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2,2-dimethyl-4-morpholinobutanenitrile

中文名称
——
中文别名
——
英文名称
2,2-dimethyl-4-morpholinobutanenitrile
英文别名
2,2-dimethyl-4-morpholin-4-ylbutanenitrile
2,2-dimethyl-4-morpholinobutanenitrile化学式
CAS
——
化学式
C10H18N2O
mdl
——
分子量
182.266
InChiKey
UZPHNZVKMQSADG-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):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    36.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2,2-dimethyl-4-morpholinobutanenitrile2-羟基吡啶盐酸氢气三乙胺 、 sodium hydroxide 作用下, 以 1,4-二氧六环乙醇 为溶剂, 反应 43.0h, 生成 (2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-4-morpholinobutyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide hydrochloride
    参考文献:
    名称:
    Discovery of highly potent renin inhibitors potentially interacting with the S3′ subsite of renin
    摘要:
    To exploit the S3' subsite of renin active site for renin inhibitor design, 42 aliskiren derivatives with modified P2' portion were designed, synthesized and biologically evaluated. Some highly potent renin inhibitors (IC50 < 3 nM) were identified, among which compounds 38 (IC50 = 0.9 nM) and 39 (IC50 = 0.7 nM) were over 2.5-fold more potent than aliskiren (IC50 = 2.3 nM). SAR analysis indicated that incorporation of polar hydrophilic moieties into the P2' portion of renin inhibitors generally enhanced the potency. Consistently with this, molecular modeling study revealed that the triazole part of 39 could provide additional interactions to the S3' subsite of renin active site. Moreover, in vivo evaluation in the double transgenic mouse hypertension model demonstrated that 39 produced greater reduction of the mean arterial blood pressure than ariskiren at the doses of 17.0 and 34.0 mu mol/kg, respectively. Taken together, the S3' subsite of renin active site merits further consideration for renin inhibitor design. (C) 2015 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2015.08.060
  • 作为产物:
    描述:
    2-(4-吗啉)乙基溴异丁腈lithium diisopropyl amide 作用下, 以 四氢呋喃 为溶剂, 反应 4.5h, 以82%的产率得到2,2-dimethyl-4-morpholinobutanenitrile
    参考文献:
    名称:
    Discovery of highly potent renin inhibitors potentially interacting with the S3′ subsite of renin
    摘要:
    To exploit the S3' subsite of renin active site for renin inhibitor design, 42 aliskiren derivatives with modified P2' portion were designed, synthesized and biologically evaluated. Some highly potent renin inhibitors (IC50 < 3 nM) were identified, among which compounds 38 (IC50 = 0.9 nM) and 39 (IC50 = 0.7 nM) were over 2.5-fold more potent than aliskiren (IC50 = 2.3 nM). SAR analysis indicated that incorporation of polar hydrophilic moieties into the P2' portion of renin inhibitors generally enhanced the potency. Consistently with this, molecular modeling study revealed that the triazole part of 39 could provide additional interactions to the S3' subsite of renin active site. Moreover, in vivo evaluation in the double transgenic mouse hypertension model demonstrated that 39 produced greater reduction of the mean arterial blood pressure than ariskiren at the doses of 17.0 and 34.0 mu mol/kg, respectively. Taken together, the S3' subsite of renin active site merits further consideration for renin inhibitor design. (C) 2015 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2015.08.060
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文献信息

  • Discovery of highly potent renin inhibitors potentially interacting with the S3′ subsite of renin
    作者:Xiaowei Sun、Xiaoan Wen、Yan-yan Chen、Chen Shi、Chengzhe Gao、Yong Wu、Li-jun Wang、Xiu-hong Yang、Hongbin Sun
    DOI:10.1016/j.ejmech.2015.08.060
    日期:2015.10
    To exploit the S3' subsite of renin active site for renin inhibitor design, 42 aliskiren derivatives with modified P2' portion were designed, synthesized and biologically evaluated. Some highly potent renin inhibitors (IC50 < 3 nM) were identified, among which compounds 38 (IC50 = 0.9 nM) and 39 (IC50 = 0.7 nM) were over 2.5-fold more potent than aliskiren (IC50 = 2.3 nM). SAR analysis indicated that incorporation of polar hydrophilic moieties into the P2' portion of renin inhibitors generally enhanced the potency. Consistently with this, molecular modeling study revealed that the triazole part of 39 could provide additional interactions to the S3' subsite of renin active site. Moreover, in vivo evaluation in the double transgenic mouse hypertension model demonstrated that 39 produced greater reduction of the mean arterial blood pressure than ariskiren at the doses of 17.0 and 34.0 mu mol/kg, respectively. Taken together, the S3' subsite of renin active site merits further consideration for renin inhibitor design. (C) 2015 Elsevier Masson SAS. All rights reserved.
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