Name | (Z)-1-Methyl-2-(tridec-8-en-1-yl)quinolin-4(1H)-one |
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Synonyms |
4(1H)-Quinolinone, 1-methyl-2-(8-tridecenyl)-, (Z)-
4(1H)-Quinolinone, 1-methyl-2-[(8Z)-8-tridecen-1-yl]- 1-Methyl-2-[(8Z)-8-tridecen-1-yl]-4(1H)-quinolinone evocarpine |
Description | Evocarpine, a quinolone alkaloid that could be isolated from Evodiae fructus, inhibitss Ca2+ influx through voltage-dependent calcium channels. Antimycobacterial activity[1][2]. |
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Related Catalog | |
In Vitro | Cumulative application of evocarpine (1-100 μM) inhibits the sustained contraction induced by 60 mM K+ in a concentration-dependent manner[1]. Evocarpine is found to induce apoptotic cell death in promyelocytic leukaemia HL‐60 cells in dose- and time-dependent manners[3]. |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 456.2±45.0 °C at 760 mmHg |
Melting Point | 34-38℃ |
Molecular Formula | C23H33NO |
Molecular Weight | 339.514 |
Flash Point | 156.1±18.1 °C |
Exact Mass | 339.256226 |
PSA | 22.00000 |
LogP | 7.70 |
Vapour Pressure | 0.0±1.1 mmHg at 25°C |
Index of Refraction | 1.526 |
Storage condition | 2-8C |
~90% 15266-38-3 |
Literature: Coppola, Gary M. Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 491 - 494 |
~% 15266-38-3 |
Literature: Journal of Heterocyclic Chemistry, , vol. 22, p. 491 - 494 |
~% 15266-38-3 |
Literature: Journal of Heterocyclic Chemistry, , vol. 22, p. 491 - 494 |
~% 15266-38-3 |
Literature: Journal of Heterocyclic Chemistry, , vol. 22, p. 491 - 494 |
~% 15266-38-3 |
Literature: Journal of Heterocyclic Chemistry, , vol. 22, p. 491 - 494 |
Precursor 3 | |
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