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3-meo-pcp in 1979

In 1979, 3-meo-pcp was integrated keeping in mind the end goal to concentrate the relationship of phencyclidine subordinates with regards to the structure action as a ketamine elective. Amid early research, 3-meo-pcp was just led in vitro utilizing different substances to take in more about the new research concoction that was made utilizing manufactured substances. In 1999, John Q. Beagle scientific expert, composed a report depicting that 3-meo-pcp was fundamentally the same as PCP in power.
Despite the fact that examination has been directed on 3-meo-pcp it is not found in any standard logical reviews, be that as it may, physicist's that have done testing depict this compound for research as being more intense yet reduces the pain relieving impact that is found with ketamine. The greater part of the investigations of these analogs in a similar gathering of psychoactive mixes have been directed in the United Kingdom.

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4-meo-pcp

4-meo-pcp also known as 4-Methoxyphencyclidine was synthesized in 1965 by Parke-Davis and was further studied by John Q. Beagle in 1999. The research chemical is listed as a dissociative anesthetic with a chemical formula of C18H27N0. The IUPAC name for this chemical is 1-[1-(4-methoxyphenyl)cyclohexyl]-piperidine. Research conducted in controlled laboratories shows that 4-meo-pcp is stronger than the parent chemical, pcp.

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3-meo-pcp phencyclidine derivative

In 1979, 3-meo-pcp was synthesized in order to study the relationship of phencyclidine derivatives when it comes to the structure activity as a ketamine alternative. During early research, 3-meo-pcp was only conducted in vitro using various substances to learn more about the new research chemical that was created using synthetic substances. In 1999, John Q. Beagle chemist, wrote a report describing that 3-meo-pcp was very similar to PCP in potency.
Even though research has been conducted on 3-meo-pcp it is not found in any mainstream scientific studies, however, chemist’s that have done testing describe this compound for research as being more potent but does reduce the analgesic effect that is found with ketamine. All of the studies of these analogs in the same group of psychoactive compounds have been conducted in the United Kingdom.

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