Günter Lambrecht - Concepedia

Author

Günter Lambrecht

Goethe University Frankfurt

Also Known As

G Lambrecht, Gunter Lambrecht, GüNter Lambrecht, Günter Lambrecht

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

Goethe University Frankfurt University of Bonn Karlsruhe Institute of Technology University Hospital Frankfurt Frankfurt University of Applied Sciences

About

Günter Lambrecht is an author at Goethe University Frankfurt specializing in medicine, pharmacology, and pharmacotherapy.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	38	1.9K
2	Natural Sciences	4	4	155
3	Engineering	2	2	37
4	Social Sciences	2	2	77
5	Health Sciences	1	1	18

Günter Lambrecht

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
PPADS, a novel functionally selective antagonist of P2 purinoceptor-mediated responses Günter Lambrecht, Thomas Friebe, Ulrike Grimm, European Journal of Pharmacology Selective AntagonistMolecular PhysiologySignal TransductionBiochemistryFunctional Selectivity	1992	298
PPADS selectively antagonizes P<sub>2X</sub>‐purinoceptor‐mediated responses in the rabbit urinary bladder Charles H.V. Hoyle, Xuenong Bo, Günter Lambrecht, British Journal of Pharmacology	1993	140
p-fluoro-hexahydro-sila-difenidol: The first M2β-selective muscarinic antagonist Günter Lambrecht, Roland Feifel, Bernhard Forth, European Journal of Pharmacology Molecular PharmacologyMedicineMechanism Of ActionPharmacological AgentNeuropharmacology	1988	129
Selective antagonism by PPADS at P<sub>2X</sub>‐purinoceptors in rabbit isolated blood vessels Charles H.V. Hoyle, Günter Lambrecht, E. Mutschler, British Journal of Pharmacology	1994	117
Structure–activity relationships of analogues of NF449 confirm NF449 as the most potent and selective known P2X1 receptor antagonist Matthias U. Kassack, Kirsten Braun, Matthias Ganso, European Journal of Medicinal Chemistry Molecular PharmacologyDrug TargetBiochemistryMedicineNatural Sciences	2004	106
Affinity profiles of hexahydro-sila-difenidol analogues at muscarinic receptor subtypes Günter Lambrecht, Roland Feifel, Monika Wagner-Röder, European Journal of Pharmacology Molecular PharmacologyAffinity ProfilesBiochemistryFunctional SelectivityMedicine	1989	105
Antagonistic properties of the suramin analogue NF023 at heterologously expressed P2X receptors Florentina Soto, Günter Lambrecht, Peter Nickel, Neuropharmacology BiochemistryMedicineP2x ReceptorsAntagonistic PropertiesMechanism Of Action	1999	99
Vasoconstrictor and vasodilator responses to various agonists in the rat perfused mesenteric arterial bed: selective inhibition by PPADS of contractions mediated via P<sub>2x</sub>‐purinoceptors Ursula Windscheif, Vera Ralevic, Hans G. Bäumert, British Journal of Pharmacology	1994	88
The suramin analogue NF279 is a novel and potent antagonist selective for the P2X1 receptor Jürgen Rettinger, Günther Schmalzing, Susanne Damer, Neuropharmacology Molecular PharmacologyMedicineP2x1 ReceptorMolecular BiologyPharmacological Agent	2000	84
Inhibitory action of PPADS on relaxant responses to adenine nucleotides or electrical field stimulation in guinea‐pig taenia coli and rat duodenum Ursula Windscheif, O. Pfaff, Charles H.V. Hoyle, British Journal of Pharmacology	1995	81

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