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Amisulpride hydrochloride

CAS No.: 81342-13-4

Amisulpride is an antagonist of 5-HT7 receptor and dopamine D2 and D3 receptors. It modulates beta 2- arresting signalin
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Description Amisulpride is an antagonist of 5-HT7 receptor and dopamine D2 and D3 receptors. It modulates beta 2- arresting signaling and increases neurite outgrowth.
Target activity D3 receptor:3.2 nM (Ki), D2 receptor:2.8 nM (Ki)
Synonyms APD-421, Amisulpride HCl, APD 421, APD421, Sultopride, 氨磺必利盐酸盐
molecular weight 405.94
Molecular formula C17H28ClN3O4S
CAS 81342-13-4
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
References 1. Jang YJ, Jeong TC, Noh K, Baek IW, Kwon KI, Kim E, Yoon YR, Kang W. Prandial effect on the systemic exposure of amisulpride. Arch Pharm Res. 2014 Oct;37(10):1325-8. doi: 10.1007/s12272-014-0331-7. Epub 2014 Jan 29. PubMed PMID: 24469600. 2. Huang LC, Huang LY, Tseng SY, Hou YM, Hsiao CC. Amisulpride and symptomatic bradycardia: a case report. Gen Hosp Psychiatry. 2015 Sep-Oct;37(5):497.e1-2. doi: 10.1016/j.genhosppsych.2013.12.005. Epub 2013 Dec 16. PubMed PMID: 26162544. 3. Donahue TJ, Hillhouse TM, Webster KA, Young R, De Oliveira EO, Porter JH. (S)-amisulpride as a discriminative stimulus in C57BL/6 mice and its comparison to the stimulus effects of typical and atypical antipsychotics. Eur J Pharmacol. 2014 Jul 5;734:15-22. doi: 10.1016/j.ejphar.2014.03.047. Epub 2014 Apr 12. PubMed PMID: 24726559. 4. Loy F, Isola M, Isola R, Lilliu MA, Solinas P, Conti G, Godoy T, Riva A, Ekström J. The antipsychotic amisulpride: ultrastructural evidence of its secretory activity in salivary glands. Oral Dis. 2014 Nov;20(8):796-802. doi: 10.1111/odi.12209. Epub 2013 Dec 10. PubMed PMID: 24245711.