AR062234A1 - Derivados de ester de nitrato de piperidinas sustituidas y metodos de preparacion - Google Patents
Derivados de ester de nitrato de piperidinas sustituidas y metodos de preparacionInfo
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- AR062234A1 AR062234A1 ARP070103476A ARP070103476A AR062234A1 AR 062234 A1 AR062234 A1 AR 062234A1 AR P070103476 A ARP070103476 A AR P070103476A AR P070103476 A ARP070103476 A AR P070103476A AR 062234 A1 AR062234 A1 AR 062234A1
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- alkoxy
- alkyl
- alq
- alkylamino
- pyridyl
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- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
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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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
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- A61P3/06—Antihyperlipidemics
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—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 no double bonds between ring members or between ring members and non-ring members
- C07D211/36—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 no 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
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/52—Oxygen atoms attached in position 4 having an aryl radical as the second substituent in position 4
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
La presente se refiere a un proceso para su preparacion, y el uso de estos compuestos como un agente terapéutico para enfermedades cardiovasculares, en particular en casos de presion arterial elevada y dano vascular y orgánico concomitante con la presion arterial elevada. Reivindicacion 1: Compuesto de la formula general (1) donde R1 es arilo o heterociclilo, en particular benzimidazolilo, benzo[1,3]dioxolilo, benzofuranilo, benzooxazolilo, benzotiazolilo, benzo[b]tienilo, quinazolinilo, quinolilo, quinoxalinilo, 2H-cromenilo, 3,4-dihidro-2H-benzo[1,4]oxazinilo, dihidro-3H-benzo-[1,4]oxazinilo, dihidro-2H-benzo[1,4]tiazinilo, 1a,7b-dihidro-1H-ciclopropa[c]cromenilo, 2,3-dihidro-1H-indolilo, dihidro-1H-pirido[2,3-b][1,4]oxazinilo, imidazo[1,2-a]piridilo, imidazo[1,5-a]piridilo, indazolilo, indolilo, isobenzofuranilo, isoquinolilo, [1,5]naftiridilo, fenilo, ftalazinilo, piridilo, pirimidinilo, 1H-pirrolo[2,3-b]piridilo, 1H-pirrolo[2,3-c]piridilo, 1H-pirrolo[3,2-b]piridilo, tetrahidro-quinolilo, tetrahidroquinoxalinilo, 1,1a,2,7b-tetrahidro-ciclopropa[c]cromenilo, tetrahidroimidazo[1,2-a]-piridilo, tetrahidroimidazo[1,5-a]piridilo, tetrahidro-isoquinolilo, [1,2,3]triazolo[1,5-a]piridilo o [1,2,4]triazolo[4,3- a]piridilo, que están sustituidos con 1-4 sustituyentes acil-alcoxi C1-8-alcoxi C1-8, acil-alcoxi C1-8-alquilo C1-8, (N-acil)-alcoxi C1-8-alquilamino C1-8, alcanoilo C1-8, alcoxi C1-8, aIcoxi C1-8-alcanoilo C1-8, alcoxi C1-8-alcoxi C1-8, alcoxi C1-8- alcoxi C1-8-alquilo C1-8, alcoxi C1-8-alquilo C1-8, (N-alcoxi C1-8)-alquilamino C1-8-carbonil-alcoxi C1-8, (N-alcoxi C1-8)-alquilamino C1-8-carbonil-alquilo C1-8, alcoxi C1-8-alquilcarbamoilo C1-8, alcoxi C1-8-alquilcarbonilo C1-8, alcoxi C1-8- alquilcarbonil-amino C1-8, 1-alcoxi C1-8-alquilheterociclilo C1-8, alcoxiaminocarbonil C1-8-alcoxi C1-8, alcoxiamino C1-8-carbonil-alquilo C1-8, alcoxicarbonilo C1-8, alcoxi C1-8-carbonil-alcoxi C1-8, alcoxicarbonil C1-8-alquilo C1-8, alcoxicarbonilamino C1-8-alcoxi C1-8, alcoxicarbonil C1-8-amino-alquilo C1-8, alquilo C1-8, (N-alquilo C1-8)-alcoxiC1-8-alquilcarbamoilo C1-8, (N-alquilo C1-8)-alcoxi C1-8-alquilcarbonil-amino C1-8, (N-alquilo C1-8)-alcoxicarbonilamino C1-8, (N- alquilo C1-8)-alquilcarbonilamino C1-8-alcoxi C1-8, (N-alquil C1-8)-alquilcarbonilamino C1-8-alquilo C1-8, (N-alquilo C1-8)-alquilsulfonilamino C1-8-alcoxi C1-8, (N-alquilo C1-8)-alquilsulfonilamino C1-8-alquilo C1-8, alquilamidinilo C1-8, alquilamino C1-8-alcoxi C1-8, di-alquilamino C1-8-alcoxi C1-8, alquilamino C1-8-alquilo C1-8, di-alquilamino C1-8-alquilo C1-8, alquilamino C1-8-carbonil-alcoxi C1-8, di-alquilamino C1-8-carbonil-alcoxi C1-8, alquilamino C1-8-carbonil-alcoxi C1-8- alquilo C1-8, alquilamino C1-8-carbonil-alquilo C1-8, di-alquilamino C1-8-carbonil-alquilo C1-8, alquilamino C1-8-carbonilamino-alcoxi C1-8, alquilamino C1-8-carbonilamino-alquilo C1-8, alquilcarbonilamino C1-8, alquilcarbonilamino C1-8-alcoxi C1-8, alquilcarbonilamino C1-8-alquilo C1-8, alquilcarboniloxi C1-8-alcoxi C1-8, alquilcarboniloxi C1-8-alquilo C1-8, alquilsulfonilo C1-8, alquilsulfonil C1-8-alcoxi C1-8, alquilsulfonil C1-8-alquilo C1-8, alquil C1-8-sulfonilamino-alcoxi C1-8, alquilsulfonilamino C1-8-alquilo C1-8, amino opcionalmente N-mono- o N,N-di-alquilado C1-8, aril-alcoxi C0-8, aril-alquilo C0-8, carbamoil alcoxi C0-8 opcionalmente N-mono- o N,N-di-alquilado C1-8, carbamoilalquilo C0-8 opcionalmente N-mono- o N,N- di-alquilado C1-8, carboxi-alcoxi C1-8, carboxi-alcoxi C1-8-alquilo C1-8, carboxi-alquilo C1-8, ciano, ciano-alcoxi C1-8, ciano-alquilo C1-8, cicloalquil C3-8-alcoxi C1-8, cicloalquil C3-8-alquilo C1-8, cicloalquilcarbonilamino C3-8-alcoxi C1-8, cicloalquilcarbonilamino C3-8-alquilo C1-8, O,N-dimetilhidroxiamino-alquilo C1-8, halogeno, halo-alcoxi C1-8, halo-alquilo C1-8, heterociclil-alcoxi C0-8, heterociclil-alquilo C0-8, heterociclilcarbonilo, hidroxi-alcoxi C1-8-alcoxi C1-8, hidroxi- alcoxi C1-8-alquilo C1-8, hidroxi-alquilo C1-8, O-metiloximil-alquilo C1-8, oxido u oxo; R2 es alqueniloxi C2-8-alcoxi C1-8, alqueniloxi C2-8-alquilo C1-8, alcoxi C1-8, alcoxi C1-8-alcoxi C1-8, alcoxi C1-8-alcoxi C1-8-alquilo C1-8 sustituido de modo opcional con halogeno, alcoxi C1-8-alquilo C1-8, alcoxi C1-8-alquilamino C1-8-alcoxi C1-8, alcoxi C1-8-alquilamino C1-8-alquilo C1-8, alcoxi C1-8-alquilsulfanil C1-8-alcoxi C1-8, alcoxi C1-8-alquilsulfanil-C1-8-alquilo C1-8, alcoxi C1-8-alquil-C0-8- cicloalquil-C3-8-alcoxi C0-8-alquilo C1-8, alquilo C1-8, alquil C1-8-sulfanil-alcoxi C1-8, alquilsulfanil C 1-8-alcoxi C1-8-alcoxi C1-8, alquilsulfanil C1-8-alcoxi C1-8-alquilo C1-8, alquilsulfanil C1-8-alquilo C1-8, alquilsulfonil C1-8-alcoxi C1-8- alcoxi C1-8, alquilsulfonil C1-8-alcoxi C1-8-alquilo C1-8, aril-alcoxi C0-8-alcoxi C1-8, aril-alcoxi C0-8-alquilo C1-8, ariloxi, cicloalquil-C3-8-alcoxi C0-8-alcoxi C1-8, cicloalquil C3-8-alcoxi C0-8-alcoxi C1-8-alquilo C1-8, cicloalquil C3-8-alcoxi C0-8-alquilo C1-8, heterociclil-alcoxi C0-8-alcoxi C1-8, heterociclil-alcoxi C0-8-alquilo C1-8 o heterocicliloxi; R3 es halogeno, R4 es acilo, alquenilo C2-8, alquilo C1-8, aril-alquilo C1-8 o hidrogeno; X es -alq-, -O-alq-, -alq-O-, -O-alq-O-, -S- alq-, -alq-S-, -alq-NR4-, -NR4-alq-, -C(O)-NR4, -alq-C(O)-NR4-, -O-alq-C(O)-NR4-, -C(O)-NR4-alq-, -alq-C(O)-NR4-alq-, NR4-C(O)-, -alq-NR4-C(O)-, -NR4-C(O)-alq-, -alq-NR4-C(O)-alq-, -O-alq-C(O)NR4-, -O-alq-NR4-C(O)-, -S(O)2-NR4-, -alq-S(O)2-NR4-, - S(O)2-NR4-alq-, -alq-S(O)2-NR4-alq-, -NR4-S(O)2-, -alq-NR4-S(O)2-, -NR4-S(O)2-alq- o -alq-NR4-S(O)2-alq-, donde alq indica alquileno C1-8 que puede estar sustituido de modo opcional con halogeno; Y es a) -alq-, -alq-O-alq-, -alq-NR4-alq-, -alq-C(O)- alq-,alq-C(O)-NR4-alq-, -alq-C(O)-alq-NR4-alq-, -alq-NR4-C(O)-alq-, -alq-NR4-alq-C(O)-alq-, no sustituido o sustituido con heterociclilo y/o halogeno y/o hidroxi y/o alcoxi, donde alq indica alquileno C1-8 lineal o ramificado; o b) si p = 0, es adicionalmente i) una union, ii) -alq-O, -alq-NR4-, -alq-C(O)-, alq-NR4-C(O)-alq-O-, no sustituido o sustituido con heterociclilo y/o halogeno y/o hidroxi y/o alcoxi donde alq indica alquileno C1-8 lineal o ramificado; Z0 es igual a -U-Z1- donde Z, es -C(O)-O-, -O-C(O)O-, -C(O)-NR7-C(O) u -O-C(O)-NR7-C(O)-, donde R7 es como se definio a continuacion; U es un radical bivalente que tiene el siguiente significado: a) -alquileno C1-8, de preferencia alquileno C1-8 que está sustituido de modo opcional con uno o más de los sustituyentes seleccionados del grupo formado por: halogeno, hidroxi, -ONO2 o To, donde To es -OC(O)-(alquilo C1-8)-ONO2 u -O-(alquilo C1-8)-ONO2; -cicloalquileno C3-8, donde el anillo está sustituido de modo opcional con cadenas laterales T, donde T es alquilo C1-8; b) un grupo de formula (2) donde v es un numero entero de 0 a 20, y v1 es un numero entero de 1 a 20; c) un grupo de formula (3) donde v es un numero entero de 0 a 20, y v1 es un numero entero de 1 a 20; d) un grupo de formula (4) donde: v1 es como se definio antes y v2 es un numero entero de 0 a 2; Z2 = -O-C(O)- o -C(O)-O- y R5 es H o CH3; e) un grupo de formula (5) donde: v1, v2, R5 y Z2 son como se definio antes; U1 es -CH2-CH2- o -CH=CH- (CH2)v2-; f) un grupo de formula (6) donde: v1 y R5 son como se definio antes, R6 es H o -C(O)CH3; g) grupo de formulas (7) donde Z3 es -O-, o -S-, v3 es un numero entero de 1 a 6, de preferencia de 1 a 4, R5 es como se definio antes; o h) un grupo de formula (8) donde: v4 es un numero entero de 0 a 10; v5 es un numero entero de 1 a 10; R7, R8, R9, R10 son iguales o diferentes, y son H o alquilo C1-4; U2 es un anillo heterocíclico saturado, no saturado o aromático de 5 o 6 miembros, que contiene uno o más heteroátomos seleccionados de nitrogeno, oxigeno y azufre, y de preferencia se seleccionan del grupo de formulas (9); m es 0, 1 o 2; n es 0 o 1; p es 0 o 1; q es 0 o 1; donde si p es = 0, q es = 1 y si p es =1, q es = 0, y sus sales, de preferencia sus sales aceptables para uso farmacéutico.
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CH12792006 | 2006-08-08 |
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AR062234A1 true AR062234A1 (es) | 2008-10-22 |
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ARP070103476A AR062234A1 (es) | 2006-08-08 | 2007-08-07 | Derivados de ester de nitrato de piperidinas sustituidas y metodos de preparacion |
Country Status (15)
Country | Link |
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US (1) | US20090325947A1 (es) |
EP (1) | EP2049514B1 (es) |
JP (1) | JP2010500327A (es) |
KR (1) | KR20090061000A (es) |
CN (1) | CN101501020A (es) |
AR (1) | AR062234A1 (es) |
AT (1) | ATE496904T1 (es) |
AU (1) | AU2007283631A1 (es) |
BR (1) | BRPI0715412A2 (es) |
CA (1) | CA2660538A1 (es) |
DE (1) | DE602007012260D1 (es) |
MX (1) | MX2009001404A (es) |
RU (1) | RU2009107891A (es) |
TW (1) | TW200821303A (es) |
WO (1) | WO2008017685A1 (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2008074450A2 (en) * | 2006-12-20 | 2008-06-26 | Nicox S.A. | Non-peptidic renin inhibitors nitroderivatives |
CA2674237C (en) | 2006-12-28 | 2015-11-24 | Rigel Pharmaceuticals, Inc. | N-substituted-heterocycloalkyloxybenzamide compounds and methods of use |
CN101910131B (zh) | 2007-11-16 | 2014-04-23 | 里格尔药品股份有限公司 | 甲酰胺、磺酰胺和胺化合物及其使用方法 |
WO2009076631A1 (en) | 2007-12-12 | 2009-06-18 | Rigel Pharmaceuticals, Inc. | Carboxamide, sulfonamide and amine compounds for metabolic disorders |
CA2708866A1 (en) | 2007-12-19 | 2009-06-25 | Hiroyuki Nakahira | Bicyclic heterocyclic derivative |
JP5658138B2 (ja) | 2008-04-23 | 2015-01-21 | ライジェル ファーマシューティカルズ, インコーポレイテッド | 代謝障害の処置のためのカルボキサミド化合物 |
US8658639B2 (en) | 2009-06-24 | 2014-02-25 | Dainippon Sumitomo Pharma Co., Ltd | N-substituted-cyclic amino derivative |
EP2560634A1 (en) * | 2010-04-23 | 2013-02-27 | Piramal Enterprises Limited | Nitric oxide releasing prodrugs of therapeutic agents |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
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DE3433383A1 (de) * | 1984-09-12 | 1986-03-20 | Boehringer Mannheim Gmbh, 6800 Mannheim | Neue phenyl-acetonitril-derivate |
IT1243367B (it) * | 1990-07-26 | 1994-06-10 | Italfarmaco Spa | Derivati acidi benzoici sostituiti ad attivita' cardiovascolare |
US6376672B1 (en) * | 1999-04-27 | 2002-04-23 | Hoffmann-La Roche Inc. | Naphthalenylmethoxypiperidines as renin inhibitors |
US20040204455A1 (en) * | 2003-04-10 | 2004-10-14 | Cody Wayne Livingston | Piperidine derivative rennin inhibitors |
AU2004260830B2 (en) * | 2003-07-31 | 2010-04-29 | Nicox S.A. | Nitrooxy derivatives of losartan, valsatan, candesartan, telmisartan, eprosartan and olmesartan as angiotensin-II receptor blockers for the treatment of cardiovascular diseases |
RU2374228C2 (ru) * | 2003-11-26 | 2009-11-27 | Новартис Аг | Производные 4-фенилпиперидина в качестве ингибиторов ренина |
AR053406A1 (es) * | 2004-07-09 | 2007-05-09 | Speedel Experimenta Ag | Derivados de piperidina como inhibidores de renina. composiciones farmaceuticas |
TW200722424A (en) * | 2005-03-31 | 2007-06-16 | Speedel Experimenta Ag | Substituted piperidines |
BRPI0609534A2 (pt) * | 2005-03-31 | 2010-04-13 | Speedel Experimenta Ag | piperidinas 3,4,5-substituìdas |
TW200833687A (en) * | 2005-03-31 | 2008-08-16 | Speedel Experimenta Ag | Substituted piperidines |
TW200804359A (en) * | 2006-01-19 | 2008-01-16 | Speedel Experimenta Ag | Substituted 4-phenylpiperidines |
TW200831463A (en) * | 2006-09-12 | 2008-08-01 | Speedel Experimenta Ag | Nitrate esters of aminoalcohols |
-
2007
- 2007-08-06 TW TW096128820A patent/TW200821303A/zh unknown
- 2007-08-07 AU AU2007283631A patent/AU2007283631A1/en not_active Abandoned
- 2007-08-07 WO PCT/EP2007/058207 patent/WO2008017685A1/en active Application Filing
- 2007-08-07 KR KR1020097004738A patent/KR20090061000A/ko not_active Application Discontinuation
- 2007-08-07 DE DE602007012260T patent/DE602007012260D1/de active Active
- 2007-08-07 AT AT07788301T patent/ATE496904T1/de not_active IP Right Cessation
- 2007-08-07 CA CA002660538A patent/CA2660538A1/en not_active Abandoned
- 2007-08-07 JP JP2009523286A patent/JP2010500327A/ja active Pending
- 2007-08-07 CN CNA2007800292065A patent/CN101501020A/zh active Pending
- 2007-08-07 EP EP07788301A patent/EP2049514B1/en not_active Not-in-force
- 2007-08-07 US US12/310,022 patent/US20090325947A1/en not_active Abandoned
- 2007-08-07 BR BRPI0715412-7A patent/BRPI0715412A2/pt not_active IP Right Cessation
- 2007-08-07 AR ARP070103476A patent/AR062234A1/es unknown
- 2007-08-07 MX MX2009001404A patent/MX2009001404A/es not_active Application Discontinuation
- 2007-08-07 RU RU2009107891/04A patent/RU2009107891A/ru not_active Application Discontinuation
Also Published As
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AU2007283631A1 (en) | 2008-02-14 |
MX2009001404A (es) | 2009-05-13 |
DE602007012260D1 (de) | 2011-03-10 |
EP2049514A1 (en) | 2009-04-22 |
JP2010500327A (ja) | 2010-01-07 |
CA2660538A1 (en) | 2008-02-14 |
KR20090061000A (ko) | 2009-06-15 |
WO2008017685A1 (en) | 2008-02-14 |
TW200821303A (en) | 2008-05-16 |
EP2049514B1 (en) | 2011-01-26 |
US20090325947A1 (en) | 2009-12-31 |
BRPI0715412A2 (pt) | 2013-07-02 |
ATE496904T1 (de) | 2011-02-15 |
RU2009107891A (ru) | 2010-09-20 |
CN101501020A (zh) | 2009-08-05 |
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