Page last updated: 2024-11-08

norbelladine

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

Description

norbelladine: common metabolic intermediate [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

norbelladine : A phenethylamine alkaloid that is tyramine in which one of the amino hydrogens has been replaced by a 3,4-dihydroxybenzyl group.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 CID416247
CHEMBL ID3359303
CHEBI ID80666
SCHEMBL ID5066630

Synonyms (11)

Synonym
NCIOPEN2_004541
norbelladine
4-[[2-(4-hydroxyphenyl)ethylamino]methyl]benzene-1,2-diol
AKOS010487570
CHEBI:80666 ,
4-({[2-(4-hydroxyphenyl)ethyl]amino}methyl)benzene-1,2-diol
SCHEMBL5066630
4-(([2-(4-hydroxyphenyl)ethyl]amino)methyl)-1,2-benzenediol #
YJYUDTAJVLORNV-UHFFFAOYSA-N
CHEMBL3359303
Q27149708

Research Excerpts

Overview

Norbelladine is an amine compound, a precursor for Amaryllidaceae alkaloids. It is found in plants traditionally used for treating a variety of human diseases.

ExcerptReferenceRelevance
"Norbelladine is an amine compound, a precursor for Amaryllidaceae alkaloids (e.g., belladine, crinamine, lycorine, and galanthamine) found in plants traditionally used for treating a variety of human diseases."( Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound.
Park, JB, 2014
)
1.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[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 (4)

ClassDescription
phenethylamine alkaloid
polyphenolMembers of the class of phenols that contain 2 or more benzene rings each of which is substituted by at least one hydroxy group.
secondary amino compoundA compound formally derived from ammonia by replacing two hydrogen atoms by organyl groups.
catecholsAny compound containing an o-diphenol component.
[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]

Pathways (1)

PathwayProteinsCompounds
Amaryllidacea alkaloids biosynthesis225
Amaryllidacea alkaloids biosynthesis236

Bioassays (5)

Assay IDTitleYearJournalArticle
AID1172900Inhibition of COX2 (unknown origin) using arachidonic acid as substrate at 0.25 uM after 10 mins by luminometry2014Bioorganic & medicinal chemistry letters, Dec-01, Volume: 24, Issue:23
Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound.
AID1172902Inhibition of LPS-induced NF-kappaB p65 activation in human THP1 cells preincubated at 10 uM for 15 mins before LPS treatment measured after 16 hrs2014Bioorganic & medicinal chemistry letters, Dec-01, Volume: 24, Issue:23
Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound.
AID1172898Antioxidant activity assessed as superoxide anion radical scavenging activity at 5 to 20 uM by xanthine/xanthine oxidase assay2014Bioorganic & medicinal chemistry letters, Dec-01, Volume: 24, Issue:23
Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound.
AID1172899Inhibition of COX1 (unknown origin) using arachidonic acid as substrate at 0.25 uM after 10 mins by luminometry2014Bioorganic & medicinal chemistry letters, Dec-01, Volume: 24, Issue:23
Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound.
AID1172897Antioxidant activity assessed as DPPH scavenging activity at 5 to 20 uM after 15 mins by UV-visible spectrophotometry2014Bioorganic & medicinal chemistry letters, Dec-01, Volume: 24, Issue:23
Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (40.00)24.3611
2020's3 (60.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 26.46

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 Index26.46 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.92 (4.65)
Search Engine Demand Index26.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (26.46)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]