Page last updated: 2024-11-08

lenticin

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

Description

lenticin: found in extracts of lentils [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

hypaphorine : An amino acid betaine obtaine by exhaustive methylation of the alpha-amino group of L-tryptophan with concomitant deprotonation of the carboxy group. [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]

Cross-References

ID SourceID
PubMed CID442106
CHEMBL ID2235164
CHEBI ID5832
SCHEMBL ID1460893
MeSH IDM0041759

Synonyms (30)

Synonym
c14h18n2o2
C09213
hypaphorine
487-58-1
lenticin
(2s)-3-(1h-indol-3-yl)-2-(trimethylazaniumyl)propanoate
SCHEMBL1460893
1h-indole-3-ethanaminium, alpha-carboxy-n,n,n-trimethyl-, inner salt, (s)-
gj3358u63l ,
(+)-hypaphorine
unii-gj3358u63l
tryptophan betaine
l-hypaphorine
hypaforin
lenticine
glyyunnanenine
chebi:5832 ,
CHEMBL2235164
l-tryptophan betaine
n,n,n-trimethyltryptophan betaine
1h-indole-3-ethanaminium, .alpha.-carboxy-n,n,n-trimethyl-, inner salt, (.alpha.s)-
hypaphorine [mi]
hypaphorine, (+)-
(.alpha.s)-.alpha.-carboxy-n,n,n-trimethyl-1h-indole-3-ethanaminium inner salt
tryptophan, trimethylbetaine
(2s)-3-(1h-indol-3-yl)-2-(trimethylammonio)propionate
AKOS030531239
Q27106905
DTXSID70964100
(s)-3-(1h-indol-3-yl)-2-(trimethylammonio)propanoate

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" (Fabaceae), a plant highly toxic for lambs and goats."( Role of hypaphorine in the toxicity of Astragalus lusitanicus.
Abdennebi, el H; Bel-Kassaoui, H; Bodo, B; Charrouf, Z; Jossang, A; Lamnaouer, D, 2008
)
0.35

Pharmacokinetics

ExcerptReferenceRelevance
" The method was applied to a pharmacokinetic study of Abrus cantoniensis Hance in rats."( Simultaneous determination of abrine, hypaphorine, schaftoside and soyasaponin Bb in rat plasma by UPLC-MS/MS and its application to a pharmacokinetic study after oral administration of Abrus cantoniensis Hance extract.
Bu, Q; Huang, B; Li, C; Liu, C; Lu, P; Zhang, C, 2023
)
0.91

Bioavailability

ExcerptReferenceRelevance
" Based on the antibacterial properties of chitosan, the angiogenesis promoting effect of vaccarin (VAC) and the anti-inflammatory effect of hypaphorine (HYP), nanoparticles with high bioavailability were prepared."( Preparation and characterization of vaccarin, hypaphorine and chitosan nanoparticles and their promoting effects on chronic wounds healing.
Cai, W; Du, B; Hou, B; Qi, M; Qiu, L; Sun, H; Wen, Y; Zhu, X, 2022
)
0.72
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
xenobioticA xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
fungal metaboliteAny eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
[role 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]

Drug Classes (3)

ClassDescription
amino-acid betaineAny amino acid-derived zwitterion - such as glycine betaine (N,N,N-trimethylammonioacetate) - in which the ammonium nitrogen carries methyl substituents and bears no hydrogen atoms.
L-tryptophan derivativeA proteinogenic amino acid derivative resulting from reaction of L-tryptophan at the amino group or the carboxy group, or from the replacement of any hydrogen of L-tryptophan by a heteroatom.
indole alkaloidAn alkaloid containing an indole skeleton.
[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 (28)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (10.71)18.7374
1990's1 (3.57)18.2507
2000's11 (39.29)29.6817
2010's6 (21.43)24.3611
2020's7 (25.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.20

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 Index23.20 (24.57)
Research Supply Index3.40 (2.92)
Research Growth Index4.96 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.20)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (3.57%)5.53%
Reviews1 (3.57%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other26 (92.86%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]