BR9916005A - Derivados de hidrazina cìclicos como inibidores do tnf-alfa - Google Patents

Derivados de hidrazina cìclicos como inibidores do tnf-alfa

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Publication number
BR9916005A
BR9916005A BR9916005-6A BR9916005A BR9916005A BR 9916005 A BR9916005 A BR 9916005A BR 9916005 A BR9916005 A BR 9916005A BR 9916005 A BR9916005 A BR 9916005A
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BR
Brazil
Prior art keywords
lower alkyl
aryl
group
optionally substituted
cycloalkyl
Prior art date
Application number
BR9916005-6A
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English (en)
Inventor
Michael John Broadhurst
William Henry Johnson
Daryl Simon Walter
Original Assignee
Hoffmann La Roche
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
Priority claimed from GBGB9827408.7A external-priority patent/GB9827408D0/en
Priority claimed from GBGB9925211.6A external-priority patent/GB9925211D0/en
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of BR9916005A publication Critical patent/BR9916005A/pt

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D419/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
    • C07D419/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D419/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • 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
    • 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
    • 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
    • A61P31/04Antibacterial agents
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • 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
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    • 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
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    • 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
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • C07D233/34Ethylene-urea
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    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/72Two oxygen atoms, e.g. hydantoin
    • C07D233/80Two oxygen atoms, e.g. hydantoin with hetero atoms or acyl radicals directly attached to ring nitrogen atoms
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    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/84Sulfur atoms
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    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
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    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
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    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/95Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
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    • C07D241/08Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
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    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
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    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
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  • Chemical & Material Sciences (AREA)
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  • Immunology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Pain & Pain Management (AREA)
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  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Communicable Diseases (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

Patente de Invenção: <B>"DERIVADOS DE HIDRAZINA CìCLICOS COMO INIBIDORES DO TNF-ALFA"<D>. Os derivados de hidrazina de fórmula (I), em que W representa O, S, CO, NR^ 5^, (CR³R^ 4^)~ m~, ou CR^ 11^; X representa CO, NR^ 6^, (CH~ 2~)~ n~, CR^ 12^ ou CHR^ 13^; Y representa CO, NR^ 7^, (CH~ 2~)~ p~, ou CHR^ 14^; Z representa CO, CS, SO~ 2~, ou CH~ 2~; m significa 0 ou 1; n e p cada um individualmente significa 0, 1 ou 2; R¹ representa alquila inferior, alquenila inferior, cicloalquila inferior, cicloalquila inferior-alquila inferior, arila ou aril-alquila inferior; R² representa alquila inferior, alquenila inferior, cicloalquila inferior, cicloalquila inferior-alquila inferior ou um grupo da fórmula V-arila, V-heterociclila ou -(CH~ 2~)~ q~-CH=CR^ 8^R^ 9^; R^ 3^, R^ 4^, R^ 5^, R^ 6^ e R^ 7^, cada um independentemente representa hidrogênio, alquila inferior opcionalmente substituída, alquenila inferior, cicloalquila inferior, cicloalquila inferior-alquila inferior, arila, aril-alquila inferior, heterociclila ou heterociclil-alquila inferior; ou R³ e R^ 4^, juntos com o átomo de carbono ao qual eles estão ligados, formam um anel com 3 a 8 elementos; ou R^ 5^ e R^ 6^ ou R^ 5^ e R^ 7^, juntos com os átomos de nitrogênio aos quais eles estão ligados, formam um anel com 3 a 8 elementos; ou R^ 11^ e R^ 12^, juntos com os átomos de carbono sp² aos quais eles estão ligados, formam um anel fundido de cicloalquenila inferior, arila ou heteroarila; ou R^ 5^ com R^ 13^ ou R^ 14^ juntos representam alquileno inferior em que um grupo CH~ 2~ é opcionalmente substituído por um heteroátomo; ou R^ 6^ ou R^ 7^ com R³ ou R^ 4^ juntos representam alquileno inferior em que um grupo CH~ 2~ é opcionalmente substituído por um heteroátomo; ou R^ 3^ e R^ 4^ juntos representam alquileno inferior em que um grupo CH~ 2~ é opcionalmente substituído por um heteroátomo; V representa um grupo espaçador; R^ 8^ e R^ 9^ juntos representam alquileno inferior em que um grupo CH~ 2~ é opcionalmente substituído por um heteroátomo; e q significa 1 ou 2; com as condições que (i) pelo menos um de W, X e Y represente um dos heteroátomos anteriormente indicados para estes substituintes ou CO, (ii) Z represente CO ou SO~ 2~ ou CS quando W representar O; (iii) W, X, Y e Z não sejam todos CO e (iv) W, X e Y não sejam todos NR^ 5^, NR^ 6^ e NR^ 7^, respectivamente; e os seus sais farmaceuticamente aceitáveis, inibem a liberação do fator de necrose de tumor alfa (TNF-<244>) a partir das células. Eles podem ser usados como medicamentos, especialmente no tratamento de doenças inflamatórias e autoimunes, osteoartrite, doenças respiratórias, tumores, caquexia, doenças cardiovasculares, febre, hemorragia e sepse.
BR9916005-6A 1998-12-11 1999-12-02 Derivados de hidrazina cìclicos como inibidores do tnf-alfa BR9916005A (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9827408.7A GB9827408D0 (en) 1998-12-11 1998-12-11 Hydrazine derivatives
GBGB9925211.6A GB9925211D0 (en) 1999-10-25 1999-10-25 Hydrazine derivatives
PCT/EP1999/009423 WO2000035885A1 (en) 1998-12-11 1999-12-02 Cyclic hydrazine derivatives as tnf-alpha inhibitors

Publications (1)

Publication Number Publication Date
BR9916005A true BR9916005A (pt) 2001-09-04

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Application Number Title Priority Date Filing Date
BR9916005-6A BR9916005A (pt) 1998-12-11 1999-12-02 Derivados de hidrazina cìclicos como inibidores do tnf-alfa

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US (1) US6281363B1 (pt)
EP (1) EP1137640B1 (pt)
JP (1) JP3913983B2 (pt)
KR (1) KR100442223B1 (pt)
CN (1) CN1132819C (pt)
AT (1) ATE305003T1 (pt)
AU (1) AU765729B2 (pt)
BR (1) BR9916005A (pt)
CA (1) CA2353924A1 (pt)
DE (1) DE69927403T2 (pt)
DK (1) DK1137640T3 (pt)
ES (1) ES2249055T3 (pt)
TR (1) TR200101644T2 (pt)
WO (1) WO2000035885A1 (pt)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1425008A (zh) * 2000-01-24 2003-06-18 沃尼尔·朗伯公司 3-氨基喹唑啉-2,4-二酮抗菌剂
PE20030701A1 (es) 2001-12-20 2003-08-21 Schering Corp Compuestos para el tratamiento de trastornos inflamatorios
US7199155B2 (en) 2002-12-23 2007-04-03 Wyeth Holdings Corporation Acetylenic aryl sulfonate hydroxamic acid TACE and matrix metalloproteinase inhibitors
EP2039695A4 (en) 2006-07-11 2010-09-15 Takeda Pharmaceutical BICYCLIC HETEROCYLIC COMPOUND AND ITS USE
JP5671453B2 (ja) 2009-04-28 2015-02-18 中外製薬株式会社 スピロイミダゾロン誘導体
KR102168738B1 (ko) 2012-12-10 2020-10-22 추가이 세이야쿠 가부시키가이샤 히단토인 유도체
KR102266021B1 (ko) 2014-06-09 2021-06-16 추가이 세이야쿠 가부시키가이샤 히단토인 유도체 함유 의약 조성물
EP3860608A1 (en) 2018-10-04 2021-08-11 INSERM (Institut National de la Santé et de la Recherche Médicale) Egfr inhibitors for treating keratodermas

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2058797A1 (en) 1991-02-01 1992-08-02 Michael John Broadhurst Amino acid derivatives
US5399589A (en) 1992-12-17 1995-03-21 Basf Aktiengesellschaft Oxalyl hydrazide-hydroxamic acid derivatives, their preparation and their use as fungicides
GB9411088D0 (en) * 1994-06-03 1994-07-27 Hoffmann La Roche Hydroxylamine derivatives
AUPO721997A0 (en) * 1997-06-06 1997-07-03 Queensland Institute Of Medical Research, The Anticancer compounds
US6235787B1 (en) * 1997-06-30 2001-05-22 Hoffmann-La Roche Inc. Hydrazine derivatives
AU2298399A (en) 1998-02-06 1999-08-23 Yoshitomi Pharmaceutical Industries, Ltd. Novel azapeptide type hydroxamic acid derivatives
US6239151B1 (en) 1998-06-26 2001-05-29 Hoffmann-La Roche Inc. Compounds as inhibitor of tumor necrosis factor alpha release

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JP2002532478A (ja) 2002-10-02
KR100442223B1 (ko) 2004-07-30
JP3913983B2 (ja) 2007-05-09
ES2249055T3 (es) 2006-03-16
DK1137640T3 (da) 2006-02-06
DE69927403T2 (de) 2006-07-06
AU765729B2 (en) 2003-09-25
DE69927403D1 (de) 2006-02-02
AU2095000A (en) 2000-07-03
ATE305003T1 (de) 2005-10-15
TR200101644T2 (tr) 2001-11-21
WO2000035885A1 (en) 2000-06-22
CN1132819C (zh) 2003-12-31
CA2353924A1 (en) 2000-06-22
KR20010086096A (ko) 2001-09-07
EP1137640A1 (en) 2001-10-04
US6281363B1 (en) 2001-08-28
CN1330640A (zh) 2002-01-09
EP1137640B1 (en) 2005-09-21

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