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EnglishIn a recent paper the first selective inhibitors of HSV1 uracil-DNA glycosylase (UDG) acting in the micromolar range have been reported. A 28.5 kDa catalytic fragment of HSV1 UDG has been crystallized in the presence of uracil, and the structure was recently solved. Starting with the optimized model of binding between 6-(4'-n-octylanilino)uracil (octAU) and UDG some new derivatives have been predicted to be active. In vitro studies with the novel synthetized compounds confirm the plausibility of the model and define the structure features for UDG inhibitors.
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| Titolo: | Synthesis and molecular modeling of novel HSV1 uracil-DNA glycosylase inhibitors |
| Autori: | |
| Data di pubblicazione: | 1999 |
| Rivista: | |
| Citazione: | Synthesis and molecular modeling of novel HSV1 uracil-DNA glycosylase inhibitors / MASSIMO PREGNOLATO; D. UBIALI; ANNALISA VERRI; FEDERICO FOCHER; SILVIO SPADARI; HONGMAO SUN; CHENGXIN ZHI; GEORGE E. WRIGHT. - In: NUCLEOSIDES & NUCLEOTIDES. - ISSN 0732-8311. - STAMPA. - 18:4-5(1999), pp. 709-711. |
| Abstract: | In a recent paper the first selective inhibitors of HSV1 uracil-DNA glycosylase (UDG) acting in the micromolar range have been reported. A 28.5 kDa catalytic fragment of HSV1 UDG has been crystallized in the presence of uracil, and the structure was recently solved. Starting with the optimized model of binding between 6-(4'-n-octylanilino)uracil (octAU) and UDG some new derivatives have been predicted to be active. In vitro studies with the novel synthetized compounds confirm the plausibility of the model and define the structure features for UDG inhibitors. |
| Handle: | http://hdl.handle.net/11571/100928 |
| Appare nelle tipologie: | 1.1 Articolo in rivista |
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