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Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2662
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dc.contributor.authorYadav, Rohanen_US
dc.contributor.authorBen Arye, Shani Leviatanen_US
dc.contributor.authorSUBRAMANI, BALAMURUGANen_US
dc.contributor.authorPadler-Karavani, Vereden_US
dc.contributor.authorKIKKERI, RAGHAVENDRAen_US
dc.date.accessioned2019-04-29T10:14:35Z
dc.date.available2019-04-29T10:14:35Z
dc.date.issued2016-09en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, 14(46), 10812-10815.en_US
dc.identifier.issn1477-0520en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2662-
dc.identifier.urihttps://doi.org/10.1039/C6OB01688Jen_US
dc.description.abstractSialic acids (Sias) are important terminal sugars on cell surfaces involved in a wide range of protein–carbohydrate interactions. Hence, agents modulating sias-mediated protein interactions are promising inhibitors or vaccine candidates. Here, we report the synthesis of Neu5Acα(2–6)Gal structural analogs and their binding to a series of siglecs. The results showed distinct binding patterns with conserved siglecs (hCD22 and mCD22) compared to rapid evolving siglecs (Siglecs -3 & -10).en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectScreening of Neu5Ac?en_US
dc.subjectSialic acid microarrayen_US
dc.subjectGlycoproteinsen_US
dc.subjectImmune responsesen_US
dc.subjectTumorigenesisen_US
dc.subject2016en_US
dc.titleScreening of Neu5Acα(2–6)gal isomer preferences of siglecs with a sialic acid microarrayen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic and Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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