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- W2019108739 abstract "Abstract Novel 3′-ureidoadenosine analogues were synthesized from 1,2:5,6-di-O-isopropylidene-D-glucose in order to lead to stronger hydrogen bonding at the A3 adenosine receptor than the corresponding 3′-aminoadenosine derivatives. However, all synthesized 3′-ureidoadenosine analogues have lost their binding affinities to the all subtypes of adenosine receptors, indicating that bulky 3′-urea moiety led to conformational distortion." @default.
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- W2019108739 date "2005-04-01" @default.
- W2019108739 modified "2023-10-15" @default.
- W2019108739 title "SYNTHESIS OF 3′-UREIDOADENOSINE ANALOGUES AND THEIR BINDING AFFINITY TO THE A<sub>3</sub> ADENOSINE RECEPTOR" @default.
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- W2019108739 doi "https://doi.org/10.1081/ncn-200060079" @default.
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