AR049545A1 - Cis-imidazolinas - Google Patents
Cis-imidazolinasInfo
- Publication number
- AR049545A1 AR049545A1 ARP050101998A ARP050101998A AR049545A1 AR 049545 A1 AR049545 A1 AR 049545A1 AR P050101998 A ARP050101998 A AR P050101998A AR P050101998 A ARP050101998 A AR P050101998A AR 049545 A1 AR049545 A1 AR 049545A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- lower alkyl
- lower alkoxy
- nx8x9
- substituted
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic 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
- C07D233/20—Heterocyclic 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 substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/22—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic 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
- C07D233/20—Heterocyclic 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 substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/26—Radicals substituted by carbon atoms having three bonds to hetero atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Compuestos, las sales y ésteres farmacéuticamente aceptables de los mismos que inhiben la interaccion de la proteína MDM2 con los péptidos similares al p53 y por ello tienen una actividad antiproliferante. Reivindicacion 1: Un compuesto de formula (1) y las sales y ésteres farmacéuticamente aceptables del mismo, en la que X1 se elige entre el grupo formado por alcoxi inferior y alcoxi inferior sustituido por trifluorometilo o fluor; X2 se elige entre el grupo formado por hidrogeno, halogeno, alquilo inferior y -C(X4X5)-X6; X3 se elige entre el grupo formado por hidrogeno, alcoxi inferior, halogeno y -C(X4X5)-X6; con la condicion de que cuando X2 es hidrogeno, halogeno o alquilo inferior, entonces X3 sea -C(X4X5)-X6; X4 y X5 son alquilo inferior y pueden estar unidos entre sí para formar un cicloalquilo; X6 se elige entre el grupo formado por alquilo inferior, ciano, -CH2-OH, -CH2-O-alquilo inferior, -CH2-O-alquilo inferior sustituido por alcoxi inferior, -C(O)X7 y -CH2-NX8X9; X7 se elige entre el grupo formado por hidroxi, alcoxi inferior, morfolino y -NX8X9; X8 y X9 se eligen con independencia entre sí entre el grupo formado por hidrogeno, alquilo inferior, alquilo inferior sustituido por alcoxi inferior o ciano y alcoxi inferior; Y1 e Y2 se eligen con independencia entre sí entre el grupo formado por halogeno, ciano y acetileno; R se elige entre el grupo formado por piperidinilo sustituido por un heterociclo de cinco o seis eslabones, piperidinilo sustituido por - NX8X9, y un resto de formula (2), en la que n = 1 o 2; R1 puede ser uno o varios sustituyentes elegidos entre el grupo formado por hidrogeno, oxo, alquilo inferior sustituido por R2, -C(O)R3 y -SO2-alquilo inferior; R2 se elige entre el grupo formado por hidroxi, alcoxi inferior, trifluorometilo, ciano, -NH-SO2-alquilo inferior, -NH-C(O)-alquilo inferior, -C(O)-alquilo inferior, -C(O)R4, -C(O)-NX8X9, -SO2-alquilo inferior, -SO2-NX8X9; R3 se elige entre el grupo formado por un heterociclo de cinco eslabones, alquilo inferior, alcoxi inferior y alquilo inferior sustituido por alcoxi inferior; y R4 se elige entre el grupo formado por hidroxi, alcoxi inferior, morfolino y -NX8X9.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US57227504P | 2004-05-18 | 2004-05-18 | |
US61553404P | 2004-10-01 | 2004-10-01 | |
US66877205P | 2005-04-06 | 2005-04-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR049545A1 true AR049545A1 (es) | 2006-08-16 |
Family
ID=35058746
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP050101998A AR049545A1 (es) | 2004-05-18 | 2005-05-16 | Cis-imidazolinas |
Country Status (21)
Country | Link |
---|---|
US (2) | US7964724B2 (es) |
EP (1) | EP1753727B1 (es) |
JP (1) | JP4814228B2 (es) |
KR (3) | KR20080027969A (es) |
CN (1) | CN1953965B (es) |
AR (1) | AR049545A1 (es) |
AT (1) | ATE414693T1 (es) |
AU (1) | AU2005243465B2 (es) |
BR (1) | BRPI0511328A (es) |
CA (1) | CA2565189A1 (es) |
DE (1) | DE602005011132D1 (es) |
ES (1) | ES2314660T3 (es) |
IL (1) | IL178884A (es) |
MX (1) | MXPA06013246A (es) |
MY (1) | MY143800A (es) |
NO (1) | NO20065730L (es) |
PE (1) | PE20060679A1 (es) |
RU (1) | RU2006144811A (es) |
TW (1) | TW200600501A (es) |
WO (1) | WO2005110996A1 (es) |
ZA (1) | ZA200609595B (es) |
Families Citing this family (66)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7893278B2 (en) | 2004-06-17 | 2011-02-22 | Hoffman-La Roche Inc. | CIS-imidazolines |
RU2411238C2 (ru) * | 2005-03-16 | 2011-02-10 | Ф.Хоффманн-Ля Рош Аг | Цис-2,4,5-триарилимидазолины и их применение в качестве противораковых лекарственных средств |
BRPI0619236A2 (pt) * | 2005-12-01 | 2011-09-20 | Hoffmann La Roche | derivados de 2,4,5-trifenil imidazolina, composição farmacêutica que os compreende, uso e processo para a sìntese dos mesmos |
KR101015073B1 (ko) * | 2006-01-18 | 2011-02-16 | 에프. 호프만-라 로슈 아게 | Mdm2 억제제로서의시스-4,5-비아릴-2-헤테로시클릭-이미다졸린 |
EP2035416A1 (en) | 2006-06-30 | 2009-03-18 | Schering Corporation | Substituted piperidines that increase p53 activity and the uses thereof |
CN101541759A (zh) * | 2006-11-27 | 2009-09-23 | 诺瓦提斯公司 | 取代的二氢咪唑类及其在治疗肿瘤中的用途 |
MX2009006397A (es) | 2006-12-14 | 2009-08-13 | Daiichi Sankyo Co Ltd | Derivados de imidazotiazol. |
EP2118123B1 (en) * | 2007-01-31 | 2015-10-14 | Dana-Farber Cancer Institute, Inc. | Stabilized p53 peptides and uses thereof |
WO2008121767A2 (en) | 2007-03-28 | 2008-10-09 | President And Fellows Of Harvard College | Stitched polypeptides |
US7625895B2 (en) | 2007-04-12 | 2009-12-01 | Hoffmann-Le Roche Inc. | Diphenyl-dihydro-imidazopyridinones |
RU2487127C2 (ru) | 2007-10-09 | 2013-07-10 | Ф.Хоффманн-Ля Рош Аг | Хиральные цис-имидазолины |
WO2009151069A1 (ja) | 2008-06-12 | 2009-12-17 | 第一三共株式会社 | 4,7-ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体 |
DE102008047128A1 (de) | 2008-09-15 | 2010-04-15 | Johann Wolfgang Goethe-Universität Frankfurt am Main | Verwendung von cis-Imidazolinen, insbesondere Nutlinen, zur Behandlung von chemoresistenten Krebserkrankungen |
MX2011007598A (es) | 2009-01-16 | 2011-08-08 | Daiichi Sankyo Co Ltd | Derivados de imidazotiazol que tienen estructura de anillo de prolina. |
BR112012008849A2 (pt) | 2009-10-14 | 2015-09-22 | Schering Corp | composto, composição farmacêutica, e, uso de um composto |
KR20120099462A (ko) | 2009-11-12 | 2012-09-10 | 더 리젠츠 오브 더 유니버시티 오브 미시건 | 스피로-옥신돌 mdm2 길항제 |
US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
WO2011106650A2 (en) * | 2010-02-27 | 2011-09-01 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Novel p53-mdm2/p53-mdm4 antagonists to treat proliferative disease |
JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
WO2012021876A2 (en) | 2010-08-13 | 2012-02-16 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles |
CA2813256A1 (en) | 2010-09-30 | 2012-04-05 | St. Jude Children's Research Hospital | Aryl-substituted imidazoles |
UY33725A (es) | 2010-11-12 | 2012-06-29 | Sanofi Sa | Antagonistas de mdm2 de espiro-oxindol |
PL2684880T3 (pl) | 2011-03-10 | 2018-07-31 | Daiichi Sankyo Company, Limited | Pochodna dispiropirolidyny |
SG194873A1 (en) | 2011-05-11 | 2013-12-30 | Sanofi Sa | Spiro-oxindole mdm2 antagonists |
MX352672B (es) | 2011-09-27 | 2017-12-04 | Amgen Inc | Compuestos heterocíclicos como inhibidores de mdm2 para el tratamiento del cáncer. |
US20140328893A1 (en) | 2011-10-11 | 2014-11-06 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Nutlin compounds for use in the treatment of pulmonary hypertension |
AU2012326026B2 (en) | 2011-10-18 | 2017-04-13 | Aileron Therapeutics, Inc. | Peptidomimetic macrocyles |
US8987274B2 (en) | 2011-10-28 | 2015-03-24 | Merck Sharp & Dohme Corp | Macrocycles that increase p53 activity and the uses thereof |
WO2013080141A1 (en) | 2011-11-29 | 2013-06-06 | Novartis Ag | Pyrazolopyrrolidine compounds |
US9062071B2 (en) | 2011-12-21 | 2015-06-23 | Merck Sharp & Dohme Corp. | Substituted piperidines as HDM2 inhibitors |
UY34591A (es) | 2012-01-26 | 2013-09-02 | Novartis Ag | Compuestos de imidazopirrolidinona |
KR102112373B1 (ko) | 2012-02-15 | 2020-05-18 | 에일러론 테라퓨틱스 인코포레이티드 | 펩티드모방체 마크로사이클 |
US8987414B2 (en) | 2012-02-15 | 2015-03-24 | Aileron Therapeutics, Inc. | Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles |
JP6171003B2 (ja) | 2012-05-24 | 2017-07-26 | ノバルティス アーゲー | ピロロピロリジノン化合物 |
TWI586668B (zh) | 2012-09-06 | 2017-06-11 | 第一三共股份有限公司 | 二螺吡咯啶衍生物之結晶 |
SG11201503052RA (en) | 2012-11-01 | 2015-05-28 | Aileron Therapeutics Inc | Disubstituted amino acids and methods of preparation and use thereof |
WO2014100065A1 (en) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as hdm2 inhibitors |
EP2948453B1 (en) | 2013-01-22 | 2017-08-02 | Novartis AG | Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction |
EP2948451B1 (en) | 2013-01-22 | 2017-07-12 | Novartis AG | Substituted purinone compounds |
WO2014120748A1 (en) | 2013-01-30 | 2014-08-07 | Merck Sharp & Dohme Corp. | 2,6,7,8 substituted purines as hdm2 inhibitors |
US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
MX368703B (es) | 2013-02-28 | 2019-10-11 | Amgen Inc | Un inhibidor de mdm2 derivado de acido benzoico para el tratamiento del cancer. |
CA2906538C (en) | 2013-03-14 | 2021-02-02 | Ana Gonzalez Buenrostro | Heteroaryl acid morpholinone compounds as mdm2 inhibitors for the treatment of cancer |
WO2014165816A1 (en) | 2013-04-05 | 2014-10-09 | North Carolina Central University | Compounds useful for the treatment of metabolic disorders and synthesis of the same |
US8975417B2 (en) | 2013-05-27 | 2015-03-10 | Novartis Ag | Pyrazolopyrrolidine derivatives and their use in the treatment of disease |
EP3412675A1 (en) | 2013-05-27 | 2018-12-12 | Novartis AG | Imidazopyrrolidinone derivatives and their use in the treatment of disease |
US9624247B2 (en) | 2013-05-28 | 2017-04-18 | Novartis Ag | Pyrazolo-pyrrolidin-4-one derivatives as bet inhibitors and their use in the treatment of disease |
PT3004112T (pt) | 2013-05-28 | 2017-12-11 | Novartis Ag | Derivados de pirazolo-pirrolidin-4-ona e sua utilização no tratamento de doença |
CN104208066B (zh) * | 2013-06-03 | 2016-06-15 | 中国科学院遗传与发育生物学研究所 | 哌嗪衍生物作为p53分子调节剂的用途 |
JOP20200296A1 (ar) | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
CN105916857B (zh) | 2013-11-21 | 2018-06-22 | 诺华股份有限公司 | 吡咯并吡咯酮衍生物及其作为bet抑制剂的用途 |
CN107106642B (zh) | 2014-09-24 | 2021-02-26 | 艾瑞朗医疗公司 | 拟肽大环化合物及其制剂 |
WO2016049359A1 (en) | 2014-09-24 | 2016-03-31 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles and uses thereof |
CA2974449C (en) | 2015-01-22 | 2023-08-29 | Sanofi-Aventis Deutschland Gmbh | Process for the production of 2-[4-(cyclopropanecarbonyl)phenyl]-2-methyl-propanenitrile |
AU2016235424A1 (en) | 2015-03-20 | 2017-10-05 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles and uses thereof |
CN108368161A (zh) | 2015-09-10 | 2018-08-03 | 艾瑞朗医疗公司 | 作为mcl-1调节剂的拟肽大环化合物 |
US11192898B2 (en) | 2016-04-06 | 2021-12-07 | The Regents Of The University Of Michigan | MDM2 protein degraders |
CA3020281A1 (en) | 2016-04-06 | 2017-10-12 | The Regents Of The University Of Michigan | Monofunctional intermediates for ligand-dependent target protein degradation |
WO2017201449A1 (en) | 2016-05-20 | 2017-11-23 | Genentech, Inc. | Protac antibody conjugates and methods of use |
WO2019079677A1 (en) * | 2017-10-20 | 2019-04-25 | Corbus Pharmaceuticals, Inc. | METHODS AND COMPOSITIONS RELATING TO 5- (1,1-DIMETHYLHEPTYL) -ORRESORCINOL ULTRAPUR |
EP3863720A1 (en) | 2018-10-08 | 2021-08-18 | The Regents Of The University Of Michigan | Small molecule mdm2 protein degraders |
JP2023518423A (ja) | 2020-03-19 | 2023-05-01 | カイメラ セラピューティクス, インコーポレイテッド | Mdm2分解剤およびそれらの使用 |
WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
US11548866B1 (en) | 2021-11-22 | 2023-01-10 | Ligature Therapeutics Pte. Ltd. | Therapeutic compounds and methods of use thereof |
US11504381B1 (en) * | 2021-11-22 | 2022-11-22 | Ligature Therapeutics Pte. Ltd. | Therapeutic compounds and methods of use thereof |
KR20230087856A (ko) | 2021-12-10 | 2023-06-19 | 교촌 에프 앤 비(주) | 생체이용율과 이미다졸 펩타이드가 증가된 수용성 닭가슴살 가수분해물 및 그 제조방법 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02101065A (ja) | 1988-10-06 | 1990-04-12 | Tanabe Seiyaku Co Ltd | イミダゾリン誘導体及びその製法 |
DE4203547A1 (de) * | 1992-02-07 | 1993-08-12 | Knoll Ag | Verfahren zur racemattrennung von verapamil |
FR2756560A1 (fr) * | 1996-12-04 | 1998-06-05 | Adir | Nouveaux derives de l'imidazoline, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
GB2351082A (en) | 1999-06-18 | 2000-12-20 | Lilly Forschung Gmbh | Synthesis of Cyclic Substituted Amidines |
US6653501B2 (en) * | 2001-06-27 | 2003-11-25 | Napro Biotherapeutics, Inc. | Chiral resolution method for producing compounds useful in the synthesis of taxanes |
WO2003051359A1 (en) * | 2001-12-18 | 2003-06-26 | F.Hoffmann-La Roche Ag | Cis-2,4,5- triphenyl-imidazolines and their use in the treatment of tumors |
RU2312101C2 (ru) * | 2001-12-18 | 2007-12-10 | Ф.Хоффманн-Ля Рош Аг | Цис-имидазолины в качестве ингибиторов mdm2 |
-
2005
- 2005-05-10 KR KR1020087005155A patent/KR20080027969A/ko not_active Application Discontinuation
- 2005-05-10 WO PCT/EP2005/005046 patent/WO2005110996A1/en active Application Filing
- 2005-05-10 MX MXPA06013246A patent/MXPA06013246A/es active IP Right Grant
- 2005-05-10 BR BRPI0511328-8A patent/BRPI0511328A/pt not_active IP Right Cessation
- 2005-05-10 CA CA002565189A patent/CA2565189A1/en not_active Abandoned
- 2005-05-10 EP EP05742255A patent/EP1753727B1/en active Active
- 2005-05-10 JP JP2007517027A patent/JP4814228B2/ja not_active Expired - Fee Related
- 2005-05-10 ES ES05742255T patent/ES2314660T3/es active Active
- 2005-05-10 KR KR1020067024089A patent/KR100832277B1/ko not_active IP Right Cessation
- 2005-05-10 CN CN200580015663XA patent/CN1953965B/zh not_active Expired - Fee Related
- 2005-05-10 RU RU2006144811/04A patent/RU2006144811A/ru not_active Application Discontinuation
- 2005-05-10 KR KR1020117006619A patent/KR20110033964A/ko not_active IP Right Cessation
- 2005-05-10 AU AU2005243465A patent/AU2005243465B2/en not_active Ceased
- 2005-05-10 DE DE602005011132T patent/DE602005011132D1/de active Active
- 2005-05-10 AT AT05742255T patent/ATE414693T1/de active
- 2005-05-13 US US11/129,621 patent/US7964724B2/en not_active Expired - Fee Related
- 2005-05-16 MY MYPI20052212A patent/MY143800A/en unknown
- 2005-05-16 AR ARP050101998A patent/AR049545A1/es not_active Application Discontinuation
- 2005-05-16 PE PE2005000539A patent/PE20060679A1/es not_active Application Discontinuation
- 2005-05-16 TW TW094115741A patent/TW200600501A/zh unknown
-
2006
- 2006-10-26 IL IL178884A patent/IL178884A/en not_active IP Right Cessation
- 2006-11-17 ZA ZA200609595A patent/ZA200609595B/xx unknown
- 2006-12-12 NO NO20065730A patent/NO20065730L/no not_active Application Discontinuation
-
2009
- 2009-02-05 US US12/366,381 patent/US20090143364A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
KR100832277B1 (ko) | 2008-05-26 |
IL178884A0 (en) | 2007-03-08 |
IL178884A (en) | 2010-12-30 |
KR20070011516A (ko) | 2007-01-24 |
EP1753727B1 (en) | 2008-11-19 |
MXPA06013246A (es) | 2007-02-08 |
TW200600501A (en) | 2006-01-01 |
EP1753727A1 (en) | 2007-02-21 |
PE20060679A1 (es) | 2006-08-11 |
JP4814228B2 (ja) | 2011-11-16 |
ES2314660T3 (es) | 2009-03-16 |
BRPI0511328A (pt) | 2007-12-04 |
US7964724B2 (en) | 2011-06-21 |
KR20080027969A (ko) | 2008-03-28 |
ATE414693T1 (de) | 2008-12-15 |
MY143800A (en) | 2011-07-15 |
US20090143364A1 (en) | 2009-06-04 |
DE602005011132D1 (de) | 2009-01-02 |
JP2007538022A (ja) | 2007-12-27 |
AU2005243465A1 (en) | 2005-11-24 |
CN1953965A (zh) | 2007-04-25 |
RU2006144811A (ru) | 2008-06-27 |
CN1953965B (zh) | 2012-07-04 |
US20050288287A1 (en) | 2005-12-29 |
AU2005243465B2 (en) | 2011-08-25 |
WO2005110996A1 (en) | 2005-11-24 |
NO20065730L (no) | 2007-01-19 |
KR20110033964A (ko) | 2011-04-01 |
CA2565189A1 (en) | 2005-11-24 |
ZA200609595B (en) | 2008-06-25 |
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