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短叶老鹤草素A

更新时间:2025-08-23 18:35:25

短叶老鹤草素A结构式
短叶老鹤草素A结构式
品牌特惠专场
常用名 短叶老鹤草素A 英文名 Brevilin A
CAS号 16503-32-5 分子量 346.417
密度 1.2±0.1 g/cm3 沸点 494.0±45.0 °C at 760 mmHg
分子式 C20H26O5 熔点 N/A
MSDS N/A 闪点 216.0±28.8 °C

 短叶老鹤草素A用途


Brevilin A 是一种从 Centipeda minima 中分离的倍半萜内酯,具有抗癌活性。Brevilin A 是一种选择性的 JAK-STAT 信号通路抑制剂,通过减弱 JAK 信号和 阻塞 STAT3 信号起作用。Brevilin A 通过线粒体途径和 PI3K/AKT/mTOR 失活诱导结肠腺癌细胞 CT26 的凋亡和自噬。

 短叶老鹤草素A名称

中文名 短叶老鹤草素 A
英文名 Brevilin A
英文别名 更多

 短叶老鹤草素A生物活性

描述 Brevilin A 是一种从 Centipeda minima 中分离的倍半萜内酯,具有抗癌活性。Brevilin A 是一种选择性的 JAK-STAT 信号通路抑制剂,通过减弱 JAK 信号和 阻塞 STAT3 信号起作用。Brevilin A 通过线粒体途径和 PI3K/AKT/mTOR 失活诱导结肠腺癌细胞 CT26 的凋亡和自噬。
相关类别
靶点实验

IC50: 10.6 µM (STAT3 signaling)[1]

参考文献

[1]. Chen X, et al. Brevilin A, a novel natural product, inhibits janus kinase activity and blocks STAT3 signaling in cancer cells. PLoS One. 2013 May 21;8(5):e63697.

[2]. You P, et al. Brevilin A induces apoptosis and autophagy of colon adenocarcinoma cell CT26 via mitochondrial pathway and PI3K/AKT/mTOR inactivation. Biomed Pharmacother. 2018 Feb;98:619-625.

 短叶老鹤草素A物理化学性质

密度 1.2±0.1 g/cm3
沸点 494.0±45.0 °C at 760 mmHg
分子式 C20H26O5
分子量 346.417
闪点 216.0±28.8 °C
精确质量 346.178009
PSA 69.67000
LogP 2.98
InChIKey KUPPZVXLWANEJJ-UXPPPGSFSA-N
SMILES CC=C(C)C(=O)OC1C2C(CC(C)C3C=CC(=O)C31C)OC(=O)C2C
外观性状 粉末
蒸汽压 0.0±1.3 mmHg at 25°C
折射率 1.535
储存条件 2-8℃,干燥,密闭

 短叶老鹤草素A安全信息

危害码 (欧洲) Xi

 短叶老鹤草素A靶点实验

查看更多实验

实验名称:Inhibition of STAT3 in human LX2 cells assessed as reduction in TGF-1beta-induced STA...
来源:ChEMBL
靶标:Signal transducer and activator of transcription 3
External Id:CHEMBL4818129
实验名称:Inhibition of STAT3 in human LX2 cells assessed as reduction in TGF-1beta-induced CTG...
来源:ChEMBL
靶标:Signal transducer and activator of transcription 3
External Id:CHEMBL4818130
实验名称:Anti-fibrotic activity against human LX2 cells assessed as reduction in TGF-1beta-ind...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4818127
实验名称:Anti-fibrotic activity against human LX2 cells assessed as reduction in TGF-1beta-ind...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4818128
实验名称:Primary qHTS for inhibitors of NSP2Pro chikungunya virus (CHIKV)
来源:NCGC
External Id:APP-Toga-CHIKV-nsp2-p
实验名称:Anticancer activity against human nasopharyngeal carcinoma cells measured upto 72 hrs...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4818131
实验名称:Antiviral activity against influenza A virus infected in MDCK cells assessed as reduc...
来源:ChEMBL
靶标:Influenza A virus
External Id:CHEMBL4818132
实验名称:Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubat...
来源:ChEMBL
靶标:HeLa
External Id:CHEMBL4815370
实验名称:qHTS assay to identify novel small-molecules to repurpose for Merkel cell carcinoma t...
来源:NCGC
靶标:N/A
External Id:MCC011
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 短叶老鹤草素A英文别名

(3S,3aR,4S,4aR,7aR,8R,9aR)-3,4a,8-Trimethyl-2,5-dioxo-2,3,3a,4,4a,5,7a,8,9,9a-decahydroazuleno[6,5-b]furan-4-yl (2Z)-2-methyl-2-butenoate
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