CL2008001537A1 - Compuestos heterociclo derivados de 1h-pirimidin-2,4-diona, dihidro-pirimidin-2,4-diona e imidazol-2,4-diona, inhibidores no nucleosidos de la transcriptasa inversa (nnrti) del vih-1; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar enfermedades mediadas por vih, sida o arc. - Google Patents
Compuestos heterociclo derivados de 1h-pirimidin-2,4-diona, dihidro-pirimidin-2,4-diona e imidazol-2,4-diona, inhibidores no nucleosidos de la transcriptasa inversa (nnrti) del vih-1; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar enfermedades mediadas por vih, sida o arc.Info
- Publication number
- CL2008001537A1 CL2008001537A1 CL2008001537A CL2008001537A CL2008001537A1 CL 2008001537 A1 CL2008001537 A1 CL 2008001537A1 CL 2008001537 A CL2008001537 A CL 2008001537A CL 2008001537 A CL2008001537 A CL 2008001537A CL 2008001537 A1 CL2008001537 A1 CL 2008001537A1
- Authority
- CL
- Chile
- Prior art keywords
- dione
- pyrimidin
- hiv
- compounds
- dihydro
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 title abstract 2
- 201000010099 disease Diseases 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 230000001404 mediated effect Effects 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 102100034343 Integrase Human genes 0.000 title 1
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 title 1
- DWRDBJCTLDOPFZ-UHFFFAOYSA-N imidazole-2,4-dione Chemical compound O=C1NC(=O)N=C1 DWRDBJCTLDOPFZ-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 239000002777 nucleoside Substances 0.000 title 1
- 150000003833 nucleoside derivatives Chemical class 0.000 title 1
- 208000030507 AIDS Diseases 0.000 abstract 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D239/22—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4174—Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/72—Two oxygen atoms, e.g. hydantoin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/76—Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
- C07D233/78—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
- C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
- C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/553—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms with halogen atoms or nitro radicals directly attached to ring carbon atoms, e.g. fluorouracil
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- General Chemical & Material Sciences (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Compuestos derivados de 1h-pirimidin-2,4-diona, dihidro-pirimidin-2,4-diona e imidazolin-2,4-diona; composición farmacéutica que comprende a dichos compuestos; y su uso para tratar enfermedades mediadas por VIH, Sida o arc.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US93225107P | 2007-05-30 | 2007-05-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2008001537A1 true CL2008001537A1 (es) | 2008-12-05 |
Family
ID=39712538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2008001537A CL2008001537A1 (es) | 2007-05-30 | 2008-05-28 | Compuestos heterociclo derivados de 1h-pirimidin-2,4-diona, dihidro-pirimidin-2,4-diona e imidazol-2,4-diona, inhibidores no nucleosidos de la transcriptasa inversa (nnrti) del vih-1; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar enfermedades mediadas por vih, sida o arc. |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8026362B2 (es) |
| EP (1) | EP2155692B1 (es) |
| JP (1) | JP5167350B2 (es) |
| KR (1) | KR101542629B1 (es) |
| CN (1) | CN101679294B (es) |
| AR (1) | AR066743A1 (es) |
| AU (1) | AU2008257771B2 (es) |
| BR (1) | BRPI0811645A2 (es) |
| CA (1) | CA2687747C (es) |
| CL (1) | CL2008001537A1 (es) |
| EA (1) | EA016386B1 (es) |
| ES (1) | ES2542153T3 (es) |
| IL (1) | IL202143A (es) |
| MX (1) | MX2009012704A (es) |
| PE (1) | PE20090296A1 (es) |
| TW (1) | TWI425946B (es) |
| WO (1) | WO2008145562A1 (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200901969A (en) * | 2007-06-06 | 2009-01-16 | Smithkline Beecham Corp | Chemical compounds |
| DE102008030091B4 (de) * | 2008-06-25 | 2011-03-03 | Resprotect Gmbh | Uracilderivate und deren Verwendung |
| EP3774804A1 (en) | 2018-03-26 | 2021-02-17 | Novartis AG | N-(3-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)benzamide derivatives |
| US11925643B2 (en) | 2018-05-23 | 2024-03-12 | Mor Research Applications Ltd. | Toll-like receptor 4 (TLR4) inhibitors and use thereof |
| EA202191711A1 (ru) | 2018-12-18 | 2021-10-04 | Мерк Шарп И Доум Корп. | Производные пиримидона в качестве селективных цитотоксических агентов против вич-инфицированных клеток |
| EP4031247A1 (en) * | 2019-09-16 | 2022-07-27 | Novartis AG | Bifunctional degraders and their methods of use |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4110470A (en) * | 1965-10-07 | 1978-08-29 | Horst Kummer | Pharmaceutical composition comprising d,l-α-methyl-thyroxine ethyl ester and the salts thereof and the control of cholesterol and triglyceride blood level therewith |
| US4949314A (en) | 1966-08-16 | 1990-08-14 | The United States Of America As Represented By The Secretary Of The Navy | Method and means for increasing echo-ranging-search rate |
| GB1601310A (en) * | 1978-05-23 | 1981-10-28 | Lilly Industries Ltd | Aryl hydantoins |
| US4518584A (en) | 1983-04-15 | 1985-05-21 | Cetus Corporation | Human recombinant interleukin-2 muteins |
| GB8327880D0 (en) | 1983-10-18 | 1983-11-16 | Ajinomoto Kk | Saccharomyces cerevisiae |
| US4604377A (en) | 1984-03-28 | 1986-08-05 | Cetus Corporation | Pharmaceutical compositions of microbially produced interleukin-2 |
| US4569790A (en) | 1984-03-28 | 1986-02-11 | Cetus Corporation | Process for recovering microbially produced interleukin-2 and purified recombinant interleukin-2 compositions |
| US4530787A (en) | 1984-03-28 | 1985-07-23 | Cetus Corporation | Controlled oxidation of microbially produced cysteine-containing proteins |
| IL76360A0 (en) | 1984-09-26 | 1986-01-31 | Takeda Chemical Industries Ltd | Mutual separation of proteins |
| US4752585A (en) | 1985-12-17 | 1988-06-21 | Cetus Corporation | Oxidation-resistant muteins |
| US4748234A (en) | 1985-06-26 | 1988-05-31 | Cetus Corporation | Process for recovering refractile bodies containing heterologous proteins from microbial hosts |
| AU622926B2 (en) | 1988-09-09 | 1992-04-30 | Nippon Kayaku Kabushiki Kaisha | Pyrimidine or purine cyclobutane derivatives |
| US5925643A (en) | 1990-12-05 | 1999-07-20 | Emory University | Enantiomerically pure β-D-dioxolane-nucleosides |
| US5489697A (en) | 1994-08-03 | 1996-02-06 | Medichem Research, Inc. | Method for the preparation of (+)-calanolide A and intermediates thereof |
| IL117574A0 (en) | 1995-04-03 | 1996-07-23 | Bristol Myers Squibb Co | Processes for the preparation of cyclobutanone derivatives |
| US7166730B2 (en) | 2000-01-27 | 2007-01-23 | Fine Tech Laboratories, Ltd | Process for the preparation of prostaglandin derivatives |
| JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
| TW200505441A (en) | 2003-03-24 | 2005-02-16 | Hoffmann La Roche | Non-nucleoside reverse transcriptase inhibitorsⅠ |
| CA2518823A1 (en) * | 2003-03-24 | 2004-10-07 | F.Hoffmann-La Roche Ag | Benzyl-pyridazinons as reverse transcriptase inhibitors |
| JP4107658B2 (ja) | 2003-07-23 | 2008-06-25 | インターナショナル・ビジネス・マシーンズ・コーポレーション | 分類因子検出装置、分類因子検出方法、プログラム、及び記録媒体 |
| DE602005019694D1 (de) | 2004-02-27 | 2010-04-15 | Inst Curie | Neue proliferationsmarker in der klinischen praxis und deren verwendung zur krebsprognose oder -diagnose |
| CA2559552A1 (en) | 2004-03-23 | 2005-09-29 | F. Hoffmann-La Roche Ag | Benzyl-pyridazinone derivatives as non-nucleoside reverse transcriptase inhibitors |
| CA2563225A1 (en) | 2004-04-15 | 2005-10-27 | F. Hoffmann-La Roche Ag | Process for preparing pyridazinone compounds |
| US7625949B2 (en) | 2004-04-23 | 2009-12-01 | Roche Palo Alto Llc | Methods for treating retroviral infections |
| US7166738B2 (en) | 2004-04-23 | 2007-01-23 | Roche Palo Alto Llc | Non-nucleoside reverse transcriptase inhibitors |
| CA2471006A1 (en) * | 2004-06-23 | 2005-12-23 | Bayer Inc. | Silica reinforced elastomer compounds prepared with dry liquid modifiers |
| CN1993332B (zh) | 2004-07-27 | 2011-04-06 | 弗·哈夫曼-拉罗切有限公司 | 作为非核苷逆转录酶抑制剂的苄基三唑酮化合物 |
| EP2135608B8 (en) | 2004-08-25 | 2012-03-21 | Ardea Biosciences, Inc. | S-triazolyl alpha -mercaptoacetanilides as inhibitors of HIV reverse transcriptase |
| EP1799696B1 (en) | 2004-09-17 | 2008-11-12 | IDENIX Pharmaceuticals, Inc. | Phosphoindoles as hiv inhibitors |
| EP1797062B8 (en) | 2004-09-30 | 2011-05-25 | Boehringer Ingelheim International GmbH | Alkynyl based dervatives of benzophenone as non-nucleoside reverse transcriptase inhibitors |
| JP4423166B2 (ja) | 2004-10-29 | 2010-03-03 | 富士通株式会社 | 電子部品の超音波実装方法および超音波実装装置 |
| JP2008525419A (ja) | 2004-12-22 | 2008-07-17 | ファイザー・リミテッド | Hiv−1逆転写酵素の非ヌクレオシド阻害剤 |
| JP2008534456A (ja) | 2005-03-24 | 2008-08-28 | エフ.ホフマン−ラ ロシュ アーゲー | ヘテロ環式逆転写酵素インヒビターとしての1,2,4−トリアゾール−5−オン化合物 |
| US20060225874A1 (en) | 2005-04-11 | 2006-10-12 | Shives Gary D | Sandwiched thermal article |
| AR057455A1 (es) | 2005-07-22 | 2007-12-05 | Merck & Co Inc | Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica |
| EP1937651B1 (en) * | 2005-09-30 | 2008-12-24 | F.Hoffmann-La Roche Ag | Nnrt inhibitors |
| JP2009515826A (ja) | 2005-10-19 | 2009-04-16 | エフ.ホフマン−ラ ロシュ アーゲー | フェニル−アセトアミドnnrt阻害剤 |
| EP1940782B1 (en) | 2005-10-19 | 2009-03-11 | F.Hoffmann-La Roche Ag | N-phenyl phenylacetamide non-nucleoside reverse transcriptase inhibitors |
| BRPI0813404A2 (pt) * | 2007-06-22 | 2014-12-30 | Hoffmann La Roche | Derivados de uréia e carbamato como inibidores de transcriptase reversa de não-nucleosídeo |
-
2008
- 2008-05-20 MX MX2009012704A patent/MX2009012704A/es active IP Right Grant
- 2008-05-20 EP EP08759780.3A patent/EP2155692B1/en not_active Not-in-force
- 2008-05-20 EA EA200901599A patent/EA016386B1/ru not_active IP Right Cessation
- 2008-05-20 JP JP2010509787A patent/JP5167350B2/ja not_active Expired - Fee Related
- 2008-05-20 WO PCT/EP2008/056165 patent/WO2008145562A1/en not_active Ceased
- 2008-05-20 CA CA2687747A patent/CA2687747C/en not_active Expired - Fee Related
- 2008-05-20 AU AU2008257771A patent/AU2008257771B2/en not_active Ceased
- 2008-05-20 BR BRPI0811645-8A2A patent/BRPI0811645A2/pt not_active IP Right Cessation
- 2008-05-20 KR KR1020097027313A patent/KR101542629B1/ko not_active Expired - Fee Related
- 2008-05-20 CN CN2008800179226A patent/CN101679294B/zh not_active Expired - Fee Related
- 2008-05-20 ES ES08759780.3T patent/ES2542153T3/es active Active
- 2008-05-27 PE PE2008000903A patent/PE20090296A1/es not_active Application Discontinuation
- 2008-05-28 AR ARP080102236A patent/AR066743A1/es unknown
- 2008-05-28 CL CL2008001537A patent/CL2008001537A1/es unknown
- 2008-05-29 TW TW097119955A patent/TWI425946B/zh not_active IP Right Cessation
- 2008-05-30 US US12/156,228 patent/US8026362B2/en not_active Expired - Fee Related
-
2009
- 2009-11-15 IL IL202143A patent/IL202143A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| KR20100028584A (ko) | 2010-03-12 |
| AR066743A1 (es) | 2009-09-09 |
| US20090076045A1 (en) | 2009-03-19 |
| CN101679294A (zh) | 2010-03-24 |
| CA2687747A1 (en) | 2008-12-04 |
| US8026362B2 (en) | 2011-09-27 |
| TW200911260A (en) | 2009-03-16 |
| IL202143A0 (en) | 2010-06-16 |
| ES2542153T3 (es) | 2015-07-31 |
| EP2155692B1 (en) | 2015-06-17 |
| WO2008145562A1 (en) | 2008-12-04 |
| CA2687747C (en) | 2015-11-17 |
| AU2008257771A1 (en) | 2008-12-04 |
| IL202143A (en) | 2014-06-30 |
| BRPI0811645A2 (pt) | 2014-11-11 |
| EP2155692A1 (en) | 2010-02-24 |
| AU2008257771B2 (en) | 2015-02-19 |
| JP2010528083A (ja) | 2010-08-19 |
| PE20090296A1 (es) | 2009-03-27 |
| EA200901599A1 (ru) | 2010-06-30 |
| EA016386B1 (ru) | 2012-04-30 |
| KR101542629B1 (ko) | 2015-08-06 |
| TWI425946B (zh) | 2014-02-11 |
| CN101679294B (zh) | 2012-08-08 |
| MX2009012704A (es) | 2009-12-08 |
| JP5167350B2 (ja) | 2013-03-21 |
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