| 中文名称 | 交沙霉素 |
| 英文名称 | Josamycin |
| CAS号 | 16846-24-5 |
| 分子式 | C42H69NO15 |
| 分子量 | 827.99 |
| EINECS号 | 240-871-6 |
| 熔点 | 131.5℃ |
| 比旋光度 | D25 -70° (c = 1 in ethanol) |
| 沸点 | 763.27°C (rough estimate) |
| 密度 | 1.1547 (rough estimate) |
| 折射率 | 1.6220 (estimate) |
| 溶解度 | 溶于乙醇 |
| 形态 | 粉末 |
| 酸度系数(pKa) | 7.1 (40% aq methanol) |
| 颜色 | 白色至微黄色 |
| 默克索引编号 | 13,5286 |
| 稳定性 | 吸湿性 |
| WGK Germany | 2 |
| RTECS号 | OH4725810 |
| 毒性 | LD50 oral in rat: > 7gm/kg |
Kd: 5.5 nM (ribosome)
Studies show that the average lifetime on the ribosome is 3 h for Josamycin and that the dissociation constants for Josamycin binding to the ribosome is 5.5 nM. Josamycin slows down formation of the first peptide bond of a nascent peptide in an amino acid-dependent way and completely inhibits formation of the second or third peptide bond, depending on peptide sequence at a saturating drug concentration, synthesis of fulllength proteins is completely shut down by Josamycin. At a saturating drug concentration, synthesis of fulllength proteins is completely shut down by Josamycin.
Blood and tissue levels of Josamycin after oral administration are 200 mg/kg to rabbits. Tissue levels are generally much higher than the blood levels, and 3 h after the administration, when the blood level is very low, the tissue levels are rather higher than those 1 h after the dose. One hour after the medication, the level in the lungs is the highest of all the tissue levels.