RU2005121491A - Производные диарилметилиденпиперидина, их препараты и их применение - Google Patents
Производные диарилметилиденпиперидина, их препараты и их применение Download PDFInfo
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- RU2005121491A RU2005121491A RU2005121491/04A RU2005121491A RU2005121491A RU 2005121491 A RU2005121491 A RU 2005121491A RU 2005121491/04 A RU2005121491/04 A RU 2005121491/04A RU 2005121491 A RU2005121491 A RU 2005121491A RU 2005121491 A RU2005121491 A RU 2005121491A
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- Prior art keywords
- alkyl
- nrc
- phenyl
- cycloalkyl
- optionally substituted
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- 125000000217 alkyl group Chemical group 0.000 claims 28
- 150000001875 compounds Chemical class 0.000 claims 14
- 229910052739 hydrogen Inorganic materials 0.000 claims 14
- 239000001257 hydrogen Substances 0.000 claims 14
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 10
- 125000001246 bromo group Chemical group Br* 0.000 claims 10
- 125000001309 chloro group Chemical group Cl* 0.000 claims 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000001072 heteroaryl group Chemical group 0.000 claims 6
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 238000000034 method Methods 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 125000002346 iodo group Chemical group I* 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 125000000168 pyrrolyl group Chemical group 0.000 claims 3
- 125000000335 thiazolyl group Chemical group 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- 208000018522 Gastrointestinal disease Diseases 0.000 claims 2
- -1 diastereomers Chemical class 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- RLTIINYXRJMMCB-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-(1-benzylpiperidin-4-ylidene)methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC=2C=CC=CC=2)CC1 RLTIINYXRJMMCB-UHFFFAOYSA-N 0.000 claims 1
- AOIABXSUGFHWJJ-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-[1-(1,3-thiazol-4-ylmethyl)piperidin-4-ylidene]methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC=2N=CSC=2)CC1 AOIABXSUGFHWJJ-UHFFFAOYSA-N 0.000 claims 1
- SXEAFQJGHPVRTQ-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-[1-(1,3-thiazol-5-ylmethyl)piperidin-4-ylidene]methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC=2SC=NC=2)CC1 SXEAFQJGHPVRTQ-UHFFFAOYSA-N 0.000 claims 1
- VGNVIKBFRCEHRY-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-[1-(pyridin-2-ylmethyl)piperidin-4-ylidene]methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC=2N=CC=CC=2)CC1 VGNVIKBFRCEHRY-UHFFFAOYSA-N 0.000 claims 1
- MDVVKIYWARQZNM-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-[1-(pyridin-3-ylmethyl)piperidin-4-ylidene]methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC=2C=NC=CC=2)CC1 MDVVKIYWARQZNM-UHFFFAOYSA-N 0.000 claims 1
- FFIPMCKXTBYFQV-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-[1-(pyridin-4-ylmethyl)piperidin-4-ylidene]methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC=2C=CN=CC=2)CC1 FFIPMCKXTBYFQV-UHFFFAOYSA-N 0.000 claims 1
- YAZKAXXYJYZBNR-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-[1-(thiophen-2-ylmethyl)piperidin-4-ylidene]methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC=2SC=CC=2)CC1 YAZKAXXYJYZBNR-UHFFFAOYSA-N 0.000 claims 1
- XNMIACUFNRTUPM-UHFFFAOYSA-N 4-[(3-acetamidophenyl)-[1-(thiophen-3-ylmethyl)piperidin-4-ylidene]methyl]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1C(C=1C=C(NC(C)=O)C=CC=1)=C1CCN(CC2=CSC=C2)CC1 XNMIACUFNRTUPM-UHFFFAOYSA-N 0.000 claims 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 1
- 208000019901 Anxiety disease Diseases 0.000 claims 1
- 208000027520 Somatoform disease Diseases 0.000 claims 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 1
- 230000036506 anxiety Effects 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 208000027753 pain disease Diseases 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
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- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/70—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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Claims (13)
1. Соединение формулы I, его фармацевтически приемлемая соль, диастереомеры, энантиомеры или их смеси
где R1 выбран из С6-10арила и С2-6гетероарила, где указанные С6-10арил и С2-6гетероарил возможно замещены одной или более чем одной группой, выбранной из -R, -NO2, -OR, -Cl, -Br, -I, -F, -CF3, -C(=O)R, -C(=O)OH, -NH2, -SH, -NHR, -NR2, -SR, -SO3Н, -SO2R, -S(=O)R, -CN, -ОН, -C(=O)OR, -C(=O)NR2, -NRC(=O)R и -NRC(=O)-OR, где R независимо представляет собой водород или С1-6алкил; и
R2, R3, R4 и R5 независимо выбраны из водорода, С1-6алкила, и С3-6циклоалкила, где указанные С1-6алкил и С3-6циклоалкил возможно замещены одной или более чем одной группой, выбранной из -R, -NO2, -OR, -Cl, -Br, -I, -F, -CF3, -C(=O)R, -C(=O)OH, -NH2, -SH, -NHR, -NR2, -SR, -SO3H, -SO2R, -S(=O)R, -CN, -OH, -C(=O)OR, -C(=O)NR2, -NRC(=O)R и -NRC(=O)-OR, где R независимо представляет собой водород или С1-6алкил.
2. Соединение по п.1,
где R1 выбран из фенила, пиридила, тиенила, фурила, имидазолила, триазолила, пирролила, тиазолила и N-оксидопиридила, где R1 возможно замещен одной или более чем одной группой, выбранной из С1-6алкила, галогенированного С1-6алкила, -NO2, -CF3, С1-6алкокси, хлора, фтора, брома и йода;
R2, R3 и R4 независимо представляют собой С1-3алкил или галогенированный С1-3алкил;
R5 выбран из водорода, С1-6алкила и С3-6циклоалкила, где указанные С1-3алкил и С3-6циклоалкил возможно замещены одной или более чем одной группой, выбранной из С1-6алкила, галогенированного С1-6алкила, -NO2, -CF3, С1-6алкокси, хлора, фтора, брома и йода.
3. Соединение по п.1,
где R1 выбран из фенила, пиридила, тиенила, фурила, имидазолила, пирролила и тиазолила, где R1 возможно замещен одной или более чем одной группой, выбранной из С1-6алкила, галогенированного С1-6алкила, -NO2, -CF3, С1-6алкокси, хлора, фтора, брома и йода;
R2, R3 и R4 независимо представляют собой С1-3алкил или галогенированный С1-3алкил; и
R5 представляет собой водород.
4. Соединение по п.1,
где R1 выбран из фенила, пиридила, тиенила, фурила, имидазолила, пирролила и тиазолила;
R2 и R3 представляют собой этил;
R4 представляет собой С1-3алкил; и
R5 представляет собой водород.
5. Соединение по п.1, выбранное из:
4-{[3-(ацетиламино)фенил][1-(тиен-2-илметил)пиперидин-4-илиден]-метил}-N,N-диэтилбензамид;
4-{[3-(ацетиламино)фенил][1-(2-фурилметил)пипердин-4-илиден]метил}-N,N-диэтилбензамид;
4-[[3-(ацетиламино)фенил][1-(фенилметил)-4-пиперидинилиден]метил]-N,N-диэтилбензамид;
4-[[3-(ацетиламино)фенил][1-(3-тиенилметил)-4-пиперидинилиден]-метил]-N,N-диэтилбензамид;
4-[[3-(ацетиламино)фенил][1-(3-пиридинилметил)-4-пиперидинилиден]-метил]-N,N-диэтилбензамид;
4-[[3-(ацетиламино)фенил][1-(4-пиридинилметил)-4-пиперидинилиден]-метил]-N,N-диэтилбензамид;
4-{[3-(ацетиламино)фенил][1-(пиридин-2-илметил)пиперидин-4-илиден]-метил}-N,N-диэтилбензамид;
4-{[3-(ацетиламино)фенил][1-(1,3-тиазол-4-илметил)пиперидин-4-илиден]метил}-N,N-диэтилбензамид;
4-{[3-(ацетиламино)фенил][1-(1,3-тиазол-5-илметил)пиперидин-4-илиден]метил}-N,N-диэтилбензамид;
и его фармацевтически приемлемые соли.
6. Соединение по любому из пп.1-5 для применения в качестве лекарства.
7. Применение соединения по любому из пп.1-5 в изготовлении лекарства для лечения боли, тревоги или функциональных желудочно-кишечных расстройств.
8. Фармацевтическая композиция, содержащая соединение по любому из пп.1-5 и фармацевтически приемлемый носитель.
9. Способ лечения боли у теплокровного животного, включающий стадию введения указанному животному, нуждающемуся в таком лечении, терапевтически эффективного количества соединения по любому из пп.1-5.
10. Способ лечения функциональных желудочно-кишечных расстройств у теплокровного животного, включающий стадию введения указанному животному, нуждающемуся в таком лечении, терапевтически эффективного количества соединения по любому из пп.1-5.
11. Способ получения соединения формулы I
включающий взаимодействие соединения формулы II
с X-C(=O)-R4 или R4C(=O)-OC(=O)R4,
где R1 выбран из С6-10арила и С2-6гетероарила, где указанные С1-6арил и С2-6гетероарил возможно замещены одной или более чем одной группой, выбранной из -R, -NO2, -OR, -Cl, -Br, -I, -F, -CF3, -C(=O)R, -C(=O)OH, -NH2, -SH, -NHR, -NR2, -SR, -SO3Н, -SO2R, -S(=O)R, -CN, -OH, -C(=O)OR, -C(=O)NR2, -NRC(=O)R и -NRC(=O)-OR, где R независимо представляет собой водород или С1-6алкил; и
R2, R3, R4 и R5 независимо выбраны из водорода, С1-6алкила и С3-6циклоалкила, где указанные C1-6алкил и С3-6циклоалкил возможно замещены одной или более чем одной группой, выбранной из -R, -NO2, -OR, -Cl, -Br, -I, -F, -CF3, -C(=O)R, -C(=O)OH, -NH2, -SH, -NHR, -NR2, -SR, -SO3H, -SO2R, -S(=O)R, -CN, -ОН, -C(=O)OR, -C(=O)NR2, -NRC(=O)R и -NRC(=O)-OR, где R независимо представляет собой водород или C1-6алкил; и
Х представляет собой Cl, Br или I.
12. Способ получения соединения формулы I
включающий взаимодействие соединения формулы III
с R1-CHO или R1-CH2X,
где R1 выбран из С6-10арила и С2-6гетероарила, где указанные С6-10арил и С2-6гетероарил возможно замещены одной или более чем одной группой, выбранной из -R, -NO2, -OR, -Cl, -Br, -I, -F, -CF3, -C(=O)R, -C(=O)OH, -NH2, -SH, -NHR, -NR2, -SR, -SO3Н, -SO2R, -S(=O)R, -CN, -ОН, -C(=O)OR, -C(=O)NR2, -NRC(=O)R и -NRC(=O)-OR, где R независимо представляет собой водород или C1-6алкил;
R2, R3, R4 и R5 независимо выбраны из водород, С1-6алкила и С3-6циклоалкила, где указанные С1-6алкил и С3-6циклоалкил возможно замещены одной или более чем одной группой, выбранной из -R, -NO2, -OR, -Cl, -Br, -I, -F, -CF3, -C(=O)R, -C(=O)OH, -NH2, -SH, -NHR, -NR2, -SR, -SO3H, -SO2R, -S(=O)R, -CN, -OH, -C(=O)OR, -C(=O)NR2, -NRC(=O)R и -NRC(=O)-OR, где R независимо представляет собой водород или С1-6алкил; и Х представляет собой Cl, Br или I.
13. Соединение формулы III
где R2, R3, R4 и R5 независимо выбраны из водорода, С1-6алкила и С3-6циклоалкила, где указанные С1-6алкил и С3-6циклоалкил возможно замещены одной или более чем одной группой, выбранной из -R, -NO2, -OR, -Cl, -Br, -I, -F, -CF3, -C(=O)R, -C(=O)OH, -NH2, -SH, -NHR, -NR2, -SR, -SO3Н, -SO2R, -S(=O)R, -CN, -OH, -C(=O)OR, -C(=O)NR2, -NRC(=O)R и -NRC(=O)-OR, где R независимо представляет собой водород или С1-6алкил.
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| SE0300105A SE0300105D0 (sv) | 2003-01-16 | 2003-01-16 | Diarylmethylidene piperdine derivatives, preparations thereof and uses thereof |
| SE0300105-4 | 2003-01-16 |
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| PT1395567E (pt) | 2001-05-18 | 2009-03-26 | Astrazeneca Ab | Derivados de 4(fenil-piperazinil-metil)benzamida e sua utilização para o tratamento da ansiedade da dor ou de distúrbios gastrointestinais |
| SE0203303D0 (sv) | 2002-11-07 | 2002-11-07 | Astrazeneca Ab | Novel Compounds |
| SE0203300D0 (sv) | 2002-11-07 | 2002-11-07 | Astrazeneca Ab | Novel Compounds |
| SE0203301D0 (sv) * | 2002-11-07 | 2002-11-07 | Astrazeneca Ab | Novel Compounds |
| JP2007503457A (ja) * | 2003-05-16 | 2007-02-22 | アストラゼネカ・アクチエボラーグ | ジアリールメチリデンピペリジン誘導体、その製造およびその使用 |
| AU2004278414B2 (en) | 2003-10-01 | 2012-05-24 | Adolor Corporation | Spirocyclic heterocyclic derivatives and methods of their use |
| DK1781631T3 (da) | 2004-08-02 | 2012-05-14 | Astrazeneca Ab | Diarylmethylpiperazinderivater, præparater dermed og anvendelser deraf |
| JP2008531683A (ja) * | 2005-02-28 | 2008-08-14 | アストラゼネカ・アクチエボラーグ | ジアリールメチルピペラジン誘導体、その製造及びその使用 |
| US7598261B2 (en) | 2005-03-31 | 2009-10-06 | Adolor Corporation | Spirocyclic heterocyclic derivatives and methods of their use |
| US7576207B2 (en) | 2006-04-06 | 2009-08-18 | Adolor Corporation | Spirocyclic heterocyclic derivatives and methods of their use |
| MY148880A (en) * | 2006-10-20 | 2013-06-14 | Astrazeneca Ab | N-(2-hydroxyethyl)-n-methyl-4-(quinolin-8-yl(1-(thiazol-4-ylmethyl)piperidin-4-ylidene)methyl)benzamide, the process of making it as well as its use for the treatment of pain, anxiety and depression |
| RS60744B1 (sr) * | 2014-12-19 | 2020-10-30 | Pharmnovo Ab | Derivati diarilmetilideni pipiredina i njihova upotreba kao agonista delta opioidnih receptora |
| CN111825654A (zh) * | 2019-04-19 | 2020-10-27 | 北京酷瓴生物技术有限公司 | 苯甲烯哌啶衍生物及其制备方法、中间体和用途 |
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| US2898339A (en) * | 1957-07-29 | 1959-08-04 | Wm S Merrell Co | N-substituted benzhydrol, benzhydryl, and benzhydrylidene piperidine |
| US4581171A (en) * | 1983-07-27 | 1986-04-08 | Janssen Pharmaceutica, N.V. | [[Bis(aryl)methylene]-1-piperidinyl]alkyl-pyrimidinones useful for treating psychotropic disorders |
| US4816586A (en) * | 1987-07-29 | 1989-03-28 | Regents Of The University Of Minnesota | Delta opioid receptor antagonists |
| US5140029A (en) * | 1989-01-09 | 1992-08-18 | Janssen Pharmaceutica N.V. | 2-aminopyrimidinone derivatives |
| US4939137A (en) * | 1989-06-28 | 1990-07-03 | Ortho Pharmaceutical Corporation | Ring-fused thienopyrimidinedione derivatives |
| US5683998A (en) * | 1991-04-23 | 1997-11-04 | Toray Industries, Inc. | Tricyclic triazolo derivatives, processes for producing the same and the uses of the same |
| US5574159A (en) * | 1992-02-03 | 1996-11-12 | Delta Pharmaceuticals, Inc. | Opioid compounds and methods for making therefor |
| ZA979781B (en) * | 1996-11-14 | 1998-06-08 | Akzo Nobel Nv | Piperidine derivatives. |
| TW548271B (en) * | 1996-12-20 | 2003-08-21 | Astra Pharma Inc | Novel piperidine derivatives having an exocyclic double bond with analgesic effects |
| KR20030009376A (ko) * | 2000-03-03 | 2003-01-29 | 오르토-맥네일 파마슈티칼, 인코퍼레이티드 | 3-(디아릴메틸렌)-8-아자비사이클로[3.2.1]옥탄 유도체 |
| US6556387B1 (en) * | 2000-03-31 | 2003-04-29 | Seagate Technology Llc | Controlling mechanical response characteristics of a disc drive actuator by adjusting a fastener engaging the actuator shaft to vary axial force on the bearing assembly |
| SE0001207D0 (sv) * | 2000-04-04 | 2000-04-04 | Astrazeneca Canada Inc | Novel compounds |
| SE0101766D0 (sv) * | 2001-05-18 | 2001-05-18 | Astrazeneca Ab | Novel compounds |
| US7589103B2 (en) * | 2003-06-27 | 2009-09-15 | Janssen Pharmaceutica N.V. | Tricyclic-bridged piperidinylidene derivatives as 8-opioid modulators |
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| Publication number | Publication date |
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| WO2004062562A2 (en) | 2004-07-29 |
| IS7980A (is) | 2005-08-12 |
| AU2004204390A1 (en) | 2004-07-29 |
| AR042887A1 (es) | 2005-07-06 |
| KR20050096137A (ko) | 2005-10-05 |
| MXPA05007484A (es) | 2005-09-21 |
| CN100422151C (zh) | 2008-10-01 |
| PL378336A1 (pl) | 2006-03-20 |
| NO20053809L (no) | 2005-10-17 |
| US20060154964A1 (en) | 2006-07-13 |
| CN1738801A (zh) | 2006-02-22 |
| SE0300105D0 (sv) | 2003-01-16 |
| ZA200505186B (en) | 2006-04-26 |
| TW200504059A (en) | 2005-02-01 |
| UA80012C2 (en) | 2007-08-10 |
| NO20053809D0 (no) | 2005-08-12 |
| RU2324680C2 (ru) | 2008-05-20 |
| CA2510382A1 (en) | 2004-07-29 |
| WO2004062562A3 (en) | 2004-09-16 |
| BRPI0406614A (pt) | 2005-12-06 |
| IL169366A0 (en) | 2007-07-04 |
| AU2004204390B2 (en) | 2007-09-06 |
| JP2006516559A (ja) | 2006-07-06 |
| EP1587790A2 (en) | 2005-10-26 |
| NZ540758A (en) | 2008-03-28 |
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