Synthesis of novel N-1 (allyloxymethyl) analogues of 6-benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, emivirine) with improved activity against HIV-1 and its mutants.
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Molecular docking studies of marine diterpenes as inhibitors of wild-type and mutants HIV-1 reverse transcriptase.N-1 regioselective Michael-type addition of 5-substituted uracils to (2-hydroxyethyl) acrylate.Synthesis of novel 2-(substituted amino)alkylthiopyrimidin-4(3H)-ones as potential antimicrobial agents.Synthesis and anti-HIV-1 activity of new fluoro-HEPT analogues: an investigation on fluoro versus hydroxy substituents.One pot synthesis, antimicrobial and antioxidant activities of fused uracils: pyrimidodiazepines, lumazines, triazolouracil and xanthines.Nucleoside analogues exerting antiviral activity through a non-nucleoside mechanism.
P2860
Synthesis of novel N-1 (allyloxymethyl) analogues of 6-benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, emivirine) with improved activity against HIV-1 and its mutants.
description
2002 nî lūn-bûn
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2002年の論文
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2002年論文
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2002年論文
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2002年論文
@zh-hk
2002年論文
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2002年論文
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2002年论文
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2002年论文
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2002年论文
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name
Synthesis of novel N-1 (allylo ...... against HIV-1 and its mutants.
@en
type
label
Synthesis of novel N-1 (allylo ...... against HIV-1 and its mutants.
@en
prefLabel
Synthesis of novel N-1 (allylo ...... against HIV-1 and its mutants.
@en
P2093
P356
P1476
Synthesis of novel N-1 (allylo ...... against HIV-1 and its mutants.
@en
P2093
Anne Marie Boel
Berit Dahan
Claus Nielsen
Nasser R El-Brollosy
P304
P356
10.1021/JM020949R
P407
P577
2002-12-01T00:00:00Z