5-(Piperazine-1-sulfonyl)isoquinolin-1(2H)-one | 105628-87-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异喹啉及其衍生物
• 英文名称: 5-(Piperazine-1-sulfonyl)isoquinolin-1(2H)-one
• 英文别名: 5-piperazin-1-ylsulfonyl-2H-isoquinolin-1-one
• CAS: 105628-87-3
• 化学式: C₁₃H₁₅N₃O₃S
• 分子量: 293.34
• InChiKey: STDZGCHUVZWDNY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.2
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  86.9
• 氢给体数：
  2
• 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。
• 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。
• Compositions comprising a mast cell degranulation-blocking agent for treatment of endogenous, painful gastrointestinal conditions of non-inflammatory, non-ulcerative origin.
  申请人：KOS PHARMACEUTICALS, INC.

  公开号：EP1203586A2

  公开（公告）日：2002-05-08

  A method for treating endogenous, painful gastrointestinal condition of non-inflammatory, non-ulcerative origin, such as abdominal migraine and irritable bowel syndrome, entails administering a pharmacologically effective amount of a mast cell degranulation-blocking agent, e.g. a histamine-3 receptor agonist.

  一种治疗非炎症性、非溃疡性内源性胃肠道疼痛病症（如腹型偏头痛和肠易激综合征）的方法，需要给药有效量的肥大细胞脱颗粒阻断剂，如组胺-3 受体激动剂。
• 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。
• Substituted isoquinolinesulfonyl compounds
  申请人：Asahi Kasei Kogyo Kabushiki Kaisha

  公开号：EP0187371B1

  公开（公告）日：1991-06-19