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  • BioBioPha
  • China
  • Product Name: Kusunokinin
  • Price: ¥3400.0/5mg
  • Purity: 97.0%
  • Stocking Period: 10 Day
  • Contact: Xueping-Zheng

58311-20-9

58311-20-9 structure
58311-20-9 structure

Name (3R,4R)-3-(1,3-Benzodioxol-5-ylmethyl)-4-(3,4-dimethoxybenzyl)dihydro-2(3H)-furanone
Synonyms (3R,4R)-3-(1,3-Benzodioxol-5-ylmethyl)-4-(3,4-dimethoxybenzyl)dihydro-2(3H)-furanone
2(3H)-Furanone, 3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]dihydro-, (3R,4R)-
Description Kusunokinin ((-)-Kusunokinin) is a nature product that could be isolated form P. nigrum. Kusunokinin has anticancer activity. Kusunokinin arrests cell cycle at G2/M phase and induce apoptosis[1].
Related Catalog
In Vitro Kusunokinin ((-)-Kusunokinin; 0.625-10 µg/mL; 72 h) 抑制癌细胞的活力,对 MCF-7、HT-29、MDA-MB-468、SW-620、A-549 和 MDA-MB-231 细胞的 IC50 值分别为 3.08、3.59、3.98、5.75、5.77 和 7.86 µM[1]。 Cell Viability Assay[1] Cell Line: Cancer cells Concentration: 0.625, 1.25, 2.5, 5 and 10 µg/mL Incubation Time: 72 hours Result: Had anticancer activity and inhibited cancer cells growth.
In Vivo Kusunokinin ((-)-Kusunokinin; 7 和 14 mg/kg; i.h.; 每周 3 次, 持续 2 周) 通过下调信号分子 (c-Src、PI3K、Akt 和 Erk1/2) 抑制 NMU 诱导的乳腺癌大鼠的肿瘤生长[1]。 Animal Model: Female Sprague Dawley rats (7 weeks of age)[1] Dosage: 7 and 14 mg/kg Administration: Subcutaneous injection, 3 times a week for 2 weeks Result: Inhibited the mammary tumor growth and decreased tumor volume. Down-regulated c-Src, Erk1/2 and PI3K proteins and decreased Akt proteins. Inhibited downstream molecules in the cell cycle (c-Myc, E2f-1, CDK1 and cyclin B1) and metastasis (E-cadherin, MMP-2 and MMP-9).
References

[1]. Tedasen A, et, al. (-)-Kusunokinin inhibits breast cancer in N-nitrosomethylurea-induced mammary tumor rats. Eur J Pharmacol. 2020 Sep 5;882:173311.  

Density 1.3±0.1 g/cm3
Boiling Point 543.6±45.0 °C at 760 mmHg
Molecular Formula C21H22O6
Molecular Weight 370.396
Flash Point 238.5±28.8 °C
Exact Mass 370.141632
LogP 3.36
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.586