ANGIOTENSIN II RECEPTOR ANTAGONISTS
    1.
    发明申请
    ANGIOTENSIN II RECEPTOR ANTAGONISTS 失效
    ANGIOTENSIN II受体拮抗剂

    公开(公告)号:US20100273845A1

    公开(公告)日:2010-10-28

    申请号:US12743402

    申请日:2008-11-21

    CPC分类号: C07D403/10

    摘要: A compound having the structure wherein R is an angiotensin receptor antagonist active group, and Y is 1) —(CH2)3R5, 2) —C(O)(CH2)2R5, 3) —C(R1R2)OC(O)O(CH2)nR5, wherein n is 1 or 2, 4) —C(R1R2)OC(O)CH2CH2R5, 5) —C(R1R2)OC(O)OCH2CH2C(R3R4)R5, provided that when Y is —C(O)(CH2)2R5, then R is R1, R2, R3 and R4 are independently selected from the group consisting of hydrogen and C1-4 alkyl; R5 is —CH(ONO2)CH(ONO2)R6; R6 is selected from CH3, CH2CH3 and CH(CH3)2; or a pharmaceutically acceptable salt or hydrate thereof, which is useful for treating hypertension.

    摘要翻译: 具有结构的化合物,其中R是血管紧张素受体拮抗剂活性基团,Y是1) - (CH 2)3 R 5,2)-C(O)(CH 2)2 R 5,3)-C(R 1 R 2)OC(O)O (CH 2)n R 5,其中n为1或2,4)-C(R 1 R 2)OC(O)CH 2 CH 2 R 5,5)-C(R 1 R 2)OC(O)OCH 2 CH 2 C(R 3 R 4) O)(CH 2)2 R 5,则R 1是R 1,R 2,R 3和R 4独立地选自氢和C 1-4烷基; R5是-CH(ONO2)CH(ONO2)R6; R 6选自CH 3,CH 2 CH 3和CH(CH 3)2; 或其药学上可接受的盐或水合物,其可用于治疗高血压。

    Angiotensin II receptor antagonists
    7.
    发明授权
    Angiotensin II receptor antagonists 失效
    血管紧张素II受体拮抗剂

    公开(公告)号:US08293777B2

    公开(公告)日:2012-10-23

    申请号:US12629419

    申请日:2009-12-02

    摘要: A compound having the structure wherein R is an angiotensin receptor antagonist active group, and Y is Y is selected from the group consisting of R1 is selected from the group consisting of —O—C1-6 alkyl, —O-aryl, —O-heteroaryl, —O—C3-8 cycloalkyl, —C1-6 alkyl, -aryl, -heteroaryl, and —C3-8 cycloalkyl; R2 and R3 are independently selected from the group consisting of hydrogen and C1-4 alkyl, or a pharmaceutically acceptable salt or hydrate thereof, which is useful for treating hypertension.

    摘要翻译: 具有其中R为血管紧张素受体拮抗剂活性基团且Y为Y的结构的化合物选自R 1选自-O-C 1-6烷基,-O-芳基,-O- 杂芳基,-O-C 3-8环烷基,-C 1-6烷基, - 芳基, - 杂芳基和-C 3-8环烷基; R2和R3独立地选自氢和C 1-4烷基,或其药学上可接受的盐或水合物,其可用于治疗高血压。

    ANGIOTENSIN II RECEPTOR ANTAGONISTS
    8.
    发明申请
    ANGIOTENSIN II RECEPTOR ANTAGONISTS 有权
    ANGIOTENSIN II受体拮抗剂

    公开(公告)号:US20100292192A1

    公开(公告)日:2010-11-18

    申请号:US12812547

    申请日:2009-01-08

    摘要: A compound having the structure wherein R is an angiotensin receptor antagonist active group, Y is selected from the group consisting of and 2) —C(R1H)OC(O)X((CR12R13)—(CHR10)m—(CH2)n—Zp—(CH2)q—(CHR11)r—(CR16R17))—R5;Z is —O— or —(CR14R15)_; m, n, p, q, and r are independently selected from the group consisting of 0 and 1; X is —O— or —(CR18R19)—; R1 is selected from the group consisting of hydrogen, C1-4 alkyl, aryl and C1-4 alkylaryl; R5 is —O—N═N(O)—NR3R4; or a pharmaceutically acceptable salt or hydrate thereof, which is useful for treating hypertension.

    摘要翻译: 具有结构的化合物,其中R是血管紧张素受体拮抗剂活性基团,Y选自和:2)-C(R 1 H)OC(O)X((CR 12 R 13) - (CHR 10)m - (CH 2)n -Z-(CH 2)q - (CHR 11)r - (CR 16 R 17)) - R 5; Z是-O-或 - (CR14R15)_; m,n,p,q和r独立地选自0和1组成的组; X是-O-或 - (CR 18 R 19) - ; R1选自氢,C1-4烷基,芳基和C1-4烷基芳基; R5是-O-N = N(O)-NR3R4; 或其药学上可接受的盐或水合物,其可用于治疗高血压。

    Diazeniumdiolate cyclohexyl derivatives
    9.
    发明授权
    Diazeniumdiolate cyclohexyl derivatives 有权
    二氮烯二硫代环己基衍生物

    公开(公告)号:US09272987B2

    公开(公告)日:2016-03-01

    申请号:US14115139

    申请日:2012-04-27

    摘要: A compound having the structure or a pharmaceutically acceptable salt thereof, wherein R6 is hydrogen, —OH, —C1-6alkyl, —OC1-6alkyl, aryl, or halogen, or together with R7, forms an oxo group, or together with R7 and the atom to which they are attached, form a 5-7-membered carbocycle ring or a 5-7-membered heterocyclic ring having 1, 2, or 3 heteroatoms, wherein alkyl and aryl are unsubstituted or independently mono-, di-, or tri-substituted with R14; R7 is hydrogen, C1-6alkyl, —CF3, aryl, —O-aryl, —O—C1-6alkyl, —C(O)OC1-6alkyl, —C(R15R16)OH, a 5-7-membered heteroaryl having 1, 2, 3 or 4 nitrogen atoms, or halogen, or together with R6, forms an oxo group, or together with R6 and the atom to which they are attached, form a 5-7-membered carbocycle ring or a 5-7-membered heterocyclic ring having 1, 2, or 3 heteroatoms wherein alkyl, aryl and heteroaryl are unsubstituted or independently mono-, di- or tri-substituted with R14; R12 is hydrogen, C1-6alkyl, or —(CH2)1-2OH, or together with R13 and the nitrogen atom to which they are attached, form a 4- to 7-membered heterocyclic ring containing one nitrogen atom and 0 or 1 oxygen atoms, wherein said ring is unsubstituted or independently mono-, di- or tri-substituted with halogen or —C1-6alkyl; R13 is —C1-6alkyl or —(CH2)1-2OH, or together with R12 and the nitrogen atom to which they are attached, form a 4- to 7-membered heterocyclic ring containing one nitrogen atom and 0 or 1 oxygen atoms, wherein said ring is unsubstituted or independently mono-, di- or tri-substituted with halogen or —C1-6alkyl.

    摘要翻译: 具有结构或其药学上可接受的盐的化合物,其中R 6是氢,-OH,-C 1-6烷基,-OC 1-6烷基,芳基或卤素,或与R 7一起形成氧代基,或与R 7和 它们连接的原子形成5-7元碳环或具有1,2或3个杂原子的5-7元杂环,其中烷基和芳基是未取代的或独立地是单 - ,二 - 或 用R14三取代; R 7是氢,C 1-6烷基,-CF 3,芳基,-O-芳基,-O-C 1-6烷基,-C(O)OC 1-6烷基,-C(R 15 R 16)OH,5- ,2,3或4个氮原子,或卤素,或与R6一起形成氧代基团,或与R6及其连接的原子一起形成5-7元碳环或5-7元碳环, 其中烷基,芳基和杂芳基是未取代的或独立地被R 14取代或被二取代或三取代的杂环基; R 12是氢,C 1-6烷基或 - (CH 2)1-2 OH,或者与R 13和它们所连接的氮原子一起形成含有一个氮原子和0或1个氧的4-至7-元杂环 原子,其中所述环是未取代的或独立地被卤素或-C 1-6烷基单,二或三取代; R 13是-C 1-6烷基或 - (CH 2)1-2 OH,或与R 12和它们所连接的氮原子一起形成含有一个氮原子和0或1个氧原子的4-至7-元杂环, 其中所述环是未取代的或独立地被卤素或-C 1-6烷基单,二或三取代。