AR045700A1 - Derivados de combretastatina que presentan actividad citotoxica - Google Patents
Derivados de combretastatina que presentan actividad citotoxicaInfo
- Publication number
- AR045700A1 AR045700A1 ARP040102518A ARP040102518A AR045700A1 AR 045700 A1 AR045700 A1 AR 045700A1 AR P040102518 A ARP040102518 A AR P040102518A AR P040102518 A ARP040102518 A AR P040102518A AR 045700 A1 AR045700 A1 AR 045700A1
- Authority
- AR
- Argentina
- Prior art keywords
- hydrogen
- phenyl
- methoxy
- trimethoxy
- double
- Prior art date
Links
- 230000001472 cytotoxic effect Effects 0.000 title abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 118
- 239000001257 hydrogen Substances 0.000 abstract 78
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 39
- 150000002431 hydrogen Chemical class 0.000 abstract 38
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 33
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 7
- 229910052794 bromium Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 4
- -1 3,4-methylenedioxy Chemical group 0.000 abstract 3
- 101100240517 Caenorhabditis elegans nhr-11 gene Proteins 0.000 abstract 3
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 3
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 abstract 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 2
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000000539 amino acid group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000006237 oxymethylenoxy group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 2
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 abstract 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- YKYIFUROKBDHCY-ONEGZZNKSA-N (e)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one Chemical group CCO\C=C\C(=O)C(F)(F)F YKYIFUROKBDHCY-ONEGZZNKSA-N 0.000 abstract 1
- JDLXKGIMAJACBQ-UHFFFAOYSA-N 2-[2-(3,4,5-trimethoxyphenyl)ethenyl]furan Chemical compound COC1=C(OC)C(OC)=CC(C=CC=2OC=CC=2)=C1 JDLXKGIMAJACBQ-UHFFFAOYSA-N 0.000 abstract 1
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 abstract 1
- YTVCXBVFGQEBAL-ARJAWSKDSA-N 2-methoxy-5-[(z)-2-(7-methoxy-1,3-benzodioxol-5-yl)ethenyl]phenol Chemical compound C=1C=2OCOC=2C(OC)=CC=1\C=C/C1=CC=C(OC)C(O)=C1 YTVCXBVFGQEBAL-ARJAWSKDSA-N 0.000 abstract 1
- OFJKTVSCJDMVRG-UHFFFAOYSA-N 3-[2-(3,4,5-trimethoxyphenyl)ethenyl]furan Chemical compound COC1=C(OC)C(OC)=CC(C=CC2=COC=C2)=C1 OFJKTVSCJDMVRG-UHFFFAOYSA-N 0.000 abstract 1
- YPPXIXDROOBVMA-UHFFFAOYSA-N 3-[2-(3,4,5-trimethoxyphenyl)ethenyl]thiophene Chemical compound COC1=C(OC)C(OC)=CC(C=CC2=CSC=C2)=C1 YPPXIXDROOBVMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- HHVKSKQBTCZYRU-ZRDIBKRKSA-N 5-[(e)-2-(1-benzofuran-2-yl)ethenyl]-4-phenyl-1,3-benzodioxole Chemical compound C=12OCOC2=CC=C(\C=C\C=2OC3=CC=CC=C3C=2)C=1C1=CC=CC=C1 HHVKSKQBTCZYRU-ZRDIBKRKSA-N 0.000 abstract 1
- YAOJHTHFCXXIDX-ZRDIBKRKSA-N 5-[(e)-2-(1-benzothiophen-2-yl)ethenyl]-4-phenyl-1,3-benzodioxole Chemical compound C=12OCOC2=CC=C(\C=C\C=2SC3=CC=CC=C3C=2)C=1C1=CC=CC=C1 YAOJHTHFCXXIDX-ZRDIBKRKSA-N 0.000 abstract 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 abstract 1
- HVXBOLULGPECHP-WAYWQWQTSA-N Combretastatin A4 Chemical compound C1=C(O)C(OC)=CC=C1\C=C/C1=CC(OC)=C(OC)C(OC)=C1 HVXBOLULGPECHP-WAYWQWQTSA-N 0.000 abstract 1
- 239000004471 Glycine Substances 0.000 abstract 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 abstract 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 abstract 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-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
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 abstract 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 abstract 1
- 102000004243 Tubulin Human genes 0.000 abstract 1
- 108090000704 Tubulin Proteins 0.000 abstract 1
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 239000004037 angiogenesis inhibitor Substances 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 229960005537 combretastatin A-4 Drugs 0.000 abstract 1
- 229930192183 combretastatin A1 Natural products 0.000 abstract 1
- YUSYSJSHVJULID-UHFFFAOYSA-N combretastatin A1 Z Natural products OC1=C(O)C(OC)=CC=C1C=CC1=CC(OC)=C(OC)C(OC)=C1 YUSYSJSHVJULID-UHFFFAOYSA-N 0.000 abstract 1
- HRRAOGKGGZFKSW-UHFFFAOYSA-N combretastatin A2 Natural products COc1ccc(C=C/c2cc(O)c3OCOc3c2)cc1OC HRRAOGKGGZFKSW-UHFFFAOYSA-N 0.000 abstract 1
- HVXBOLULGPECHP-UHFFFAOYSA-N combretastatin A4 Natural products C1=C(O)C(OC)=CC=C1C=CC1=CC(OC)=C(OC)C(OC)=C1 HVXBOLULGPECHP-UHFFFAOYSA-N 0.000 abstract 1
- YUSYSJSHVJULID-WAYWQWQTSA-N combretastatin a-1 Chemical compound OC1=C(O)C(OC)=CC=C1\C=C/C1=CC(OC)=C(OC)C(OC)=C1 YUSYSJSHVJULID-WAYWQWQTSA-N 0.000 abstract 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 abstract 1
- 235000018417 cysteine Nutrition 0.000 abstract 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical class [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 abstract 1
- 230000007717 exclusion Effects 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 230000000771 oncological effect Effects 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- CDRPUGZCRXZLFL-OWOJBTEDSA-N piceatannol Chemical compound OC1=CC(O)=CC(\C=C\C=2C=C(O)C(O)=CC=2)=C1 CDRPUGZCRXZLFL-OWOJBTEDSA-N 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 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
- 239000004474 valine Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/12—Oxygen atoms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/215—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring having unsaturation outside the six-membered aromatic rings
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three 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
- C07D307/58—One oxygen atom, e.g. butenolide
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three 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
- C07D307/70—Nitro radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three 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
- C07D307/70—Nitro radicals
- C07D307/71—Nitro radicals attached in position 5
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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
- C07D333/30—Hetero atoms other than halogen
- C07D333/32—Oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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
- C07D333/42—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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 with nitro or nitroso radicals directly attached to ring carbon atoms
- C07D333/44—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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 with nitro or nitroso radicals directly attached to ring carbon atoms attached in position 5
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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Abstract
Dichos compuestos, aunque están relacionados químicamente con la estructura de cis/trans-combretastatina, no siempre ligan a la tubulina, pero sin embargo presentan actividad citotóxica de interés en el campo oncológico como agentes anticáncer y/o antiangiogénicos. Reivindicación 1: Compuestos de fórmula (1) caracterizados porque: los diversos R1, R2, R3 y R4, que pueden ser iguales o diferentes, son H, OH, OPO3H2 u OCH2OPO3H2 y su sal disódica, OMe, OCH2O, NO2, F, Cl, Br; -R1-R2- también pueden ser juntos: -CR8=CR9-X-; Y es un radical seleccionado del grupo (2); R5 y R6, que pueden ser iguales o diferentes, son H o halógeno; R7 es H, OMe, SO2Ph; Ar es una estructura seleccionada del grupo (3); R8, R9 y R10, que pueden ser iguales o diferentes, son H, OH, OPO3H2 o OCH2OPO3H2 y su sal disódica, OR11, OCH2O, NH2, NHR11, NO2, alquilo C1-4, C6H5, C5H4N o halógeno; R11 es alquilo C1-4 o acilo, residuo de aminoácidos; X es O, S, N, NR12; R12 es H, CH3, CH2Ph; Z es CH, N; con la condición de que el compuesto de fórmula (1) no sea combretastatina A-1, combretastatin A-2, combretastatin A-4, y sus derivados fosfatos disódicos y con la exclusión de los siguientes compuestos: 2-fenil-6-trans-estiril-benzo[b]furano; 2,3-difenil- 6-trans-estiril-benzo[b]furano; 2-fenil-6-(4-metoxi)-trans-estiril-benzo[b]furano; 2-fenil-6-(3,4-dimetoxi)-trans-estiril-benzo[b]furano; 2-fenil-6-(3,4,5-trimetoxi)-trans-estiril-benzo[b]furano; 2-fenil-6-(3,4-metilendioxi)-trans-estiril- benzo[b]furano; 2,3-difenil-6-(4-metoxi)-trans-estiril-benzo[b]furano; 2-fenil-5-(3,4-metilendioxi)-trans-estiril-benzo[b]tiofeno; 2-fenil-6-trans-estiril-benzo[b]tiofeno; 2-fenil-6-(4-metoxi)-trans-estiril-benzo[b]tiofeno; 2-fenil-6-(4-cloro)-trans- estiril-benzo[b]tiofeno; Piceatanol; 1-(3-furanil)-2-(3,4,5-trimetoxifenil)eteno; 1-(3-tiofenil)-2-(3,4,5-trimetoxifenil)eteno; 1-(2-furanil)-2-(3,4,5-trimetoxifenil)eteno; y con la condición de que: - cuando R1 es hidrógeno y R2-R4 son 3,4,5- trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 y R9 son hidrógeno, R10 no es metoxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 2-cloro, R10 no es 4-metoxi; - cuando R1 es hidrógeno y R2-R4 son trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, por lo menos uno de R8-R10 no es hidrógeno; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 y R9 son hidrógeno, R10 no es ninguno de 4-cloro, 4-bromo, 4-nitro, 4-hidroxi, 4-acetilo, 4-etoxi, 4-alquilo C1-4; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 4-nitro o 4-amino, R10 no es ninguno de 3-cloro, 3-metoxi, 3-metilo; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-nitro o 3-amino, R10 no es ninguno de 3- cloro, 3-metoxi, 3-metilo; - cuando R1 es hidrógeno y R2-R4 son 2,3,4-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 y R9 son hidrógeno, R10 no es 4-metoxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, por lo menos uno de R8 es hidrógeno, R9 es 3-metoxi, R10 no es 5-metoxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8-R10 no son metoxi; - cuando R1 y R2 son hidrógeno y R3-R4 son 3,4-dimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 y R9 son hidrógeno, R10 no es 4-metoxi; - cuando R1 y R2 son hidrógeno y R3-R4 son 3,4-dimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9-R10 no son 3,5-dimetoxi; - cuando R1 y R2 son hidrógeno y R3-R4 son 3, 4-dimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, por lo menos uno de R8-R10 no es hidrógeno; - cuando R1 y R2 son hidrógeno y R3-R4 son 3,5-metoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 y R9 son hidrógeno, R10 no es 4-metoxi; - cuando R1 y R2 son hidrógeno y R3-R4 son 3,5-metoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 y R9 son hidrógeno, Rio no es 4-acetilo; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar no es piridilo; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-amino, R10 es 4-NHR11, R11 no es el residuo de serina; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-amino, R10 no es 4-metoxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-amino, R10 no es un grupo 4-alquiloxi que tiene de 1 a 3 átomos de carbono, o un grupo 4-alquilo que tiene de 1 a 4 átomos de carbono, o un átomo de halógeno; - cuando R1 es hidrógeno y R2-R3 son 3,4-metilendioxi, R4 es 5-metoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-amino, R10 no es 4-metoxi; - cuando R1 es hidrógeno y R2-R4 son 2,3, 4-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-amino, R10 no es 4-metoxi;- cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es NHR11, R11 es el residuo de serina, R10 no es 4-metoxi; - cuando R1 es hidrógeno y R2-R3 son 3,4-metilendioxi, R4 es 4- metoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es NHR11, R11 es el residuo del aminoácido cisteina, glicina, fenilalanina, serina, triptofano, tirosina, valina, R10 no es 4- metoxi; - cuando R1 es hidrógeno y R2-R3 son 3,4-metilendioxi, R4 es 4-metoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es NO2 o NH2, R10 no es 4-metoxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, por lo menos uno de R8-R10 no es hidrógeno;- cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 4-metoxi, R10 no es 3-fluoro; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 4-metilo, R10 no es 3-fluoro o 3-hidroxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 4-metoxi, R10 no es 3-metoxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es 3-fluoro, R9 es 4-metoxi, R10 no es 2- o 5-fluoro; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 4-metoxi, R10 no es 3-hidroxi o 3-amino; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 4-metoxi, R10 no es 3-fluoro o 3-bromo; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 y R9 son hidrógeno, R10 no es 4-hidroxi; - cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-metilo, R10 no es 4-metilo;- cuando R1 es hidrógeno y R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace cis, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 4-metoxi, R10 no es 3-hidroxi;- cuando R1-R2 son hidrógeno y R3-R4 son 3,5-dihidroxi, Y es un doble enlace trans, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 es 3-hidroxi, R10 no es 5-hidroxi; - cuando R1-R3 son hidrógeno, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 y R10 son 3,4-dimetilo, y R4 no es 4-metoxi;- cuando R1-R2 son hidrógeno, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8 es hidrógeno, R9 y R10 son 3,4-dimetilo, R4 es 4-metoxi,R3 no es 3-fluoro o 3-bromo o 3-nitro o 3-hidroxi; - cuando R1-R2 son hidrógeno, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8-R10 son 3,4,5-trietoxi, R4 es 4-metoxi, R3 no es 3-fluoro o 3-cloro o 3-bromo o 3-hidroxi;- cuando R1-R2 son hidrógeno, R4 es 4-metoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8-R9 son 4,5-dimetoxi, R10 es 3-hidroxi, R3 no es 3-fluoro o 3- hidroxi; - cuando R1-R2 son hidrógeno, R4 es 4-metoxi, Y es un doble enlace, R5 y R6 son H, Ar es fenilo, R8-R9 son 4,5-dimetoxi, R10 es 3-metoxi, R3 no es 3-fluoro; - cuando R1 es hidrógeno, R2-R4 son 3,4,5-trimetoxi, Y es un doble enlace, R5 y R6 son H, Ar es 2-naftilo, por lo menos uno de R8-R10 no es hidrógeno; - cuando R1 y R2 son hidrógeno, R3 es 3-hidroxi, R4 es 4-metoxi, Y es un doble enlace, R5 y R6 son H, Ar es 2-naftilo, por lo menos uno de R8-R10 no es hidrógeno; - cuando R1 es hidrógeno, R2-R4 son 3,4,5-trimetoxi, Y es de fórmula (4), Ar es indolilo, en donde por lo menos uno de R8-R10 es diferente de hidrógeno; sus enantiómeros, diastereoisómeros, las mezclas respectivas y sus sales farmacéuticamente aceptables.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT000355A ITRM20030355A1 (it) | 2003-07-18 | 2003-07-18 | Composti ad attivita' citotossica derivati della combretastatina. |
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| Publication Number | Publication Date |
|---|---|
| AR045700A1 true AR045700A1 (es) | 2005-11-09 |
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| ARP040102518A AR045700A1 (es) | 2003-07-18 | 2004-07-16 | Derivados de combretastatina que presentan actividad citotoxica |
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| Country | Link |
|---|---|
| US (1) | US20060160773A1 (es) |
| EP (1) | EP1646616A2 (es) |
| JP (1) | JP2007530427A (es) |
| KR (1) | KR20060039001A (es) |
| CN (1) | CN1826330A (es) |
| AR (1) | AR045700A1 (es) |
| AU (1) | AU2004257011A1 (es) |
| BR (1) | BRPI0412744A (es) |
| CA (1) | CA2531389A1 (es) |
| IT (1) | ITRM20030355A1 (es) |
| MX (1) | MXPA06000625A (es) |
| TW (1) | TW200504042A (es) |
| WO (1) | WO2005007635A2 (es) |
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| MX2007009888A (es) | 2005-02-17 | 2007-10-16 | Synta Pharmaceuticals Corp | Compuestos para el tratamiento de trastornos proliferativos. |
| JP5149177B2 (ja) * | 2005-07-25 | 2013-02-20 | シンタ ファーマシューティカルズ コーポレーション | 増殖性疾患の治療のための、チューブリンポリマー化の1,2,3−トリアゾール系抑制剤 |
| US7781580B2 (en) * | 2007-04-23 | 2010-08-24 | Virginia Commonwealth University | Stilbene derivatives as new cancer therapeutic agents |
| WO2009067706A1 (en) | 2007-11-21 | 2009-05-28 | Oxigene, Inc. | Method for treating hematopoietic neoplasms |
| CN104043125B (zh) | 2008-04-10 | 2018-01-12 | 弗吉尼亚州立邦联大学 | 诱导肿瘤缺氧以治疗癌症 |
| CN102249987B (zh) * | 2011-05-06 | 2013-07-24 | 兰州大学 | 一种考布他汀类化合物及其制备方法和用途 |
| CN102863388B (zh) * | 2011-07-05 | 2015-04-29 | 南京圣和药业股份有限公司 | 肿瘤靶向药物Combretastatin A4衍生物 |
| WO2013047813A1 (ja) | 2011-09-30 | 2013-04-04 | 大鵬薬品工業株式会社 | 1,2,4-トリアジン-6-カルボキサミド誘導体 |
| PL220039B1 (pl) | 2012-03-29 | 2015-08-31 | Univ Medyczny Im Karola Marcinkowskiego W Poznaniu | Nowe pochodne (Z)-1,2-difenyloetenu |
| CN102993115B (zh) * | 2012-12-08 | 2015-09-30 | 南京师范大学 | 一种3,5–二取代异噁唑啉衍生物及其合成方法和应用 |
| US11419934B2 (en) | 2015-08-18 | 2022-08-23 | Oncotelic Therapeutics, Inc. | Use of VDAS to enhance immunomodulating therapies against tumors |
| CN110536685A (zh) * | 2016-12-23 | 2019-12-03 | 昆士兰大学 | Sox18蛋白活性的抑制剂用于治疗血管生成相关疾病和/或淋巴管生成相关疾病 |
| PE20211268A1 (es) * | 2017-10-25 | 2021-07-19 | Bayer Pharma AG | Proceso para preparar el benzotiofen-2-il boronato |
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| CH540247A (de) * | 1967-04-21 | 1973-09-28 | Ciba Geigy Ag | Verfahren zur Herstellung von heterocyclischen, Asthylendoppelbindungen enthaltenden Verbindungen |
| FR2558158B1 (fr) * | 1984-01-13 | 1986-05-16 | Roussel Uclaf | Derives de l'indole ethenyl phenol, leurs sels, procede de preparation, application a titre de medicaments, compositions les renfermant et intermediaires |
| US5468898A (en) * | 1990-09-10 | 1995-11-21 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Substituted naphthylene compounds exhibiting selective leukotriene B4 antagonist activity |
| GB9408577D0 (en) * | 1994-04-29 | 1994-06-22 | Fujisawa Pharmaceutical Co | New compound |
| YU54202A (sh) * | 2000-01-18 | 2006-01-16 | Agouron Pharmaceuticals Inc. | Jedinjenja indazola, farmaceutske smeše i postupci za stimulisanje i inhibiranje ćelijske proliferacije |
| US6897231B2 (en) * | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
| WO2003087072A1 (en) * | 2002-03-29 | 2003-10-23 | Mochida Pharmaceutical Co., Ltd. | Therapeutic agent for endothelial disorder |
-
2003
- 2003-07-18 IT IT000355A patent/ITRM20030355A1/it unknown
-
2004
- 2004-07-06 EP EP04745198A patent/EP1646616A2/en not_active Withdrawn
- 2004-07-06 AU AU2004257011A patent/AU2004257011A1/en not_active Abandoned
- 2004-07-06 KR KR1020067001052A patent/KR20060039001A/ko not_active Ceased
- 2004-07-06 US US10/563,465 patent/US20060160773A1/en not_active Abandoned
- 2004-07-06 BR BRPI0412744-7A patent/BRPI0412744A/pt not_active IP Right Cessation
- 2004-07-06 WO PCT/IT2004/000373 patent/WO2005007635A2/en not_active Ceased
- 2004-07-06 JP JP2006520106A patent/JP2007530427A/ja not_active Withdrawn
- 2004-07-06 CA CA002531389A patent/CA2531389A1/en not_active Abandoned
- 2004-07-06 MX MXPA06000625A patent/MXPA06000625A/es unknown
- 2004-07-06 CN CNA2004800207571A patent/CN1826330A/zh active Pending
- 2004-07-12 TW TW093120812A patent/TW200504042A/zh unknown
- 2004-07-16 AR ARP040102518A patent/AR045700A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| TW200504042A (en) | 2005-02-01 |
| WO2005007635A8 (en) | 2005-05-12 |
| AU2004257011A1 (en) | 2005-01-27 |
| ITRM20030355A0 (it) | 2003-07-18 |
| BRPI0412744A (pt) | 2006-09-26 |
| US20060160773A1 (en) | 2006-07-20 |
| ITRM20030355A1 (it) | 2005-01-19 |
| JP2007530427A (ja) | 2007-11-01 |
| MXPA06000625A (es) | 2006-04-19 |
| CN1826330A (zh) | 2006-08-30 |
| WO2005007635A2 (en) | 2005-01-27 |
| WO2005007635A3 (en) | 2005-08-11 |
| EP1646616A2 (en) | 2006-04-19 |
| CA2531389A1 (en) | 2005-01-27 |
| KR20060039001A (ko) | 2006-05-04 |
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