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(2RS)-3-[(3-phenoxyphenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol | 263264-10-4

中文名称
——
中文别名
——
英文名称
(2RS)-3-[(3-phenoxyphenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol
英文别名
3-[[3-(phenoxy)phenyl][[3-(1,1,2,2-tetrafluoroethoxy)-phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol;1,1,1-Trifluoro-3-((3-phenoxyphenyl)(3-(1,1,2,2-tetrafluoroethoxy)benzyl)amino)propan-2-ol;1,1,1-trifluoro-3-[3-phenoxy-N-[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]anilino]propan-2-ol
(2RS)-3-[(3-phenoxyphenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol化学式
CAS
263264-10-4
化学式
C24H20F7NO3
mdl
——
分子量
503.417
InChiKey
XNYMOOHZPFZFJE-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):
    7.2
  • 重原子数:
    35
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    41.9
  • 氢给体数:
    1
  • 氢受体数:
    11

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (2RS)-3-[(3-phenoxyphenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol 在 (diethylamino)sulfur trifluoride 作用下, 以 正己烷二氯甲烷 为溶剂, 以240 mg (50%)的产率得到N-(3-phenoxyphenyl)-N-(3,3,3,2-tetrafluoropropyl)-3-(1,1,2,2-tetrafluoroethoxy)benzenemethanamine
    参考文献:
    名称:
    Substituted N, N-disubstituted diamino compounds useful for inhibiting cholesteryl ester transfer protein activity
    摘要:
    这项发明涉及替代多环芳基和杂环芳基的三级杂烷基胺化合物,可用作胆固醇酯转移蛋白(CETP;血浆脂质转移蛋白-I)的抑制剂,以及用于治疗动脉粥样硬化和其他冠状动脉疾病的化合物、组合物和方法。首选的三级杂烷基胺化合物是取代的N,N-二取代二胺。首选的具体N,N-二取代二胺化合物是:1
    公开号:
    US20020120011A1
  • 作为产物:
    描述:
    1,1,1-三氟-2,3-环氧丙烷(3-phenoxyphenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amineytterbium(III) triflate 作用下, 反应 24.0h, 以70.8%的产率得到(2RS)-3-[(3-phenoxyphenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol
    参考文献:
    名称:
    Substituted tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity
    摘要:
    该发明涉及用作胆固醇酯转移蛋白(CETP;血浆脂质转移蛋白-I)抑制剂的取代三级杂代烷基胺化合物,以及用于治疗动脉粥样硬化和其他冠状动脉疾病的化合物、组合物和方法。
    公开号:
    US06924313B1
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文献信息

  • Nitrosated and nitrosylated diuretic compounds, compositions and methods of use
    申请人:Garvey S. David
    公开号:US20050059655A1
    公开(公告)日:2005-03-17
    The invention describes novel nitrosated and/or nitrosylated diuretic compounds or pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated and/or nitrosylated diuretic compound, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides novel compositions and kits comprising at least one diuretic compound of the invention, that is optionally nitrosated and/or nitrosylated, and, optionally, at least one nitric oxide donor compound and/or at least one therapeutic agent. The invention also provides methods for (a) treating conditions resulting from excessive water and/or electrolyte retention; (b) treating cardiovascular diseases; (c) treating renovascular diseases; (d) treating diabetes; (e) treating diseases resulting from oxidative stress; (f) treating endothelial dysfunctions; (g) treating diseases caused by endothelial dysfunctions; (h) treating cirrhosis; (j) treating pre-eclampsia; (k) treating osteoporosis; and (l) treating nephropathy.
    该发明描述了新颖的亚硝基化和/或亚硝酰化利尿化合物或其药用盐,以及包含至少一种亚硝基化和/或亚硝酰化利尿化合物的新型组合物,以及可选地至少一种一氧化氮供体和/或至少一种治疗剂。该发明还提供了包含该发明中至少一种利尿化合物的新型组合物和试剂盒,该利尿化合物可选择地亚硝基化和/或亚硝酰化,并且可选地至少一种一氧化氮供体化合物和/或至少一种治疗剂。该发明还提供了用于(a)治疗由于过多分和/或电解贮留引起的疾病;(b)治疗心血管疾病;(c)治疗肾血管疾病;(d)治疗糖尿病;(e)治疗由氧化应激引起的疾病;(f)治疗内皮功能障碍;(g)治疗由内皮功能障碍引起的疾病;(h)治疗肝硬化;(j)治疗子痫前期;(k)治疗骨质疏松症;和(l)治疗肾病的方法。
  • Nitric oxide enhancing diuretic compounds, compositions and methods of use
    申请人:Garvey S. David
    公开号:US20060189603A1
    公开(公告)日:2006-08-24
    The invention describes novel compositions and kits comprising at least one nitric oxide enhancing diuretic compound, or pharmaceutically acceptable salts thereof, and, optionally, at least one nitric oxide enhancing compound and/or at least one therapeutic agent. The invention also provides methods for (a) treating conditions resulting from excessive water and/or electrolyte retention; (b) treating cardiovascular diseases; (c) treating renovascular diseases; (d) treating diabetes; (e) treating diseases resulting from oxidative stress; (f) treating endothelial dysfunctions; (g) treating diseases caused by endothelial dysfunctions; (h) treating cirrhosis; (j) treating pre-eclampsia; (k) treating osteoporosis; (l) treating nephropathy; (m) treating peripheral vascular diseases; (n) treating portal hypertension; (o) treating central nervous system disorders; (p) treating metabolic syndrome; (q) treating sexual dysfunctions; and (r) hyperlipidemia. The nitric oxide enhancing diuretic compounds comprise at least one nitric oxide enhancing group linked to the diuretic compound through one or more sites such as carbon, oxygen and/or nitrogen via a bond or moiety that cannot be hydrolyzed.
    该发明描述了包含至少一种增强一氧化氮利尿化合物或其药用盐的新型组合物和试剂盒,以及可选地,至少一种增强一氧化氮化合物和/或至少一种治疗剂的试剂盒。该发明还提供了以下方法:(a)治疗由过多分和/或电解贮留引起的症状;(b)治疗心血管疾病;(c)治疗肾血管疾病;(d)治疗糖尿病;(e)治疗由氧化应激引起的疾病;(f)治疗内皮功能障碍;(g)治疗由内皮功能障碍引起的疾病;(h)治疗肝硬化;(j)治疗子痫前期;(k)治疗骨质疏松症;(l)治疗肾病;(m)治疗外周血管疾病;(n)治疗门静脉高压;(o)治疗中枢神经系统疾病;(p)治疗代谢综合征;(q)治疗性功能障碍;以及(r)高脂血症。增强一氧化氮利尿化合物包括至少一种增强一氧化氮基团,通过碳、氧和/或氮等一个或多个位点与利尿化合物连接,连接通过不能解的键或基团。
  • (R)-chiral halogenated substituted N-benzyl-N-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity
    申请人:——
    公开号:US20020177708A1
    公开(公告)日:2002-11-28
    The invention relates to substituted aryl and heteroaryl (R)-Chiral Halogenated 1-Substitutedamino-(n+1)-Alkanol compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating atherosclerosis and other coronary artery diseases. Novel high yield, stereoselective processes for the preparation of the chiral substituted alkanol compounds from chiral and achiral intermediates are described.
    这项发明涉及取代芳基和杂环芳基的(R)-手性卤代1-取代基-(n+1)-烷醇化合物,用作胆固醇酯转移蛋白(CETP;血浆脂质转移蛋白-I)的抑制剂,以及用于治疗动脉粥样硬化和其他冠状动脉疾病的化合物、组合物和方法。描述了从手性和不对映体中间体制备手性取代烷醇化合物的新型高产率、立体选择性过程。
  • Nitric oxide enhancing angiotensin II antagonist compounds, compositions and methods of use
    申请人:Garvey S. David
    公开号:US20070032533A1
    公开(公告)日:2007-02-08
    The invention describes compositions and kits comprising at least one nitric oxide enhancing angiotensin II antagonist compound, or pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitric oxide enhancing angiotensin II antagonist compound, and, optionally, at least one nitric oxide enhancing compound and/or at least one therapeutic agent. The invention also provides methods for (a) treating cardiovascular diseases; (b) treating renovascular diseases; (c) treating diabetes; (d) treating diseases resulting from oxidative stress; (e) treating endothelial dysfunctions; (f) treating diseases caused by endothelial dysfunctions; (g) treating cirrhosis; (h) treating pre-eclampsia; (j) treating osteoporosis; (k) treating nephropathy; (l) treating peripheral vascular diseases; (m) treating portal hypertension (o) treating central nervous system disorders; (p) treating metabolic syndrome; and (q) treating hyperlipidemia. The nitric oxide enhancing angiotensin II antagonist compounds comprise at least one nitric oxide enhancing group linked to the angiotensin II antagonist compound through one or more sites such as carbon, oxygen and/or nitrogen via a bond or moiety that cannot be hydrolyzed.
    该发明描述了包含至少一种一氧化氮增强的血管紧张素II拮抗剂化合物或其药用盐的组合物和试剂盒,以及包含至少一种一氧化氮增强的血管紧张素II拮抗剂化合物的新型组合物,还可以包含至少一种一氧化氮增强化合物和/或至少一种治疗剂。该发明还提供了用于(a)治疗心血管疾病;(b)治疗肾血管疾病;(c)治疗糖尿病;(d)治疗由氧化应激导致的疾病;(e)治疗内皮功能障碍;(f)治疗由内皮功能障碍引起的疾病;(g)治疗肝硬化;(h)治疗子痫前症;(j)治疗骨质疏松症;(k)治疗肾病;(l)治疗外周血管疾病;(m)治疗门静脉高压症;(o)治疗中枢神经系统疾病;(p)治疗代谢综合征;和(q)治疗高脂血症的方法。一氧化氮增强的血管紧张素II拮抗剂化合物包括至少一种一氧化氮增强基团,通过碳、氧和/或氮等一个或多个位点与血管紧张素II拮抗剂化合物连接,连接方式是通过一种不能解的键或基团。
  • Nitric Oxide Releasing Pyruvate Compounds, Compositions and Methods of Use
    申请人:Garvey David S.
    公开号:US20080287407A1
    公开(公告)日:2008-11-20
    The invention describes novel nitrosated and/or nitrosylated pyruvate compounds and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated and/or nitrosylated pyruvate compound, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel compositions comprising at least one pyruvate compound and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one pyruvate compound, that is optionally nitrosated and/or nitrosylated, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides methods for treating diseases resulting from oxidative stress, diabetes, reperfusion injury following ischemia, preservation of tissues, organs, organ parts and/or limbs.
    该发明描述了新颖的硝化和/或亚硝化丙酮酸盐及其药用可接受盐,以及包含至少一种硝化和/或亚硝化丙酮酸化合物的新型组合物,以及可选地,至少一种捐赠、转移或释放一氧化氮、刺激内源性一氧化氮合成、提高内源性内皮源性舒张因子平或是一氧化氮合酶底物的化合物,和/或至少一种治疗剂。该发明还提供了包含至少一种丙酮酸化合物和至少一种捐赠、转移或释放一氧化氮、提高内源性内皮源性舒张因子平、刺激内源性一氧化氮合成或是一氧化氮合酶底物和/或至少一种治疗剂的新型组合物。该发明还提供了包含至少一种丙酮酸化合物的新型试剂盒,该丙酮酸化合物可选地硝化和/或亚硝化,以及可选地至少一种一氧化氮供体和/或至少一种治疗剂。该发明还提供了治疗由氧化应激、糖尿病、缺血后再灌注损伤、组织、器官、器官部分和/或肢体保护引起的疾病的方法。
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