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33627-41-7

中文名称 旋覆花内酯
英文名称 inulicin
CAS 33627-41-7
分子式 C17H24O5
分子量 308.37
MOL 文件 33627-41-7.mol
更新日期 2025/05/12 11:20:20
33627-41-7 结构式 33627-41-7 结构式

基本信息

中文别名
旋覆花素
旋复花内酯
旋覆花内酯
旋覆花次内酯
乙酰旋覆花内酯
1-O-乙酰基大花旋覆花内酯
英文别名
inulicin
Britannilactone
inulicin USP/EP/BP
Inulicin(1-O-acetyl Britannilactone)
1-O-Acetylbritannilactone (Inulicin)
6-(3-acetoxy-propyl)-4-hydroxy-5,7-dimethyl-3-methylene-3,3a,4,5,8,8a-hexahydro-cyclohepta[b]furan-2-one
(3aS)-6-(3-Acetoxypropyl)-3,3aα,4,5,8,8aα-hexahydro-4α-hydroxy-5α,7-dimethyl-3-methylene-2H-cyclohepta[b]furan-2-one
(3aS)-3,3aα,4,5,8,8aα-Hexahydro-4α-hydroxy-6-(3-acetoxypropyl)-5α,7-dimethyl-3-methylene-2H-cyclohepta[b]furan-2-one
(3aS,4S,7aR)-5-[(1S)-4-(Acetyloxy)-1-methylbutyl]-3a,4,7,7a-tetrahydro-4-hydroxy-6-methyl-3-methylene-2(3H)-benzofuranone
2(3H)-Benzofuranone,5-[(1S)-4-(acetyloxy)-1-methylbutyl]-3a,4,7,7a-tetrahydro-4-hydroxy-6-methyl-3-methylene-,(3aS,4S,7aR)-
所属类别
生物化工:中草药成分

物理化学性质

熔点124.0-126.1 °C
沸点481.7±45.0 °C(Predicted)
密度1.16
储存条件4°C, protect from light
溶解度可溶于DMSO
酸度系数(pKa)13.71±0.60(Predicted)
形态固体
颜色White to off-white
生物来源plant
旋覆花内酯价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2025/02/08HY-N0896旋覆花内酯
Inulicin
33627-41-71mg430元
2025/02/08HY-N0896旋覆花内酯
Inulicin
33627-41-75mg990元
2025/02/08HY-N0896旋覆花内酯
Inulicin
33627-41-710 mM * 1 mLin DMSO1089元

常见问题列表

生物活性
Inulicin (1-O-Acetylbritannilactone) 是从 Inula Britannica L 分离的一种活性化合物。Inulicin (1-O-Acetylbritannilactone) 抑制 VEGF 介导的 Src 和 FAK 活化。Inulicin (1-O-Acetylbritannilactone) 还抑制 LPS 诱导的 PGE2 产生和 COX-2 表达,以及抑制 NF-κB 活化和易位。
靶点

NF-κB

COX-2

体外研究

Inulicin (1-O-Acetylbritannilactone) inhibits angiogenesis and lung cancer cell growth through regulating VEGF-Src-FAK signaling. Inulicin dose-dependently inhibits vascular endothelial growth factor (VEGF)-induced proliferation, migration, and capillary structure formation of cultured human umbilical vascular endothelial cells (HUVECs). Treatment of A549 NSCLC cells with Inulicin results in cell growth inhibition and Src-FAK in-activation. The potential effect of Inulicin is tested ton Src and FAK phosphorylation in A549 lung cancer cells. Significant high levels of Src and FAK phosphorylations are noticed a in A549 cells, which are both inhibited by treatment of Inulicin (5 μM and 10 μM). Src and FAK are both important for cancer cell proliferation. Thus, A549 cell growth, tested by MTT assay and clonogenicity assay,is remarkably inhibited by corresponding Inulicin treatment. The anti-A549 cell growth activity of Inulicin is again dose-dependent. Inulicin (1-O-Acetylbritannilactone) isolated from Inula britannica-F. , inhibits inflammatory responses in vascular smooth muscle cells (VSMCs). Inulicin (5, 10, 20 μM) has several concentration dependent effects, including inhibition of lipopolysaccharide (LPS)-induced PGE 2 production and COX-2 expression, and blockade of NF-κB activation and translocation. In addition, Inulicin directly inhibits the binding of active NF-κB to specific DNA cis-element.

体内研究

Administration of a single dose of Inulicin (1-O-Acetylbritannilactone; 12 mg/kg/day) remarkably suppresses growth of A549 xenografts in nude mice. In vivo microvessels formation and Src activation are also significantly inhibited in Inulicin-treated xenograft tumors. To investigate the potential activity of Inulicin in vivo, a nude mice xenograft model is applied. A single dose of Inulicin (12 mg/kg/day, i.p.) dramatically inhibits the growth of A549 xenografts in nude mice. Further, the weights of Inulicin-treated tumors are remarkably lighter than that of vehicle-treated tumors. Notably, Inulicin administration does not affect mice body weights.

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