Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones
(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.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/72789704-9db0-48ce-ade8-bcd234927350
- author
- Ellervik, Ulf LU and Magnusson, Göran LU
- organization
- publishing date
- 1994
- 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}}, }