Page last updated: 2024-12-11

volkensin

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

Description

volkensin: a type 2 ribosome-inactivating protein; 1569-bp ORF (523 amino acid residues) without introns, with an internal linker sequence of 45 bp; from roots of Adenia volkensii Harms (kilyambiti plant); contains two free cysteinyl residues out of 14 derived from the gene sequence [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
Adeniagenus[no description available]PassifloraceaeA plant family of the order Violales, subclass Dilleniidae, class Magnoliopsida that are herbaceous or woody vines, shrubs, and trees, mostly of warm regions. Many have tendrils in leaf axils. Leaves are alternate. Flowers have 3-5 sepals, petals and stamens. Nearly all species have seeds that bear a fleshy appendage called an aril.[MeSH]
Adenia volkensiispecies[no description available]PassifloraceaeA plant family of the order Violales, subclass Dilleniidae, class Magnoliopsida that are herbaceous or woody vines, shrubs, and trees, mostly of warm regions. Many have tendrils in leaf axils. Leaves are alternate. Flowers have 3-5 sepals, petals and stamens. Nearly all species have seeds that bear a fleshy appendage called an aril.[MeSH]

Cross-References

ID SourceID
PubMed CID6438338
CHEMBL ID4872878
MeSH IDM0140931

Synonyms (9)

Synonym
adenia volkesii toxin
volkensin
ribosome-inactivating protein type 2, adenia volkensii
rip protein, a volkensii harms
protein volkensin
volkensin (protein)
volkensin (glycoprotein)
91933-11-8
CHEMBL4872878

Research Excerpts

Overview

Volkensin is a galactose-specific lectin. It is a potent inhibitor of eukaryotic protein synthesis in whole cells as well as in a cell-free system.

ExcerptReferenceRelevance
"Volkensin is a galactose-specific lectin and is a potent inhibitor of eukaryotic protein synthesis in whole cells as well as in a cell-free system (a rabbit reticulocyte lysate)."( Properties of volkensin, a toxic lectin from Adenia volkensii.
Abbondanza, A; Barbieri, L; Brown, AN; Falasca, AI; Olsnes, S; Pihl, A; Sandvig, K; Stirpe, F, 1985
)
1.35

Treatment

Volkensin treatment caused significant losses in Fr1/Fr2 of neocortex in the number of infragranular pyramidal neurones. It also reduced binding to muscarinic cholinergic m1 receptors.

ExcerptReferenceRelevance
"Volkensin treatment caused significant loss of pyramidal neurones which was accompanied by reduced binding to muscarinic cholinergic m1 receptors."( An aspect of Alzheimer neuropathology after suicide transport damage.
Bowen, DM; Chessell, IP; Francis, PT; Heath, PR; Pearson, RC; Procter, AW; Webster, MT, 1994
)
1.01
"Volkensin treatment caused significant losses in Fr1/Fr2 of neocortex in the number of infragranular pyramidal neurones and binding to deep cortical layers of both [3H]pirenzepine (muscarinic cholinergic m1 receptors) and [3H]kainate (kainate sensitive glutamate receptors)."( Localisation of muscarinic (m1) and other neurotransmitter receptors on corticofugal-projecting pyramidal neurones.
Bowen, DM; Chessell, IP; Francis, PT; Pangalos, MN; Pearson, RC, 1993
)
1.01

Toxicity

ExcerptReferenceRelevance
" Thus, the damage observed after in vivo experiments could be partly related to diffusion of toxic substances from early-affected glial cells."( Toxicity of ricin and volkensin, two ribosome-inactivating proteins, to microglia, astrocyte, and neuron cultures.
Battelli, MG; Buonamici, L; Ceccarelli, G; Ciani, E; Contestabile, A; Sparapani, M; Stirpe, F, 1997
)
0.61
" Both RIPs resulted toxic for glial cells in culture by MTT test, killing 50% of microglia, the most sensitive cell type, at concentrations around 10(-14)M."( In vitro and in vivo toxicity of type 2 ribosome-inactivating proteins lanceolin and stenodactylin on glial and neuronal cells.
Battelli, MG; Bolognesi, A; Contestabile, A; D'Alessandro, C; Farini, V; Monti, B; Polazzi, E; Stirpe, F, 2007
)
0.34
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1781219Inhibition of NO production in LPS-stimulated mouse RAW264.7 cells
AID1781220Cytotoxicity against human MCF7-DOX cells measured after 48 hrs by MTT assay
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (43)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (6.98)18.7374
1990's28 (65.12)18.2507
2000's9 (20.93)29.6817
2010's2 (4.65)24.3611
2020's1 (2.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 20.75

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 Index20.75 (24.57)
Research Supply Index3.83 (2.92)
Research Growth Index5.28 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.75)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (4.44%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other43 (95.56%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]