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Submit Review2S,6S-Hydroxynorketamine hydrochloride is a ketamine metabolite. Decreases intracellular D-serine (a NMDA co-agonist) concentrations in PC-12 cells (IC50 = 0.18 nM). Exerts antidepressant effects in mice.
2R,6R-Enantiomer and Racemate also available.
Sold under license from the NIH, US patent 62/313,309
M. Wt | 276.16 |
Formula | C12H14ClNO2.HCl |
Storage | Store at RT |
Purity | ≥98% (HPLC) |
CAS Number | 1430202-70-2 |
PubChem ID | 124201855 |
InChI Key | ZQJVHBJDLMIKJK-JGAZGGJJSA-N |
Smiles | ClC1=C([C@]2(N)C([C@@H](O)CCC2)=O)C=CC=C1.Cl |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
water | 13.81 | 50 | |
DMSO | 27.62 | 100 |
The following data is based on the product molecular weight 276.16. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3.62 mL | 18.11 mL | 36.21 mL |
5 mM | 0.72 mL | 3.62 mL | 7.24 mL |
10 mM | 0.36 mL | 1.81 mL | 3.62 mL |
50 mM | 0.07 mL | 0.36 mL | 0.72 mL |
References are publications that support the biological activity of the product.
Singh et al (2016) KA metabolites enantioselectively decrease intracellular D-serine concentrations in PC-12 cells. PLoS One 11 e0149499 PMID: 27096720
Zanos et al (2016) NMDAR inhibition-independent antidepressant actions of KA metabolites. Nature 533 481 PMID: 27144355
If you know of a relevant reference for 2S,6S-Hydroxynorketamine hydrochloride, please let us know.
Keywords: 2S,6S-Hydroxynorketamine hydrochloride, 2S,6S-Hydroxynorketamine hydrochloride supplier, Potent, AMPA, agonists, agonism, ketamine, metabolites, antidepressants, enantiomer, 2S,6S-HNK, depression, Receptors, NMDA, Ketamine, and, Metabolites, 6095, Tocris Bioscience
Citations are publications that use Tocris products. Selected citations for 2S,6S-Hydroxynorketamine hydrochloride include:
Ago et al (2019) (R)-Ketamine induces a greater increase in prefrontal 5-HT release than (S)-Ketamine and Ketamine Metabolites via an AMPA receptor-independent mechanism. Int J Neuropsychopharmacol 22 665 PMID: 31325908
Ye et al (2019) KA metabolite (2R,6R)-hydroxynorKA enhances aggression via periaqueductal gray glutamatergic transmission. Neuropharmacology 157 PMID: 31207251
Eero et al (2022) Antidepressant and Antipsychotic Drugs Reduce Viral Infection by SARS-CoV-2 and Fluoxetine Shows Antiviral Activity Against the Novel Variants in vitro. Front Pharmacol 12 755600 PMID: 35126106
Chou et al (2018) (2R,6R)-hydroxynorKA rescues chronic stress-induced depression-like behavior through its actions in the midbrain periaqueductal gray. Neuropharmacology 139 1 PMID: 29953886
Do you know of a great paper that uses 2S,6S-Hydroxynorketamine hydrochloride from Tocris? Please let us know.
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
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The key feature of drug addiction is the inability to stop using a drug despite clear evidence of harm. This poster describes the brain circuits associated with addiction, and provides an overview of the main classes of addictive drugs and the neurotransmitter systems that they target.
Major depressive disorder is characterized by depressed mood and a loss of interest and/or pleasure. Updated in 2015 this poster highlights presynaptic and postsynaptic targets for the potential treatment of major depressive disorder, as well as outlining the pharmacology of currently approved antidepressant drugs.