4-Prenyloxypsoralen 4-((3-甲基丁-2-烯-1-基)氧基)-7H-呋喃[3,2-g]苯并吡喃-7-酮

CAS 482-45-1 MFCD00272155

化学结构图

482-45-1
SMILES: CC(C)=CCOc1c2ccoc2cc2oc(=O)ccc12

化学属性

Mol. FormulaC16H14O4
Mol. Weight270
Density1.242

别名和识别编码

Chemical Name4-Prenyloxypsoralen
CAS Number482-45-1
Synonym ISOIMPERATORIN(P) 4-(3-Methylbut-2-enoxy)furo[3,2-g]chromen-7-one 4-(3-Methylbut-2-enyloxy)furo[3,2-g]chromen-7-one 4-[(3-Methyl-2-buten-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one 4-(3-Methyl-but-2-enyloxy-furo[3,2-g]chromen-7-one Isomperatorin 4-(3-Methyl-but-2-enyloxy-furo[3,2-γ],chromen-7-one buten-1-yl)oxy]- 4-PRENYLOXYPSORALEN ISOIMPERATORIN 4-(Isopentenyloxy)-7H-furo[3,2-g][1]benzopyran-7-one 7H-Furo[3,2-g][1]benzopyran-7-one, 4-[(3-methyl-2- 异欧芹属素乙 4-(3-甲基丁-2-烯氧基)呋喃并[3,2-g]苯并吡喃-7-酮 Isoimperatoin 白芷甲素 4-[(3-Methyl-2-butenyl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one 异欧前胡素
MDL NumberMFCD00272155
Chemical Name Translation4-((3-甲基丁-2-烯-1-基)氧基)-7H-呋喃[3,2-g]苯并吡喃-7-酮
Beilstein Registry Number1291723
LabNetwork Molecule IDLN00358320
PubChem Substance ID68081
InChIInChI=1S/C16H14O4/c1-10(2)5-7-19-16-11-3-4-15(17)20-14(11)9-13-12(16)6-8-18-13/h3-6,8-9H,7H2,1-2H3
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分类

  • {SNA} Alphabetical Index of Phytochemical Standards, Analytical Standards, Angelica, Citrus, I - M, Phenylpropanes, Phytochemical Standards, Phytochemical Standards by Plant Genus, 分析/色谱
  • {SNA} Alphabetical, Analytical Standards, Analytical/Chromatography, Angelica, Chromatography,
  • {SNA} Alphabetical, Analytical Standards, Angelica, Chromatography, Citrus, I - M, Life Sciences Standards, Phytopharma Standards, Standards by Plant Genus, 分析/色谱
  • {uni_hamburg} no charge; oxygen heterocycle; carbocycle; aromatic; large ring; fused rings; 5ring; 6ring; 9ring; 10ring; 13ring; ester; lactone; ether; 1fragment

产品应用

  • Anti-inflammatory. Effect on proliferation.

相关文献及参考

  • Short: III/35D4 Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts for Carbon-13, Part 4: Natural Products Author: Dobhal, M.P. Editor: Gupta, R.R.; Lechner, M.D. Source: Landolt-Börnstein, New Series Volume: III/35D4 Year: 2006 Keyword: aromatic compounds; carbon-13; chemical shift; coupling constant; molecular structure ISBN: 978-3-540-29732-1 ISBN: 3-540-29732-4 Internet Resource: DOI:10.1007/b13179 RefComment: VIII, 417 p., 1925 illus., Hardcover RefComment: Written for Scientists and engineers in the fields of physics, chemistry and physical chemistry who intend to use NMR to study the structure and the binding of molecules Abstract: Nuclear Magnetic Resonance (NMR) is based on the fact that certain nuclei exhibit a magnetic moment, oriented by a magnetic field, and absorb characteristic frequencies in the radiofrequency part of the spectrum. The spectral lines of the nuclei are highly influenced by the chemical environment i.e. the structure and interaction of the molecules. NMR is now the leading technique and a powerful tool for the investigation of the structure and interaction of molecules. The present Landolt-Börnstein volume III/35 Nuclear Magnetic Resonance (NMR) Data is therefore of major interest to all scientists and engineers who intend to use NMR to study the structure and the binding of molecules. Volume III/35 "NMR-Data" is divided into several subvolumes and parts. Subvolume III/35A contains the nuclei 11B and 31P, subvolume III/35B contains the nuclei 19F and 15N, subvolume III/35C contains the nucleus 1H, subvolume III/35D contains the nucleus 13C, subvolume III/35E contains the nucleus 17O, and subvolume III/35G contains the nucleus 77Se. More nuclei will be presented later.

安全信息

RTECSLV1513000
Storage condition 储存温度2-8℃
WGK Germany3
GHS Symbol
Safety Statements
  • S24/25 Avoid contact with skin and eyes 避免皮肤和眼睛接触;
Precautionary statements
  • P262 Do not get in eyes, on skin, or on clothing. 不要接触眼睛,皮肤或衣服。

其他信息

  • MOL 文件:482-45-1.mol
  • 药理作用:分子式C16H14O4,分子量270.27,无色针状结晶(乙醇),熔点110~111℃。 异欧前胡素具有降压、解痉、抗癌的作用,还可以治疗银屑病。
  • 羌活中异欧前胡素的含量测定:[色谱条件] 色谱柱:μbondapak C18柱(150mm×6mm, 5μm);流动相:甲醇-乙腈-0.25mol/L磷酸溶液(9:5:10);流速:1.0ml/min;检测波长:322nm;柱温:室温。 [供试品的制备] 取本品粗粉约50g,用8倍量90%乙醇回流提取3次,每次1.5h,合并提取液,回收乙醇,得浸膏13.70g,并将其与适量经处理过的大孔吸附树脂拌匀,置于经处理过的大孔吸附树脂柱上,依次用水,20%、30%、40%、50%、60%、70%、80%、90%的乙醇冲洗,每次冲至洗脱液无色,水浴蒸干,得膏状物,分别用50%乙醇溶解,定容至50ml。按本法色谱条件进行测定。

系列性分类


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