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256925-03-8

中文名称 AL 082D06游离态
英文名称 D 06
CAS 256925-03-8
分子式 C23H24ClN3O2
分子量 409.91
MOL 文件 256925-03-8.mol
更新日期 2024/07/12 16:05:06
256925-03-8 结构式 256925-03-8 结构式

基本信息

中文别名
AL 082D06游离态
英文别名
D 06
AL082D06
AL-082D06
AL 082D06
AL 082D06(D-06)
AL-082D06
D06
D-06
AL082D06
4,4'-[(2-Chloro-5-nitrophenyl)methylene]bis[N,N-dimethylbenzenamine]
Benzenamine, 4,4'-[(2-chloro-5-nitrophenyl)methylene]bis[N,N-dimethyl-
4-[(2-Chloro-5-nitrophenyl)-[4-(dimethylamino)phenyl]methyl]-N,N-dimethylaniline
所属类别
生物化工:激动剂抑制剂

物理化学性质

沸点543.7±50.0 °C(Predicted)
密度1.232±0.06 g/cm3(Predicted)
储存条件Sealed in dry,2-8°C
溶解度DMSO:6.25(Max Conc. mg/mL);15.25(Max Conc. mM)
DMF:10.0(Max Conc. mg/mL);24.4(Max Conc. mM)
DMF:PBS (pH 7.2) (1:2):0.33(Max Conc. mg/mL);0.81(Max Conc. mM)
酸度系数(pKa)5.36±0.24(Predicted)
形态结晶固体
颜色Light yellow to yellow
AL 082D06游离态价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-15709AL 082D06游离态
AL 082D06
256925-03-82mg2000元
2024/04/30S6608AL 082D06游离态
AL082D06
256925-03-82mg2269.2元
2024/04/30HY-15709AL 082D06游离态
AL 082D06
256925-03-85mg3000元

常见问题列表

生物活性
AL082D06是非类固醇的糖皮质激素受体拮抗剂,而对与其高度相关受体如盐皮质激素、雄激素、雌激素和孕酮等无显著结合亲和力。
靶点
TargetValue
Glucocorticoid receptor
()
210 nM(Ki)
体外研究

AL 082D06 (D06) binds specifically to GR with nanomolar affinity. Addition of AL 082D06 causes a dose-dependent decrease in transcriptional activation from the MMTV:Luc reporter stimulated with half-maximal DEX concentrations. AL 082D06 acts to antagonize reporter activity using several glucocorticoid-responsive promoter- reporter systems including the 3-kb tyrosine amino transferase (TAT) promoter and less complex promoters comprised of isolated glucocorticoid response element (GRE) sequences. AL 082D06 competes with 3 H-Dex for baculovirus-expressed GR with nanomolar affinity. Other intracellular receptors (AR, ER, PR, and MR) have no affinity for AL 082D06 in a similarly structured binding assay with the appropriate receptor and tritiated ligand (>2500 nM). AL 082D06 has no activation efficacy on the progesterone, androgen, mineralocorticoid, retinoid, glucocorticoid, or estrogen receptors. AL 082D06 is very efficacious at antagonizing GR activity but exhibits much weaker efficacy when tested against the other steroid receptors in contrast to the reference antagonists used as controls.

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