6027-91-4
6027-91-4 结构式
基本信息
GUVACINE HYDROCHLORIDE >96% \ GABA UPTAK
1,2,5,6-Tetrahydro-3-pyridinecarboxylic Acid Hydrochloride
3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-, hydrochloride
物理化学性质
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2024/04/30 | HY-100809 | 去甲槟榔次碱 Guvacine hydrochloride | 6027-91-4 | 5 mg | 600元 |
| 2024/04/30 | HY-100809 | 去甲槟榔次碱 Guvacine hydrochloride | 6027-91-4 | 10 mM * 1 mLin Water | 660元 |
| 2024/04/30 | HY-100809 | 去甲槟榔次碱 Guvacine hydrochloride | 6027-91-4 | 10 mg | 800元 |
常见问题列表
IC50: 14 μM (human GAT-1), 39 μM (rat GAT-1), 58 μM (rat GAT-2), 119 μM (human GAT-3), 378 μM (rat GAT-3), 1870 μM (human BGT-3)
Guvacine hydrochloride is a potent inhibitor of GABA transporter, dispalys modest selectivity for cloned GABA transporters with IC 50 s of 14 μM (human GAT-1), 39 μM (rat GAT-1), 58 μM (rat GAT-2), 119 μM (human GAT-3), 378 μM (rat GAT-3), and 1870 μM (human BGT-3). Guvacine has low affinity at hBGT-1 (IC 50 >1 mM). Guvacine hydrochloride is a potent inhibitor of GABA uptake, but does not inhibit sodium-independent GABA binding, and is weak or inactive as a GABA receptor agonist. Guvacine inhibits the uptake GABA and β-alanine with IC 50 s of 23 ± 2 μM, 66 ± 11 μM in the Cat spinal cord, and 8 ± 1 μM, 123 ± 28 μM in the rat cerebral cortex, respectively.