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1001600-56-1

中文名称 BV 6
英文名称 BV6
CAS 1001600-56-1
分子式 C70H96N10O8.xCF3COOH
分子量 1205.57
MOL 文件 1001600-56-1.mol
更新日期 2024/01/31 11:06:36
1001600-56-1 结构式 1001600-56-1 结构式

基本信息

中文别名
化合物BV6
BV-6游离态
英文别名
BV6
CS-1501
CS-2877
BV-6
BV6
BV-6 TFA
CHEBI:47924
BV6 USP/EP/BP
CHEBI:47924
BV-6 BV 6
4,4'-(1,6-Hexanediyl)bis[N-methyl-L-alanyl-(2S)-2-cyclohexylglycyl-L-prolyl-β-phenyl-L-Phenylalanin
L-Phenylalaninamide, 4,4'-(1,6-hexanediyl)bis[N-methyl-L-alanyl-(2S)-2-cyclohexylglycyl-L-prolyl-β-phenyl-
所属类别
生物化工:IAP 抑制剂

物理化学性质

沸点1376.7±65.0 °C(Predicted)
密度1.177±0.06 g/cm3(Predicted)
储存条件Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
溶解度≥60.28 mg/mL in DMSO; insoluble in H2O; ≥12.6 mg/mL in EtOH with ultrasonic
酸度系数(pKa)12.89±0.20(Predicted)
形态固体

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

常见问题列表

生物活性
BV-6是一种SMAC模拟的cIAP和XIAP的双重抑制剂。
体外研究
BV6抑制HCC193 NSCLC细胞的细胞活性,IC50 为 7.2 μM,在HCC193 和H460细胞系引起细胞凋亡,并通过分别激活裂解的caspase-8 和caspase-9显著增加这些细胞系的放射敏感性。在不成熟的树突细胞中,BV-6治疗导致经典的NF-kB通路适度激活。此外,BV-6增加CIK细胞介导的血液病(H9,THP-1,和Tanoue)和固体肿瘤(RH1,RH30,和TE671)的消退。BV-6也会增强外周血单核细胞的凋亡,并且对免疫细胞限制其细胞毒性潜能具有显著的抑制作用。
靶点

IAP

体内研究

Murine cIAP-1, cIAP-2 and XIAP expressions are clearly observed in the cytoplasm of both epithelial and stromal cells of implants, whereas Survivin is mainly expressed in the nuclei BV6 treatment for 4 weeks attenuated the intensity of IAPs expression. The size of lesions range from ~2 to 7 mm in diameter. The monolayer epithelial cell lining of the cyst is shown. After immunohistochemical staining, cytokeratin and vimentin are positively stained, whereas calretinin is negative. After BV6 treatment for 4 weeks, the total number of lesions (4.6 versus 2.8/mouse), the average weight (78.1 versus 32.0 mg/mouse) and the surface area (44.5 versus 24.6 mm 2 /mouse) of lesions are significantly less than in the controls. In the endometrial gland epithelia or stroma, the percentage of Ki67-positive cells decreases after BV6 treatment.

图谱信息

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