What is 3-HO-PCE HCL?
3-HO-PCE HCL stands for 3-Hydroxyeticyclidine. This chemical falls into the arylcyclohexylamine class. It is a synthetic dissociative that is relatively new on the research chemical market. It is very similar to 3-HO-PCP in structural nature.
Early research reports have shown that this chemical produces research findings of stimulation, sedation, pain relief, motor control loss, changes in the perception of gravity, tactile disconnection, conceptual thinking, euphoria, disinhibition, time distortion, internal hallucination, and immersion enhancement. 3?HO-PCE is an excellent addition to any lab.
Where to Buy 3-HO-PCE?
Multiplescaners is one of the top3-HO-PCE HCL vendors in the world. We sell extremely high-quality 3-HO-PCE, typically in powder form. However, if you would like a different form, please feel free to contact us, because we often have different forms available.
You must be at least 18 years old to buy it from us, and you must be in full legal compliance with the research chemical laws of your nation. Our chemicals are not designed for human or animal consumption, they are only designed for research experiments.
3-HO-PCE Legality
It is illegal in the United Kingdom. It is unscheduled in most other countries since it is so new. However, it could potentially be considered illegal in nations with strong analogue laws, such as the United States.
3-HO-PCP acts as a high-affinity uncompetitive antagonist of the NMDA receptor via the dizocilpine (MK-801) site (Ki = 30 nM). It has much higher affinity than PCP for this site (Ki = 250 nM, for comparison; 8-fold difference). The drug also has high affinity for the μ-opioid receptor (MOR) (Ki = 39–60 nM) in animal test subjects, the κ-opioid receptor (KOR) (Ki = 140 nM), and the sigma σ1 receptor (Ki = 42 nM; IC50 = 19 nM), whereas it has only low affinity for the δ-opioid receptor (Ki = 2,300 nM).The high affinity of 3-HO-PCP for opioid receptors is unique among arylcyclohexylamines and is in contrast to PCP, which has only very low affinity for the MOR (Ki = 11,000–26,000 nM; 282- to 433-fold difference) and the other opioid receptors (Ki = 4,100 nM for the KOR and 73,000 nM for the DOR).
Although it was hypothesized that 3-HO-PCP might be a metabolite of PCP in humans, there is no evidence that this is the case
Reviews
There are no reviews yet.