4,4'-diaminoazobenzene : Azobenzene substituted at each of the phenyl 4-positions by an amino group.
ID Source | ID |
---|---|
PubMed CID | 10855 |
CHEMBL ID | 1337483 |
CHEMBL ID | 3186630 |
CHEBI ID | 53616 |
SCHEMBL ID | 16556 |
MeSH ID | M0075633 |
Synonym |
---|
unii-rck8poj999 |
rck8poj999 , |
benzenamine, 4,4'-(1,2-diazenediyl)bis- |
EN300-17405 |
4-[2-(4-aminophenyl)diazen-1-yl]aniline |
4,4'-diaminoazobenzene |
4,4'-(e)-diazene-1,2-diyldianiline |
brn 0745553 |
aniline, 4,4'-azodi- |
einecs 208-690-7 |
ccris 3448 |
4,4'-azobisbenzenamine |
p-diaminoazobenzene |
4-4'-diaminoazobenzene |
benzenamine, 4,4'-azobis- |
nsc 17103 |
smr000343277 |
MLS000517108 |
wln: zr dnunr dz |
nsc-17103 |
nsc17103 |
4,4'-(diaminoazo)benzene |
p-(diaminoazo)benzene |
aniline,4'-azodi- |
azodianiline |
4,4'-azodianiline |
p'-amino-p-aminoazobenzene |
benzenamine,4'-azobis- |
p-azoaniline |
538-41-0 |
4-[(4-aminophenyl)diazenyl]aniline |
CHEBI:53616 , |
4,4'-azobis(benzenamine) |
4,4'-diazenediylbisaniline |
AKOS000120621 |
NCGC00246076-01 |
HMS2666A12 |
dtxcid80399 |
dtxsid2020399 , |
cas-538-41-0 |
tox21_202586 |
NCGC00260673-01 |
AKOS024348849 |
4-[(e)-2-(4-aminophenyl)diazen-1-yl]aniline |
4-(4-aminophenyl)azoaniline |
A829790 |
4-[(4-aminophenyl)diazenyl]phenylamine |
FT-0616998 |
EPITOPE ID:116059 |
p-diaminoazobenzene [mi] |
4,4-azodianiline |
4-(4-aminophenylazo)-phenylamine |
KQIKKETXZQDHGE-UHFFFAOYSA-N |
SCHEMBL16556 |
sr-01000044610 |
SR-01000044610-1 |
CHEMBL1337483 |
KQIKKETXZQDHGE-FOCLMDBBSA-N |
CHEMBL3186630 |
mfcd00041892 |
4-[(e)-(4-aminophenyl)diazenyl]phenylamine |
diaminoazobenzol |
F1196-0308 |
4-[(e)-(4-aminophenyl)azo]aniline |
Q27124116 |
YSWG109 |
(e)-4,4'-(diazene-1,2-diyl)dianiline |
D78184 |
AS-56804 |
CS-0369377 |
4,4'-diazenediyldianiline |
DTXSID50859469 |
CS-0132346 |
4-[(1e)-2-(4-aminophenyl)diazen-1-yl]aniline |
Z56926520 |
SY062010 |
4,4 inverted exclamation mark -azodianiline |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, TYROSYL-DNA PHOSPHODIESTERASE | Homo sapiens (human) | Potency | 100.0000 | 0.0040 | 23.8416 | 100.0000 | AID485290 |
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 6.0231 | 0.0072 | 15.7588 | 89.3584 | AID1224835; AID588342 |
RAR-related orphan receptor gamma | Mus musculus (house mouse) | Potency | 0.8654 | 0.0060 | 38.0041 | 19,952.5996 | AID1159521; AID1159523 |
ATAD5 protein, partial | Homo sapiens (human) | Potency | 16.3535 | 0.0041 | 10.8903 | 31.5287 | AID504466; AID504467 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 17.7267 | 0.0007 | 14.5928 | 83.7951 | AID1259369; AID1259392 |
Microtubule-associated protein tau | Homo sapiens (human) | Potency | 11.2202 | 0.1800 | 13.5574 | 39.8107 | AID1460 |
AR protein | Homo sapiens (human) | Potency | 13.9703 | 0.0002 | 21.2231 | 8,912.5098 | AID1259243; AID1259247; AID743040; AID743042; AID743054 |
nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 0.8686 | 0.0010 | 22.6508 | 76.6163 | AID1224838; AID1224893 |
retinoic acid nuclear receptor alpha variant 1 | Homo sapiens (human) | Potency | 0.6078 | 0.0030 | 41.6115 | 22,387.1992 | AID1159552; AID1159553; AID1159555 |
estrogen-related nuclear receptor alpha | Homo sapiens (human) | Potency | 8.7293 | 0.0015 | 30.6073 | 15,848.9004 | AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403 |
bromodomain adjacent to zinc finger domain 2B | Homo sapiens (human) | Potency | 79.4328 | 0.7079 | 36.9043 | 89.1251 | AID504333 |
euchromatic histone-lysine N-methyltransferase 2 | Homo sapiens (human) | Potency | 70.7946 | 0.0355 | 20.9770 | 89.1251 | AID504332 |
aryl hydrocarbon receptor | Homo sapiens (human) | Potency | 11.5066 | 0.0007 | 23.0674 | 1,258.9301 | AID743122 |
Histone H2A.x | Cricetulus griseus (Chinese hamster) | Potency | 32.9224 | 0.0391 | 47.5451 | 146.8240 | AID1224845; AID1224896 |
NPC intracellular cholesterol transporter 1 precursor | Homo sapiens (human) | Potency | 0.5012 | 0.0126 | 2.4518 | 25.0177 | AID485313 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 100.0000 | 0.0060 | 26.1688 | 89.1251 | AID540317 |
thyroid hormone receptor beta isoform 2 | Rattus norvegicus (Norway rat) | Potency | 34.3517 | 0.0003 | 23.4451 | 159.6830 | AID743067 |
histone deacetylase 9 isoform 3 | Homo sapiens (human) | Potency | 13.4775 | 0.0376 | 17.0823 | 61.1927 | AID1259364; AID1259388 |
ras-related protein Rab-9A | Homo sapiens (human) | Potency | 0.5623 | 0.0002 | 2.6215 | 31.4954 | AID485297 |
nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 4.6430 | 0.0006 | 27.2152 | 1,122.0200 | AID743202; AID743219 |
peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Homo sapiens (human) | Potency | 39.8107 | 0.4256 | 12.0591 | 28.1838 | AID504891 |
DNA polymerase iota isoform a (long) | Homo sapiens (human) | Potency | 89.1251 | 0.0501 | 27.0736 | 89.1251 | AID588590 |
urokinase-type plasminogen activator precursor | Mus musculus (house mouse) | Potency | 4.4668 | 0.1585 | 5.2879 | 12.5893 | AID540303 |
plasminogen precursor | Mus musculus (house mouse) | Potency | 4.4668 | 0.1585 | 5.2879 | 12.5893 | AID540303 |
urokinase plasminogen activator surface receptor precursor | Mus musculus (house mouse) | Potency | 4.4668 | 0.1585 | 5.2879 | 12.5893 | AID540303 |
nuclear receptor ROR-gamma isoform 1 | Mus musculus (house mouse) | Potency | 3.9811 | 0.0079 | 8.2332 | 1,122.0200 | AID2546 |
lethal(3)malignant brain tumor-like protein 1 isoform I | Homo sapiens (human) | Potency | 28.1838 | 0.0752 | 15.2253 | 39.8107 | AID485360 |
survival motor neuron protein isoform d | Homo sapiens (human) | Potency | 14.1254 | 0.1259 | 12.2344 | 35.4813 | AID1458 |
muscleblind-like protein 1 isoform 1 | Homo sapiens (human) | Potency | 28.1838 | 0.0041 | 9.9625 | 28.1838 | AID2675 |
Guanine nucleotide-binding protein G | Homo sapiens (human) | Potency | 50.1187 | 1.9953 | 25.5327 | 50.1187 | AID624287 |
ATPase family AAA domain-containing protein 5 | Homo sapiens (human) | Potency | 6.3523 | 0.0119 | 17.9420 | 71.5630 | AID651632; AID720516 |
Ataxin-2 | Homo sapiens (human) | Potency | 5.4444 | 0.0119 | 12.2221 | 68.7989 | AID651632 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
rac GTPase-activating protein 1 isoform a | Homo sapiens (human) | IC50 (µMol) | 21.9500 | 7.3900 | 57.8904 | 301.2400 | AID624330 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
G protein activity | Guanine nucleotide-binding protein G | Homo sapiens (human) |
adenylate cyclase activator activity | Guanine nucleotide-binding protein G | Homo sapiens (human) |
protein binding | ATPase family AAA domain-containing protein 5 | Homo sapiens (human) |
ATP binding | ATPase family AAA domain-containing protein 5 | Homo sapiens (human) |
ATP hydrolysis activity | ATPase family AAA domain-containing protein 5 | Homo sapiens (human) |
DNA clamp unloader activity | ATPase family AAA domain-containing protein 5 | Homo sapiens (human) |
DNA binding | ATPase family AAA domain-containing protein 5 | Homo sapiens (human) |
RNA binding | Ataxin-2 | Homo sapiens (human) |
epidermal growth factor receptor binding | Ataxin-2 | Homo sapiens (human) |
protein binding | Ataxin-2 | Homo sapiens (human) |
mRNA binding | Ataxin-2 | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Process | via Protein(s) | Taxonomy |
---|---|---|
plasma membrane | Guanine nucleotide-binding protein G | Homo sapiens (human) |
Elg1 RFC-like complex | ATPase family AAA domain-containing protein 5 | Homo sapiens (human) |
nucleus | ATPase family AAA domain-containing protein 5 | Homo sapiens (human) |
cytoplasm | Ataxin-2 | Homo sapiens (human) |
Golgi apparatus | Ataxin-2 | Homo sapiens (human) |
trans-Golgi network | Ataxin-2 | Homo sapiens (human) |
cytosol | Ataxin-2 | Homo sapiens (human) |
cytoplasmic stress granule | Ataxin-2 | Homo sapiens (human) |
membrane | Ataxin-2 | Homo sapiens (human) |
perinuclear region of cytoplasm | Ataxin-2 | Homo sapiens (human) |
ribonucleoprotein complex | Ataxin-2 | Homo sapiens (human) |
cytoplasmic stress granule | Ataxin-2 | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, 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] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (12.50) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (12.50) | 29.6817 |
2010's | 4 (50.00) | 24.3611 |
2020's | 2 (25.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (19.92) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 8 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |