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(R)-4-(1-氨基乙基)-N-1H-吡咯并[2,3-B]吡啶-4-基苯甲酰胺盐酸盐 | 471843-75-1

中文名称
(R)-4-(1-氨基乙基)-N-1H-吡咯并[2,3-B]吡啶-4-基苯甲酰胺盐酸盐
中文别名
——
英文名称
Y-39983
英文别名
(R)-(+)-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-4-(1-aminoethyl)benzamide monohydrochloride;hydrochloric acid salt of (R)-(+)-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-4-(1-aminoethyl)benzamide;(R)-(+)-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-4-(1-aminoethyl)benzamide hydrochloride;Benzamide, 4-((1R)-1-aminoethyl)-N-1H-pyrrolo(2,3-b)pyridin-4-yl-, hydrochloride (1:1);4-[(1R)-1-aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide;hydrochloride
(R)-4-(1-氨基乙基)-N-1H-吡咯并[2,3-B]吡啶-4-基苯甲酰胺盐酸盐化学式
CAS
471843-75-1
化学式
C16H16N4O*ClH
mdl
——
分子量
316.79
InChiKey
IILQESWQPZIAGP-HNCPQSOCSA-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

物化性质

  • 溶解度:
    可溶于DMSO

计算性质

  • 辛醇/水分配系数(LogP):
    3.26
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    83.8
  • 氢给体数:
    4
  • 氢受体数:
    3

SDS

SDS:21c22769b55109309e0faac7deb1d086
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制备方法与用途

Y-33075盐酸盐(Y-39983)是一种选择性ROCK抑制剂,源自于Y-27632,并且比后者更为有效,其IC50值为3.6 nM。

反应信息

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文献信息

  • N-heterocyclic substituted benzamide derivatives with antihypertensive activity
    申请人:Mitsubishi Pharma Corporation
    公开号:EP1195372A1
    公开(公告)日:2002-04-10
    Benzamide compounds of the formula wherein each symbol is as defined in the specification, isomers thereof and pharmaceutically acceptable acid addition salts thereof. Pharmaceutical compositions comprising a therapeutically effective amount of this compound and a pharmaceutically acceptable additive, and therapeutic agents for hypertension, therapeutic agents for angina pectoris, therapeutic agent for asthma, therapeutic agents for renal and peripheral circulatory disturbances and inhibitor of cerebral vasospasm, which comprise this compound. The compound of the present invention has strong smooth muscle relaxing action, and shows hypotensive action and cerebral • coronary vasodilating action like conventional calcium antagonists, as well as long-lasting renal and peripheral circulation improving action. Unlike calcium antagonists, it permits oral administration to suppress vascular contraction caused by various agonists, and is useful as a strong and long-acting agent for prophylaxis and treatment of circulatory diseases in coronary, cerebral, renal and peripheral arteries, as a therapeutic agent for hypertension, angina pectoris, and renal and peripheral circulation disorder, an inhibitor of cerebral vasospasm and the like. Moreover, the compound of the present invention is useful as a therapeutic agent for asthma.
    苯甲酰胺化合物的化学式如规范中所定义的每个符号,其异构体和药学上可接受的酸盐。包括该化合物的治疗有效量和药学上可接受的添加剂的药物组合物,以及治疗高血压、心绞痛、哮喘、肾脏和外周循环障碍以及脑血管痉挛抑制剂的治疗剂,其中包括该化合物。本发明的化合物具有强大的平滑肌松弛作用,表现出类似于传统钙拮抗剂的降压作用和脑冠脉扩张作用,以及持久的肾脏和外周循环改善作用。与钙拮抗剂不同,它允许口服给药以抑制各种激动剂引起的血管收缩,并可用作冠状动脉、脑部、肾脏和外周动脉循环疾病的预防和治疗的强效长效药物,作为治疗高血压、心绞痛、肾脏和外周循环障碍的治疗剂,脑血管痉挛抑制剂等。此外,本发明的化合物还可用作哮喘的治疗剂。
  • Kinase inhibitors
    申请人:Leysen Casimir Maria Dirk
    公开号:US20070191420A1
    公开(公告)日:2007-08-16
    The invention provides the use of a compound or a composition comprising said compound for inhibiting the activity of at least one kinase, other than ROCK kinase, in vitro or in vivo, pharmaceutical and/or veterinary compositions comprising such compounds, medical and veterinary uses of such compounds and the compounds themselves.
    本发明提供了使用一种化合物或含有该化合物的组合物来抑制体外或体内至少一种激酶的活性(ROCK激酶除外),以及含有该类化合物的药物和/或兽医组合物,该类化合物的医学和兽医用途以及化合物本身。
  • Visual function disorder improving agents
    申请人:——
    公开号:US20040106646A1
    公开(公告)日:2004-06-03
    The present invention provides a visual function disorder improving agent containing a compound having Rho kinase inhibitory activity, particularly (R)-(+)-N-( 1 H-pyrrolo[2,3-b]pyridin-4-yl)-4-(1-aminoethyl)benzamide, as an effective component. This agent has axon of the retinal ganglion cellal extension promoting action and optic nerve cell regeneration promoting action, and is useful for the treatment of a visual function disorder associated with various eye diseases caused by damage, defects, degeneration and the like in the retinal or optic nerve.
    本发明提供了一种含有具有Rho激酶抑制活性的化合物的视觉功能障碍改善剂,特别是(R)-(+)-N-(1H-吡咯[2,3-b]吡啶-4-基)-4-(1-氨基乙基)苯甲酰胺作为有效成分。该剂具有促进视网膜神经节细胞轴突延伸和视神经细胞再生的作用,可用于治疗与视网膜或视神经的损伤、缺陷、退化等引起的各种眼部疾病相关的视觉功能障碍。
  • VISUAL FUNCTION IMPROVING AGENTS
    申请人:Senju Pharmaceutical Co., Ltd.
    公开号:EP1378247A1
    公开(公告)日:2004-01-07
    The present invention provides a visual function disorder improving agent containing a compound having Rho kinase inhibitory activity, particularly (R)-(+)-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-4-(1-aminoethyl)benzamide, as an effective component. This agent has axon of the retinal ganglion cellal extension promoting action and optic nerve cell regeneration promoting action, and is useful for the treatment of a visual function disorder associated with various eye diseases caused by damage, defects, degeneration and the like in the retinal or optic nerve.
    本发明提供了一种视功能紊乱改善剂,其有效成分含有具有 Rho 激酶抑制活性的化合物,特别是(R)-(+)-N-(1H-吡咯并[2,3-b]吡啶-4-基)-4-(1-氨基乙基)苯甲酰胺。这种药剂具有促进视网膜神经节细胞轴突延伸的作用和促进视神经细胞再生的作用,可用于治疗因视网膜或视神经系统损伤、缺损、变性等引起的与各种眼病相关的视觉功能障碍。
  • CORNEAL PERCEPTION RECOVERY DRUG CONTAINING AMIDE COMPOUND
    申请人:Senju Pharmaceutical Co., Ltd.
    公开号:EP1752456A1
    公开(公告)日:2007-02-14
    The amide compound of the formula (I) [each symbol is as defined in the description] has a promoting action on neuritogenesis of trigeminal nerve cells, and the compound is useful as a corneal neuritogenesis promoter, an agent for recovering corneal sensitivity by promotion of corneal neuritogenesis, and an agent for treating dry eye.
    式(I)[各符号如描述中所定义]的酰胺化合物对三叉神经细胞的神经元发生具有促进作用,该化合物可用作角膜神经元发生促进剂、通过促进角膜神经元发生恢复角膜敏感性的制剂以及治疗干眼症的制剂。
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