- Evocarpine
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- $52.00 / 1mg
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2026-01-30
- CAS:15266-38-3
- Min. Order:
- Purity: 99.82%
- Supply Ability: 10g
- evocarpine
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- $0.00 / 25kg
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2024-04-12
- CAS:15266-38-3
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 2000ton
- evocarpine
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- $1.00 / 1kg
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2019-07-06
- CAS:15266-38-3
- Min. Order: 1g
- Purity: 99%
- Supply Ability: 100KG
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| | 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 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 | | pka | 2.52±0.70(Predicted) | | form | Solid | | color | White to off-white | | CAS DataBase Reference | 15266-38-3 |
| | evocarpine Usage And Synthesis |
| Chemical Properties | White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO. It is derived from Evodia rutaecarpa (Juss.) Benth. | | Uses | Evocarpine, a quinolone alkaloid that could be isolated from Evodiae fructus, inhibitss Ca2+ influx through voltage-dependent calcium channels. Antimycobacterial activity[1][2]. | | Definition | ChEBI: 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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