金精三羧酸
中文名称 | 金精三羧酸 |
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中文同义词 | 金精三羧酸;金黄三羧羧;金黄三羧酸;金精三羧酸|ATA |
英文名称 | AURINTRICARBOXYLIC ACID |
英文同义词 | TIMTEC-BB SBB005410;LABOTEST-BB LT00080677;ATA;5,5-(3-carboxy-4-oxocyclohexa-2,5-dienylidenemethylene)di(salicylic acid);aurinetricarboxylic acid;AURINTRICARBOXYLIC ACID FREE ACIDPRACTIC AL GRADE;Aurintricarboxylic Acid (Ata);AURINTRICARBONIC ACID |
CAS号 | 4431-00-9 |
分子式 | C22H14O9 |
分子量 | 422.34 |
EINECS号 | 224-628-1 |
相关类别 | 色素类;生化试剂-色素类;化学试剂;通用生化试剂-生物染色剂与化学指示剂;有机化工原料;Colours, Dyes, Indicators & Pigments |
Mol文件 | 4431-00-9.mol |
结构式 |
金精三羧酸 性质
熔点 | 300 °C(lit.) |
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沸点 | 458.99°C (rough estimate) |
密度 | 1.3860 (rough estimate) |
折射率 | 1.6230 (estimate) |
储存条件 | +15C to +30C |
溶解度 | 1 M NH4OH:10 mg/mL |
形态 | 粉末 |
酸度系数(pKa) | 2.20±0.20(Predicted) |
颜色 | 暗红色至棕色 |
水溶解性 | Insoluble in water. |
BRN | 2228904 |
CAS 数据库 | 4431-00-9(CAS DataBase Reference) |
EPA化学物质信息 | Benzoic acid, 5-[(3-carboxy-4-hydroxyphenyl)(3-carboxy-4-oxo-2,5-cyclohexadien-1-ylidene)methyl]-2-hydroxy- (4431-00-9) |
Topoisomerase II
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rP2X1R 8.6 nM (IC 50 ) |
rP2X3R 72.9 nM (IC 50 ) |
Apoptosis
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miRNA 0.47 μM (IC 50 ) |
Aurintricarboxylic acid strongly inhibits rP2X1Rs and rP2X3Rs with IC
50
values of 8.6 nM and 72.9 nM, respectively, and more weakly inhibits P2X2/3Rs, P2X2Rs, P2X4Rs or P2X7Rs.
Aurintricarboxylic acid inhibition of ATP-induced currents is concentration dependent.
Aurintricarboxylic acid is a non-competitive antagonist of P2X3R.
Aurintricarboxylic acid can inhibit the severe acute respiratory syndrome-associated coronavirus (SARS-CoV) and vaccinia virus.
Aurintricarboxylic acid protects MDCK cells from infection with influenza A strains PR8, NY or N.
Aurintricarboxylic acid inhibits replication of influenza A and B viruses.
Aurintricarboxylic acid inhibits neuraminidase activities of influenza A and B viruses.
Aurintricarboxylic acid inhibits TWEAK-Fn14-mediated NF-κB activation.
Aurintricarboxylic acid (10 μM;0.5-2 hours) suppresses TWEAK-Fn14-mediated NF-κB, Akt, and Src phosphorylation in GBM cells.
Aurintricarboxylic acid blocks TWEAK-stimulated Rac1 activation and TRAF2 recruitment to Fn14 cytoplasmic domain in glioma cells.
Aurintricarboxylic acid represses TWEAK-stimulated glioma cell migration and invasion without causing cell cytotoxicity.
Aurintricarboxylic acid (Compound 8) cannot regulate loading of endogenous let-7 onto AGO2 inside cultured cells, whereas can inhibit RISC loading of exogenous siRNA.
Western Blot Analysis
Cell Line: | T98G, A172, GBM44 glioma cells |
Concentration: | 10 μM |
Incubation Time: | 0.5 hour, 1 hour, 2 hours |
Result: | Abrogated TWEAK activation of downstream signals including phosphorylation of the NF-κB family member p65, Akt, and Src in all three GBM cell lines. |
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