Authors:
Allender, CJ
Brain, KR
Ballatore, C
Cahard, D
Siddiqui, A
McGuigan, C
Citation: Cj. Allender et al., Separation of individual antiviral nucleotide prodrugs from synthetic mixtures using cross-reactivity of a molecularly imprinted stationary phase, ANALYT CHIM, 435(1), 2001, pp. 107-113
Authors:
McGuigan, C
Bidois, L
Hiouni, A
Ballatore, C
De Clercq, E
Balzarini, J
Citation: C. Mcguigan et al., Phosphoramidate derivatives of stavudine as inhibitors of HIV: unnatural amino acids may substitute for alanine, ANTIVIR CHE, 11(2), 2000, pp. 111-116
Authors:
Siddiqui, AQ
McGuigan, C
Ballatore, C
Wedgwood, O
De Clercq, E
Balzarini, J
Citation: Aq. Siddiqui et al., Simple mono-derivatisation of the aryl moiety of d4A and ddA-based phosphoramidate prodrugs significantly enhances their anti-HIV potency in cell culture., BIOORG MED, 9(17), 1999, pp. 2555-2560
Authors:
Ballatore, C
McGuigan, C
De Clercq, E
Balzarini, J
Citation: C. Ballatore et al., An in situ pig liver esterase assay as a useful predictive tool for the likely in vitro anti viral activity of phosphoramidate pro-drugs., NUCLEOS NUC, 18(4-5), 1999, pp. 967-969
Authors:
Siddiqui, AQ
Ballatore, C
McGuigan, C
De Clercq, E
Balzarini, J
Citation: Aq. Siddiqui et al., The presence of substituents on the aryl moiety of the aryl phosphoramidate derivative of d4T enhances anti-HIV efficacy in cell culture: A structure-activity relationship, J MED CHEM, 42(3), 1999, pp. 393-399
Authors:
Siddiqui, AQ
McGuigan, C
Ballatore, C
Zuccotto, F
Gilbert, IH
De Clercq, E
Balzarini, J
Citation: Aq. Siddiqui et al., Design and synthesis of lipophilic phospharamidate d4T-MP prodrugs expressing high potency against HIV in cell culture: Structural determinants for in vitro activity and QSAR, J MED CHEM, 42(20), 1999, pp. 4122-4128