朝藿定B

更新时间：2024-01-02 07:29:03

朝藿定B结构式	常用名	朝藿定B	英文名	Epimedin B
	CAS号	110623-73-9	分子量	808.776
	密度	1.6±0.1 g/cm3	沸点	1066.1±65.0 °C at 760 mmHg
	分子式	C₃₈H₄₈O₁₉	熔点	N/A
	MSDS	N/A	闪点	325.6±27.8 °C

朝藿定B用途

朝藿定B (Epimedin B)是淫羊藿中的一种天然活性成分，据报道有抗骨质疏松症的潜能。

中文名	淫羊藿定 B
英文名	3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
中文别名	朝藿定 B \| 朝藿定B
英文别名	更多

描述	朝藿定B (Epimedin B)是淫羊藿中的一种天然活性成分,据报道有抗骨质疏松症的潜能。
相关类别	信号通路 >> 其他 >> 其他天然产物 >> 黄酮类化合物研究领域 >> 其他
参考文献	[1]. ZHAN Yang, et al. Evaluation of Antiosteoporotic Activity for Micro Amount Icariin and Epimedin B Based on the Osteoporosis Model Using Zebrafish. Chinese Pharmaceutical Journal, 2014-01 [2]. Cui L, et al. Metabolite profiles of epimedin B in rats by ultraperformance liquid chromatography/quadrupole-time-of-flight mass spectrometry. J Agric Food Chem. 2013 Apr 17;61(15):3589-99. [3]. ZHANG Hua-feng, et al. Effects of microwave radiation on extraction of epimedin B from Epimedii Folium. Chinese Traditional and Herbal Drugs, 2011-09

描述

朝藿定B (Epimedin B)是淫羊藿中的一种天然活性成分,据报道有抗骨质疏松症的潜能。

相关类别

信号通路 >> 其他 >> 其他

天然产物 >> 黄酮类化合物

研究领域 >> 其他

参考文献

[1]. ZHAN Yang, et al. Evaluation of Antiosteoporotic Activity for Micro Amount Icariin and Epimedin B Based on the Osteoporosis Model Using Zebrafish. Chinese Pharmaceutical Journal, 2014-01

[2]. Cui L, et al. Metabolite profiles of epimedin B in rats by ultraperformance liquid chromatography/quadrupole-time-of-flight mass spectrometry. J Agric Food Chem. 2013 Apr 17;61(15):3589-99.

[3]. ZHANG Hua-feng, et al. Effects of microwave radiation on extraction of epimedin B from Epimedii Folium. Chinese Traditional and Herbal Drugs, 2011-09

密度	1.6±0.1 g/cm3
沸点	1066.1±65.0 °C at 760 mmHg
分子式	C₃₈H₄₈O₁₉
分子量	808.776
闪点	325.6±27.8 °C
精确质量	808.278992
PSA	297.12000
LogP	2.87
蒸汽压	0.0±0.3 mmHg at 25°C
折射率	1.685
储存条件	2~8°C，避光，干燥

危害码 (欧洲)	Xi

Epmedin B

4H-1-Benzopyran-4-one, 3-[(6-deoxy-2-O-β-D-xylopyranosyl-α-L-mannopyranosyl)oxy]-7-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-

3-{[6-Deoxy-2-O-(β-D-xylopyranosyl)-α-L-mannopyranosyl]oxy}-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4-oxo-4H-chromen-7-yl β-D-glucopyranoside

3-{[6-Deoxy-2-O-(β-D-xylopyranosyl)-α-L-mannopyranosyl]oxy}-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-4-oxo-4H-chromen-7-yl β-D-glucopyranoside

EpimedinB

4H-1-Benzopyran-4-one, 3-((6-deoxy-2-O-β-D-xylopyranosyl-α-L-mannopyranosyl)oxy)-7-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-butenyl)-

Epimedin B