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ICRF-193

产品号 I4659 公司名称 Sigma Aldrich
CAS号 21416-88-6 公司网站 http://www.sigmaaldrich.com
分子式 C12H18N4O4 电 话 1-800-521-8956
分子量 282.29572 传 真
纯 度 ≥95% 电子邮件
保 存 Chembase数据库ID: 153963

产品价格信息

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产品别名

标题
ICRF-193
IUPAC标准名
4-[(2S,3R)-3-(3,5-dioxopiperazin-1-yl)butan-2-yl]piperazine-2,6-dione
IUPAC传统名
4-[(2S,3R)-3-(3,5-dioxopiperazin-1-yl)butan-2-yl]piperazine-2,6-dione
别名
meso-4,4′-(3,2-butanediyl)-bis(2,6-piperazinedione)

产品登记号

MDL号 MFCD01702964
PubChem SID 24896062
CAS号 21416-88-6

产品性质

Empirical Formula (Hill Notation) C12H18N4O4
纯度 ≥95%
溶解度 DMSO: soluble4 mg/mL
GHS危险品标识 GHS06
GHS警示词 Danger
GHS危险声明 H301-H317
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS警示性声明 P280-P301 + P310
RID/ADR UN 2811 6.1/PG 3
危险公开号 22-43
RTECS编号 TL6380200
安全公开号 36/37
保存温度 -20°C
联合国危险货物等级 6.1
联合国危险货物编号 2811
联合国危险货物包装类别(PG) 3
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
ICRF-193 induces a G2 checkpoint that is associated with an ATR-dependent inhibition of polo-like kinase 1 (plk1) activity and a decrease in cyclin B1 phosphorylation.1 Induces apoptosis in several cell lines including K562 and Molt-4 cells.2,,,1 ICRF-193 is a topoisomerase II inhibitor, more potent against topoisomerase II-β than topoisomerase II-α3, and may in addition cause DNA strand breaks.4
详细说明 (简体中文)
Biochem/physiol Actions
ICRF-193 induces a G2 checkpoint that is associated with an ATR-dependent inhibition of polo-like kinase 1 (plk1) activity and a decrease in cyclin B1 phosphorylation.1 Induces apoptosis in several cell lines including K562 and Molt-4 cells.2,,,1 ICRF-193 is a topoisomerase II inhibitor, more potent against topoisomerase II-β than topoisomerase II-α3, and may in addition cause DNA strand breaks.4

参考文献