(S)-6-(2-(Benzo[D][1,3]Dioxol-5-Yl)Ethyl)-4-Methoxy-5,6-Dihydro-2H-Pyran-2-One (S)-6-(2-(苯并[d][1,3]二氧戊环-5-基)乙基)-4-甲氧基-5,6-二氢-2H-吡喃-2-酮

CAS 19902-91-1 MFCD00221731

化学结构图

19902-91-1
SMILES: COC1C[C@H](CCC2C=C3OCOC3=CC=2)OC(=O)C=1

化学属性

Mol. FormulaC15H16O5
Mol. Weight276.31

别名和识别编码

Chemical Name(S)-6-(2-(Benzo[D][1,3]Dioxol-5-Yl)Ethyl)-4-Methoxy-5,6-Dihydro-2H-Pyran-2-One
Synonym 2H-Pyran-2-one, 6-(2-(1,3-benzodioxol-5-yl)ethyl)-5,6-dihydro-4-methoxy-, 7,8-Dihydromethysticin Dihydromethysticin (+)-Dihydromethysticin 6-[2-(1,3-Benzodioxol-5-yl)ethyl]-4-methoxy-5,6-dihydro-2H-pyran-2-one DHM
CAS Number19902-91-1
MDL NumberMFCD00221731
Beilstein Registry Number91699
Chemical Name Translation(S)-6-(2-(苯并[d][1,3]二氧戊环-5-基)乙基)-4-甲氧基-5,6-二氢-2H-吡喃-2-酮
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分类

  • {SNA} A - D, Alphabetical, Analytical Standards, Analytical/Chromatography, Chromatography, Life Sciences Standards, Phenylpropanes, Phytopharma Standards, Piper, Standards by Plant Genus, Substance Classification

相关文献及参考

  • [2]. Walden J, et al. Effects of kawain and dihydromethysticin on field potential changes in the hippocampus. Prog Neuropsychopharmacol Biol Psychiatry. 1997 May;21(4):697-706.
  • [3]. Sarris J, et al. Kava: a comprehensive review of efficacy, safety, and psychopharmacology. Aust N Z J Psychiatry. 2011 Jan;45(1):27-35.
  • [1]. Ma Y, et al. Desmethoxyyangonin and dihydromethysticin are two major pharmacological kavalactones with marked activity on the induction of CYP3A23. Drug Metab Dispos. 2004 Nov;32(11):1317-24.
  • [1]. Ma Y, et al. Desmethoxyyangonin and dihydromethysticin are two major pharmacological kavalactones with marked activity on the induction of CYP3A23. Drug Metab Dispos. 2004 Nov;32(11):1317-24.
  • [2]. Walden J, et al. Effects of kawain and dihydromethysticin on field potential changes in the hippocampus. Prog Neuropsychopharmacol Biol Psychiatry. 1997 May;21(4):697-706.
  • [3]. Sarris J, et al. Kava: a comprehensive review of effica

安全信息

WGK Germany3
RTECSUQ0516000
TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Oral
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 1050 mg/kg
TOXIC EFFECTS :
   Behavioral - muscle weakness
   Behavioral - ataxia
   Lungs, Thorax, or Respiration - other changes
REFERENCE :
   AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans
   Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium)  V.4-   
   1898-  Volume(issue)/page/year: 138,505,1962

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intraperitoneal
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 420 mg/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   EXPEAM Experientia.  (Birkhaeuser Verlag, POB 133, CH-4010 Basel,
   Switzerland)  V.1-    1945-  Volume(issue)/page/year: 26,283,1970

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intraperitoneal
SPECIES OBSERVED        : Rodent - rabbit
DOSE/DURATION           : 300 mg/kg
TOXIC EFFECTS :
   Behavioral - muscle weakness
   Behavioral - muscle contraction or spasticity
   Gastrointestinal - nausea or vomiting
REFERENCE :
   AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans
   Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium)  V.4-   
   1898-  Volume(issue)/page/year: 138,505,1962

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intraperitoneal
SPECIES OBSERVED        : Mammal - dog
DOSE/DURATION           : >200 mg/kg
TOXIC EFFECTS :
   Behavioral - muscle weakness
   Behavioral - muscle contraction or spasticity
   Gastrointestinal - nausea or vomiting
REFERENCE :
   AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans
   Institute of Pharmacology,

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