RU2013127155A - Новые замещенные бициклические ароматические соединения в качестве ингибиторов s-нитрозоглутатион-редуктазы - Google Patents
Новые замещенные бициклические ароматические соединения в качестве ингибиторов s-нитрозоглутатион-редуктазы Download PDFInfo
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- RU2013127155A RU2013127155A RU2013127155/04A RU2013127155A RU2013127155A RU 2013127155 A RU2013127155 A RU 2013127155A RU 2013127155/04 A RU2013127155/04 A RU 2013127155/04A RU 2013127155 A RU2013127155 A RU 2013127155A RU 2013127155 A RU2013127155 A RU 2013127155A
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- hydroxynaphthalen
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- benzoic acid
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- 0 CC(C)=CC(C)=CC=C(*)N Chemical compound CC(C)=CC(C)=CC=C(*)N 0.000 description 3
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Abstract
1. Соединение Формулы 1:Формула 1где Rвыбран из группы, состоящей из Н, F и Cl;Rи Rнезависимо выбраны из группы, состоящей из Н, F, Cl, Br, Me, ОСНи циано;Rвыбран из группы, состоящей из Н, F, Cl, Br, Me и ОСН;Х выбран из группы, состоящей из,,,,,,,,,,, и;А выбран из группы, состоящей из,,,,,,, и;Rвыбран из группы, состоящей из F, Cl, Br, СН, CF, ОСН, циано, N(СН)и морфолино;n выбран из группы, состоящей из 0, 1 и 2;Rвыбран из группы, состоящей из Н, F, Cl, Br, СН, CF, ОСН, циано, N(СН)и морфолино;при условии, что если Х является, а A является СООН, то по меньшей мере один из R, R, R, Rи Rне является водородом, или n должен быть >0, и R, будучи в мета-положении к нафталину, не может быть СН.2. Соединение по п.1, отличающееся тем, чтоХ выбран из группы, состоящей из,,, и.3. Соединение по п.1, отличающееся тем, что Х является.4. Соединение по п.3, отличающееся тем, что Rявляется водородом.5. Соединение по п.3, отличающееся тем, что Rявляется водородом.6. Соединение по п.1, отличающееся тем, что соединением является соединение Формулы 2Формула 27. Соединение по п.6, отличающееся тем, чтоRвыбран из группы, состоящей из Н и F;Rвыбран из группы, состоящей из Н, F, Cl, Br и циано;Rвыбран из группы, состоящей из Н, F и Cl;Rявляется Н; иRвыбран из группы, состоящей из Н, F, Cl и циано.8. Соединение по п.6, отличающееся тем, что Rвыбран из группы, состоящей из F и Cl.9. Соединение по п.6, отличающееся тем, что Rвыбран из группы, состоящей из F, Cl, Br, Me, ОСНи циано.10. Соединение по п.6, отличающееся тем, что Rвыбран из группы, состоящей из F, Cl, Br, Me, ОСНи циано.11. Соединение по п.6, отличающееся тем, что Rвыбран из группы, состоящей из F, Cl, Br, Me и ОСН;12. Соединение по п.6, отличающееся тем, что Rвыбран из группы, состоящей из F, Cl, Br, СН, CF, ОСН, циано, N(СН)и морфолин�
Claims (32)
1. Соединение Формулы 1:
Формула 1
где R1 выбран из группы, состоящей из Н, F и Cl;
R2a и R2b независимо выбраны из группы, состоящей из Н, F, Cl, Br, Me, ОСН3 и циано;
R2c выбран из группы, состоящей из Н, F, Cl, Br, Me и ОСН3;
Х выбран из группы, состоящей из
А выбран из группы, состоящей из
R3 выбран из группы, состоящей из F, Cl, Br, СН3, CF3, ОСН3, циано, N(СН3)2 и морфолино;
n выбран из группы, состоящей из 0, 1 и 2;
R4 выбран из группы, состоящей из Н, F, Cl, Br, СН3, CF3, ОСН3, циано, N(СН3)2 и морфолино;
4. Соединение по п.3, отличающееся тем, что R2c является водородом.
5. Соединение по п.3, отличающееся тем, что R2b является водородом.
7. Соединение по п.6, отличающееся тем, что
R1 выбран из группы, состоящей из Н и F;
R2a выбран из группы, состоящей из Н, F, Cl, Br и циано;
R2b выбран из группы, состоящей из Н, F и Cl;
R2c является Н; и
R4 выбран из группы, состоящей из Н, F, Cl и циано.
8. Соединение по п.6, отличающееся тем, что R1 выбран из группы, состоящей из F и Cl.
9. Соединение по п.6, отличающееся тем, что R2a выбран из группы, состоящей из F, Cl, Br, Me, ОСН3 и циано.
10. Соединение по п.6, отличающееся тем, что R2b выбран из группы, состоящей из F, Cl, Br, Me, ОСН3 и циано.
11. Соединение по п.6, отличающееся тем, что R2c выбран из группы, состоящей из F, Cl, Br, Me и ОСН3;
12. Соединение по п.6, отличающееся тем, что R4 выбран из группы, состоящей из F, Cl, Br, СН3, CF3, ОСН3, циано, N(СН3)2 и морфолино.
15. Соединение по п.14, отличающееся тем, что А является СООН.
17. Соединение по п.16, отличающееся тем, что R2c является Н.
18. Соединение по п.16, отличающееся тем, что R2b является Н.
19. Соединение по п.16, отличающееся тем, что
R1 выбран из группы, состоящей из Н и F;
R2b выбран из группы, состоящей из Н, F и Cl;
R2c является Н; и
R4 выбран из группы, состоящей из Н, F, Cl и циано.
22. Соединение по п.21, отличающееся тем, что А является СООН.
24. Соединение по п.23, отличающееся тем, что R2c является Н.
25. Соединение по п.23, отличающееся тем, что K2b является Н.
26. Соединение по п.23, отличающееся тем, что
R2a выбран из группы, состоящей из Н, F, Cl, Br и циано;
R2a выбран из группы, состоящей из Н, F и Cl;
R2c является H; и
R4 выбран из группы, состоящей из Н, F, Cl и циано.
27. Соединение по п.1, отличающееся тем, что соединение выбрано из группы, состоящей из
3-хлор-4-(6-гидроксинафталин-2-ил)бензойной кислоты;
3-фтор-4-(6-гидроксинафталин-2-ил)бензойной кислоты;
4-(6-гидроксинафталин-2-ил)-3-метоксибензойной кислоты;
3-(диметиламино)-4-(6-гидроксинафталин-2-ил)бензойной кислоты;
3-циано-4-(6-гидроксинафталин-2-ил)бензойной кислоты;
4-(6-гидроксинафталин-2-ил)-3-морфолинобензойной кислоты;
4-(1-бром-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(6-гидрокси-1-метилнафталин-2-ил)бензойной кислоты;
4-(1-циано-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(6-гидрокси-3-метоксинафталин-2-ил)бензойной кислоты;
4-(1-хлор-6-гидроксинафталин-2-ил)бензойной кислоты;
6-(4-(1Н-тетразол-5-ил)фенил)нафталин-2-ола;
5-(6-гидроксинафталин-2-ил)пиколиновой кислоты;
6-(6-гидроксинафталин-2-ил)никотиновой кислоты;
5-(6-гидроксинафталин-2-ил)пиразин-2-карбоновой кислоты;
2-(6-гидроксинафталин-2-ил)пиримидин-5-карбоновой кислоты;
6-(6-гидроксинафталин-2-ил)пиридазин-3-карбоновой кислоты;
5-(6-гидроксинафталин-2-ил)пиримидин-2-карбоновой кислоты;
6-(1H-бензо[d][1,2,3]триазол-6-ил)нафталин-2-ола;
4-(6-гидроксинафталин-2-ил)-3-(трифторметил)бензойной кислоты;
3-хлор-4-(3-фтор-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(3-хлор-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(3-фтор-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(6-гидрокси-1-метоксинафталин-2-ил)бензойной кислоты;
4-(1-фтор-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(6-гидрокси-3-метилнафталин-2-ил)бензойной кислоты;
4-(1-циано-5-фтор-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(1-циано-6-гидроксинафталин-2-ил)-3-фторбензойной кислоты;
3-хлор-4-(5-фтор-6-гидроксинафталин-2-ил)бензойной кислоты;
4-(5-фтор-6-гидроксинафталин-2-ил)бензойной кислоты;
3-фтор-4-(5-фтор-6-гидроксинафталин-2-ил)бензойной кислоты; и
4-(5-фтор-6-гидроксинафталин-2-ил)-3-метилбензойной кислоты.
28. Применение соединения Формулы 1 по п.1 или его фармацевтически приемлемой соли в качестве ингибитора GSNOR.
29. Применение соединения по п.27 или его фармацевтически приемлемой соли в качестве ингибитора GSNOR.
30. Фармацевтическая композиция, включающая терапевтически эффективное количество соединения по п.1 вместе с фармацевтически приемлемым носителем или формообразующим средством.
31. Способ лечения заболевания или состояния, который включает введение терапевтически эффективного количества соединения Формулы 1 по п.1 пациенту, нуждающемуся в этом.
32. Способ получения соединения Формулы 1 по п.1.
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| WO2012170371A1 (en) * | 2011-06-10 | 2012-12-13 | N30 Pharmaceuticals, Llc | Compounds as s-nitrosoglutathione reductase inhibitors |
| WO2016128905A1 (en) * | 2015-02-10 | 2016-08-18 | Glenmark Pharmaceuticals S.A. | Thienopyrrole compounds as s-nitrosoglutathione reductase inhibitors |
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-
2011
- 2011-12-16 AU AU2011343518A patent/AU2011343518B2/en not_active Ceased
- 2011-12-16 WO PCT/US2011/065502 patent/WO2012083171A1/en not_active Ceased
- 2011-12-16 US US13/991,972 patent/US8785643B2/en not_active Expired - Fee Related
- 2011-12-16 US US13/991,973 patent/US9249132B2/en not_active Expired - Fee Related
- 2011-12-16 BR BR112013014681A patent/BR112013014681A2/pt not_active IP Right Cessation
- 2011-12-16 EP EP11849550.6A patent/EP2651871A4/en not_active Withdrawn
- 2011-12-16 JP JP2013544827A patent/JP5898230B2/ja not_active Expired - Fee Related
- 2011-12-16 CN CN201180065419XA patent/CN103328430A/zh active Pending
- 2011-12-16 RU RU2013127155/04A patent/RU2013127155A/ru not_active Application Discontinuation
- 2011-12-16 WO PCT/US2011/065490 patent/WO2012083165A1/en not_active Ceased
- 2011-12-16 KR KR1020137017883A patent/KR20130138292A/ko not_active Ceased
- 2011-12-16 CA CA2821412A patent/CA2821412A1/en not_active Abandoned
- 2011-12-16 JP JP2013544825A patent/JP5990187B2/ja not_active Expired - Fee Related
- 2011-12-16 EP EP11849278.4A patent/EP2651223A4/en not_active Withdrawn
-
2013
- 2013-06-09 IL IL226834A patent/IL226834A/en not_active IP Right Cessation
-
2014
- 2014-07-09 US US14/326,686 patent/US9012646B2/en not_active Expired - Fee Related
-
2015
- 2015-03-03 US US14/637,223 patent/US9221810B2/en not_active Expired - Fee Related
- 2015-11-18 US US14/944,468 patent/US9364481B2/en not_active Expired - Fee Related
- 2015-12-21 US US14/977,448 patent/US20160108011A1/en not_active Abandoned
-
2016
- 2016-06-06 US US15/173,926 patent/US20160279117A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| JP2014506875A (ja) | 2014-03-20 |
| EP2651223A1 (en) | 2013-10-23 |
| US20130261123A1 (en) | 2013-10-03 |
| KR20130138292A (ko) | 2013-12-18 |
| US9012646B2 (en) | 2015-04-21 |
| US9364481B2 (en) | 2016-06-14 |
| US20160108011A1 (en) | 2016-04-21 |
| US20140329821A1 (en) | 2014-11-06 |
| AU2011343518B2 (en) | 2016-11-10 |
| IL226834A (en) | 2016-09-29 |
| JP5990187B2 (ja) | 2016-09-07 |
| WO2012083171A1 (en) | 2012-06-21 |
| US20130261122A1 (en) | 2013-10-03 |
| US20160067254A1 (en) | 2016-03-10 |
| CN103328430A (zh) | 2013-09-25 |
| EP2651871A1 (en) | 2013-10-23 |
| US20160279117A1 (en) | 2016-09-29 |
| AU2011343518A1 (en) | 2013-07-04 |
| US8785643B2 (en) | 2014-07-22 |
| US20150183774A1 (en) | 2015-07-02 |
| BR112013014681A2 (pt) | 2016-10-04 |
| JP2013545821A (ja) | 2013-12-26 |
| US9221810B2 (en) | 2015-12-29 |
| CA2821412A1 (en) | 2012-06-21 |
| EP2651223A4 (en) | 2015-07-22 |
| US9249132B2 (en) | 2016-02-02 |
| WO2012083165A1 (en) | 2012-06-21 |
| EP2651871A4 (en) | 2015-07-22 |
| JP5898230B2 (ja) | 2016-04-06 |
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