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106577-39-3

中文名稱 黑海常春藤苷A1
英文名稱 Hederacolchiside A1
CAS 106577-39-3
分子式 C47H76O16
分子量 897.1
MOL 文件 106577-39-3.mol
更新日期 2024/02/02 15:50:15
106577-39-3 結(jié)構(gòu)式 106577-39-3 結(jié)構(gòu)式

基本信息

中文別名
黑海常春藤苷A1
黑海常春藤皂苷A1
竹節(jié)香附皂苷R13
革葉常春藤皂苷A1
HEDERACOLCHISIDE A1(標(biāo)準(zhǔn)品)
齊墩果酸-3-O-Α-L鼠李吡喃糖基-(1→2)[Β-D-葡萄吡喃糖基-(1→4)] -Α-L-吡喃阿拉伯糖苷
齊墩果酸-3-O-Β-D-吡喃鼠李糖基-(1→2)-[Β-D-吡喃葡萄糖基-(1→4)]-Α-L-吡喃阿拉伯糖苷
英文別名
Raddeanoside R13
Hederacolchiside A1
HEDERACOLCHISIDE A1

Hederacolchiside A1 USP/EP/BP
Oleanolic acid-3-O-β-D-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→4)-]-α-L-arabinopyranoside,Hederacolchiside A1
Olean-12-en-28-oicacid, 3-[(O-6-deoxy-a-L-mannopyranosyl-(12)-O-[b-D-glucopyranosyl-(14)]-a-L-arabinopyranosyl)oxy]-, (3b)-
Olean-12-en-28-oic acid, 3-[(O-6-deoxy-α-L-mannopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl)oxy]-, (3β)-
所屬類別
生物化工:植物提取物

物理化學(xué)性質(zhì)

熔點(diǎn)253-255℃ (methanol , water )
沸點(diǎn)967.2±65.0 °C(Predicted)
密度1.36±0.1 g/cm3 (20 ºC 760 Torr)
儲(chǔ)存條件4°C, protect from light
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)4?+-.0.70(Predicted)
形態(tài)Solid
顏色White to off-white

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302
防范說(shuō)明P264-P270-P301+P312-P501

常見(jiàn)問(wèn)題列表

生物活性
Hederacolchiside A1 是從白頭翁中分離的,通過(guò)調(diào)節(jié) PI3K/Akt/mTOR 信號(hào)通路誘導(dǎo)凋亡,從而抑制腫瘤細(xì)胞的增殖。Hederacolchiside A1 具有抗血吸蟲(chóng)病活性,影響體內(nèi)和體外的寄生蟲(chóng)生存力。
靶點(diǎn)

PI3K

Akt

mTOR

體外研究

Hederacolchiside A1 reduces the mitochondrial membrane potential and Bcl-2 protein levels, whereas cleaved caspase-3 was higher.
Hederacolchiside A1 effectively inhibits the phosphorylations of phosphatidylinositol 3 kinase (PI3K), protein kinase B (Akt), and mammalian target of rapamycin (mTOR) .

體內(nèi)研究

hederacolchiside A1 (3.0, 4.5, and 6.0?mg/kg, ip) can significantly inhibit the weight of tumor in an H22 xenograft model.
Hederacolchiside A1 (3.25, 7.5, and 15.0?mg/kg, ig) can significantly inhibit the weight of tumor in nude mice xenograft tumor models using human breast carcinoma MCF-7 cells.

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