Page last updated: 2024-12-05

n,n'-diacetylbenzidine

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

Description

N,N'-diacetylbenzidine: induces glomerular epithelial cell lesions; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID11942
CHEMBL ID1567221
CHEBI ID82308
SCHEMBL ID3818831
MeSH IDM0050393

Synonyms (74)

Synonym
CBDIVE_014211
HMS2587G07
n,n'-diacetylbenzidine
n,4'-biphenylylenebisacetamide
613-35-4
acetamide,n'-[1,1'-biphenyl]-4,4'-diylbis-
acetamide,n'-4,4'-biphenylylenebis-
nsc-4717
diacetylbenzidine
4,4'-diacetamidobiphenyl
benzidine,n'-diacetyl-
4,4'-diacetylaminobiphenyl
wln: 1vmr dr dmv1
nsc4717
n,1'-biphenyl)-4,4'-diylbis-acetamide
4,4'-diacetylbenzidine
4',4'''-biacetanilide
acetamide, n,n'-[1,1'-biphenyl]-4,4'-diylbis-
n,n'-diacetyl benzidine
n-[4'-(acetylamino)-1,1'-biphenyl-4-yl]acetamide
MLS000682798
smr000312155
nsc 12409
brn 2217711
biphenyl, 4,4'-diacetamido-
n,n'-(1,1'-biphenyl)-4,4'-diylbisacetamide
n,n'-4,4'-biphenylylenebisacetamide
benzidine, n,n'-diacetyl-
ai3-08917
ccris 197
nsc 4717
acetamide, n,n'-4,4'-biphenylylenebis-
acetamide, n,n'-(1,1'-biphenyl)-4,4'-diylbis-
n,n'-(1,1'-biphenyl)-4,4'-diylbis-acetamide
hsdb 5078
einecs 210-338-2
n,n'-(1,1'-biphenyl)-4,4'-diylbis-acetamide 4',4'''-biacetanilide
nsc12409
nsc-12409
OPREA1_870996
OPREA1_734946
MAYBRIDGE4_003199
NCGC00176103-01
n,n'-biphenyl-4,4'-diyldiacetamide
STK122403
HMS1530B09
AKOS000495581
n-[4-(4-acetamidophenyl)phenyl]acetamide
C19217
unii-2ee5599gqs
4-13-00-00373 (beilstein handbook reference)
2ee5599gqs ,
FT-0632558
diacetylbenzidine, n,n-
4,4'-diacetylbenzidine [hsdb]
n,n'-diacetylbenzidine [iarc]
CHEBI:82308 ,
CHEMBL1567221
SCHEMBL3818831
n-[4'-(acetylamino)[1,1'-biphenyl]-4-yl]acetamide #
CZVHCFKUXGRABC-UHFFFAOYSA-N
4,4'-diacetylamino-1,1'-biphenyl
n-(4'-acetylamino-biphenyl-4-yl)-acetamide
DTXSID9036854
sr-01000596885
SR-01000596885-1
mfcd00048194
4,4-bis(methoxycarbonyl)-2,2-bipyridine
n,n'-(biphenyl-4,4'-diyl)diacetamide
Q26840865
n,n'-([1,1'-biphenyl]-4,4'-diyl)diacetamide
CS-0362407
n,n'-[1,1'-biphenyl]-4,4'-diylbis-acetamide
n-{4'-acetamido-[1,1'-biphenyl]-4-yl}acetamide

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" A preliminary dose-response test showed that NOHDABZ was the most toxic compound; it caused chemical peritonitis and death in each of 4 animals given 70 mumol/kg body weight/injected."( Carcinogenicity of benzidine, N,N'-diacetylbenzidine, and N-hydroxy-N,N'-diacetylbenzidine for female CD rats.
Garner, CD; Morton, KC; Shirai, T; Wang, CY, 1981
)
0.55
" The nonspecific cytochrome P450 inhibitor SKF-525A (10 microM) exhibited a partial dose-response inhibition (maximum 41% of complete reaction mixture) of N'HA formation, but did not alter NHA formation."( Rat liver cytochrome P450 metabolism of N-acetylbenzidine and N,N'-diacetylbenzidine.
Davis, BB; Lakshmi, VM; Zenser, TV, 1997
)
0.54
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
biphenylsBenzenoid aromatic compounds containing two phenyl or substituted-phenyl groups which are joined together by a single bond.
[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]

Protein Targets (8)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
WRNHomo sapiens (human)Potency39.81070.168331.2583100.0000AID651768
ATAD5 protein, partialHomo sapiens (human)Potency29.08100.004110.890331.5287AID504467
nuclear factor erythroid 2-related factor 2 isoform 2Homo sapiens (human)Potency20.59620.00419.984825.9290AID504444
huntingtin isoform 2Homo sapiens (human)Potency1.99530.000618.41981,122.0200AID1688
DNA polymerase iota isoform a (long)Homo sapiens (human)Potency89.12510.050127.073689.1251AID588590
lethal(3)malignant brain tumor-like protein 1 isoform IHomo sapiens (human)Potency14.12540.075215.225339.8107AID485360
survival motor neuron protein isoform dHomo sapiens (human)Potency15.84890.125912.234435.4813AID1458
DNA dC->dU-editing enzyme APOBEC-3F isoform aHomo sapiens (human)Potency6.30960.025911.239831.6228AID602313
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (15)

Assay IDTitleYearJournalArticle
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (20)

TimeframeStudies, This Drug (%)All Drugs %
pre-199010 (50.00)18.7374
1990's2 (10.00)18.2507
2000's2 (10.00)29.6817
2010's5 (25.00)24.3611
2020's1 (5.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.36

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 Index11.36 (24.57)
Research Supply Index3.14 (2.92)
Research Growth Index4.50 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.36)

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%
Other22 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]