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

9 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-HT_2A/5-HT_2C receptor profile of novel analogues 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 analogues 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 - 16 nov. 2016

Adgang til dokumentet

10.1021/acschemneuro.6b00265

Citationsformater

@article{ba748a670b364f27b9086408a63b576d,

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

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 analogues 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 analogues 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}",

year = "2016",

month = nov,

day = "16",

doi = "10.1021/acschemneuro.6b00265",

language = "English",

pages = "1--6",

journal = "ACS Chemical Neuroscience",

issn = "1948-7193",

publisher = "American Chemical Society",

}

TY - JOUR

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 - 2016/11/16

Y1 - 2016/11/16

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 analogues 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 analogues 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 analogues 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 analogues 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

SP - 1

EP - 6

JO - ACS Chemical Neuroscience

JF - ACS Chemical Neuroscience

ER -

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

Abstract

Adgang til dokumentet

Fingeraftryk

Citationsformater