( en | de | ru )

 

Disambiguation of "Kachler, S."

Author of the publication

copydeleteadd this publication to your clipboard
3HHEMADO--a novel tritiated agonist selective for the human adenosine A3 receptor

, , , , , , and . Eur J Pharmacol, 556 (1-3): 14-8 (February 2007)Klotz, Karl-Norbert Falgner, Nico Kachler, Sonja Lambertucci, Catia Vittori, Sauro Volpini, Rosaria Cristalli, Gloria Research Support, Non-U.S. Gov't Netherlands European journal of pharmacology Eur J Pharmacol. 2007 Feb 5;556(1-3):14-8. Epub 2006 Oct 27..

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

Marco Kachler

Uwe Kächler

Hilde Kachler

Helmut Horst Kachler

Thomas Victor Kachler

 

Other publications of authors with the same name

3HHEMADO--a novel tritiated agonist selective for the human adenosine A3 receptor, , , , , , and . Eur J Pharmacol, 556 (1-3): 14-8 (February 2007)Klotz, Karl-Norbert Falgner, Nico Kachler, Sonja Lambertucci, Catia Vittori, Sauro Volpini, Rosaria Cristalli, Gloria Research Support, Non-U.S. Gov't Netherlands European journal of pharmacology Eur J Pharmacol. 2007 Feb 5;556(1-3):14-8. Epub 2006 Oct 27..2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A3 adenosine receptors, , , , , and . Naunyn Schmiedebergs Arch Pharmacol, 360 (2): 103-8 (August 1999)Klotz, K N Camaioni, E Volpini, R Kachler, S Vittori, S Cristalli, G N0IMH30003/MH/NIMH NIH HHS/United States Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Germany Naunyn-Schmiedeberg's archives of pharmacology Naunyn Schmiedebergs Arch Pharmacol. 1999 Aug;360(2):103-8..Combining selectivity and affinity predictions using an integrated Support Vector Machine (SVM) approach: An alternative tool to discriminate between the human adenosine A(2A) and A(3) receptor pyrazolo-triazolo-pyrimidine antagonists binding sites, , , , , , , , , and 2 other author(s). Bioorg Med Chem, 17 (14): 5259-74 (July 2009)Michielan, Lisa Bolcato, Chiara Federico, Stephanie Cacciari, Barbara Bacilieri, Magdalena Klotz, Karl-Norbert Kachler, Sonja Pastorin, Giorgia Cardin, Riccardo Sperduti, Alessandro Spalluto, Giampiero Moro, Stefano Research Support, Non-U.S. Gov't England Bioorganic & medicinal chemistry Bioorg Med Chem. 2009 Jul 15;17(14):5259-74. Epub 2009 May 21..Synthesis, biological and modeling studies of 1,3-di-n-propyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro 1,2,4-triazolo 3,4-f-purines as adenosine receptor antagonists, , , , , , , and . Farmaco, 60 (8): 643-51 (August 2005)Pastorin, G Bolcato, C Cacciari, B Kachler, S Klotz, K-N Montopoli, C Moro, S Spalluto, G Research Support, Non-U.S. Gov't France Farmaco (Societa chimica italiana : 1989) Farmaco. 2005 Aug;60(8):643-51..Synthesis, biological studies and molecular modeling investigation of 1,3-dimethyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro 1,2,4-triazolo 3,4-f-purines as potential adenosine receptor antagonists, , , , , , , and . Farmaco, 60 (4): 299-306 (April 2005)Pastorin, Giorgia Bolcato, Chiara Cacciari, Barbara Kachler, Sonja Klotz, Karl-Norbert Montopoli, Christian Moro, Stefano Spalluto, Giampiero Research Support, Non-U.S. Gov't Italy Farmaco (Societa chimica italiana : 1989) Farmaco. 2005 Apr;60(4):299-306..9-Ethyladenine derivatives as adenosine receptor antagonists: 2- and 8-substitution results in distinct selectivities, , , , , and . Naunyn Schmiedebergs Arch Pharmacol, 367 (6): 629-34 (June 2003)Klotz, Karl-Norbert Kachler, Sonja Lambertucci, Catia Vittori, Sauro Volpini, Rosaria Cristalli, Gloria Research Support, Non-U.S. Gov't Germany Naunyn-Schmiedeberg's archives of pharmacology Naunyn Schmiedebergs Arch Pharmacol. 2003 Jun;367(6):629-34. Epub 2003 May 7..N6-Cycloalkyl- and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice, , , , , , , , , and 1 other author(s). J Med Chem, 52 (8): 2393-406 (April 2009)Franchetti, Palmarisa Cappellacci, Loredana Vita, Patrizia Petrelli, Riccardo Lavecchia, Antonio Kachler, Sonja Klotz, Karl-Norbert Marabese, Ida Luongo, Livio Maione, Sabatino Grifantini, Mario Research Support, Non-U.S. Gov't United States Journal of medicinal chemistry J Med Chem. 2009 Apr 23;52(8):2393-406..