For research use only. Not for therapeutic Use.
Paroxetine hydrochloride is a serotonin uptake inhibitor that is effective in the treatment of depression. It is a highly potent and selective ST (serotonin transporter/5-HT) uptake inhibitor. It acts by binding to ST (serotonin transporter/SERT) with high affinity. Paroxetine binds to the pre-synaptic serotonin transporter complex resulting in negative allosteric modulation of the complex thereby blocking reuptake of serotonin by the pre-synaptic transporter. Paroxetine HCl has also displayed a high affinity for muscarinic acetylcholine receptors.
Catalog Number | A000195 |
CAS Number | 78246-49-8 |
Synonyms | 78246-49-8; Paroxetine Hcl; Paroxat; Aropax 20; (3S,4R)-3-((Benzo[d][1,3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)piperidine hydrochloride |
Molecular Formula | C19H21ClFNO3 |
Purity | ≥95% |
Target | Autophagy |
Solubility | Soluble in DMSO > 10 mM |
Storage | -20°C |
InChI | 1S/C19H20FNO3.ClH/c20-15-3-1-13(2-4-15)17-7-8-21-10-14(17)11-22-16-5-6-18-19(9-16)24-12-23-18;/h1-6,9,14,17,21H,7-8,10-12H2;1H/t14-,17-;/m0./s1 |
InChIKey | GELRVIPPMNMYGS-RVXRQPKJSA-N |
SMILES | C1CNCC(C1C2=CC=C(C=C2)F)COC3=CC4=C(C=C3)OCO4.Cl |
Reference | 1: Brittain HG. Paroxetine hydrochloride: polymorphs and solvatomorphs. Profiles <br> 3: Khatavkar UN, Shimpi SL, Jayaram Kumar K, Deo KD. Development and comparative 4: Pae CU, Misra A, Ham BJ, Han C, Patkar AA, Masand PS. Paroxetine mesylate: 5: Jin SJ, Yoo YH, Kim MS, Kim JS, Park JS, Hwang SJ. Paroxetine hydrochloride 6: Venkatachalam A, Chatterjee VS. Stability-indicating high performance thin 7: Alarfaj N, Razeq SA, Sultan M. Spectrofluorimetric determination of paroxetine <br> 9: Roscoe JA, Morrow GR, Hickok JT, Mustian KM, Griggs JJ, Matteson SE, Bushunow 10: Erk N, Biryol I. Voltammetric and HPLC techniques for the determination of |