Synthesis of glycoconjugated chlorin p6 cycloimide

Lebedeva, Viktoriya S.; Ruziev, Ramzes D.; Popov, Anton; Sebyakin, Yu. L.; Mironov, A. F.

doi:10.1016/j.mencom.2007.06.008

Cited by 6 publications

(2 citation statements)

References 6 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…(Steiner, et al, 2007) Amphiphilic cyclic disaccharide analogues TOF Two phosphodiester links, four lipophilic chains (Coppola, et al, 2007) TOF Biotinylated glyconanoparticles Reduction with poly(ethyleneglycol), and HAuCl 4 via a photochemical process gives biotinylated gold nanoparticles. (Miyagawa, et al, 2007) bis-(α , β-D-glucopyranosyl)-polyisobutylene To study self-association TOF (Orosz, et al, 2007) 1-Deoxygalactonojirimycinlysine hybrids As potent TOF D-galactosidase inhibitors (Steiner, et al, 2008a) Fused bicyclic thioglycosides of GlcNAc As mycothiol biosynthesis inhibitors TOF (Slättegård, et al, 2007) Galactosecyclohexenephosphonates TOF (3,5-DHB, ATT, To find competitive inhibitors of the trans-sialidase of the pathogen (Busse, et al, 2007) Poly 1,6-dithio-D (Lebedeva, et al, 2007) Synthesis by cross-metathesis reaction TOF Glycoporphyrins (da TOF Glyco nanoribbons Carbohydrate, PEG spacer and β-sheetforming peptide for self assembly (Lim, et al, 2007b) Lactose-conjugated psoralen TOF (CHCA) For preparation of spherical DNA microassemblies (Kim, et al, 2007e) N 4 -β-D-glycoside cytosines (Ali, et al, 2007) Click chemistry to obtain photosensitizers for cancer chemotherapy (Grin, et al, 2008) TOF (DHB) Salacinol analogues…”

Section: R-tof (Dhb)mentioning

confidence: 99%

Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2007–2008

Harvey

2011

Mass Spectrometry Reviews

View full text Add to dashboard Cite

This review is the fifth update of the original review, published in 1999, on the application of MALDI mass spectrometry to the analysis of carbohydrates and glycoconjugates and brings coverage of the literature to the end of 2008. The first section of the review covers fundamental studies, fragmentation of carbohydrate ions, use of derivatives and new software developments for analysis of carbohydrate spectra. Among newer areas of method development are glycan arrays, MALDI imaging and the use of ion mobility spectrometry. The second section of the review discusses applications of MALDI MS to the analysis of different types of carbohydrate. Specific compound classes that are covered include carbohydrate polymers from plants, N- and O-linked glycans from glycoproteins, biopharmaceuticals, glycated proteins, glycolipids, glycosides and various other natural products. There is a short section on the use of MALDI mass spectrometry for the study of enzymes involved in glycan processing and a section on the use of MALDI MS to monitor products of the chemical synthesis of carbohydrates with emphasis on carbohydrate-protein complexes and glycodendrimers. Corresponding analyses by electrospray ionization now appear to outnumber those performed by MALDI and the amount of literature makes a comprehensive review on this technique impractical. However, most of the work relating to sample preparation and glycan synthesis is equally relevant to electrospray and, consequently, those proposing analyses by electrospray should also find material in this review of interest.

show abstract