猩红酸
中文名称 | 猩红酸 |
---|---|
中文同义词 | 6,6'-(1,3-亚脲基)双(1,1'-萘酚)-3,3'-磺酸;猩红酸;7,7-(羰基二亚氨基)二(4-羟基-2-萘磺酸);腥红酸;7,7'-(羰基双(氮杂二基))双(4-羟基萘-2-磺酸);化合物 T22239 |
英文名称 | 6,6'-Ureylene-bis(1-naphthol-3-sulfonic acid) |
英文同义词 | 4,4'-dihydroxy-7,7'-ureylenedi(naphthalene-2-sulphonic acid);7,7'-(Carbonyldiimino)bis[4-hydroxy-2-naphthalenesulfonic acid];6,6'-ureylene-bis(1-naphthol-3-sulfonic acid);phosgenated;N,N'-bis(4-hydroxy-2-sulfonaphthalene-7-yl)urea;7,7'-Ureylenebis(4-hydroxy-2-naphthalenesulfonic acid);N,N'-Bis[6-(1-naphthol-3-sulfonic acid)]urea;6,6'-ureylenbis-1-naphthol-3-sulfonic acid |
CAS号 | 134-47-4 |
分子式 | C21H16N2O9S2 |
分子量 | 504.49 |
EINECS号 | 205-142-9 |
相关类别 | 化工原料;染料中间体;Intermediates of Dyes and Pigments |
Mol文件 | 134-47-4.mol |
结构式 |
猩红酸 性质
密度 | 1.798±0.06 g/cm3(Predicted) |
---|---|
储存条件 | Sealed in dry,Room Temperature |
溶解度 | 二甲基亚砜:83.33 mg/mL(165.18 mM) |
酸度系数(pKa) | -0.17±0.40(Predicted) |
CAS 数据库 | 134-47-4(CAS DataBase Reference) |
EPA化学物质信息 | 7,7'-(Carbonyldiimino)bis[4-hydroxy-2-naphthalenesulfonic acid] (134-47-4) |
Target | Value |
HMT
() | |
human PRMT1
() | |
yeast Hmt1p
(Cell-free assay) | 3.0 μM |
AMI-1 free acid can inhibit the in vitro methylation reactions performed by all five recombinantly active PRMTs (PRMT1, -3, -4, and -6 and Hmt1p).
AMI-1 free acid not only inhibits type I PRMTs (PRMT1, 3, 4 and 6) but also type II PRMT5.
AMI-1 free acid specifically inhibits arginine, but not lysine, methyltransferase activity in vitro and does not compete for the AdoMet binding site.
AMI-1 free acid inhibits methylation of GFP-Npl3 and cellular proteins.
AMI-1 free acid (0.6-2.4 mM; 48-96 hours) inhibits the cell viability of sarcoma in S180 and U2OS cells in a time-dependent and dose-dependent manner in vitro.
AMI-1 free acid (1.2-2.4 mM; 48-72 hours) reduces S180 cell viability through the induction of cell apoptosis.
Cell Viability Assay
Cell Line: | S180 cells, U2OS cells |
Concentration: | 0.6 mM, 1.2 mM, 2.4 mM |
Incubation Time: | 48 hours, 72 hours, 96 hours |
Result: | Inhibited the cell viability. |
Apoptosis Analysis
Cell Line: | S180 cells |
Concentration: | 1.2 mM, 2.4 mM |
Incubation Time: | 48 hours, 72 hours |
Result: | Increased the percentages of cells undergoing apoptosis. |
AMI-1 free acid (0.5 mg; intratumorally; daily; for 7 days) inhibits S180 viability in vivo.
AMI-1 free acid (0.5 mg; intratumorally; daily; for 7 days) downregulates PRMT5 but does not regulate the expression of PRMT7 in a tumor xenograft model.
AMI-1 free acid (0.5 mg; intratumorally; daily; for 7 days) decreases the levels of H4R3me2s and H3R8me2s in a tumor xenograft model.
Animal Model: | 6-7 weeks old male Kunming mice (18-22 g), with S180 cells xenograft |
Dosage: | 0.5 mg |
Administration: | Intratumorally, daily, for 7 days |
Result: | Decreased tumor weight. |