PE20130005A1 - Compuestos triciclicos novedosos - Google Patents
Compuestos triciclicos novedososInfo
- Publication number
- PE20130005A1 PE20130005A1 PE2012000736A PE2012000736A PE20130005A1 PE 20130005 A1 PE20130005 A1 PE 20130005A1 PE 2012000736 A PE2012000736 A PE 2012000736A PE 2012000736 A PE2012000736 A PE 2012000736A PE 20130005 A1 PE20130005 A1 PE 20130005A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- ora
- compounds
- tricyclic compounds
- imidazo
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- FFNVQNRYTPFDDP-UHFFFAOYSA-N 2-cyanopyridine Chemical compound N#CC1=CC=CC=N1 FFNVQNRYTPFDDP-UHFFFAOYSA-N 0.000 abstract 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 abstract 1
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 208000026278 immune system disease Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 210000000952 spleen Anatomy 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
-
- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/12—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 three hetero rings
- C07D513/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
SE REFIERE A COMPUESTOS HETEROCICLICOS DE FORMULA (Ia), (Ib), ENTRE OTROS, DONDE R1 ES H, HALOGENO, CF3, CN, -C(O)-ALQUILO(C1-C6) OPCIONALMENTE SUSTITUIDO, ENTRE OTROS; R2 ES H, CN, -C(O)-CICLOALQUILO(C3-C6), -S-ALQUILO(C1-C6), ENTRE OTROS; R3 ES H, CF3, CN, HETEROCICLILO(C1-C10), ARILO(C6-C10), ENTRE OTROS; R5 ES H, HALOGENO, CF3, -S-ALQUILO(C1-C6), ALCOXI(C1-C6), ENTRE OTROS; R6 ES H, OCF3, -C(O)-ALQUILO(C1-C6), -C(O)-CICLOALQUILO(C3-C6), ENTRE OTROS; R7 ES H, -(CH2)n-P(=O)(ORa)(ORa), CH=CH-P(=O)(ORa)(ORa), ENTRE OTROS, EN DONDE n ES DE 1 A 3; Ra ES H, ALQUILO(C1-C10), ALQUENILO(C2-C10), ALQUIL(C1-C10)-O-ALQUILO(C1-C10), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: (E)-3-(1-CICLOHEXIL-6H-IMIDAZO[1,5-a]PIRROLO[2,3-e]PIRAZIN-3-IL)ACRILICO; 3-(3-(4-(2-HIDROXIPROPAN-2-IL)FENIL)-6H-IMIDAZO[1,5-a]PIRROLO[2,3-e]PIRAZIN-1-IL)PICOLINONITRILO; ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE LA TIROSINA DEL BAZO (SYK) SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDADES INFLAMATORIAS E INMUNES
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26559109P | 2009-12-01 | 2009-12-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20130005A1 true PE20130005A1 (es) | 2013-02-16 |
Family
ID=44115273
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2012000736A PE20130005A1 (es) | 2009-12-01 | 2010-12-01 | Compuestos triciclicos novedosos |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US8785639B2 (es) |
| EP (1) | EP2506713A4 (es) |
| JP (1) | JP2013512282A (es) |
| KR (1) | KR20120102724A (es) |
| CN (1) | CN102711470A (es) |
| AU (1) | AU2010326030A1 (es) |
| CA (1) | CA2781010A1 (es) |
| CL (1) | CL2012001396A1 (es) |
| CR (1) | CR20120294A (es) |
| DO (1) | DOP2012000149A (es) |
| EC (1) | ECSP12011968A (es) |
| GT (1) | GT201200167A (es) |
| IL (1) | IL220053A0 (es) |
| MX (1) | MX2012006381A (es) |
| NZ (1) | NZ599938A (es) |
| PE (1) | PE20130005A1 (es) |
| PH (1) | PH12012501000A1 (es) |
| RU (1) | RU2012127368A (es) |
| SG (1) | SG181147A1 (es) |
| WO (1) | WO2011068899A1 (es) |
| ZA (1) | ZA201203588B (es) |
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| HUE028347T2 (en) | 2008-06-10 | 2016-12-28 | Abbvie Inc | Tricyclic compounds |
| US20100277320A1 (en) * | 2009-06-30 | 2010-11-04 | Gold Steven K | RFID Keypad Assemblies |
| PH12012501076B1 (en) * | 2009-12-01 | 2018-07-04 | Abbvie Inc | Novel tricyclic compounds |
| WO2011156698A2 (en) | 2010-06-11 | 2011-12-15 | Abbott Laboratories | NOVEL PYRAZOLO[3,4-d]PYRIMIDINE COMPOUNDS |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| AU2012244549B2 (en) | 2011-04-21 | 2017-04-20 | Origenis Gmbh | Heterocyclic compounds as kinase inhibitors |
| MX365311B (es) * | 2011-08-12 | 2019-05-29 | Nissan Chemical Ind Ltd | Compuestos heterocíclicos tricíclicos inhibidores de jak. |
| CN102603743B (zh) * | 2012-02-24 | 2014-05-28 | 南京天易生物科技有限公司 | 抗肿瘤的氮杂苯并[f]薁衍生物其制备方法及其用途 |
| PH12019502809B1 (en) | 2012-06-13 | 2024-04-24 | Incyte Holdings Corp | Substituted tricyclic compounds as fgfr inhibitors |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| WO2014060113A1 (en) | 2012-10-19 | 2014-04-24 | Origenis Gmbh | Novel kinase inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| ES2755130T3 (es) | 2013-02-08 | 2020-04-21 | Nissan Chemical Corp | Compuesto de pirrolopiridina tricíclico, e inhibidor de JAK |
| SMT201800127T1 (it) | 2013-04-19 | 2018-05-02 | Incyte Holdings Corp | Eterocilci biciclici come inibitori di fgfr |
| WO2014169473A1 (en) * | 2013-04-19 | 2014-10-23 | Abbvie Inc. | 6H-IMIDAZO[1,5-a]PYRROLO[2,3-e]PYRAZINE COMPOUNDS |
| AU2015260349B2 (en) | 2014-05-14 | 2019-02-21 | Nissan Chemical Industries, Ltd. | Tricyclic compound and JAK inhibitor |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| SG10201913036RA (en) | 2015-02-20 | 2020-02-27 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| JP6589233B2 (ja) * | 2015-03-17 | 2019-10-16 | 株式会社カネカ | トリアリールメタノールの製造方法 |
| US11524964B2 (en) | 2015-10-16 | 2022-12-13 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| CN120483986A (zh) | 2015-10-16 | 2025-08-15 | 艾伯维公司 | 制备咪唑并[1,2-a]吡咯并[2,3-e]吡嗪类化合物及其固态形式的方法 |
| US11512092B2 (en) | 2015-10-16 | 2022-11-29 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US12365689B2 (en) | 2015-10-16 | 2025-07-22 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US11773106B2 (en) | 2015-10-16 | 2023-10-03 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US10550126B2 (en) | 2015-10-16 | 2020-02-04 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US11365198B2 (en) | 2015-10-16 | 2022-06-21 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
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| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| BR112020008850A2 (pt) * | 2017-11-03 | 2020-10-20 | Aclaris Therapeutics, Inc. | composto, composição farmacêutica e método para tratar uma doença mediada por jak1 e jak3 |
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| JP2021523121A (ja) | 2018-05-04 | 2021-09-02 | インサイト・コーポレイションIncyte Corporation | Fgfr阻害剤の固体形態及びその調製プロセス |
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| CN108707101B (zh) * | 2018-07-05 | 2022-05-17 | 深圳大学 | 光催化合成生物碱的方法 |
| JP7516365B2 (ja) * | 2018-10-23 | 2024-07-16 | イントラ-セルラー・セラピーズ・インコーポレイテッド | 新規化合物 |
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| KR20220035447A (ko) * | 2019-07-18 | 2022-03-22 | 브리스톨-마이어스 스큅 컴퍼니 | IRAK4 억제제로서 유용한 피라졸로[3,4-d]피롤로[1,2-b]피리다지닐 화합물 |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| JOP20220083A1 (ar) | 2019-10-14 | 2023-01-30 | Incyte Corp | حلقات غير متجانسة ثنائية الحلقة كمثبطات لـ fgfr |
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| US20230365544A1 (en) * | 2020-05-12 | 2023-11-16 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Small molecule inhibitors of calcium channel activity and uses thereof |
| WO2021257857A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Naphthyridinone compounds as jak2 v617f inhibitors |
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| WO2022006456A1 (en) | 2020-07-02 | 2022-01-06 | Incyte Corporation | Tricyclic pyridone compounds as jak2 v617f inhibitors |
| HRP20250814T1 (hr) * | 2020-07-02 | 2025-09-12 | Incyte Corporation | Spojevi tricikličke uree kao jak2 v617f inhibitori |
| WO2022046989A1 (en) | 2020-08-27 | 2022-03-03 | Incyte Corporation | Tricyclic urea compounds as jak2 v617f inhibitors |
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| US11958861B2 (en) | 2021-02-25 | 2024-04-16 | Incyte Corporation | Spirocyclic lactams as JAK2 V617F inhibitors |
| JP2024509587A (ja) | 2021-03-11 | 2024-03-04 | ヤンセン ファーマシューティカ エヌ.ベー. | Jak媒介性障害の治療に使用するためのlorpucitinib |
| US12065494B2 (en) | 2021-04-12 | 2024-08-20 | Incyte Corporation | Combination therapy comprising an FGFR inhibitor and a Nectin-4 targeting agent |
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-
2010
- 2010-12-01 US US12/958,291 patent/US8785639B2/en active Active
- 2010-12-01 JP JP2012542166A patent/JP2013512282A/ja active Pending
- 2010-12-01 CA CA2781010A patent/CA2781010A1/en not_active Abandoned
- 2010-12-01 EP EP10835075.2A patent/EP2506713A4/en not_active Withdrawn
- 2010-12-01 MX MX2012006381A patent/MX2012006381A/es not_active Application Discontinuation
- 2010-12-01 RU RU2012127368/04A patent/RU2012127368A/ru not_active Application Discontinuation
- 2010-12-01 AU AU2010326030A patent/AU2010326030A1/en not_active Abandoned
- 2010-12-01 SG SG2012039905A patent/SG181147A1/en unknown
- 2010-12-01 KR KR1020127016419A patent/KR20120102724A/ko not_active Withdrawn
- 2010-12-01 CN CN2010800629352A patent/CN102711470A/zh active Pending
- 2010-12-01 NZ NZ599938A patent/NZ599938A/en not_active IP Right Cessation
- 2010-12-01 WO PCT/US2010/058598 patent/WO2011068899A1/en not_active Ceased
- 2010-12-01 PE PE2012000736A patent/PE20130005A1/es not_active Application Discontinuation
- 2010-12-01 PH PH1/2012/501000A patent/PH12012501000A1/en unknown
-
2012
- 2012-05-16 ZA ZA2012/03588A patent/ZA201203588B/en unknown
- 2012-05-29 IL IL220053A patent/IL220053A0/en unknown
- 2012-05-30 GT GT201200167A patent/GT201200167A/es unknown
- 2012-05-30 CL CL2012001396A patent/CL2012001396A1/es unknown
- 2012-05-30 DO DO2012000149A patent/DOP2012000149A/es unknown
- 2012-05-30 CR CR20120294A patent/CR20120294A/es unknown
- 2012-06-12 EC ECSP12011968 patent/ECSP12011968A/es unknown
-
2014
- 2014-06-09 US US14/299,652 patent/US20140349970A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| IL220053A0 (en) | 2012-10-31 |
| JP2013512282A (ja) | 2013-04-11 |
| ECSP12011968A (es) | 2012-07-31 |
| US20110190489A1 (en) | 2011-08-04 |
| RU2012127368A (ru) | 2014-01-10 |
| DOP2012000149A (es) | 2012-09-30 |
| PH12012501000A1 (en) | 2013-02-11 |
| GT201200167A (es) | 2014-06-10 |
| EP2506713A1 (en) | 2012-10-10 |
| EP2506713A4 (en) | 2014-09-03 |
| CL2012001396A1 (es) | 2012-09-14 |
| KR20120102724A (ko) | 2012-09-18 |
| WO2011068899A1 (en) | 2011-06-09 |
| SG181147A1 (en) | 2012-07-30 |
| CA2781010A1 (en) | 2011-06-09 |
| NZ599938A (en) | 2014-08-29 |
| ZA201203588B (en) | 2015-07-29 |
| AU2010326030A1 (en) | 2012-06-07 |
| US8785639B2 (en) | 2014-07-22 |
| MX2012006381A (es) | 2012-06-19 |
| CN102711470A (zh) | 2012-10-03 |
| US20140349970A1 (en) | 2014-11-27 |
| CR20120294A (es) | 2012-09-03 |
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