Page last updated: 2024-12-06

2-nitro-7-methoxynaphtho(2-1b)furan

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

Description

2-nitro-7-methoxynaphtho(2-1b)furan: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID53424
CHEMBL ID7645
SCHEMBL ID11229865
MeSH IDM0097502

Synonyms (22)

Synonym
75965-74-1
nsc329223
naphtho[2, 7-methoxy-2-nitro-
nsc-329223
r 7000
7-methoxy-2-nitronaphtho(2,1-b)furan
ccris 4520
r7000 ,
nsc 329223
brn 5749492
naphtho(2,1-b)furan, 7-methoxy-2-nitro-
2-nitro-7-methoxynaphtho(2,1-b)furan
2-nitro-7-methoxynaphtho(2-1b)furan
CHEMBL7645 ,
7-methoxy-2-nitro-naphtho[2,1-b]furan
7-methoxy-2-nitronaphtho[2,1-b]furan
bdbm50304341
7-methoxy-2-nitrobenzo[e][1]benzofuran
2-nitro-7-methoxynaphtho[2,1-b]furan
DTXSID80226862
SCHEMBL11229865
2-nitro-7-methoxynaphtho[2,1-b]furan, bcr(r) certified reference material
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Hepatocyte nuclear factor 4-alphaHomo sapiens (human)EC50 (µMol)2.57002.09002.33002.5700AID455458
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (27)

Processvia Protein(s)Taxonomy
positive regulation of transcription by RNA polymerase IIHepatocyte nuclear factor 4-alphaHomo sapiens (human)
regulation of transcription by RNA polymerase IIHepatocyte nuclear factor 4-alphaHomo sapiens (human)
transcription by RNA polymerase IIHepatocyte nuclear factor 4-alphaHomo sapiens (human)
ornithine metabolic processHepatocyte nuclear factor 4-alphaHomo sapiens (human)
lipid metabolic processHepatocyte nuclear factor 4-alphaHomo sapiens (human)
xenobiotic metabolic processHepatocyte nuclear factor 4-alphaHomo sapiens (human)
sex differentiationHepatocyte nuclear factor 4-alphaHomo sapiens (human)
blood coagulationHepatocyte nuclear factor 4-alphaHomo sapiens (human)
negative regulation of cell population proliferationHepatocyte nuclear factor 4-alphaHomo sapiens (human)
response to glucoseHepatocyte nuclear factor 4-alphaHomo sapiens (human)
regulation of gastrulationHepatocyte nuclear factor 4-alphaHomo sapiens (human)
regulation of lipid metabolic processHepatocyte nuclear factor 4-alphaHomo sapiens (human)
signal transduction involved in regulation of gene expressionHepatocyte nuclear factor 4-alphaHomo sapiens (human)
negative regulation of cell growthHepatocyte nuclear factor 4-alphaHomo sapiens (human)
intracellular receptor signaling pathwayHepatocyte nuclear factor 4-alphaHomo sapiens (human)
glucose homeostasisHepatocyte nuclear factor 4-alphaHomo sapiens (human)
cholesterol homeostasisHepatocyte nuclear factor 4-alphaHomo sapiens (human)
regulation of circadian rhythmHepatocyte nuclear factor 4-alphaHomo sapiens (human)
negative regulation of DNA-templated transcriptionHepatocyte nuclear factor 4-alphaHomo sapiens (human)
positive regulation of DNA-templated transcriptionHepatocyte nuclear factor 4-alphaHomo sapiens (human)
positive regulation of transcription by RNA polymerase IIHepatocyte nuclear factor 4-alphaHomo sapiens (human)
rhythmic processHepatocyte nuclear factor 4-alphaHomo sapiens (human)
regulation of insulin secretionHepatocyte nuclear factor 4-alphaHomo sapiens (human)
lipid homeostasisHepatocyte nuclear factor 4-alphaHomo sapiens (human)
phospholipid homeostasisHepatocyte nuclear factor 4-alphaHomo sapiens (human)
triglyceride homeostasisHepatocyte nuclear factor 4-alphaHomo sapiens (human)
anatomical structure developmentHepatocyte nuclear factor 4-alphaHomo sapiens (human)
cell differentiationHepatocyte nuclear factor 4-alphaHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (15)

Processvia Protein(s)Taxonomy
transcription cis-regulatory region bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
DNA-binding transcription factor activity, RNA polymerase II-specificHepatocyte nuclear factor 4-alphaHomo sapiens (human)
DNA-binding transcription activator activity, RNA polymerase II-specificHepatocyte nuclear factor 4-alphaHomo sapiens (human)
DNA bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
chromatin bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
DNA-binding transcription factor activityHepatocyte nuclear factor 4-alphaHomo sapiens (human)
signaling receptor bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
fatty acid bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
protein bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
zinc ion bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
protein homodimerization activityHepatocyte nuclear factor 4-alphaHomo sapiens (human)
RNA polymerase II-specific DNA-binding transcription factor bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
sequence-specific double-stranded DNA bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
RNA polymerase II cis-regulatory region sequence-specific DNA bindingHepatocyte nuclear factor 4-alphaHomo sapiens (human)
nuclear receptor activityHepatocyte nuclear factor 4-alphaHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (4)

Processvia Protein(s)Taxonomy
nucleusHepatocyte nuclear factor 4-alphaHomo sapiens (human)
nucleoplasmHepatocyte nuclear factor 4-alphaHomo sapiens (human)
cytoplasmHepatocyte nuclear factor 4-alphaHomo sapiens (human)
chromatinHepatocyte nuclear factor 4-alphaHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (9)

Assay IDTitleYearJournalArticle
AID455696Cytotoxicity against human HepG2/C3A cells after 48 hrs by MTT assay2009Bioorganic & medicinal chemistry, Oct-01, Volume: 17, Issue:19
Identification of small molecule regulators of the nuclear receptor HNF4alpha based on naphthofuran scaffolds.
AID201366Mutagenicity in Salmonella Typhimurium TA100 was determined1993Journal of medicinal chemistry, Apr-16, Volume: 36, Issue:8
Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis.
AID201368Mutagenicity in Salmonella Typhimurium TA98 was determined1993Journal of medicinal chemistry, Apr-16, Volume: 36, Issue:8
Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis.
AID455697Agonist activity at AF1 deleted human HNF4alpha7 nuclear receptor expressed in human HepG2/C3A cells co-transfected with LexADBD assessed as increase in transcriptional activity after 16 hrs by beta-galactosidase one hybrid assay2009Bioorganic & medicinal chemistry, Oct-01, Volume: 17, Issue:19
Identification of small molecule regulators of the nuclear receptor HNF4alpha based on naphthofuran scaffolds.
AID23231Calculated partition coefficient (clogP)1993Journal of medicinal chemistry, Apr-16, Volume: 36, Issue:8
Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis.
AID70453Genotoxicity (SOSIP) on Escherichia coli PQ37 (SOS induction potential data, as a measure of genotoxicity)1993Journal of medicinal chemistry, Apr-16, Volume: 36, Issue:8
Mechanistic interpretation of the genotoxicity of nitrofurans (antibacterial agents) using quantitative structure-activity relationships and comparative molecular field analysis.
AID455698Agonist activity at human HNF4alpha7 nuclear receptor LBDdetaF expressed in human HepG2/C3A cells co-transfected with LexADBD assessed as increase in transcriptional activity after 16 hrs by beta-galactosidase one hybrid assay2009Bioorganic & medicinal chemistry, Oct-01, Volume: 17, Issue:19
Identification of small molecule regulators of the nuclear receptor HNF4alpha based on naphthofuran scaffolds.
AID455462Agonist activity at human full length HNF4alpha nuclear receptor expressed in human HepG2/C3A cells co-transfected with LexADBD assessed as increase in transcriptional activity at 9.3 uM by beta-galactosidase one hybrid assay relative to control2009Bioorganic & medicinal chemistry, Oct-01, Volume: 17, Issue:19
Identification of small molecule regulators of the nuclear receptor HNF4alpha based on naphthofuran scaffolds.
AID455458Agonist activity at human full length HNF4alpha nuclear receptor expressed in human HepG2/C3A cells co-transfected with LexADBD assessed as increase in transcriptional activity after 16 hrs by beta-galactosidase one hybrid assay2009Bioorganic & medicinal chemistry, Oct-01, Volume: 17, Issue:19
Identification of small molecule regulators of the nuclear receptor HNF4alpha based on naphthofuran scaffolds.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (31)

TimeframeStudies, This Drug (%)All Drugs %
pre-199017 (54.84)18.7374
1990's10 (32.26)18.2507
2000's4 (12.90)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.65

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index10.65 (24.57)
Research Supply Index3.47 (2.92)
Research Growth Index4.12 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.65)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (3.23%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other30 (96.77%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]