Page last updated: 2024-11-10

ophiopogonin d

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

Description

ophiopogonin D: RN given refers to (1beta,3beta,25R)-isomer; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID46173859
CHEBI ID80883
MeSH IDM0135893

Synonyms (23)

Synonym
41753-55-3
ophiopogonin d
C17042
E0022
diosgenin 3-o-(alpha-l-rhamnopyranosyl-(1-2))(beta-d-xylopyranosyl-(1-3))-beta-d-glucopyranoside
945619-74-9
CHEBI:80883
deacetylophiopogonin c
deacetylophiopogonin c,ojv-v
ophiopogonin d, >=98% (hplc)
ophiopogonind
ojv-vi
AKOS032949041
Q27151383
FS-9595
mfcd09970543
125150-67-6
HY-N0515
CS-0009054
i(2)-d-gulopyranoside, i(2)-d-xylopyranosyl o-6-deoxy-i+/--l-mannopyranosyl-(1->2)-6-deoxy-1-c-[(3i(2),14i(3/4),25r)-3-hydroxyspirost-5-en-1-yl]-
(2s,3r,4r,5r,6s)-2-[(2r,3r,4s,5s,6r)-5-hydroxy-2-[(1s,2s,4s,5'r,6r,7s,8r,9s,12s,13r,14r,16r)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyl-4-[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-y
A859337
DTXSID401317339

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" The pharmacokinetic study of ophiopogonin D in rats was then defined using the method after intravenous dosing (77."( Quantitative determination of ophiopogonin d by liquid chromatography/electrospray ionization mass spectrometry and its pharmacokinetics in rat.
Gu, SH; Hao, HP; Roberts, MS; Shang, LL; Sun, JG; Wang, GJ; Xia, CH; Yan, B; Zheng, CN, 2008
)
0.35

Bioavailability

ExcerptReferenceRelevance
" It suggested that the potential interactions of SMS with CYP 3A drug substrates should be noticed, especially the drugs whose bioavailability depends heavily on intestinal CYP3A."( Effects of Shengmai San on key enzymes involved in hepatic and intestinal drug metabolism in rats.
Chia-Hui Tan, E; Chiang, TY; Lee, IJ; Ueng, YF; Wang, HJ; Wang, YC; Yun, CH, 2021
)
0.62

Dosage Studied

ExcerptRelevanceReference
" The pharmacokinetic study of ophiopogonin D in rats was then defined using the method after intravenous dosing (77."( Quantitative determination of ophiopogonin d by liquid chromatography/electrospray ionization mass spectrometry and its pharmacokinetics in rat.
Gu, SH; Hao, HP; Roberts, MS; Shang, LL; Sun, JG; Wang, GJ; Xia, CH; Yan, B; Zheng, CN, 2008
)
0.35
"Rats were divided into 7 groups and dosed consecutively for 7 days with mono and combined-therapy administrations."( A metabonomic study of cardioprotection of ginsenosides, schizandrin, and ophiopogonin D against acute myocardial infarction in rats.
Jiang, M; Kang, L; Li, Z; Liu, X; Wang, Y; Xu, L; Zhao, X, 2014
)
0.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
steroid saponinAny saponin derived from a hydroxysteroid.
[compound class information is derived from 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]

Research

Studies (38)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (2.63)18.7374
1990's0 (0.00)18.2507
2000's3 (7.89)29.6817
2010's18 (47.37)24.3611
2020's16 (42.11)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 Studies1 (2.63%)4.05%
Observational0 (0.00%)0.25%
Other37 (97.37%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]