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N-[2-[(4,5-Dihydro-1H-imidazol-2-yl)amino]ethyl]-5-isoquinolinesulfonamide | 92564-35-7

中文名称
——
中文别名
——
英文名称
N-[2-[(4,5-Dihydro-1H-imidazol-2-yl)amino]ethyl]-5-isoquinolinesulfonamide
英文别名
N-[2-(4,5-dihydro-1H-imidazol-2-ylamino)ethyl]isoquinoline-5-sulfonamide
N-[2-[(4,5-Dihydro-1H-imidazol-2-yl)amino]ethyl]-5-isoquinolinesulfonamide化学式
CAS
92564-35-7
化学式
C14H17N5O2S
mdl
——
分子量
319.38
InChiKey
FZPOLUKNIDSPGU-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.1
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    104
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • Pharmaceutical agent containing Rho kinase inhibitor
    申请人:——
    公开号:US20020032148A1
    公开(公告)日:2002-03-14
    A Rho kinase inhibitor is provided as a novel pharmaceutical agent, particularly as a therapeutic agent of hypertension, a therapeutic agent of angina pectoris, a suppressive agent of cerebrovascular contraction, a therapeutic agent of asthma, a therapeutic agent of peripheral circulation disorder, a prophylactic agent of immature birth, a therapeutic agent of arteriosclerosis, an anti-cancer drug, an anti-inflammatory agent, an immunosuppressant, a therapeutic agent of autoimmune disease, an anti-AIDS drug, a contraceptive, a prophylactic agent of digestive tract infection, a therapeutic agent of osteoporosis, a therapeutic agent of retinopathy and a brain function improving drug. In addition, the Rho kinase inhibitor is provided as a reagent and a diagnostic.
    提供了一种新型药物代理——Rho激酶抑制剂,特别用于治疗高血压、心绞痛、脑血管收缩抑制剂、哮喘、周围循环障碍的治疗剂、早产预防剂、动脉硬化的治疗剂、抗癌药物、抗炎剂、免疫抑制剂、自身免疫疾病的治疗剂、抗艾滋病药物、避孕药、消化道感染预防剂、骨质疏松症的治疗剂、视网膜病的治疗剂和脑功能改善药物。此外,Rho激酶抑制剂还可作为试剂和诊断工具。
  • Isoquinolinesulfonamide derivatives and process for the preparation thereof
    申请人:Asahi Kasei Kogyo Kabushiki Kaisha
    公开号:EP0109023A1
    公开(公告)日:1984-05-23
    This invention relates to novel isoquinolinesulfonamide derivates of Formula (I): wherein A is a C0-10 alkylene group or a C0-10 alkylene group having a C1-10 alkyl group, a phenyl group, a substituted phenyl group or a phenylalkyl group; R1 and R2 each is a hydrogen atom; or R1 and R2 are linked directly to form an ethylene group unsubstituted or substituted with a C1-4 alkyl group; R3 and R4 each is a hydrogen atom, a C1-6 alkyl group or linked directly to form a C2-6 alkylene group; and the pharmaceutically acceptable acid addition salt thereof, and to a precess for preparing them. The isoquinoline derivatives possess a relaxatory action for vascular smooth muscle and action for increasing blood flow and are useful as a vasodilator and a hypotensor.
    本发明涉及式(I)的新型异喹啉磺酰胺衍生物: 其中 A 为 C0-10 烯基或具有 C1-10 烷基的 C0-10 烯基、苯基、取代苯基或苯基烷基;R1 和 R2 各为氢原子;或 R1 和 R2 直接连接形成未取代或被 C1-4 烷基取代的乙烯基; R3和R4各自为氢原子、C1-6烷基或直接连接形成C2-6亚烷基;及其药学上可接受的酸加成盐,以及制备它们的预处理方法。异喹啉衍生物具有松弛血管平滑肌和增加血流量的作用,可用作血管扩张剂和降压剂。
  • CARDIAC PROTECTIVE
    申请人:Asahi Kasei Kogyo Kabushiki Kaisha
    公开号:EP0654266A1
    公开(公告)日:1995-05-24
    A cardiac protective containing an isoquinolinesulfonamide derivative represented by general formula (I) or a salt thereof, suitable for treating myocardial diseases and myocardial cytopathy, wherein R¹ represents H, Cl or OH; A, R², R³, and R⁴ represent each a group selected dependent on R¹; A represents C₂-C₆ alkylene which may be substituted by alkyl, cinnamyl, phenyl or benzyl; R² and R³ represent each independently H, C₁-C₆ alkyl, C₆ or lower cycloalkyl, cinnamyl, phenyl or benzyl, or alternatively R² and R³ may be combined together to represent alkylene which may be alkylated; R⁴ represents H, C₁-C₆ alkyl, phenyl, benzyl, benzoyl, cinnamyl, cinnamoyl, furoyl (a) or (b), or alternatively R⁴ may be combined with R³ to represent a chain which may contain an interposed oxygen atom; R⁵ represents C₁-C₆ alkyl; and R⁶ and R⁷ are each independently selected dependent on R¹ and represent each H or CH₃. or alternatively R⁶ and R⁷ may be combined together to represent C₂-C₄ alkylene.
    一种心脏保护剂,含有通式(I)代表的异喹啉磺酰胺衍生物或其盐,适用于治疗心肌疾病和心肌细胞病变,其中R¹代表H、Cl或OH;A、R²、R³和R⁴各自代表根据R¹选择的基团;A代表C₂-C₆亚烷基,可被烷基、肉桂基、苯基或苄基取代;R² 和 R³ 各自独立地代表 H、C₁-C₆ 烷基、C₆ 或低级环烷基、肉桂基、苯基或苄基,或者 R² 和 R³ 可组合在一起,代表可被烷基化的亚烷基;R⁴ 代表 H、C₁-C₆ 烷基、苯基、苄基、苯甲酰基、肉桂酰基、肉桂酰基、呋喃基 (a) 或 (b),或者 R⁴ 可与 R³ 结合在一起,代表可包含一个中间氧原子的链;R⁵ 代表 C₁-C₆烷基;以及 R⁶ 和 R⁷ 各自独立地根据 R¹ 进行选择,并各自代表 H 或 CH₃。或者,R⁶ 和 R⁷ 可以组合在一起代表 C₂-C₄ 亚烷基。
  • Use of isoquinoline-derivatives for treating and preventing pigmentary disorders
    申请人:Switch Biotech Aktiengesellschaft
    公开号:EP1479386A1
    公开(公告)日:2004-11-24
    The invention relates to the use of isoquinoline-derivatives for treating and/or preventing pigmentary disorders.
    本发明涉及使用异喹啉衍生物治疗和/或预防色素性疾病。
  • Novel 5-acyl-2-(1H)-pyridinones
    申请人:MERRELL DOW PHARMACEUTICALS INC.
    公开号:EP0124089B1
    公开(公告)日:1987-03-04
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