rac-Paroxetine-d4 Hydrochloride manufacturers
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| | rac-Paroxetine-d4 Hydrochloride Basic information |
| Product Name: | rac-Paroxetine-d4 Hydrochloride | | Synonyms: | (3S,4R)-3-(1,3-benzodioxol-5-yloxymethyl)-4-(2,3,5,6-tetradeuterio-4-fluorophenyl)piperidine;rac-3-[(1,3-Benzod-d4-ioxol-5-yloxy)methyl]-4-(4-fluorophenyl-d4)piperidine Hydrochloride;rac-Aropax-d4;rac-Deroxat-d4;rac-Paxil-d4;rac-Seroxat-d4;rel-Paroxetine (hydrochloride);D4-Paroxetine HCl | | CAS: | 2714485-95-5 | | MF: | C19H16D4FNO3.ClH | | MW: | 369.85 | | EINECS: | | | Product Categories: | | | Mol File: | 2714485-95-5.mol |  |
| | rac-Paroxetine-d4 Hydrochloride Chemical Properties |
| form | Solid | | color | White to off-white |
| | rac-Paroxetine-d4 Hydrochloride Usage And Synthesis |
| Uses | Paroxetine-d4 (hydrochloride) is deuterium labeled Paroxetine (hydrochloride). Paroxetine hydrochloride is a potent selective serotonin-reuptake inhibitor, commonly prescribed as an and has GRK2 inhibitory ability with IC50 of 14μM. Paroxetine hydrochloride can be used for the research of depressive disorder[1][2][3]. | | References | [1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Liu RP, et al. Paroxetine ameliorates lipopolysaccharide-induced microglia activation via differential regulation of MAPK signaling. J Neuroinflammation. 2014 Mar 12;11:47. DOI:10.1186/1742-2094-11-47
[3] Wang Q, et al. Paroxetine alleviates T lymphocyte activation and infiltration to joints of collagen-induced arthritis. Sci Rep. 2017 Mar 28;7:45364. DOI:10.1038/srep45364
[4] Lassen TR, et al. Effect of paroxetine on left ventricular remodeling in an in vivo rat model of myocardial infarction. Basic Res Cardiol. 2017 May;112(3):26. DOI:10.1007/s00395-017-0614-5
[5] Zarei M, et al. Paroxetine attenuates the development and existing pain in a rat model of neurophatic pain. Iran Biomed J. 2014;18(2):94-100. DOI:10.6091/ibj.1282.2013
[6] Waldschmidt HV, et al. Structure-Based Design of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors Based on Paroxetine. J Med Chem. 2017 Apr 13;60(7):3052-3069. DOI:10.1021/acs.jmedchem.7b00112 |
| | rac-Paroxetine-d4 Hydrochloride Preparation Products And Raw materials |
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