For research use only. Not for therapeutic Use.
Venlafaxine-d6 hydrochloride (CAS: 1062606-12-5), a premium pharmaceutical research compound designed for advanced psychopharmacological and antidepressant studies. As a deuterated analog of Venlafaxine hydrochloride, it offers enhanced stability and improved pharmacokinetic properties. Venlafaxine-d6 hydrochloride is ideal for use in pharmacological and biochemical research, providing precise and reliable data for your studies. This high-purity compound ensures consistent results, aiding in the development of novel therapies for depression and anxiety disorders. Trusted by leading laboratories, Venlafaxine-d6 hydrochloride is your go-to solution for cutting-edge mental health research. Unlock new possibilities in the treatment of psychiatric disorders with Venlafaxine-d6 hydrochloride, where innovation meets reliability.
| Catalog Number | S000165 |
| CAS Number | 1062606-12-5 |
| Molecular Formula | C17H22D6ClNO2 |
| Purity | ≥95% |
| Target | Serotonin Transporter |
| IUPAC Name | 1-[2-[bis(trideuteriomethyl)amino]-1-(4-methoxyphenyl)ethyl]cyclohexan-1-ol;hydrochloride |
| InChI | InChI=1S/C17H27NO2.ClH/c1-18(2)13-16(17(19)11-5-4-6-12-17)14-7-9-15(20-3)10-8-14;/h7-10,16,19H,4-6,11-13H2,1-3H3;1H/i1D3,2D3; |
| InChIKey | QYRYFNHXARDNFZ-TXHXQZCNSA-N |
| SMILES | [2H]C([2H])([2H])N(CC(C1=CC=C(C=C1)OC)C2(CCCCC2)O)C([2H])([2H])[2H].Cl |
| Reference | [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [2]. Bymaster FP, et al. Comparative affinity of duloxetine and venlafaxine for serotonin and norepinephrine transporters in vitro and in vivo, human serotonin receptor subtypes, and other neuronal receptors. Neuropsychopharmacology. 2001 Dec;25(6):871-80. [3]. Goeringer KE, et al. Postmortem tissue concentrations of venlafaxine. Forensic Sci Int. 2001 Sep 15;121(1-2):70-5. |
