Adenosine receptor agonists: Synthesis and biological evaluation of 1-deaza analogues of adenosine
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: In: Journal of medicinal chemistry (1988) 6, 31, 1179-1183.
- Schlagwort
-
Toxikologie
Arzneimittelentwicklung
Arzneimitteldesign
- Ereignis
-
Veröffentlichung
- (wo)
-
Würzburg
- (wer)
-
Universität Würzburg
- (wann)
-
2011
- Urheber
-
Cristalli, G.
Franchetti, P.
Grifantini, M.
Vittori, S.
Klotz, Karl-Norbert
Lohse, M. J.
- URN
-
urn:nbn:de:bvb:20-opus-60262
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:49 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Cristalli, G.
- Franchetti, P.
- Grifantini, M.
- Vittori, S.
- Klotz, Karl-Norbert
- Lohse, M. J.
- Universität Würzburg
Entstanden
- 2011
Ähnliche Objekte (12)
The glycoprotein nature of A1 adenosine receptors
2-Alkynyl derivatives of adenosine and adenosine-5'-N-ethyluronamides as selective agonists at A2 adenosine receptors
Mechanism of A2 adenosine receptor activation. I. Blockade of A2 adenosine receptors by photoaffinity labeling
Effects of barbiturates on A1 adenosine receptors of rat brain
Regulation von G-Protein-gekoppelten Rezeptoren
Eigenschaften des Insulinrezeptors in isolierten Rattenhepatocyten, Untersuchungen zur Struktur des Rezeptors und zur Internalisierung von Insulin und Rezeptor
Adenosine receptors and singnaling in the kidney
Characterization of the solubilized A1 adenosine receptor from rat brain membranes
Agonist photoaffinity labeling of A1 adenosine receptors: Persistent activation reveals spare receptors
2',3'-Dideoxy-N6-cyclohexyladenosine: an adenosine derivative with antagonist properties at adenosine receptors
Barbiturates are selective antagonists at A1 adenosine receptors
A\(_2B}\) adenosine receptor signaling in MDA-MB-231 breast cancer cells: Mechanism of A\(_2B}\)-mediated reduction of ERK1/2 phosphorylation
The glycoprotein nature of A1 adenosine receptors
2-Alkynyl derivatives of adenosine and adenosine-5'-N-ethyluronamides as selective agonists at A2 adenosine receptors
Mechanism of A2 adenosine receptor activation. I. Blockade of A2 adenosine receptors by photoaffinity labeling
Effects of barbiturates on A1 adenosine receptors of rat brain
Regulation von G-Protein-gekoppelten Rezeptoren
Eigenschaften des Insulinrezeptors in isolierten Rattenhepatocyten, Untersuchungen zur Struktur des Rezeptors und zur Internalisierung von Insulin und Rezeptor
Adenosine receptors and singnaling in the kidney
Characterization of the solubilized A1 adenosine receptor from rat brain membranes
Agonist photoaffinity labeling of A1 adenosine receptors: Persistent activation reveals spare receptors
2',3'-Dideoxy-N6-cyclohexyladenosine: an adenosine derivative with antagonist properties at adenosine receptors
Barbiturates are selective antagonists at A1 adenosine receptors
A\(_2B}\) adenosine receptor signaling in MDA-MB-231 breast cancer cells: Mechanism of A\(_2B}\)-mediated reduction of ERK1/2 phosphorylation
The glycoprotein nature of A1 adenosine receptors
2-Alkynyl derivatives of adenosine and adenosine-5'-N-ethyluronamides as selective agonists at A2 adenosine receptors
Mechanism of A2 adenosine receptor activation. I. Blockade of A2 adenosine receptors by photoaffinity labeling
Effects of barbiturates on A1 adenosine receptors of rat brain
Regulation von G-Protein-gekoppelten Rezeptoren
Eigenschaften des Insulinrezeptors in isolierten Rattenhepatocyten, Untersuchungen zur Struktur des Rezeptors und zur Internalisierung von Insulin und Rezeptor
Adenosine receptors and singnaling in the kidney
Characterization of the solubilized A1 adenosine receptor from rat brain membranes
Agonist photoaffinity labeling of A1 adenosine receptors: Persistent activation reveals spare receptors
2',3'-Dideoxy-N6-cyclohexyladenosine: an adenosine derivative with antagonist properties at adenosine receptors
Barbiturates are selective antagonists at A1 adenosine receptors