Bioactivity | Ampreloxetine (TD-9855) hydrochloride is an orally active and CNS-penetrant inhibitor of Norepinephrine transporter (NET) and Serotonin 5-HT uptake transporter (SERT), but not Dopamine transporter (DAT). Ampreloxetine hydrochloride binds norepinephrine transporters (NET) and serotonin transporters (SERT) with EC50 values of 11.7 ng/mL and 50.8 ng/mL, respectively, in plasma[1]. |
In Vivo | Ampreloxetine hydrochloride (0.3- 60mg /kg;口服;单剂量) 在大鼠模型中,其血浆浓度和剂量水平无关[1]。 Animal Model: |
Name | Ampreloxetine hydrochloride |
CAS | 1227056-87-2 |
Formula | C18H19ClF3NO |
Molar Mass | 357.80 |
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]. Smith JA, et al. Preclinical to clinical translation of CNS transporter occupancy of TD-9855, a novel norepinephrine and serotonin reuptake inhibitor. Int J Neuropsychopharmacol. 2014 Dec 13;18(2):pyu027. |