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Cucurbitacin B hydrate

产品号 C8499 公司名称 Sigma Aldrich
CAS号 6199-67-3(anhydrous) 公司网站 http://www.sigmaaldrich.com
分子式 C32H48O9 电 话 1-800-521-8956
分子量 576.71812 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 Chembase数据库ID: 154800

产品价格信息

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产品别名

标题
Cucurbitacin B hydrate
IUPAC标准名
(6R)-6-[(1R,2R,4S,10S,11S,13R,14R,15R)-4,13-dihydroxy-1,6,6,11,15-pentamethyl-5,17-dioxotetracyclo[8.7.0.02,7.011,15]heptadec-7-en-14-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl acetate hydrate
IUPAC传统名
(6R)-6-[(1R,2R,4S,10S,11S,13R,14R,15R)-4,13-dihydroxy-1,6,6,11,15-pentamethyl-5,17-dioxotetracyclo[8.7.0.02,7.011,15]heptadec-7-en-14-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl acetate hydrate
别名
(2β,9β,10α,16α,23E)-25-(acetyloxy)-2,16,20-trihydroxy-9-methyl-19-Norlanosta-5,23-diene-3,11,22-trione

产品登记号

MDL号 MFCD18432707
CAS号 6199-67-3(anhydrous)

产品性质

Empirical Formula (Hill Notation) C32H46O8 · xH2O
纯度 ≥98% (HPLC)
外观 off-white to light brown powder
溶解度 DMSO: ≥20 mg/mL
GHS危险品标识 GHS06
GHS警示词 Danger
GHS危险声明 H300
欧盟危险性物质标志 有毒(Toxic) 有毒(Toxic) (T)
MSDS下载 下载链接
GHS警示性声明 P264-P301 + P310
危险公开号 25
安全公开号 45
保存温度 2-8°C
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
Cucurbitacin B is a triterpenoid constituent of Cucurbitaceae plant species. Cucurbitacin B inhibits proliferation in a wide variety of tumor cell lines (IC50 15-30 nM) by inducing apoptosis and inducing cell cycle arrest at G2/M phase. Although the mechanism of action is unclear, Cucurbitacin B inhibits STAT 3 phosphorylation and expression levels and has been shown to block JAK2 activity. Curcubitacin B also inhibits the transcriptional activity of HIF1a and Nf-KB. Curcubitacin B is structurally similar to the JAK inhibitor Curcubitacin I.
详细说明 (简体中文)
Biochem/physiol Actions
Cucurbitacin B is a triterpenoid constituent of Cucurbitaceae plant species. Cucurbitacin B inhibits proliferation in a wide variety of tumor cell lines (IC50 15-30 nM) by inducing apoptosis and inducing cell cycle arrest at G2/M phase. Although the mechanism of action is unclear, Cucurbitacin B inhibits STAT 3 phosphorylation and expression levels and has been shown to block JAK2 activity. Curcubitacin B also inhibits the transcriptional activity of HIF1a and Nf-KB. Curcubitacin B is structurally similar to the JAK inhibitor Curcubitacin I.

参考文献