547740-66-9Relevant articles and documents
New results on the reactivity of 5,6-diamino-4-hydroxy-2-mercaptopyrimidine
Cosimelli, Barbara,Iadanza, Manuela,Spisani, Raffaella,Novellino, Ettore
, p. 883 - 886 (2004)
The reaction of 5,6-diamino-4-hydroxy-2-mercaptopyrimidine with mono- and α,ω-dihalocompounds has been reinvestigated. Alkyl derivatives of 5-amino group, not previously described, have been obtained as reaction products. A comparison with the reactivity of 6-amino-4-hydroxy-2- mercaptopyrimidine has been also performed.
Preliminary finding on a new calcium channel entry blocker chemotype: 5,6-diamino-4-hydroxy-2-mercaptopyrimidine derivatives
Cosimelli, Barbara,Severi, Elda,Novellino, Ettore,Cavaccini, Anna,Cataldi, Mauro,Budriesi, Roberta,Micucci, Matteo,Chiarini, Alberto,Ioan, Pierfranco
scheme or table, p. 5597 - 5601 (2011/10/02)
We report the preliminary in vitro characterization of a series of pyrimidines as a new chemotype that modulates cardiovascular parameters and relaxes ileum smooth muscle according to classical calcium entry blockers. Tested compounds showed an interestin
Syntheses of highly functionalised 6-substituted pteridines.
Guiney, Donie,Gibson, Colin L,Suckling, Colin J
, p. 664 - 675 (2007/10/03)
Methods for the synthesis of polyfunctional 6-substituted pteridines from the corresponding 6-aldehydes are described. Alkene, ester, ketone, amide, cyano, oxime, bromo, methoxy and dihydroxy functional groups have all been introduced principally through