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公开(公告)号:AT380054T
公开(公告)日:2007-12-15
申请号:AT01945236
申请日:2001-06-01
Applicant: PENTAPHARM LTD , EZAKI GLICO CO
Inventor: KURIKI TAKASHI , NAKAE TAKASHI , NISHIMURA TAKAHISA , NAKAYAMA HIROKI
IPC: A61Q19/02 , A61K8/00 , A61K8/19 , A61K8/23 , A61K8/30 , A61K8/33 , A61K8/34 , A61K8/35 , A61K8/36 , A61K8/362 , A61K8/365 , A61K8/368 , A61K8/40 , A61K8/41 , A61K8/42 , A61K8/44 , A61K8/46 , A61K8/49 , A61K8/60 , A61K8/64 , A61K8/67 , A61K8/68 , A61K8/72 , A61K8/73 , A61K8/86 , A61K8/96 , A61K8/97 , A61K8/98 , A61K31/198 , A61K31/355 , A61K31/375 , A61K31/70 , A61K31/7048 , A61K31/715 , A61K36/06 , A61Q5/00 , A61Q19/00 , C07D201/00
Abstract: The objective of the present invention was to enhance the skin whitening effects and blackening prevention effects and supply safe topical agents for dermatological use. For that purpose a topical composition comprising 4-hydroxyphenyl-alpha-D-glucopyranoside and UV absorber is manufactured.
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公开(公告)号:EA008705B1
公开(公告)日:2007-06-29
申请号:EA200501582
申请日:2004-04-08
Applicant: ALGORX PHARMACEUTICALS INC
Inventor: MCINVAIN SHARON , CHEN WEI , RAMIYA PREMCHANDRAN H , BIRCH RONALD , CARTER RICHARD B , ANDERSON TIMOTHY A , ZHANG HEPING
IPC: A61K31/165 , A61K31/05 , A61K31/16 , A61K31/5415 , A61K31/551 , A61K45/06 , C07C51/36 , C07C231/02 , C07C233/20 , C07D201/00
Abstract: Внастоящемизобретениипредложенспособсинтезатранс-изомеракапсаицинаи/иликапсаициноподобныхсоединений, путемиспользованияпроцесса, вкоторомтранс-конфигурациюзадаютс самогоначалареакциисинтезаи сохраняютеенапротяжениивсегопроцессасинтеза.
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公开(公告)号:ES2245594B1
公开(公告)日:2006-12-01
申请号:ES200401285
申请日:2004-05-27
Applicant: ESTEVE LABOR DR
Inventor: NOHEDA MARIN PEDRO , BERNABE PAJARES MANUEL , MAROTO QUINTANA SERGIO , TABARES CANTERO NURIA
IPC: C07D205/12 , C07D201/00
Abstract: La invención proporciona azetidinonas espirocondensadas sumamente funcionalizadas que tienen un resto ciclohexano con el número deseado de grupos hidroxilo protegidos o sin proteger, que se introducen con alta estereo y regioselectividad, así como procedimientos para su obtención.
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公开(公告)号:BRPI0409748A
公开(公告)日:2006-10-24
申请号:BRPI0409748
申请日:2004-04-08
Applicant: ALGORX PHARMACEUTICALS INC
Inventor: MCIIVAIN SHARON , CHEN WEI , RAMIYA PREMCHANDRAN H , BURCH RONALD , CARTER RICHARD , ANDERSON TIMOTHY A
IPC: A61K31/05 , A61K31/16 , A61K31/165 , A61K31/5415 , A61K31/551 , A61K45/06 , C07C51/36 , C07C231/02 , C07C233/20 , C07D201/00
Abstract: The present invention provides methods for synthesizing the trans isomer of capsaicin and/or capsaicin-like compounds by utilizing a process wherein the trans geometry is set from the beginning of the synthesis reaction and carried through the entire synthesis process.
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公开(公告)号:EA200501582A1
公开(公告)日:2006-06-30
申请号:EA200501582
申请日:2004-04-08
IPC: A61K31/165 , A61K31/05 , A61K31/16 , A61K31/5415 , A61K31/551 , A61K45/06 , C07C51/36 , C07C231/02 , C07C233/20 , C07D201/00
Abstract: Внастоящемизобретениипредложенспособсинтезатрансизомеракапсаицинаи/иликапсаициноподобныхсоединенийпутемиспользованияпроцесса, вкоторомтрансконфигурациюзадаютс самогоначалареакциисинтезаи сохраняютеенапротяжениивсегопроцессасинтеза.
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公开(公告)号:DK1280757T3
公开(公告)日:2005-12-12
申请号:DK01947234
申请日:2001-04-23
Applicant: HOFFMANN LA ROCHE
Inventor: LAPIERRE JEAN-MARC , BELLONI PAULA NANETTE , JOLIDON SYNESE , KLAUS MICHAEL
IPC: A61K31/045 , A61K31/11 , A61K31/165 , A61K31/19 , A61K31/192 , A61K31/20 , A61K31/23 , A61K31/235 , A61K31/27 , A61K31/275 , A61K31/353 , A61K31/381 , A61K31/382 , A61K31/421 , A61K31/4704 , A61P3/02 , A61P11/00 , A61P17/00 , A61P17/02 , A61P17/06 , A61P17/16 , A61P35/00 , A61P43/00 , C07C63/49 , C07C63/64 , C07C63/66 , C07C63/74 , C07C65/26 , C07C65/28 , C07C69/616 , C07C69/635 , C07C69/734 , C07C69/76 , C07C69/80 , C07C69/82 , C07C69/90 , C07C69/94 , C07C255/33 , C07C271/58 , C07C323/56 , C07C403/20 , C07D213/30 , C07D215/12 , C07D215/14 , C07D215/22 , C07D261/08 , C07D263/00 , C07D263/38 , C07D271/06 , C07D277/24 , C07D307/42 , C07D311/00 , C07D311/58 , C07D333/40 , C07D335/06 , C07D201/00
Abstract: New compounds containing bicyclic fused rings, one of which being a phenyl moiety connected by an aliphatic chain to a cycloalkyl or aryl moiety, and pharmaceutically active salts thereof are useful as RAR selective retinoid agonists. Furthermore, such retinoic acid receptor agonists, particularly retinoic acid receptor gamma (RARgamma) selective agonists, are useful for the treatment of emphysema and associated pulmonary diseases, as well as for the therapy and prophylaxis of dermatological disorders, for the therapy and prophylaxis of malignant and premalignant epithelial lesions, tumors and precancerous changes of the mucous membrane in the mouth, tongue, larynx, esophagus, bladder, cervix and colon.
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公开(公告)号:NO20053910D0
公开(公告)日:2005-08-22
申请号:NO20053910
申请日:2005-08-22
Applicant: UCB FARCHIM SA
Inventor: ATES CELAL , CAVOY EMILE , BOUVY DIDIER
IPC: C07D201/00 , C07D271/06 , C07D271/07 , C07D295/15 , C07D
Abstract: The present invention relates to new enantiomerically pure piperazine derivatives of formula (I) wherein Y represents hydroxy or a leaving group and n is 1, 2, 3, 4 or 5, and to their use as synthesis intermediates, especially for the preparation of pharmaceutically active compounds
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公开(公告)号:DK1235831T3
公开(公告)日:2005-06-27
申请号:DK00971960
申请日:2000-10-13
Applicant: ASTRAZENECA AB
Inventor: BJOERE ANNIKA , STRANDLUND GERT , WILSTERMANN MICHAEL , PONTEN FRITIOF , BJOERSNE MAGNUS , CLADINGBOEL DAVID , HOFFMAN KURT-JUERGEN , PAVEY JOHN , SVENSSON PEDER , THOMSON COLIN
IPC: C07D303/36 , A61K20060101 , A61K31/535 , A61K31/537 , A61K31/538 , A61K31/5386 , A61P20060101 , A61P9/06 , C07B61/00 , C07D20060101 , C07D265/30 , C07D295/16 , C07D295/26 , C07D303/48 , C07D498/00 , C07D498/08 , C07D513/00 , C07D515/02 , C07D519/00 , C07D201/00
Abstract: The present invention relates to a combination comprising component (a) being a compound of formula I, and component (b), being, at least one other drug useful in the treatment of arrhythmias and / or at least one other drug useful in the treatment of a cardiovascular disorder.
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公开(公告)号:HK1051046B
公开(公告)日:2005-04-29
申请号:HK03101833
申请日:2003-03-13
Applicant: ALLERGAN PHARMACEUTICALS INT LTD
Inventor: FREDRICK DANA CAZER , GREGORY EUGENE PERRY , DENNIS MICHAEL BILLINGS , NANCY LEE REDMAN-FUREY
IPC: A61K31/663 , C07F20060101 , A61K20060101 , A61K31/675 , A61P20060101 , A61P3/14 , A61P19/00 , A61P19/02 , A61P19/08 , A61P19/10 , A61P25/00 , A61P29/00 , C07D201/00 , C07F9/58
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公开(公告)号:TR200402435T4
公开(公告)日:2004-12-21
申请号:TR200402435
申请日:2001-02-01
Applicant: PROCTER & GAMBLE
Inventor: CAZER FREDRICK DANA , PERRY GREGORY EUGENE , BILLINGS DENNIS MICHEAL , FUREY NANCY LEE REDMAN
IPC: A61K31/663 , A61K31/675 , A61P3/14 , A61P19/00 , A61P19/02 , A61P19/08 , A61P19/10 , A61P25/00 , A61P29/00 , C07D201/00 , C07F9/58
Abstract: The present invention discloses 3-pyridyl-1-hydroxyethylidene-1,1-bisphosphonic acid sodium hemipentahydrate and monohydrate, methods of preparing the hemipentahydrate or monohydrate through control of the nucleation temperature and rate of crystallization and pharmaceutical compositions containing one or both of the hydrate forms.
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