TY - JOUR
T1 - Effects of 5′-phosphate derivatives of 2-hexynyl adenosine and 2-phenylethynyl adenosine on responses of human platelets mediated by P2Y receptors
AU - Cristalli, Gloria
AU - Podda, Gian Marco
AU - Costanzi, Stefano
AU - Lambertucci, Catia
AU - Lecchi, Anna
AU - Vittori, Sauro
AU - Volpini, Rosaria
AU - Zighetti, Maddalena L.
AU - Cattaneo, Marco
PY - 2005/4/21
Y1 - 2005/4/21
N2 - Newly synthesized mono-, di-, and triphosphate of 2-alkynyl adenosines showed very different behavior in human platelet P2Y receptor models, according to the different alkynyl chains. In fact, 2-hexynyladenosine di- (5) and triphosphate (7) induced platelet shape change and aggregation and inhibited PGE1-induced increase in platelet cyclic AMP. On the contrary, the corresponding 2-phenylethynyladenosine di- (6) and triphosphate (8) did not induce platelet shape change or aggregation, but inhibited platelet aggregation induced by ADP.
AB - Newly synthesized mono-, di-, and triphosphate of 2-alkynyl adenosines showed very different behavior in human platelet P2Y receptor models, according to the different alkynyl chains. In fact, 2-hexynyladenosine di- (5) and triphosphate (7) induced platelet shape change and aggregation and inhibited PGE1-induced increase in platelet cyclic AMP. On the contrary, the corresponding 2-phenylethynyladenosine di- (6) and triphosphate (8) did not induce platelet shape change or aggregation, but inhibited platelet aggregation induced by ADP.
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U2 - 10.1021/jm0493562
DO - 10.1021/jm0493562
M3 - Article
C2 - 15828813
AN - SCOPUS:17544368426
VL - 48
SP - 2763
EP - 2766
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
SN - 0022-2623
IS - 8
ER -