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WO1998050346A3 - Derives d'acetamide et d'uree, procede de preparation et utilisation de ces derives dans le traitement des troubles du systeme nerveux central - Google Patents

Derives d'acetamide et d'uree, procede de preparation et utilisation de ces derives dans le traitement des troubles du systeme nerveux central Download PDF

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Publication number
WO1998050346A3
WO1998050346A3 PCT/EP1998/002263 EP9802263W WO9850346A3 WO 1998050346 A3 WO1998050346 A3 WO 1998050346A3 EP 9802263 W EP9802263 W EP 9802263W WO 9850346 A3 WO9850346 A3 WO 9850346A3
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WIPO (PCT)
Prior art keywords
group
alkyl
oxygen
sulphur
nitrogen
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Ceased
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PCT/EP1998/002263
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WO1998050346A2 (fr
Inventor
Laramie Mary Gaster
Paul Adrian Wyman
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SmithKline Beecham Ltd
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SmithKline Beecham Ltd
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Filing date
Publication date
Priority claimed from GBGB9707874.5A external-priority patent/GB9707874D0/en
Priority claimed from GBGB9801632.2A external-priority patent/GB9801632D0/en
Application filed by SmithKline Beecham Ltd filed Critical SmithKline Beecham Ltd
Priority to AU75267/98A priority Critical patent/AU7526798A/en
Publication of WO1998050346A2 publication Critical patent/WO1998050346A2/fr
Publication of WO1998050346A3 publication Critical patent/WO1998050346A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36Radicals substituted by singly-bound nitrogen atoms
    • C07D213/40Acylated substituent nitrogen atom
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/16Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C07C233/24Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/29Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/40Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
    • C07C271/58Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/32Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
    • C07C275/34Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/32Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
    • C07C275/34Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C275/36Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with at least one of the oxygen atoms further bound to a carbon atom of a six-membered aromatic ring, e.g. N-aryloxyphenylureas
    • CCHEMISTRY; METALLURGY
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/40Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
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    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/39Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
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    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/08Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

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  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Composés ayant la formule (I), leurs procédés de préparation et leur utilisation en tant qu'agents CNS, formule dans laquelle Ra est un groupe ayant la formule (i) dans laquelle P1 représente phényle, aryle bicyclique, un anneau hétérocyclique de 5 à 7 membres et contenant de 1 à 3 hétéroatomes sélectionnés parmi oxygène, azote et soufre, ou un anneau hétérocyclique bicyclique contenant de 1 à 3 hétéroatomes sélectionnés parmi oxygène, azote et soufre; ou Ra est un groupe de formule (ii); L est un groupe de formule -Y-C(=V)-DG-, dans laquelle Y représente -NH-, NR5 où R5 représente C¿1-6? alkyle, ou Y représente -CH2-, ou -O-; V représente oxygène ou soufre; B représente azote, carbone ou un groupe CH, G représente hydrogène ou C1-6 alkyle à condition que D soit azote ou un groupe CH, ou G forme avec R?b1¿ un groupe W qui est (CR16R17)t, t valant 2, 3 ou 4 et R?16 et R17¿ représente indépendamment hydrogène ou C¿1-6? alkyle ou W représente (CR?16R17)¿u-J où u vaut 0, 1, 2 ou 3 et J représente oxygène, soufre, CR?16=CR17, CR16=N, =CR16O, =CR16¿S ou =CR16-NR17; B représente CH¿2?, oxygène, S(O)p où p vaut 0, 1 ou 2, NR?6 où R6¿ est hydrogène ou C¿1-6? alkyle ou B est CR?7=CR8 où R7 et R8¿ sont indépendamment hydrogène ou C¿1-6? alkyle; R?c et Rd¿ représentent indépendamment hydrogène ou C¿1-6? alkyle; R?y¿ est un anneau hétérocyclique ayant de 5 à 7 membres et contenant de 1 à 3 hétéroatomes sélectionnés parmi oxygène, azote et soufre, ou Ry est un groupe ayant la formule NReRf dans laquelle Re et Rf représentent indépendamment hydrogène, C¿1-6? alkyle ou aralkyle; R?b1 et Rb2¿ représentent indépendamment hydrogène, halogène, hydroxy, C¿1-6? alkyle, trifluorométhyle, C1-6 alcoxy ou aryle, ou R?b1¿ forment ensemble avec G un groupe W tel que défini ci-dessus; et n représente 0, 1, 2, 3 ou 4.
PCT/EP1998/002263 1997-04-18 1998-04-14 Derives d'acetamide et d'uree, procede de preparation et utilisation de ces derives dans le traitement des troubles du systeme nerveux central Ceased WO1998050346A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU75267/98A AU7526798A (en) 1997-04-18 1998-04-14 Acetamide and urea derivatives, process for their preparation and their use in the treatment of cns disorders

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GBGB9707874.5A GB9707874D0 (en) 1997-04-18 1997-04-18 Novel compounds
GB9707874.5 1997-04-18
GB9801632.2 1998-01-26
GBGB9801632.2A GB9801632D0 (en) 1998-01-26 1998-01-26 Novel compounds

Publications (2)

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WO1998050346A2 WO1998050346A2 (fr) 1998-11-12
WO1998050346A3 true WO1998050346A3 (fr) 1999-03-11

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AR (1) AR012450A1 (fr)
AU (1) AU7526798A (fr)
CO (1) CO4950609A1 (fr)
WO (1) WO1998050346A2 (fr)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7229986B2 (en) 2000-05-16 2007-06-12 Takeda Pharmaceutical Company Ltd. Melanin-concentrating hormone antagonist
US7388111B2 (en) 2005-10-19 2008-06-17 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
US8865737B2 (en) 2006-08-28 2014-10-21 Eisai R&D Management Co., Ltd. Antitumor agent for undifferentiated gastric cancer
US8952035B2 (en) 2007-11-09 2015-02-10 Eisai R&D Management Co., Ltd. Combination of anti-angiogenic substance and anti-tumor platinum complex
US8962655B2 (en) 2007-01-29 2015-02-24 Eisai R&D Management Co., Ltd. Composition for treatment of undifferentiated gastric cancer
US8962650B2 (en) 2011-04-18 2015-02-24 Eisai R&D Management Co., Ltd. Therapeutic agent for tumor
US8969344B2 (en) 2005-08-02 2015-03-03 Eisai R&D Management Co., Ltd. Method for assay on the effect of vascularization inhibitor
US9006256B2 (en) 2006-05-18 2015-04-14 Eisai R&D Management Co., Ltd. Antitumor agent for thyroid cancer
US9012458B2 (en) 2010-06-25 2015-04-21 Eisai R&D Management Co., Ltd. Antitumor agent using compounds having kinase inhibitory effect in combination
US9334239B2 (en) 2012-12-21 2016-05-10 Eisai R&D Management Co., Ltd. Amorphous form of quinoline derivative, and method for producing same
US9504746B2 (en) 2004-09-17 2016-11-29 Eisai R&D Management Co., Ltd. Pharmaceutical compositions of 4-(3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy)-7-methoxy-6-quinolinecarboxamide

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU6123699A (en) * 1998-10-16 2000-05-08 Takeda Chemical Industries Ltd. Nitrogenous fused heterocycle compounds, process for the preparation thereof andagents containing the same
CZ20013289A3 (cs) * 1999-03-12 2002-01-16 Boehringer Ingelheim Pharmaceuticals, Inc. Sloučeniny výhodné jako protizánětové prostředky
US6492393B1 (en) * 1999-11-16 2002-12-10 Boehringer Ingelheim Pharmaceuticals, Inc. Compounds useful as anti-inflammatory agents
ATE307127T1 (de) * 2000-08-16 2005-11-15 Neurogen Corp 2,4-substituierte pyridinderivate
HU230302B1 (hu) 2000-10-20 2015-12-28 Eisai R&D Management Co., Ltd. Nitrogéntartalmú aromás származékok és ezeket tartalmazó gyógyászati készítmények
US6525091B2 (en) * 2001-03-07 2003-02-25 Telik, Inc. Substituted diarylureas as stimulators for Fas-mediated apoptosis
JP4323810B2 (ja) 2001-04-20 2009-09-02 ワイス 5−ヒドロキシトリプトアミン−6リガンドとしてのヘテロシクリルオキシ−、−チオキシ−および−アミノベンザゾール誘導体
CA2444036A1 (fr) * 2001-04-20 2002-10-31 Yanfang Li Derives de heterocyclylalcoxy-, -alkylthio- et -alkylaminobenzazole en tant que ligands de la 5-hydroxytryptamine-6
US20030073681A1 (en) * 2001-08-21 2003-04-17 Hauske James R. 2-substituted piperidines that are ligands for monoamine receptors and transporters
JP2005526723A (ja) 2002-02-15 2005-09-08 グラクソ グループ リミテッド バニロイド受容体モジュレーター
PE20040522A1 (es) 2002-05-29 2004-09-28 Novartis Ag Derivados de diarilurea dependientes de la cinasa de proteina
US7056925B2 (en) 2002-08-13 2006-06-06 Abbott Laboratories Urea kinase inhibitors
KR20050100615A (ko) * 2003-01-14 2005-10-19 싸이토키네틱스, 인코포레이티드 화합물, 조성물 및 방법
CN101337930B (zh) 2003-11-11 2010-09-08 卫材R&D管理有限公司 脲衍生物的制备方法
US7166738B2 (en) 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
US7625949B2 (en) 2004-04-23 2009-12-01 Roche Palo Alto Llc Methods for treating retroviral infections
CA2570999C (fr) 2004-06-17 2014-01-07 Cytokinetics, Inc. Composes, compositions et methodes
US7176222B2 (en) 2004-07-27 2007-02-13 Cytokinetics, Inc. Syntheses of ureas
US7625931B2 (en) 2005-01-14 2009-12-01 Cgi Pharmaceuticals, Inc. Certain substituted diphenyl ureas, as modulators of kinase activity
US7777040B2 (en) 2005-05-03 2010-08-17 Cgi Pharmaceuticals, Inc. Certain substituted ureas, as modulators of kinase activity
US7538223B2 (en) 2005-08-04 2009-05-26 Cytokinetics, Inc. Compounds, compositions and methods
TW200808321A (en) 2005-12-15 2008-02-16 Cytokinetics Inc Certain chemical entities, compositions and methods
US7825120B2 (en) 2005-12-15 2010-11-02 Cytokinetics, Inc. Certain substituted ((piperazin-1-ylmethyl)benzyl)ureas
EP1959962A2 (fr) 2005-12-16 2008-08-27 Cytokinetics, Inc. Entites chimiques, compositions et methodes
US7989455B2 (en) 2005-12-19 2011-08-02 Cytokinetics, Inc. Compounds, compositions and methods
KR101446499B1 (ko) 2006-01-27 2014-10-06 피브로겐, 인크. 저산소증 유발가능 인자(hif)를 안정시키는 시아노이소퀴놀린 화합물
CA2647596C (fr) 2006-04-04 2012-06-12 Fibrogen, Inc. Composes de pyrrolo- et de thiazolopyridine et procedes d'utilisation
EP2370422B1 (fr) 2008-11-14 2019-06-05 Fibrogen, Inc. Dérivés de thiochromène utiles en tant qu'inhibiteurs de l'hydroxylase hif
GB201106817D0 (en) 2011-04-21 2011-06-01 Astex Therapeutics Ltd New compound
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GB201218864D0 (en) 2012-10-19 2012-12-05 Astex Therapeutics Ltd Bicyclic heterocycle compounds and their uses in therapy
US9980973B2 (en) 2012-10-19 2018-05-29 Astex Therapeutics Limited Bicyclic heterocycle compounds and their uses in therapy
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SG11201801083UA (en) 2015-08-20 2018-03-28 Eisai R&D Man Co Ltd Tumor therapeutic agent
US12303505B2 (en) 2017-02-08 2025-05-20 Eisai R&D Management Co., Ltd. Tumor-treating pharmaceutical composition
US20200197384A1 (en) 2017-05-16 2020-06-25 Eisai R&D Management Co., Ltd. Treatment of hepatocellular carcinoma

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1176918A (fr) * 1955-06-29 1959-04-17 Rech S Et Tech Appliquees Composés nitrés, aminés et amidés de la série aromatique et leur préparation
DE2226009A1 (de) * 1971-05-28 1973-01-25 Squibb & Sons Inc Phenylharnstoffe, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
DE4036782A1 (de) * 1990-11-17 1992-05-21 Basf Ag Substituierte anilide
WO1995015954A1 (fr) * 1993-12-07 1995-06-15 Smithkline Beecham Plc Biphenylylamides heterocycliques utilisables comme antagonistes du 5ht1d
EP0790240A1 (fr) * 1996-02-15 1997-08-20 Tanabe Seiyaku Co., Ltd. Dérivés de phénol ayant une activité pharmaceutique et procédés pour leur préparation

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1176918A (fr) * 1955-06-29 1959-04-17 Rech S Et Tech Appliquees Composés nitrés, aminés et amidés de la série aromatique et leur préparation
DE2226009A1 (de) * 1971-05-28 1973-01-25 Squibb & Sons Inc Phenylharnstoffe, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
DE4036782A1 (de) * 1990-11-17 1992-05-21 Basf Ag Substituierte anilide
WO1995015954A1 (fr) * 1993-12-07 1995-06-15 Smithkline Beecham Plc Biphenylylamides heterocycliques utilisables comme antagonistes du 5ht1d
EP0790240A1 (fr) * 1996-02-15 1997-08-20 Tanabe Seiyaku Co., Ltd. Dérivés de phénol ayant une activité pharmaceutique et procédés pour leur préparation

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
C. HANEGRAAFF ET AL, ANN. PHARM. FR., vol. 27, no. 11, 1969, pages 663 - 672, XP002084135 *
P.G. WYATT ET AL, J. MED. CHEM., vol. 38, no. 10, 1995, pages 1657 - 1665, XP002084134 *

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US9504746B2 (en) 2004-09-17 2016-11-29 Eisai R&D Management Co., Ltd. Pharmaceutical compositions of 4-(3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy)-7-methoxy-6-quinolinecarboxamide
US8969344B2 (en) 2005-08-02 2015-03-03 Eisai R&D Management Co., Ltd. Method for assay on the effect of vascularization inhibitor
US9006240B2 (en) 2005-08-02 2015-04-14 Eisai R&D Management Co., Ltd. Method for assay on the effect of vascularization inhibitor
US7388111B2 (en) 2005-10-19 2008-06-17 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
US9006256B2 (en) 2006-05-18 2015-04-14 Eisai R&D Management Co., Ltd. Antitumor agent for thyroid cancer
US8865737B2 (en) 2006-08-28 2014-10-21 Eisai R&D Management Co., Ltd. Antitumor agent for undifferentiated gastric cancer
US8962655B2 (en) 2007-01-29 2015-02-24 Eisai R&D Management Co., Ltd. Composition for treatment of undifferentiated gastric cancer
US8952035B2 (en) 2007-11-09 2015-02-10 Eisai R&D Management Co., Ltd. Combination of anti-angiogenic substance and anti-tumor platinum complex
US9012458B2 (en) 2010-06-25 2015-04-21 Eisai R&D Management Co., Ltd. Antitumor agent using compounds having kinase inhibitory effect in combination
US8962650B2 (en) 2011-04-18 2015-02-24 Eisai R&D Management Co., Ltd. Therapeutic agent for tumor
US9334239B2 (en) 2012-12-21 2016-05-10 Eisai R&D Management Co., Ltd. Amorphous form of quinoline derivative, and method for producing same

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AU7526798A (en) 1998-11-27

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