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氧化前胡素

更新时间:2025-08-27 12:06:54

氧化前胡素结构式
氧化前胡素结构式
品牌特惠专场
常用名 氧化前胡素 英文名 Oxypeucedanin
CAS号 737-52-0 分子量 286.279
密度 1.4±0.1 g/cm3 沸点 469.6±45.0 °C at 760 mmHg
分子式 C16H14O5 熔点 141-142 °C
MSDS N/A 闪点 237.8±28.7 °C

 氧化前胡素用途


Oxypeucedanin 是从 Angelica dahurica 中分离出来的呋喃香豆素衍生物。Oxypeucedanin 是一种选择性的开放通道阻滞剂,可抑制 hKv1.5 通道电流,IC50 值为 76 nM。Oxypeucedanin 延长心脏动作电位持续时间 (APD),是一种潜在的抗心律失常试剂。Oxypeucedanin 通过抑制癌细胞迁移来诱导细胞凋亡 (apoptosis )。

 氧化前胡素名称

中文名 氧化前胡素
英文名 oxypeucedanin
中文别名 淫羊藿素
英文别名 更多

 氧化前胡素生物活性

描述 Oxypeucedanin 是从 Angelica dahurica 中分离出来的呋喃香豆素衍生物。Oxypeucedanin 是一种选择性的开放通道阻滞剂,可抑制 hKv1.5 通道电流,IC50 值为 76 nM。Oxypeucedanin 延长心脏动作电位持续时间 (APD),是一种潜在的抗心律失常试剂。Oxypeucedanin 通过抑制癌细胞迁移来诱导细胞凋亡 (apoptosis )。
相关类别
靶点实验

IC50: HKv1.5 current; apoptosis[1]

参考文献

[1]. Eun JS, et al. Effects of oxypeucedanin on hKv1.5 and action potential duration.Biol Pharm Bull. 2005 Apr;28(4):657-60.

[2]. Yu Liu, et al. Oxypeucedanin hydrate monoacetate isolated from Angelica dahurica induces apoptosis in Caco-2 colon carcinoma cells through the mediation of PI3K-signalling pathway and inhibition of cancer cell migration

 氧化前胡素物理化学性质

密度 1.4±0.1 g/cm3
沸点 469.6±45.0 °C at 760 mmHg
熔点 141-142 °C
分子式 C16H14O5
分子量 286.279
闪点 237.8±28.7 °C
精确质量 286.084137
PSA 65.11000
LogP 2.17
InChIKey QTAGQHZOLRFCBU-UHFFFAOYSA-N
SMILES CC1(C)OC1COc1c2ccoc2cc2oc(=O)ccc12
蒸汽压 0.0±1.2 mmHg at 25°C
折射率 1.634
储存条件 2-8°C

 氧化前胡素安全信息

危害码 (欧洲) Xi

 氧化前胡素合成线路

~86%

氧化前胡素结构式

氧化前胡素

737-52-0

文献:Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610

~%

氧化前胡素结构式

氧化前胡素

737-52-0

文献:Organic and Biomolecular Chemistry, , vol. 4, # 8 p. 1604 - 1610

~%

氧化前胡素结构式

氧化前胡素

737-52-0

文献:Organic and Biomolecular Chemistry, , vol. 4, # 8 p. 1604 - 1610

~%

氧化前胡素结构式

氧化前胡素

737-52-0

文献:Organic and Biomolecular Chemistry, , vol. 4, # 8 p. 1604 - 1610

 氧化前胡素靶点实验

查看更多实验

实验名称:Antiproliferative activity against serum-stimulated primary rat aortic VSMC at 30 uM ...
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL1817331
实验名称:Antioxidant activity assessed as inhibition of ferrous chloride-induced lipid peroxid...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4133602
实验名称:Inhibition of recombinant human CYP1A1 expressed in baker's yeast-derived microsomes ...
来源:ChEMBL
靶标:Cytochrome P450 1A1
External Id:CHEMBL4257963
实验名称:Inhibition of recombinant human BACE1 using Rh-EVNLDAEFK as substrate after 60 mins b...
来源:ChEMBL
靶标:Beta-secretase 1
External Id:CHEMBL1936881
实验名称:Antiausteritic activity against human MIAPaCa2 cells in nutrient-deprived medium meas...
来源:ChEMBL
靶标:MIA PaCa-2
External Id:CHEMBL4200159
实验名称:Antiausteritic activity against human PANC1 cells in nutrient-deprived medium measure...
来源:ChEMBL
靶标:PANC-1
External Id:CHEMBL4200158
实验名称:Larvicidal activity against Aedes aegypti larvae after 24 hrs by TLC bioassay
来源:ChEMBL
靶标:Aedes aegypti
External Id:CHEMBL1013844
实验名称:Cytotoxicity against human PANC1 cells in DMEM measured after 24 hrs by WST8 assay
来源:ChEMBL
靶标:PANC-1
External Id:CHEMBL4200161
实验名称:Antifungal activity against Cladosporium cucumerinum assessed as inhibition of spore ...
来源:ChEMBL
靶标:Cladosporium cucumerinum
External Id:CHEMBL1013843
实验名称:Antiausteritic activity against human PSN1 cells in nutrient-deprived medium measured...
来源:ChEMBL
靶标:PSN1
External Id:CHEMBL4200160
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 氧化前胡素英文别名

4-(3,3-Dimethyl-oxiranylmethoxy)-furo[3,2-g]chromen-7-one
5-[(3,3-Dimethyl-2-oxiranyl)methoxy]-7H-furo[3,2-g]chromen-7-one
4-[(3,3-Dimethyl-2-oxiranyl)methoxy]-7H-furo[3,2-g]chromen-7-one
Oxypencedanin
5-[(3,3-Dimethyloxiran-2-yl)methoxy]-7H-furo[3,2-g]chromen-7-one
oxypeucadanin
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