Synthesis and evaluation of double-prodrugs against HIV. Conjugation of D4T with 6-benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, emivirine)-type reverse transcriptase inhibitors via the SATE prodrug approach.
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Design, Synthesis, and Antiviral Evaluation of Chimeric Inhibitors of HIV Reverse Transcriptase.[d4U]-spacer-[HI-236] double-drug inhibitors of HIV-1 reverse-transcriptase.C-2-aryl O-substituted HI-236 derivatives as non-nucleoside HIV-1 reverse-transcriptase inhibitors.Design, synthesis, and biological evaluation of novel trifluoromethyl indoles as potent HIV-1 NNRTIs with an improved drug resistance profile.Identification of novel bifunctional HIV-1 reverse transcriptase inhibitors.Virtual Screening for Potential Substances for the Prophylaxis of HIV Infection in Libraries of Commercially Available Organic Compounds
P2860
Synthesis and evaluation of double-prodrugs against HIV. Conjugation of D4T with 6-benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, emivirine)-type reverse transcriptase inhibitors via the SATE prodrug approach.
description
2005 nî lūn-bûn
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2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Synthesis and evaluation of do ...... via the SATE prodrug approach.
@en
type
label
Synthesis and evaluation of do ...... via the SATE prodrug approach.
@en
prefLabel
Synthesis and evaluation of do ...... via the SATE prodrug approach.
@en
P2093
P50
P356
P1476
Synthesis and evaluation of do ...... via the SATE prodrug approach.
@en
P2093
Claus Nielsen
Lene Petersen
Thomas H Hansen
P304
P356
10.1021/JM040845B
P407
P577
2005-02-01T00:00:00Z