5-HT2A/5-HT2C receptor pharmacology and intrinsic clearance of N-benzylphenethylamines modified at the primary site of metabolism

Sebastian Leth-Petersen; Ida Nymann Petersen; Anders A Jensen; Christoffer Bundgaard; Mathias Bæk; Jan Kehler; Jesper L Kristensen

doi:10.1021/acschemneuro.6b00265

5-HT2A/5-HT2C receptor pharmacology and intrinsic clearance of N-benzylphenethylamines modified at the primary site of metabolism

Sebastian Leth-Petersen, Ida Nymann Petersen, Anders A Jensen, Christoffer Bundgaard, Mathias Bæk, Jan Kehler, Jesper L Kristensen

LUKKET: Medicinal Chemistry Research

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

16 Citationer (Scopus)

Abstract

The toxic hallucinogen 25B-NBOMe is very rapidly degraded by human liver microsomes and has low oral bioavailability. Herein we report on the synthesis, microsomal stability and 5-HT2A/5-HT2C receptor profile of novel analogs of 25B-NBOMe modified at the primary site of metabolism. Although microsomal stability could be increased while maintaining potent 5-HT2 receptor agonist properties, all analogs had an intrinsic clearance above 1.3 L/kg/h predictive of high first-pass metabolism.

Originalsprog	Engelsk
Tidsskrift	A C S Chemical Neuroscience
Sider (fra-til)	1-6
Antal sider	6
ISSN	1948-7193
DOI	https://doi.org/10.1021/acschemneuro.6b00265
Status	Udgivet - 26 aug. 2016

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Citationsformater

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abstract = "The toxic hallucinogen 25B-NBOMe is very rapidly degraded by human liver microsomes and has low oral bioavailability. Herein we report on the synthesis, microsomal stability and 5-HT2A/5-HT2C receptor profile of novel analogs of 25B-NBOMe modified at the primary site of metabolism. Although microsomal stability could be increased while maintaining potent 5-HT2 receptor agonist properties, all analogs had an intrinsic clearance above 1.3 L/kg/h predictive of high first-pass metabolism.",

author = "Sebastian Leth-Petersen and Petersen, {Ida Nymann} and Jensen, {Anders A} and Christoffer Bundgaard and Mathias B{\ae}k and Jan Kehler and Kristensen, {Jesper L}",

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T1 - 5-HT2A/5-HT2C receptor pharmacology and intrinsic clearance of N-benzylphenethylamines modified at the primary site of metabolism

AU - Leth-Petersen, Sebastian

AU - Petersen, Ida Nymann

AU - Jensen, Anders A

AU - Bundgaard, Christoffer

AU - Bæk, Mathias

AU - Kehler, Jan

AU - Kristensen, Jesper L

PY - 2016/8/26

Y1 - 2016/8/26

N2 - The toxic hallucinogen 25B-NBOMe is very rapidly degraded by human liver microsomes and has low oral bioavailability. Herein we report on the synthesis, microsomal stability and 5-HT2A/5-HT2C receptor profile of novel analogs of 25B-NBOMe modified at the primary site of metabolism. Although microsomal stability could be increased while maintaining potent 5-HT2 receptor agonist properties, all analogs had an intrinsic clearance above 1.3 L/kg/h predictive of high first-pass metabolism.

AB - The toxic hallucinogen 25B-NBOMe is very rapidly degraded by human liver microsomes and has low oral bioavailability. Herein we report on the synthesis, microsomal stability and 5-HT2A/5-HT2C receptor profile of novel analogs of 25B-NBOMe modified at the primary site of metabolism. Although microsomal stability could be increased while maintaining potent 5-HT2 receptor agonist properties, all analogs had an intrinsic clearance above 1.3 L/kg/h predictive of high first-pass metabolism.

U2 - 10.1021/acschemneuro.6b00265

DO - 10.1021/acschemneuro.6b00265

M3 - Journal article

C2 - 27564969

SN - 1948-7193

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JO - A C S Chemical Neuroscience

JF - A C S Chemical Neuroscience

ER -