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柏木双黄酮

更新时间:2025-08-25 01:54:50

柏木双黄酮结构式
柏木双黄酮结构式
品牌特惠专场
常用名 柏木双黄酮 英文名 Cupressuflavone
CAS号 3952-18-9 分子量 538.46
密度 N/A 沸点 1083.4ºC at 760mmHg
分子式 C30H18O10 熔点 >400ºC
MSDS N/A 闪点 609ºC

 柏木双黄酮用途


咖啡黄酮是一种天然产物,可以在大果咖啡中找到。咖啡黄酮具有抗炎和抗溃疡的活性。Cupressuflavone对CCl4诱导的小鼠肝肾毒性也具有保护作用[1][2][3]。

 柏木双黄酮名称

中文名 柏木双黄酮
英文名 cupressuflavone
英文别名 更多

 柏木双黄酮生物活性

描述 咖啡黄酮是一种天然产物,可以在大果咖啡中找到。咖啡黄酮具有抗炎和抗溃疡的活性。Cupressuflavone对CCl4诱导的小鼠肝肾毒性也具有保护作用[1][2][3]。
相关类别
体外研究 咖啡黄酮(40-160 mg/kg;口服,每天一次,持续5天)在肝脏和肾脏组织中通过增强抗氧化防御状态、减少脂质过氧化和防止 四氯化碳诱导的病理变化来对抗氧化应激[1] 咖啡黄酮(40-160 mg/kg;口服)在40、100、160毫克/千克剂量下分别抑制角叉菜胶诱导的炎症爪水肿 55%、60%和 64%[2]
参考文献

[1]. Al-Sayed E, et, al. Protective role of Cupressuflavone from Cupressus macrocarpa against carbon tetrachloride-induced hepato- and nephrotoxicity in mice. Planta Med. 2014 Dec;80(18):1665-71.  

[2]. Al-Sayed E, et, al. Anti-inflammatory and analgesic activities of cupressuflavone from Cupressus macrocarpa: Impact on pro-inflammatory mediators. Drug Dev Res. 2018 Feb;79(1):22-28.  

[3]. Koriem KMM, et, al. Protective effect of Cupressus sempervirens extract against indomethacin-induced gastric ulcer in rats. Interdiscip Toxicol. 2015 Mar;8(1):25-34.  

 柏木双黄酮物理化学性质

沸点 1083.4ºC at 760mmHg
熔点 >400ºC
分子式 C30H18O10
分子量 538.46
闪点 609ºC
精确质量 538.09000
PSA 181.80000
LogP 5.13400
InChIKey LADPNODMUXOPRG-UHFFFAOYSA-N
SMILES O=c1cc(-c2ccc(O)cc2)oc2c(-c3c(O)cc(O)c4c(=O)cc(-c5ccc(O)cc5)oc34)c(O)cc(O)c12
折射率 1.793
储存条件 2-8°C,密封,干燥

 柏木双黄酮靶点实验

查看更多实验

实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
实验名称:Absorbance-based primary biochemical high throughput screening assay to identify acti...
来源:The Scripps Research Institute Molecular Screening Center
靶标:caspase-3 preproprotein [Homo sapiens]
External Id:PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule modulators of NR3A
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1015-NR3A-Primary-Assay
实验名称:uHTS identification of small molecule modulators of Rev-erb Alpha.
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1016-RevErbaLBD-Primary-Assay
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 柏木双黄酮英文别名

8-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
8,8'-Biapigenin
Cupressuflavone
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