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Chemical constituents and anti-inflammatory activities of Triplostegia glandulifera
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Chinese Traditional and Herbal Drugs | 2026, 57(8) : 2989 - 2999
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Chinese Traditional and Herbal Drugs | 2026, 57(8): 2989-2999
Chemical constituents and anti-inflammatory activities of Triplostegia glandulifera
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DENG Maoxin, ZHANG Hongchuan, MA Kaiyue, WANG Haiming, ZHANG Ying, SHI Qiongxian, LIU Jing, LI Weijiao, DONG Fawu
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doi: 10.7501/j.issn.0253-2670.2026.08.012
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Objective To systematically investigate the chemical constituents and in vitro anti-inflammatory activities of the dried tuberous roots of Triplostegia glandulifera. Method Compounds were isolated and purified by silica gel, Sephadex LH-20, ODS column chromatography and semi-preparative HPLC. Their structures were identified by physicochemical properties and spectroscopic data. The cytotoxicity and inhibitory effects on nitric oxide (NO) production were evaluated by CCK-8 assay and Griess method, respectively. Results Twenty-four compounds were isolated and identified as 3,4-dimethoxybenzyl alcohol-O-[β-D-apiofuranosyl-(1→6)-β-D-glucopyranoside] (1), sysamarin B (2), primulagenin A (3), oleanolic acid-3-O-[α-L-rhamnopyranosyl-(1→3)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranoside] (4), oleanolic acid-3-O-α-L-arabinopyranoside (5), caffeic acid (6), ethyl caffeate (7), (2'R,3'R)-2',3'-dihydroxy-4'-methoxy caffeoyl butyrate (8), 5-O-[(E)-caffeoyl]-quinic acid (9), methyl 4,5-di-O-caffeoyl quinate (10), eugenyl-O-D-gucopyranoside (11), rel-(2α,3β)-7-O-methylcedrusin (12), (7S,8R)-erythro-7,9,9'-trihydroxy-3,3'-dimethoxy-8-O-4'-neolignan-4-O-D-glucopyranoside (13), (+)-pinoresinol (14), (-)-pinoresinol (15), (+)-syringaresinol-O-D-diglucopyranoside (16), ethyl protocatechuate (17), tangeretin (18), hesperidin (19), (1S,3S)-1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (20), nonialkaloid B (21), strych-novoline (22), 1-(β-D-ribofuranosyl)-1H-1,2,4-triazone (23), and inosine (24). Compounds 2, 4, 5 and 19 showed significant inhibitory activities against NO production. The IC50 values of compounds 4 and 5 were (23.76 ± 1.22) and (23.87 ± 0.23) μmol/L, respectively, which were comparable to that of dexamethasone. Conclusion Compound 1 is a new compound. Compounds 2-5 and 7-24 were isolated from the genus Triplostegia for the first time. Compounds 2, 4, 5 and 19 possess potent in vitro anti-inflammatory activities.
Triplostegia glandulifera Wall. ex DC.  /  anti-inflammatory activity  /  triplostegia phenolic glycoside A  /  oleanolic acid-3-O-α-L-arabinopyranoside  /  ethyl caffeate  /  hesperidin
DENG Maoxin, ZHANG Hongchuan, MA Kaiyue, WANG Haiming, ZHANG Ying, SHI Qiongxian, LIU Jing, LI Weijiao, DONG Fawu. Chemical constituents and anti-inflammatory activities of Triplostegia glandulifera[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (8) : 2989 -2999 . DOI: 10.7501/j.issn.0253-2670.2026.08.012
Year 2026 volume 57 Issue 8
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doi: 10.7501/j.issn.0253-2670.2026.08.012
  • Receive Date:2026-01-07
  • Online Date:2026-09-09
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  • Received:2026-01-07
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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