扁蓄苷结构式
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常用名 | 扁蓄苷 | 英文名 | Avicularin |
|---|---|---|---|---|
| CAS号 | 572-30-5 | 分子量 | 434.350 | |
| 密度 | 1.9±0.1 g/cm3 | 沸点 | 855.4±65.0 °C at 760 mmHg | |
| 分子式 | C20H18O11 | 熔点 | 240-243ºC | |
| MSDS | 中文版 美版 | 闪点 | 305.8±27.8 °C |
扁蓄苷用途Avicularin 是一种存在多种植物中有生物活性的黄酮类化合物,具有抗炎、抗过敏、抗氧化、保肝、抗肿瘤等作用。在 LPS 刺激的 RAW 264.7 巨噬细胞中,Avicularin 通过抑制 ERK 信号通路产生抗炎活性。Avicularin 能通过调节 NF-κB(p65)、COX-2 和 PPAR-γ 的活性来改善人类肝细胞癌。 |
| 中文名 | 扁蓄苷 |
|---|---|
| 英文名 | avicularin |
| 中文别名 | 蓄苷 | 蓄苷 |
| 英文别名 | 更多 |
| 描述 | Avicularin 是一种存在多种植物中有生物活性的黄酮类化合物,具有抗炎、抗过敏、抗氧化、保肝、抗肿瘤等作用。在 LPS 刺激的 RAW 264.7 巨噬细胞中,Avicularin 通过抑制 ERK 信号通路产生抗炎活性。Avicularin 能通过调节 NF-κB(p65)、COX-2 和 PPAR-γ 的活性来改善人类肝细胞癌。 |
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| 相关类别 | |
| 参考文献 |
| 密度 | 1.9±0.1 g/cm3 |
|---|---|
| 沸点 | 855.4±65.0 °C at 760 mmHg |
| 熔点 | 240-243ºC |
| 分子式 | C20H18O11 |
| 分子量 | 434.350 |
| 闪点 | 305.8±27.8 °C |
| 精确质量 | 434.084900 |
| PSA | 190.28000 |
| LogP | 2.06 |
| InChIKey | BDCDNTVZSILEOY-UXYNSRGZSA-N |
| SMILES | O=c1c(OC2OC(CO)C(O)C2O)c(-c2ccc(O)c(O)c2)oc2cc(O)cc(O)c12 |
| 外观性状 | 白色粉末 |
| 蒸汽压 | 0.0±0.3 mmHg at 25°C |
| 折射率 | 1.802 |
| 储存条件 | 2-8C |
| 危险品运输编码 | NONH for all modes of transport |
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| 扁蓄苷上游产品 0 | |
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| 扁蓄苷下游产品 3 | |
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Protective effect of components isolated from Lindera erythrocarpa against oxidative stress-induced apoptosis of H9c2 cardiomyocytes.
Phytother Res. 25(11) , 1612-7, (2011) Eight compounds were isolated from the methanol fraction of Lindera erythrocarpa and assessed for their ability to protect H9c2 cardiomyocytes against oxidative stress-induced cell death. Three of the... |
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Inhibitory activity against urease of quercetin glycosides isolated from Allium cepa and Psidium guajava.
Biosci. Biotechnol. Biochem. 74 , 878-880, (2010) Methanolic extracts of edible plants and seaweeds were tested for their inhibitory activity against Jack bean urease. Quercetin-4'-O-beta-D-glucopyranoside was isolated from Allium cepa as a urease in... |
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[Determination of avicularin in Polygonum aviculare L].
Yao Xue Xue Bao 18(9) , 700-4, (1983)
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实验名称:Antifungal activity against Candida parapsilosis
来源:ChEMBL
靶标:Candida parapsilosis
External Id:CHEMBL4313268
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实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
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实验名称:Cytotoxicity against human SGC7901 cells by MTT assay
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL3404774
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实验名称:Cytotoxicity against human A549 cells at 20 mcg/mL after 3 days by SRB assay
来源:ChEMBL
靶标:A549
External Id:CHEMBL1001922
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实验名称:Antifungal activity against Candida albicans
来源:ChEMBL
靶标:Candida albicans
External Id:CHEMBL4313242
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实验名称:Cytotoxicity against human MCF7 cells at 20 mcg/mL after 3 days by SRB assay
来源:ChEMBL
靶标:MCF7
External Id:CHEMBL1001923
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实验名称:Antioxidant activity assessed as ABTS radical scavenging activity after 15 mins
来源:ChEMBL
靶标:N/A
External Id:CHEMBL3404778
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实验名称:Antioxidant activity assessed as FRAP values at 12.5 ug/ml incubated at 37 degC for 5...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL3404779
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| Fenicularin |
| 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl α-L-arabinofuranoside |
| Quercetin 3-α-L-arabinofuranoside |
| Avicularin |
| QUERCETIN-3-ARABINOSIDE |
| Avicularoside |
| Avicularine |
| Avicularin,Quercetin 3-alpha-L-arabinofuranoside |