Page last updated: 2024-11-08

jujuboside a

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

Cross-References

ID SourceID
PubMed CID51346169
CHEBI ID177582
MeSH IDM0232475

Synonyms (16)

Synonym
CHEBI:177582
jujuboside a
55466-04-1
C17831
AKOS025311230
Q-100636
CS-7861
jujuboside a, >=97% (hplc)
HY-N0659
alpha-l-arabinopyranoside, (3beta,16beta,23r)-16,23:16,30-diepoxy-20-hydroxydammar-24-en-3-yl o-6-deoxy-alpha-l-mannopyranosyl-(1-->2)-o-[o-beta-d-glucopyranosyl-(1-->6)-o-[beta-d-xylopyranosyl-(1-->2)]-beta-d-glucopyranosyl-(1-->3)]-
(3beta,16beta,23r)-16,23:16,30-diepoxy-20-hydroxydammar-24-en-3-yl o-6-deoxy-alpha-l-mannopyranosyl-(1-->2)-o-[o-beta-d-glucopyranosyl-(1-->6)-o-[beta-d-xylopyranosyl-(1-->2)]-beta-d-glucopyranosyl-(1-->3)]-alpha-l-arabinopyranoside
PN3SW9GZ6X
CCG-270655
S9213
DTXSID601317892
EX-A8003C

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" The developed method was successfully applied to the pharmacokinetic study in rats."( An LC-MS/MS method for determination of jujuboside A in rat plasma and its application to pharmacokinetic studies.
He, S; Huang, X; Li, N; Li, Y; Liu, C; Mi, S; Wang, N; Zheng, X; Zhong, Y, 2012
)
0.38

Dosage Studied

ExcerptRelevanceReference
"01 vs control) at a dosage of 80 mg/kg, and the genes MAP/microtubule affinity-regulating kinase3 (Mark3) and retinitis pigmentosa GTPase regulator interacting protein1 (Rpgrip1) were upregulated by JuA in the mouse hippocampus."( Upregulation of Mark3 and Rpgrip1 mRNA expression by jujuboside A in mouse hippocampus.
Wang, C; Xia, Q; Xia, Y; Xiong, T; Yao, DZ; You, ZL, 2007
)
0.34
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
triterpenoidAny terpenoid derived from a triterpene. The term includes compounds in which the C30 skeleton of the parent triterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
[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 (43)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (4.65)18.2507
2000's12 (27.91)29.6817
2010's18 (41.86)24.3611
2020's11 (25.58)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%
Other43 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]