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14513-15-6

中文名称 SIRT1/2 INHIBITOR IV
英文名称 NSC-1125476, Tetrahydro-5-[(2-hydroxy-1-naphthalenyl)methyl]-6-phenyl-2-thioxo-4(1H)-Pyrimidinone, 5-(2-Hydroxynaphthalen-1-ylmethyl)-6-phenyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one, 5-[(2-hydroxy-1-naphthyl)methyl]-2-mercapto-6-phenyl-4(3H)-Pyrimidinone
CAS 14513-15-6
分子式 C21H16N2O2S
分子量 360.435
MOL 文件 14513-15-6.mol
更新日期 2024/06/12 17:31:29
14513-15-6 结构式 14513-15-6 结构式

基本信息

中文别名
化合物CAMBINOL
SIRT1和SIRT1抑制剂(CAMBINOL)
5-[(2-羟基萘-1-基)甲基]-6-苯基-2-硫代-2,3-二氢嘧啶-4(1H)-酮
英文别名
Cambinol
NSC 112546
NSC-1125476
CAMBINOL
NSC-1125476
SIRT1/2 Inhibitor IV
Cambinol - NSC 112546
SIRT1/2 Inhibitor IV, Cambinol
5-[(2-hydroxy-1-naphthyl)methyl]-2-mercapto-6-phenyl-4(3H)-Pyrimidinone
5-[(2-Hydroxy-1-naphthyl)methyl]-6-phenyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone
5-(2-Hydroxynaphthalen-1-ylmethyl)-6-phenyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one

物理化学性质

熔点235 °C(dec.)
储存条件Room temp
储存条件room temp
溶解度二甲基亚砜:≥10mg/mL
形态白色固体
颜色白色至灰白色

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H319
防范说明P305+P351+P338
危险品标志Xn
危险类别码22
WGK Germany3
海关编码2933.59.8000
SIRT1/2 INHIBITOR IV价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30C3535Cambinol
Cambinol
14513-15-65mg250元
2024/04/30C3535Cambinol
Cambinol
14513-15-625mg990元
2024/04/30HY-100732SIRT1/2 INHIBITOR IV
Cambinol
14513-15-65mg990元

常见问题列表

生物活性
Cambinol是一种新型的、非竞争性的nSMase2抑制剂,Ki值为7 μM。
靶点
TargetValue
nSMase2
(Cell-free assay)
7 μM(Ki)
体外研究

Cambinol inhibits NAD-dependent deacetylase activity of human SIRT1 and SIRT2. Inhibition of SIRT1 activity with cambinol during genotoxic stress leads to hyperacetylation of key stress response proteins and promotes cell cycle arrest. Treatment of BCL6-expressing Burkitt lymphoma cells with cambinol as a single agent induces apoptosis, which is accompanied by hyperacetylation of BCL6 and p53. Cambinol has only weak inhibitory activity against SIRT5 (42% inhibition at 300 μM) and no activity against SIRT3.

体内研究

Cambinol is well tolerated in mice (100 mg/kg) and inhibits growth of Burkitt lymphoma xenografts. No significant weight loss occurs in cambinol-treated animals relative to controls. Inhibitors of NAD-dependent deacetylases may constitute novel anticancer agents.

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