Page last updated: 2024-12-08

peiminine

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

Description

peiminine: isolated from Fritillaria verticillata; structure given in first source; RN given refers to (3beta,5alpha)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
FritillariagenusA plant genus of the family LILIACEAE. Members of this genus produce imperialine, a steroidal alkaloid which acts at muscarinic receptors.[MeSH]LiliaceaeA monocot family within the order Liliales.[MeSH]

Cross-References

ID SourceID
PubMed CID167691
CHEBI ID5886
SCHEMBL ID5956998
MeSH IDM0136763

Synonyms (31)

Synonym
peiminine
kashmirine
verticinone
3,20-dihydroxycevan-6-one
18059-10-4
raddeanine
fritillarine
cevan-6-one, 3,20-dihydroxy-, (3beta,5alpha)-
3beta,20-dihydroxy-5alpha-cevan-6-one
zhebeinone
qub07u6vtq ,
unii-qub07u6vtq
S9148
AKOS015895686
SCHEMBL5956998
CCG-208360
CS-3732
CHEBI:5886
Q-100214
cevan-6-one, 3,20-dihydroxy-, (3.beta.,5.alpha.)-
imperialine [mi]
osnovanine
HY-N0213
AC-7988
mfcd00210542
peininine ,(s)
DTXSID80939349
Q27106924
verticinone;raddeanine
(1r,2s,6s,9s,10s,11s,14s,15s,18s,20s,23r,24s)-10,20-dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one
P2609

Research Excerpts

Overview

Peiminine is a major biologically active component of Fritillaria thunbergii Miq. It exhibits good anticancer, antiinflammatory, and anti-osteoclast effects.

ExcerptReferenceRelevance
"Peiminine is a major biologically active component of Fritillaria thunbergii Miq that exhibits good anticancer, antiinflammatory, and anti-osteoclast effects. "( Peiminine regulates bone-fat balance by canonical Wnt/β-catenin pathway in an ovariectomized rat model.
Gu, H; Wei, J, 2023
)
3.8
"Peiminine (PMI) is a biologically active component extracted from Fritillaria walujewii Regel."( Peiminine serves as an adriamycin chemosensitizer in gastric cancer by modulating the EGFR/FAK pathway.
Ding, M; Gu, Z; Li, T; Ma, L; Nie, Y; Tang, Q; Wang, Y, 2018
)
2.64
"Peiminine is a compound isolated from Bolbostemma paniculatum (Maxim) Franquet (Cucurbitaceae family), which has demonstrated antitumor activities. "( The effects and mechanism of peiminine-induced apoptosis in human hepatocellular carcinoma HepG2 cells.
Chao, X; Dong, C; Li, H; Tang, Y; Wang, B; Wang, G; Wu, J; Zhao, J, 2019
)
2.25

Pharmacokinetics

Peimine and peiminine were eliminated slowly from male rat plasma. Significant gender-related differences were observed in the pharmacokinetic parameters.

ExcerptReferenceRelevance
" extract, the pharmacokinetic parameters were calculated as well."( [Simultaneous determination of peimine and peiminine in rat plasma by LC-MS/MS and its application in the pharmacokinetic study].
Chen, LH; Liu, HN; Liu, LL; Yi, WJ; Zhao, Y; Zhu, WF, 2010
)
0.62
"A sensitive LC-MS-MS method has been successfully applied to pharmacokinetic study of peimine and peiminine in rat plasma after oral administration of Fritillaria thunbergii Miq."( Comparative pharmacokinetic studies of peimine and peiminine in rat plasma by LC-MS-MS after oral administration of Fritillaria thunbergii Miq. and Fritillaria thunbergii Miq. - Glycyrrhiza uralensis Fisch. couple extract.
Chen, L; Liu, H; Liu, L; Yan, Z; Zhang, H; Zhu, W, 2011
)
0.84
"Compared with female rats, peimine and peiminine were eliminated slowly from male rat plasma, and significant gender-related differences were observed in the pharmacokinetic parameters."( Sex dependent pharmacokinetics, tissue distribution and excretion of peimine and peiminine in rats assessed by liquid chromatography-tandem mass spectrometry.
Chen, LH; Guan, YM; Guan, ZY; Liu, HN; Wang, S; Yi, WJ; Zhang, HM; Zhu, WF, 2013
)
0.89
" The developed method was successfully applied to the pharmacokinetic study of imperialine in rats."( Novel LC-MS/MS method for analyzing imperialine in rat plasma: development, validation, and application to pharmacokinetics.
Gong, T; Lin, Q; Song, X; Sun, X; Zhang, Q; Zhang, Z, 2013
)
0.39
" The analytical method was successfully applied to a pharmacokinetic study of the multi-components after oral administration of Sanjie Zhentong Capsule in rats."( Simultaneous determination of ten bioactive constituents of Sanjie Zhentong Capsule in rat plasma by ultra-high-performance liquid chromatography tandem mass spectrometry and its application to a pharmacokinetic study.
Hu, JH; Huang, W; Li, D; Li, J; Pan, Y; Wang, Y; Wang, ZZ; Xiao, W, 2017
)
0.46

Bioavailability

ExcerptReferenceRelevance
" could decrease C(max) and prolong MRT(0-infinity) and t1/2 of peimine remarkly with the bioavailability of peimine remained practically unchanged."( Comparative pharmacokinetic studies of peimine and peiminine in rat plasma by LC-MS-MS after oral administration of Fritillaria thunbergii Miq. and Fritillaria thunbergii Miq. - Glycyrrhiza uralensis Fisch. couple extract.
Chen, L; Liu, H; Liu, L; Yan, Z; Zhang, H; Zhu, W, 2011
)
0.62
" Oral bioavailability with a dose of 1mg/kg was 31."( Novel LC-MS/MS method for analyzing imperialine in rat plasma: development, validation, and application to pharmacokinetics.
Gong, T; Lin, Q; Song, X; Sun, X; Zhang, Q; Zhang, Z, 2013
)
0.39
" Bitter almond and licorice can reduce the intestinal absorption rate ofpeimine and peiminine."( [Rat intestinal absorption trait of peimine and peiminine in Thunberg fritillary bulb extract].
Chen, LH; Guan, ZY; Liu, HN; Zhang, LH; Zhu, WF, 2013
)
0.87
" The current study was conducted to develop a sustained-release tablet for imperialine both to prolong absorption time and to improve the oral bioavailability of the drug."( A (polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer)-dispersed sustained-release tablet for imperialine to simultaneously prolong the drug release and improve the oral bioavailability.
Deng, L; Fu, Y; Gong, T; Li, J; Lin, Q; Qu, M; Zhang, Z, 2015
)
0.42

Dosage Studied

ExcerptRelevanceReference
"In the present study, male BALB/c mice received an oral dosage of sodium carboxymethylcellulose (CMC-Na) (0."( Synergistic anti-inflammatory effects of peimine, peiminine, and forsythoside a combination on LPS-induced acute lung injury by inhibition of the IL-17-NF-κB/MAPK pathway activation.
Du, H; Gong, G; Liu, C; Ma, Q; Quan, ZS; Wu, Y; Zhen, D, 2022
)
0.97
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
alkaloidAny of the naturally occurring, basic nitrogen compounds (mostly heterocyclic) occurring mostly in the plant kingdom, but also found in bacteria, fungi, and animals. By extension, certain neutral compounds biogenetically related to basic alkaloids are also classed as alkaloids. Amino acids, peptides, proteins, nucleotides, nucleic acids, amino sugars and antibiotics are not normally regarded as alkaloids. Compounds in which the nitrogen is exocyclic (dopamine, mescaline, serotonin, etc.) are usually classed as amines rather than alkaloids.
[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 (65)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (1.54)18.7374
1990's12 (18.46)18.2507
2000's10 (15.38)29.6817
2010's30 (46.15)24.3611
2020's12 (18.46)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 24.85

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 Index24.85 (24.57)
Research Supply Index4.25 (2.92)
Research Growth Index5.76 (4.65)
Search Engine Demand Index26.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (24.85)

All Compounds (24.57)

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%
Other69 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]