-
1
-
-
0033029686
-
Pharmacokinetics of the Antiviral Agent β-D-2′,3′-Didehydro-2′,3′-Dideoxy-5- Fluorocytidine
-
Li M, Selwyn J H and Junxing S et al, Pharmacokinetics of the Antiviral Agent β-D-2′,3′-Didehydro-2′,3′-Dideoxy-5- Fluorocytidine, ANTIMICROBAGENTSCH, 1999, 43:381-384.
-
(1999)
ANTIMICROBAGENTSCH
, vol.43
, pp. 381-384
-
-
Li, M.1
Selwyn, J.H.2
Junxing, S.3
-
2
-
-
0035160478
-
New developments in anti-HIV chemo therapy
-
Clercq ED, New developments in anti-HIV chemo therapy, Curr Med Chem, 1999, 8:1543-1572.
-
(1999)
Curr Med Chem
, vol.8
, pp. 1543-1572
-
-
Clercq, E.D.1
-
3
-
-
2342531101
-
Antiviral drugs in current clinical use
-
Clercq ED, Antiviral drugs in current clinical use, J Clin Viral, 2004, 30:225-133.
-
(2004)
J Clin Viral
, vol.30
, pp. 225-133
-
-
Clercq, E.D.1
-
4
-
-
33747100570
-
Pharmacology of current and promising nucleosides for the treatment of human immunodeficiency viruses
-
Schinazi RF, Hernandez BI and Hurwitz SJ et al, Pharmacology of current and promising nucleosides for the treatment of human immunodeficiency viruses, RF Antivir Res, 2006, 71:322-334.
-
(2006)
RF Antivir Res
, vol.71
, pp. 322-334
-
-
Schinazi, R.F.1
Hernandez, B.I.2
Hurwitz, S.J.3
-
5
-
-
0026720613
-
A highly stereoselective synthesis of anti-HIV 2′,3′-dideoxy- and 2′,3′-didehydro-2′, 3′-dideoxynucleosides
-
Beach WB, Kim HO and Jeong LK et al, A highly stereoselective synthesis of anti-HIV 2′,3′-dideoxy- and 2′,3′-didehydro-2′, 3′-dideoxynucleosides, J Org Chem, 1992, 57:3887-3897.
-
(1992)
J Org Chem
, vol.57
, pp. 3887-3897
-
-
Beach, W.B.1
Kim, H.O.2
Jeong, L.K.3
-
6
-
-
0344659999
-
Anti-HIV activity, biochemistry, and pharmacokinetics of β-D-2′,3′-didehydro-2′,3′- dideoxy-5-fluorocytidine (D4FC)
-
Geneva, Switzerland, July 3
-
Schinazi R F, Ma L and Shi J et al, Anti-HIV activity, biochemistry, and pharmacokinetics of β-D-2′,3′-didehydro-2′,3′- dideoxy-5-fluorocytidine (D4FC), Paper presented at 12th World AIDS Conference, Geneva, Switzerland, July 3, 1998, 27-28.
-
(1998)
Paper presented at 12th World AIDS Conference
, pp. 27-28
-
-
Schinazi, R.F.1
Ma, L.2
Shi, J.3
-
7
-
-
0032542041
-
Synthesis and compareative evaluation of two antiviral agents: β-L-Fd4C and β-D-Fd4C
-
Chen SH, Lin S and King I et al, Synthesis and compareative evaluation of two antiviral agents: β-L-Fd4C and β-D-Fd4C, Bioorg Med Chem Lett, 1998, 8:3245-3250.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 3245-3250
-
-
Chen, S.H.1
Lin, S.2
King, I.3
-
8
-
-
0025344608
-
Synthesis of 2′,3′-unsaturated and 2′,3′-dideoxy analogs of 6-azapyrimidine nucleosides as potential anti-HIV agents
-
Lin TS, Yang JH and Gao YS, Synthesis of 2′,3′-unsaturated and 2′,3′-dideoxy analogs of 6-azapyrimidine nucleosides as potential anti-HIV agents, Nucleosides & Nucleotides, 1998, 9:97-108.
-
(1998)
Nucleosides & Nucleotides
, vol.9
, pp. 97-108
-
-
Lin, T.S.1
Yang, J.H.2
Gao, Y.S.3
-
9
-
-
51649131112
-
Method for the preparation of 2′,3′-dideoxy and 2′,3′-dideoxy-didehydro nucleoside,
-
US Patent 5,455,339, 26 Oct
-
Chung CK, Method for the preparation of 2′,3′-dideoxy and 2′,3′-dideoxy-didehydro nucleoside, US Patent 5,455,339, 26 Oct. 1992.
-
(1992)
-
-
Chung, C.K.1
-
10
-
-
33747357282
-
Enzymatic synthesis of β-D-2′ 3′-unstaturated-5-fluorocytidine
-
Fu SJ, Zhu LM, Enzymatic synthesis of β-D-2′ 3′-unstaturated-5-fluorocytidine, Biocatal and Biotransform, 2006, 24:253-256.
-
(2006)
Biocatal and Biotransform
, vol.24
, pp. 253-256
-
-
Fu, S.J.1
Zhu, L.M.2
-
11
-
-
0017871516
-
-
Cardinaud R Nucleoside deoxyribosyltransferase from Lactobacillus helveticus. Methods enzymol, 1978, 51:446-455.
-
Cardinaud R Nucleoside deoxyribosyltransferase from Lactobacillus helveticus. Methods enzymol, 1978, 51:446-455.
-
-
-
|