4-(2-thiazolylazo)resorcinol: sensitive indicator for metals [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
ID Source | ID |
---|---|
PubMed CID | 75253 |
CHEMBL ID | 1433124 |
CHEMBL ID | 4296835 |
SCHEMBL ID | 1683188 |
MeSH ID | M0085972 |
Synonym |
---|
1,3-benzenediol, 4-(2-thiazolylazo)- |
4-(2-thiazolylazo) resorcinol |
nsc-298197 |
nsc298197 |
mls000757077 , |
2246-46-0 |
4-(2-thiazolylazo)resorcinol, 97% |
smr000528892 |
4-(2-thiazolylazo)resorcinol |
NCGC00246782-01 |
A816216 |
(4e)-3-hydroxy-4-(thiazol-2-ylhydrazono)cyclohexa-2,5-dien-1-one |
4-(1,3-thiazol-2-yldiazenyl)benzene-1,3-diol |
einecs 218-836-1 |
nsc 298197 |
4-(thiazol-2-ylazo)resorcinol |
HMS2862H16 |
FT-0616562 |
AKOS015903424 |
SCHEMBL1683188 |
4-(thiazol-2-yldiazenyl)benzene-1,3-diol |
CHEMBL1433124 |
SHNIKUXMZFPPCS-VAWYXSNFSA-N |
4-[(e)-1,3-thiazol-2-yldiazenyl]-1,3-benzenediol # |
mfcd00005322 |
AKOS030228182 |
AS-64484 |
4-[(1e)-2-(1,3-thiazol-2-yl)diazen-1-yl]benzene-1,3-diol |
J-014727 |
3-hydroxy-4-(1,3-thiazol-2-ylhydrazono)cyclohexa-2,5-dien-1-one |
(e)-4-(thiazol-2-yldiazenyl)benzene-1,3-diol |
tar [=4-(2-thiazolylazo)resorcinol] [metal indicator and spectrophotometric reagent for transition metals] |
T70594 |
CHEMBL4296835 , |
DTXSID40902377 |
noname_1619 |
96627-60-0 |
DTXSID701307456 |
4-(2'-thiazolylazo)resorcinol |
CAA24646 |
?4-(2-thiazolylazo)resorcinol |
bdbm50568047 |
4-[2-(2-thiazolyl)diazenyl]-1,3-benzenediol |
XM6NV2GYM9 |
1,3-benzenediol, 4-[2-(2-thiazolyl)diazenyl]- |
1,3-benzenediol, 4-(2-thiazolylazo)-, (e)- |
resorcinol, 4-(2-thiazolylazo)- |
4-[(e)-1,3-thiazol-2-yldiazenyl]-1,3-benzenediol |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, TYROSYL-DNA PHOSPHODIESTERASE | Homo sapiens (human) | Potency | 3.1623 | 0.0040 | 23.8416 | 100.0000 | AID485290 |
Chain A, Putative fructose-1,6-bisphosphate aldolase | Giardia intestinalis | Potency | 5.0000 | 0.1409 | 11.1940 | 39.8107 | AID2451 |
Chain A, JmjC domain-containing histone demethylation protein 3A | Homo sapiens (human) | Potency | 35.4813 | 0.6310 | 35.7641 | 100.0000 | AID504339 |
Chain A, 2-oxoglutarate Oxygenase | Homo sapiens (human) | Potency | 8.9125 | 0.1778 | 14.3909 | 39.8107 | AID2147 |
Chain A, Ferritin light chain | Equus caballus (horse) | Potency | 31.6228 | 5.6234 | 17.2929 | 31.6228 | AID485281 |
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 23.9341 | 0.0072 | 15.7588 | 89.3584 | AID588342 |
chaperonin-containing TCP-1 beta subunit homolog | Homo sapiens (human) | Potency | 17.7828 | 3.9811 | 27.7649 | 39.8107 | AID504842 |
phosphopantetheinyl transferase | Bacillus subtilis | Potency | 5.6234 | 0.1413 | 37.9142 | 100.0000 | AID1490 |
ATAD5 protein, partial | Homo sapiens (human) | Potency | 2.5918 | 0.0041 | 10.8903 | 31.5287 | AID504467 |
GLS protein | Homo sapiens (human) | Potency | 12.5893 | 0.3548 | 7.9355 | 39.8107 | AID624170 |
TDP1 protein | Homo sapiens (human) | Potency | 15.4594 | 0.0008 | 11.3822 | 44.6684 | AID686978; AID686979 |
Microtubule-associated protein tau | Homo sapiens (human) | Potency | 3.5481 | 0.1800 | 13.5574 | 39.8107 | AID1460 |
TSHR protein | Homo sapiens (human) | Potency | 75.6863 | 0.3381 | 19.0466 | 37.9330 | AID602292 |
Smad3 | Homo sapiens (human) | Potency | 35.4813 | 0.0052 | 7.8098 | 29.0929 | AID588855 |
apical membrane antigen 1, AMA1 | Plasmodium falciparum 3D7 | Potency | 1.1220 | 0.7079 | 12.1943 | 39.8107 | AID720542 |
nonstructural protein 1 | Influenza A virus (A/WSN/1933(H1N1)) | Potency | 2.2387 | 0.2818 | 9.7212 | 35.4813 | AID2326 |
67.9K protein | Vaccinia virus | Potency | 9.0532 | 0.0001 | 8.4406 | 100.0000 | AID720579; AID720580 |
bromodomain adjacent to zinc finger domain 2B | Homo sapiens (human) | Potency | 25.1189 | 0.7079 | 36.9043 | 89.1251 | AID504333 |
P53 | Homo sapiens (human) | Potency | 17.7828 | 0.0731 | 9.6858 | 31.6228 | AID504706 |
pyruvate kinase | Leishmania mexicana mexicana | Potency | 25.1189 | 0.3981 | 13.7447 | 31.6228 | AID1721; AID1722 |
IDH1 | Homo sapiens (human) | Potency | 9.2000 | 0.0052 | 10.8652 | 35.4813 | AID686970 |
euchromatic histone-lysine N-methyltransferase 2 | Homo sapiens (human) | Potency | 44.6684 | 0.0355 | 20.9770 | 89.1251 | AID504332 |
beta-2 adrenergic receptor | Homo sapiens (human) | Potency | 5.6234 | 0.0058 | 6.0263 | 32.6427 | AID492947 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 56.2341 | 0.0060 | 26.1688 | 89.1251 | AID540317 |
importin subunit beta-1 isoform 1 | Homo sapiens (human) | Potency | 100.0000 | 5.8048 | 36.1306 | 65.1308 | AID540263 |
DNA polymerase beta | Homo sapiens (human) | Potency | 89.1251 | 0.0224 | 21.0102 | 89.1251 | AID485314 |
mitogen-activated protein kinase 1 | Homo sapiens (human) | Potency | 28.1838 | 0.0398 | 16.7842 | 39.8107 | AID1454 |
eyes absent homolog 2 isoform a | Homo sapiens (human) | Potency | 100.0000 | 1.1998 | 14.6419 | 50.1187 | AID488837 |
snurportin-1 | Homo sapiens (human) | Potency | 100.0000 | 5.8048 | 36.1306 | 65.1308 | AID540263 |
histone-lysine N-methyltransferase 2A isoform 2 precursor | Homo sapiens (human) | Potency | 19.9526 | 0.0103 | 23.8567 | 63.0957 | AID2662 |
DNA polymerase iota isoform a (long) | Homo sapiens (human) | Potency | 100.0000 | 0.0501 | 27.0736 | 89.1251 | AID588590 |
nuclear receptor ROR-gamma isoform 1 | Mus musculus (house mouse) | Potency | 7.0795 | 0.0079 | 8.2332 | 1,122.0200 | AID2551 |
lethal(3)malignant brain tumor-like protein 1 isoform I | Homo sapiens (human) | Potency | 20.9762 | 0.0752 | 15.2253 | 39.8107 | AID485360; AID540279 |
geminin | Homo sapiens (human) | Potency | 2.9093 | 0.0046 | 11.3741 | 33.4983 | AID624297 |
Vpr | Human immunodeficiency virus 1 | Potency | 31.6228 | 1.5849 | 19.6264 | 63.0957 | AID651644 |
muscleblind-like protein 1 isoform 1 | Homo sapiens (human) | Potency | 14.1254 | 0.0041 | 9.9625 | 28.1838 | AID2675 |
neuropeptide S receptor isoform A | Homo sapiens (human) | Potency | 1.2589 | 0.0158 | 12.3113 | 615.5000 | AID1461 |
Endothelin receptor type B | Rattus norvegicus (Norway rat) | Potency | 25.1189 | 0.5623 | 15.1609 | 31.6228 | AID1721 |
Endothelin-1 receptor | Rattus norvegicus (Norway rat) | Potency | 25.1189 | 0.5623 | 15.1609 | 31.6228 | AID1721 |
Alpha-synuclein | Homo sapiens (human) | Potency | 2.2387 | 0.5623 | 9.3985 | 25.1189 | AID652106 |
Guanine nucleotide-binding protein G | Homo sapiens (human) | Potency | 50.1187 | 1.9953 | 25.5327 | 50.1187 | AID624287 |
TAR DNA-binding protein 43 | Homo sapiens (human) | Potency | 31.6228 | 1.7783 | 16.2081 | 35.4813 | AID652104 |
[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) |
---|---|---|---|---|---|---|---|
nonstructural protein 1 | Influenza A virus (A/California/07/2009(H1N1)) | IC50 (µMol) | 11.3840 | 0.2000 | 24.4540 | 100.0000 | AID504329 |
Indoleamine 2,3-dioxygenase 1 | Homo sapiens (human) | IC50 (µMol) | 45.0400 | 0.0537 | 3.0757 | 10.0000 | AID1754168 |
Tryptophan 2,3-dioxygenase | Homo sapiens (human) | IC50 (µMol) | 43.2800 | 0.1100 | 1.6692 | 9.8000 | AID1754169 |
[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) |
---|---|---|---|---|---|---|---|
heat shock protein 90 | Candida albicans | EC50 (µMol) | 16.7060 | 0.1200 | 6.4855 | 33.8530 | AID2387; AID2400; AID2423 |
calcineurin A1, putative | Candida dubliniensis CD36 | EC50 (µMol) | 180.0000 | 4.6630 | 6.3810 | 8.0990 | AID2388 |
[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) |
---|---|---|---|---|---|---|---|
FAD-linked sulfhydryl oxidase ALR | Homo sapiens (human) | AC50 | 4.5530 | 0.0050 | 3.2126 | 22.7870 | AID493248 |
POsterior Segregation | Caenorhabditis elegans | AC50 | 19.0670 | 3.2980 | 12.4649 | 24.6150 | AID493130 |
Zinc finger protein mex-5 | Caenorhabditis elegans | AC50 | 38.2600 | 0.3000 | 31.0987 | 106.7000 | AID449745 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
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. |
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. |
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. |
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. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
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. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID1754168 | Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as substrate incubated for 30 mins by methylene blue reagent based concurrent assay | |||
AID1754169 | Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptophan as substrate incubated for 30 mins by methylene blue reagent based concurrent assay | |||
AID1754173 | Selectivity index, ratio of IC50 for inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 to IC50 for inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) | |||
[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 (5.56) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (27.78) | 29.6817 |
2010's | 9 (50.00) | 24.3611 |
2020's | 3 (16.67) | 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 (18.90) 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 | 19 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |