Page last updated: 2024-11-12

akebia saponin d

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

akebia saponin D: isolated from Dipsacus asper; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

akebia saponin D : A triterpenoid saponin that is hederagenin attached to a alpha-L-arabinopyranosyl residue at position 3 via a glycosidic linkage and a 6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl residue at position 28 via an ester linkage. It is the active ingredient found in the traditional Chinese herb Radix Dipsaci. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

FloraRankFlora DefinitionFamilyFamily Definition
Dipsacusgenus[no description available]CaprifoliaceaeA plant family of the order Dipsacales, subclass Asteridae, class Magnoliopsida.[MeSH]

Cross-References

ID SourceID
PubMed CID126956703
MeSH IDM0528041

Synonyms (5)

Synonym
akebia saponin d
S5455
39524-08-8
akebia saponin d, >=98% (hplc)
CCG-270580

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" The validated method was successfully applied to a pharmacokinetic study in rats after oral administration of asperosaponin VI."( Determination of asperosaponin VI in rat plasma by HPLC-ESI-MS and its application to preliminary pharmacokinetic studies.
Ding, L; Hu, YZ; Li, K; Li, P; Liu, EH; Qi, LW; Yang, ZL, 2010
)
0.36
"15-700 ng/mL and was successfully applied to a pilot pharmacokinetic study in beagle dogs."( Determination of asperosaponin VI in dog plasma by high-performance liquid chromatography-tandem mass spectrometry and its application to a pilot pharmacokinetic study.
Ding, L; Du, XL; Qi, XM; Shakya, S; Yang, XL; Yang, ZL; Zhu, H, 2012
)
0.38
" A-VI and M1 concentrations in plasma, bile, urine and feces were determined by established LC-MS/MS to calculate the pharmacokinetic parameters."( [Study on pharmacokinetics of asperosaponin VI and its active metabolite in rats].
Cheng, L; Ding, L; Liu, RJ; Shakya, S; Yang, ZL; Zhu, H, 2013
)
0.39
" Consequently, the validated method could be successfully and precisely applied to the pharmacokinetic study of asperosaponin VI and its metabolites."( Pharmacokinetics study of asperosaponin VI and its metabolites cauloside A, HN saponin F and hederagenin.
Chang, YX; Gao, XM; Han, LF; Huo, Y; Liu, EW; Wang, JL; Wang, L; Wang, T, 2014
)
0.4
" The validated method was successfully applied to the pharmacokinetics (PK) studies of the twenty-one prototypes at pharmacodynamic doses (0."( Simultaneous determination of multiple components in rat plasma and pharmacokinetic studies at a pharmacodynamic dose of Xian-Ling-Gu-Bao capsule by UPLC-MS/MS.
Dai, Y; Dai, ZQ; Gao, MX; Tang, XY; Wu, QC; Xiao, HH; Yao, XS; Yao, ZH; Zeng, JX, 2020
)
0.56

Compound-Compound Interactions

ExcerptReferenceRelevance
" To more comprehensively evaluate the quality of wine-fried Dipsaci Radix, HPLC fingerprint combined with content of asperosaponin VI and AA may be a reasonable and practical approach."( Chromatographic fingerprint combined with content of asperosaponin VI and antioxidant activity for quality evaluation of wine-fried Dipsaci Radix.
Chu, G; Duan, X; Li, Z; Liu, X; Nie, L; Song, L; Wang, S, 2014
)
0.4

Bioavailability

ExcerptReferenceRelevance
" However, the low bioavailability of ASD limited its clinical utility."( Microcrystalline preparation of akebia saponin D for its bioavailability enhancement in rats.
Ding, G; Huang, WZ; Wang, QH; Wang, ZZ; Xiao, W; Yang, XL; Yang, ZL; Zhang, CF, 2015
)
0.42
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (58)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (3.45)29.6817
2010's39 (67.24)24.3611
2020's17 (29.31)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other58 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]