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endo-4-bromo-2-(2-pyrrolidin-1-yl-ethoxy)-aniline | 1161833-90-4

中文名称
——
中文别名
——
英文名称
endo-4-bromo-2-(2-pyrrolidin-1-yl-ethoxy)-aniline
英文别名
4-Bromo-2-(2-pyrrolidin-1-yl-ethoxy)-phenylamine;4-bromo-2-(2-pyrrolidin-1-yl-ethoxy)-aniline;4-Bromo-2-[2-(pyrrolidin-1-yl)ethoxy]aniline;4-bromo-2-(2-pyrrolidin-1-ylethoxy)aniline
endo-4-bromo-2-(2-pyrrolidin-1-yl-ethoxy)-aniline化学式
CAS
1161833-90-4
化学式
C12H17BrN2O
mdl
——
分子量
285.184
InChiKey
IEKCXQDKELIIQS-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

物化性质

  • 沸点:
    378.7±32.0 °C(Predicted)
  • 密度:
    1.396±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    38.5
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Tetrahydroisoquinoline Derivatives As Highly Selective and Potent Rho Kinase Inhibitors
    作者:Xingang Fang、Yan Yin、Yen Ting Chen、Lei Yao、Bo Wang、Michael D. Cameron、Li Lin、Susan Khan、Claudia Ruiz、Thomas Schröter、Wayne Grant、Amiee Weiser、Jennifer Pocas、Alok Pachori、Stephan Schürer、Philip LoGrasso、Yangbo Feng
    DOI:10.1021/jm100579r
    日期:2010.8.12
    Rho kinase (ROCK) is a promising drug target for the treatment of many diseases including hypertension, multiple sclerosis, cancer, and glaucoma. The structure-activity relationships (SAR) around a series of tetrahydroisoquinolines were evaluated utilizing biochemical and cell-based assays to measure ROCK inhibition. These novel ROCK inhibitors possess high potency, high selectivity, and appropriate pharmacokinetic properties for glaucoma applications. The lead compound, 35, had subnanomolar potency in enzyme ROCK-II assays as well as excellent cell-based potency (IC(50) = 51 nM). In a kinase panel profiling, 35 had an off-target hit rate of only 1.6% against 442 kinases. Pharmacology studies showed that compound 35 was efficacious in reducing intraocular pressure (IOP) in rats with reasonably long duration of action. These results suggest that compound 35 may serve as a promising agent for further development in the treatment of glaucoma.
  • Discovery of Potent and Selective Urea-Based ROCK Inhibitors and Their Effects on Intraocular Pressure in Rats
    作者:Yan Yin、Michael D. Cameron、Li Lin、Susan Khan、Thomas Schröter、Wayne Grant、Jennifer Pocas、Yen Ting Chen、Stephan Schürer、Alok Pachori、Philip LoGrasso、Yangbo Feng
    DOI:10.1021/ml1000382
    日期:2010.7.8
    A series of urea-based Rho kinase (ROCK) inhibitors were designed and evaluated. The discovered compounds had excellent enzyme and cellular potency, high kinase selectivity, high aqueous solubility, good porcine corneal penetration, and appropriate DMPK profiles for topical applications as antiglaucoma therapeutics.
  • DRUGS AND COMPOSITIONS FOR THE TREATMENT OF OCULAR DISORDERS
    申请人:Graybug Vision, Inc.
    公开号:EP3600324A1
    公开(公告)日:2020-02-05
  • [EN] DRUGS AND COMPOSITIONS FOR THE TREATMENT OF OCULAR DISORDERS<br/>[FR] COMPOSÉS ET COMPOSITIONS POUR LE TRAITEMENT DE TROUBLES OCULAIRES
    申请人:GRAYBUG VISION INC
    公开号:WO2018175922A1
    公开(公告)日:2018-09-27
    The present invention provides new prodrugs of therapeutically active compounds, including oligomeric prodrugs, and compositions to treat medical disorders, for example glaucoma, a disorder or abnormality related to an increase in intraocular pressure (IOP), a disorder requiring neuroprotection, age-related macular degeneration, or diabetic retinopathy.
    本发明提供了治疗活性化合物的新前药,包括寡聚前药,以及用于治疗医学疾病的组合物,例如青光眼,一种与眼压增高有关的疾病或异常,需要神经保护的疾病,年龄相关性黄斑变性,或糖尿病性视网膜病变。
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