JP2009541385A5 - - Google Patents
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- JP2009541385A5 JP2009541385A5 JP2009516963A JP2009516963A JP2009541385A5 JP 2009541385 A5 JP2009541385 A5 JP 2009541385A5 JP 2009516963 A JP2009516963 A JP 2009516963A JP 2009516963 A JP2009516963 A JP 2009516963A JP 2009541385 A5 JP2009541385 A5 JP 2009541385A5
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- 150000001412 amines Chemical class 0.000 claims 15
- 239000002253 acid Substances 0.000 claims 11
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 9
- 239000011780 sodium chloride Substances 0.000 claims 9
- 239000003586 protic polar solvent Substances 0.000 claims 8
- -1 trialkylsilyl halide Chemical class 0.000 claims 8
- 238000000034 method Methods 0.000 claims 7
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims 6
- 239000003814 drug Substances 0.000 claims 5
- IJOOHPMOJXWVHK-UHFFFAOYSA-N Trimethylsilyl chloride Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 claims 4
- CSRZQMIRAZTJOY-UHFFFAOYSA-N Trimethylsilyl iodide Chemical compound C[Si](C)(C)I CSRZQMIRAZTJOY-UHFFFAOYSA-N 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 3
- 229940079593 drugs Drugs 0.000 claims 3
- 150000007524 organic acids Chemical class 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N Citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 2
- 230000002921 anti-spasmodic Effects 0.000 claims 2
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 2
- IYYIVELXUANFED-UHFFFAOYSA-N bromo(trimethyl)silane Chemical compound C[Si](C)(C)Br IYYIVELXUANFED-UHFFFAOYSA-N 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 235000019253 formic acid Nutrition 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 150000002576 ketones Chemical class 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 2
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims 2
- RTGDFNSFWBGLEC-SYZQJQIISA-N 2-(morpholin-4-yl)ethyl (4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-2-benzofuran-5-yl)-4-methylhex-4-enoate Chemical compound COC1=C(C)C=2COC(=O)C=2C(O)=C1C\C=C(/C)CCC(=O)OCCN1CCOCC1 RTGDFNSFWBGLEC-SYZQJQIISA-N 0.000 claims 1
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims 1
- 229960004676 ANTITHROMBOTIC AGENTS Drugs 0.000 claims 1
- CEUORZQYGODEFX-UHFFFAOYSA-N Aripirazole Chemical compound ClC1=CC=CC(N2CCN(CCCCOC=3C=C4NC(=O)CCC4=CC=3)CC2)=C1Cl CEUORZQYGODEFX-UHFFFAOYSA-N 0.000 claims 1
- 239000005552 B01AC04 - Clopidogrel Substances 0.000 claims 1
- 239000005465 B01AC22 - Prasugrel Substances 0.000 claims 1
- SECKRCOLJRRGGV-UHFFFAOYSA-N BAY 38-9456 Chemical compound CCCC1=NC(C)=C(C(N=2)=O)N1NC=2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(CC)CC1 SECKRCOLJRRGGV-UHFFFAOYSA-N 0.000 claims 1
- WSEQXVZVJXJVFP-UHFFFAOYSA-N Citalopram Chemical compound O1CC2=CC(C#N)=CC=C2C1(CCCN(C)C)C1=CC=C(F)C=C1 WSEQXVZVJXJVFP-UHFFFAOYSA-N 0.000 claims 1
- 229960003009 Clopidogrel Drugs 0.000 claims 1
- GKTWGGQPFAXNFI-HNNXBMFYSA-N Clopidogrel Chemical compound C1([C@H](N2CC=3C=CSC=3CC2)C(=O)OC)=CC=CC=C1Cl GKTWGGQPFAXNFI-HNNXBMFYSA-N 0.000 claims 1
- 101700062901 DPP Proteins 0.000 claims 1
- 102100012353 DPP4 Human genes 0.000 claims 1
- 101700039720 DPP4 Proteins 0.000 claims 1
- 101700040453 DRD2 Proteins 0.000 claims 1
- HXGBXQDTNZMWGS-RUZDIDTESA-N Darifenacin Chemical compound C=1C=CC=CC=1C([C@H]1CN(CCC=2C=C3CCOC3=CC=2)CC1)(C(=O)N)C1=CC=CC=C1 HXGBXQDTNZMWGS-RUZDIDTESA-N 0.000 claims 1
- ADEBPBSSDYVVLD-UHFFFAOYSA-N Donepezil Chemical compound O=C1C=2C=C(OC)C(OC)=CC=2CC1CC(CC1)CCN1CC1=CC=CC=C1 ADEBPBSSDYVVLD-UHFFFAOYSA-N 0.000 claims 1
- 229940052760 Dopamine agonists Drugs 0.000 claims 1
- ZEUITGRIYCTCEM-KRWDZBQOSA-N Duloxetine Chemical compound C1([C@@H](OC=2C3=CC=CC=C3C=CC=2)CCNC)=CC=CS1 ZEUITGRIYCTCEM-KRWDZBQOSA-N 0.000 claims 1
- 208000010228 Erectile Dysfunction Diseases 0.000 claims 1
- AAKJLRGGTJKAMG-UHFFFAOYSA-N Erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 claims 1
- 229960001433 Erlotinib Drugs 0.000 claims 1
- 229960003444 IMMUNOSUPPRESSANTS Drugs 0.000 claims 1
- 239000005551 L01XE03 - Erlotinib Substances 0.000 claims 1
- TYZROVQLWOKYKF-ZDUSSCGKSA-N Linezolid Chemical compound O=C1O[C@@H](CNC(=O)C)CN1C(C=C1F)=CC=C1N1CCOCC1 TYZROVQLWOKYKF-ZDUSSCGKSA-N 0.000 claims 1
- 229940035363 MUSCLE RELAXANTS Drugs 0.000 claims 1
- BUGYDGFZZOZRHP-UHFFFAOYSA-N Memantine Chemical compound C1C(C2)CC3(C)CC1(C)CC2(N)C3 BUGYDGFZZOZRHP-UHFFFAOYSA-N 0.000 claims 1
- FABPRXSRWADJSP-MEDUHNTESA-N Moxifloxacin Chemical compound COC1=C(N2C[C@H]3NCCC[C@H]3C2)C(F)=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 FABPRXSRWADJSP-MEDUHNTESA-N 0.000 claims 1
- 229940083876 Muscle relaxants FOR TREATMENT OF HEMORRHOIDS AND ANAL FISSURES FOR TOPICAL USE Drugs 0.000 claims 1
- 229960003089 Pramipexole Drugs 0.000 claims 1
- FASDKYOPVNHBLU-ZETCQYMHSA-N Pramipexole Chemical compound C1[C@@H](NCCC)CCC2=C1SC(N)=N2 FASDKYOPVNHBLU-ZETCQYMHSA-N 0.000 claims 1
- GZUITABIAKMVPG-UHFFFAOYSA-N Raloxifene Chemical compound C1=CC(O)=CC=C1C1=C(C(=O)C=2C=CC(OCCN3CCCCC3)=CC=2)C2=CC=C(O)C=C2S1 GZUITABIAKMVPG-UHFFFAOYSA-N 0.000 claims 1
- 229960004622 Raloxifene Drugs 0.000 claims 1
- VGKDLMBJGBXTGI-SJCJKPOMSA-N Sertraline Chemical compound C1([C@@H]2CC[C@@H](C3=CC=CC=C32)NC)=CC=C(Cl)C(Cl)=C1 VGKDLMBJGBXTGI-SJCJKPOMSA-N 0.000 claims 1
- 229960002073 Sertraline Drugs 0.000 claims 1
- MFFMDFFZMYYVKS-SECBINFHSA-N Sitagliptin Chemical compound C([C@H](CC(=O)N1CC=2N(C(=NN=2)C(F)(F)F)CC1)N)C1=CC(F)=C(F)C=C1F MFFMDFFZMYYVKS-SECBINFHSA-N 0.000 claims 1
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N Terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 230000001430 anti-depressive Effects 0.000 claims 1
- 230000000843 anti-fungal Effects 0.000 claims 1
- 239000000883 anti-obesity agent Substances 0.000 claims 1
- 230000003262 anti-osteoporosis Effects 0.000 claims 1
- 239000003146 anticoagulant agent Substances 0.000 claims 1
- 239000000935 antidepressant agent Substances 0.000 claims 1
- 239000003472 antidiabetic agent Substances 0.000 claims 1
- 229940121375 antifungals Drugs 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 claims 1
- 239000000010 aprotic solvent Substances 0.000 claims 1
- 229960004372 aripiprazole Drugs 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000000812 cholinergic antagonist Substances 0.000 claims 1
- VDHAWDNDOKGFTD-MRXNPFEDSA-N cinacalcet Chemical compound N([C@H](C)C=1C2=CC=CC=C2C=CC=1)CCCC1=CC=CC(C(F)(F)F)=C1 VDHAWDNDOKGFTD-MRXNPFEDSA-N 0.000 claims 1
- 229960003315 cinacalcet Drugs 0.000 claims 1
- 229960001653 citalopram Drugs 0.000 claims 1
- 235000015165 citric acid Nutrition 0.000 claims 1
- 229960002677 darifenacin Drugs 0.000 claims 1
- 150000001991 dicarboxylic acids Chemical class 0.000 claims 1
- 229960003530 donepezil Drugs 0.000 claims 1
- 239000003136 dopamine receptor stimulating agent Substances 0.000 claims 1
- 229960002866 duloxetine Drugs 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- 230000001861 immunosuppresant Effects 0.000 claims 1
- 239000003018 immunosuppressive agent Substances 0.000 claims 1
- 201000001881 impotence Diseases 0.000 claims 1
- 238000011065 in-situ storage Methods 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 229960003907 linezolid Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229960004640 memantine Drugs 0.000 claims 1
- 229960003702 moxifloxacin Drugs 0.000 claims 1
- 229960004866 mycophenolate mofetil Drugs 0.000 claims 1
- 239000003158 myorelaxant agent Substances 0.000 claims 1
- 230000000701 neuroleptic Effects 0.000 claims 1
- 239000003176 neuroleptic agent Substances 0.000 claims 1
- DTGLZDAWLRGWQN-UHFFFAOYSA-N prasugrel Chemical compound C1CC=2SC(OC(=O)C)=CC=2CN1C(C=1C(=CC=CC=1)F)C(=O)C1CC1 DTGLZDAWLRGWQN-UHFFFAOYSA-N 0.000 claims 1
- 229960004197 prasugrel Drugs 0.000 claims 1
- 239000004089 psychotropic agent Substances 0.000 claims 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2(1H)-one Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims 1
- 239000000018 receptor agonist Substances 0.000 claims 1
- 201000000980 schizophrenia Diseases 0.000 claims 1
- 239000003772 serotonin uptake inhibitor Substances 0.000 claims 1
- 229960004034 sitagliptin Drugs 0.000 claims 1
- 239000002002 slurry Substances 0.000 claims 1
- 229960002722 terbinafine Drugs 0.000 claims 1
- 229960002381 vardenafil Drugs 0.000 claims 1
- PNVNVHUZROJLTJ-UHFFFAOYSA-N venlafaxine Chemical compound C1=CC(OC)=CC=C1C(CN(C)C)C1(O)CCCCC1 PNVNVHUZROJLTJ-UHFFFAOYSA-N 0.000 claims 1
- 229960004688 venlafaxine Drugs 0.000 claims 1
Claims (17)
- 有機アミンの結晶質ハロゲン化水素酸塩の製造方法であって、溶媒中の有機アミンにハロゲン化トリアルキルシリルが添加され、有機アミンは遊離塩基または酸付加塩の形態であり、有機アミンが酸付加塩の形態であるとき酸付加塩の共役酸はハロゲン化水素酸よりも弱い酸である、前記方法。
- 方法が、
(a)有機アミンをプロトン性溶媒中に溶解または懸濁させる段階;
(b)ハロゲン化トリアルキルシリルを添加する段階;
(c)結晶を形成させる段階;および
(d)形成された結晶を収集する段階
を含む、請求項1に記載の方法。 - 段階(a)のプロトン性溶媒はヒドロキシル基またはカルボキシル基を含む化合物であり、特にプロトン性溶媒が芳香族もしくは脂肪族アルコール、シラノール、エノール化可能なケトンまたは芳香族もしくは脂肪族カルボン酸であり、より特定的にはプロトン性溶媒がC1−C6アルキルアルコール、ギ酸または酢酸である、請求項2に記載の方法。
- 段階(b)のハロゲン化トリアルキルシリルが、トリメチルシリルクロリド、トリメチルシリルブロミドまたはトリメチルシリルヨージド、特にトリメチルシリルクロリドである、請求項2または3に記載の方法。
- 方法が、
(a)有機アミンを非プロトン性溶媒中に溶解または懸濁させる段階;
(b)少なくとも1当量のプロトン性溶媒を添加する段階;
(c)ハロゲン化トリアルキルシリルを添加する段階;
(d)結晶を形成させる段階;および
(e)形成された結晶を収集する段階
を含む、請求項1に記載の方法。 - 段階(b)のプロトン性溶媒はヒドロキシル基またはカルボキシル基を含む化合物であり、特にプロトン性溶媒が芳香族もしくは脂肪族アルコール、シラノール、エノール化可能なケトンまたは芳香族もしくは脂肪族カルボン酸であり、より特定的にはプロトン性溶媒がC1−C6アルキルアルコール、ギ酸または酢酸である、請求項5に記載の方法。
- 段階(c)のハロゲン化トリアルキルシリルが、トリメチルシリルクロリド、トリメチルシリルブロミドまたはトリメチルシリルヨージド、特にトリメチルシリルクロリドである、請求項5または6に記載の方法。
- 方法が、
(a)有機アミンの酸付加塩を溶媒中に溶解、懸濁または生成させる段階;
(b)ハロゲン化トリアルキルシリルを添加する段階;
(c)結晶を形成させる段階;および
(d)形成された結晶を収集する段階
を含む、請求項1に記載の方法。 - 段階(a)の有機アミンの酸付加塩は、共役酸が塩酸よりも弱い酸であり好ましくは有機酸である酸を、アミンの溶液またはスラリーに添加することによってその場に生成される、請求項8に記載の方法。
- 段階(a)の有機酸が、置換されているか置換されていないアルカン酸、芳香族カルボン酸、ジカルボン酸またはクエン酸から選択される、請求項8または9に記載の方法。
- 有機酸が酢酸である、請求項10に記載の方法。
- 有機アミンが医薬的に活性な化合物、特にヒト用薬剤である、請求項1〜10のいずれか一項に記載の方法。
- 薬物が一級、二級、三級または四級アミノ基を含み、特に薬物が抗欝剤、特にセロトニン再取り込みインヒビターセルトラリン、デュロキセチン、ベンラファキシンもしくはシタロプラム、精神向性薬、特にドネペジル、統合失調症治療薬、特に神経遮断薬アリピプラゾール、筋肉弛緩薬、特に鎮痙薬メマンチン、免疫抑制薬、特にミコフェノラートモフェチル、抗真菌薬、特にテルビナフィン、抗菌剤、特に例えばモキシフロキサシンもしくはオキサゾリジノンリネゾリドとしてのキノロン、カルシウム模擬薬、特にシナカルセット、ドーパミンアゴニスト、特にD2−受容体アゴニストプラミペキソール、抗肥満薬、特にリボナバント、抗血栓症薬、特にクロピドグレルおよびプラスグレル、抗骨粗鬆症薬、特にラロキシフェン、鎮痙剤、特にダリフェナシン、男性勃起機能不全治療薬、特にバルデナフィル、抗糖尿病薬、特にDPP−IVインヒビターシタグリプチンおよび抗新生物薬、特にエルロチニブからなる群から選択される、請求項12に記載の方法。
- 有機アミンの結晶質ハロゲン化水素酸塩を製造するための、ハロゲン化トリアルキルシリルの使用。
- 有機アミンの結晶質ハロゲン化水素酸塩が、前記有機アミンの既存の数種類のハロゲン化水素酸塩の中の1つの所望のハロゲン化水素酸塩である、請求項14に記載の使用。
- 有機アミンの無水結晶質ハロゲン化水素酸塩を製造するための、請求項14または15に記載の使用。
- 有機アミンの結晶質ハロゲン化水素酸塩の溶媒を製造するための、請求項14〜16に記載の使用。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06116134 | 2006-06-27 | ||
PCT/EP2007/005596 WO2008000418A2 (en) | 2006-06-27 | 2007-06-25 | New method for salt preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2009541385A JP2009541385A (ja) | 2009-11-26 |
JP2009541385A5 true JP2009541385A5 (ja) | 2010-01-14 |
Family
ID=37450796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009516963A Pending JP2009541385A (ja) | 2006-06-27 | 2007-06-25 | 塩の製造のための新規な方法 |
Country Status (14)
Country | Link |
---|---|
US (1) | US20100204470A1 (ja) |
EP (3) | EP2032521B1 (ja) |
JP (1) | JP2009541385A (ja) |
CN (1) | CN101484411A (ja) |
AT (1) | ATE446946T1 (ja) |
AU (1) | AU2007264030B2 (ja) |
CA (1) | CA2655061A1 (ja) |
DE (1) | DE602007003024D1 (ja) |
DK (1) | DK2032521T3 (ja) |
ES (1) | ES2335369T3 (ja) |
PL (1) | PL2032521T3 (ja) |
RU (1) | RU2461542C2 (ja) |
SI (1) | SI2032521T1 (ja) |
WO (1) | WO2008000418A2 (ja) |
Families Citing this family (42)
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US8524735B2 (en) | 2005-05-18 | 2013-09-03 | Mpex Pharmaceuticals, Inc. | Aerosolized fluoroquinolones and uses thereof |
WO2007108011A2 (en) * | 2006-03-20 | 2007-09-27 | Ind-Swift Laboratories Limited | Process for the preparation of highly pure donepezil |
WO2008130630A2 (en) * | 2007-04-16 | 2008-10-30 | Teva Pharmaceutical Industries Ltd. | Polymorphic form of rimonabant hydrochloride and processes for preparation thereof |
EP2218713A1 (en) * | 2007-08-17 | 2010-08-18 | Hetero Drugs Limited | Erlotinib hydrochloride polymorph Form A substantially free of polymorph Form B |
EP2257556A1 (en) | 2008-02-06 | 2010-12-08 | Helm AG | Prasugrel salts with improved properties |
WO2009125426A2 (en) * | 2008-02-08 | 2009-10-15 | Neuland Laboratories Ltd | NOVEL PROCESS FOR THE PREPARATION OF (3SM-[2-(2 J-DIHYDRO-5- BENZOFURANYLϊETHYL]-α.α -DIPHENYL-3-PYRROLIDINEACETAMIDE HYDROBROMIDE |
WO2010042549A1 (en) | 2008-10-07 | 2010-04-15 | Mpex Pharmaceuticals, Inc. | Inhalation of levofloxacin for reducing lung inflammation |
HUE038428T2 (hu) | 2008-10-07 | 2018-10-29 | Horizon Orphan Llc | Aeroszol fluorokinolon készítmények javított farmakokinetika érdekében |
WO2010109443A1 (en) | 2009-03-26 | 2010-09-30 | Ranbaxy Laboratories Limited | Process for the preparation of erlotinib or its pharmaceutically acceptable salts thereof |
EP2415774B1 (en) * | 2009-03-31 | 2014-07-09 | Shanghai Institute of Pharmaceutical Industry | Crystals of acetic acid solvate of prasugrel hydrobromate |
EP2236509A1 (en) | 2009-04-01 | 2010-10-06 | Ragactives, S.L. | Method for obtaining 1,3-difunctionalized pyrrolidine derivatives |
PT2473170T (pt) | 2009-09-04 | 2019-08-23 | Horizon Orphan Llc | Utilização de levofloxacina em aerossol para tratamento de fibrose cística |
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2007
- 2007-06-25 EP EP07785845A patent/EP2032521B1/en not_active Revoked
- 2007-06-25 CA CA002655061A patent/CA2655061A1/en not_active Abandoned
- 2007-06-25 DE DE602007003024T patent/DE602007003024D1/de active Active
- 2007-06-25 ES ES07785845T patent/ES2335369T3/es active Active
- 2007-06-25 DK DK07785845.4T patent/DK2032521T3/da active
- 2007-06-25 SI SI200730132T patent/SI2032521T1/sl unknown
- 2007-06-25 RU RU2009102279/04A patent/RU2461542C2/ru not_active IP Right Cessation
- 2007-06-25 AT AT07785845T patent/ATE446946T1/de active
- 2007-06-25 US US12/301,620 patent/US20100204470A1/en not_active Abandoned
- 2007-06-25 JP JP2009516963A patent/JP2009541385A/ja active Pending
- 2007-06-25 AU AU2007264030A patent/AU2007264030B2/en not_active Ceased
- 2007-06-25 CN CNA2007800235359A patent/CN101484411A/zh active Pending
- 2007-06-25 PL PL07785845T patent/PL2032521T3/pl unknown
- 2007-06-25 EP EP09173721A patent/EP2145890B1/en not_active Not-in-force
- 2007-06-25 WO PCT/EP2007/005596 patent/WO2008000418A2/en active Application Filing
- 2007-06-25 EP EP11193885A patent/EP2436381A1/en not_active Withdrawn
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