TY - JOUR
T1 - Characterization of a Novel Heteroglucan from the Rhizome of Cnidium officinale Exhibiting High Reticuloendothelial System-Potentiating and Anti-complementary Activities
AU - Tomoda, Masashi
AU - Ōhara, Naoko
AU - Shimizu, Noriko
AU - Gonda, Ryōko
PY - 1994/1/1
Y1 - 1994/1/1
N2 - A novel β-heteroglucan, called cnidirhan SIIA, was isolated from the rhizome of Cnidium officinale Makino. It was homogeneous on electrophoresis and gel chromatography, and its molecular mass was more than 1 x 107. It was composed of D-glucose, D-galactose and L-arabinose in the molar ratio of 85:5:8, in addition to small numbers of 0-acetyl groups. Methylation analysis and nuclear magnetic resonance studies indicated its main structural features composed of β-l,6-linked D-glucopyranosyl residues with both 3,6- and 4,6-branching points. In addition, it has both β-1,4-linked L-arabinopyranosyl and β-1,6-linked D-galactopyranosyl residues. The polysaccharide showed very pronounced reticuloendothelial system-potentiating activity in a carbon clearance test, as well as a marked anti-complementary activity.
AB - A novel β-heteroglucan, called cnidirhan SIIA, was isolated from the rhizome of Cnidium officinale Makino. It was homogeneous on electrophoresis and gel chromatography, and its molecular mass was more than 1 x 107. It was composed of D-glucose, D-galactose and L-arabinose in the molar ratio of 85:5:8, in addition to small numbers of 0-acetyl groups. Methylation analysis and nuclear magnetic resonance studies indicated its main structural features composed of β-l,6-linked D-glucopyranosyl residues with both 3,6- and 4,6-branching points. In addition, it has both β-1,4-linked L-arabinopyranosyl and β-1,6-linked D-galactopyranosyl residues. The polysaccharide showed very pronounced reticuloendothelial system-potentiating activity in a carbon clearance test, as well as a marked anti-complementary activity.
KW - Cnidium officinale
KW - cnidirhan SIIA
KW - heteroglucan
KW - immunological activity
KW - polysaccharide
KW - structure
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U2 - 10.1248/bpb.17.973
DO - 10.1248/bpb.17.973
M3 - Article
C2 - 8000388
AN - SCOPUS:0028065186
SN - 0918-6158
VL - 17
SP - 973
EP - 976
JO - Biological and Pharmaceutical Bulletin
JF - Biological and Pharmaceutical Bulletin
IS - 7
ER -