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Results:
1-14
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Results: 14
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
Vicentini, CB
Manfrini, M
Bianchi, N
Rutigliano, C
Mischiati, C
Gambari, R
Citation: S. Manfredini et al., Pyrazolo-triazoles as light activable DNA cleaving agents, BIO MED CH, 8(9), 2000, pp. 2343-2346
Authors:
Manfredini, S
Lampronti, I
Vertuani, S
Solaroli, N
Recanatini, M
Bryan, D
McKinney, M
Citation: S. Manfredini et al., Design, synthesis and binding at cloned muscarinic receptors of N-[5-(1 '-substituted-acetoxymethyl)-3-oxadiazolyl] and N-[4-(1 '-substituted-acetoxymethyl)-2-dioxolanyl] dialkyl amines, BIO MED CH, 8(7), 2000, pp. 1559-1566
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:
Manfredini, S
Vertuani, S
Manfredi, B
Rossoni, G
Calviello, G
Palozza, P
Citation: S. Manfredini et al., Novel antioxidant agents deriving from molecular combinations of vitamins C and E analogues: 3,4-dihydroxy-5(R)-[2(R,S)-(6-hydroxy-2,5,7,8-tetramethyl-chroman-2(R,S)-yl-methyl)-[1,3]dioxolan-4(S)-yl]-5H-furan-2-one and 3-O-octadecyl derivatives, BIO MED CH, 8(12), 2000, pp. 2791-2801
Authors:
Baraldi, PG
de las Infantas, MJP
Manfredini, S
Romagnoli, R
Citation: Pg. Baraldi et al., A new synthetic approach to pyrazolo[3,4-c]-1,2,5-oxadiazoles, SYNTHESIS-S, (1), 2000, pp. 72-74
Authors:
Parnigotto, PP
Conconi, MT
Bortoletto, C
Manfredini, S
Montesi, F
Schiavon, M
Cancellotti, FM
Citation: Pp. Parnigotto et al., Heterocyclic derivatives of all-trans retinoic acid: in vitro effects on fibroblast/keratinocyte growth and differentiation, and in vivo effects on guinea-pig skin, PHARM TOX, 85(2), 1999, pp. 49-55
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:
Baraldi, PG
Balboni, G
Cacciari, B
Guiotto, A
Manfredini, S
Romagnoli, R
Spalluto, G
Thurston, DE
Howard, PW
Bianchi, N
Rutigliano, C
Mischiati, C
Gambari, R
Citation: Pg. Baraldi et al., Synthesis, in vitro antiproliferative activity, and DNA-binding propertiesof hybrid molecules containing pyrrolo[2,1-c][1,4]benzodiazepine and minor-groove-binding oligopyrrole carriers, J MED CHEM, 42(25), 1999, pp. 5131-5141
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
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