TN2009000398A1 - 5,6-dihydro-1h-pyridin-2-one compounds - Google Patents
5,6-dihydro-1h-pyridin-2-one compoundsInfo
- Publication number
- TN2009000398A1 TN2009000398A1 TNP2009000398A TN2009000398A TN2009000398A1 TN 2009000398 A1 TN2009000398 A1 TN 2009000398A1 TN P2009000398 A TNP2009000398 A TN P2009000398A TN 2009000398 A TN2009000398 A TN 2009000398A TN 2009000398 A1 TN2009000398 A1 TN 2009000398A1
- Authority
- TN
- Tunisia
- Prior art keywords
- compounds
- pyridin
- dihydro
- hepatitis
- virus
- Prior art date
Links
- OXRRHYRRQWIHIV-UHFFFAOYSA-N 2,3-dihydro-1h-pyridin-6-one Chemical class O=C1NCCC=C1 OXRRHYRRQWIHIV-UHFFFAOYSA-N 0.000 title abstract 2
- 241000711549 Hepacivirus C Species 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/435—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
-
- 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
- A61K31/5415—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 ortho- or peri-condensed with carbocyclic ring systems, e.g. phenothiazine, chlorpromazine, piroxicam
-
- 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
- A61K31/549—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 having two or more nitrogen atoms in the same ring, e.g. hydrochlorothiazide
-
- 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
- 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
- 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
-
- 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
-
- 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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/18—Bridged 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)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Materials For Medical Uses (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US90747807P | 2007-04-03 | 2007-04-03 | |
PCT/US2008/059164 WO2008124450A1 (fr) | 2007-04-03 | 2008-04-02 | Composés de 5,6-dihydro-1h-pyridine-2-un |
Publications (1)
Publication Number | Publication Date |
---|---|
TN2009000398A1 true TN2009000398A1 (en) | 2010-12-31 |
Family
ID=39831340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TNP2009000398A TN2009000398A1 (en) | 2007-04-03 | 2009-09-30 | 5,6-dihydro-1h-pyridin-2-one compounds |
Country Status (23)
Country | Link |
---|---|
US (6) | US7939524B2 (fr) |
EP (1) | EP2129224B1 (fr) |
JP (2) | JP5739662B2 (fr) |
KR (1) | KR101542516B1 (fr) |
CN (2) | CN101677563B (fr) |
AR (1) | AR065927A1 (fr) |
AU (1) | AU2008237364B2 (fr) |
BR (1) | BRPI0809685A2 (fr) |
CA (1) | CA2682584C (fr) |
CL (1) | CL2008000959A1 (fr) |
EA (1) | EA017685B1 (fr) |
ES (1) | ES2578302T3 (fr) |
HK (2) | HK1137119A1 (fr) |
IL (2) | IL201312A (fr) |
MX (1) | MX2009010564A (fr) |
MY (1) | MY157961A (fr) |
NZ (1) | NZ580445A (fr) |
PE (1) | PE20090220A1 (fr) |
TN (1) | TN2009000398A1 (fr) |
TW (2) | TWI481588B (fr) |
UA (1) | UA100120C2 (fr) |
WO (1) | WO2008124450A1 (fr) |
ZA (1) | ZA200907673B (fr) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5306194B2 (ja) | 2006-06-22 | 2013-10-02 | アナディス ファーマシューティカルズ インク | ピロ[1,2−b]ピリダジノン化合物 |
UA100120C2 (en) | 2007-04-03 | 2012-11-26 | Анадис Фармасьютикалз, Инк. | 5,6-dihydro-1h-pyridin-2-one compounds |
WO2009152166A1 (fr) * | 2008-06-10 | 2009-12-17 | Anadys Pharmaceuticals, Inc. | Composés de dioxyde-1,1 de thiadiazine[1,2,4] |
WO2010042834A1 (fr) | 2008-10-09 | 2010-04-15 | Anadys Pharmaceuticals, Inc. | Procédé d'inhibition du virus de l'hépatite c par combinaison d'une 5,6-dihydro-1h-pyridin-2-one et d'un ou plusieurs composés antiviraux supplémentaires |
TW201026675A (en) * | 2008-10-09 | 2010-07-16 | Anadys Pharmaceuticals Inc | 5,6-dihydro-1H-pyridin-2-one compounds |
KR20120092142A (ko) | 2009-10-28 | 2012-08-20 | 애나디스 파마슈티칼스, 인코포레이티드 | 중수소화 5,6-다이하이드로-1h-파이리딘-2-온 화합물 |
PH12012501216A1 (en) | 2009-12-18 | 2012-11-05 | Boehringer Ingelheim Int | Hcv combination therapy |
US20120321590A1 (en) | 2011-04-06 | 2012-12-20 | Anadys Pharmaceuticals, Inc. | Bridged polycyclic compounds |
US8815847B2 (en) * | 2011-06-07 | 2014-08-26 | Anadys Pharmaceuticals, Inc. | [1,2,4]thiadiazine 1,1-dioxide compounds for lowering serum uric acid |
CN104812383A (zh) * | 2012-06-12 | 2015-07-29 | 豪夫迈·罗氏有限公司 | 治疗hcv感染的治疗剂组合 |
CN105051010B (zh) * | 2013-01-14 | 2017-07-28 | 豪夫迈·罗氏有限公司 | 制备n‑(4‑硝基‑2‑氨磺酰基‑苯基)‑丙酰胺酸甲酯和n‑(4‑氨基‑2‑氨磺酰基‑苯基)‑丙酰胺酸甲酯的新方法 |
SI3421468T1 (sl) * | 2013-11-13 | 2021-03-31 | Vertex Pharmaceuticals Incorporated | Postopki za pripravo inhibitorjev replikacije virusov influence |
WO2016130043A1 (fr) * | 2015-02-13 | 2016-08-18 | Александ Васильевич ИВАЩЕНКО | Inhibiteurs de réplication du virus de l'hépatite b à base de benzo[1,2,4]thiadiazine et compositions pharmaceutiques pour traiter l'hépatite b |
US20180126000A1 (en) | 2016-06-02 | 2018-05-10 | Abbvie Inc. | Glucocorticoid receptor agonist and immunoconjugates thereof |
WO2019106609A1 (fr) | 2017-12-01 | 2019-06-06 | Abbvie Inc. | Agoniste du récepteur des glucocorticoïdes et immunoconjugués de celui-ci |
CA3137584A1 (fr) | 2019-04-29 | 2020-11-05 | Solent Therapeutics, Llc | Derives de 1,1-dioxyde de 3-amino-4h-benzo[e][1,2,4]thiadiazine en tant qu'inhibiteurs de mrgx2 |
CN113292574B (zh) * | 2020-02-21 | 2022-05-03 | 四川大学 | 一类手性多环的托品烷化合物及其制备方法和用途 |
US12274700B1 (en) | 2020-10-30 | 2025-04-15 | Accencio LLC | Methods of treating symptoms of coronavirus infection with RNA polymerase inhibitors |
JP7435515B2 (ja) * | 2021-03-17 | 2024-02-21 | 株式会社村田製作所 | 部品収容装置 |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4171361A (en) * | 1977-03-31 | 1979-10-16 | Eli Lilly And Company | 1-Substituted-3-amino-6,7-dialkoxy-1H-1,2,4-benzothiadiazine-1-oxides |
US4889851A (en) * | 1986-11-21 | 1989-12-26 | Fujisawa Pharmaceutical Co, Ltd. | Benzothiadiazine compounds, and pharmaceutical composition comprising the same |
AU2001261377A1 (en) | 2000-05-10 | 2001-11-20 | Smith Kline Beecham Corporation | Novel anti-infectives |
AR036081A1 (es) | 2001-06-07 | 2004-08-11 | Smithkline Beecham Corp | Compuesto de 1,2-dihidroquinolina, su uso para preparar una composicion farmaceutica, metodos para prepararlo y compuestos del acido 2-aminobenzoico n-alquilado de utilidad como intermediarios en dichos metodos |
WO2003059356A2 (fr) | 2001-10-30 | 2003-07-24 | Smithkline Beecham Corporation | Nouveaux anti-infectieux |
CA2504385C (fr) | 2002-11-01 | 2012-12-18 | Abbott Laboratories | Agents anti-infectieux |
DE60335564D1 (de) * | 2002-11-01 | 2011-02-10 | Abbott Lab | Antiinfektiöse mittel |
US20050075331A1 (en) * | 2003-10-06 | 2005-04-07 | Pratt John K. | Anti-infective agents |
US7601709B2 (en) | 2003-02-07 | 2009-10-13 | Enanta Pharmaceuticals, Inc. | Macrocyclic hepatitis C serine protease inhibitors |
ES2378071T3 (es) * | 2004-03-24 | 2012-04-04 | Janssen Pharmaceutica Nv | Moduladores de cannabinoides de tetrahidro-indazol |
US7439246B2 (en) | 2004-06-28 | 2008-10-21 | Bristol-Myers Squibb Company | Fused heterocyclic kinase inhibitors |
DE602005015732D1 (de) | 2004-08-23 | 2009-09-10 | Hoffmann La Roche | Heterozyklische antivirale verbindungen |
GT200500373A (es) | 2004-12-17 | 2006-10-02 | Compuestos de piridazinones | |
WO2006093801A1 (fr) * | 2005-02-25 | 2006-09-08 | Abbott Laboratories | Derives de thiadiazine utiles en tant qu’agents anti-infectieux |
BRPI0607533A2 (pt) | 2005-04-21 | 2009-09-15 | Nippon Shinyaku Co Ltd | derivado de ftalazinona, composição farmacêutica, inibidor de fosfodiesterase do tipo 4,supressor da produção de tnf-alfa, agente preventivo ou terapêutico, preparado externo, bem como uso do referido derivado |
MX2007013415A (es) | 2005-05-04 | 2008-01-15 | Hoffmann La Roche | Compuestos antivirales heterociclicos. |
WO2008051637A2 (fr) | 2006-06-22 | 2008-05-02 | Anadys Pharmaceuticals, Inc. | Composés de pyridazinone |
JP5306194B2 (ja) * | 2006-06-22 | 2013-10-02 | アナディス ファーマシューティカルズ インク | ピロ[1,2−b]ピリダジノン化合物 |
TW200840572A (en) * | 2006-12-12 | 2008-10-16 | Anadys Pharmaceuticals Inc | 5,6-dihydro-1H-pyridin-2-one compounds |
WO2008073987A1 (fr) | 2006-12-12 | 2008-06-19 | Anadys Pharmaceuticals, Inc. | Composés [1,2-b]pyridazinone condensés saturés |
US20080188466A1 (en) | 2006-12-21 | 2008-08-07 | Anadys Pharmaceuticals, Inc. | Pyridazinone compounds |
WO2008082725A1 (fr) | 2006-12-29 | 2008-07-10 | Anadys Pharmaceuticals, Inc. | Composés de type pyridazinone |
US20080227774A1 (en) | 2007-03-15 | 2008-09-18 | Frank Ruebsam | 5,5-disubstituted-indolizinone compounds |
UA100120C2 (en) | 2007-04-03 | 2012-11-26 | Анадис Фармасьютикалз, Инк. | 5,6-dihydro-1h-pyridin-2-one compounds |
US7834009B2 (en) * | 2007-08-27 | 2010-11-16 | Anadys Pharmaceuticals, Inc. | 4-hydroxy-5,6-dihydro-1H-pyridin-2-one compounds |
-
2008
- 2008-02-04 UA UAA200910844A patent/UA100120C2/ru unknown
- 2008-04-02 WO PCT/US2008/059164 patent/WO2008124450A1/fr active Application Filing
- 2008-04-02 PE PE2008000597A patent/PE20090220A1/es active IP Right Grant
- 2008-04-02 ES ES08733076.7T patent/ES2578302T3/es active Active
- 2008-04-02 EP EP08733076.7A patent/EP2129224B1/fr active Active
- 2008-04-02 CL CL2008000959A patent/CL2008000959A1/es unknown
- 2008-04-02 BR BRPI0809685A patent/BRPI0809685A2/pt not_active Application Discontinuation
- 2008-04-02 AU AU2008237364A patent/AU2008237364B2/en not_active Ceased
- 2008-04-02 JP JP2010502271A patent/JP5739662B2/ja not_active Expired - Fee Related
- 2008-04-02 NZ NZ580445A patent/NZ580445A/en not_active IP Right Cessation
- 2008-04-02 KR KR1020097023036A patent/KR101542516B1/ko not_active Expired - Fee Related
- 2008-04-02 MY MYPI20094109A patent/MY157961A/en unknown
- 2008-04-02 CA CA2682584A patent/CA2682584C/fr active Active
- 2008-04-02 TW TW103101356A patent/TWI481588B/zh not_active IP Right Cessation
- 2008-04-02 CN CN200880018225.2A patent/CN101677563B/zh not_active Expired - Fee Related
- 2008-04-02 CN CN201410217806.6A patent/CN104086540B/zh not_active Expired - Fee Related
- 2008-04-02 EA EA200970916A patent/EA017685B1/ru unknown
- 2008-04-02 TW TW097111924A patent/TWI427079B/zh not_active IP Right Cessation
- 2008-04-02 US US12/061,499 patent/US7939524B2/en active Active
- 2008-04-02 MX MX2009010564A patent/MX2009010564A/es active IP Right Grant
- 2008-04-03 AR ARP080101383A patent/AR065927A1/es active IP Right Grant
-
2009
- 2009-09-30 TN TNP2009000398A patent/TN2009000398A1/fr unknown
- 2009-10-01 IL IL201312A patent/IL201312A/en active IP Right Grant
- 2009-11-02 ZA ZA2009/07673A patent/ZA200907673B/en unknown
-
2010
- 2010-05-13 HK HK10104667.2A patent/HK1137119A1/zh not_active IP Right Cessation
-
2011
- 2011-03-08 US US13/043,167 patent/US8101800B2/en not_active Expired - Fee Related
-
2012
- 2012-01-23 US US13/356,063 patent/US8236948B2/en not_active Expired - Fee Related
- 2012-08-06 US US13/567,667 patent/US8546602B2/en active Active
-
2013
- 2013-04-11 IL IL225694A patent/IL225694A/en active IP Right Grant
- 2013-09-30 US US14/041,376 patent/US8765741B2/en active Active
-
2014
- 2014-06-10 US US14/300,306 patent/US9156832B2/en not_active Expired - Fee Related
-
2015
- 2015-02-10 HK HK15101490.6A patent/HK1201822A1/xx not_active IP Right Cessation
- 2015-02-16 JP JP2015027744A patent/JP5934403B2/ja not_active Expired - Fee Related
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