HK1128471A1 - Heterocyclic non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents - Google Patents
Heterocyclic non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agentsInfo
- Publication number
- HK1128471A1 HK1128471A1 HK09108147.6A HK09108147A HK1128471A1 HK 1128471 A1 HK1128471 A1 HK 1128471A1 HK 09108147 A HK09108147 A HK 09108147A HK 1128471 A1 HK1128471 A1 HK 1128471A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- preparation
- pharmaceutical composition
- antiviral agents
- nucleoside compounds
- heterocyclic non
- Prior art date
Links
Classifications
-
- 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
-
- 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
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three 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
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
- C07D277/24—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Pulmonology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200610027724 | 2006-06-13 | ||
PCT/CN2007/001861 WO2007147336A1 (en) | 2006-06-13 | 2007-06-13 | Heterocyclic non-nucleoside compounds, their peparation, pharmaceutical composition and their use as antiviral agents |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1128471A1 true HK1128471A1 (en) | 2009-10-30 |
Family
ID=38833067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK09108147.6A HK1128471A1 (en) | 2006-06-13 | 2009-09-04 | Heterocyclic non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents |
Country Status (7)
Country | Link |
---|---|
US (1) | US8653115B2 (zh) |
EP (1) | EP2030974B1 (zh) |
JP (1) | JP4999923B2 (zh) |
KR (1) | KR101130380B1 (zh) |
CN (1) | CN101443330B (zh) |
HK (1) | HK1128471A1 (zh) |
WO (1) | WO2007147336A1 (zh) |
Families Citing this family (38)
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WO2010037479A1 (de) | 2008-10-01 | 2010-04-08 | Bayer Cropscience Ag | Heterocyclyl substituierte thiazole als pflanzenschutzmittel |
CN101747282A (zh) | 2008-12-10 | 2010-06-23 | 上海特化医药科技有限公司 | 一类含有嘧啶酮苯基的化合物、其药物组合物及其制备方法和用途 |
WO2010066353A1 (de) * | 2008-12-11 | 2010-06-17 | Bayer Cropscience Ag | Thiazolyoximether und -hydrazone asl pflanzenschutzmittel |
WO2010128163A2 (en) * | 2009-05-08 | 2010-11-11 | Pike Pharma Gmbh | Small molecule inhibitors of influenza a and b virus and respiratory syncytial virus replication |
EP2272846A1 (de) | 2009-06-23 | 2011-01-12 | Bayer CropScience AG | Thiazolylpiperidin Derivate als Fungizide |
JP5785560B2 (ja) | 2009-12-21 | 2015-09-30 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺真菌剤としてのビス(ジフルオロメチル)ピラゾール |
CN102106852B (zh) * | 2009-12-23 | 2013-01-16 | 中国科学院上海药物研究所 | 2',2-联噻唑非核苷类化合物作为丙型肝炎病毒抑制剂的医药用途 |
EP2542089B1 (en) | 2010-03-05 | 2017-01-18 | Karyopharm Therapeutics, Inc. | Nuclear transport modulators and uses thereof |
CN102199133B (zh) | 2010-03-24 | 2015-08-19 | 中国科学院上海药物研究所 | 2’,2-双噻唑非核苷类化合物及其制备方法、药物组合物和作为肝炎病毒抑制剂的用途 |
WO2011134969A1 (de) | 2010-04-28 | 2011-11-03 | Bayer Cropscience Ag | Ketoheteroarylpiperidin und -piperazin derivate als fungizide |
US8815775B2 (en) | 2010-05-18 | 2014-08-26 | Bayer Cropscience Ag | Bis(difluoromethyl)pyrazoles as fungicides |
BR112012030184A2 (pt) | 2010-05-27 | 2015-12-29 | Bayer Cropscience Ag | derivados de ácido piridinilcarboxílico como fungicidas |
US20120122928A1 (en) | 2010-08-11 | 2012-05-17 | Bayer Cropscience Ag | Heteroarylpiperidine and -Piperazine Derivatives as Fungicides |
EP2423210A1 (de) | 2010-08-25 | 2012-02-29 | Bayer CropScience AG | Heteroarylpiperidin- und -piperazinderivate als Fungizide |
US8759527B2 (en) | 2010-08-25 | 2014-06-24 | Bayer Cropscience Ag | Heteroarylpiperidine and -piperazine derivatives as fungicides |
BR112013010497B1 (pt) | 2010-10-27 | 2018-07-17 | Bayer Intellectual Property Gmbh | derivados de heteroaril - piperidina e - piperazina enquanto fungicidas, composição os compreendendo, bem como processo para a produção de composições para controle de fungos fitopatogênicos nocivos e método para controle de fungos fitopatogênicos nocivos |
US9303000B2 (en) | 2011-01-17 | 2016-04-05 | Karyopharm Therapeutics Inc. | Olefin containing nuclear transport modulators and uses thereof |
EP2532233A1 (en) | 2011-06-07 | 2012-12-12 | Bayer CropScience AG | Active compound combinations |
EA201490407A1 (ru) | 2011-07-29 | 2014-05-30 | Кариофарм Терапевтикс, Инк. | Содержащие гидразид модуляторы нуклеарного транспорта и их применения |
JP6006794B2 (ja) | 2011-07-29 | 2016-10-12 | カリオファーム セラピューティクス,インコーポレイテッド | 核内輸送調節因子およびその使用 |
EP2755971B1 (de) | 2011-09-15 | 2017-12-20 | Bayer Intellectual Property GmbH | Piperidinpyrazole als fungizide |
US20130267517A1 (en) | 2012-03-31 | 2013-10-10 | Hoffmann-La Roche Inc. | Novel 4-methyl-dihydropyrimidines for the treatment and prophylaxis of hepatitis b virus infection |
SG11201407268SA (en) | 2012-05-09 | 2015-01-29 | Karyopharm Therapeutics Inc | Nuclear transport modulators and uses thereof |
CN103626705B (zh) * | 2012-08-27 | 2016-12-21 | 中国科学院上海药物研究所 | 1‑(3‑苯甲酰氨基苄基)‑1h‑吲唑‑3‑甲酰胺类化合物及其制备方法和抗病毒用途 |
SG11201500377UA (en) | 2012-09-10 | 2015-02-27 | Hoffmann La Roche | 6-amino acid heteroaryldihydropyrimidines for the treatment and prophylaxis of hepatitis b virus infection |
EP2968278B8 (en) | 2013-03-15 | 2019-05-22 | Karyopharm Therapeutics Inc. | Methods of promoting wound healing using crm1 inhibitors |
DK3492455T3 (da) | 2013-06-21 | 2023-08-14 | Karyopharm Therapeutics Inc | 1,2,4-triazoler som nukleare transportmodulatorer og anvendelse til behandling af specifikke former for cancer |
AU2015301484B2 (en) | 2014-08-15 | 2020-02-20 | Karyopharm Therapeutics Inc. | Polymorphs of selinexor |
CN104628717B (zh) * | 2015-03-16 | 2017-02-15 | 湖南大学 | 3‑[5‑(1,2,4‑三唑‑1‑基)噻唑‑2‑基]苯并噁嗪及其应用 |
CN104829607B (zh) * | 2015-05-11 | 2017-04-12 | 邵阳学院 | N‑噻唑苯并噁嗪酮衍生物作为神经氨酸酶抑制剂的应用 |
CN105503730B (zh) * | 2015-12-25 | 2018-06-22 | 山东大学 | 吡唑类衍生物及其制备方法与应用 |
EP3397633A1 (en) | 2015-12-31 | 2018-11-07 | Karyopharm Therapeutics, Inc. | Nuclear transport modulators and uses thereof |
EP3397634A1 (en) | 2015-12-31 | 2018-11-07 | Karyopharm Therapeutics, Inc. | Nuclear transport modulators and uses thereof |
JOP20190024A1 (ar) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
WO2018098472A1 (en) | 2016-11-28 | 2018-05-31 | Karyopharm Therapeutics Inc. | Crm1 inhibitors for treating epilepsy |
CN108610301B (zh) * | 2016-12-12 | 2021-08-31 | 中山大学 | 一类手性芳杂胺类衍生物及其合成方法和应用 |
CN107286147B (zh) * | 2017-05-10 | 2021-02-12 | 南华大学 | N-[5-(1,2,4-三唑-1-基)噻唑-2-基]吗啉基酰胺及其医药用途 |
WO2019165374A1 (en) | 2018-02-26 | 2019-08-29 | Gilead Sciences, Inc. | Substituted pyrrolizine compounds as hbv replication inhibitors |
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US4528291A (en) | 1982-06-22 | 1985-07-09 | Schering Corporation | 2-(4'-Pyridinyl)-thiazole compounds and their use in increasing cardiac contractility |
US4499097A (en) * | 1983-03-10 | 1985-02-12 | American Cyanamid Company | 2-(Pyridyl)imidazolyl ketones |
US4746669A (en) * | 1985-12-23 | 1988-05-24 | Merck & Co., Inc. | Substituted thiazoles as immunoregulants |
JPH0725754B2 (ja) * | 1986-01-30 | 1995-03-22 | 富山化学工業株式会社 | 新規なチアゾール化合物またはその塩 |
US4732895A (en) * | 1986-05-02 | 1988-03-22 | American Cyanamid Company | α-[5-methyl-2-(pyridinyl)-1H-imidazol-4-yl]substituted-1-piperazineethanols useful for treating hypertension |
JPH01110683A (ja) * | 1986-09-27 | 1989-04-27 | Sawai Seiyaku Kk | N−テトラゾリルチアゾールカルボキシアミド誘導体およびその用途 |
US4743586A (en) * | 1986-10-29 | 1988-05-10 | American Cyanamid Company | Method of treating hypertension using substituted imidazo[1,5-d]1,2,4-triazin-1(2H)-ones |
JP2941937B2 (ja) * | 1990-01-25 | 1999-08-30 | キヤノン株式会社 | 新規化合物、これを含む液晶組成物及びこれを使用した液晶素子並びに表示装置 |
ES2092580T3 (es) * | 1990-11-30 | 1996-12-01 | Teijin Ltd | Derivado de 2-ariltiazol y composicion farmaceutica que contiene el mismo. |
JPH04247076A (ja) * | 1991-02-01 | 1992-09-03 | Canon Inc | 液晶性化合物、これを含む液晶組成物、およびその使用方法、それを使用した液晶素子、表示装置 |
GB9604242D0 (en) * | 1996-02-28 | 1996-05-01 | Glaxo Wellcome Inc | Chemical compounds |
GB9817118D0 (en) * | 1998-08-07 | 1998-10-07 | Glaxo Group Ltd | Pharmaceutical compounds |
WO2000015637A1 (en) * | 1998-09-16 | 2000-03-23 | Dow Agrosciences Llc | 2-methoxyimino -2-(pyridinyloxymethyl) phenyl acetamides with 5 membered heterocyclic rings on the pyridine ring as fungicides |
DE19858192A1 (de) * | 1998-12-17 | 2000-06-21 | Aventis Cropscience Gmbh | 4-Trifluormethyl-3-oxazolylpyridine, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel |
GB2348641A (en) * | 1999-04-06 | 2000-10-11 | Secr Defence | Liquid crystal alkenyl compounds incorporating a heterocyclic five-membered ring |
ATE252091T1 (de) * | 1999-08-27 | 2003-11-15 | Lilly Co Eli | Biaryl-oxa(thia)zolderivate und ihre verwendung als ppars modulatoren |
TWI262185B (en) * | 1999-10-01 | 2006-09-21 | Eisai Co Ltd | Carboxylic acid derivatives having anti-hyperglycemia and anti-hyperlipemia action, and pharmaceutical composition containing the derivatives |
ES2275887T3 (es) * | 2001-06-07 | 2007-06-16 | Eli Lilly And Company | Moduladores de receptores activados por proliferadores de peroxisoma (ppar). |
JP3984892B2 (ja) * | 2002-08-30 | 2007-10-03 | 株式会社資生堂 | 油中水型乳化組成物 |
JP4974463B2 (ja) * | 2002-12-20 | 2012-07-11 | ニツポネツクス・インコーポレーテツド | インダン酢酸誘導体ならびに製薬学的薬剤としてのそれらの使用、中間体及び製造方法 |
US7470713B2 (en) * | 2004-02-23 | 2008-12-30 | Bristol-Myers Squibb Company | Imidazole based kinase inhibitors |
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 |
BRPI0616187A2 (pt) * | 2005-09-21 | 2011-06-14 | Decode Genetics Ehf | composto, composiÇço farmacÊutica, e, uso de uma quantidade terapeuticamente eficaz de um composto |
JP5301286B2 (ja) * | 2006-02-03 | 2013-09-25 | イーライ リリー アンド カンパニー | Fx受容体を調節するための化合物及び方法 |
MX2008011857A (es) * | 2006-03-23 | 2008-12-15 | Prolysis Ltd | Agentes antibacterianos. |
-
2007
- 2007-06-13 WO PCT/CN2007/001861 patent/WO2007147336A1/zh active Application Filing
- 2007-06-13 EP EP07721434.4A patent/EP2030974B1/en not_active Not-in-force
- 2007-06-13 KR KR1020087032272A patent/KR101130380B1/ko not_active IP Right Cessation
- 2007-06-13 US US12/304,598 patent/US8653115B2/en not_active Expired - Fee Related
- 2007-06-13 CN CN2007800174622A patent/CN101443330B/zh active Active
- 2007-06-13 JP JP2009514619A patent/JP4999923B2/ja not_active Expired - Fee Related
-
2009
- 2009-09-04 HK HK09108147.6A patent/HK1128471A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP2030974A1 (en) | 2009-03-04 |
WO2007147336A1 (en) | 2007-12-27 |
US8653115B2 (en) | 2014-02-18 |
JP4999923B2 (ja) | 2012-08-15 |
CN101443330A (zh) | 2009-05-27 |
EP2030974B1 (en) | 2016-02-17 |
JP2009539888A (ja) | 2009-11-19 |
KR101130380B1 (ko) | 2012-04-23 |
US20100056569A1 (en) | 2010-03-04 |
KR20090016009A (ko) | 2009-02-12 |
EP2030974A4 (en) | 2009-08-19 |
CN101443330B (zh) | 2012-12-19 |
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Date | Code | Title | Description |
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PC | Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee) |
Effective date: 20170613 |