Amisulpride hydrochloride

TargetMol
Product Code: TAR-T0811L
Supplier: TargetMol
CodeSizePrice
TAR-T0811L-5mg5mg£850.00
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Quantity:
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Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Amisulpride is an antagonist of 5-HT7 receptor and dopamine D2 and D3 receptors. It modulates beta 2- arresting signaling and increases neurite outgrowth.
CAS:
81342-13-4
Formula:
C17H28ClN3O4S
Molecular Weight:
405.94
Purity:
0.98
SMILES:
Cl.CCN1CCCC1CNC(=O)c1cc(c(N)cc1OC)S(=O)(=O)CC

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, Ekstr?m 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.