Unknown

Dataset Information

0

Synthesis of Sulfo-Sialic Acid Analogues: Potent Neuraminidase Inhibitors in Regards to Anomeric Functionality.


ABSTRACT: The design, synthesis and application of N-acetylneuraminic acid-derived compounds bearing anomeric sulfo functional groups are described. These novel compounds, which we refer to as sulfo-sialic acid analogues, include 2-decarboxy-2-deoxy-2-sulfo-N-acetylneuraminic acid and its 4-deoxy-3,4-dehydrogenated pseudoglycal. While 2-decarboxy-2-deoxy-2-sulfo-N-acetylneuraminic acid contains no further modifications of the 2-deoxy-pyranose ring, it is still a more potent inhibitor of avian-origin H5N1 neuraminidase (NA) and drug-resistant His275Tyr NA as compared to the oxocarbenium ion transition state analogue 2,3-dehydro-2-deoxy-N-acetylneuraminic acid. The sulfo-sialic acid analogues described in this report are also more potent inhibitors of influenza NA (up to 40-fold) and bacterial NA (up to 8.5-fold) relative to the corresponding anomeric phosphonic acids. These results confirm that this novel anomeric sulfo modification offers great potential to improve the potency of next-generation NA inhibitors including covalent inhibitors.

SUBMITTER: Vavricka CJ 

PROVIDER: S-EPMC5557986 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis of Sulfo-Sialic Acid Analogues: Potent Neuraminidase Inhibitors in Regards to Anomeric Functionality.

Vavricka Christopher J CJ   Muto Chiaki C   Hasunuma Tomohisa T   Kimura Yoshinobu Y   Araki Michihiro M   Wu Yan Y   Gao George F GF   Ohrui Hiroshi H   Izumi Minoru M   Kiyota Hiromasa H  

Scientific reports 20170815 1


The design, synthesis and application of N-acetylneuraminic acid-derived compounds bearing anomeric sulfo functional groups are described. These novel compounds, which we refer to as sulfo-sialic acid analogues, include 2-decarboxy-2-deoxy-2-sulfo-N-acetylneuraminic acid and its 4-deoxy-3,4-dehydrogenated pseudoglycal. While 2-decarboxy-2-deoxy-2-sulfo-N-acetylneuraminic acid contains no further modifications of the 2-deoxy-pyranose ring, it is still a more potent inhibitor of avian-origin H5N1  ...[more]

Similar Datasets

| S-EPMC8073777 | biostudies-literature
| S-EPMC6600469 | biostudies-literature
| S-EPMC3818918 | biostudies-literature
| S-EPMC7488290 | biostudies-literature
| S-EPMC9049778 | biostudies-literature
| S-EPMC8895027 | biostudies-literature
| S-EPMC7069248 | biostudies-literature
| S-EPMC3857970 | biostudies-literature
| S-EPMC8060387 | biostudies-literature
| S-EPMC2906235 | biostudies-literature