AR058956A1 - Derivados de tiofeno agonistas de receptores s1p1/edg1, composiciones farmaceuticas que los contienen y usos como agentes inmunomoduladores. - Google Patents
Derivados de tiofeno agonistas de receptores s1p1/edg1, composiciones farmaceuticas que los contienen y usos como agentes inmunomoduladores.Info
- Publication number
- AR058956A1 AR058956A1 ARP070100083A ARP070100083A AR058956A1 AR 058956 A1 AR058956 A1 AR 058956A1 AR P070100083 A ARP070100083 A AR P070100083A AR P070100083 A ARP070100083 A AR P070100083A AR 058956 A1 AR058956 A1 AR 058956A1
- Authority
- AR
- Argentina
- Prior art keywords
- hydroxy
- ethyl
- alkyl
- represents hydrogen
- och2
- Prior art date
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- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/22—Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
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- 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
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Abstract
Reivindicacion 1: Un compuesto seleccionado del grupo que consiste en compuestos de tiofeno de la Formula (1), en donde A representa *-CO-CH=CH-,*-CO-CH2CH2-, *-CO-CH2-NH-,en donde los asteriscos indican el enlace que está unido al grupo tiofeno de la Formula (1); R1 representa hidrogeno, metilo, o trifluormetilo; R2 representa n-propilo, isobutilo, o ciclopropilmetilo; R3 representa hidrogeno, metilo, trifluormetilo, etilo, n-propilo, isopropilo, o isobutilo; R4 representa hidrogeno, alquilo C1-4, metoxi, o halogeno; R5 representa hidrogeno, alquilo C1-4, alcoxi C1-4, o halogeno; R6 representa hidroxi-alquilo C1-4, di-(hidroxi-alquil C1-)-alquilo C1-4, 2,3-dihidroxipropilo, -CH2-(CH2)n-NR61R62, -CH2-(CH2)n-NHCOR64, -CH2-(CH2)n- NHSO2R63, -(CH2)k-(CHR65)p-CHR66-CONR61R62, -(CH2)nCH(OH)-CH2-NR61R62, -(CH2)nCH(OH)-CH2-NHCOR64, -(CH2)nCH(OH)-CH2-NHSO2R63, -CO-NHR61, hidroxi, hidroxi-alcoxi C2-4, di-(hidroxi-alquil C1-4)-alcoxi C1-4, 1-glicerilo, 2,3-dihidroxipropoxi, 2- hidroxi-3-metoxi-propoxi, -OCH2-(CH2)mNR61 R62, -OCH2-(CH2)mNHCOR64, OCH2-(CH2)mNHSO2R63, -OCH2-CH(OH)-CH2-NR61R62, -OCH2-CH(OH)-CH2-NHCOR64, -OCH2-CH(OH)-CH2-NHSO2R63, -NR61R62, -NHCO-R64, o -SO2NH-R61; R61 representa hidrogeno, metilo, etilo, 2- hidroxietilo, 2-hidroxi-1-hidroximetil-etilo, 2,3-dihidroxi-propilo, 2-alcoxietilo C1-4, 3-hidroxipropilo, 3-alcoxipropilo C1-4, 2- aminoetilo, 2-(alquilamino C1-4)etilo, 2-(di-(alquil C1-4)amino)etilo, carboximetilo, alquilcarboximetilo C1-4, 2- carboxietilo, o 2-(alquilcarboxi C1- 4)etilo; R62 representa hidrogeno, o metilo; R63 representa metilo, etilo, 2-hidroxietilo, 2-metoxietilo, metilamino, etilamino, o dimetilamino; R64 representa hidroximetilo, aminometilo, metilaminometilo, dimetilaminometilo, 2-aminoetilo, o 2-metilamino-etilo; R65 representa hidrogeno; R66 representa hidrogeno o hidroxi; y en el caso que R66 represente hidroxi, R65 puede además representar hidroxi; m representa el entero 1 o 2; n representa 0, 1, o 2; k representa 0; p representa 0 o 1; y en el caso que p represente 1, k puede además representar 1; y R7 representa hidrogeno, alquilo C1-4, o halogeno; y las sales de los mismos.
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IB2006050103 | 2006-01-11 |
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AR058956A1 true AR058956A1 (es) | 2008-03-05 |
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ARP070100083A AR058956A1 (es) | 2006-01-11 | 2007-01-09 | Derivados de tiofeno agonistas de receptores s1p1/edg1, composiciones farmaceuticas que los contienen y usos como agentes inmunomoduladores. |
Country Status (17)
Country | Link |
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US (1) | US8003800B2 (es) |
EP (1) | EP1976512B1 (es) |
JP (1) | JP5114430B2 (es) |
KR (1) | KR101382710B1 (es) |
CN (1) | CN101370496B (es) |
AR (1) | AR058956A1 (es) |
AU (1) | AU2007204121B2 (es) |
BR (1) | BRPI0706476A2 (es) |
CA (1) | CA2635047C (es) |
ES (1) | ES2553345T3 (es) |
IL (1) | IL192657A (es) |
MY (1) | MY154909A (es) |
NO (1) | NO20083462L (es) |
NZ (1) | NZ570258A (es) |
RU (1) | RU2437877C2 (es) |
TW (1) | TWI404706B (es) |
WO (1) | WO2007080542A1 (es) |
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CN103119038B (zh) | 2010-04-23 | 2016-05-04 | 百时美施贵宝公司 | 作为1-磷酸鞘氨醇1受体激动剂的4-(5-异噁唑基或5-吡唑基-1,2,4-噁二唑基-3-基)扁桃酰胺 |
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JP5869579B2 (ja) | 2010-09-24 | 2016-02-24 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 置換オキサジアゾール化合物およびそれらのs1p1アゴニストとしての使用 |
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US10111841B2 (en) | 2015-06-19 | 2018-10-30 | University Of South Florida | Stabilization of alcohol intoxication-induced cardiovascular instability |
KR102603199B1 (ko) | 2015-06-22 | 2023-11-16 | 아레나 파마슈티칼스, 인크. | S1p1 수용체-관련 장애에서의 사용을 위한 (r)-2-(7-(4-시클로펜틸-3-(트리플루오로메틸)벤질옥시)-1,2,3,4-테트라히드로시클로-펜타[b]인돌-3-일)아세트산 (화합물 1)의 결정성 l-아르기닌 염 |
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GB0601744D0 (en) | 2006-01-27 | 2006-03-08 | Novartis Ag | Organic compounds |
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-
2007
- 2007-01-05 TW TW096100513A patent/TWI404706B/zh not_active IP Right Cessation
- 2007-01-09 AR ARP070100083A patent/AR058956A1/es unknown
- 2007-01-10 US US12/160,520 patent/US8003800B2/en not_active Expired - Fee Related
- 2007-01-10 ES ES07700562T patent/ES2553345T3/es active Active
- 2007-01-10 NZ NZ570258A patent/NZ570258A/en not_active IP Right Cessation
- 2007-01-10 EP EP07700562.7A patent/EP1976512B1/en active Active
- 2007-01-10 JP JP2008549960A patent/JP5114430B2/ja not_active Expired - Fee Related
- 2007-01-10 RU RU2008132802/04A patent/RU2437877C2/ru not_active IP Right Cessation
- 2007-01-10 AU AU2007204121A patent/AU2007204121B2/en not_active Ceased
- 2007-01-10 MY MYPI20082557A patent/MY154909A/en unknown
- 2007-01-10 WO PCT/IB2007/050070 patent/WO2007080542A1/en active Application Filing
- 2007-01-10 KR KR1020087018081A patent/KR101382710B1/ko not_active Expired - Fee Related
- 2007-01-10 BR BRPI0706476-4A patent/BRPI0706476A2/pt not_active IP Right Cessation
- 2007-01-10 CA CA2635047A patent/CA2635047C/en not_active Expired - Fee Related
- 2007-01-10 CN CN2007800022066A patent/CN101370496B/zh not_active Expired - Fee Related
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2008
- 2008-07-07 IL IL192657A patent/IL192657A/en not_active IP Right Cessation
- 2008-08-08 NO NO20083462A patent/NO20083462L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
RU2437877C2 (ru) | 2011-12-27 |
JP5114430B2 (ja) | 2013-01-09 |
NO20083462L (no) | 2008-10-09 |
BRPI0706476A2 (pt) | 2011-04-05 |
EP1976512A1 (en) | 2008-10-08 |
US8003800B2 (en) | 2011-08-23 |
WO2007080542A1 (en) | 2007-07-19 |
AU2007204121B2 (en) | 2012-06-07 |
US20100240717A1 (en) | 2010-09-23 |
MY154909A (en) | 2015-08-28 |
CA2635047C (en) | 2014-07-29 |
CA2635047A1 (en) | 2007-07-19 |
RU2008132802A (ru) | 2010-02-20 |
IL192657A (en) | 2015-09-24 |
AU2007204121A1 (en) | 2007-07-19 |
TW200804298A (en) | 2008-01-16 |
CN101370496B (zh) | 2012-07-04 |
ES2553345T3 (es) | 2015-12-07 |
JP2009523165A (ja) | 2009-06-18 |
IL192657A0 (en) | 2009-02-11 |
EP1976512B1 (en) | 2015-09-30 |
NZ570258A (en) | 2011-07-29 |
KR101382710B1 (ko) | 2014-04-08 |
KR20080083010A (ko) | 2008-09-12 |
CN101370496A (zh) | 2009-02-18 |
TWI404706B (zh) | 2013-08-11 |
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