AR077316A2 - Compuestos heterociclicos apropiados para tratar trastornos que responden a la modulacion del receptor de serotonina 5ht6 - Google Patents
Compuestos heterociclicos apropiados para tratar trastornos que responden a la modulacion del receptor de serotonina 5ht6Info
- Publication number
- AR077316A2 AR077316A2 ARP100102573A ARP100102573A AR077316A2 AR 077316 A2 AR077316 A2 AR 077316A2 AR P100102573 A ARP100102573 A AR P100102573A AR P100102573 A ARP100102573 A AR P100102573A AR 077316 A2 AR077316 A2 AR 077316A2
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- fluorinated
- alkoxy
- halogen
- radical
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 7
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- -1 pyridylsulfonyl Chemical group 0.000 abstract 4
- 150000003254 radicals Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 3
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 abstract 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 2
- 108010081348 HRT1 protein Hairy Proteins 0.000 abstract 2
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 abstract 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 abstract 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 abstract 1
- 101100097467 Arabidopsis thaliana SYD gene Proteins 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 101100495925 Schizosaccharomyces pombe (strain 972 / ATCC 24843) chr3 gene Proteins 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 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
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- UHCBBWUQDAVSMS-UHFFFAOYSA-N fluoroethane Chemical compound CCF UHCBBWUQDAVSMS-UHFFFAOYSA-N 0.000 abstract 1
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 abstract 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
- C07D207/09—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
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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
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
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- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- 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
- C07D211/08—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
- C07D211/28—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms to which a second hetero atom is attached
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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
- C07D401/12—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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- 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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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Psychology (AREA)
- Diabetes (AREA)
- Anesthesiology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
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- Urology & Nephrology (AREA)
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- Hospice & Palliative Care (AREA)
- Nutrition Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Métodos de preparacion, composiciones farmacéuticas y uso de los mismos. Reivindicacion 1: Un compuesto de la formula 1 caracterizado porque n es 0,1 o 2; G es CH2 o CHR3; R1 es H, alquilo C1-6, alquilo C1-6 sustituido por cicloalquilo C3-6, hidroxialquilo C1-6, alquilo fluorado C1-6, cicloalquilo C3-6, cicloalquilo fluorado C3-6, alquenilo C3-6, alquenilo fluorado C3-6, formilo, acetilo, propionilo o bencilo; R2, R3 y R4 son, en forma independiente entre sí, H, metilo, fluorometilo, difluorometilo, o trifluorometilo; A es 1,4-fenileno o 1,3-fenileno, que es opcionalmente sustituido por uno, dos, tres o cuatro sustituyentes seleccionados entre halogeno, alquilo C1-4, alcoxi C1-4, alquilo fluorado C1-4 y alcoxi fluorado C1-4; E es NR5 o CH2, en donde R5 es H o alquilo C1-3; Ar es un radical de la formula A, B, C, D, E, F o G en donde Ra es halogeno, hidroxilo, alquilo C1-6, alquilo fluorado C1-6, hidroxialquilo C1-6, alcoxi C1-6-alquilo C1-6, alquenilo C2-6, alquenilo fluorado C2-6, cicloalquilo C3-6, cicloalquilo fluorado C3-6, alcoxi C1-6, hidroxialcoxi C1-6, alcoxi C1-6-alcoxi C1-6, alcoxi C1-6 fluorado, alquiltio C1-6, alquiltio fluorado C1-6, alquilsulfinilo C1-6, alquilsulfinilo fluorado C1-6, alquilsulfonilo C1-6, alquilsulfonilo fluorado C1-6, fenilsulfonilo, piridilsulfonilo, benciloxi, fenoxi, fenilo, donde el fenilo y el radical piridilo en los ultimos 5 radicales pueden no estar sustituidos o pueden tener entre 1 y 3 sustituyentes seleccionados entre alquilo C1-4, alquilo fluorado C1-4 y halogeno, CN, nitro, alquilcarbonilo C1-6, alquilcarbonilo fluorado C1-6, alquilcarbonilamino C1-6, alquilcarbonilamino fluorado C1-6, carboxi, NH-C(O)-NR6R7, NR6R7, NR6R7-C1-6-alquileno, O-NR6R7, donde R6 y R7 son, en forma independiente entre sí, H, alquilo C1-4, alquilo fluorado C1-4 o alcoxi C1-4 o pueden formar, junto con N, un anillo saturado o insaturado de 4, 5, o 6 miembros, R9-CO-NR6-C1-6-alquileno, donde R6 tiene los valores que se han definido y R9 es alquilo C1-4 o fenilo, donde el radical fenilo puede no estar sustituido o puede tener entre 1 y 3 sustituyentes seleccionados entre alquilo C1-4, alquilo fluorado C1-4 y halogeno, CH2-piridilo, donde el radical piridilo puede no estar sustituido o puede tener entre 1 y 3 sustituyentes seleccionados entre alquilo C1-4, alquilo fluorado C1-4 y halogeno, o es un anillo heterocíclico saturado o insaturado, aromático o no aromático de 3 a 7 miembros que comprende como miembros del anillo 1, 2, 3 o 4 heteroátomos seleccionados entre N, O y S y/o 1, 2 o 3 grupos que contienen heteroátomos seleccionados entre NR8, donde R8 es H, alquilo C1-4, alquilo fluorado C1-4, alquilcarbonilo C1-4 o alquilcarbonilo fluorado C1-4, SO, SO2 y CO, y donde el heterociclo puede tener 1, 2 o 3 sustituyentes seleccionados entre hidroxi, halogeno, alquilo C1-6, alquilo fluorado C1-6, alcoxi C1-6, alcoxi fluorado C1-6, alquiltio C1-6, alquiltio fluorado C1-6, NR6R7-C1-6-alquileno, donde R6 y R7 tienen los valores que se han definido, carboxilo y alquiloxicarbonilo C1-4; Rb y Rc, en forma independiente entre sí, son H, halogeno, CH3, OCH3, CH2F, OCH2F, CHF2, OCHF2, CF3, OCF3, CH2CH2F, OCH2CH2F, CH2CHF2, OCH2CHF2, CH2CF3 o OCH2CF3; Rd se define como Ra; Re es H o se define como Ra; Rf se define como Ra; k es 0, 1, 2 o 3; y j es 0, 1, 2, 3 o 4; con la salvedad de que Ra no es F, CH2F, CHF2, CF3 o OCF3 si A es 1,4-fenileno, Ar es un radical de la formula (A) y Rb y Rc son H o halogeno; excepto los compuestos, donde R1 es propilo, G es CH2, n es 1, A es 1,4-fenileno, E es NH, Ar es un radical de formula (F) y Rd es halogeno, alquilo C1-6, alquenilo C2-6 o un atillo heteroaromático de 5 miembros; y sales de adicion ácida de los mismos toleradas fisiologicamente.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79313906P | 2006-04-19 | 2006-04-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR077316A2 true AR077316A2 (es) | 2011-08-17 |
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
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| ARP070101658A AR060526A1 (es) | 2006-04-19 | 2007-04-18 | Compuestos heterociclicos para tratar trastornos que responden a la modulacion del receptor de serotonina 5ht6 |
| ARP100102573A AR077316A2 (es) | 2006-04-19 | 2010-07-15 | Compuestos heterociclicos apropiados para tratar trastornos que responden a la modulacion del receptor de serotonina 5ht6 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
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| ARP070101658A AR060526A1 (es) | 2006-04-19 | 2007-04-18 | Compuestos heterociclicos para tratar trastornos que responden a la modulacion del receptor de serotonina 5ht6 |
Country Status (19)
| Country | Link |
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| US (1) | US8642642B2 (es) |
| EP (1) | EP2029528A1 (es) |
| JP (1) | JP2009534354A (es) |
| KR (1) | KR20080112394A (es) |
| CN (1) | CN101421234A (es) |
| AR (2) | AR060526A1 (es) |
| AU (1) | AU2007239494A1 (es) |
| BR (1) | BRPI0710177A2 (es) |
| CA (1) | CA2648891A1 (es) |
| CR (1) | CR10371A (es) |
| DO (1) | DOP2007000077A (es) |
| EC (1) | ECSP088826A (es) |
| MX (1) | MX2008013434A (es) |
| NZ (1) | NZ572761A (es) |
| PE (1) | PE20080191A1 (es) |
| RU (1) | RU2451012C2 (es) |
| TW (1) | TW200812961A (es) |
| UY (1) | UY30295A1 (es) |
| WO (1) | WO2007118899A1 (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ555123A (en) * | 2004-10-14 | 2011-01-28 | Abbott Gmbh & Co Kg | Heterocyclic compounds suitable for treating disorders that respond to modulation of the dopamine D3 receptor |
| ATE495153T1 (de) * | 2006-11-09 | 2011-01-15 | Hoffmann La Roche | Arylsulfonylpyrrolidine als 5-ht6-inhibitoren |
| WO2009109042A1 (en) * | 2008-03-06 | 2009-09-11 | Horbay Roger P | A system, method and computer program for retention and optimization of gaming revenue and amelioration of negative gaming behaviour |
| KR20120016639A (ko) * | 2009-04-30 | 2012-02-24 | 애보트 게엠베하 운트 콤파니 카게 | 세로토닌 5-ht6 수용체의 조절에 반응하는 장애를 치료하는 데 적합한 n-페닐-(피페라지닐 또는 호모피페라지닐)-벤젠설폰아미드 또는 벤젠설포닐-페닐-(피페라진 또는 호모피페라진) 화합물 |
| WO2012059432A1 (en) | 2010-11-01 | 2012-05-10 | Abbott Gmbh & Co. Kg | N-phenyl-(homo)piperazinyl-benzenesulfonyl or benzenesulfonamide compounds suitable for treating disorders that respond to the modulation of the 5-ht6 receptor |
| WO2012059431A1 (en) | 2010-11-01 | 2012-05-10 | Abbott Gmbh & Co. Kg | Benzenesulfonyl or sulfonamide compounds suitable for treating disorders that respond to the modulation of the serotonin 5-ht6 receptor |
| PL395470A1 (pl) * | 2011-06-29 | 2013-01-07 | Adamed Spólka Z Ograniczona Odpowiedzialnoscia | Sulfonamidowe pochodne amin alicyklicznych do leczenia chorób osrodkowego ukladu nerwowego |
| CN106902112B (zh) * | 2017-03-07 | 2019-06-04 | 中国医学科学院医药生物技术研究所 | Imb-a6作为雄激素受体拮抗剂的应用 |
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| AU7513494A (en) | 1993-08-06 | 1995-02-28 | Upjohn Company, The | 2-aminoindans as selective dopamine d3 ligands |
| DK0807101T3 (da) | 1995-02-01 | 2001-09-10 | Upjohn Co | 2-Aminoindaner som selektive dopamin-D3-ligander |
| US5646180A (en) * | 1995-12-05 | 1997-07-08 | Vertex Pharmaceuticals Incorporated | Treatment of the CNS effects of HIV |
| ES2192677T3 (es) | 1996-05-30 | 2003-10-16 | Baker Hughes Inc | Control de la corrosion por el acido naptenico con compuestos de tiofosforo. |
| DZ2376A1 (fr) | 1996-12-19 | 2002-12-28 | Smithkline Beecham Plc | Dérivés de sulfonamides nouveaux procédé pour leurpréparation et compositions pharmaceutiques les c ontenant. |
| TW450954B (en) | 1998-05-14 | 2001-08-21 | Pharmacia & Amp Upjohn Company | Phenylsulfonamide-phenylethylamines useful as dopamine receptors |
| BR9912299A (pt) | 1998-07-20 | 2001-11-20 | Merck Patent Gmbh | Derivados de bifenila |
| US20040127502A1 (en) * | 2001-01-31 | 2004-07-01 | Synaptic Pharmaceutical Corporation | Use of GAL3 antagonist for treatment of depression |
| WO2002083863A2 (en) * | 2001-04-17 | 2002-10-24 | Sepracor, Inc. | Thiazole and other heterocyclic ligands and use thereof |
| EP1406884A1 (en) * | 2001-05-11 | 2004-04-14 | Biovitrum Ab | Arylsusfonamide compounds for the treatment of obesity, type ii diabetes and cns-disorders |
| GB0321473D0 (en) | 2003-09-12 | 2003-10-15 | Glaxo Group Ltd | Novel compounds |
| WO2005037830A1 (en) | 2003-10-10 | 2005-04-28 | Wyeth | Piperidinylchromen-6-ylsulfonamide compounds as 5-hydroxytryptamine-6 ligands |
| GB0411421D0 (en) | 2004-05-21 | 2004-06-23 | Glaxo Group Ltd | Novel compounds |
| NZ555123A (en) * | 2004-10-14 | 2011-01-28 | Abbott Gmbh & Co Kg | Heterocyclic compounds suitable for treating disorders that respond to modulation of the dopamine D3 receptor |
| KR100909318B1 (ko) | 2004-12-16 | 2009-07-24 | 에프. 호프만-라 로슈 아게 | 항비만제로서 피페라지닐 피리딘 유도체 |
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| WO2006096439A2 (en) * | 2005-03-04 | 2006-09-14 | Boehringer Ingelheim International Gmbh | Pharmaceutical compositions for the treatment and/or prevention of schizophrenia and related diseases |
| US8497273B2 (en) * | 2006-04-19 | 2013-07-30 | Abbott Gmbh & Co. Kg | Heterocyclic compounds suitable for treating disorders that respond to modulation of the serotonin 5HT6 receptor |
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2007
- 2007-04-18 PE PE2007000479A patent/PE20080191A1/es not_active Application Discontinuation
- 2007-04-18 CA CA002648891A patent/CA2648891A1/en not_active Abandoned
- 2007-04-18 US US12/297,350 patent/US8642642B2/en active Active
- 2007-04-18 KR KR1020087028322A patent/KR20080112394A/ko not_active Ceased
- 2007-04-18 RU RU2008145597/04A patent/RU2451012C2/ru not_active IP Right Cessation
- 2007-04-18 MX MX2008013434A patent/MX2008013434A/es not_active Application Discontinuation
- 2007-04-18 NZ NZ572761A patent/NZ572761A/en not_active IP Right Cessation
- 2007-04-18 DO DO2007000077A patent/DOP2007000077A/es unknown
- 2007-04-18 EP EP07728269A patent/EP2029528A1/en not_active Withdrawn
- 2007-04-18 AU AU2007239494A patent/AU2007239494A1/en not_active Abandoned
- 2007-04-18 BR BRPI0710177-5A patent/BRPI0710177A2/pt not_active IP Right Cessation
- 2007-04-18 CN CNA2007800135172A patent/CN101421234A/zh active Pending
- 2007-04-18 JP JP2009505887A patent/JP2009534354A/ja active Pending
- 2007-04-18 TW TW096113699A patent/TW200812961A/zh unknown
- 2007-04-18 UY UY30295A patent/UY30295A1/es not_active Application Discontinuation
- 2007-04-18 AR ARP070101658A patent/AR060526A1/es not_active Application Discontinuation
- 2007-04-18 WO PCT/EP2007/053807 patent/WO2007118899A1/en not_active Ceased
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2008
- 2008-10-16 EC EC2008008826A patent/ECSP088826A/es unknown
- 2008-10-16 CR CR10371A patent/CR10371A/es not_active Application Discontinuation
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2010
- 2010-07-15 AR ARP100102573A patent/AR077316A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US8642642B2 (en) | 2014-02-04 |
| DOP2007000077A (es) | 2008-01-15 |
| PE20080191A1 (es) | 2008-03-10 |
| EP2029528A1 (en) | 2009-03-04 |
| KR20080112394A (ko) | 2008-12-24 |
| US20090306175A1 (en) | 2009-12-10 |
| CN101421234A (zh) | 2009-04-29 |
| CR10371A (es) | 2008-12-11 |
| NZ572761A (en) | 2011-09-30 |
| WO2007118899A1 (en) | 2007-10-25 |
| RU2008145597A (ru) | 2010-05-27 |
| ECSP088826A (es) | 2008-11-27 |
| CA2648891A1 (en) | 2007-10-25 |
| TW200812961A (en) | 2008-03-16 |
| AR060526A1 (es) | 2008-06-25 |
| AU2007239494A1 (en) | 2007-10-25 |
| JP2009534354A (ja) | 2009-09-24 |
| MX2008013434A (es) | 2009-01-26 |
| UY30295A1 (es) | 2007-11-30 |
| RU2451012C2 (ru) | 2012-05-20 |
| BRPI0710177A2 (pt) | 2012-05-29 |
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