MX2010001745A - Imidazoles fusionados para el tratamiento del cancer. - Google Patents
Imidazoles fusionados para el tratamiento del cancer.Info
- Publication number
- MX2010001745A MX2010001745A MX2010001745A MX2010001745A MX2010001745A MX 2010001745 A MX2010001745 A MX 2010001745A MX 2010001745 A MX2010001745 A MX 2010001745A MX 2010001745 A MX2010001745 A MX 2010001745A MX 2010001745 A MX2010001745 A MX 2010001745A
- Authority
- MX
- Mexico
- Prior art keywords
- cancer treatment
- fused imidazoles
- fused
- imidazoles
- pi3k
- Prior art date
Links
Classifications
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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 two hetero rings
- C07D401/10—Heterocyclic 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 two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Compuestos de fórmula (I) (ver fórmula I) tautórneros o estereoisómeros de éstos, o sus sales, donde el anillo B y el imidazol al que está fusionado, R4, R6, y R7 tienen los significados indicados en la descripción y las reivindicaciones, que son inhibidores eficaces de la vía Pi3K/Akt.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1573MU2007 | 2007-08-14 | ||
EP07118733A EP2062893A1 (en) | 2007-10-18 | 2007-10-18 | Fused imidazoles for cancer treatment |
PCT/EP2008/060686 WO2009021990A1 (en) | 2007-08-14 | 2008-08-14 | Fused imidazoles for cancer treatment |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2010001745A true MX2010001745A (es) | 2010-03-10 |
Family
ID=39876840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2010001745A MX2010001745A (es) | 2007-08-14 | 2008-08-14 | Imidazoles fusionados para el tratamiento del cancer. |
Country Status (24)
Country | Link |
---|---|
US (2) | US8592591B2 (es) |
EP (1) | EP2176259B1 (es) |
JP (1) | JP5327652B2 (es) |
KR (1) | KR20100049589A (es) |
CN (1) | CN101835776A (es) |
AR (1) | AR067946A1 (es) |
AT (1) | ATE503757T1 (es) |
AU (1) | AU2008288390A1 (es) |
CA (1) | CA2695251C (es) |
CL (1) | CL2008002397A1 (es) |
CR (1) | CR11271A (es) |
DE (1) | DE602008005894D1 (es) |
DO (1) | DOP2010000057A (es) |
EA (1) | EA201000297A1 (es) |
EC (1) | ECSP109965A (es) |
MA (1) | MA31609B1 (es) |
MX (1) | MX2010001745A (es) |
PA (1) | PA8793301A1 (es) |
PE (1) | PE20090596A1 (es) |
SV (1) | SV2010003482A (es) |
TN (1) | TN2010000071A1 (es) |
TW (1) | TW200924761A (es) |
UY (1) | UY31292A1 (es) |
WO (1) | WO2009021990A1 (es) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ576570A (en) * | 2006-10-19 | 2010-11-26 | Takeda Pharmaceutical | 7-sulfonylamino-2-thiazol and 2-thiadiazol -indole compounds |
PA8793301A1 (es) * | 2007-08-14 | 2009-04-23 | Bayer Schering Pharma Ag | Imidazoles bicíclicos fusionados |
WO2009046448A1 (en) | 2007-10-04 | 2009-04-09 | Intellikine, Inc. | Chemical entities and therapeutic uses thereof |
US7868001B2 (en) * | 2007-11-02 | 2011-01-11 | Hutchison Medipharma Enterprises Limited | Cytokine inhibitors |
US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US8637542B2 (en) | 2008-03-14 | 2014-01-28 | Intellikine, Inc. | Kinase inhibitors and methods of use |
BRPI0915231A2 (pt) | 2008-07-08 | 2018-06-12 | Intellikine Inc | compostos inibidores de quinase e métodos de uso |
US8476282B2 (en) | 2008-11-03 | 2013-07-02 | Intellikine Llc | Benzoxazole kinase inhibitors and methods of use |
EP2396331B1 (en) * | 2009-02-13 | 2013-10-16 | Bayer Intellectual Property GmbH | Fused pyrimidines as akt inhibitors |
AU2010226490A1 (en) | 2009-03-20 | 2011-10-06 | Amgen Inc. | Inhibitors of PI3 kinase |
TW201103943A (en) | 2009-04-27 | 2011-02-01 | Shionogi & Co | Urea derivative having pi3k inhibitory activity |
GEP201706639B (en) | 2009-08-17 | 2017-03-27 | Intellikine Llc | Heterocyclic compounds and uses thereof |
NZ599597A (en) | 2009-10-30 | 2013-05-31 | Janssen Pharmaceutica Nv | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
WO2011053476A1 (en) * | 2009-11-02 | 2011-05-05 | Abbott Laboratories | Imidazopyridines as a novel scaffold for multi-targeted kinase inhibition |
EP2526102B1 (en) | 2010-01-22 | 2017-03-08 | Fundación Centro Nacional de Investigaciones Oncológicas Carlos III | Inhibitors of PI3 kinase |
UY33213A (es) | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
CN103097384B (zh) * | 2010-07-12 | 2017-02-15 | 拜耳知识产权有限责任公司 | 取代的咪唑并[1,2‑a]嘧啶和吡啶 |
CN103384670B (zh) | 2010-07-28 | 2016-05-25 | 拜耳知识产权有限责任公司 | 取代的咪唑并[1,2-b]哒嗪 |
EP2463289A1 (en) | 2010-11-26 | 2012-06-13 | Almirall, S.A. | Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors |
DE102011008352A1 (de) * | 2011-01-12 | 2012-07-12 | Merck Patent Gmbh | 5-([1,2,3]Triazol-4-yl)-7H-pyrrolo-[2,3-d]pyrimidinderivate |
AR085397A1 (es) | 2011-02-23 | 2013-09-25 | Intellikine Inc | Combinacion de inhibidores de quinasa y sus usos |
PL2698372T3 (pl) * | 2011-04-06 | 2016-07-29 | Taiho Pharmaceutical Co Ltd | Nowy związek imidazooksazynowy lub jego sól |
JO3068B1 (ar) * | 2011-04-07 | 2017-03-15 | Bayer Ip Gmbh | إيميدازوبيريميدينات كمثبطات كيناز akt |
MX344600B (es) | 2011-06-27 | 2016-12-20 | Janssen Pharmaceutica Nv | Derivados de 1-aril-4-metil-[1,2,4]triazolo[4,3-a]quinoxalina. |
EP2554544A1 (en) | 2011-08-01 | 2013-02-06 | Almirall, S.A. | Pyridin-2(1h)-one derivatives as jak inhibitors |
US9260435B2 (en) * | 2012-01-10 | 2016-02-16 | Bayer Pharma Aktiengesellschaft | Substituted imidazopyrazines as Akt kinase inhibitors |
CN104066736B (zh) | 2012-01-10 | 2017-03-08 | 拜耳知识产权有限责任公司 | 作为akt激酶抑制剂的取代的吡唑并嘧啶 |
RU2657540C2 (ru) | 2012-06-26 | 2018-06-14 | Янссен Фармацевтика Нв | Комбинации, содержащие ингибиторы pde 2, такие как 1-арил-4-метил-[1,2,4]триазоло[4,3-а]хиноксалиновые соединения, и ингибиторы pde 10, для применения в лечении неврологических или метаболических расстройств |
JP5855250B2 (ja) * | 2012-07-02 | 2016-02-09 | 大鵬薬品工業株式会社 | イミダゾオキサジン化合物による抗腫瘍効果増強剤 |
RU2667058C2 (ru) | 2012-07-09 | 2018-09-14 | Янссен Фармацевтика Нв | Ингибиторы фермента фосфодиэстеразы 10 |
CN105209042B (zh) | 2013-03-22 | 2019-03-08 | 米伦纽姆医药公司 | 催化性mtorc 1/2抑制剂与选择性极光a激酶抑制剂的组合 |
GB201321732D0 (en) * | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic agents |
WO2016136928A1 (ja) | 2015-02-27 | 2016-09-01 | 大鵬薬品工業株式会社 | イミダゾオキサジンの結晶、当該結晶を含む医薬組成物、及び当該結晶の製造方法 |
US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
WO2018081167A1 (en) * | 2016-10-24 | 2018-05-03 | Yumanity Therapeutics | Compounds and uses thereof |
CA3083000A1 (en) | 2017-10-24 | 2019-05-02 | Yumanity Therapeutics, Inc. | Compounds and uses thereof |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6908929B2 (en) | 2000-03-31 | 2005-06-21 | Ortho-Mcneil Pharmaceutical, Inc. | Phenyl-substituted imidazopyridines |
EP1277754B8 (en) * | 2000-04-27 | 2005-09-28 | Astellas Pharma Inc. | Imidazopyridine derivatives |
WO2004096131A2 (en) | 2003-04-24 | 2004-11-11 | Merck & Co., Inc. | Inhibitors of akt activity |
EA009038B1 (ru) * | 2003-07-30 | 2007-10-26 | Лабораториос С.А.Л.В.А.Т., С.А. | Замещенные имидазопиримидины для предупреждения и лечения рака |
DE602005026509D1 (de) | 2004-04-09 | 2011-04-07 | Merck Sharp & Dohme | Hemmer der akt aktivität |
WO2006036395A2 (en) * | 2004-08-23 | 2006-04-06 | Merck & Co., Inc. | Inhibitors of akt activity |
CA2589084A1 (en) * | 2004-12-15 | 2006-06-22 | Merck & Co., Inc. | Inhibitors of akt activity |
BRPI0610863A2 (pt) * | 2005-05-20 | 2010-08-03 | Array Biopharma Inc | compostos inibidores de raf e métodos para sua utilização |
US20070049591A1 (en) * | 2005-08-25 | 2007-03-01 | Kalypsys, Inc. | Inhibitors of MAPK/Erk Kinase |
TW200800213A (en) * | 2005-09-02 | 2008-01-01 | Abbott Lab | Novel imidazo based heterocycles |
PE20070978A1 (es) * | 2006-02-14 | 2007-11-15 | Novartis Ag | COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks) |
US7530313B2 (en) | 2006-05-12 | 2009-05-12 | Day & Zimmerman, Inc. | Self-destruct fuze delay mechanism |
PA8793301A1 (es) * | 2007-08-14 | 2009-04-23 | Bayer Schering Pharma Ag | Imidazoles bicíclicos fusionados |
-
2008
- 2008-08-14 PA PA20088793301A patent/PA8793301A1/es unknown
- 2008-08-14 CL CL2008002397A patent/CL2008002397A1/es unknown
- 2008-08-14 PE PE2008001379A patent/PE20090596A1/es not_active Application Discontinuation
- 2008-08-14 JP JP2010520584A patent/JP5327652B2/ja not_active Expired - Fee Related
- 2008-08-14 CA CA2695251A patent/CA2695251C/en not_active Expired - Fee Related
- 2008-08-14 AT AT08787222T patent/ATE503757T1/de not_active IP Right Cessation
- 2008-08-14 AU AU2008288390A patent/AU2008288390A1/en not_active Abandoned
- 2008-08-14 TW TW097131067A patent/TW200924761A/zh unknown
- 2008-08-14 UY UY31292A patent/UY31292A1/es not_active Application Discontinuation
- 2008-08-14 KR KR1020107003250A patent/KR20100049589A/ko not_active Application Discontinuation
- 2008-08-14 CN CN200880103578A patent/CN101835776A/zh active Pending
- 2008-08-14 MX MX2010001745A patent/MX2010001745A/es not_active Application Discontinuation
- 2008-08-14 WO PCT/EP2008/060686 patent/WO2009021990A1/en active Application Filing
- 2008-08-14 EP EP08787222A patent/EP2176259B1/en active Active
- 2008-08-14 DE DE602008005894T patent/DE602008005894D1/de active Active
- 2008-08-14 EA EA201000297A patent/EA201000297A1/ru unknown
- 2008-08-14 US US12/191,706 patent/US8592591B2/en not_active Expired - Fee Related
- 2008-08-15 AR ARP080103563A patent/AR067946A1/es unknown
-
2010
- 2010-02-12 SV SV2010003482A patent/SV2010003482A/es not_active Application Discontinuation
- 2010-02-12 MA MA32618A patent/MA31609B1/fr unknown
- 2010-02-12 CR CR11271A patent/CR11271A/es not_active Application Discontinuation
- 2010-02-12 EC EC2010009965A patent/ECSP109965A/es unknown
- 2010-02-12 DO DO2010000057A patent/DOP2010000057A/es unknown
- 2010-02-12 TN TNP2010000071A patent/TN2010000071A1/fr unknown
-
2013
- 2013-11-26 US US14/090,367 patent/US9387204B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
PE20090596A1 (es) | 2009-06-07 |
CL2008002397A1 (es) | 2009-09-25 |
EA201000297A1 (ru) | 2010-08-30 |
TN2010000071A1 (en) | 2011-09-26 |
AU2008288390A1 (en) | 2009-02-19 |
DOP2010000057A (es) | 2010-04-15 |
US9387204B2 (en) | 2016-07-12 |
MA31609B1 (fr) | 2010-08-02 |
JP2010535847A (ja) | 2010-11-25 |
CA2695251A1 (en) | 2009-02-19 |
US8592591B2 (en) | 2013-11-26 |
CR11271A (es) | 2010-05-19 |
EP2176259B1 (en) | 2011-03-30 |
KR20100049589A (ko) | 2010-05-12 |
CN101835776A (zh) | 2010-09-15 |
US20140088110A1 (en) | 2014-03-27 |
AR067946A1 (es) | 2009-10-28 |
DE602008005894D1 (de) | 2011-05-12 |
JP5327652B2 (ja) | 2013-10-30 |
PA8793301A1 (es) | 2009-04-23 |
CA2695251C (en) | 2016-06-21 |
ECSP109965A (es) | 2010-03-31 |
SV2010003482A (es) | 2010-07-06 |
EP2176259A1 (en) | 2010-04-21 |
UY31292A1 (es) | 2009-03-31 |
ATE503757T1 (de) | 2011-04-15 |
US20090156604A1 (en) | 2009-06-18 |
WO2009021990A1 (en) | 2009-02-19 |
TW200924761A (en) | 2009-06-16 |
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