Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/1735
Title: Presentation of the β-carboxamidophosphonate arrangement in substrate structures targeting HIV-1 PR
Author(s): Bligh, Annie Sim Wan 
Author(s): Wardle, N. J.
Hudson, H. R.
Matthews, R. W.
Nunn, C.
Vella, C.
Issue Date: 2009
Publisher: Bentham Science
Journal: Letters in Drug Design & Discovery 
Volume: 6
Issue: 2
Start page: 139
End page: 145
Abstract: 
Novel O,O-diethyl 1-benzamido-2,2-biscarbamoylethanephosphonates were synthesised as putative substrates to HIV-1 PR, to exploit the state of activation of the phosphonate electrophilic function in β-carboxamidophosphonate arrangements. O,O-Diethyl 1-benzamido-2,2-bis[(1S)-N-(1-benzyl-2-hydroxyethyl)carbamoyl]ethanephosphonate exhibited moderate anti-HIV activity in vitro (EC50 = 53 μrbamoyl]ethanephosphonate inhibited HIV-1 PR (IC50 = 31 μM).
URI: https://repository.cihe.edu.hk/jspui/handle/cihe/1735
DOI: 10.2174/157018009787582660
CIHE Affiliated Publication: No
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