JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001197
Submitter
The Noguchi Institute
Reaction ID
R-0000-001203
Regist Date
2012/06/21 16:44:44
REACTANT
MOLECULE ID
JCGG-COM0001299 (Reaction Tree)
Mol
0.27 mmol
MOLECULE ID
JCGG-COM0001277
Reactant Type
(BrC6H4)3NSbCl6
Mol
0.34 + 0.08 mmol
MOLECULE ID
JCGG-COM0001273 (Reaction Tree)
Mol
0.09 mmol
PRODUCT
MOLECULE ID
JCGG-COM0001296 (Reaction Tree)
Yield
71%
REACTION DETAIL
Reaction Time
40 minutes, 12 hours
Reaction Temp
15 degree C, room temp
Solvent
dry MeCN, dry MeCN
Comment
1) 30+(BrC6H4)3NSbCl6, 4, 2) the second addition of (BrC6H4)3NSbCl6
The reaction mixture was protected from light.
COMMENT
Keywords: prostate specific antigen, PSA, N-linked glycan, peptide backbone, antibody, cancer, amino acid, keyhole limpet hemocyanin, KLH
There are two phases in this reaction.
REFERENCE
Reference Id
REF-0000-000061
Issn
Electronic
Doi
10.1021/ja8028137
PubMed ID
18798614
Journal Name
Journal of the American Chemical Society. (2008) 130 (41): 13598-607.
Article Title
Toward a prostate specific antigen-based prostate cancer diagnostic assay: preparation of keyhole limpet hemocyanin-conjugated normal and transformed prostate specific antigen fragments.
Author
Vadim Y, Dudkin; Justin S, Miller; Anna S, Dudkina; Christophe, Antczak; David A, Scheinberg; Samuel J, Danishefsky
Affiliation
Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, New York, New York 10065, USA.
Reference Id
REF-0000-000062
Source
J. AM. CHEM. SOC. 2008, 130, 13598-13607
Doi
10.1021/ja8028137

©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)