HK1091831A1 - Isoxazole compounds as inhibitors of heat shock proteins - Google Patents
Isoxazole compounds as inhibitors of heat shock proteinsInfo
- Publication number
- HK1091831A1 HK1091831A1 HK06112447.8A HK06112447A HK1091831A1 HK 1091831 A1 HK1091831 A1 HK 1091831A1 HK 06112447 A HK06112447 A HK 06112447A HK 1091831 A1 HK1091831 A1 HK 1091831A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- inhibitors
- heat shock
- shock proteins
- isoxazole compounds
- isoxazole
- Prior art date
Links
- 150000002545 isoxazoles Chemical class 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102000002812 Heat-Shock Proteins Human genes 0.000 title 1
- 108010004889 Heat-Shock Proteins Proteins 0.000 title 1
- 101710113864 Heat shock protein 90 Proteins 0.000 abstract 1
- 102100034051 Heat shock protein HSP 90-alpha Human genes 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- 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
-
- 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
- A61K31/42—Oxazoles
-
- 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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Reproductive Health (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0303105A GB0303105D0 (en) | 2003-02-11 | 2003-02-11 | Isoxazole compounds |
GBGB0306560.4A GB0306560D0 (en) | 2003-03-21 | 2003-03-21 | Isoxazole compounds |
GB0313751A GB0313751D0 (en) | 2003-06-13 | 2003-06-13 | Isoxazole compounds |
PCT/GB2004/000506 WO2004072051A1 (fr) | 2003-02-11 | 2004-02-09 | Composes d'isoxazole utiles comme inhibiteurs des proteines de choc thermique |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1091831A1 true HK1091831A1 (en) | 2007-01-26 |
Family
ID=32872455
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK06112447.8A HK1091831A1 (en) | 2003-02-11 | 2006-11-10 | Isoxazole compounds as inhibitors of heat shock proteins |
Country Status (19)
Country | Link |
---|---|
US (6) | US7705027B2 (fr) |
EP (1) | EP1611112B1 (fr) |
JP (1) | JP4921162B2 (fr) |
KR (1) | KR101166749B1 (fr) |
CN (1) | CN1771235B (fr) |
AU (1) | AU2004210779B2 (fr) |
BR (1) | BRPI0407403B1 (fr) |
CA (1) | CA2515726C (fr) |
CY (1) | CY1113761T1 (fr) |
DK (1) | DK1611112T3 (fr) |
EA (1) | EA009919B1 (fr) |
ES (1) | ES2393483T3 (fr) |
HK (1) | HK1091831A1 (fr) |
MX (1) | MXPA05008335A (fr) |
NO (1) | NO335001B1 (fr) |
NZ (1) | NZ541479A (fr) |
PT (1) | PT1611112E (fr) |
SI (1) | SI1611112T1 (fr) |
WO (1) | WO2004072051A1 (fr) |
Families Citing this family (114)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI332943B (en) | 2001-07-10 | 2010-11-11 | Synta Pharmaceuticals Corp | Taxol enhancer compounds |
TWI297335B (en) | 2001-07-10 | 2008-06-01 | Synta Pharmaceuticals Corp | Taxol enhancer compounds |
TWI252847B (en) | 2001-07-10 | 2006-04-11 | Synta Pharmaceuticals Corp | Synthesis of taxol enhancers |
TWI330079B (en) | 2003-01-15 | 2010-09-11 | Synta Pharmaceuticals Corp | Treatment for cancers |
MXPA05008335A (es) | 2003-02-11 | 2006-05-04 | Vernalis Cambridge Ltd | Compuestos de isoxazol como inhibidores de las proteinas de choque por calor. |
GB0315111D0 (en) * | 2003-06-27 | 2003-07-30 | Cancer Rec Tech Ltd | Substituted 5-membered ring compounds and their use |
US7538241B2 (en) | 2003-12-26 | 2009-05-26 | Kyowa Hakko Kogyo Co., Ltd. | Hsp90 family protein inhibitors |
WO2005117849A1 (fr) | 2004-05-28 | 2005-12-15 | Unigen Pharmaceuticals, Inc. | Diarylalcanes constituant des inhibiteurs puissants d'enzymes binucleaires |
GB0412769D0 (en) | 2004-06-08 | 2004-07-07 | Novartis Ag | Organic compounds |
KR101313027B1 (ko) | 2004-06-23 | 2013-10-02 | 신타 파마슈티칼스 코프. | 암 치료용 비스(티오-히드라지드 아미드) 염 |
ES2410591T3 (es) | 2004-09-22 | 2013-07-02 | Nippon Kayaku Kabushiki Kaisha | Nuevo copolímero en bloque, preparación micelar y agente antineoplásico que lo contiene como principio activo |
US7781485B2 (en) | 2004-11-09 | 2010-08-24 | Kyowa Hakko Kirin Co., Ltd. | Hsp90 family protein inhibitors |
EP1817295B1 (fr) | 2004-11-18 | 2012-11-07 | Synta Pharmaceuticals Corp. | Composes triazole modulant l'activite de hsp90 |
CA2597430C (fr) | 2005-02-17 | 2014-08-05 | Synta Pharmaceuticals Corp. | Derives de combretastine et d'isoxazole pour le traitement de troubles |
DE102005007304A1 (de) * | 2005-02-17 | 2006-08-24 | Merck Patent Gmbh | Triazolderivate |
FR2882361A1 (fr) * | 2005-02-22 | 2006-08-25 | Aventis Pharma Sa | Nouveaux derives de 3-aryl-1,2-benzisoxazole, compositions les contenant et leur utilisation |
JP4956737B2 (ja) * | 2005-02-23 | 2012-06-20 | 国立大学法人名古屋大学 | 抗ポリグルタミン病剤 |
US8399464B2 (en) | 2005-03-09 | 2013-03-19 | Nippon Kayaku Kabushiki Kaisha | HSP90 inhibitor |
CN1834095B (zh) * | 2005-03-18 | 2011-04-20 | 中国科学院上海药物研究所 | 一类非核苷类抗病毒抑制剂及其制备方法和用途 |
JP2008137894A (ja) * | 2005-03-22 | 2008-06-19 | Nippon Kayaku Co Ltd | 新規なアセチレン誘導体 |
FR2884252B1 (fr) | 2005-04-08 | 2007-05-18 | Aventis Pharma Sa | Nouveaux derives d'isoindoles, compositions les contenant, leur preparation et leurs utilisations pharmaceutiques notamment en tant qu'inhibiteurs d'activites de la proteine chaperone hsp90 |
WO2006109085A1 (fr) | 2005-04-13 | 2006-10-19 | Astex Therapeutics Limited | Derives d'hydroxybenzamide et leur utilisation comme inhibteurs de hsp90 |
BRPI0610219A2 (pt) | 2005-04-15 | 2010-06-08 | Synta Pharmaceuticals Corp | métodos de tratamento de um ser humano com cáncer e composição de farmacêutica |
FR2885904B1 (fr) | 2005-05-19 | 2007-07-06 | Aventis Pharma Sa | Nouveaux derives du fluorene, compositions les contenant et utilisation |
WO2006126751A1 (fr) * | 2005-05-25 | 2006-11-30 | Korea Research Institute Of Bioscience And Biotechnology | Nouveaux derives diaryl-isoxazole ainsi que compositions pharmaceutiques contenant ces derives pour la prevention et le traitement de cancers |
CA2618628C (fr) | 2005-08-18 | 2014-11-18 | Synta Pharmaceuticals Corp. | Derives de triazole modulant l'activite de hsp90 |
GB0603880D0 (en) * | 2006-02-27 | 2006-04-05 | Novartis Ag | Organic compounds |
US7754725B2 (en) | 2006-03-01 | 2010-07-13 | Astex Therapeutics Ltd. | Dihydroxyphenyl isoindolymethanones |
JP5249016B2 (ja) | 2006-03-28 | 2013-07-31 | 日本化薬株式会社 | タキサン類の高分子結合体 |
WO2007131034A1 (fr) * | 2006-05-03 | 2007-11-15 | The Regents Of The University Of Michigan | Derives de pyrimidone actifs en tant que modulateurs de la proteine de choc thermique (hsp) 70 |
US8940332B2 (en) | 2006-05-18 | 2015-01-27 | Nippon Kayaku Kabushiki Kaisha | High-molecular weight conjugate of podophyllotoxins |
JP2010501562A (ja) | 2006-08-21 | 2010-01-21 | シンタ ファーマシューティカルズ コーポレーション | 増殖性障害を治療するための化合物 |
WO2008027445A2 (fr) | 2006-08-31 | 2008-03-06 | Synta Pharmaceuticals Corp. | Combinaisons de bis(thio-hydrazide amides) traitant le cancer |
WO2008033449A2 (fr) * | 2006-09-14 | 2008-03-20 | Synta Pharmaceuticals Corp. | Composés pour le traitement de l'angiogenèse |
EP2070971B1 (fr) | 2006-10-03 | 2016-06-22 | Nippon Kayaku Kabushiki Kaisha | Mélange d'un dérivé de résorcinol avec un polymère |
EP2073803B1 (fr) | 2006-10-12 | 2018-09-19 | Astex Therapeutics Limited | Combinaisons pharmaceutiques |
JP5721949B2 (ja) | 2006-10-12 | 2015-05-20 | アステックス、セラピューティックス、リミテッドAstex Therapeutics Limited | 複合薬剤 |
GB0620259D0 (en) | 2006-10-12 | 2006-11-22 | Astex Therapeutics Ltd | Pharmaceutical compounds |
US9730912B2 (en) | 2006-10-12 | 2017-08-15 | Astex Therapeutics Limited | Pharmaceutical compounds |
US8883790B2 (en) | 2006-10-12 | 2014-11-11 | Astex Therapeutics Limited | Pharmaceutical combinations |
WO2008044027A2 (fr) | 2006-10-12 | 2008-04-17 | Astex Therapeutics Limited | Composés pharmaceutiques |
JP5503872B2 (ja) | 2006-11-06 | 2014-05-28 | 日本化薬株式会社 | 核酸系代謝拮抗剤の高分子誘導体 |
US8188222B2 (en) | 2006-11-08 | 2012-05-29 | Nippon Kayaku Kabushiki Kaisha | High molecular weight derivative of nucleic acid antimetabolite |
US7799954B2 (en) | 2006-11-17 | 2010-09-21 | Abraxis Bioscience, Llc | Dicarbonyl derivatives and methods of use |
CA2678043A1 (fr) | 2007-03-01 | 2008-09-04 | Novartis Ag | Sels d'addition acides, hydrates et polymorphes d'ethylamide d'acide 5-(2,4-dihydroxy-5-isopropyl-phenyl)-4-(4-morpholin-4-ylmethyl-phenyl)-isoxazole-3-carboxylique et preparations comprenant ces formes |
KR20100027231A (ko) | 2007-07-25 | 2010-03-10 | 에프. 호프만-라 로슈 아게 | 벤조퓨란- 및 벤조[b]티오펜-2-카복실산 아마이드 유도체 및 이의 히스타민 3 수용체 조절제로서의 용도 |
CA2974477C (fr) | 2007-08-27 | 2019-12-31 | Dart Neuroscience (Cayman) Ltd. | Composes isoxazole therapeutiques |
WO2009026658A1 (fr) * | 2007-08-29 | 2009-03-05 | The University Of Sydney | Agonistes de ppar |
JP5349318B2 (ja) | 2007-09-28 | 2013-11-20 | 日本化薬株式会社 | ステロイド類の高分子結合体 |
WO2009049305A2 (fr) | 2007-10-12 | 2009-04-16 | Arqule, Inc. | Composés de tétrazole substitués et leurs utilisations |
TW200922595A (en) * | 2007-10-12 | 2009-06-01 | Novartis Ag | Organic compounds |
CN101918389A (zh) * | 2007-11-02 | 2010-12-15 | 梅特希尔基因公司 | 组蛋白脱乙酰酶抑制剂 |
GB0722680D0 (en) * | 2007-11-19 | 2007-12-27 | Topotarget As | Therapeutic compounds and their use |
EP2258397B1 (fr) | 2008-03-18 | 2017-10-11 | Nippon Kayaku Kabushiki Kaisha | Conjugué de polymère et de substance physiologiquement active |
GB0806527D0 (en) | 2008-04-11 | 2008-05-14 | Astex Therapeutics Ltd | Pharmaceutical compounds |
LT5623B (lt) | 2008-04-30 | 2010-01-25 | Biotechnologijos Institutas, , | 5-aril-4-(5-pakeistieji 2,4-dihidroksifenil)-1,2,3-tiadiazolai kaip hsp90 šaperono slopikliai ir tarpiniai junginiai jiems gauti |
EP2284209B1 (fr) | 2008-05-08 | 2016-08-31 | Nippon Kayaku Kabushiki Kaisha | Conjugué de polymère avec l'acide folique ou un dérivé de l'acide folique |
EP2273882A4 (fr) * | 2008-05-13 | 2011-07-13 | Poniard Pharmaceuticals Inc | Composés bioactifs pour le traitement du cancer et des maladies neurodégénératives |
TWI450898B (zh) * | 2008-07-04 | 2014-09-01 | Sigma Tau Res Switzerland Sa | 具有抗腫瘤活性之芳基異唑化合物 |
EP3542780B1 (fr) | 2008-07-21 | 2022-01-19 | Unigen, Inc. | Famille de composés permettant le blanchiment (éclaircissement) de la peau |
CN102227221A (zh) * | 2008-11-28 | 2011-10-26 | 诺瓦提斯公司 | 包含hsp90抑制剂和mtor抑制剂的药物组合 |
CN102227227B (zh) * | 2008-11-28 | 2014-05-28 | 诺华股份有限公司 | 包含吡啶并[4,3-d]嘧啶衍生的HSP90抑制剂和HER2抑制剂的药物组合 |
ES2533954T3 (es) | 2009-04-21 | 2015-04-16 | Nerviano Medical Sciences S.R.L. | Derivados de resorcinol como inhibidores de HSP90 |
JP5544357B2 (ja) | 2009-05-15 | 2014-07-09 | 日本化薬株式会社 | 水酸基を有する生理活性物質の高分子結合体 |
JPWO2011040421A1 (ja) | 2009-09-29 | 2013-02-28 | 武田薬品工業株式会社 | スクリーニング方法 |
ES2552157T3 (es) | 2009-10-16 | 2015-11-26 | Novartis Ag | Biomarcadores de respuesta farmacodinámica tumoral |
JP2013519727A (ja) * | 2010-02-17 | 2013-05-30 | イルドン ファーム シーオー.,エルティーディー. | 新規の5員複素環誘導体及びその製造方法 |
EP2560640A1 (fr) | 2010-04-19 | 2013-02-27 | Synta Pharmaceuticals Corp. | Thérapie anticancéreuse à l'aide d'une combinaison d'un composé inhibiteur de hsp90 et d'un inhibiteur d'egfr |
JP5856069B2 (ja) | 2010-11-17 | 2016-02-09 | 日本化薬株式会社 | 新規なシチジン系代謝拮抗剤の高分子誘導体 |
BR112013024413B1 (pt) | 2011-03-24 | 2020-02-18 | Unigen, Inc. | Compostos e métodos para a preparação de diarilpropanos |
WO2013015661A2 (fr) * | 2011-07-28 | 2013-01-31 | Ildong Pharm Co.,Ltd. | Nouveaux promédicaments de 5-(2,4-dihydroxy-5-isopropylphényl)-n-éthyl-4-(5-méthyl1-1,2,4-oxadiazol-3-yl)isoxazole-3-carboxamide |
CN102351655A (zh) * | 2011-08-18 | 2012-02-15 | 杭州澳赛诺化工有限公司 | 一种4-异丙基间苯二酚的合成方法 |
RU2623426C2 (ru) | 2011-09-11 | 2017-06-26 | Ниппон Каяку Кабусики Кайся | Способ получения блок-сополимера |
RU2624493C2 (ru) | 2011-10-14 | 2017-07-04 | Новартис Аг | 2-КАРБОКСАМИД ЦИКЛОАМИНО ПРОИЗВОДНЫЕ МОЧЕВИНЫ В КОМБИНАЦИИ С ИНГИБИТОРАМИ Hsp90 ДЛЯ ЛЕЧЕНИЯ ПРОЛИФЕРАТИВНЫХ ЗАБОЛЕВАНИЙ |
CN103086994A (zh) * | 2011-10-31 | 2013-05-08 | 上海壹志医药科技有限公司 | 异噁唑衍生物的盐 |
JP2014532712A (ja) | 2011-11-02 | 2014-12-08 | シンタ ファーマシューティカルズ コーポレーション | トポイソメラーゼi阻害剤とhsp90阻害剤の組合せを使用する癌療法 |
JP2014534228A (ja) | 2011-11-02 | 2014-12-18 | シンタ ファーマシューティカルズ コーポレーション | 白金含有剤とhsp90阻害剤の組合せ療法 |
AU2012339679A1 (en) | 2011-11-14 | 2014-06-12 | Synta Pharmaceuticals Corp. | Combination therapy of Hsp90 inhibitors with BRAF inhibitors |
WO2014074580A1 (fr) | 2012-11-07 | 2014-05-15 | Novartis Ag | Polythérapie |
EP2917181B1 (fr) * | 2012-11-09 | 2019-09-25 | Jacobus Pharmaceutical Company, Inc. | Dérivés hétéroaryles et leurs utilisations |
EP2917200A1 (fr) | 2012-11-09 | 2015-09-16 | Jacobus Pharmaceutical Company, Inc. | Dérivés aryle et leurs utilisations |
JP2016512812A (ja) * | 2013-03-15 | 2016-05-09 | ノバルティス アーゲー | バイオマーカー |
AU2014302458A1 (en) * | 2013-06-26 | 2015-12-24 | Proteostasis Therapeutics, Inc. | Methods of modulating CFTR activity |
JOP20200094A1 (ar) | 2014-01-24 | 2017-06-16 | Dana Farber Cancer Inst Inc | جزيئات جسم مضاد لـ pd-1 واستخداماتها |
JOP20200096A1 (ar) | 2014-01-31 | 2017-06-16 | Children’S Medical Center Corp | جزيئات جسم مضاد لـ tim-3 واستخداماتها |
SI3116909T1 (sl) | 2014-03-14 | 2020-03-31 | Novartis Ag | Molekule protiteles na LAG-3 in njih uporaba |
CA2952862A1 (fr) * | 2014-06-19 | 2015-12-23 | Proteostasis Therapeutics, Inc. | Composes, compositions et procedes pour augmenter l'activite du cftr |
AU2015325279B2 (en) | 2014-10-01 | 2020-02-27 | Daiichi Sankyo Company, Limited | Isoxazole derivative as mutant isocitrate dehydrogenase 1 inhibitor |
MA41044A (fr) | 2014-10-08 | 2017-08-15 | Novartis Ag | Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer |
CA2964367C (fr) | 2014-10-14 | 2024-01-30 | Novartis Ag | Molecules d'anticorps de pd-l1 et leurs utilisations |
EP3233918A1 (fr) | 2014-12-19 | 2017-10-25 | Novartis AG | Polythérapies |
CN104725329B (zh) * | 2015-01-13 | 2017-01-18 | 陕西科技大学 | 一种具有抗肿瘤活性的异恶唑羧酸类化合物及其合成方法 |
CA2974756A1 (fr) * | 2015-01-22 | 2016-07-28 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Derive de resorcinol utilise en tant qu'inhibiteur de hsp90 |
EP3268035A4 (fr) | 2015-03-10 | 2018-10-31 | Aduro Biotech, Inc. | Compositions et procédés d'activation de la signalisation dépendante de « stimulateur de gènes d'interféron » |
CN106349180B (zh) * | 2015-07-14 | 2020-05-19 | 上海翰森生物医药科技有限公司 | 4,5-二苯基异噁唑衍生物及其制备方法和应用 |
US20180207273A1 (en) | 2015-07-29 | 2018-07-26 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
WO2017019896A1 (fr) | 2015-07-29 | 2017-02-02 | Novartis Ag | Traitements combinés comprenant des molécules d'anticorps qui se lient à pd-1 |
PL3317301T3 (pl) | 2015-07-29 | 2021-11-15 | Novartis Ag | Terapie skojarzone zawierające cząsteczki przeciwciał przeciw lag-3 |
BR112018008867A8 (pt) | 2015-11-03 | 2019-02-26 | Janssen Biotech Inc | anticorpos que se ligam especificamente a pd-1 e seus usos |
CA3007671A1 (fr) | 2015-12-17 | 2017-06-22 | Novartis Ag | Molecules d'anticorps anti-pd-1 et leurs utilisations |
CN107540624B (zh) * | 2016-06-29 | 2020-06-16 | 广州市恒诺康医药科技有限公司 | 热休克蛋白抑制剂及其制备方法和应用 |
CN106146466A (zh) * | 2016-06-30 | 2016-11-23 | 珠海赛隆药业股份有限公司(长沙)医药研发中心 | 富马酸沃诺拉赞中间体、其制备方法和制备富马酸沃诺拉赞的方法 |
EP3507367A4 (fr) | 2016-07-05 | 2020-03-25 | Aduro BioTech, Inc. | Composés dinucléotidiques cycliques d'acide nucléique bloqué et leurs utilisations |
CN109641858B (zh) * | 2016-07-21 | 2021-06-25 | 正大天晴药业集团股份有限公司 | 间苯二酚类衍生物的结晶、盐及其制备方法 |
UY37695A (es) | 2017-04-28 | 2018-11-30 | Novartis Ag | Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo |
CN111217762B (zh) * | 2018-11-23 | 2021-08-20 | 华中师范大学 | 多卤代5-(2-羟基苯基)异噁唑类化合物及其制备方法和应用 |
WO2020231979A1 (fr) * | 2019-05-13 | 2020-11-19 | The Trustees Of Princeton University | Inhibiteurs à petites molécules de réplication virale |
CN110283080A (zh) * | 2019-07-05 | 2019-09-27 | 山西大学 | 一种含氟的二苯甲酮衍生物及其制备方法和应用 |
WO2021152113A1 (fr) | 2020-01-31 | 2021-08-05 | Bayer Aktiengesellschaft | Dérivés de 2,3-benzodiazépines substitués |
KR102676631B1 (ko) * | 2020-10-07 | 2024-06-19 | 광주과학기술원 | 과민성 방광의 예방 또는 치료용 약학적 조성물 |
CN115160250B (zh) * | 2021-04-02 | 2024-06-04 | 沈阳药科大学 | 4,6-联苯二酚类衍生物及其用途 |
US11324737B1 (en) * | 2021-05-25 | 2022-05-10 | Louis Habash | Modulating expression level of a gene encoding a heat shock protein by treating a human subject with a nitroxide |
US11729925B2 (en) | 2021-06-15 | 2023-08-15 | Erico International Corporation | Mounting bracket with angled mounting openings for electrical boxes |
CN114751870B (zh) * | 2022-02-28 | 2023-10-20 | 贵州医科大学 | 一种2-(异噁唑-5-基)苯基-3,4-二羟基苯甲酸酯及其衍生物及合成方法和应用 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0418667B1 (fr) * | 1989-09-22 | 1995-08-16 | BASF Aktiengesellschaft | Amides d'acides carboxyliques |
EP0633254A1 (fr) * | 1991-05-01 | 1995-01-11 | Taiho Pharmaceutical Co., Ltd. | Nouveau derive d'isoxazole et sel de ce derive |
WO1994024095A1 (fr) * | 1993-04-16 | 1994-10-27 | Abbott Laboratories | Agents immunosuppresseurs |
IL154501A0 (en) * | 1996-10-15 | 2003-09-17 | Searle & Co | Use of cyclooxygenase-2 inhibitors for the manufacture of a medicament for the treatment and prevention of neoplasia |
US6187797B1 (en) * | 1996-12-23 | 2001-02-13 | Dupont Pharmaceuticals Company | Phenyl-isoxazoles as factor XA Inhibitors |
AU6645998A (en) * | 1996-12-23 | 1998-07-17 | Du Pont Pharmaceuticals Company | Oxygen or sulfur containing heteroaromatics as factor xa inhibitors |
DE69929345T2 (de) | 1998-08-07 | 2006-09-21 | Chiron Corp. (N.D.Ges.D. Staates Delaware), Emeryville | Substituierte isoxal-derivate als östrogenrezeptormodulatoren |
SK286080B6 (sk) * | 1998-09-09 | 2008-03-05 | Metabasis Therapeutics, Inc. | Heterocyklické aromatické zlúčeniny obsahujúce fosfonátovú skupinu, ich použitie a farmaceutická kompozícia obsahujúca uvedené zlúčeniny |
HUP0402506A3 (en) * | 1998-12-24 | 2007-05-29 | Metabasis Therapeutics Inc | A combination of fbpase inhibitors and insulin sensitizers for the treatment of diabetes |
PL366110A1 (en) * | 1999-08-13 | 2005-01-24 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases |
HUP0204092A3 (en) * | 1999-12-22 | 2005-02-28 | Metabasis Therapeutics Inc San | Novel bisamidate phosphononate prodrugs |
US6673818B2 (en) * | 2001-04-20 | 2004-01-06 | Pharmacia Corporation | Fluoro-substituted benzenesulfonyl compounds for the treatment of inflammation |
JP2002363079A (ja) * | 2001-05-31 | 2002-12-18 | National Cancer Center-Japan | モフェゾラクを有効成分とする、消化管ポリープおよび/または消化管がんの予防または治療のための薬剤 |
EP1456180B1 (fr) * | 2001-12-21 | 2007-10-03 | Vernalis (Cambridge) Limited | 3-(2,4)dihydroxyphenyl-4-phenylpyrazoles et leur utilisation medicale |
MXPA05008335A (es) * | 2003-02-11 | 2006-05-04 | Vernalis Cambridge Ltd | Compuestos de isoxazol como inhibidores de las proteinas de choque por calor. |
US20110201587A1 (en) * | 2010-02-16 | 2011-08-18 | Bio Holding, Inc. | Hsp90 inhibitors and methods of use |
-
2004
- 2004-02-09 MX MXPA05008335A patent/MXPA05008335A/es active IP Right Grant
- 2004-02-09 SI SI200431954T patent/SI1611112T1/sl unknown
- 2004-02-09 PT PT04709273T patent/PT1611112E/pt unknown
- 2004-02-09 AU AU2004210779A patent/AU2004210779B2/en not_active Expired
- 2004-02-09 CA CA2515726A patent/CA2515726C/fr not_active Expired - Lifetime
- 2004-02-09 BR BRPI0407403-3A patent/BRPI0407403B1/pt not_active IP Right Cessation
- 2004-02-09 KR KR1020057014738A patent/KR101166749B1/ko active IP Right Grant
- 2004-02-09 NZ NZ541479A patent/NZ541479A/en not_active IP Right Cessation
- 2004-02-09 ES ES04709273T patent/ES2393483T3/es not_active Expired - Lifetime
- 2004-02-09 EA EA200501272A patent/EA009919B1/ru active IP Right Revival
- 2004-02-09 US US10/544,443 patent/US7705027B2/en not_active Expired - Lifetime
- 2004-02-09 DK DK04709273.9T patent/DK1611112T3/da active
- 2004-02-09 EP EP04709273A patent/EP1611112B1/fr not_active Expired - Lifetime
- 2004-02-09 JP JP2006502254A patent/JP4921162B2/ja not_active Expired - Lifetime
- 2004-02-09 WO PCT/GB2004/000506 patent/WO2004072051A1/fr active Search and Examination
- 2004-02-09 CN CN2004800093392A patent/CN1771235B/zh not_active Expired - Lifetime
-
2005
- 2005-09-09 NO NO20054195A patent/NO335001B1/no unknown
-
2006
- 2006-11-10 HK HK06112447.8A patent/HK1091831A1/xx not_active IP Right Cessation
-
2010
- 2010-02-19 US US12/708,686 patent/US8507480B2/en not_active Expired - Lifetime
-
2012
- 2012-06-18 US US13/525,409 patent/US8450310B2/en not_active Expired - Lifetime
- 2012-11-09 CY CY20121101068T patent/CY1113761T1/el unknown
-
2013
- 2013-06-27 US US13/929,098 patent/US9718793B2/en not_active Expired - Lifetime
-
2017
- 2017-06-23 US US15/631,059 patent/US10413550B2/en not_active Expired - Lifetime
-
2019
- 2019-07-31 US US16/528,278 patent/US11234987B2/en not_active Expired - Lifetime
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HK1091831A1 (en) | Isoxazole compounds as inhibitors of heat shock proteins | |
GB2392154B (en) | Protein Kinase Inhibitors | |
GB2398781B (en) | Kinase inhibitors | |
DE60112974D1 (en) | Carbolinderivate | |
IL165434A0 (en) | Compounds having DPP-IV inhibitory activity | |
MXPA04002931A (es) | Heterociclos que contienen nitrogeno de 5 miembros sustituidos con fenilo para el tratamiento de la obesidad. | |
MY135477A (en) | 2-(2,6-dichlorophenyl)-diarylimidazoles | |
HK1096549A1 (en) | Imidazopyridine-derivatives as inducible no-synthase inhibitors | |
DE60216233D1 (en) | Carbolinderivate | |
PH12009500610A1 (en) | 4-imidazolin-2-one compounds | |
NO20044526L (no) | Hemisterlinderivater og anvendelser derav | |
AU2001266575A1 (en) | Chemical compounds | |
GB0308201D0 (en) | Novel compounds | |
HK1096548A1 (en) | Imidazopyridine-derivatives as inductible no-synthase inhibitors | |
DE602004005881D1 (de) | Substituierte pyrazinonverbindungen zur behandlung von entzündungen | |
MXPA02012470A (es) | Inhibidores de fosfodiesterasa especificos para gmp ciclico. | |
RS20060206A (en) | Aminopyridine-derivatives as inducible no-synthase inhibitors | |
RS20060195A (en) | Imidazopyridine-derivatives as inducible no-synthase inhibitors | |
NO20001751L (no) | Nye forbindelser til bruk som neuroprotektive midler | |
MY136854A (en) | Crystalline n-formyl hydroxylamine compounds | |
DE60014915D1 (de) | Hypoxanthin- und thiohypxanthin-verbindungen | |
SG145572A1 (en) | Intermediates useful in the synthesis of hiv-protease inhibitors and methods for preparing the same | |
UA84603C2 (ru) | Производные тетрагидронафтиридина и способ их получения | |
MY140520A (en) | TRICYCLIC 6-ALKYLIDE-PENEMS AS ß-LACTAMASE INHIBITORS |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PE | Patent expired |
Effective date: 20240212 |