Bioactivity | TC-2153 is a selective inhibitor of striatal-enriched protein tyrosine phosphatase (STEP), with psychotropic activity and low acute toxicity. TC-2153 increases the expression of brain-derived neurotropic factor (BDNF) in the brain. And it decreases MAOA and 5-HT1A receptors mRNA level in midbrain. TC-2153 also inhibits 5-HT2A receptor-mediated signaling[1]. |
Invitro | TC-2153 (10 μM; 3 h) 减少皮层和海马神经元体外培养中 DOI (HY-103124) 诱导的 c-fos 阳性神经元百分比[1]。 |
In Vivo | 慢性 TC-2153 处理: TC-2153 (20 mg/kg; 腹腔注射; 每天 1 次,连续 7 天) 显示抗抑郁类效果,不改变运动,探索活动和焦虑情况[1]。 急性 TC-2153 处理: TC-2153 (10 mg/kg和20 mg/kg; 单次剂量) 抑制小鼠体内 5-HT2A 受体的功能活性[1]。 Animal Model: |
Name | TC-2153 |
CAS | 1381769-23-8 |
Formula | C7H5ClF3NS5 |
Molar Mass | 355.89 |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Reference | [1]. Walters JM, et al. Pharmacological inhibition of STriatal-Enriched protein tyrosine Phosphatase by TC-2153 reduces hippocampal excitability and seizure propensity. Epilepsia. 2022 May;63(5):1211-1224. |