ES2188194T3 - 1,8-naftiridin-4(1h)-onas sustituidas como inhibidores de la fosfodiesterasa 4. - Google Patents

1,8-naftiridin-4(1h)-onas sustituidas como inhibidores de la fosfodiesterasa 4.

Info

Publication number
ES2188194T3
ES2188194T3 ES99933078T ES99933078T ES2188194T3 ES 2188194 T3 ES2188194 T3 ES 2188194T3 ES 99933078 T ES99933078 T ES 99933078T ES 99933078 T ES99933078 T ES 99933078T ES 2188194 T3 ES2188194 T3 ES 2188194T3
Authority
ES
Spain
Prior art keywords
alkyl
aminosulfonyl
amino
uncle
phosphodesterase
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.)
Expired - Lifetime
Application number
ES99933078T
Other languages
English (en)
Inventor
Edward Fox Kleinman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Products Inc
Original Assignee
Pfizer Products 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 Pfizer Products Inc filed Critical Pfizer Products Inc
Application granted granted Critical
Publication of ES2188194T3 publication Critical patent/ES2188194T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic 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

Abstract

Un compuesto de fórmula**(Fórmula)** o una sal farmacéuticamente aceptable del mismo, en la que R1 se selecciona del grupo constituido por hidrógeno, alquilo(C1-C6), clocloalquilo(C3-C7), arilo(C6-C10), heteroarilo(C5-C9) y heterocicloalquilo(C2-C9), en la que los grupos alquilo, cicloalquilo, arilo, heteroarilo o heterocicloalquilo están opcionalmente sustituidos por halo, hidroxilo, alquilo(C1-C6), alcoxilo(C1-C6), amino, alquil(C1-C6)amino, (alquil(C1-C6))2-amino, tío, alquil(C1-C6)tío, ciano, carboxilo, carboxialquilo(C1-C6), hidroxialquilo(C1-C6), acilo(C1-C6), aminosulfonilo, alquil(C1-C6)aminosulfonilo o (alquil(C1-C6)2-aminosulfonilo. R2 es arilo(C6-C10) o heteroarilo(C5-C9); y R3 es hidrógeno, halo, hidroxilo, alquilo(C1-C6), alcoxilo(C1-C6), amino, alquil(C1-C6)amino, (alquil(C1-C6))2-amino, tío, alquil(C1-C6)tío, carboxilo, carboxialquilo(C1-C6), hidroxialquilo(C1-C6), acilo(C1-C6), aminosulfonilo, alquil(C1-C6)-aminosulfonilo o (alquil(C1-C6)2-aminosulfonilo.
ES99933078T 1998-08-11 1999-08-05 1,8-naftiridin-4(1h)-onas sustituidas como inhibidores de la fosfodiesterasa 4. Expired - Lifetime ES2188194T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9617698P 1998-08-11 1998-08-11

Publications (1)

Publication Number Publication Date
ES2188194T3 true ES2188194T3 (es) 2003-06-16

Family

ID=22256080

Family Applications (1)

Application Number Title Priority Date Filing Date
ES99933078T Expired - Lifetime ES2188194T3 (es) 1998-08-11 1999-08-05 1,8-naftiridin-4(1h)-onas sustituidas como inhibidores de la fosfodiesterasa 4.

Country Status (44)

Country Link
US (1) US6174895B1 (es)
EP (1) EP1104420B1 (es)
JP (1) JP2002522541A (es)
KR (1) KR20010072368A (es)
CN (1) CN1312810A (es)
AP (1) AP2001002068A0 (es)
AR (1) AR015557A1 (es)
AT (1) ATE229955T1 (es)
AU (1) AU4924999A (es)
BG (1) BG105321A (es)
BR (1) BR9912902A (es)
CA (1) CA2340180A1 (es)
CO (1) CO5130004A1 (es)
CZ (1) CZ2001485A3 (es)
DE (1) DE69904602T2 (es)
DK (1) DK1104420T3 (es)
DZ (1) DZ2866A1 (es)
EA (1) EA200100124A1 (es)
EE (1) EE200100085A (es)
ES (1) ES2188194T3 (es)
GE (1) GEP20033029B (es)
GT (1) GT199900128A (es)
HK (1) HK1038917A1 (es)
HN (1) HN1999000130A (es)
HR (1) HRP20010107A2 (es)
HU (1) HUP0103466A3 (es)
ID (1) ID27843A (es)
IL (1) IL140868A0 (es)
IS (1) IS5815A (es)
MA (1) MA26669A1 (es)
NO (1) NO20010684L (es)
NZ (1) NZ509297A (es)
OA (1) OA11591A (es)
PA (1) PA8480001A1 (es)
PE (1) PE20000950A1 (es)
PL (1) PL346005A1 (es)
PT (1) PT1104420E (es)
SK (1) SK1822001A3 (es)
SV (1) SV1999000120A (es)
TN (1) TNSN99155A1 (es)
TR (1) TR200100433T2 (es)
TW (1) TW542835B (es)
WO (1) WO2000009504A1 (es)
ZA (1) ZA200101040B (es)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8815951B2 (en) 1996-08-13 2014-08-26 The Regents Of The University Of California Inhibitors of epoxide hydrolases for the treatment of inflammation
EP1343528A2 (en) * 2000-11-02 2003-09-17 Research Foundation of City University of New York Methods for stimulating nervous system regeneration and repair by inhibition phosphodiesterase type 4
WO2002088079A2 (en) * 2001-05-01 2002-11-07 Bristol-Myers Squibb Company Dual inhibitors of pde 7 and pde 4
JO2311B1 (en) * 2001-08-29 2005-09-12 ميرك فروست كندا ليمتد Alkyl inhibitors Ariel phosphodiesterase-4
US7323460B2 (en) 2002-03-15 2008-01-29 Merck & Co., Inc. N-(substituted benzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamides useful as HIV integrase inhibitors
KR100454750B1 (ko) * 2002-06-20 2004-11-03 삼성에스디아이 주식회사 유기 전계 발광 소자용 청색 발광 화합물 및 이를 사용한유기 전계 발광 소자
US20060079540A1 (en) * 2002-11-27 2006-04-13 Altana Pharma Ag Pde4 and pde3/4 inhibitors for use in the treatment of cachexia
US6861422B2 (en) * 2003-02-26 2005-03-01 Boehringer Ingelheim Pharma Gmbh & Co. Kg Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions
DE10349497A1 (de) * 2003-10-23 2005-05-25 Bayer Cropscience Ag N-substituierte Pyrazolylcarboxanilide
JP2007517828A (ja) * 2004-01-17 2007-07-05 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 気道の疾患を治療するための置換プテリジンの使用
DE102004002557A1 (de) * 2004-01-17 2005-08-04 Boehringer Ingelheim Pharma Gmbh & Co. Kg Verwendung von substituierten Pyrimido(5,4-d)pyrimidinen zur Behandlung von Atemwegserkrankungen
DE102004029784A1 (de) * 2004-06-21 2006-01-05 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue 2-Benzylaminodihydropteridinone, Verfahren zur deren Herstellung und deren Verwendung als Arzneimittel
DE102004033670A1 (de) * 2004-07-09 2006-02-02 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Pyridodihydropyrazinone, Verfahren zu Ihrer Herstellung und Ihre Verwendung als Arzneimittel
US20060058311A1 (en) * 2004-08-14 2006-03-16 Boehringer Ingelheim International Gmbh Combinations for the treatment of diseases involving cell proliferation
US20060035903A1 (en) * 2004-08-14 2006-02-16 Boehringer Ingelheim International Gmbh Storage stable perfusion solution for dihydropteridinones
US20060074088A1 (en) * 2004-08-14 2006-04-06 Boehringer Ingelheim International Gmbh Dihydropteridinones for the treatment of cancer diseases
US7728134B2 (en) * 2004-08-14 2010-06-01 Boehringer Ingelheim International Gmbh Hydrates and polymorphs of 4[[(7R)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-pteridinyl]amino]-3-methoxy-N-(1-methyl-4-piperidinyl)-benzamide, process for their manufacture and their use as medicament
US7759485B2 (en) * 2004-08-14 2010-07-20 Boehringer Ingelheim International Gmbh Process for the manufacture of dihydropteridinones
EP1632493A1 (de) * 2004-08-25 2006-03-08 Boehringer Ingelheim Pharma GmbH & Co.KG Dihydropteridinonderivative, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
EP1630163A1 (de) * 2004-08-25 2006-03-01 Boehringer Ingelheim Pharma GmbH & Co.KG Dihydropteridinonderivative, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
DE102004058337A1 (de) * 2004-12-02 2006-06-14 Boehringer Ingelheim Pharma Gmbh & Co. Kg Verfahren zur Herstellung von annelierten Piperazin-2-on Derivaten
EP1915155A1 (en) * 2005-08-03 2008-04-30 Boehringer Ingelheim International GmbH Dihydropteridinones in the treatment of respiratory diseases
US7439358B2 (en) * 2006-02-08 2008-10-21 Boehringer Ingelheim International Gmbh Specific salt, anhydrous and crystalline form of a dihydropteridione derivative
WO2009019205A1 (en) * 2007-08-03 2009-02-12 Boehringer Ingelheim International Gmbh Crystalline form of a dihydropteridione derivative
US8546566B2 (en) 2010-10-12 2013-10-01 Boehringer Ingelheim International Gmbh Process for manufacturing dihydropteridinones and intermediates thereof
US9358233B2 (en) 2010-11-29 2016-06-07 Boehringer Ingelheim International Gmbh Method for treating acute myeloid leukemia
US9370535B2 (en) 2011-05-17 2016-06-21 Boehringer Ingelheim International Gmbh Method for treatment of advanced solid tumors
ES2773272T3 (es) * 2012-08-08 2020-07-10 Merck Patent Gmbh Derivados de (aza-)isoquinolinona
JP6440625B2 (ja) 2012-11-14 2018-12-19 ザ・ジョンズ・ホプキンス・ユニバーシティー 精神分裂病を処置するための方法および組成物
WO2015011236A1 (en) 2013-07-26 2015-01-29 Boehringer Ingelheim International Gmbh Treatment of myelodysplastic syndrome
US9867831B2 (en) 2014-10-01 2018-01-16 Boehringer Ingelheim International Gmbh Combination treatment of acute myeloid leukemia and myelodysplastic syndrome

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU165405B (es) * 1972-06-29 1974-08-28
US3856800A (en) * 1973-02-26 1974-12-24 Sterling Drug Inc Process of preparing 1,4-dihydro-4-oxo-7-q-3-unsubstituted-1,8-naphthyridines from cyclic alkylidenyl n-(6-q-2-pyridyl) aminomethylenemalonates
US3882132A (en) * 1973-03-08 1975-05-06 Sterling Drug Inc Preparation of 1-alkyl-1,4-dihydro-7-substituted-4-oxo-1,8-naphthyridine-3-carboxylic acids via the 3-aminomethyl analogs
US5817670A (en) * 1994-08-29 1998-10-06 Yamanouchi Pharmaceutical Co., Ltd. Naphthyridine derivatives and pharmaceutical compositions thereof
JP4323574B2 (ja) * 1995-12-13 2009-09-02 大日本住友製薬株式会社 抗腫瘍剤

Also Published As

Publication number Publication date
ID27843A (id) 2001-04-26
NZ509297A (en) 2003-11-28
GEP20033029B (en) 2003-07-25
PL346005A1 (en) 2002-01-14
IL140868A0 (en) 2002-02-10
HN1999000130A (es) 2000-11-22
CA2340180A1 (en) 2000-02-24
EA200100124A1 (ru) 2001-10-22
PT1104420E (pt) 2003-03-31
OA11591A (en) 2004-07-30
BR9912902A (pt) 2001-05-08
CZ2001485A3 (cs) 2002-05-15
PE20000950A1 (es) 2000-09-27
MA26669A1 (fr) 2004-12-20
TW542835B (en) 2003-07-21
IS5815A (is) 2001-01-16
ATE229955T1 (de) 2003-01-15
DE69904602D1 (en) 2003-01-30
HK1038917A1 (zh) 2002-04-04
HUP0103466A3 (en) 2002-11-28
AU4924999A (en) 2000-03-06
PA8480001A1 (es) 2000-09-29
DE69904602T2 (de) 2003-04-30
DK1104420T3 (da) 2003-01-13
CO5130004A1 (es) 2002-02-27
EP1104420B1 (en) 2002-12-18
HRP20010107A2 (en) 2002-02-28
EE200100085A (et) 2002-08-15
TR200100433T2 (tr) 2001-07-23
HUP0103466A2 (hu) 2002-02-28
DZ2866A1 (fr) 2003-12-01
JP2002522541A (ja) 2002-07-23
BG105321A (en) 2001-12-29
SK1822001A3 (en) 2002-08-06
GT199900128A (es) 2001-01-30
EP1104420A1 (en) 2001-06-06
NO20010684D0 (no) 2001-02-09
WO2000009504A1 (en) 2000-02-24
ZA200101040B (en) 2003-01-07
CN1312810A (zh) 2001-09-12
NO20010684L (no) 2001-04-09
AP2001002068A0 (en) 2001-03-31
AR015557A1 (es) 2001-05-02
KR20010072368A (ko) 2001-07-31
TNSN99155A1 (fr) 2005-11-10
SV1999000120A (es) 2000-09-05
US6174895B1 (en) 2001-01-16

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