fenazox: RN given refers to parent cpd without isomeric designation; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
trans-azoxybenzene : An azoxybenzene with a trans-configuration. [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]
cis-azoxybenzene : An azoxybenzene with a cis-configuration. [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]
ID Source | ID |
---|---|
PubMed CID | 10316 |
CHEMBL ID | 1442921 |
CHEMBL ID | 2356614 |
CHEBI ID | 51866 |
CHEBI ID | 51868 |
CHEBI ID | 51865 |
SCHEMBL ID | 14179802 |
MeSH ID | M0133776 |
Synonym |
---|
unii-x2k99tm19q |
diazene, 1,2-diphenyl-, 1-oxide |
x2k99tm19q , |
azoxybenzol |
nsc1796 |
azoxybenzene |
azoxybenzide |
azobenzene, oxide |
azoxybenzeen |
nsc-1796 |
495-48-7 |
azossibenzene |
ordinary azoxybenzene |
wln: onr&unr |
benzene, azoxydi- |
diazene, diphenyl-, 1-oxide |
fenazox |
ccris 5965 |
einecs 207-802-1 |
hsdb 2861 |
brn 0743984 |
azoxybenzeen [dutch] |
azoxydibenzene |
fenazox [german] |
nsc 1796 |
ai3-00476 |
azossibenzene [italian] |
azoxybenzol [german] |
diphenyldiazene 1-oxide |
fentoxan |
n,n'-diphenyl-diazene n-oxide |
(z)-oxido-phenyl-phenylimino-ammonium |
NCGC00091251-01 |
[(e)-phenyl-nno-azoxy]benzene |
CHEBI:51866 |
diphenyldiazene oxide |
CHEBI:51868 , |
trans-azoxybenzene |
CHEBI:51865 , |
[(e)-nno-azoxy]benzene |
[(z)-nno-azoxy]benzene |
1,2-diphenyldiazene 1-oxide |
(phenyl-nno-azoxy)benzene |
cis-azoxybenzene |
A0571 |
oxido-phenyl-phenyliminoazanium |
NCGC00091251-02 |
tox21_201167 |
NCGC00258719-01 |
AKOS006228960 |
cas-495-48-7 |
dtxcid904555 |
dtxsid0024555 , |
tox21_111108 |
[(z)-phenyl-nno-azoxy]benzene |
STL280266 |
FT-0622535 |
trans-diphenyldiazene oxide |
azoxybenzene cis-form |
benzenamine, n-(oxidophenylimino)-, (n(z))- |
unii-dc1p3je72o |
diazene, 1,2-diphenyl-, 1-oxide, (1e)- |
dc1p3je72o , |
azoxybenzene, (e)- |
20972-43-4 |
azoxybenzene, (z)- |
azoxybenzene cis-form [mi] |
2cyq7pt9ss , |
azoxybenzene trans-form [mi] |
unii-2cyq7pt9ss |
21650-65-7 |
GAUZCKBSTZFWCT-UHFFFAOYSA-N |
SCHEMBL14179802 |
CHEMBL1442921 |
CHEMBL2356614 |
mfcd00019925 |
Q5715108 |
1,2-diphenyldiazene oxide |
zoxybenzene |
(z)-1,2-diphenyldiazene oxide |
(e)-azoxybenzene |
Q27122876 |
(z)-azoxybenzene |
Q27122880 |
(e)-1,2-diphenyldiazene 1-oxide |
A913989 |
D88279 |
Excerpt | Reference | Relevance |
---|---|---|
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs." | ( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019) | 0.51 |
Class | Description |
---|---|
azoxy compound | An N-oxide of an azo compound of structure RN=N(+)(O(-))R. |
[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 | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 12.0382 | 0.0072 | 15.7588 | 89.3584 | AID1224835; AID624030 |
pregnane X receptor | Rattus norvegicus (Norway rat) | Potency | 25.1189 | 0.0251 | 27.9203 | 501.1870 | AID651751 |
RAR-related orphan receptor gamma | Mus musculus (house mouse) | Potency | 20.5105 | 0.0060 | 38.0041 | 19,952.5996 | AID1159521; AID1159523 |
TDP1 protein | Homo sapiens (human) | Potency | 26.1679 | 0.0008 | 11.3822 | 44.6684 | AID686978; AID686979 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 35.8558 | 0.0007 | 14.5928 | 83.7951 | AID1259368; AID1259392 |
AR protein | Homo sapiens (human) | Potency | 39.2098 | 0.0002 | 21.2231 | 8,912.5098 | AID743042; AID743054 |
nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 27.7442 | 0.0010 | 22.6508 | 76.6163 | AID1224838; AID1224839; AID1224893 |
retinoic acid nuclear receptor alpha variant 1 | Homo sapiens (human) | Potency | 5.3453 | 0.0030 | 41.6115 | 22,387.1992 | AID1159552; AID1159553; AID1159555 |
estrogen-related nuclear receptor alpha | Homo sapiens (human) | Potency | 17.1926 | 0.0015 | 30.6073 | 15,848.9004 | AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403 |
pregnane X nuclear receptor | Homo sapiens (human) | Potency | 21.6899 | 0.0054 | 28.0263 | 1,258.9301 | AID1346982 |
estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 18.6348 | 0.0002 | 29.3054 | 16,493.5996 | AID1259244; AID1259248; AID743075; AID743079; AID743080; AID743091 |
peroxisome proliferator-activated receptor delta | Homo sapiens (human) | Potency | 61.6599 | 0.0010 | 24.5048 | 61.6448 | AID743215 |
aryl hydrocarbon receptor | Homo sapiens (human) | Potency | 33.6905 | 0.0007 | 23.0674 | 1,258.9301 | AID651777; AID743085; AID743122 |
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_a | Homo sapiens (human) | Potency | 22.1651 | 0.0017 | 23.8393 | 78.1014 | AID743083 |
thyroid stimulating hormone receptor | Homo sapiens (human) | Potency | 51.4350 | 0.0016 | 28.0151 | 77.1139 | AID1224895 |
potassium voltage-gated channel subfamily H member 2 isoform d | Homo sapiens (human) | Potency | 50.1187 | 0.0178 | 9.6374 | 44.6684 | AID588834 |
thyroid hormone receptor beta isoform 2 | Rattus norvegicus (Norway rat) | Potency | 76.9588 | 0.0003 | 23.4451 | 159.6830 | AID743065; AID743067 |
histone deacetylase 9 isoform 3 | Homo sapiens (human) | Potency | 9.8781 | 0.0376 | 17.0823 | 61.1927 | AID1259364; AID1259388 |
nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 19.9712 | 0.0006 | 27.2152 | 1,122.0200 | AID651741; AID720636; AID743202; AID743219 |
peripheral myelin protein 22 | Rattus norvegicus (Norway rat) | Potency | 36.1254 | 0.0056 | 12.3677 | 36.1254 | AID624032 |
Voltage-dependent calcium channel gamma-2 subunit | Mus musculus (house mouse) | Potency | 24.3365 | 0.0015 | 57.7890 | 15,848.9004 | AID1259244 |
Glutamate receptor 2 | Rattus norvegicus (Norway rat) | Potency | 24.3365 | 0.0015 | 51.7393 | 15,848.9004 | AID1259244 |
Nuclear receptor ROR-gamma | Homo sapiens (human) | Potency | 4.7308 | 0.0266 | 22.4482 | 66.8242 | AID651802 |
ATPase family AAA domain-containing protein 5 | Homo sapiens (human) | Potency | 16.7855 | 0.0119 | 17.9420 | 71.5630 | AID651632 |
Ataxin-2 | Homo sapiens (human) | Potency | 16.7855 | 0.0119 | 12.2221 | 68.7989 | AID651632 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID504749 | qHTS profiling for inhibitors of Plasmodium falciparum proliferation | 2011 | Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043 | Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets. |
AID1296008 | Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening | 2020 | SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1 | Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening. |
AID1346987 | P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5 | A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1346986 | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5 | A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 4 (25.00) | 18.7374 |
1990's | 2 (12.50) | 18.2507 |
2000's | 1 (6.25) | 29.6817 |
2010's | 6 (37.50) | 24.3611 |
2020's | 3 (18.75) | 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 (17.75) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 1 (6.25%) | 6.00% |
Case Studies | 1 (6.25%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 14 (87.50%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |