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Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones

Ellervik, Ulf LU orcid and Magnusson, Göran LU (1994) In Bioorganic and Medicinal Chemistry 2(11). p.1261-1266
Abstract
The minimum energy conformations of the four sterically reasonable SLex and SLea lactones were calculated using the molecular mechanics force-field MM2(91). The tetrasaccharide lactone involving the 3- and 2-position of the Gal moiety was found to be more stable than the 3,4-lactone both for SLex and SLea. © 1994.
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author
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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Bioorganic and Medicinal Chemistry
volume
2
issue
11
pages
1261 - 1266
publisher
Elsevier
external identifiers
  • scopus:0028542912
ISSN
0968-0896
DOI
10.1016/S0968-0896(00)82077-5
language
English
LU publication?
yes
id
72789704-9db0-48ce-ade8-bcd234927350
date added to LUP
2023-08-10 15:04:09
date last changed
2024-01-05 04:06:26
@article{72789704-9db0-48ce-ade8-bcd234927350,
  abstract     = {{The minimum energy conformations of the four sterically reasonable SLex and SLea lactones were calculated using the molecular mechanics force-field MM2(91). The tetrasaccharide lactone involving the 3- and 2-position of the Gal moiety was found to be more stable than the 3,4-lactone both for SLex and SLea. © 1994.}},
  author       = {{Ellervik, Ulf and Magnusson, Göran}},
  issn         = {{0968-0896}},
  language     = {{eng}},
  number       = {{11}},
  pages        = {{1261--1266}},
  publisher    = {{Elsevier}},
  series       = {{Bioorganic and Medicinal Chemistry}},
  title        = {{Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones}},
  url          = {{http://dx.doi.org/10.1016/S0968-0896(00)82077-5}},
  doi          = {{10.1016/S0968-0896(00)82077-5}},
  volume       = {{2}},
  year         = {{1994}},
}