| Molecular Formula | C21H16N2O9S2 |
| Molar Mass | 504.49 |
| Density | 1.798±0.06 g/cm3(Predicted) |
| Melting Point | 86-88 ℃ |
| Appearance | Dry gray-white powder |
| pKa | -0.17±0.40(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.822 |
| Use | As an intermediate for azo dyes, used in the manufacture of direct Orange S, direct acid fast red 4BS, etc |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| Biological activity | AMI-1 free acid is an effective, cell-permeable, reversible protein arginine N-methyltransferase (PRMTs) inhibitor, The IC50 values for human PRMT1 and yeast Hmt1p are 8.8 μM and 3.0 μM respectively. AMI-1 free acid exerts an inhibitory effect on PRMTs by blocking peptide-substrate binding. |
| Target | Value |
| HMT () | |
| human PRMT1 () | |
| yeast Hmt1p (Cell-free assay) | 3.0 μM |
| Cell Line: | S180 cells, U2OS cells S180 cells |
| Concentration: | 0.6 mM, 1.2 mM, 2.4 mM 1.2 mM, 2.4 mM |
| Incubation Time: | 48 hours, 72 hours, 96 hours 48 hours, 72 hours |
| Result: | Inhibited the cell viability. Increased the percentages of cells undergoing apoptosis. Decreased tumor weight. |
| 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 |
| use | is an intermediate for azo dyes, used to make direct orange s, direct acid-resistant red 4BS, etc. |