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Ketamine salts solubility

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Int J Neuropsychopharmacol. 2019 Sep; 22(9): 601–607.
Published online 2019 Jul 29. doi: 10.1093/ijnp/pyz042
PMCID: PMC6754733
PMID: 31353393
Opportunities in Novel Psychotropic Drug Design from Natural Compounds

Abstract

Multiple initiatives at the national and international level support natural drug discovery. Psychiatrists and patients are not well informed about natural psychotropics in general. Existing antidepressant and antipsychotic drugs were developed from atropine, a natural product. Subsequent drug developments were largely based on extension and modification of earlier molecular scaffolds. This limits their mechanisms of action to similar neuropathways. Natural psychotropic substances, particularly those with hallucinogenic and psychedelic properties and different chemical structures, may serve as new paths to novel psychotropic drug development.

Keywords: natural psychoactive substances, botanical psychotropics, designer drugs, psychotropic designs


Introduction

Natural psychotropic research has not been at the forefront of psychopharmacology until recently. In 2019, the World Health Organization will include traditional medicine (TM) into its global compendium. The US National Cancer Institute (NCI) announced a new initiative for drug discovery from natural products (Thornburg et al., 2018). The NCI’s natural product repository consists of over 230 000 natural product extracts collected from biodiverse areas in different parts of the world. The US National Center for Complementary and Integrative Health of the National Institutes of Health announced a similar program on natural product drug discovery (NCCIH, 2016). All of these initiatives have generated much interest and discussion regarding medicines and psychotropics derived from plants, animals, and minerals.

The recent increase in interest regarding natural psychotropics has been fueled by the emerging threat of new psychoactive substances worldwide, as alerted by the United Nations Office on Drugs and Crime (UNODC, 2019). New psychoactive substances are mostly available as natural products, such as cacti and animal venom or from modification of their active ingredients, such as synthetic cannabinoids.

Health supplements containing TM are a big business. The absence of strict regulation and the adulteration of some of these products has triggered repeated warnings from the US Food and Drug Administration (FDA, 2019a) and the implementation of stricter oversight this year (FDA, 2019b). Yet based on the sales figures of these supplements, it is clear that TM is highly popular. One of the reasons why patients have resorted to TM may be related to the belief that TM products are “natural” and therefore “safe.” As a result, patient concerns about the safety of manmade drugs may lead to noncompliance, especially during long-term drug maintenance. A significant number of patients suffering from mood disorders failed to respond to existing antidepressant drugs according to large-scale studies such as Star* D (Trivedi et al., 2006). Desperate patients understandably might resort to other forms of medicine that claim efficacy. The success of TM has shown that there is an unmet need for new psychiatric drugs to serve many patients who are not satisfied with current psychiatric drugs. The US National Institute of Mental Health psychoactive drug screening program (NIMH, 2017) represents an effort to stimulate innovative research to discover novel tools and potential therapeutic agents for the treatment of psychiatric disorders, complementary to the NCI and National Institutes of Health initiatives.

Many patients and clinicians alike, however, are not well-informed about TM and may not know that existing antidepressant and antipsychotic drugs in fact are based on plant molecules. Later generations of antidepressant and antipsychotics were mostly synthesized from drug molecules modified from earlier scaffolds. Discovery of psychotropic molecules, natural or synthetic, has mostly been serendipitous. New molecules with targets different from the current are urgently needed. We review in this manuscript the evolution of psychiatric drugs from natural molecules, the merits of this approach, and future opportunities in designer drugs.

...

Conclusion

Natural medicine is popular, but its true value is found in its active ingredients and novel molecules. Phytochemicals like atropine have proven to be valuable scaffolds or chemical platforms from which new drugs were developed. Our existing antipsychotics and antidepressants originated from atropine through serendipity, but serendipity only occurs with the prepared mind. Many of the important drug discoveries have occurred through careful clinical observation of unexpected or unusual effects of compounds with other indications. The recent surge in neuroscience and neuropharmacology research related to new psychoactive substances may open new paths to novel compounds, with alternate mechanisms of action on psychiatric disorders. Neuropsychopharmacologists and clinicians together will continue to play critical but cooperative roles in future discoveries.

Full Medical Journal Paper: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754733/
 
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yeah, there are actually more.... crazy shit

i would totally rock the raver Death patch tho for real.. shades of terry pratchett... i guess Death needs to unwind sometimes too
 
A novel multipatient intranasal diamorphine spray for use in acute pain in children: pharmacovigilance data from an observational study
Jason Kendall, Ian Maconochie, Ian C K Wong, Richard Howard, on behalf of the DIASAFE study
https://emj.bmj.com/content/32/4/269


Objectives To establish the safety of an intranasal diamorphine (IND) spray in children.

Design An open-label, single-dose pharmacovigilance trial.

Setting Emergency departments in eight UK hospitals.

Participants Children aged 2–16 years with a fracture or other trauma.

Outcome measures Adverse events (AE) specifically related to nasal irritation, respiratory and central nervous system depression.

Results 226 patients received 0.1 mg/kg IND. No serious or severe AEs occurred. The incidence of treatment-emergent AEs (TEAEs) was 26.5% (95% CI 20.9% to 32.8% ), 93% being mild. 89% were related to treatment, all being known effects of the drug or route of administration except for three events in two patients. 20.4% (95% CI 15.3% to 26.2% ) patients reported nasal irritation, all mild except one moderate and one ‘unknown’ severity. No respiratory depression was reported. Three AEs related to reduced Glasgow Coma Score (GCS) occurred, all mild.

Conclusions There were no safety concerns raised during the conduct of the study. In addition to expected side effects, IND can cause mild nasal irritation in a proportion of patients.

"Your arm hurts little Billy? Here, have a sniff of this shit"... start em young huh?
 
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Multimodal imaging of hallucinogens 25C‐ and 25I‐NBOMe on blotter papers
Elias Lützen, Michael Holtkamp, Imke Stamme, Robin Schmid, Michael Sperling, Michael Pütz, Uwe Karst
First published: 17 December 2019
https://doi.org/10.1002/dta.2751
Due to the much lower production costs but similar effects to lysergic acid diethylamide (LSD), phenethylamine derivatives are sold as a cheaper replacement or deceptively as LSD itself. These potent hallucinogenic substances can lead to severe intoxication, thus a more profound understanding of their use is required. This includes the elucidation of the manufacturing processes for the commonly used blotter papers and the assessment of the risk of overdosing because of a heterogeneous distribution on the blotter papers. Besides the rapid detection of the analytes, the manufacturing process was elucidated by three different imaging techniques and liquid chromatography‐mass spectrometry (LC–MS). A blotter paper sample, containing the two hallucinogenic phenethylamine derivatives 25I‐NBOMe and 25C‐NBOMe, was analyzed by complementary techniques such as micro x‐ray fluorescence (μXRF), laser ablation (LA)‐inductively coupled plasma‐optical emission spectroscopy (ICP‐OES), matrix assisted laser desorption ionization (MALDI)‐MS, and with LC–MS after extraction. Using the signal from chlorine and iodine within the compounds, μXRF proved to be the fastest, cheapest and easiest method for identification, requiring no sample preparation at all. LA‐ICP‐OES provided three‐dimensional information of the elements in the blotter paper. These results helped to confirm the assumption that manufacturers spray the compounds onto the paper. Whereas μXRF and LA‐ICP‐OES detected signals for chlorine and iodine, MALDI‐MS‐imaging showed the molecular distribution of both analytes. LC–MS analyses as a complementary method support the imaging results. Quantitative results for different drug hotspots revealed a heterogeneous distribution of the drugs on the blotter paper implying an inherent risk of overdosing for consumers.


dta2751-fig-0004-m.png

Obtained iodine and chlorine distribution of a certain area of the blotter paper (see red rectangle in Figure 1B, 1C and Figure 2B 2C and 3) of the blotter paper via LA‐ICP‐OES. Figure 3C shows a depth profile of the chlorine signal from a hotspot (small rectangle in Figure 4B), which was obtained by ablating the same area six times via LA‐ICP‐OES. Experiments were performed using a spot size of 50 μm and a scan rate of 100 μm/s

Very cool - not all blotters are equal...
 
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I guess I should have made my post prison stint return 'hello' here. Funny how my eyes glaze over whenever the name of that MDMA function group appears.
 
I guess I should have made my post prison stint return 'hello' here. Funny how my eyes glaze over whenever the name of that MDMA function group appears.

Hey, I haven't posted here much until recently, but I remember you well from Opiophile. Glad you're still with us and back in the semi-free world.
 
Hey, I haven't posted here much until recently, but I remember you well from Opiophile. Glad you're still with us and back in the semi-free world.
Opiophile, years back, glad to have been a part of it & good to hear the well wishes.
 
Simultaneous Production of Psilocybin and a Cocktail of β‐Carboline Monoamine Oxidase Inhibitors in “Magic” Mushrooms
Felix Blei, Sebastian Dörner, Janis Fricke, Dr. Florian Baldeweg, Felix Trottmann, Dr. Anna Komor , Dr. Florian Meyer, Prof. Dr. Christian Hertweck , Prof. Dr. Dirk Hoffmeister
First published: 14 November 2019
https://doi.org/10.1002/chem.201904363
The psychotropic effects of Psilocybe “magic” mushrooms are caused by the l‐tryptophan‐derived alkaloid psilocybin. Despite their significance, the secondary metabolome of these fungi is poorly understood in general. Our analysis of four Psilocybe species identified harmane, harmine, and a range of other l‐tryptophan‐derived β‐carbolines as their natural products, which was confirmed by 1D and 2D NMR spectroscopy. Stable‐isotope labeling with 13C11‐l‐tryptophan verified the β‐carbolines as biosynthetic products of these fungi. In addition, MALDI‐MS imaging showed that β‐carbolines accumulate toward the hyphal apices. As potent inhibitors of monoamine oxidases, β‐carbolines are neuroactive compounds and interfere with psilocybin degradation. Therefore, our findings represent an unprecedented scenario of natural product pathways that diverge from the same building block and produce dissimilar compounds, yet contribute directly or indirectly to the same pharmacological effects.
 
Simultaneous Production of Psilocybin and a Cocktail of β‐Carboline Monoamine Oxidase Inhibitors in “Magic” Mushrooms
Felix Blei, Sebastian Dörner, Janis Fricke, Dr. Florian Baldeweg, Felix Trottmann, Dr. Anna Komor , Dr. Florian Meyer, Prof. Dr. Christian Hertweck , Prof. Dr. Dirk Hoffmeister
First published: 14 November 2019
https://doi.org/10.1002/chem.201904363
Now this is cool. The effects of using synthesized/extracted pure psilocybin used in clinical trials versus the whole array of mushroom alkaloids used in naturalistic settings would certainly be an interesting investigation. Something that struck me was the researchers' definitive statement that these MAO inhibitory compounds have no effects: "Despite the co-occurrence of 1 and MAO inhibitors in Psilocybe, numerous studies with pure synthetic compound have shown that the somatic, endocrinic, and psychotropic effects are the sole consequence of 1 uptake." More work to be done I suppose...
 
It could just be the dose is too low for the MAOI to function.
 
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Aromatic–Amine Pendants Produce Highly Potent and Efficacious Mixed Efficacy μ-Opioid Receptor (MOR)/δ-Opioid Receptor (DOR) Peptidomimetics with Enhanced Metabolic Stability
Corresponding author: Henry I. Mosberg (Department of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, United States)
Journal of Medicinal Chemistry 2020, Volume 63, Issue 4, Pages 1671-1683
Published online January 27th, 2020
https://doi.org/10.1021/acs.jmedchem.9b01818
We previously reported a novel SAR campaign that converted a metabolically unstable series of μ-opioid receptor (MOR) agonist/δ-opioid receptor (DOR) antagonist bicyclic core peptidomimetics with promising analgesic activity and reduced abuse liabilities into a more stable series of benzylic core analogues. Herein, we expanded the SAR of that campaign and determined that the incorporation of amines into the benzylic pendant produces enhanced MOR-efficacy in this series, whereas the reincorporation of an aromatic ring into the pendant enhanced MOR-potency. Two compounds, which contain a piperidine (14) or an isoindoline (17) pendant, retained the desired opioid profile in vitro, possessed metabolic half-lives of greater than 1 h in mouse liver microsomes (MLMs), and were active antinociceptive agents in the acetic acid stretch assay (AASA) at subcutaneous doses of 1 mg/kg.
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Piperidine propionamide as a scaffold for potent sigma-1 receptor antagonists and mu opioid receptor agonists for treating neuropathic pain
Corresponding authors: Yin Chen and Guisen Zhang (Jiangsu Key Laboratory of Marine Biological Resources and Environment, Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening, School of Pharmacy, Jiangsu Ocean University, Lianyungang, China)
European Journal of Medicinal Chemistry 2020, Volume 191, Page 112144
Published online February 14th, 2020
https://doi.org/10.1016/j.ejmech.2020.112144
We designed and synthesized a novel series of piperidine propionamide derivatives as potent sigma-1 (σ1) receptor antagonists and mu (μ) opioid receptor agonists, and measured their affinity for σ1 and μ receptors in vitro through binding assays. The basic scaffold of the new compounds contained a 4-substituted piperidine ring and N-aryl propionamide. Compound 44, N-(2-(4-(4-fluorobenzyl) piperidin-1-yl) ethyl)-N-(4-methoxy-phenyl) propionamide, showed the highest affinity for σ1 receptor (Ki σ1 = 1.86 nM) and μ receptor (Ki μ = 2.1 nM). It exhibited potent analgesic activity in the formalin test (ED50 = 15.1 ± 1.67 mg/kg) and had equivalent analgesic effects to S1RA (σ1 antagonist) in a CCI model. Therefore, Compound 44, which has mixed σ1/μ receptor profiles, may be a potential candidate for treating neuropathic pain.
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Synthesis and Biological Evaluation of Tryptamines Found in Hallucinogenic Mushrooms: Norbaeocystin, Baeocystin, Norpsilocin, and Aeruginascin
Corresponding author: Alexander M. Sherwood (Usona Institute, Madison, United States)
Journal of Natural Products 2020, Volume 83, Issue 2, Pages 461-467
Published online February 20th, 2020
https://doi.org/10.1021/acs.jnatprod.9b01061
A general synthetic method was developed to access known tryptamine natural products present in psilocybin-producing mushrooms. In vitro and in vivo experiments were then conducted to inform speculations on the psychoactive properties, or lack thereof, of the natural products. In animal models, psychedelic activity by baeocystin alone was not evident using the mouse head twitch response assay, despite its putative dephosphorylated metabolite, norpsilocin, possessing potent agonist activity at the 5-HT2A receptor.
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I know the old adage if you want something done correct do it yourself. It never hurts to ask, though.

If anyone has found articles newer than J Pharmacol Exp Ther. 2012 Nov; 343(2): 413–425. on the subject (cocaine analogues). Eight years is a long time, a few new ones are sure to have come along.
Here are a couple more-recent papers:

2-Substituted 3β-Aryltropane Cocaine Analogs Produce Atypical Effects without Inducing Inward-Facing Dopamine Transporter Conformations

DAT Conformation Does Not Predict the Ability of Atypical Dopamine Uptake Inhibitors to Substitute for Cocaine
 
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