AR044825A1 - Derivados de 5,6-diaril-pirazinas-2-carboxamida y -2-sulfonamidas -3-sustituidas como moduladores de cb1 - Google Patents
Derivados de 5,6-diaril-pirazinas-2-carboxamida y -2-sulfonamidas -3-sustituidas como moduladores de cb1Info
- Publication number
- AR044825A1 AR044825A1 ARP040102135A ARP040102135A AR044825A1 AR 044825 A1 AR044825 A1 AR 044825A1 AR P040102135 A ARP040102135 A AR P040102135A AR P040102135 A ARP040102135 A AR P040102135A AR 044825 A1 AR044825 A1 AR 044825A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- alkyl
- optionally substituted
- groups
- hydroxy
- Prior art date
Links
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 12
- 125000000623 heterocyclic group Chemical group 0.000 abstract 10
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 9
- 125000001153 fluoro group Chemical group F* 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 229920006395 saturated elastomer Chemical group 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- -1 carboxy, cyano, carbamoyl Chemical group 0.000 abstract 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 3
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000002252 acyl group Chemical group 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 3
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 abstract 1
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 abstract 1
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 abstract 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 abstract 1
- 125000006553 (C3-C8) cycloalkenyl group Chemical group 0.000 abstract 1
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004849 alkoxymethyl group Chemical group 0.000 abstract 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
- 150000003216 pyrazines Chemical class 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 abstract 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D241/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms
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- C07D—HETEROCYCLIC COMPOUNDS
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- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
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- 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
- C07D401/12—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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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
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- Veterinary Medicine (AREA)
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- Pharmacology & Pharmacy (AREA)
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- General Health & Medical Sciences (AREA)
- Public Health (AREA)
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- Neurosurgery (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Diabetes (AREA)
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- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
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- Oncology (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Compuestos de pirazina, procesos para preparar dichos compuestos, su uso en el tratamiento de la obesidad, trastornos psiquiátricos y neurológicos, y composiciones farmacéuticas que los contienen. Reivindicación 1: Un compuesto caracterizado porque responde a la fórmula (1) y sales aceptables para uso farmacéutico del mismo, en donde R1 y R2 representan en forma independiente fenilo, tienilo o piridilo donde cada uno de los cuales está sustituido opcionalmente en forma independiente con uno o más grupos representados por Z; Z representa un grupo C1-6 alquilo opcionalmente sustituido con uno o más hidroxi o por un grupo NR10R11 en donde R10 y R11 representan en forma independiente H, un grupo C1-6 alquilo, un grupo C1-6 alcanoilo, un grupo C1-6alcoxicarbonilo, o Z representa un grupo C3-8 cicloalquilo, un grupo C1-6 alcoxi, hidroxi, halo, trifluorometilo, trifluorometiltio,, trifluorometoxi, trifluorometilsulfonilo, nitro, mono o di C1-3 alquilamido, C1-3 alquiltio, C1-3alquilsulfonilo, C1-3 alquilsulfoniloxi, C1-3 alcoxicarbonilo, carboxi, ciano, carbamoilo, mono o di C1-3 alquilo carbamoilo, sulfamoilo, acetilo, un grupo aromático heterocíclico que está opcionalmente sustituido con uno o más halo, C1-4 alquilo, trifluorometilo o trifluorometoxi y un grupo heterocíclico saturado o parcialmente insaturado de entre 5 y 8 miembros que contiene uno o más heteroátomos seleccionados entre N, O o S donde el grupo heterocíclico está opcionalmente sustituido con uno o más grupos C1-3 alquilo, hidroxi, fluoro, bencilo o un grupo amino-NRxRy en donde Rx y Ry representan en forma independiente H o C1-4 alquilo; R3 representa un grupo de la fórmula X-Y-NR5R6 en donde X es CO o SO2 y Y está ausente o representa NH opcionalmente sustituido con un grupo C1-3 alquilo y R5 y R6 representan en forma independiente un grupo C1-6 alquilo opcionalmente sustituido con uno o más hidroxi; un grupo (amino)C1-4 alquilo en donde el amino está opcionalmente sustituido con uno o más grupos C1-3 alquilo; un grupo (C3-12 cicloalquil)(CH2)g- donde g es 0, 1, 2 o 3 donde el cicloalquilo está opcionalmente sustituido con uno o más fluoro, hidroxi, (C1-3) alquilo-(C1-3)alcoxi, trifluorometilo o trifluorometoxi; un grupo (CH2)r(fenil)s en donde r es 0, 1,2 3 o 4, s es 1 cuando r es 0, en caso contrario s es 1 0 2 y los grupos fenilo están sustituidos opcionalmente en forma independiente con uno o más grupos representados por Z; naftilo; antracenilo; un grupo heterocíclico saturado o parcialmente insaturado de entre 5 y 8 miembros que contiene uno o más heteroátomos seleccionados entre N, O, o S donde el grupo heterocíclico está opcionalmente sustituido con uno o más grupos C1-3 alquilo, hidroxi, fluoro, trifluorometilo, bencilo o un grupo amino-NRxRy en donde Rx y Ry representan en forma independiente H o C1-4 alquilo; 1-adamantilmetilo; un grupo (CH2)t Het en donde t es 0, 1, 2, 3 o 4, y la cadena alquileno está opcionalmente sustituida con uno o más grupos C1-3 alquilo y Het representa un grupo aromático heterocíclico opcionalmente sustituido con uno, dos o tres grupos seleccionados entre un grupo C1-5 alquilo, un grupo C1-5 alcoxi o halo; o R5 representa H y R6 tiene los valores que se han definido; o R5 y R6 junto con el átomo de N al cual están unidos representan un grupo heterocíclico saturado o parcialmente insaturado de entre 5 y 8 miembros que contiene un N y opcionalmente uno de los siguientes: O, S o un N adicional; donde el grupo heterocíclico está opcionalmente sustituido con uno o más grupos C1-3 alquilo, hidroxi, fluoro, trifluorometilo, trifluorometoxi, bencilo, C1-6 alcanoilo o un grupo amino-NRxRy en donde Rx y Ry representan en forma independiente H o C1-4 alquilo; R4 representa un grupo de la fórmula (CH2)nCOOR7 en donde n es 0, 1, 2, 3 o 4; y R7 representa un grupo C4-12 alquilo, un grupo C3-12 cicloalquilo o un grupo (C3-12)cicloalquil)C1-3 alquilo donde cada uno de los cuales está opcionalmente sustituido con uno o más de los siguientes: un grupo C1-6 alquilo; fluoro, amino o hidroxi, o R7 representa un grupo -(CH2)aféenlo en donde a es 0, 1, 2, 3 o 4 y el grupo fenilo está opcionalmente sustituido con uno o más grupos representados por Z que pueden ser iguales o diferentes o R7 representa un grupo heterocíclico saturado o parcialmente insaturado de entre 5 y 8 miembros que contiene uno o más de los siguientes: O, S o N; donde el grupo heterocíclico está opcionalmente sustituido con uno o más grupos C1-3 alquilo, C1-3 acilo, hidroxi, amino o bencilo; o R4 representa un grupo de la fórmula -(CH2)o-O-(CH2)pR8 en donde o y p representan en forma independiente un entero 0, 1, 2, 3 o 4 y cada una de las cadenas alquilo está sustituida opcionalmente en forma independiente con uno o más grupos C1-6 alquilo, grupos C1-6 alcoxi o hidroxi y R8 representa un grupo C1-12 alquilo o un grupo C1-12 alcoxi o R8 representa fenilo sustituido opcionalmente en forma independiente con uno o más grupos Z o R8 representa un grupo aromático heterocíclico o un grupo heterocíclico saturado o parcialmente insaturado de entre 5 y 8 miembros que contiene uno o más de los siguientes: O, S o N donde cada uno de estos anillos está opcionalmente sustituido con uno o más grupos representados por Z que pueden ser iguales o diferentes; con la condición de que R4 no es un grupo C1-3 alcoximetilo salvo que R3 represente un grupo de la fórmula X-Y-NR5R6 en donde X es CO y Y esté ausente y R5 sea H y R6 sea un grupo C3-8 cicloalquilo sustituido con uno o más fluoro o X sea CO y Y sea NH y NR5R6 juntos representen un grupo piperidino sustituido con uno o más fluoro; o R8 representa un grupo C3-8 cicloalquilo o un grupo C3-8 cicloalquenilo opcionalmente sustituido con uno o más grupos representados por Z que pueden ser iguales o diferentes; R4 representa un grupo C4-12 alquilo opcionalmente sustituido con uno o más fluoro, hidroxi, o amino; o R4 representa un grupo de la fórmula -(CH2)gR9 en donde g es 0, 1, 2, 3 o 4 y R9 representa un grupo C3-12 cicloalquilo, un grupo C3-12 cicloalquenilo, fenilo, un grupo aromático heterocíclico o u grupo heterocíclico saturado o parcialmente insaturado de entre 5 y 8 miembros que contiene uno o más de los siguientes: O, S o N donde cada uno de estos anillos está opcionalmente sustituido con uno o más grupos representados por Z que pueden ser iguales o diferentes; o R4 representa un grupo de la fórmula -L1R9 en donde L1 representa una cadena C2-6 alquenileno opcionalmente sustituida con uno o más grupos C1-4 alquilo y R9 tiene los valores que se han definido; o R4 representa un grupo de la fórmula -(CH2)m O-(CO)-R10 en donde m representa un entero 0, 1, 2, 3 o 4, en donde R10 representa un grupo C1-12 alquilo opcionalmente sustituido con uno o más fluoro, hidroxi, o amino o R10 representa un grupo de la fórmula -(CH2)gR9 en donde g y R9 tienen los valores que se han descrito; o R4 representa un grupo de la fórmula CONR11R12 en donde R11 y R12 representan en forma independiente H o un grupo C1-8 alquilo o un grupo C1-8 alquilo sustituido con uno o más grupos hidroxi con la condición de que al menos uno de R11 y R12 sea un grupo hidroxi C1-8 alquilo; o R4 representa un grupo de la fórmula -L2CN en donde L2 representa una cadena C1-6 alquileno.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0314057.1A GB0314057D0 (en) | 2003-06-18 | 2003-06-18 | Therapeutic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR044825A1 true AR044825A1 (es) | 2005-10-05 |
Family
ID=27636738
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040102135A AR044825A1 (es) | 2003-06-18 | 2004-06-18 | Derivados de 5,6-diaril-pirazinas-2-carboxamida y -2-sulfonamidas -3-sustituidas como moduladores de cb1 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US20070093484A1 (es) |
| EP (1) | EP1638953B1 (es) |
| JP (1) | JP2006527771A (es) |
| KR (1) | KR20060023152A (es) |
| CN (1) | CN1809554A (es) |
| AR (1) | AR044825A1 (es) |
| AT (1) | ATE406361T1 (es) |
| AU (1) | AU2004247616A1 (es) |
| BR (1) | BRPI0411508A (es) |
| CA (1) | CA2527035A1 (es) |
| DE (1) | DE602004016158D1 (es) |
| ES (1) | ES2311159T3 (es) |
| GB (1) | GB0314057D0 (es) |
| IL (1) | IL171983A0 (es) |
| IS (1) | IS8226A (es) |
| MX (1) | MXPA05013711A (es) |
| NO (1) | NO20055919L (es) |
| RU (1) | RU2005138365A (es) |
| TW (1) | TW200524605A (es) |
| UY (1) | UY28376A1 (es) |
| WO (1) | WO2004111034A1 (es) |
| ZA (1) | ZA200510101B (es) |
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| WO2004029204A2 (en) | 2002-09-27 | 2004-04-08 | Merck & Co., Inc. | Substituted pyrimidines |
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| GB0230087D0 (en) * | 2002-12-24 | 2003-01-29 | Astrazeneca Ab | Therapeutic agents |
| GB0302672D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
| GB0302671D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
| US20060135523A1 (en) * | 2003-06-18 | 2006-06-22 | Astrazeneca Ab | 2-substituted 5,6-diaryl-pyrazine derivatives as cb1 modulator |
| GB0314261D0 (en) * | 2003-06-19 | 2003-07-23 | Astrazeneca Ab | Therapeutic agents |
| ES2326280T3 (es) | 2005-04-06 | 2009-10-06 | F. Hoffmann-La Roche Ag | Derivados de piridin-3-carboxamida como agonistas inversos de cb1. |
| TW200716594A (en) * | 2005-04-18 | 2007-05-01 | Neurogen Corp | Substituted heteroaryl CB1 antagonists |
| TW200804338A (en) * | 2005-11-24 | 2008-01-16 | Astrazeneca Ab | New compounds |
| US7629346B2 (en) | 2006-06-19 | 2009-12-08 | Hoffmann-La Roche Inc. | Pyrazinecarboxamide derivatives as CB1 antagonists |
| US7781593B2 (en) | 2006-09-14 | 2010-08-24 | Hoffmann-La Roche Inc. | 5-phenyl-nicotinamide derivatives |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| FR2922209B1 (fr) | 2007-10-12 | 2010-06-11 | Sanofi Aventis | 5,6-DIARYLES PYRIDINES SUBSTITUES EN POSITION 2 et 3, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE. |
| CA2741125A1 (en) | 2008-10-22 | 2010-04-29 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| WO2010051206A1 (en) | 2008-10-31 | 2010-05-06 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| US8895596B2 (en) | 2010-02-25 | 2014-11-25 | Merck Sharp & Dohme Corp | Cyclic benzimidazole derivatives useful as anti-diabetic agents |
| US8410107B2 (en) | 2010-10-15 | 2013-04-02 | Hoffmann-La Roche Inc. | N-pyridin-3-yl or N-pyrazin-2-yl carboxamides |
| US8669254B2 (en) | 2010-12-15 | 2014-03-11 | Hoffman-La Roche Inc. | Pyridine, pyridazine, pyrimidine or pyrazine carboxamides as HDL-cholesterol raising agents |
| BR112013021236B1 (pt) | 2011-02-25 | 2021-05-25 | Merck Sharp & Dohme Corp | composto derivado de benzimidazol, e, composição |
| WO2012120057A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US9403808B2 (en) * | 2011-10-28 | 2016-08-02 | Hoffmann-La Roche Inc. | Pyrazine derivatives |
| US9527875B2 (en) | 2012-08-02 | 2016-12-27 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
| MX2015010935A (es) | 2013-02-22 | 2015-10-29 | Merck Sharp & Dohme | Compuestos biciclicos antidiabeticos. |
| US9650375B2 (en) | 2013-03-14 | 2017-05-16 | Merck Sharp & Dohme Corp. | Indole derivatives useful as anti-diabetic agents |
| WO2015051496A1 (en) | 2013-10-08 | 2015-04-16 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
| TWI806832B (zh) | 2016-07-12 | 2023-07-01 | 美商銳新醫藥公司 | 作為異位shp2抑制劑之2,5-雙取代型3-甲基吡嗪及2,5,6-三取代型3-甲基吡嗪 |
| EP3551176A4 (en) | 2016-12-06 | 2020-06-24 | Merck Sharp & Dohme Corp. | Antidiabetic heterocyclic compounds |
| AU2018210770B2 (en) | 2017-01-23 | 2022-03-24 | Revolution Medicines, Inc. | Bicyclic compounds as allosteric SHP2 inhibitors |
| BR112019014527A2 (pt) | 2017-01-23 | 2020-02-27 | Revolution Medicines, Inc. | Compostos de piridina como inibidores de shp2 alostéricos |
| SG11202001282UA (en) | 2017-09-07 | 2020-03-30 | Revolution Medicines Inc | Shp2 inhibitor compositions and methods for treating cancer |
| BR112020007058A2 (pt) | 2017-10-12 | 2020-10-06 | Revolution Medicines, Inc. | compostos de piridina, pirazina, e triazina como inibidores de shp2 alostéricos |
| WO2019118909A1 (en) | 2017-12-15 | 2019-06-20 | Revolution Medicines, Inc. | Polycyclic compounds as allosteric shp2 inhibitors |
| CN118978535A (zh) | 2018-05-01 | 2024-11-19 | 锐新医药公司 | 作为mTOR抑制剂的C40-、C28-及C-32连接的雷帕霉素类似物 |
| AR131658A1 (es) * | 2023-01-30 | 2025-04-16 | Eurofarma Laboratorios S A | Hidrazidas bloqueadoras de nav 1.7 y/o nav 1.8, sus procesos de obtención, composiciones, usos, métodos de tratamiento de los mismos y sus kits |
| CN118852308B (zh) * | 2024-09-24 | 2024-12-10 | 德州学院 | 一种红光发射凝胶因子、纤维状凝胶软材料及其制备方法和应用 |
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| GB9319129D0 (en) * | 1993-09-15 | 1993-11-03 | Dowelanco Ltd | Storage and dilution of stable aqueous dispersions |
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| SE9403846D0 (sv) * | 1994-11-09 | 1994-11-09 | Univ Ohio State Res Found | Small particle formation |
| DE4440337A1 (de) * | 1994-11-11 | 1996-05-15 | Dds Drug Delivery Services Ges | Pharmazeutische Nanosuspensionen zur Arzneistoffapplikation als Systeme mit erhöhter Sättigungslöslichkeit und Lösungsgeschwindigkeit |
| US5665331A (en) * | 1995-01-10 | 1997-09-09 | Nanosystems L.L.C. | Co-microprecipitation of nanoparticulate pharmaceutical agents with crystal growth modifiers |
| AU4807197A (en) * | 1996-10-03 | 1998-04-24 | Paul Bunn | Hydrophilic microparticles and methods to prepare same |
| US6127520A (en) * | 1997-04-15 | 2000-10-03 | Regents Of The University Of Michigan | Compositions and methods for the inhibition of neurotransmitter uptake of synaptic vesicles |
| FR2766368B1 (fr) * | 1997-07-24 | 2000-03-31 | Univ Claude Bernard Lyon | Procede de preparation de nanocapsules de type vesiculaire, utilisables notamment comme vecteurs colloidaux de principes actifs pharmaceutiques ou autres |
| US6375986B1 (en) * | 2000-09-21 | 2002-04-23 | Elan Pharma International Ltd. | Solid dose nanoparticulate compositions comprising a synergistic combination of a polymeric surface stabilizer and dioctyl sodium sulfosuccinate |
| FR2789079B3 (fr) * | 1999-02-01 | 2001-03-02 | Sanofi Synthelabo | Derive d'acide pyrazolecarboxylique, sa preparation, les compositions pharmaceutiques en contenant |
| US6383471B1 (en) * | 1999-04-06 | 2002-05-07 | Lipocine, Inc. | Compositions and methods for improved delivery of ionizable hydrophobic therapeutic agents |
| PT1268435E (pt) * | 2000-03-23 | 2007-02-28 | Solvay Pharm Bv | Derivados de 4,5-diidro-1h-pirazol tendo actividade cb1-antagonista |
| ES2287293T3 (es) * | 2001-08-06 | 2007-12-16 | Astrazeneca Ab | Dispersion acuosa que comprende nanoparticulas estables de trigliceridos de cadena media (mct) activos, insolubles en agua y de tipo excipiente. |
| US20060003012A9 (en) * | 2001-09-26 | 2006-01-05 | Sean Brynjelsen | Preparation of submicron solid particle suspensions by sonication of multiphase systems |
| SE0104332D0 (sv) * | 2001-12-19 | 2001-12-19 | Astrazeneca Ab | Therapeutic agents |
| SE0104330D0 (sv) * | 2001-12-19 | 2001-12-19 | Astrazeneca Ab | Therapeutic agents |
| GB0216700D0 (en) * | 2002-07-18 | 2002-08-28 | Astrazeneca Ab | Process |
| GB0302671D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
| GB0302673D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
| GB0302672D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
| US20060135523A1 (en) * | 2003-06-18 | 2006-06-22 | Astrazeneca Ab | 2-substituted 5,6-diaryl-pyrazine derivatives as cb1 modulator |
| GB0314261D0 (en) * | 2003-06-19 | 2003-07-23 | Astrazeneca Ab | Therapeutic agents |
-
2003
- 2003-06-18 GB GBGB0314057.1A patent/GB0314057D0/en not_active Ceased
-
2004
- 2004-06-16 BR BRPI0411508-2A patent/BRPI0411508A/pt not_active Application Discontinuation
- 2004-06-16 RU RU2005138365/04A patent/RU2005138365A/ru not_active Application Discontinuation
- 2004-06-16 CN CNA2004800172002A patent/CN1809554A/zh active Pending
- 2004-06-16 US US10/560,862 patent/US20070093484A1/en not_active Abandoned
- 2004-06-16 KR KR1020057024072A patent/KR20060023152A/ko not_active Withdrawn
- 2004-06-16 JP JP2006517044A patent/JP2006527771A/ja not_active Withdrawn
- 2004-06-16 WO PCT/SE2004/000970 patent/WO2004111034A1/en not_active Ceased
- 2004-06-16 ES ES04749012T patent/ES2311159T3/es not_active Expired - Lifetime
- 2004-06-16 EP EP04749012A patent/EP1638953B1/en not_active Expired - Lifetime
- 2004-06-16 AU AU2004247616A patent/AU2004247616A1/en not_active Abandoned
- 2004-06-16 DE DE602004016158T patent/DE602004016158D1/de not_active Expired - Fee Related
- 2004-06-16 MX MXPA05013711A patent/MXPA05013711A/es unknown
- 2004-06-16 AT AT04749012T patent/ATE406361T1/de not_active IP Right Cessation
- 2004-06-16 CA CA002527035A patent/CA2527035A1/en not_active Abandoned
- 2004-06-18 UY UY28376A patent/UY28376A1/es unknown
- 2004-06-18 TW TW093117694A patent/TW200524605A/zh unknown
- 2004-06-18 AR ARP040102135A patent/AR044825A1/es unknown
-
2005
- 2005-11-15 IL IL171983A patent/IL171983A0/en unknown
- 2005-12-12 ZA ZA200510101A patent/ZA200510101B/en unknown
- 2005-12-13 NO NO20055919A patent/NO20055919L/no not_active Application Discontinuation
-
2006
- 2006-01-11 IS IS8226A patent/IS8226A/is unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN1809554A (zh) | 2006-07-26 |
| KR20060023152A (ko) | 2006-03-13 |
| IL171983A0 (en) | 2006-04-10 |
| JP2006527771A (ja) | 2006-12-07 |
| TW200524605A (en) | 2005-08-01 |
| ATE406361T1 (de) | 2008-09-15 |
| EP1638953B1 (en) | 2008-08-27 |
| HK1088003A1 (en) | 2006-10-27 |
| ZA200510101B (en) | 2006-12-27 |
| CA2527035A1 (en) | 2004-12-23 |
| WO2004111034A1 (en) | 2004-12-23 |
| EP1638953A1 (en) | 2006-03-29 |
| IS8226A (is) | 2006-01-11 |
| ES2311159T3 (es) | 2009-02-01 |
| US20070093484A1 (en) | 2007-04-26 |
| MXPA05013711A (es) | 2006-03-08 |
| UY28376A1 (es) | 2005-01-31 |
| DE602004016158D1 (de) | 2008-10-09 |
| RU2005138365A (ru) | 2006-07-27 |
| GB0314057D0 (en) | 2003-07-23 |
| NO20055919L (no) | 2006-02-16 |
| BRPI0411508A (pt) | 2006-07-25 |
| AU2004247616A1 (en) | 2004-12-23 |
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