| 中文名称 | 氢化可的松琥珀酸酯 |
| 英文名称 | Hydrocortisone 21-hemisuccinate |
| CAS号 | 2203-97-6 |
| 分子式 | C25H34O8 |
| 分子量 | 462.53 |
| EINECS号 | 218-612-3 |
| 熔点 | 170~172℃ |
| 比旋光度 | [α]D20 +147~+153° (c=1, C2H5OH) (After Drying) |
| 沸点 | 685.5±55.0 °C(Predicted) |
| 密度 | 1.33±0.1 g/cm3(Predicted) |
| 溶解度 | 几乎不溶于水,易溶于丙酮和无水乙醇。溶于碱金属碳酸盐和碱金属氢氧化物的稀溶液。 |
| 形态 | 固体 |
| 酸度系数(pKa) | pKa 5.10/5.64(20% aq EtOH/50% aq EtOH) (Uncertain) |
| 颜色 | 白色至类白色 |
| 安全说明 | 22-24/25 |
| WGK Germany | 3 |
| RTECS号 | TU5010147 |
氢化可的松琥珀酸酯是一种皮质类固醇,用作分析和色谱试剂。
Hydrocortisone hemisuccinate (Hydrocortisone 21-hemisuccinate),一种糖皮质激素, 是口服活性的甾体抗炎剂 (SAID)。Hydrocortisone hemisuccinate 抑制 IL-6 和 IL-3 的生物活性,IC50 值分别为 6.7 和 21.4 μM。Hydrocortisone hemisuccinate 可用于溃疡性结肠炎 (UC) 的研究。|
IL-6 6.7 μM (IC 50 ) |
IL-3 21.4 μM (IC 50 ) |
Hydrocortisone hemisuccinate inhibits IL-6 and IL-3 bioactivity, with IC
50
s of 6.7 and 21.4 μM, respectively, and shows no cytotoxic effects on IL-6-independent MH60 cells.
Hydrocortisone hemisuccinate (0.12-60 μM; 72 h) inhibits phytohemagglutinin (PHA) response in peripheral lymphocytes (PBL) and T-lymphocytes cultures.
Hydrocortisone hemisuccinate (30 mg/kg; p.o. twice daily for 5 d) reduces the weight loss and increases the food intake in mice.
| Animal Model: | Male Sprague-Dawley rats (200-220 g, 10-11 weeks) are induced colitis |
| Dosage: | 30 mg/kg |
| Administration: | P.o. twice daily for 5 days |
| Result: |
Significantly decreased the disease activity index (DAI) scores and myeloperoxidase (MPO) activity compared to the 2, 4, 6-trinitrobenzenesulfonic acid (TNBS) group.
Increased the body weight. |