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8-[2-(Dimethylamino)ethyl]-3,5-dimethoxyphenanthrene-2,6-diol | 66396-17-6

中文名称
——
中文别名
——
英文名称
8-[2-(Dimethylamino)ethyl]-3,5-dimethoxyphenanthrene-2,6-diol
英文别名
——
8-[2-(Dimethylamino)ethyl]-3,5-dimethoxyphenanthrene-2,6-diol化学式
CAS
66396-17-6
化学式
C20H23NO4
mdl
——
分子量
341.407
InChiKey
GMXXEYOMDIZADE-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

  • 熔点:
    227-229 °C
  • 沸点:
    558.2±50.0 °C(Predicted)
  • 密度:
    1.238±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    62.2
  • 氢给体数:
    2
  • 氢受体数:
    5

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

点击查看最新优质反应信息

文献信息

  • Reactive Oxygen Species (ROS) Generation Inhibited by Aporphine and Phenanthrene Alkaloids Semi-Synthesized from Natural Boldine
    作者:Lara Milián、Rossana Estellés、Belén Abarca、Rafael Ballesteros、María Jesús Sanz、María Amparo Blázquez
    DOI:10.1248/cpb.52.696
    日期:——
    Four phenanthrene and one aporphine alkaloids semi-synthesized from boldine were evaluated for their inhibitory effect on reactive oxygen species (ROS) generation. ROS generation by neutrophils stimulated with N-formyl-methionyl-leucyl-phenylalanine was inhibited in a concentration dependent manner. Alkaloids exerted similar inhibitory effect in the hypoxanthine–xanthine oxidase system than in stimulated neutrophils, which could be attributed to a direct ROS scavenging activity. None of the alkaloids assayed had any effect on xanthine oxidase activity. Therefore the synthesized alkaloids might constitute an alternative therapy in inflammation disorders in which ROS generation is involved.
    研究人员评估了从粗碱半合成的四种菲生物碱和一种卟吩生物碱对活性氧(ROS)生成的抑制作用。在 N-甲酰基-蛋氨酰-亮氨酰-苯丙氨酸的刺激下,中性粒细胞产生的 ROS 会受到浓度依赖性抑制。生物碱对次黄嘌呤-黄嘌呤氧化酶系统的抑制作用与对受刺激的中性粒细胞的抑制作用相似,这可能是由于生物碱具有直接清除 ROS 的活性。没有一种生物碱对黄嘌呤氧化酶的活性有任何影响。因此,合成的生物碱可作为一种替代疗法,用于治疗与 ROS 生成有关的炎症疾病。
  • BOLDINE COMPOUNDS FOR PROMOTING BONE GROWTH
    申请人:Ellies Debra
    公开号:US20100092559A1
    公开(公告)日:2010-04-15
    The present invention provides a method of promoting bone growth in a subject in need thereof, by administering to the subject a therapeutically effective amount of a compound of Formula I. The present invention also provides methods for the treatment of renal disease and cancer.
  • BOLDLINE COMPOUNDS FOR PROMOTING BONE GROWTH
    申请人:Ellies Debra
    公开号:US20120301509A1
    公开(公告)日:2012-11-29
    The present invention provides a method of promoting bone growth in a subject in need thereof, by administering to the subject a therapeutically effective amount of a compound of Formula I. The present invention also provides methods for the treatment of renal disease and cancer.
  • US8188065B2
    申请人:——
    公开号:US8188065B2
    公开(公告)日:2012-05-29
  • US8460642B2
    申请人:——
    公开号:US8460642B2
    公开(公告)日:2013-06-11
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同类化合物

防己菲碱 绿唐松草酮 N-去甲基芒籽宁 N,N-二甲基-2-芘-1-基乙胺 ATM44-乙酰氧基类似物 3,4-二甲氧基-N,N-二甲基-1-菲乙胺 trimethyl-(2-oxo-2-pyrene-1-yl-ethyl)-ammonium bromide dimethyl-(2-[1]phenanthryl-ethyl)-amine secocrebanine N-allylsecoboldine 4-Phenanthrenol, 1-(2-(dimethylamino)ethyl)-3,5,6-trimethoxy- 1-(2-Dimethylaminoethyl)-3,6,7-trimethoxyphenanthren-4-ol [2-(5,6-Dihydroxy-phenanthren-1-yl)-ethyl]-methyl-cyanamide 8-[2-[ethyl(methyl)amino]ethyl]-9,10-dihydrophenanthrene-3,4-diol;hydron;bromide 3,4-Phenanthrenediol, 8-(2-(ethylmethylamino)ethyl)-, hydrobromide Acetic acid 5-[2-(cyano-methyl-amino)-ethyl]-10-methoxy-phenanthro[3,4-d][1,3]dioxol-11-yl ester 3,4,5,6-Tetramethoxy-1-(dimethylamino-ethyl)-phenanthren 8-(2-Dimethylamino-ethyl)-phenanthrene-3,4-diol 3,4-Phenanthrenediol, 8-(2-(dimethylamino)ethyl)-, hydrobromide 2.3.5.6-Tetramethoxy-8-<2-dimethylamino-aethyl>-phenanthren-methojodid Dicentrin-methin II N-[2-(9-methoxynaphtho[2,1-g][1,3]benzodioxol-5-yl)ethyl]-N-methylhydroxylamine 1-<2-ethyl>-3,4,6,7-tetramethoxyphenantrene N-carbethoxy-N-methyl-2-(3',4'-dimethoxy-1'-phenanthryl)ethylamine N-benzylsecoboldine [2-(10,11-dimethoxy-phenanthro[3,4-d][1,3]dioxol-5-yl)-ethyl]-dimethyl-amine secoroemerine N-carbethoxysecoglaucine Ethyl-methyl-(2-naphtho[2,1-g][1,3]benzodioxol-5-ylethyl)azanium N-benzyl-2-(3,7-dibutoxy-4,6-dimethoxyphenanthren-1-yl)-N-methylethanamine Dimethyl-[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]azanium Dimethyl(2-naphtho[2,1-g][1,3]benzodioxol-5-ylethyl)azanium 8-[2-(dimethylamino)ethyl]-9,10-dihydrophenanthrene-3,4-diol;hydron;bromide N,N-dimethyl-2-pyren-1-ylpropan-1-amine 2-(3,4-Dihydroxyphenanthren-1-yl)ethyl-trimethylazanium N,N-dimethyl-2-[(6R)-6-methyl-6,7-dihydronaphtho[2,1-g][1,3]benzodioxol-5-yl]ethanamine N,N-dimethyl-2-(3,4,6,7-tetramethoxy-6,7-dihydrophenanthren-1-yl)ethanamine N,N-dimethyl-2-[(10R)-3,4,6,7-tetramethoxy-10-methyl-9,10-dihydrophenanthren-1-yl]ethanamine Trimethyl(2-naphtho[2,1-g][1,3]benzodioxol-5-ylethyl)azanium Ethyl-methyl-(2-phenanthro[3,4-d][1,3]dioxol-5-yl-ethyl)-amine (1S)-2-(dimethylamino)-1-naphtho[2,1-g][1,3]benzodioxol-5-ylethanol Trimethyl-[2-(2,3,4-trimethoxyphenanthren-1-yl)ethyl]azanium 3,6-Dimethoxy-4-hydroxy-8-<2-(N-methyl-N-ethylamino)ethyl>phenanthrene [2-(5,6-dimethoxy-9,10-dihydro-[1]phenanthryl)-ethyl]-dimethyl-amine 8-[2-(Dimethylamino)ethyl]-3,5-dimethoxyphenanthrene-2,6-diol 2-bromosecoboldine 2-bromo-N,N-dimethylsecoboldine iodide 2-bromo-3,7-dimethoxy-N,N-dimethylsecoboldine iodide 2-bromo-N-methylsecoboldine