Page last updated: 2024-11-07

liensinine

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

Description

liensinine: RN given for (R-(R*,R*))-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID160644
CHEBI ID186021
SCHEMBL ID12807599
MeSH IDM0214144

Synonyms (18)

Synonym
2586-96-1
phenol, 4-[[(1r)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl]methyl]-2-[[(1r)-1,2,3,4-tetrahydro-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-7-isoquinolinyl]oxy]-
liensinine
4-[[(1r)-6,7-dimethoxy-2-methyl-3,4-dihydro-1h-isoquinolin-1-yl]methyl]-2-[[(1r)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1h-isoquinolin-7-yl]oxy]phenol
CHEBI:186021
phenol, 4-((1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)methyl)-2-((1,2,3,4-tetrahydro-1-((4-hydroxyphenyl)methyl)-6-methoxy-2-methyl-7-isoquinolinyl)oxy)-, (r-(r*,r*))-
S9411
AKOS015903080
SCHEMBL12807599
AC-34403
HY-N0484
mfcd03427702
CCG-270234
H10631
CS-0009003
DTXSID80948754
AS-56226
EX-A8013N

Research Excerpts

Overview

Liensinine (LIE) is a bisbenzylisoquinoline-type alkaloid extracted from the seed embryo of Nelumbo nucifera.

ExcerptReferenceRelevance
"Liensinine (LIE) is a bisbenzylisoquinoline-type alkaloid extracted from the seed embryo of Nelumbo nucifera."( Liensinine attenuates inflammation and oxidative stress in spleen tissue in an LPS-induced mouse sepsis model.
Chu, M; Dong, J; Dong, Z; Fan, H; Pan, E; Qiang, J; Shi, J; Tan, X; Wang, H; Wang, Y; Xu, B; Yang, Y; Zhang, X, 2023
)
3.07
"Liensinine (LSN) is a naturally derived bisbenzylisoquinoline alkaloid that is known to exhibit numerous antioxidative and cardiovascular beneficial effects."( Liensinine prevents ischemic injury following myocardial infarction via inhibition of Wnt/β‑catenin signaling activation.
Ma, E; Peng, J; Ren, DN; Shen, F; Wo, D; Wu, C; Zhong, X; Zhu, W, 2023
)
3.07

Effects

ExcerptReferenceRelevance
"Liensinine has been proved to have hypotensive effect."( Liensinine induces gallbladder cancer apoptosis and G2/M arrest by inhibiting ZFX-induced PI3K/AKT pathway.
Bian, R; Gao, Y; Li, Y; Liu, Y; Shen, Y; Song, X; Xu, Y; Zhang, Y, 2019
)
2.68

Pharmacokinetics

The method was successfully applied to a pharmacokinetic study involving intravenous administration of liensinine, isoliensinine and neferine to rats.

ExcerptReferenceRelevance
"A method for the determination of plasma concentration of liensinine with HPLC and pharmacokinetic study of liensinine in rabbits were reported."( [Pharmacokinetics of liensinine in rabbits].
Cai, H; Hu, X; Lou, S; Yin, W; Zhang, X, 1992
)
0.85
" This developed method was applied in the plasma pharmacokinetic study of total bisbenzylisoquinoline alkaloids (TAL) of the lotus flower (Lian Zi Xin) following a single oral and intravenous administration of TAL in rats."( Simultaneous determination of liensinine, isoliensinine and neferine from seed embryo of Nelumbo nucifera Gaertn. in rat plasma by a rapid HPLC method and its application to a pharmacokinetic study.
Bai, Y; Huang, Y; Liu, P; Wang, J; Xiang, J; Zhao, L, 2011
)
0.66
"The method was successfully applied to a pharmacokinetic study involving intravenous administration of liensinine, isoliensinine and neferine to rats."( Simultaneous determination of liensinine, isoliensinine and neferine in rat plasma by UPLC-MS/MS and application of the technique to pharmacokinetic studies.
Bu, T; Chen, D; Chen, ZC; Dong, YY; Ge, RS; Hu, G; Wang, YY; Xu, RA; Yao, WW, 2015
)
0.92
" The method was also successfully applied to the pharmacokinetic study of liensinine in rats."( Quantification of liensinine in rat plasma using ultra-performance liquid chromatography tandem mass spectrometry and its application to a pharmacokinetic study.
Li, HW; Lv, SF; Wang, B; Wang, XH; Zhang, XL, 2015
)
0.98
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
isoquinolinesA class of organic heteropolycyclic compound consisting of isoquinoline and its substitution derivatives.
[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 (51)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (7.84)18.7374
1990's6 (11.76)18.2507
2000's7 (13.73)29.6817
2010's20 (39.22)24.3611
2020's14 (27.45)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 28.35

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index28.35 (24.57)
Research Supply Index3.95 (2.92)
Research Growth Index5.11 (4.65)
Search Engine Demand Index34.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (28.35)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.96%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other50 (98.04%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]