K. Nilsson

发表

Phenyl ureas of creatinine as mGluR5 antagonists. A structure-activity relationship study of fenobam analogues.

Karolina Nilsson, A. Wallberg, P. Raboisson, 2006, Bioorganic & medicinal chemistry letters.

Transient lower esophageal sphincter relaxations in dogs are inhibited by a metabotropic glutamate receptor 5 antagonist.

L. Blackshaw, J. Jensen, J. Mattsson, 2005, European journal of pharmacology.

Discovery of agonists of cannabinoid receptor 1 with restricted central nervous system penetration aimed for treatment of gastroesophageal reflux disease.

A. Plowright, J. Ulander, J. Jensen, 2013, Journal of medicinal chemistry.

Structure-activity relationship of thiopyrimidines as mGluR5 antagonists.

Karolina Nilsson, David Wensbo, A. Wallberg, 2006, Bioorganic & medicinal chemistry letters.

Different in vitro and in vivo profiles of substituted 3‐aminopropylphosphinate and 3‐aminopropyl(methyl)phosphinate GABAB receptor agonists as inhibitors of transient lower oesophageal sphincter relaxation

L. Blackshaw, J. Jensen, S. Oja, 2012, British journal of pharmacology.

Effects of (2R)‐(3‐amino‐2‐fluoropropyl)sulphinic acid (AFPSiA) on transient lower oesophageal sphincter relaxation in dogs and mechanism of hypothermic effects in mice

J. Jensen, B. Olsson, J. Mattsson, 2005, British journal of pharmacology.

A new series of pyridinyl-alkynes as antagonists of the metabotropic glutamate receptor 5 (mGluR5).

A. Wallberg, David Wensbo, P. Bach, 2006, Bioorganic & medicinal chemistry letters.

Identification and design of a novel series of MGAT2 inhibitors.

Malin Lemurell, Zhong-Qing Yuan, Öjvind Davidsson, 2013, Bioorganic & medicinal chemistry letters.

A Novel Allosteric Activator of Free Fatty Acid 2 Receptor Displays Unique Gi-functional Bias*

Ashley M. Miller, G. Milligan, A. Tobin, 2016, The Journal of Biological Chemistry.

The orphan receptor GPR55 is a novel cannabinoid receptor

S. Hjorth, P. Greasley, T. Drmota, 2007, British journal of pharmacology.

Aminomethyl-2,6-difluorophenols as a novel class of increased lipophilicity GABA(C) receptor antagonists.

R. Silverman, G. Johnston, J. Mattsson, 1999, Bioorganic & Medicinal Chemistry Letters.

Aminomethyl-2,6-difluorophenols as a Novel Class of Increased Lipophilicity GABAc Receptor Antagonists.

R. Silverman, G. Johnston, J. Mattsson, 2000 .

(R)-(3-Amino-2-fluoropropyl) Phosphinic Acid (AZD3355), a Novel GABAB Receptor Agonist, Inhibits Transient Lower Esophageal Sphincter Relaxation through a Peripheral Mode of Action

Jacobson, J. Dent, A. Page, 2009, Journal of Pharmacology and Experimental Therapeutics.

Synthesis and pharmacological evaluation of novel gamma-aminobutyric acid type B (GABAB) receptor agonists as gastroesophageal reflux inhibitors.

Christer Alstermark, Ola Fjellström, Karolina Nilsson, 2008, Journal of medicinal chemistry.

376 AZD3355, a Novel GABAB Receptor Agonist, Inhibits Transient Lower Esophageal Sphincter Relaxations in the Dog

J. Jensen, J. Mattsson, K. Nilsson, 2008 .

W1789 The New Reflux Inhibitor Azd3355 Has a Low Propensity for Inducing Central Side Effects Due to Its Affinity for the GABA Carrier

L. Blackshaw, J. Jensen, J. Mattsson, 2008 .

Recent advances in non-competitive mGlu5 receptor antagonists and their potential therapeutic applications.

Karolina Nilsson, David Wensbo, Louise Edwards, 2005, Current topics in medicinal chemistry.

Structure-activity relationships for the linker in a series of pyridinyl-alkynes that are antagonists of the metabotropic glutamate receptor 5 (mGluR5).

A. Wallberg, David Wensbo, P. Bach, 2006, Bioorganic & medicinal chemistry letters.