AR085014A1 - Derivados de acido 3-heteroaroilamino-propionico amino-sustituidos y su uso como composiciones farmaceuticas - Google Patents
Derivados de acido 3-heteroaroilamino-propionico amino-sustituidos y su uso como composiciones farmaceuticasInfo
- Publication number
- AR085014A1 AR085014A1 ARP120100226A ARP120100226A AR085014A1 AR 085014 A1 AR085014 A1 AR 085014A1 AR P120100226 A ARP120100226 A AR P120100226A AR P120100226 A ARP120100226 A AR P120100226A AR 085014 A1 AR085014 A1 AR 085014A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- series consisting
- optionally substituted
- halogen
- different substituents
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 239000002253 acid Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 17
- 125000001424 substituent group Chemical group 0.000 abstract 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 16
- 229910052736 halogen Inorganic materials 0.000 abstract 16
- 150000002367 halogens Chemical class 0.000 abstract 16
- 125000000217 alkyl group Chemical group 0.000 abstract 14
- 229910052739 hydrogen Inorganic materials 0.000 abstract 12
- 239000001257 hydrogen Substances 0.000 abstract 12
- 229910052757 nitrogen Inorganic materials 0.000 abstract 12
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 10
- 150000002431 hydrogen Chemical class 0.000 abstract 9
- 229910052760 oxygen Inorganic materials 0.000 abstract 9
- 229910052717 sulfur Inorganic materials 0.000 abstract 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 8
- 125000005842 heteroatom Chemical group 0.000 abstract 8
- 239000001301 oxygen Substances 0.000 abstract 8
- 239000011593 sulfur Substances 0.000 abstract 8
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 229910052731 fluorine Inorganic materials 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- 102000005572 Cathepsin A Human genes 0.000 abstract 1
- 108010059081 Cathepsin A Proteins 0.000 abstract 1
- 206010019280 Heart failures Diseases 0.000 abstract 1
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 208000017169 kidney disease Diseases 0.000 abstract 1
- 208000019423 liver disease Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 abstract 1
Classifications
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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
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings 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
- C07D231/38—Nitrogen atoms
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- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings 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
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
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- A61K31/415—1,2-Diazoles
- A61K31/4152—1,2-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. antipyrine, phenylbutazone, sulfinpyrazone
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- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
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- 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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- C07D401/12—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 linked by a chain containing hetero atoms as chain links
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Abstract
La presente se refiere a compuestos de fórmula (1) que son valiosos compuestos farmacéuticos activos. Se trata de inhibidores de la proteasa catepsina A y son útiles para el tratamiento de enfermedades tales como, por ejemplo, aterosclerosis, insuficiencia cardiaca, enfermedades renales, enfermedades hepáticas o enfermedades inflamatorias. La presente se refiere además a procedimientos para la preparación de los compuestos de fórmula (1), a su uso y a composiciones farmacéuticas que los comprenden.Reivindicación 1: Un compuesto de fórmula (1), en cualquiera de sus formas estereoisoméricas o una mezcla de formas estereoisoméricas en cualquier proporción, o una de sus sales fisiológicamente aceptables o un solvato fisiológicamente aceptable de cualquiera de ellos: en la que: A se selecciona de la serie que consiste en C(R1) y N; D se selecciona de la serie que consiste en N(R2), O y S; E se selecciona de la serie que consiste en C(R3) y N; G se selecciona de la serie que consiste en R71-O-C(O)-, R72-N(R73)-C(O)-, NC- y tetrazol-5-ilo; R1 se selecciona de la serie que consiste en hidrógeno, halógeno, alquilo C1-6, Ar, HO-, alquil C1-6-O-, alquil C1-6-S(O)m- y NC-; R2 se selecciona de la serie que consiste en alquilo C1-7, cicloalquil C3-7-CsH2s- y Ar-CsH2s-, en los que s es un número entero seleccionado de la serie que consiste en 0, 1, 2 y 3; o R2 y R11 son conjuntamente -C(R18)=C(R19)-; R3 se selecciona de la serie que consiste en hidrógeno, halógeno, alquilo C1-6, alquil C1-6-O-, alquil C1-6-S(O)m- y NC-; R10 se selecciona de la serie que consiste en R11, R12-N(R13)-C(O)- y Het2-C(O)-, R14-C(O)- y alquil C1-4-S(O)m; R11 se selecciona de la serie que consiste en hidrógeno, R14, cicloalquilo C3-7, Ar y Het3 o R10 y R11 forman Het2; R12 y R13 se seleccionan independientemente entre sí de la serie que consiste en hidrógeno, R15 y Ar; R14 es alquilo C1-10 que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, HO-, R16-O-, R17-O-, oxo, cicloalquilo C3-7, Ar, Het1, Het3, NC-, H2N-C(O)-, alquil C1-4-NH-C(O)-, di(alquil C1-4)N-C(O)-, Het1-C(O)-, alquil C1-4-C(O)-NH- y alquil C1-4-S(O)m-; R15 es alquilo C1-6 que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, HO- y alquil C1-6-O-; R16 es alquilo C1-6 que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en HO-, alquil C1-4-O- y NC-; R17 es cicloalquil C3-7-CuH2u- que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-6, HO- y alquil C1-6-O-, en el que u es un número entero seleccionado de la serie que consiste en 0, 1, 2 y 3; R18 se selecciona de la serie de hidrógeno, halógeno, alquilo C1-6, HO- y alquil C1-6 O-; R19 se selecciona de la serie de hidrógeno, halógeno, alquilo C1-6, HO- y alquil C1-6-O-; o R18 y R19 conjuntamente se seleccionan de la serie de -(CH2)-(CH2)-(CH2)-, -(CH2)-(CH2)-(CH2)-(CH2)-, -(CH2)-(CH)=(CH)- y -(CH)=(CH)-(CH)=(CH)-; R30 se selecciona de la serie que consiste en R31, cicloalquilo C3-7, R32-CuH2u- y Het3-CuH2u-, en los que u es un número entero seleccionado de la serie que consiste en 0, 1, 2 y 3; R31 es alquilo C1-10 que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, cicloalquilo C3-7, HO-, alquil C1-6-O-, alquil C1-6-S(O)m- y NC-; R32 se selecciona de la serie que consiste en fenilo y un heterociclo monocíclico aromático de 5 ó 6 miembros que comprende uno, dos o tres heteroátomos del anillo idénticos o diferentes seleccionados de la serie que consiste en nitrógeno, oxígeno y azufre, y se une mediante un átomo de carbono del anillo, estando tanto el fenilo como el heterociclo opcionalmente sustituidos con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-6, cicloalquilo C3-7, R33, HO-, alquil C1-6-O-, R33-O-, R33-alquil C1-4-O-, -O-CH2-O-, -O-CF2-O-, alquil C1-6-S(O)m-, H2N-S(O)2-, alquil C1-4-NH-S(O)2-, di(alquil C1-4)N-S(O)2-, H2N-, alquil C1-6-NH-, di(alquil C1-6)N-, Het1, alquil C1-4-C(O)-NH-, Ar-C(O)-NH-, alquil C1-4-S(O)2-NH- y NC-; R33 se selecciona de la serie que consiste en fenilo y un heterociclo monocíclico aromático de 5 ó 6 miembros que comprende uno, dos o tres heteroátomos del anillo idénticos o diferentes seleccionados de la serie que consiste en nitrógeno, oxígeno y azufre, y se une mediante un átomo de carbono del anillo, estando tanto el fenilo como el heterociclo opcionalmente sustituidos con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-6, cicloalquilo C3-7, HO-, alquil C1-6-O-, alquil C1-6-S(O)m, H2N-S(O)2-, alquil C1-4-NH-S(O)2-, di(alquil C1-4)N-S(O)2- y NC-; R40 se selecciona de la serie que consiste en hidrógeno y alquilo C1-4; o R30 y R40 son conjuntamente (CH2)x que está opcionalmente sustituido con uno o más sustituyentes alquilo C1-4 idénticos o diferentes, en el que x es un número entero seleccionado de la serie que consiste en 2, 3, 4 y 5; R50 se selecciona de la serie que consiste en hidrógeno, alquilo C1-6, HO- y alquil C1-6-O-; R60 se selecciona de la serie que consiste en hidrógeno y alquilo C1-6; o R50 y R60 son conjuntamente (CH2)y que está opcionalmente sustituido con uno o más sustituyentes alquilo C1-4 idénticos o diferentes, en el que y es un número entero seleccionado de la serie que consiste en 2, 3, 4 y 5; o R30 y R50 son conjuntamente (CH2)z que está opcionalmente sustituido con uno o más sustituyentes alquilo C1-4 idénticos o diferentes, en el que z es un número entero seleccionado de la serie que consiste en 2, 3, 4 y 5; R71 se selecciona de la serie que consiste en hidrógeno y alquilo C1-8 que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en alquil C1-6-O- y alquil C1-6-C(O)-O-; R72 se selecciona de la serie que consiste en hidrógeno, alquilo C1-6, cicloalquilo C3-6, -CH2-(CH2)b-cicloalquilo C3-6, Het4 y -(CH2)b-Het4, estando alquilo o cicloalquilo opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, HO-, HOOC-, alquil C1-6-O- y alquil C1-6-C(O)-O-, NC-, N(alquilo C1-4)2 y b es 0, 1 ó 2; R73 se selecciona de la serie que consiste en hidrógeno, alquilo C1-6; o R72 y R73 junto con el átomo de nitrógeno al que están unidos forman a heterociclo monocíclico saturado de 4 a 7 miembros, que opcionalmente contiene un heteroátomo más del anillo seleccionado de la serie que consiste en nitrógeno, oxígeno y azufre, que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-4, HO- y alquil C1-4-O-; Ar, independientemente del resto de grupos Ar, se selecciona de la serie que consiste en fenilo y un heterociclo monocíclico aromático de 5 ó 6 miembros que comprende uno, dos o tres heteroátomos del anillo idénticos o diferentes seleccionados de la serie que consiste en nitrógeno, oxígeno y azufre, y se une mediante un átomo de carbono del anillo, estando tanto el fenilo como el heterociclo opcionalmente sustituidos con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-6, alquil C1-6-O-, -O-CH2-O-, -O-CF2-O-, alquil C1-6-S(O)m-, H2N-S(O)2- y NC-; Het1, independientemente del resto de grupos Het1, es un heterociclo monocíclico saturado o insaturado de 4 a 8 miembros que comprende un átomo de nitrógeno del anillo mediante el que Het1 se une y, opcionalmente, uno o dos heteroátomos más del anillo idénticos o diferentes seleccionados de la serie que consiste en nitrógeno, oxígeno y azufre, que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-4, HO-, alquil C1-4-O-, oxo y NC-; Het2 es un heterociclo monocíclico saturado de 4 a 7 miembros que comprende un átomo de nitrógeno del anillo mediante el que Het2 se une y, opcionalmente, un heteroátomo más del anillo seleccionado de la serie que consiste en nitrógeno, oxígeno y azufre, que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-4, HO-, oxo y alquil C1-4-O-; Het3, independientemente del resto de grupos Het3, es un heterociclo monocíclico saturado de 4 a 7 miembros que comprende uno o dos heteroátomos del anillo idénticos o diferentes seleccionados de la serie que consiste en nitrógeno, oxígeno y azufre y se une mediante un átomo de carbono del anillo, que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en flúor, alquilo C1-4 y oxo; Het4, independientemente del resto de grupos Het4, es un heterociclo monocíclico saturado o insaturado de 4 a 8 miembros que comprende de uno a cuatro heteroátomos del anillo seleccionados de la serie que consiste en nitrógeno, oxígeno y azufre, que está opcionalmente sustituido con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en halógeno, alquilo C1-4, HO-, alquil C1-4-O-, oxo y NC-; m, independientemente del resto de números m, es un número entero seleccionado de la serie que consiste en 0, 1 y 2; en el que todos los grupos cicloalquilo, independientemente entre sí, están opcionalmente sustituidos con uno o más sustituyentes idénticos o diferentes seleccionados de la serie que consiste en flúor y alquilo C1-4; en la que todos los grupos alquilo, CsH2s, CuH2u, alquilo (CH2)x y alquilo (CH2)y, independientemente entre sí, e independientemente de cualquier otro sustituyente, están opcionalmente sustituidos con uno o
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| CA2835216A1 (en) * | 2011-05-31 | 2012-12-06 | Theravance, Inc. | Neprilysin inhibitors |
| KR20140049020A (ko) * | 2011-07-26 | 2014-04-24 | 사노피 | 치환된 3-(티아졸-4-카보닐)- 또는 3-(티아졸-2-카보닐)아미노프로피온산 유도체 및 이의 약제로서의 용도 |
| WO2014053533A1 (en) | 2012-10-05 | 2014-04-10 | Sanofi | Use of substituted 3-heteroaroylamino-propionic acid derivatives as pharmaceuticals for prevention/treatment of atrial fibrillation |
| TW201514158A (zh) * | 2013-03-28 | 2015-04-16 | Sanofi Sa | 二芳基-丙酸衍生物及其作為醫藥之用途 |
| CN105073720B (zh) * | 2013-03-28 | 2017-10-13 | 赛诺菲 | 联芳基‑丙酸衍生物及其作为药物的用途 |
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| DE10143858A1 (de) | 2001-09-07 | 2003-03-27 | Degussa | Verfahren zur Herstellung von Enolaten von alpha-Ketoestern |
| FR2830192B1 (fr) | 2001-09-28 | 2004-08-20 | Oreal | Composition tinctoriale comprenant une base d'oxydation du type diaminopyrazole et un coupleur pyrazolo-azole |
| US20040072802A1 (en) | 2002-10-09 | 2004-04-15 | Jingwu Duan | Beta-amino acid derivatives as inhibitors of matrix metalloproteases and TNF-alpha |
| JP4585448B2 (ja) | 2002-12-23 | 2010-11-24 | サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 第Xa因子阻害剤としてのピラゾール−誘導体 |
| JP2005145839A (ja) | 2003-11-12 | 2005-06-09 | Japan Science & Technology Agency | 新規なカテプシンa阻害剤 |
| AU2006205220B2 (en) | 2005-01-10 | 2012-09-13 | Exelixis, Inc. | Heterocyclic carboxamide compounds as steroid nuclear receptors ligands |
| ATE553090T1 (de) * | 2005-07-06 | 2012-04-15 | Merck Canada Inc | Cathepsincysteinproteasehemmer |
| FR2908409B1 (fr) * | 2006-11-10 | 2009-01-09 | Sanofi Aventis Sa | Pyrazoles substituees,compositions les contenant,procede de fabrication et utilisation |
| EP2238127B1 (en) | 2007-12-26 | 2012-08-15 | Sanofi | Pyrazole-carboxamide derivatives as p2y12 antagonists |
| JP5504171B2 (ja) | 2007-12-26 | 2014-05-28 | サノフイ | P2y12アンタゴニストとしてのヘテロサイクリックピラゾール−カルボキサミド |
| WO2010012793A1 (en) * | 2008-08-01 | 2010-02-04 | Bayer Cropscience Sa | Fungicide aminothiazole derivatives |
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| Publication number | Publication date |
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| SG191828A1 (en) | 2013-08-30 |
| TWI523844B (zh) | 2016-03-01 |
| KR20140006916A (ko) | 2014-01-16 |
| CN103459374B (zh) | 2015-11-25 |
| RU2605600C2 (ru) | 2016-12-27 |
| AU2012210515B2 (en) | 2016-05-12 |
| EP2668167B1 (en) | 2014-12-17 |
| WO2012101199A1 (en) | 2012-08-02 |
| TW201240969A (en) | 2012-10-16 |
| MY161165A (en) | 2017-04-14 |
| US20120232112A1 (en) | 2012-09-13 |
| JP5957468B2 (ja) | 2016-07-27 |
| AU2012210515A1 (en) | 2013-08-15 |
| HK1187335A1 (en) | 2014-04-04 |
| CN103459374A (zh) | 2013-12-18 |
| MX2013007987A (es) | 2013-08-21 |
| IL227024A (en) | 2015-10-29 |
| US8962671B2 (en) | 2015-02-24 |
| EP2668167A1 (en) | 2013-12-04 |
| JP2014503572A (ja) | 2014-02-13 |
| BR112013018170A2 (pt) | 2018-09-18 |
| RU2013139352A (ru) | 2015-03-10 |
| CA2823277A1 (en) | 2012-08-02 |
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