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108477-18-5

中文名称:
108477-18-5
中文同义词:
半胱天冬酶和细胞凋亡激活剂(UBIQUITIN ISOPEPTIDASE INHIBITOR I, G5)
英文名称:
4H-Thiopyran-4-one,tetrahydro-3,5-bis[(4-nitrophenyl)methylene]-1,1-dioxide
英文同义词:
4H-Thiopyran-4-one,tetrahydro-3,5-bis[(4-nitrophenyl)methylene]-1,1-dioxide;NSC-144303;Ubiquitin Isopeptidase Inhibitor I;Ubiquitin Isopeptidase Inhibitor I, G5;G5, Ubiquitin Isopeptidase Inhibitor I;Ubiquitin Isopeptidase-IN-G5;Ubiquitin Isopeptidase Inhibitor I, G5 (NSC144303)
CAS号:
108477-18-5
分子式:
C19H14N2O7S
分子量:
414.39
EINECS号:
相关类别:
细胞生物学试剂
Mol文件:
108477-18-5.mol
熔点 
233.5-234.5 °C
沸点 
693.0±55.0 °C(Predicted)
密度 
1.541±0.06 g/cm3(Predicted)
生物活性
Ubiquitin Isopeptidase Inhibitor I, G5 (NSC 144303)是凋亡不依赖的半胱天冬酶和细胞凋亡的激活剂,对E1A和E1A/C9DN细胞的IC50值分别为1.76和1.6 μM。
靶点
IC50: 1.76 μM (E1A cells), 1.6 μM (E1A/C9DN cells)
体外研究
G5 is capable of activating an apoptosome-independent apoptotic pathway. It targets the ubiquitinproteasome system by inhibiting the ubiquitin isopeptidases. G5 induces a rather unique apoptotic pathway, which includes a Bcl-2-dependent but apoptosome-independent mitochondrial pathway with upregulation of the BH3-only protein Noxa, stabilization of the inhibitor of apoptosis antagonist Smac, but also the involvement of the death receptor pathway. G5 is a potent apoptotic inducer showing IC 50 s of 1.76 and 1.6 μM in E1A and E1A/C9DN cells, respectively.
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CAS    号: 108477-18-5
规       格:10g/20g/100g/1kg
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详细介绍
英文名:
4H-Thiopyran-4-one,tetrahydro-3,5-bis[(4-nitrophen
外观:
纯度:
请咨询卖家
分子式:
C19H14N2O7S
分子量:
414.39
中文名称:
108477-18-5
中文同义词:
半胱天冬酶和细胞凋亡激活剂(UBIQUITIN ISOPEPTIDASE INHIBITOR I, G5)
英文名称:
4H-Thiopyran-4-one,tetrahydro-3,5-bis[(4-nitrophenyl)methylene]-1,1-dioxide
英文同义词:
4H-Thiopyran-4-one,tetrahydro-3,5-bis[(4-nitrophenyl)methylene]-1,1-dioxide;NSC-144303;Ubiquitin Isopeptidase Inhibitor I;Ubiquitin Isopeptidase Inhibitor I, G5;G5, Ubiquitin Isopeptidase Inhibitor I;Ubiquitin Isopeptidase-IN-G5;Ubiquitin Isopeptidase Inhibitor I, G5 (NSC144303)
CAS号:
108477-18-5
分子式:
C19H14N2O7S
分子量:
414.39
EINECS号:
相关类别:
细胞生物学试剂
Mol文件:
108477-18-5.mol
熔点 
233.5-234.5 °C
沸点 
693.0±55.0 °C(Predicted)
密度 
1.541±0.06 g/cm3(Predicted)
生物活性
Ubiquitin Isopeptidase Inhibitor I, G5 (NSC 144303)是凋亡不依赖的半胱天冬酶和细胞凋亡的激活剂,对E1A和E1A/C9DN细胞的IC50值分别为1.76和1.6 μM。
靶点
IC50: 1.76 μM (E1A cells), 1.6 μM (E1A/C9DN cells)
体外研究
G5 is capable of activating an apoptosome-independent apoptotic pathway. It targets the ubiquitinproteasome system by inhibiting the ubiquitin isopeptidases. G5 induces a rather unique apoptotic pathway, which includes a Bcl-2-dependent but apoptosome-independent mitochondrial pathway with upregulation of the BH3-only protein Noxa, stabilization of the inhibitor of apoptosis antagonist Smac, but also the involvement of the death receptor pathway. G5 is a potent apoptotic inducer showing IC 50 s of 1.76 and 1.6 μM in E1A and E1A/C9DN cells, respectively.
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