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evocarpine

evocarpine Suppliers list
Company Name: BioBioPha Co., Ltd.  
Tel: 0871-65217109
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Company Name: Shanghai Winherb Medical Technology Co., Ltd.  
Tel: 17301719108 13341702378
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Company Name: Wuxi Zhongkun Biochemical Technology Co., Ltd.  
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evocarpine manufacturers

  • Evocarpine
  • Evocarpine pictures
  • $52.00
  • 2026-07-15
  • CAS:15266-38-3
  • Purity: 99.81%
  • Supply Ability: 10g
  • evocarpine
  • evocarpine pictures
  • 2024-04-12
  • CAS:15266-38-3
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 2000ton
  • evocarpine
  • evocarpine pictures
  • $1.00
  • 2019-07-06
  • CAS:15266-38-3
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: 100KG
evocarpine Basic information
Product Name:evocarpine
Synonyms:1-Methyl-2-[(Z)-8-tridecene-1-yl]quinoline-4(1H)-one;1-Methyl-2-[(Z)-8-tridecenyl]-4(1H)-quinolinone;1-Methyl-2-[(Z)-8-tridecenyl]-4(1H)-quinolone;1-Methyl-2-[(Z)-8-tridecenyl]quinoline-4(1H)-one;evocarpine;1-Methyl-2-(8Z)-8-tridecenyl-4(1H)-quinolinone;(Z)-1-Methyl-2-(tridec-8-en-1-yl)quinolin-4(1H)-one;4(1H)-Quinolinone,1-Methyl-2-(8Z)-8-tridecen-1-yl-
CAS:15266-38-3
MF:C23H33NO
MW:339.51
EINECS:
Product Categories:
Mol File:15266-38-3.mol
evocarpine Structure
evocarpine Chemical Properties
Melting point 34-38℃
Boiling point 456.2±45.0 °C(Predicted)
density 0.975±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. 2-8°C
form Solid
pka2.52±0.70(Predicted)
color White to off-white
CAS DataBase Reference15266-38-3
Safety Information
MSDS Information
evocarpine Usage And Synthesis
Chemical PropertiesWhite crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO. It is derived from Evodia rutaecarpa (Juss.) Benth.
UsesEvocarpine, a quinolone alkaloid that could be isolated from Evodiae fructus, inhibitss Ca2+ influx through voltage-dependent calcium channels. Antimycobacterial activity[1][2].
DefinitionChEBI: Evocarpine is a member of quinolines.
References[1] J Yamahar, et al. The vasorelaxant effect of evocarpine in isolated aortic strips: mode of action. Eur J Pharmacol. 1988 Oct 11;155(1-2):139-43. DOI:10.1016/0014-2999(88)90411-6
[2] C Hochfellner, et al. Antagonistic effects of indoloquinazoline alkaloids on antimycobacterial activity of evocarpine. J Appl Microbiol. 2015 Apr;118(4):864-72. DOI:10.1111/jam.12753
[3] N Y Kim, et al. Cyclic adenosine monophosphate inhibits quinolone alkaloid evocarpine-induced apoptosis via activation of protein kinase A in human leukaemic HL-60 cells. Pharmacol Toxicol. 2000 Jul;87(1):1-5. DOI:10.1111/j.0901-9928.2000.870101.x
evocarpine Preparation Products And Raw materials
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