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

Ulf Ellervik; Göran Magnusson

doi:10.1016/S0968-0896(00)82077-5

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

Ulf Ellervik, Göran Magnusson

Faculty of Engineering, LTH

Research output: Contribution to journal › Article › peer-review

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.

Original language	English
Pages (from-to)	1261-1266
Journal	Bioorganic and Medicinal Chemistry
Volume	2
Issue number	11
DOIs	https://doi.org/10.1016/S0968-0896(00)82077-5
Publication status	Published - 1994

Subject classification (UKÄ)

Organic Chemistry

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10.1016/S0968-0896(00)82077-5

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title = "Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones",

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. {\textcopyright} 1994.",

author = "Ulf Ellervik and G{\"o}ran Magnusson",

year = "1994",

doi = "10.1016/S0968-0896(00)82077-5",

language = "English",

volume = "2",

pages = "1261--1266",

journal = "Bioorganic and Medicinal Chemistry",

issn = "0968-0896",

publisher = "Elsevier",

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TY - JOUR

T1 - Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones

AU - Ellervik, Ulf

AU - Magnusson, Göran

PY - 1994

Y1 - 1994

N2 - 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.

AB - 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.

U2 - 10.1016/S0968-0896(00)82077-5

DO - 10.1016/S0968-0896(00)82077-5

M3 - Article

SN - 0968-0896

VL - 2

SP - 1261

EP - 1266

JO - Bioorganic and Medicinal Chemistry

JF - Bioorganic and Medicinal Chemistry

IS - 11

ER -

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

Abstract

Subject classification (UKÄ)

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