouveaux dérivés de guanidine et leur utilisation comme inhibiteurs de l'adhésion des cellules

Also Published As

Publication number Publication date
KR980009241A (ko) 1998-04-30
IL121359A0 (en) 1998-01-04
US20030050314A1 (en) 2003-03-13
KR100541172B1 (ko) 2006-10-24
US6399620B1 (en) 2002-06-04
HRP970404A2 (en) 1998-04-30
HK1006779A1 (en) 1999-03-19
TW490461B (en) 2002-06-11
JPH1143476A (ja) 1999-02-16
NO973399L (no) 1998-01-26
ID17615A (id) 1998-01-15
EP0820991A3 (fr) 2000-05-17
BR9704072A (pt) 1999-01-05
PL321254A1 (en) 1998-02-02
ZA976532B (en) 1998-04-16
AR007961A1 (es) 1999-11-24
HUP9701264A1 (hu) 1998-05-28
AU2941897A (en) 1998-02-05
CA2211270C (fr) 2009-02-10
EP0820991B1 (fr) 2007-08-29
NO973399D0 (no) 1997-07-23
JP4077535B2 (ja) 2008-04-16
DE59712879D1 (de) 2007-10-11
SK100597A3 (en) 1998-02-04
ATE371650T1 (de) 2007-09-15
RU2180331C2 (ru) 2002-03-10
CA2211270A1 (fr) 1998-01-24
CN1179418A (zh) 1998-04-22
CZ234397A3 (cs) 1998-03-18
AU726376B2 (en) 2000-11-02
HU9701264D0 (en) 1997-09-29
EP0820991A2 (fr) 1998-01-28
DE19629816A1 (de) 1998-01-29
US20080021055A1 (en) 2008-01-24
PL189189B1 (pl) 2005-07-29
HUP9701264A3 (en) 2001-02-28
US7348333B2 (en) 2008-03-25
NZ328388A (en) 1998-07-28
CN1064352C (zh) 2001-04-11

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