| 中文名称 | 亚牛磺酸 |
| 英文名称 | HYPOTAURINE |
| CAS号 | 300-84-5 |
| 分子式 | C2H7NO2S |
| 分子量 | 109.15 |
| EINECS号 | 200-258-5 |
| 熔点 | 175-177 °C |
| 沸点 | 354.9±44.0 °C(Predicted) |
| 密度 | 1.511±0.06 g/cm3(Predicted) |
| LogP | -2.030 (est) |
| 溶解度 | H2O:100 mg/mL |
| 形态 | 固体 |
| 酸度系数(pKa) | 2.54±0.10(Predicted) |
| 颜色 | 白色 |
| 水溶解性 | Soluble to 100 mM in water |
| 危险品标志 | Xi |
| 危险类别码 | 36/37/38 |
| 安全说明 | 26-36 |
| WGK Germany | 3 |
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Human Endogenous Metabolite
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Hypotaurine and taurine are found to reside within the cytosolic compartment of the cell. The ratio of taurine to hypotaurine is approx 50:1. The cytosolic concentration of taurine is approx. 50 mM. The concentration of hypotaurine decreases by 80% when resting neutrophils are converted into actively respiring cells by exposure to opsonized zymosan. Hypotaurine activates hypoxia signaling through the competitive inhibition of prolyl hydroxylase domain-2. This leads to the activation of hypoxia signaling as well as to the enhancement of glioma cell proliferation and invasion.
Hypotaurine has antinociceptive effects on thermal, mechanical, and chemical nociception in the spinal cord. In CCI rats, hypotaurine alleviates mechanical allodynia and thermal hyperalgesia. Intrathecal hypotaurine suppresses acute, inflammatory, and neuropathic pain. Hypotaurine may regulate nociceptive transmission physiologically by activating glycinergic neurons in the spinal cord.