1-(2,5-Dioxo-2,5-dihydro-1H-imidazol-4-YL)urea

Details

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Internal ID d92b8980-fb90-49a0-b1b5-72e8f41c3d68
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name (2,5-dioxoimidazol-4-yl)urea
SMILES (Canonical) C1(=O)C(=NC(=O)N1)NC(=O)N
SMILES (Isomeric) C1(=O)C(=NC(=O)N1)NC(=O)N
InChI InChI=1S/C4H4N4O3/c5-3(10)6-1-2(9)8-4(11)7-1/h(H4,5,6,7,8,9,10,11)
InChI Key MFAONEQLPARJAO-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C4H4N4O3
Molecular Weight 156.10 g/mol
Exact Mass 156.02834000 g/mol
Topological Polar Surface Area (TPSA) 114.00 Ų
XlogP -1.60
Atomic LogP (AlogP) -1.70
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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105245-87-2
(2,5-dioxoimidazol-4-yl)urea
[2,5-dioxo-imidazolidin-(4e)-ylidene]-urea
SCHEMBL9203157
SCHEMBL23212141
DTXSID00425870
(2,5-dioxo-2,5-dihydro-1H-imidazol-4-yl)urea
A927680
Q27452843
Benzotriazol-1-yloxytris(dimethylamino)phosphonium Hexafluorophosphate (BOP)

2D Structure

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2D Structure of 1-(2,5-Dioxo-2,5-dihydro-1H-imidazol-4-YL)urea

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9590 95.90%
Caco-2 - 0.7689 76.89%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4211 42.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9756 97.56%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9771 97.71%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.9211 92.11%
CYP3A4 substrate - 0.6787 67.87%
CYP2C9 substrate - 0.5624 56.24%
CYP2D6 substrate - 0.8860 88.60%
CYP3A4 inhibition - 0.9684 96.84%
CYP2C9 inhibition - 0.9487 94.87%
CYP2C19 inhibition - 0.9295 92.95%
CYP2D6 inhibition - 0.9397 93.97%
CYP1A2 inhibition - 0.8538 85.38%
CYP2C8 inhibition - 0.9839 98.39%
CYP inhibitory promiscuity - 0.9968 99.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7943 79.43%
Carcinogenicity (trinary) Non-required 0.6764 67.64%
Eye corrosion - 0.9719 97.19%
Eye irritation - 0.7714 77.14%
Skin irritation - 0.8382 83.82%
Skin corrosion - 0.9517 95.17%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7447 74.47%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.8783 87.83%
skin sensitisation - 0.9154 91.54%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6572 65.72%
Acute Oral Toxicity (c) III 0.5747 57.47%
Estrogen receptor binding - 0.9187 91.87%
Androgen receptor binding - 0.7830 78.30%
Thyroid receptor binding - 0.6385 63.85%
Glucocorticoid receptor binding - 0.7554 75.54%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.7441 74.41%
Honey bee toxicity - 0.9684 96.84%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.9324 93.24%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.42% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.07% 85.14%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.87% 89.34%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 85.30% 83.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.35% 91.11%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.82% 81.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.25% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.60% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.75% 95.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Aristolochia contorta
Aristolochia debilis
Cistanche deserticola
Dioscorea polystachya
Fibraurea recisa
Triticum aestivum
Typha domingensis

Cross-Links

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PubChem 6852197
NPASS NPC264726