Literature DB >> 23727703

Synthesis of 6'-acylamido-6'-deoxy-α-D-galactoglycerolipids.

Chunxia Li1, Yihua Sun, Jun Zhang, Zhimin Zhao, Guangli Yu, Huashi Guan.   

Abstract

Aminoglycoglycerolipid 1a isolated from an algal extract showed activity against the enzyme Myt1 kinase with an IC50 value of 0.12 μg/mL. Its analogues, 6'-acylamido-6'-deoxy-α-D-galactoglycerolipids (2a-g) were synthesized in an efficient way with high stereoselectivity. The key step was to employ a 4-OAc protecting group of the galactosyl donor 14 as a remote neighboring participation group to give the glycoside with high α-anomeric selectivity (α:β=32:1) in the glycosylation. The preliminary bioactivity screening showed that compound 2g exhibited good inhibition against Myt1 kinase.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23727703     DOI: 10.1016/j.carres.2013.02.008

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  5 in total

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Review 3.  Chemistry and Biology of Bioactive Glycolipids of Marine Origin.

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4.  Influence of Configuration at the 4- and 6-Positions on the Conformation and Anomeric Reactivity and Selectivity of 7-Deoxyheptopyranosyl Donors: Discovery of a Highly Equatorially Selective l-glycero-d-gluco-Heptopyranosyl Donor.

Authors:  Kapil Upadhyaya; Rahul S Bagul; David Crich
Journal:  J Org Chem       Date:  2021-08-03       Impact factor: 4.198

Review 5.  Total synthesis and structure-activity relationship of glycoglycerolipids from marine organisms.

Authors:  Jun Zhang; Chunxia Li; Guangli Yu; Huashi Guan
Journal:  Mar Drugs       Date:  2014-06-18       Impact factor: 5.118

  5 in total

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