簡(jiǎn)介:高車(chē)前素,Hispidulin是具有廣泛生物活性的天然黃酮。 Hispidulin是Pim-1的抑制劑,IC50值為2.71 μM。
高車(chē)前素物理化學(xué)性質(zhì):
密度 |
1.5±0.1 g/cm3 |
沸點(diǎn) |
601.5±55.0 °C at 760 mmHg |
分子式 |
C16H12O6 |
分子量 |
300.263 |
閃點(diǎn) |
230.1±25.0 °C |
精確質(zhì)量 |
300.063385 |
PSA |
100.13 |
LogP |
1.6 |
外觀性狀 |
white to beige |
蒸汽壓 |
0.0±1.8 mmHg at 25°C |
折射率 |
1.697 |
儲(chǔ)存條件 |
Desiccate at -20°C |
水溶解性 |
DMSO: soluble20mg/mL, clear |
高車(chē)前素詳細(xì)介紹:
中文名稱(chēng): |
高車(chē)前素 |
中文別名: |
高車(chē)前素;4',5,7-三羥基-6-甲氧基黃酮;粗毛豚草素;1,3-二氯丙烷;高車(chē)前素 粗毛豚草素;高車(chē)前素(4',5,7-三羥基-6-甲氧基黃酮);高車(chē)前素,hispidulin,植物提取物,標(biāo)準(zhǔn)品,對(duì)照品;高車(chē)前素標(biāo)準(zhǔn)品;高車(chē)前素對(duì)照品;[ "4',5,7-Trihydroxy-6-methoxyflavone", " 高車(chē)前素" ] |
英文名稱(chēng): |
Hispidulin |
英文別名: |
4',5,7-Trihydroxy-6-methoxyflavone;HISPIDULIN;SCUTELLAREIN 6-METHYL ETHER;5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one;6-Methoxyapigenin;6-Methylscutellarein;Hispidulin(Dinatin);Methoxyapigenin;4H-1-Benzopyran-4-one,5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-;5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxychromen-4-one;Dinatin;5,7,4'-trihydroxy-6-methoxyflavone;6-O-Methylapigenin;4′,5,7-Trihydroxy-6-methoxyflavone;Salvitin;5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one;4H-1-BENZOPYRAN-4-ONE, 5,7-DIHYDROXY-2-(4-HYDROXYPHENYL)-6-METHOXY-;NSC122415;Flavone, 4',5,7-trihydroxy-6-methoxy-;N7F61604C2;5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-1-b |
CAS號(hào): |
1447-88-7 |
分子式: |
C16H12O6 |
分子量: |
300.26 |
詳細(xì)描述: |
博飛美科提供1447-88-7,高車(chē)前素,Hispidulin,Perfemiker,上海現(xiàn)貨。 Medlife,致力于提供高品質(zhì)、高性?xún)r(jià)比小分子化合物的產(chǎn)品。 Medlife小分子化合物大量庫(kù)存,提供超過(guò)2萬(wàn)種的抑制劑、激動(dòng)劑、拮抗劑等產(chǎn)品,是藥物及疾病研究的重要原料供應(yīng)商。 苯二氮卓受體部分正向變構(gòu)調(diào)節(jié)劑,Hispidulin是具有廣泛生物活性的天然黃酮。 Hispidulin是Pim-1的抑制劑,IC50值為2.71 μM。 查詢(xún)關(guān)鍵詞:“1447-88-7,高車(chē)前素,Hispidulin,PC12256,Perfemiker,上?,F(xiàn)貨”。 |
高車(chē)前素參考文獻(xiàn):
[1]. Chao SW, et al. Total Synthesis of Hispidulin and the Structural Basis for Its Inhibition of Proto-oncogene KinasePim-1. J Nat Prod. 2015 Aug 28;78(8):1969-76.
[2]. Gao H, et al. Hispidulin induces apoptosis through mitochondrial dysfunction and inhibition of P13k/Akt signalling pathway in HepG2 cancer cells. Cell Biochem Biophys. 2014 May;69(1):27-34.
[3]. Zhou R, et al. Hispidulin exerts anti-osteoporotic activity in ovariectomized mice via activating AMPK signaling pathway. Cell Biochem Biophys. 2014 Jun;69(2):311-7.
[4]. Lin TY, et al. Protective effect of hispidulin on kainic acid-induced seizures and neurotoxicity in rats. Eur J Pharmacol. 2015 May 15;755:6-15.