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Physalin B

更新时间:2025-08-25 18:38:39

Physalin B结构式
Physalin B结构式
品牌特惠专场
常用名 Physalin B 英文名 Physalin B
CAS号 23133-56-4 分子量 510.53200
密度 N/A 沸点 N/A
分子式 C28H30O9 熔点 N/A
MSDS N/A 闪点 N/A

 Physalin B用途


Physalin B 是 Cape gooseberry 中主要的甾体活性成分之一,通过调节 p53 依赖的凋亡途径,诱导乳腺癌细胞周期阻滞和诱导凋亡 (apoptosis)。Physalin B 抑制人结肠癌细胞泛素-蛋白酶体通路并诱导不完全自噬反应。

 Physalin B名称

中文名 酸浆苦味B
英文名 physalin B

 Physalin B生物活性

描述 Physalin B 是 Cape gooseberry 中主要的甾体活性成分之一,通过调节 p53 依赖的凋亡途径,诱导乳腺癌细胞周期阻滞和诱导凋亡 (apoptosis)。Physalin B 抑制人结肠癌细胞泛素-蛋白酶体通路并诱导不完全自噬反应。
相关类别
参考文献

[1]. Wang A, et al. Physalin B induces cell cycle arrest and triggers apoptosis in breast cancer cells through modulating p53-dependent apoptotic pathway. Biomed Pharmacother. 2018;101:334-341.

[2]. Ma YM, et al. Physalin B not only inhibits the ubiquitin-proteasome pathway but also induces incomplete autophagic response in human colon cancer cells in vitro. Acta Pharmacol Sin. 2015;36(4):517-527.

 Physalin B物理化学性质

分子式 C28H30O9
分子量 510.53200
精确质量 510.18900
PSA 125.43000
LogP 1.55700
InChIKey HVTFEHJSUSPQBK-DNJDGUCCSA-N
SMILES CC12C(=O)C=CCC1=CCC1C2CCC2(O)C(=O)OC3(C)C4CC5(C)C(COC16OC23C5C6=O)C(=O)O4
储存条件 2-8°C,干燥,密封

 Physalin B安全信息

危害码 (欧洲) Xi

 Physalin B靶点实验

查看更多实验

实验名称:Inhibition of peptide-glutamyl-peptide-hydrolyzing activity of 20S proteasome in huma...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1942848
实验名称:Inhibition of chymotrypsin-like activity of 20S proteasome in human DLD1 cells transf...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1942849
实验名称:Cytotoxicity against human NCI-H460 cells assessed as cell growth inhibition measured...
来源:ChEMBL
靶标:NCI-H460
External Id:CHEMBL4815641
实验名称:Cytotoxicity against human SF-268 cells assessed as cell growth inhibition measured a...
来源:ChEMBL
靶标:SF-268
External Id:CHEMBL4815642
实验名称:Cytotoxicity against human PC-3 cells assessed as cell growth inhibition measured aft...
来源:ChEMBL
靶标:PC-3
External Id:CHEMBL4815639
实验名称:Cytotoxicity against human MCF7 cells assessed as cell growth inhibition measured aft...
来源:ChEMBL
靶标:MCF7
External Id:CHEMBL4815640
实验名称:Cytotoxicity against human WI-38 cells assessed as cell growth inhibition measured af...
来源:ChEMBL
靶标:WI-38
External Id:CHEMBL4815643
实验名称:Inhibition of GLI1 (unknown origin) transcriptional activity
来源:ChEMBL
靶标:Zinc finger protein GLI1
External Id:CHEMBL5250706
实验名称:Antitumor activity against human LNCAP cells
来源:ChEMBL
靶标:LNCaP
External Id:CHEMBL889079
实验名称:Antitumor activity against human KB cells
来源:ChEMBL
靶标:KB
External Id:CHEMBL889080
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