AR039566A1 - Inhibidores de la histona deacetilasa, composicion farmaceutica que los contiene y sus procesos de preparacion - Google Patents
Inhibidores de la histona deacetilasa, composicion farmaceutica que los contiene y sus procesos de preparacionInfo
- Publication number
- AR039566A1 AR039566A1 ARP030100854A ARP030100854A AR039566A1 AR 039566 A1 AR039566 A1 AR 039566A1 AR P030100854 A ARP030100854 A AR P030100854A AR P030100854 A ARP030100854 A AR P030100854A AR 039566 A1 AR039566 A1 AR 039566A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- amino
- aminoalkyl
- alkyloxy
- 4alkyl
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract 2
- 108010033040 Histones Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 52
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 35
- -1 methylimidazolyl Chemical group 0.000 abstract 22
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 20
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 14
- 125000003545 alkoxy group Chemical group 0.000 abstract 13
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000002541 furyl group Chemical group 0.000 abstract 4
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 125000002431 aminoalkoxy group Chemical group 0.000 abstract 3
- 229910052799 carbon Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000004104 aryloxy group Chemical group 0.000 abstract 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 2
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 125000002757 morpholinyl group Chemical group 0.000 abstract 2
- 125000006542 morpholinylalkyl group Chemical group 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 125000002971 oxazolyl group Chemical group 0.000 abstract 2
- 125000004193 piperazinyl group Chemical group 0.000 abstract 2
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000001544 thienyl group Chemical group 0.000 abstract 2
- 125000004385 trihaloalkyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 102000003964 Histone deacetylase Human genes 0.000 abstract 1
- 108090000353 Histone deacetylase Proteins 0.000 abstract 1
- 125000000815 N-oxide group Chemical group 0.000 abstract 1
- 230000002159 abnormal effect Effects 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000005122 aminoalkylamino group Chemical group 0.000 abstract 1
- 125000005001 aminoaryl group Chemical group 0.000 abstract 1
- 125000005097 aminocarbonylalkyl group Chemical group 0.000 abstract 1
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 1
- 125000005160 aryl oxy alkyl group Chemical group 0.000 abstract 1
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 230000010261 cell growth Effects 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 125000002349 hydroxyamino group Chemical group [H]ON([H])[*] 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 230000004614 tumor growth Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- A61K31/402—1-aryl substituted, e.g. piretanide
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
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- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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Abstract
Compuestos de la fórmula (1) que presentan actividad enzimática inhibidora sobre la histona desacetilasa; su proceso de preparación y uso del compuesto para la manufactura de un medicamento. Estos compuestos poseen acción terapéutica inhibiendo el crecimiento anormal de células y el crecimiento de los tumores. Reivindicación 1: Un compuesto de formula (1), las formas N-óxido, las sales farmacéuticamente aceptables obtenidas mediante la adición de ácidos, o sus formas estereoquímicamente isómeras caracterizados porque en la fórmula (1), n vale 0,1, 2 o 3 y cuando n es 0 entonces se tiene un enlace directo; t vale 0, 1, 2, 3 ó 4 y cuando t es 0 entonces se tiene un enlace directo; cada uno de los Q es nitrógeno o carbono; cada uno de los X es nitrógeno o carbono; cada uno de los Y es nitrógeno o carbono; cada uno de los Z es nitrógeno o -CH<; R1 es -C(O)NR7R8, -NHC(O)R9, -C(O)- alcanodiil C1-6SR9, -NR10C(O)N(OH)R9, -NR10C(O)alcanodiil C1-6SR9, -NR10C(O)C=N (OH)R9 u otro grupo Zn-quelante siendo R7 y R8 independientemente entre si, seleccionados de entre hidrógeno, hidroxi, alquilo C1-6, hidroxialquilo C1-6, aminoalquilo C1-6 o aminoarilo; R9 es independientemente seleccionado de entre hidrógeno, alquilo C1-6, alquil C1-6carbonilo, arilalquilo C1-6, alquil C1-6pirazinilo, piridinona, pirrolidinona o metilimidazolilo; R10 es independientemente seleccionado entre hidrógeno o alquilo C1-6; R2 es hidrógeno, halo, hidroxi, amino, nitro, alquilo C1-6, alquiloxi C1-6, trifluorometilo, di (alquil C1-6)-amino, hidroxiamino o naftalensulfonilpirazinilo; -L- es un enlace directo o un radical bivalente seleccionado de entre alcanodiilo C1-6, alcanodiiloxi C1-6, amino, carbonilo o aminocarbonilo cada uno de los R3 independientemente de los demás representa un átomo de hidrógeno y un átomo de hidrógeno puede estar substituido por un substituyente seleccionado entre arilo; R4 es hidrógeno, hidroxilo, amino, hidroxialquilo C1-6, alquilo C1-6, alquiloxilo C1-6, arilalquilo C1-6, aminocarbonilo, hidroxicarbonilo, aminoalquilo C1-6, aminocarbonilalquilo C1-6, hidroxicarbonilalquilo C1-6, hidroxiaminocarbonilo, alquiloxi C1-6carbonilo, alquil C1-6aminoalquilo C1-6 o di (alquil C1-6)aminoalquilo C1-6 ; la parte cíclica A es un radical seleccionado entre (a-1), a (a-51) en los cuales cada s es independientemente 0,1, 2,3, 4 o 5; cada R5 y R6 son independientemente seleccionados de hidrógeno; halo; hidroxilo; amino; nitro; trihaloalquilo C1-6; trihaloalquiloxilo C1-6; alquilo C1-6; alquilo C1-6 substituido con arilo y cicloalquilo C3-10; alquiloxilo C1-6; alquiloxi C1-6alquiloxilo C1-6; alquil C1-6carbonilo; alquiloxi C1-6carbonilo; alquil C1-6sulfonilo; cianoalquilo C1-6; hidroxialquilo C1-6; hidroxialquiloxilo C1-6; hidroxialquil C1-6amino; aminoalquiloxilo C1-6; di (alquil C1-6) aminocarbonilo; di(hidroxialquil C1-6) amino; (aril) (alquil C1-6)amino; di (alquil C1-6)aminoalquiloxilo C1-6; di (alquil C1-6)aminoalquilamino C1-6; di (alquil C1-6)aminoalquilo C1-6; arilsulfonilo; arilsulfonilamino; ariloxilo; ariloxialquilo C1-6; arilalquenodiilo C2-6; di (alquil C1-6)amino; di (alquil C1-6)aminoalquilo C1-6; di(alquil C1-6) amino (alquil C1-6) amino; di(alquil C1-6) amino(alquil C1-6) alquilo C1-6; di (alquil C1-6)aminoalquilo C1-6(alquil C1-6)amino; di (alquil C1-6)aminoalquil C1-6(alquil C1-6)aminoalquilo C1-6; aminosulfonilamino (alquil C1-6) amino; aminosulfonilamino(alquil C1-6) aminoalquilo C1-6; di (alquil C1-6)aminosulfonilamino(alquil C1-6) amino; di (alquil C1-6)aminosulfonilamino(alquil C1-6)aminoalquilo C1-6; ciano; tiofenilo; tiofenilo substituido con di (alquil C1-6)aminoalquil C1-6aminoalquilo C1-6, di (alquil C1-6)aminoalquilo C1-6, alquil C1-6piperazinilalquilo C1-6, hidroxialquil C1-6piperazinilalquilo C1-6, hidroxialquiloxi C1-6alquil C1-6piperazinilalquilo C1-6, di(alquil C1-6) aminosulfonilpiperazinilalquilo C1-6, alquiloxi C1-6piperidinilo, alquiloxi C1-6piperidinilalquilo C1-6, morfolinilalquilo C1-6, hidroxialquil C1-6(alquil C1-6)aminoalquilo C1-6, o di(hidroxialquil C1-6)aminoalquilo C1-6 ; furanilo; furanilo substituido con hidroxialquilo C1-6; benzofuranilo; imidazolilo; oxazolilo; oxazolilo substituido con arilo y alquilo C1-6; alquil C1-6triazolilo; tetrazolilo; pirrolidinilo; pirrolilo; piperidinilalquiloxilo C1-6; morfolinilo; alquil C1-6morfolinilo; morfolinilalquiloxilo C1-6; morfolinilalquilo C1-6; morfolinilalquil C1-6amino; morfolinilalquilamino C1-6alquilo C1-6; piperazinilo; alquil C1-6piperazinilo; alquil C1-6piperazinilalquiloxilo C1-6; piperazinilalquilo C1-6; naftalenilsulfonilpiperazinilo; naftalenilsulfonilpiperidinilo; naftalenilsulfonilo; alquil C1-6piperazinilalquilo C1-6; alquil C1-6piperazinilalquil C1-6amino; alquil C1-6piperazinilalquil C1-6aminoalquilo C1-6; alquil C1-6piperazinilsulfonilo; aminosulfonilpiperazinilalquiloxilo C1-6; aminosulfonilpiperazinilo; aminosulfonilpiperazinilalquilo C1-6; di(alquilo C1-6) aminosulfonilpiperazinilo; di (alquil C1-6)aminosulfonilpiperazinilalquilo C1-6; hidroxialquil C1-6piperazinilo; hidroxialquil C1-6piperazinilalquilo C1-6; alquiloxi C1-6piperidinilo; alquiloxi C1-6piperidinilalquilo C1-6; piperidinilaminoalquil C1-6amino; piperdinilaminoalquil C1-6aminoalquilo C1-6; (alquil C1-6piperidinil)(hidroxialquil C1-6)aminoalquilo C1-6; (alquil C1-6piperidinil)(hidroxialquilo C1-6) aminoalquilo C1-6; hidroxialquiloxi C1-6alquil C1-6piperazinilo; (hidroxialquil C1-6)piperidinilalquilo C1-6; (hidroxialquil C1-6)amino; (hidroxialquil C1-6)(alquil C1-6)aminoalquilo C1-6; hidroxialquil C1-6aminoalquilo C1-6; di(hidroxialquil C1-6 aminoalquilo C1-6; pirrolidinilalquilo C1-6; pirrolidinilalquiloxilo C1-6; pirazolilo; tiopirazolilo; pirazolilo substituido con dos substituyentes seleccionados de alquilo C1-6 o trihaloalquilo C1-6; piridinilo; piridinilo substituido con alquiloxilo C1-6, ariloxilo o arilo; pirimidinilo; tetrahidropiridinilpiperazinilo; tetrahidropirimidinilpiperazinilalquilo C1-6; quinolinilo; indol; fenilo; o fenilo substituido con uno, dos o tres substituyentes independientemente seleccionados de halo, amino, nitro, alquilo C1-6, alquiloxilo C1-6, hidroxialquilo C1-4, trifluorometilo, trifluorometiloxilo, hidroxialquiloxilo C1-4, alquil C1-4sulfonilo, alquiloxi C1-4alquiloxilo C1-4, alquiloxi C1-4carbonilo, aminoalquiloxilo C1-4, di (alquil C1-4)aminoalquiloxilo C1-4, di(alquil C1-4) amino, di (alquil C1-4) aminocarbonilo, di (alquil C1-4)aminoalquilo C1-4, (alquil C1-4)aminoalquil C1-4aminoalquilo C1-4, di (alquil C1-4)aminoalquil C1-4 amino, di (alquil C1-4)aminoalquil C1-4aminoalquilo C1-4, di (alquil C1-4)aminoalquil C1-4amino; di (alquil C1-4)aminoalquil C1-4aminoalquilo C1-4; aminosulfonilamino(alquil C1-4) amino, aminosulfonilamino (alquil C1-4)aminoalquilo C1-4, di (alquil C1-4)aminosulfonilamino(alquil C1-4)amino, di (alquil C1-4)aminosulfonilamino(alquil C1-4)aminoalquilo C1-6, ciano, piperidinilalquiloxilo C1-4, pirrolidinilalquiloxilo C1-4, aminosulfonilpiperazinilo, aminosulfonilpiperazinilalquilo C1-4, di(alquil C1-4) aminosulfonilpiperazinilo, di (alquil C1-4)aminosulfonilpiperazinilalquilo C1-4, hidroxialquil C1-4piperazinilo, hidroxialquil C1-4piperazinilalquilo C1-4, alquiloxi C1-4piperidinilo, alquiloxi C1-4piperidinilalquilo C1-4, hidroxialquiloxi C1-4alquil C1-4piperazinilo, hidroxialquiloxi C1-4alquil C1-4piperaziniloalquilo C1-4, (hidroxialquil C1-4)(alquil C1-4) amino, (hidroxialquil C1-4)(alquil C1-4)aminoalquilo C1-4, di(hidroxialquil C1-4) arnino, di(hidroxialquil C1-4) aminoalquilo C1-4, furanilo, furanilo substituido con -CH=CH-CH=CH-, pirrolidinilalquilo C1-4, pirrolidiniloalquiloxilo C1-4, morfolinilo, morfolinilalquiloxilo C1-4, morfolinilalquilo C1-4, morfolinilalquil C1-4amino, piperazinilo, alquil C1-4piperazinilo, alquil C1-4piperazinilalquiloxilo C1-4, piperazinilalquilo C1-4, alquil C1-4piperazinilalquilo C1-4, alquil C1-4piperazinilalquil C1-4arnino, alquil C1-4piperazinilalquil C1-4aminoalquilo C1-4, tetrahidropirimidinilpiperazinilo, tetrahidropirimidinilpiperazinilalquilo C1-4, piperidinilaminoalquil C1-4amino, piperidinilaminoalquil C1-4aminoC1-4alquilo, (alquil C1-4piperidinil)(hidroxialquil C1-4)amino, (alquil C1-4piperidinil)(hidroxialquil C1-4)aminoalquil C1-4aminoalquilo C1-4, piridinilalquiloxilo C1-4, hidroxialquil C1-4amino, (hidroxialquil C1-4)aminoalquilo C1-4, di (alquil C1-4)aminoalquil C1-4amino, aminotiadiazolilo, aminosulfonilpiperazinilalquiloxilo C1-4, o tiofenilalquil C1-4amino ; pudiendo cada R5 y R6 estar ubicado sobre el nitrógeno en reemplazo del hidrógeno; arilo en la anterior es fenilo, o fenilo substituido con uno o más substituyentes seleccionados cada uno independientemente de halo, alquilo C1-6, alquiloxilo C1-6, trifluorometilo, ciano o hidroxicarbonilo.
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| US36379902P | 2002-03-13 | 2002-03-13 |
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- 2003-03-11 CA CA2475764A patent/CA2475764C/en not_active Expired - Fee Related
- 2003-03-11 IL IL16400403A patent/IL164004A0/xx unknown
- 2003-03-11 AU AU2003212335A patent/AU2003212335B8/en not_active Ceased
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- 2003-03-11 EA EA200401201A patent/EA007272B1/ru not_active IP Right Cessation
- 2003-03-11 EP EP03711980A patent/EP1485353B1/en not_active Expired - Lifetime
- 2003-03-11 KR KR10-2004-7011509A patent/KR20040090985A/ko not_active Withdrawn
- 2003-03-11 DE DE60333260T patent/DE60333260D1/de not_active Expired - Lifetime
- 2003-03-12 TW TW092105284A patent/TW200400822A/zh unknown
- 2003-03-12 AR ARP030100854A patent/AR039566A1/es not_active Application Discontinuation
- 2003-11-03 UA UA20041008334A patent/UA78031C2/uk unknown
- 2003-11-03 UA UA20041008337A patent/UA78033C2/uk unknown
- 2003-11-03 UA UA20040907276A patent/UA77263C2/uk unknown
- 2003-11-03 UA UA20041008336A patent/UA78032C2/uk unknown
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2004
- 2004-09-09 ZA ZA200407235A patent/ZA200407235B/en unknown
- 2004-09-09 ZA ZA200407234A patent/ZA200407234B/en unknown
- 2004-09-09 IL IL164006A patent/IL164006A/en not_active IP Right Cessation
- 2004-09-09 ZA ZA200407232A patent/ZA200407232B/en unknown
- 2004-09-09 ZA ZA200407237A patent/ZA200407237B/en unknown
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- 2004-09-09 IL IL164007A patent/IL164007A/en not_active IP Right Cessation
- 2004-09-28 NO NO20044113A patent/NO20044113L/no not_active Application Discontinuation
- 2004-10-01 NO NO20044194A patent/NO20044194L/no not_active Application Discontinuation
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2009
- 2009-01-27 US US12/360,139 patent/US8114999B2/en not_active Expired - Fee Related
- 2009-02-18 US US12/372,785 patent/US8343988B2/en not_active Expired - Fee Related
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- 2009-04-24 US US12/429,838 patent/US20090227558A1/en not_active Abandoned
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2011
- 2011-12-30 US US13/341,316 patent/US20120108603A1/en not_active Abandoned
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2012
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2013
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2014
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2015
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