Page last updated: 2024-11-05

n-methyl-n-nitrosotoluene-p-sulfonamide

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

Description

diazalo: noncarcinogenic cpd involved in transnitrosating activity in rats & human gastric juice [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6628
CHEMBL ID1606452
CHEBI ID143725
SCHEMBL ID105447
MeSH IDM0377082

Synonyms (76)

Synonym
nsc-5290
nsc5290
benzenesulfonamide, n,4-dimethyl-n-nitroso-
toluene-p-sulfonylmethylnitrosamide
p-tolylsulfonyl-methyl-nitrosamid
n-nitroso-n-methyl-p-toluenesulfamide
p-tolylsulfonylmethylnitrosamide
nsc313
methylnitroso-p-toluenesulfonamide
wln: onn1&swr d1
n-nitroso-n-methyl-4-tolylsulfonamide
diazale
nsc-313
benzenesulfonamide,4-dimethyl-n-nitroso-
n-methyl-n-nitroso-p-tolylsulfonylamide
80-11-5
p-toluenesulfonamide, n-methyl-n-nitroso-
n-methyl-n-nitroso-p-toluenesulfonamide
p-tolylsulfonylmethylnitrosamine
diazald
diazald(r), 99%
brn 2214345
n-methyl-n-nitrosotoluene-4-sulphonamide
einecs 201-252-6
nsc 313
p-tolylsulfonyl-methyl-nitrosamid [german]
diazalo
ai3-52479
hsdb 5234
MLS001361349
smr000875348
n,4-dimethyl-n-nitrosobenzenesulfonamide
CHEBI:143725
n,4-dimethyl-n-nitroso-benzenesulfonamide
A839839
NCGC00247025-01
AKOS005720984
T0323
p-toluenesulfonyl-n-methyl-n-nitrosamide
HMS2230C22
STL146734
4-11-00-00478 (beilstein handbook reference)
unii-k3089966la
n-nitroso-n-methyl-4-toluenesulfonamide
k3089966la ,
FT-0631355
AB00201
p-tolylsulfonylmethylnitrosamide [mi]
p-tolylsulfonylmethylnitrosamide [hsdb]
methyl-n-nitroso-p-toluenesulfonamide, n-
102832-11-1
HMS3369J17
n-methyl-n-nitrosotoluene-p-sulphonamide
n-methyl-n-nitroso-p-toluenesul-fonamide
n-methyl n-nitroso-p-toluenesulfonamide
n-methyl-n-nitroso-p-toluene sulfonamide
n-methyl-n-nitroso-4-toluenesulfonamide
n-methyl-n-nitroso-p-toluenesulphonamide
SCHEMBL105447
DTXSID8058827
W-104248
CHEMBL1606452
n-nitroso-n-methyl-p-toluenesulfonamide
n-methyl-n-nitrosotoluene-4-sulfonamide
p-tolylsulfonylmethylnitrosoamide
n-methyl-n-nitroso, p-toluene sulfonamide
n,4-dimethyl-n'-oxobenzenesulfonohydrazide #
diazogen
n-methyl-n-nitroso-p-toluenesulfonamide, purum, >=98.0% (hplc)
n,4-dimethyl-n'-oxobenzene-1-sulfonohydrazide
AS-64766
n-methyl-n-nitrosotoluene-4-sulphonamide (ntols)
Q20650189
AMY41341
n-methyl-n-nitroso-p-toluensulfonamide
diazald(r)-n-methyl-13c
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
sulfonamideAn amide of a sulfonic acid RS(=O)2NR'2.
[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 (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency23.93410.007215.758889.3584AID588342
thioredoxin glutathione reductaseSchistosoma mansoniPotency50.11870.100022.9075100.0000AID485364
67.9K proteinVaccinia virusPotency28.18380.00018.4406100.0000AID720580
chromobox protein homolog 1Homo sapiens (human)Potency63.09570.006026.168889.1251AID540317
nuclear factor erythroid 2-related factor 2 isoform 2Homo sapiens (human)Potency6.51310.00419.984825.9290AID504444
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (13)

Assay IDTitleYearJournalArticle
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.
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.
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.
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.
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID651635Viability Counterscreen for Primary 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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (11.11)18.7374
1990's1 (11.11)18.2507
2000's2 (22.22)29.6817
2010's4 (44.44)24.3611
2020's1 (11.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.59

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 Index12.59 (24.57)
Research Supply Index2.30 (2.92)
Research Growth Index4.90 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.59)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (11.11%)4.05%
Observational0 (0.00%)0.25%
Other8 (88.89%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]