BR9901208A - Derivados de ácido acético de fenóxi e de tetrazol de fenóximetila, tendo propriedades anti-tumor, que atuam como antagonistas de atividade mdm2.. - Google Patents
Derivados de ácido acético de fenóxi e de tetrazol de fenóximetila, tendo propriedades anti-tumor, que atuam como antagonistas de atividade mdm2..Info
- Publication number
- BR9901208A BR9901208A BR9901208-1A BR9901208A BR9901208A BR 9901208 A BR9901208 A BR 9901208A BR 9901208 A BR9901208 A BR 9901208A BR 9901208 A BR9901208 A BR 9901208A
- Authority
- BR
- Brazil
- Prior art keywords
- group
- alkyl
- groups
- hydrogen
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/62—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by hydrogenation of carbon-to-carbon double or triple bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C07C45/74—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with dehydration
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
- C07C49/83—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
- C07C49/835—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups having unsaturation outside an aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/76—Unsaturated compounds containing keto groups
- C07C59/90—Unsaturated compounds containing keto groups containing singly bound oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/708—Ethers
- C07C69/712—Ethers the hydroxy group of the ester being etherified with a hydroxy compound having the hydroxy group bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Patente de Invenção: <B>"DERIVADOS DE áCIDO ACéTICO DE FENóXI E DE TETRAZOL DE FENóXIMETILA, TENDO PROPRIEDADES ANTI-TUMOR, QUE ATUAM COMO ANTAGONISTAS DE ATIVIDADE MDM2"<D>. A presente invenção refere-se a derivados de ácido acético de fenóxi e de tetrazol de fenóximetila de fórmula (I): onde: - o grupo -O-C(R1)(R2)-(CH~ 2~)~ p~-A pode ser em posição orto, meta ou para; - A é selecionado de -COOH, -COO-(C~ 1~-C~ 4~)alquila, -CN ou um grupo de fórmula: em que R' é hidrogênio ou (C~ 1~-C~ 4~)alquila; ou o grupo A-(CH~ 2~)~ p~-C(R1)(R2)- é selecionado de fenila, benzila ou (indolil)metila, que pode ser substituído por grupos R4; - p é 0, 1 ou 2; - R1 e R2 são independentemente selecionados de hidrogênio ou (C~ 1~-C~ 8~)alquila ou eles formam, juntos com o átomo de carbono ao qual eles são ligados, um grupo (C~ 3~-C~ 7~)cicloalquila; - R4 são de 0 a 2 substituentes independentemente selecionados de cloro, bromo, iódo, flúor, grupos (C~ 1~-C~ 8~)alquila, hidróxi, (C~ 1~-C~ 4~) alcóxi, (C~ 1~-C~ 4~)acila, lineares ou ramificados; ou o grupo na fórmula (I) é um grupo naftila que por sua vez pode ser substituído por grupos R4; - n é um número inteiro de 1 a 4; - m é 0 ou 1; - B é selecionado de C~ 1~-C~ 10~ alquila linear ou ramificada, -CO-C(R3)=CH-R, -CH=C(R3)-CO-Ar, -CO-CH(R3)-CH~ 2~-R ou -CO-CH(R3)-CH~ 2~-NR5R6 quando m é 0, ou é -CH=C(R3)-CO-Ar quando m é 1; - R é selecionado de hidrogênio, <B>-Ar<D> ou -CO-<B>Ar<D>; - R3 é hidrogênio ou um grupo (C~ 1~-C~ 8~)alquila; -R5 e R6 são independentemente um grupo (C~ 1~-C~ 4~)alquila, ou eles formam, juntos com o átomo de nitrogênio ao qual eles são ligados, um grupo piperidino, piperazino, (C~ 1~-C~ 8~)alquilpiperazino, morfolino ou tiomorfolino; - <B>Ar<D> é um grupo fenila que pode ser não substituído ou substituído com de 1 a 3 grupos independentemente selecionados de cloro, bromo, iódo, flúor, grupos (C~ 1~-C~ 4~)alquila, hidróxi, (C~ 1~-C~ 4~) alcóxi, (C~ 1~-C~ 4~)acila, lineares ou ramificados, os estereoisómeros deles ou os sais deles com ácidos ou bases farmaceuticamente aceitáveis, para as preparação de um medicamento tendo atividade antagónica de MDM2, novos compostos da fórmula acima mencionada, e composições farmacêuticas contendo pelo menos um daqueles compostos.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98105726A EP0947511A1 (en) | 1998-03-30 | 1998-03-30 | Derivatives of phenoxy acetic acid and of phenoxymethyl tetrazole having antitumor activity |
Publications (1)
Publication Number | Publication Date |
---|---|
BR9901208A true BR9901208A (pt) | 2000-04-25 |
Family
ID=8231677
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR9901208-1A BR9901208A (pt) | 1998-03-30 | 1999-03-29 | Derivados de ácido acético de fenóxi e de tetrazol de fenóximetila, tendo propriedades anti-tumor, que atuam como antagonistas de atividade mdm2.. |
Country Status (20)
Country | Link |
---|---|
EP (1) | EP0947511A1 (pt) |
JP (1) | JP2000063340A (pt) |
KR (1) | KR19990078366A (pt) |
CN (1) | CN1232028A (pt) |
AR (1) | AR018170A1 (pt) |
AU (1) | AU2250299A (pt) |
BR (1) | BR9901208A (pt) |
CA (1) | CA2267047A1 (pt) |
HR (1) | HRP990093A2 (pt) |
HU (1) | HUP9900804A3 (pt) |
ID (1) | ID22335A (pt) |
IL (1) | IL129191A0 (pt) |
MA (1) | MA26616A1 (pt) |
NO (1) | NO991526L (pt) |
NZ (1) | NZ334874A (pt) |
PE (1) | PE20000341A1 (pt) |
PL (1) | PL332273A1 (pt) |
SG (1) | SG81972A1 (pt) |
TR (1) | TR199900719A2 (pt) |
ZA (1) | ZA992407B (pt) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2841784B1 (fr) * | 2002-07-08 | 2007-03-02 | Composition a base de derives de 1,3-diphenylprop-2en-1-one substitues, preparation et utilisations | |
FR2841900B1 (fr) | 2002-07-08 | 2007-03-02 | Genfit S A | Nouveaux derives de 1,3-diphenylprop-2-en-1-one substitues, preparation et utilisations |
FR2857361B1 (fr) * | 2003-07-08 | 2005-09-09 | Genfit S A | PREPARATION DE DERIVES DE 1,3-DIPHENYPROP-2-¼n-1-one |
WO2005063774A1 (en) * | 2003-12-22 | 2005-07-14 | Johns Hopkins University | Boronic acid aryl analogs |
JP2007297283A (ja) * | 2004-07-28 | 2007-11-15 | Santen Pharmaceut Co Ltd | 新規桂皮酸関連化合物 |
SG174107A1 (en) * | 2006-08-30 | 2011-09-29 | Univ Michigan | New small molecule inhibitors of mdm2 and the uses thereof |
DE602007006519D1 (de) | 2006-09-21 | 2010-06-24 | Hoffmann La Roche | Oxindolderivate als antikrebsmittel |
US7638548B2 (en) | 2006-11-09 | 2009-12-29 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
US7553833B2 (en) | 2007-05-17 | 2009-06-30 | Hoffmann-La Roche Inc. | 3,3-spiroindolinone derivatives |
US7928233B2 (en) | 2009-02-10 | 2011-04-19 | Hoffmann-La Roche Inc. | Spiroindolinone pyridine derivatives |
US8217051B2 (en) | 2009-02-17 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
US8076482B2 (en) | 2009-04-23 | 2011-12-13 | Hoffmann-La Roche Inc. | 3,3′-spiroindolinone derivatives |
US8017607B2 (en) | 2009-10-14 | 2011-09-13 | Hoffmann-La Roche Inc. | N-substituted-pyrrolidines as inhibitors of MDM2-P-53 interactions |
US8088815B2 (en) | 2009-12-02 | 2012-01-03 | Hoffman-La Roche Inc. | Spiroindolinone pyrrolidines |
US8288431B2 (en) | 2010-02-17 | 2012-10-16 | Hoffmann-La Roche Inc. | Substituted spiroindolinones |
US8217044B2 (en) | 2010-04-28 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone pyrrolidines |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3255241A (en) * | 1961-01-19 | 1966-06-07 | Merck & Co Inc | (2-alkylidene acyl)phenoxy-and (2-alkylidene acyl)phenylmercaptocarboxylic acids |
BE639727A (pt) * | 1962-11-13 | |||
US3251064A (en) * | 1962-11-13 | 1966-05-10 | Everett M Schultz | beta-aminoacylphenoxy-and beta-aminoacylphenylmercapto-derivatives of monocarboxylicacids |
US3994955A (en) * | 1975-01-20 | 1976-11-30 | G. D. Searle & Co. | Substituted phenoxydialkylacetic acids and esters |
US4904697A (en) * | 1987-04-09 | 1990-02-27 | Merrell Dow Pharmaceuticals Inc. | Controlling the growth of certain tumor tissue with chalcone derivatives |
JPH0624975A (ja) * | 1992-05-12 | 1994-02-01 | Dainippon Ink & Chem Inc | 制癌活性増強剤 |
DE4327365A1 (de) * | 1993-08-14 | 1995-02-16 | Boehringer Mannheim Gmbh | Verwendung von Phenolen und Phenolderivaten als Arzneimittel mit fibrinogensenkender Wirkung |
-
1998
- 1998-03-30 EP EP98105726A patent/EP0947511A1/en not_active Withdrawn
-
1999
- 1999-03-26 PE PE1999000244A patent/PE20000341A1/es not_active Application Discontinuation
- 1999-03-26 TR TR1999/00719A patent/TR199900719A2/xx unknown
- 1999-03-26 CA CA002267047A patent/CA2267047A1/en not_active Abandoned
- 1999-03-26 ID IDP990274D patent/ID22335A/id unknown
- 1999-03-26 NZ NZ334874A patent/NZ334874A/xx unknown
- 1999-03-26 IL IL12919199A patent/IL129191A0/xx unknown
- 1999-03-26 AR ARP990101366A patent/AR018170A1/es unknown
- 1999-03-26 MA MA25510A patent/MA26616A1/fr unknown
- 1999-03-27 SG SG9901555A patent/SG81972A1/en unknown
- 1999-03-29 NO NO991526A patent/NO991526L/no not_active Application Discontinuation
- 1999-03-29 KR KR1019990010823A patent/KR19990078366A/ko not_active Application Discontinuation
- 1999-03-29 PL PL99332273A patent/PL332273A1/xx unknown
- 1999-03-29 HR HR98105726.8A patent/HRP990093A2/hr not_active Application Discontinuation
- 1999-03-29 ZA ZA9902407A patent/ZA992407B/xx unknown
- 1999-03-29 HU HU9900804A patent/HUP9900804A3/hu unknown
- 1999-03-29 BR BR9901208-1A patent/BR9901208A/pt not_active Application Discontinuation
- 1999-03-30 JP JP11087932A patent/JP2000063340A/ja active Pending
- 1999-03-30 AU AU22502/99A patent/AU2250299A/en not_active Abandoned
- 1999-03-30 CN CN99104509A patent/CN1232028A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
PE20000341A1 (es) | 2000-05-08 |
TR199900719A2 (xx) | 1999-10-21 |
ID22335A (id) | 1999-09-30 |
JP2000063340A (ja) | 2000-02-29 |
SG81972A1 (en) | 2001-07-24 |
CA2267047A1 (en) | 1999-09-30 |
AR018170A1 (es) | 2001-10-31 |
CN1232028A (zh) | 1999-10-20 |
IL129191A0 (en) | 2000-02-17 |
HUP9900804A3 (en) | 2001-08-28 |
NO991526D0 (no) | 1999-03-29 |
KR19990078366A (ko) | 1999-10-25 |
AU2250299A (en) | 1999-10-14 |
HUP9900804A2 (hu) | 1999-11-29 |
EP0947511A1 (en) | 1999-10-06 |
ZA992407B (en) | 1999-09-30 |
PL332273A1 (en) | 1999-10-11 |
HU9900804D0 (en) | 1999-05-28 |
NZ334874A (en) | 2000-08-25 |
HRP990093A2 (en) | 2000-02-29 |
MA26616A1 (fr) | 2004-12-20 |
NO991526L (no) | 1999-10-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR9901208A (pt) | Derivados de ácido acético de fenóxi e de tetrazol de fenóximetila, tendo propriedades anti-tumor, que atuam como antagonistas de atividade mdm2.. | |
KR0126768B1 (ko) | 메틸렌 포스포노알킬포스피네이트 및 이를 함유하는 약제학적 조성물 | |
ATE325094T1 (de) | Sulfonamide enthaltende indolderivate | |
DE60018135D1 (de) | Benzothiophenderivate, Benzofuranderivate und Indolderivate, Verfahren zu ihrer Herstellung und sie enthaltende pharmazeutische Zubereitungen | |
DE69415445D1 (de) | Zytotoxische Stilben-Derivate und diese enthaltende pharmazeutische Zusammensetzungen | |
DE122009000040I1 (de) | Naphthalin-Derivate, Verfahren zu ihrer Herstellung und sie enthaltende pharmazeutische Zusammensetzungen. | |
CY1106276T1 (el) | Παραγωγα υποκατεστημενου φαινυλπροπιονικου οξεος ως ανταγωνιστες σε υποδοχεις αλφα που ενepγοποιουνται απο παραγοντες που επαγουν τον πολλαπλασιασμο των ανθρωπινων υπepοξεισωματων (ppar) | |
DK0928788T3 (da) | Imidazolidin-4-on-derivater, der er nyttige som anticancer-midler | |
NZ241568A (en) | Amide, sulphonamide and phosphonamide derivatives and pharmaceutical compositions | |
HUP0401235A2 (hu) | 5-HT6 receptor affinitással rendelkező arilszulfonil-származékok, eljárás előállításukra és a vegyületeket tartalmazó gyógyászati készítmények | |
NZ239115A (en) | Substituted piperazine derivatives and pharmaceutical compositions | |
HRP20060023A2 (en) | Use of bicyclo[2.2.1]heptane derivatives for the preparation of neuroprotective pharmaceutical compositions | |
DK0952159T3 (da) | Anvendelse af phenylhydrazonderivater som antiinflammatoriske eller analgetiske midler | |
JPH051257B2 (pt) | ||
ATE214064T1 (de) | Indane-1-ol derivate, verfahren zu deren herstellung und diese enthaltende pharmazeutische zusammenstellungen | |
ATE106734T1 (de) | Pharmazeutische zusammensetzung zur verhinderung der plättchenaggregation. | |
BR0109573A (pt) | Composto ou uma pró-droga ou um sal farmacologicamente aceitável do mesmo, agente, composição farmacêutica, e, uso de um composto ou uma pró-droga ou um sal farmacologicamente aceitável do mesmo | |
BR0013375A (pt) | Composições farmacêuticas contendo derivados tiazolidinodiona e processo para sua preparação | |
HUP0002715A2 (hu) | Benzotiofénszármazékok alkalmazása trombocitaszám csökkentésére szolgáló gyógyszerkészítmények előállítására | |
HRP20090054T3 (en) | Piperazine derivatives of alkyl oxindoles | |
HUP9902270A1 (hu) | Analgetikus hatású akridinszármazékok, előállításuk és alkalmazásuk | |
ECSP992900A (es) | Derivados de acido fenoxiacetico y fenoximetil tetrazol con actividad antitumoral | |
BR0004066A (pt) | Composto ou um éster ou sal deste farmaceuticamente aceitáveis, uso do mesmo, composição farmacêutica, e, composto ou um derivado de acetal deste | |
PT92579A (pt) | Processo para a preparacao de composicoes farmaceuticas para o tratamento do cancro | |
DE69016378T2 (de) | Substituierte Benzothiazolinone, ihre Herstellung und sie enthaltende pharmazeutische Zusammenstellungen. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA10 | Dismissal: dismissal - article 33 of industrial property law | ||
B11Y | Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette] |