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Citation: R. Alvarez et al., SYNTHESIS AND ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ACTIVITY OF NOVEL 3'-SPIRO NUCLEOSIDE ANALOGS OF TSAO-T, Antiviral chemistry & chemotherapy, 8(6), 1997, pp. 507-517
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Citation: C. Mcguigan et al., SYNTHESIS AND EVALUATION OF 5-HALO 2',3'-DIDEHYDRO-2',3'-DIDEOXYNUCLEOSIDES AND THEIR BLOCKED PHOSPHORAMIDATES AS POTENTIAL ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS AGENTS - AN EXAMPLE OF KINASE BYPASS, Antiviral chemistry & chemotherapy, 8(6), 1997, pp. 519-527
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Citation: A. Chimirri et al., STRUCTURAL FEATURES AND ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) ACTIVITY OF THE ISOMERS OF IFLUOROPHENYL)-1H,3H-THIAZOLO[3,4-A]BENZIMIDAZOLE, A POTENT NONNUCLEOSIDE HIV-1 REVERSE-TRANSCRIPTASE INHIBITOR, Antiviral chemistry & chemotherapy, 8(4), 1997, pp. 363-370
Citation: J. Balzarini et E. Declercq, THE THIOCARBOXANILIDES UC-10 AND UC-781 HAVE AN ADDITIVE INHIBITORY EFFECT AGAINST HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE AND REPLICATION IN CELL-CULTURE WHEN COMBINED WITH OTHER ANTIRETROVIRAL DRUGS, Antiviral chemistry & chemotherapy, 8(3), 1997, pp. 197-204
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Citation: R. Song et al., ANTI-HIV ACTIVITIES OF ANIONIC METALLOPORPHYRINS AND RELATED-COMPOUNDS, Antiviral chemistry & chemotherapy, 8(2), 1997, pp. 85-97
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Citation: L. Naesens et al., HPMPC (CIDOFOVIR), PMEA (ADEFOVIR) AND RELATED ACYCLIC NUCLEOSIDE PHOSPHONATE ANALOGS - A REVIEW OF THEIR PHARMACOLOGY AND CLINICAL POTENTIAL IN THE TREATMENT OF VIRAL-INFECTIONS, Antiviral chemistry & chemotherapy, 8(1), 1997, pp. 1-23
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Citation: S. Aquaro et al., INHIBITION OF REPLICATION OF HIV IN PRIMARY MONOCYTE MACROPHAGES BY DIFFERENT ANTIVIRAL DRUGS AND COMPARATIVE EFFICACY IN LYMPHOCYTES/, Journal of leukocyte biology, 62(1), 1997, pp. 138-143
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Citation: R. Alvarez et al., NOVEL ANALOGS OF THE ANTI HIV-1 AGENT TSAO-T MODIFIED AT THE 3'-SPIROMOIETY, Nucleosides & nucleotides, 16(7-9), 1997, pp. 1033-1036
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Citation: Ne. Poopeiko et al., SYNTHESIS AND BIOLOGICAL EVALUATION OF 2',3'-DIDEOXY-3'-FLUORORIBOFURANOSYL PURINE NUCLEOSIDES, Nucleosides & nucleotides, 16(7-9), 1997, pp. 1083-1086
Citation: Rla. Devrueh et al., LIPOPHILIC DERIVATIZATION OF THE ANTIVIRAL DRUG 9-(2-PHOSPHONYLMETHOXYETHYL)ADENINE AND ITS INCORPORATION INTO A LACTOSYLATED LIPID CARRIERTO IMPROVE ITS LIVER UPTAKE, Nucleosides & nucleotides, 16(7-9), 1997, pp. 1279-1282
Citation: C. Meier et al., ,3'-DIDEOXY-2',3'-DIDEHYDROYTHYMIDINEMONOPHOSPHATE (CYCLOSAL-D4TMP) -A NEW PRO-NUCLEOTIDE APPROACH, Nucleosides & nucleotides, 16(7-9), 1997, pp. 1303-1306
Citation: M. Lorey et al., LO-SALIGENYL-5-FLUORO-2'-DEOXYURIDINEMONOPHOSPHATE (CYCLOSAL-FDUMP) -A NEW PRODRUG APPROACH FOR FDUMP, Nucleosides & nucleotides, 16(7-9), 1997, pp. 1307-1310
Citation: M. Lorey et al., NEW SYNTHESIS AND ANTITUMOR-ACTIVITY OF CYCLOSAL-DERIVATIVES OF 5-FLUORO-2'-DEOXYURIDINEMONOPHOSPHATE, Nucleosides & nucleotides, 16(5-6), 1997, pp. 789-792
Citation: C. Meier et al., ENYL-3'-AZIDO-2',3'-DIDEOXY-THYMIDINEMONOPHOSPHATE (CYCLOSAL-AZTMP) -A NEW PRO-NUCLEOTIDE APPROACH, Nucleosides & nucleotides, 16(5-6), 1997, pp. 793-796
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Citation: En. Olsufyeva et al., DAUNORUBICIN DERIVATIVES OBTAINED FROM DAUNORUBICIN AND NUCLEOSIDE DIALDEHYDES, Nucleosides & nucleotides, 16(1-2), 1997, pp. 87-95
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Citation: Jm. Blanco et al., SYNTHESIS AND ANTIVIRAL AND CYTOSTATIC ACTIVITIES OF CARBOCYCLIC NUCLEOSIDES INCORPORATING A MODIFIED CYCLOPENTANE RING .1. GUANOSINE ANALOGS, Nucleosides & nucleotides, 16(1-2), 1997, pp. 159-171
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Citation: C. Balo et al., NOVEL CARBOCYCLIC NUCLEOSIDES CONTAINING A CYCLOPENTYL RING - ADENOSINE AND URIDINE ANALOGS, Archiv der pharmazie, 330(8), 1997, pp. 265-267
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Citation: Jr. Dimmock et al., MANNICH-BASES OF PHENOLIC AZOBENZENES POSSESSING CYTOTOXIC ACTIVITY, European journal of medicinal chemistry, 32(7-8), 1997, pp. 583-594
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Citation: C. Mcguigan et al., PHOSPHORAMIDATE DERIVATIVES OF D4T AS INHIBITORS OF HIV - THE EFFECT OF AMINO-ACID VARIATION, Antiviral research, 35(3), 1997, pp. 195-204
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BALESTRA E
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CALIO R
Citation: Cf. Perno et al., RED-BLOOD-CELLS MEDIATED DELIVERY OF 9-(2-PHOSPHONYLMETHOXYETHYL)ADENINE TO PRIMARY MACROPHAGES - EFFICIENCY, METABOLISM AND ACTIVITY AGAINST HUMAN-IMMUNODEFICIENCY-VIRUS OR HERPES-SIMPLEX VIRUS, Antiviral research, 33(3), 1997, pp. 153-164
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Citation: J. Balzarini et al., ANTIRETROVIRAL ACTIVITIES OF ACYCLIC NUCLEOSIDE PHOSPHONATES [9-(2-PHOSPHONYLMETHOXYETHYL)ADENINE, 9-(2-PHOSPHONYLMETHOXYETHYL) GUANINE, (R)-9-(2-PHOSPHONYLMETHOXYPROPYL)ADENINE, AND MDL-74,968] IN CELL-CULTURES AND MURINE SARCOMA VIRUS-INFECTED NEWBORN NMRI MICE, Antimicrobial agents and chemotherapy, 41(3), 1997, pp. 611-616
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Citation: M. Witvrouw et al., SRR-SB3, A DISULFIDE-CONTAINING MACROLIDE THAT INHIBITS A LATE-STAGE OF THE REPLICATIVE CYCLE OF HUMAN-IMMUNODEFICIENCY-VIRUS, Antimicrobial agents and chemotherapy, 41(2), 1997, pp. 262-268