ID Source | ID |
---|---|
PubMed CID | 6828 |
CHEMBL ID | 1566472 |
SCHEMBL ID | 263716 |
MeSH ID | M0060263 |
Synonym |
---|
n,n'-diethyl-n,n'-diphenylurea |
nsc44038 |
nsc-44038 |
1,3-diethyl-1,3-diphenyl-urea |
85-98-3 |
nsc28779 |
s-diethyldiphenylurea |
carbamite |
n,n'-diethylcarbanilide |
urea,3-diethyl-1,3-diphenyl- |
centralite 1 |
centralite1 |
nsc-28779 |
urea,n'-diethyl-n,n'-diphenyl- |
wln: 2nr&vn2&r |
n,n-diethylcarbanilide |
usaf ek-1047 |
centralite i |
ethyl centralite |
centralite-1 |
bis(n-ethyl-n-phenyl)urea |
centralite |
carbanilide,n'-diethyl- |
NCGC00091392-01 |
einecs 201-645-2 |
nsc 44038 |
brn 2751977 |
carbanilide, n,n'-diethyl- |
bis-(n-ethyl-n-fenyl)mocovina [czech] |
urea, 1,3-diethyl-1,3-diphenyl- |
ai3-01942 |
1,3-diethyldiphenylurea |
1,3-diethyl-1,3-diphenylurea |
1,3-diethyl-1,3-difenylmocovina [czech] |
urea, n,n'-diethyl-n,n'-diphenyl- |
ccris 4618 |
sym-diethyldiphenylurea |
1,3-diethyl-1,3-diphenylurea, 99% |
pzimiyvozbtarw-uhfffaoysa- |
inchi=1/c17h20n2o/c1-3-18(15-11-7-5-8-12-15)17(20)19(4-2)16-13-9-6-10-14-16/h5-14h,3-4h2,1-2h3 |
1,3-diethyl-1,3-di(phenyl)urea |
MLS002415749 |
smr001370912 |
NCGC00091392-02 |
HMS3039F11 |
tox21_200369 |
NCGC00257923-01 |
cas-85-98-3 |
dtxcid705040 |
dtxsid8025040 , |
1,3-diethylcarbanilide |
D0485 |
1,3-diethyl-1,3-difenylmocovina |
ec 201-645-2 |
bis-(n-ethyl-n-fenyl)mocovina |
unii-4169z9sdjg |
4169z9sdjg , |
FT-0623546 |
AKOS015913312 |
SCHEMBL263716 |
n,n'-diethylcarbanilide [mi] |
CHEMBL1566472 |
W-104072 |
n,n'-diethyldiphenylurea |
PZIMIYVOZBTARW-UHFFFAOYSA-N |
mfcd00035794 |
AS-59399 |
Q5062193 |
n,n'-diphenyl-n,n'-diethylurea |
diethylcarbanilide |
D70352 |
CS-W010105 |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
ATAD5 protein, partial | Homo sapiens (human) | Potency | 16.3535 | 0.0041 | 10.8903 | 31.5287 | AID504467 |
TDP1 protein | Homo sapiens (human) | Potency | 16.3601 | 0.0008 | 11.3822 | 44.6684 | AID686978 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 43.2771 | 0.0007 | 14.5928 | 83.7951 | AID1259369; AID1259392 |
AR protein | Homo sapiens (human) | Potency | 34.1858 | 0.0002 | 21.2231 | 8,912.5098 | AID1259243; AID1259247; AID743035; AID743063 |
aldehyde dehydrogenase 1 family, member A1 | Homo sapiens (human) | Potency | 25.1189 | 0.0112 | 12.4002 | 100.0000 | AID1030 |
thyroid stimulating hormone receptor | Homo sapiens (human) | Potency | 15.8489 | 0.0013 | 18.0743 | 39.8107 | AID926; AID938 |
nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 15.5815 | 0.0010 | 22.6508 | 76.6163 | AID1224839; AID1224893 |
progesterone receptor | Homo sapiens (human) | Potency | 30.6379 | 0.0004 | 17.9460 | 75.1148 | AID1346795 |
glucocorticoid receptor [Homo sapiens] | Homo sapiens (human) | Potency | 44.6684 | 0.0002 | 14.3764 | 60.0339 | AID588533 |
estrogen-related nuclear receptor alpha | Homo sapiens (human) | Potency | 58.0111 | 0.0015 | 30.6073 | 15,848.9004 | AID1224841; AID1224848; AID1224849; AID1259401; AID1259403 |
farnesoid X nuclear receptor | Homo sapiens (human) | Potency | 50.1187 | 0.3758 | 27.4851 | 61.6524 | AID588526 |
pregnane X nuclear receptor | Homo sapiens (human) | Potency | 20.3189 | 0.0054 | 28.0263 | 1,258.9301 | AID1346982; AID720659 |
peroxisome proliferator activated receptor gamma | Homo sapiens (human) | Potency | 31.6228 | 0.0010 | 19.4141 | 70.9645 | AID588537 |
alpha-galactosidase | Homo sapiens (human) | Potency | 35.4813 | 4.4668 | 18.3916 | 35.4813 | AID2107 |
thyroid stimulating hormone receptor | Homo sapiens (human) | Potency | 56.2828 | 0.0016 | 28.0151 | 77.1139 | AID1224843; AID1224895 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 89.1251 | 0.0060 | 26.1688 | 89.1251 | AID540317 |
thyroid hormone receptor beta isoform 2 | Rattus norvegicus (Norway rat) | Potency | 43.2771 | 0.0003 | 23.4451 | 159.6830 | AID743067 |
nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 54.8442 | 0.0006 | 27.2152 | 1,122.0200 | AID743202; AID743219 |
geminin | Homo sapiens (human) | Potency | 1.1582 | 0.0046 | 11.3741 | 33.4983 | AID624296 |
Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) | Potency | 35.4813 | 3.9811 | 46.7448 | 112.2020 | AID720708 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
guanyl-nucleotide exchange factor activity | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
protein binding | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
cAMP binding | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
protein-macromolecule adaptor activity | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
small GTPase binding | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Process | via Protein(s) | Taxonomy |
---|---|---|
cytosol | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
plasma membrane | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
membrane | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
hippocampal mossy fiber to CA3 synapse | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
plasma membrane | Rap guanine nucleotide exchange factor 4 | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
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. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
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. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
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. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (25.00) | 29.6817 |
2010's | 5 (62.50) | 24.3611 |
2020's | 1 (12.50) | 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 weak demand-to-supply ratio for research on this compound.
| This Compound (12.85) 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] |