Abstract
Synthetic lipid A analogs which have two amide-bound and two ester-bound (R)-3-hydroxytetradecanoyl groups at the C-2 and -2' and C-3 and -3' positions of beta(1-6)glucosamine disaccharide mono- or diphosphates showed high activities in most in vitro assays, and the lethality of a diphosphate derivative to galactosamine-treated mice was almost comparable to that of natural lipid A. The pyrogenicity and Shwartzman induction activity of the synthetic analogs, however, were much less than those of natural lipid A.
Dates
Type | When |
---|---|
Created | 5 years, 8 months ago (Jan. 2, 2020, 10:04 p.m.) |
Deposited | 3 years, 6 months ago (March 4, 2022, 5:18 p.m.) |
Indexed | 1 year, 4 months ago (April 27, 2024, 7:50 a.m.) |
Issued | 41 years, 2 months ago (July 1, 1984) |
Published | 41 years, 2 months ago (July 1, 1984) |
Published Print | 41 years, 2 months ago (July 1, 1984) |
@article{Kotani_1984, title={Immunobiologically active lipid A analogs synthesized according to a revised structural model of natural lipid A}, volume={45}, ISSN={1098-5522}, url={http://dx.doi.org/10.1128/iai.45.1.293-296.1984}, DOI={10.1128/iai.45.1.293-296.1984}, number={1}, journal={Infection and Immunity}, publisher={American Society for Microbiology}, author={Kotani, S and Takada, H and Tsujimoto, M and Ogawa, T and Harada, K and Mori, Y and Kawasaki, A and Tanaka, A and Nagao, S and Tanaka, S}, year={1984}, month=jul, pages={293–296} }