Authors:
Manfredini, S
Baraldi, PG
Durini, E
Porcu, L
Angusti, A
Vertuani, S
Solaroli, N
De Clercq, E
Karlsson, A
Balzarini, J
Citation: S. Manfredini et al., Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitors, BIOORG MED, 11(10), 2001, pp. 1329-1332
Authors:
Dalpiaz, A
Scatturin, A
Menegatti, E
Bortolotti, F
Pavan, B
Biondi, C
Durini, E
Manfredini, S
Citation: A. Dalpiaz et al., Synthesis and study of 5 '-ester prodrugs of N-6-cyclopentgladenosine, a selective A(1) receptor agonist, PHARM RES, 18(4), 2001, pp. 531-536
Authors:
Balzarini, J
Degreve, B
Zhu, CY
Durini, E
Porcu, L
De Clercq, E
Karlsson, A
Manfredini, S
Citation: J. Balzarini et al., 2 '-O-acyl/alkyl-substituted arabinosyl nucleosides as inhibitors of humanmitochondrial thymidine kinase, BIOCH PHARM, 61(6), 2001, pp. 727-732
Authors:
Manfredini, S
Baraldi, PG
Bazzanini, R
Durini, E
Vertuani, S
Pani, A
Marceddu, T
Demontis, F
Vargiu, L
La Colla, P
Citation: S. Manfredini et al., Pyrazole related nucleosides 5. Synthesis and biological activity of 2 '-deoxy-2 ',3 '-dideoxy- and acyclo-analogues of 4-iodo-1-beta-D-ribofuranosyl-3-carboxymethyl pyrazole (IPCAR)., NUCLEOS NUC, 19(4), 2000, pp. 705-722
Authors:
Manfredini, S
Marastoni, M
Tomatis, R
Durini, E
Spisani, S
Pani, A
Marceddu, T
Musiu, C
Marongiu, ME
La Colla, P
Citation: S. Manfredini et al., Peptide T-araC conjugates: Solid-phase synthesis and biological activity of N-4-(acylpeptidyl)-araC, BIO MED CH, 8(3), 2000, pp. 539-547
Authors:
Bazzanini, R
Manfredini, S
Durini, E
Groschel, B
Cinatl, J
Balzarini, J
De Clercq, E
Imbach, JL
Perigaud, C
Gosselin, G
Citation: R. Bazzanini et al., Prodrugs of Ara-CMP and Ara-AMP with a S-acyl-2-thioethyl (SATE) biolabilephosphate protecting group: Synthesis and biological evaluation, NUCLEOS NUC, 18(4-5), 1999, pp. 971-972
Authors:
Manfredini, S
Baraldi, PG
Durini, E
Balzarini, J
De Clercq, E
Karlsson, A
Buzzoni, V
Thelander, L
Citation: S. Manfredini et al., Synthesis, cytostatic activity and inhibition of ribonucleotide reductase by 5 '-phosphoramidates and 5 '-diphosphates, of 2 '-O-allyl-arabinofuranosyl nucleosides, NUCLEOS NUC, 18(4-5), 1999, pp. 1007-1008
Authors:
Manfredini, S
Baraldi, PG
Durini, E
Vertuani, S
Balzarini, J
De Clercq, E
Karlsson, A
Buzzoni, V
Thelander, L
Citation: S. Manfredini et al., 5 '-phosphoramidates and 5 '-diphosphates of 2 '-O-allyl-beta-D-arabinofuranosyluracil, -cytosine, and -adenine: Inhibition of ribonucleotide reductase, J MED CHEM, 42(17), 1999, pp. 3243-3250