橙皮苷甲基查尔酮结构式
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常用名 | 橙皮苷甲基查尔酮 | 英文名 | Hesperidin methylchalcone |
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CAS号 | 24292-52-2 | 分子量 | 624.587 | |
密度 | 1.6±0.1 g/cm3 | 沸点 | 953.0±65.0 °C at 760 mmHg | |
分子式 | C29H36O15 | 熔点 | 120 °C (dec.)(lit.) | |
MSDS | 中文版 美版 | 闪点 | 309.5±27.8 °C |
橙皮苷甲基查尔酮用途Hesperidin methylchalcone (Hesperidin methyl chalcone) 抑制氧化应激,细胞因子产生和 NF-κB 活化。Hesperidin methylchalcone 抑制炎症和疼痛。且具有血管保护活性。 |
中文名 | 甲基橙皮甙查尔酮 |
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英文名 | Hesperidin methylchalcone |
中文别名 | 甲基橙皮苷查尔酮 | 橙皮甙甲基查尔酮 |
英文别名 | 更多 |
描述 | Hesperidin methylchalcone (Hesperidin methyl chalcone) 抑制氧化应激,细胞因子产生和 NF-κB 活化。Hesperidin methylchalcone 抑制炎症和疼痛。且具有血管保护活性。 |
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相关类别 | |
靶点 |
NF-κB |
参考文献 |
密度 | 1.6±0.1 g/cm3 |
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沸点 | 953.0±65.0 °C at 760 mmHg |
熔点 | 120 °C (dec.)(lit.) |
分子式 | C29H36O15 |
分子量 | 624.587 |
闪点 | 309.5±27.8 °C |
精确质量 | 624.205444 |
PSA | 234.29000 |
LogP | 1.86 |
外观性状 | 黄色粉末 |
蒸汽压 | 0.0±0.3 mmHg at 25°C |
折射率 | 1.672 |
储存条件 | 密闭,阴凉,通风干燥处 |
稳定性 | 遵照规格使用和储存 避免氧化剂 |
计算化学 | 1.疏水参数计算参考值(XlogP):-0.3 2.氢键供体数量:8 3.氢键受体数量:15 4.可旋转化学键数量:10 5.互变异构体数量:15 6.拓扑分子极性表面积234 7.重原子数量:44 8.表面电荷:0 9.复杂度:952 10.同位素原子数量:0 11.确定原子立构中心数量:10 12.不确定原子立构中心数量:0 13.确定化学键立构中心数量:1 14.不确定化学键立构中心数量:0 15.共价键单元数量:1 |
更多 | 1. 性状:固体 2. 密度(g/mL,25℃):未确定 3. 相对蒸汽密度(g/mL,空气=1):未确定 4. 熔点(ºC):120 5. 沸点(ºC,):未确定 6. 沸点(ºC,5.2kPa):未确定 7. 折射率:未确定 8. 闪点(ºC):未确定 9. 比旋光度(º):[α]20/D −71°, c =1 in ethanol 10. 自燃点或引燃温度(ºC):未确定 11. 蒸气压(mmHg,78ºC):未确定 12. 饱和蒸气压(kPa,60ºC):未确定 13. 燃烧热(KJ/mol):未确定 14. 临界温度(oC):未确定 15. 临界压力(KPa):未确定 16. 油水(辛醇/水)分配系数的对数值:未确定 17. 爆炸上限(%,V/V):未确定 18. 爆炸下限(%,V/V):未确定 19. 溶解性(g/l,at 20 ºC:未确定 |
个人防护装备 | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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危险品运输编码 | NONH for all modes of transport |
WGK德国 | 3 |
RTECS号 | FL7085000 |
Assessment of the antineoplastic potential of chalcones in animal models.
Curr. Med. Chem. 20(2) , 186-221, (2013) One part of chemical space that is endowed with interesting biological properties is the area of the chalcones. With this review, we provide a comprehensive overview of the numerous in vivo animal stu... |
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Absorption and elimination of (14C) hesperidin methylchalcone in the rat.
Eur. J. Drug Metab. Pharmacokinet. 6(3) , 171-7, (1981) Hesperidin methylchalcone resorption and excretion were studied in rats, using 14C-labelling. The level of radioactivity in the blood showed a peak 1-2 hours after oral administration of the labelled ... |
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Inhibitory effect of the Ruscus extract and of the flavonoid hesperidine methylchalcone on increased microvascular permeability induced by various agents in the hamster cheek pouch.
J. Cardiovasc. Pharmacol. 22(2) , 225-30, (1993) The Ruscus extract and the flavonoid hesperidine methylchalcone (HMC) are used in treatment of venous insufficiency. In the present study, we used the hamster cheek pouch preparation and investigated ... |
2-Propen-1-one, 1-[4-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2-hydroxy-6-methoxyphenyl]-3-(3-hydroxy-4-methoxyphenyl)- |
3-Hydroxy-4-[3-(3-hydroxy-4-methoxyphenyl)acryloyl]-5-methoxyphenyl 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside |
HESPERIDIN METHYL CHALCONE |
HESPERIDIN METHYL CHALCONE*PRACTICAL GRA DE |
EINECS 246-128-2 |
MFCD00010438 |
Hesperidine Methyl Chalcone |
(e)-osyl]oxy]-2-hydroxy-6-methoxyphenyl]-3-(3-hydroxy-4-methoxyphenyl) |