[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Pett et al., 2014 - Google Patents

A Convergent Strategy for the Synthesis of Type‐1 Elongated Mucin Cores 1–3 and the Corresponding Glycopeptides

Pett et al., 2014

Document ID
14854610153223117177
Author
Pett C
Westerlind U
Publication year
Publication venue
Chemistry–A European Journal

External Links

Snippet

Mucins are a class of highly O‐glycosylated proteins found on the surface of cells in epithelial tissues. O‐Glycosylation is crucial for the functionality of mucins and changes therein can have severe consequences for an organism. With that in mind, the elucidation of …
Continue reading at chemistry-europe.onlinelibrary.wiley.com (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02—Acyclic radicals, not substituted by cyclic structures
    • C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
    • C07H5/08—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to sulfur, selenium or tellurium
    • C07H5/10—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to sulfur, selenium or tellurium to sulfur
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
    • C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids

Similar Documents

Publication Publication Date Title
Kulkarni et al. “One-pot” protection, glycosylation, and protection–glycosylation strategies of carbohydrates
Sun et al. Pre‐activation‐based one‐pot synthesis of an α‐(2, 3)‐sialylated core‐fucosylated complex type bi‐antennary N‐glycan dodecasaccharide
Tanaka et al. One‐Pot Synthesis of Sialo‐Containing Glycosyl Amino Acids by Use of an N‐Trichloroethoxycarbonyl‐β‐thiophenyl Sialoside
Imamura et al. Extended Applications of Di‐tert‐butylsilylene‐Directed α‐Predominant Galactosylation Compatible with C2‐Participating Groups toward the Assembly of Various Glycosides
Dziadek et al. Biomimetic Synthesis of the Tumor‐Associated (2, 3)‐Sialyl‐T Antigen and Its Incorporation into Glycopeptide Antigens from the Mucins MUC1 and MUC4
Geurtsen et al. Chemoselective glycosylations. 2. Differences in size of anomeric leaving groups can be exploited in chemoselective glycosylations
Karelin et al. Synthesis of oligosaccharides related to cell wall polysaccharides of the fungi Candida and Aspergillus
Denavit et al. Synthetic inhibitors of galectins: Structures and syntheses
Pett et al. A Convergent Strategy for the Synthesis of Type‐1 Elongated Mucin Cores 1–3 and the Corresponding Glycopeptides
Pett et al. A unified strategy for the synthesis of mucin cores 1–4 saccharides and the assembled multivalent glycopeptides
Singh et al. Positional scanning MUC1 glycopeptide library reveals the importance of PDTR epitope glycosylation for lectin binding
Reintjens et al. Synthesis of C‐glycosyl amino acid building blocks suitable for the solid‐phase synthesis of multivalent glycopeptide mimics
Yoshida et al. Synthesis of the Core Oligosaccharides of Lipooligosaccharides from Campylobacter jejuni: A Putative Cause of Guillain–Barré Syndrome
Holm et al. Glycopeptide specificity of helper T cells obtained in mouse models for rheumatoid arthritis
Pokorny et al. Synthesis of 5-O-oligoglucosyl extended α-(2→ 4)-Kdo disaccharides corresponding to inner core fragments of Moraxellaceae lipopolysaccharides
Grube et al. Synthesis of galactosylated glycosylphosphatidylinositol derivatives from trypanosoma brucei
Hsieh et al. Two‐step functionalization of oligosaccharides using glycosyl iodide and trimethylene oxide and its applications to multivalent glycoconjugates
D'Alonzo et al. A semisynthetic approach to new immunoadjuvant candidates: Site‐selective chemical manipulation of Escherichia coli monophosphoryl lipid A
Kuir et al. Aggregation of a tetrasaccharide acceptor observed by NMR: synthesis of pentasaccharide fragments of the LeaLex tumor-associated hexasaccharide antigen
Mong et al. Application of 2‐azido‐2‐deoxythioglycosides for β‐glycoside formation and oligosaccharide synthesis
Chinoy et al. Chemical synthesis of a glycopeptide derived from Skp1 for probing protein specific glycosylation
Ni Cheallaigh et al. Synthesis of building blocks for an iterative approach towards oligomers of the Streptococcus pneumoniae type 1 zwitterionic capsular polysaccharide repeating unit
Kanaya et al. Synthetic studies on glycosphingolipids from protostomia phyla: Synthesis of glycosphingolipids and related carbohydrate moieties from the parasite Schistosoma mansoni
Hendel et al. Convergent preparation of dimLex hexasaccharide analogues
Ozaki et al. Blockwise synthesis of polylactosamine fragments and keratan sulfate oligosaccharides comprised of dimeric Galβ (1→ 4) GlcNAc6Sβ