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218136-59-5

中文名称 ALPHA,ALPHA-二苯基-4-[(3-吡啶亚甲基)氨基]-1-吡嗪戊腈
英文名称 α,α-Diphenyl-4-[(3-pyridinylmethylene)amino]-1-piperazinepentanenitrile
CAS 218136-59-5
分子式 C27H29N5
分子量 423.55
MOL 文件 218136-59-5.mol
更新日期 2023/03/20 15:41:23
218136-59-5 结构式 218136-59-5 结构式

基本信息

中文别名
ALPHA,ALPHA-二苯基-4-[(3-吡啶亚甲基)氨基]-1-吡嗪戊腈
英文别名
CS-117
SC 26196
PF-o6341724
SC26196
SC 26196
SC 26196 - PF 06341724
α,α-Diphenyl-4-[(3-pyridinylMethylene)aMino]-1-piperazine
a,a-diphenyl-4-[(3-pyridinylmethylene)amino]-1-piperazinepentanenitrile
α,α-Diphenyl-4-[(3-pyridinylmethylene)amino]-1-piperazinepentanenitrile
1-Piperazinepentanenitrile, α,α-diphenyl-4-[(3-pyridinylmethylene)amino]-
alpha,alpha-Diphenyl-4-[(3-pyridinylmethylene)amino]-1-piperazinepentanenitrile
所属类别
生物化工:抑制剂

物理化学性质

储存条件2-8°C
溶解度二甲基亚砜:≥10mg/mL
形态粉末
颜色白色至棕褐色

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335
WGK Germany3

常见问题列表

应用
SC-26196 是一种有效的,具有口服活性的 Delta6 去饱和酶 (D6D, FADS2) 抑制剂 (在大鼠肝微粒体中,IC50=0.2 µM)。具有抗炎活性。
生物活性
SC-26196 是一种有效的,具有口服活性的 Delta6 去饱和酶 (D6D, FADS2) 抑制剂 (在大鼠肝微粒体中,IC50=0.2 µM)。具有抗炎活性。
靶点

IC50: 0.2 µM (Delta6 desaturase in a rat liver microsomal assay)

体外研究

SC-26196 (200 nM) inhibits proliferation of peripheral blood mononuclear cells (PBMCs), but Not Jurkat Cells.

Cell Proliferation Assay

Cell Line: PBMCs and Jurkat cells
Concentration: 200 nM
Incubation Time: 96 hours for PBMCs; 144 hours for Jurkat cells
Result: Treatment of PBMCs significantly decreased the proportion of cells that underwent division, the division index and proliferation index.
Did not alter cell proliferation significantly in Jurkat cells.
体内研究

SC-26196 ( included in the diet at 0, 0.07, 0.21, or 0.7 mg/kg diet to achieve dosages of 0, 10, 30, and 100 mg/kg per day) causes a decrease in the calculated Δ6-desaturase index in both adipose tissue and liver. Feeding 100 mg SC-26196 per kg BW per day inhibits the Δ6-desaturase enzyme.

Animal Model: Male mice (12- or 15-week-old)
Dosage: 0, 10, 30, and 100 mg/kg per day
Administration: Included in the diet at 0, 0.07, 0.21, or 0.7mg/kg diet to achieve dosages of 0, 10, 30, and 100mg/kg per day.
Result: Caused a decrease in the calculated Δ6-desaturase index in both adipose tissue and liver.
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