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RU2008135153A - Применение нитрооксипроизводного лекарственного средства для лечения мышечной дистрофии - Google Patents

Применение нитрооксипроизводного лекарственного средства для лечения мышечной дистрофии Download PDF

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RU2008135153A
RU2008135153A RU2008135153/15A RU2008135153A RU2008135153A RU 2008135153 A RU2008135153 A RU 2008135153A RU 2008135153/15 A RU2008135153/15 A RU 2008135153/15A RU 2008135153 A RU2008135153 A RU 2008135153A RU 2008135153 A RU2008135153 A RU 2008135153A
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Эмилио КЛЕМЕНТИ (IT)
Эмилио КЛЕМЕНТИ
Джулио КОССУ (IT)
Джулио КОССУ
Сильвия БРУНЕЛЛИ (IT)
Сильвия БРУНЕЛЛИ
Эннио ОНГИНИ (IT)
Эннио Онгини
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Никокс С.А.
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Abstract

1. Применение высвобождающих оксид азота соединений формулы (Ia) ! ! или их энантиомеров или диастереомеров для приготовления лекарственных средств для лечения мышечных дистрофий, где в общей формуле (Ia) M, Х и Y имеют следующие значения: ! М - остаток, выбранный из: ! , , ! где RA - атом водорода или -С(O)СН3, ! , ! ! , ! , ! , ! ! , ! , ! , ! , ! , ! , ! , ! , ! , ! ! ! Х представляет собой -О-, -S- или -NR1-, где R1 представляет Н или линейный или разветвленный C1-C6алкил; ! Y - двухвалентный радикал, имеющий следующие значения: ! a) прямой или разветвленный С1-С20алкилен, преимущественно С1-С10, необязательно замещенный одним или более заместителями, выбранными из группы, состоящей из: атома галогена, гидрокси, -ONO2 или Т, где Т представляет собой -OC(O)(C1-C10алкил)-ONO2 или -O(C1-C10алкил)-ONO2; более предпочтительно Y представляет собой -C1-С10алкилен; ! -C5-C7циклоалкилен, необязательно замещенный линейной или разветвленной группой С1-С10алкил, предпочтительно СН3; ! b) ! c) ! где n - целое число от 0 до 20, предпочтительно n - целое число от 0 до 5, более предпочтительно n равно 0; ! n1 - целое число от 1 до 20, предпочтительно n1 - целое число от 1 до 5, более предпочтительно n1 равно 1; ! при условии, что когда Y выбран из двухвалентных радикалов, указанных под b) и с), тогда группа -ONO2 в формуле (I) связана с -(CH2)n1-; ! d) ! где X1=-ОСО- или -COO-, и R2 означает Н или СН3; ! na - целое число от 0 до 20; предпочтительно n - целое число от 1 до 5; ! n2 - целое число от 0 до 2; ! е) ! где Y1 означает -СН2-СН2-(СН2)n2-; или -CH=CH-(CH2)n2-; ! X1, na, n2 и R2 как указано выше; ! f) ! где na и R2 как указано выше, R3 означает Н или -СОСН3; ! при условии, что когда Y выбран из двухвалентных радикалов, указанных под d) и f), тогда группа -ONO2 в формуле (I) связана с -(СН2)na-; ! при условии, ч�

Claims (5)

1. Применение высвобождающих оксид азота соединений формулы (Ia)
Figure 00000001
или их энантиомеров или диастереомеров для приготовления лекарственных средств для лечения мышечных дистрофий, где в общей формуле (Ia) M, Х и Y имеют следующие значения:
М - остаток, выбранный из:
Figure 00000002
,
Figure 00000003
,
где RA - атом водорода или -С(O)СН3,
Figure 00000004
,
Figure 00000005
Figure 00000006
Figure 00000007
,
Figure 00000008
Figure 00000009
,
Figure 00000010
Figure 00000011
,
Figure 00000012
Figure 00000013
Figure 00000014
Figure 00000015
,
Figure 00000016
Figure 00000017
,
Figure 00000018
Figure 00000019
,
Figure 00000020
Figure 00000021
,
Figure 00000022
Figure 00000023
,
,
Figure 00000025
Figure 00000026
,
Figure 00000027
Figure 00000028
,
Figure 00000029
Figure 00000030
,
Figure 00000031
Figure 00000032
Х представляет собой -О-, -S- или -NR1-, где R1 представляет Н или линейный или разветвленный C1-C6алкил;
Y - двухвалентный радикал, имеющий следующие значения:
a) прямой или разветвленный С120алкилен, преимущественно С110, необязательно замещенный одним или более заместителями, выбранными из группы, состоящей из: атома галогена, гидрокси, -ONO2 или Т, где Т представляет собой -OC(O)(C1-C10алкил)-ONO2 или -O(C1-C10алкил)-ONO2; более предпочтительно Y представляет собой -C110алкилен;
-C5-C7циклоалкилен, необязательно замещенный линейной или разветвленной группой С110алкил, предпочтительно СН3;
b)
Figure 00000033
c)
Figure 00000034
где n - целое число от 0 до 20, предпочтительно n - целое число от 0 до 5, более предпочтительно n равно 0;
n1 - целое число от 1 до 20, предпочтительно n1 - целое число от 1 до 5, более предпочтительно n1 равно 1;
при условии, что когда Y выбран из двухвалентных радикалов, указанных под b) и с), тогда группа -ONO2 в формуле (I) связана с -(CH2)n1-;
d)
Figure 00000035
где X1=-ОСО- или -COO-, и R2 означает Н или СН3;
na - целое число от 0 до 20; предпочтительно n - целое число от 1 до 5;
n2 - целое число от 0 до 2;
е)
Figure 00000036
где Y1 означает -СН2-СН2-(СН2)n2-; или -CH=CH-(CH2)n2-;
X1, na, n2 и R2 как указано выше;
f)
Figure 00000037
где na и R2 как указано выше, R3 означает Н или -СОСН3;
при условии, что когда Y выбран из двухвалентных радикалов, указанных под d) и f), тогда группа -ONO2 в формуле (I) связана с -(СН2)na-;
при условии, что когда Х означает -NR1-, где R1 как указано выше, Y не может быть f);
g)
Figure 00000038
,
Figure 00000039
где Х2 означает -О- или -S-;
n3 - целое число от 1 до 6, предпочтительно от 1 до 4, и
R2 как определено выше.
2. Применение по п.1, где соединение формулы (Ia) представляет собой 3-(нитрооксиметил) фениловый эфир 2-(ацетилокси) бензойной кислоты формулы (Ib)
Figure 00000040
3. Применение по п.1, где соединение формулы (Iа) представляет собой 4-нитрооксибутиловый эфир 2-фтор-альфа-метил-4[1,1'-бифенил]4-уксусной кислоты формулы (IIIb)
Figure 00000041
4. Применение по п.1, где в формуле (Ia) M выбирают из:
Figure 00000028
,
Figure 00000042
Figure 00000030
,
Figure 00000031
Figure 00000043
Х представляет атом кислорода,
Y выбирают из:
прямой C110алкилен;
b)
Figure 00000044
где n - целое число от 0 до 5; и
n1 - целое число от 1 до 5, более предпочтительно n1 равно 1;
5. Применение по п.4, где соединение формулы (Ia) выбирают из:
4-(нитроокси)бутилового эфира правастатина
Figure 00000045
4-(нитрооксиметил)бензилового эфира правастатина
Figure 00000046
3-(нитроокси)бутилового эфира аторвастатина
Figure 00000047
3-(нитрооксиметил)бензилового эфира аторвастатина
Figure 00000048
RU2008135153/15A 2006-02-03 2007-01-23 Применение нитрооксипроизводного лекарственного средства для лечения мышечной дистрофии RU2429828C2 (ru)

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IL192299A0 (en) 2009-08-03
AU2007211508B2 (en) 2012-08-23
RU2429828C2 (ru) 2011-09-27
US8575222B2 (en) 2013-11-05
EP1978947A2 (en) 2008-10-15
CN101378739B (zh) 2014-06-04
KR20080097989A (ko) 2008-11-06
RU2011118522A (ru) 2012-11-20
NZ569396A (en) 2011-06-30
WO2007088123A3 (en) 2007-09-20
SI1978947T1 (sl) 2014-12-31
EP1978947B1 (en) 2014-08-13
WO2007088123A2 (en) 2007-08-09
RU2560144C2 (ru) 2015-08-20
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AU2007211508A1 (en) 2007-08-09
HK1129592A1 (en) 2009-12-04
CA2641816A1 (en) 2007-08-09
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US20090093510A1 (en) 2009-04-09
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CA2641816C (en) 2016-01-05

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