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Luseogliflozin is an orally active second-generation sodium-glucose co-transporter 2 (SGLT2) inhibitor developed by Taisho Pharmaceutical for the treatment of patients with type 2 diabetes mellitus (T2DM).
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 23.01 mL | 115.06 mL | 230.12 mL |
| 0.5 mM | 4.6 mL | 23.01 mL | 46.02 mL |
| 1 mM | 2.3 mL | 11.51 mL | 23.01 mL |
| 5 mM | 0.46 mL | 2.3 mL | 4.6 mL |
*The above data is based on the productmolecular weight 434.55. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Catalog Num | A13476 |
|---|---|
| Actions | Inhibitor |
| M. Wt | 434.55 |
| Formula | C23H30O6S |
| Solubility | DMSO |
| Purity | >98% |
| Storage | at -20°C 3 years Powder |
| CAS No. | 898537-18-3 |
| Synonyms | TS 071, TS071, TS-71 |
| SMILES | CCOC1=CC=C(C=C1)CC2=C(C=C(C(=C2)[[email protected]]3[[email protected]@H]([[email protected]]([[email protected]@H]([[email protected]](S3)CO)O)O)O)OC)C |
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