Immunobiologically active lipid A analogs synthesized according to a revised structural model of natural lipid A.

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.

journal_name

Infect Immun

journal_title

Infection and immunity

authors

Kotani S,Takada H,Tsujimoto M,Ogawa T,Harada K,Mori Y,Kawasaki A,Tanaka A,Nagao S,Tanaka S

doi

10.1128/IAI.45.1.293-296.1984

subject

Has Abstract,Author List Incomplete

pub_date

1984-07-01 00:00:00

pages

293-6

issue

1

eissn

0019-9567

issn

1098-5522

journal_volume

45

pub_type

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