1H-Imidazole, 1-(2-methyl-1-oxo-2-propenyl)-

Details

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Internal ID 2ff42a36-05c2-4e7a-8403-5b8333bf6b9b
Taxonomy Organoheterocyclic compounds > Azoles > Imidazoles > Substituted imidazoles > Carbonylimidazoles
IUPAC Name 1-imidazol-1-yl-2-methylprop-2-en-1-one
SMILES (Canonical) CC(=C)C(=O)N1C=CN=C1
SMILES (Isomeric) CC(=C)C(=O)N1C=CN=C1
InChI InChI=1S/C7H8N2O/c1-6(2)7(10)9-4-3-8-5-9/h3-5H,1H2,2H3
InChI Key OMRBLVYISVXTDL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8N2O
Molecular Weight 136.15 g/mol
Exact Mass 136.063662883 g/mol
Topological Polar Surface Area (TPSA) 34.90 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1H-Imidazole, 1-(2-methyl-1-oxo-2-propenyl)-
1-Methacryloyl imidazole
N-(2-Methylacryloyl)imidazola
SCHEMBL2346666
1-Methacryloyl-1H-imidazole #
DTXSID70336484
OMRBLVYISVXTDL-UHFFFAOYSA-N
MFCD30062950
1-(1H-Imidazol-1-yl)-2-methylprop-2-en-1-one

2D Structure

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2D Structure of 1H-Imidazole, 1-(2-methyl-1-oxo-2-propenyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9845 98.45%
Caco-2 + 0.7527 75.27%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5875 58.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9622 96.22%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9431 94.31%
OCT2 inhibitior - 0.7848 78.48%
BSEP inhibitior - 0.9195 91.95%
P-glycoprotein inhibitior - 0.9835 98.35%
P-glycoprotein substrate - 0.9476 94.76%
CYP3A4 substrate - 0.7183 71.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8813 88.13%
CYP3A4 inhibition - 0.6565 65.65%
CYP2C9 inhibition - 0.5972 59.72%
CYP2C19 inhibition - 0.5848 58.48%
CYP2D6 inhibition - 0.8065 80.65%
CYP1A2 inhibition - 0.5356 53.56%
CYP2C8 inhibition - 0.9197 91.97%
CYP inhibitory promiscuity + 0.6073 60.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Warning 0.4040 40.40%
Eye corrosion + 0.6491 64.91%
Eye irritation + 0.9542 95.42%
Skin irritation - 0.5493 54.93%
Skin corrosion - 0.8189 81.89%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6540 65.40%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.8648 86.48%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5857 58.57%
Acute Oral Toxicity (c) III 0.5653 56.53%
Estrogen receptor binding - 0.9520 95.20%
Androgen receptor binding - 0.7681 76.81%
Thyroid receptor binding - 0.8277 82.77%
Glucocorticoid receptor binding - 0.8652 86.52%
Aromatase binding - 0.7478 74.78%
PPAR gamma - 0.8877 88.77%
Honey bee toxicity - 0.9512 95.12%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6732 67.32%
Fish aquatic toxicity - 0.5541 55.41%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.25% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 96.16% 83.82%
CHEMBL1951 P21397 Monoamine oxidase A 96.12% 91.49%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 91.37% 92.29%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 87.55% 93.10%
CHEMBL2581 P07339 Cathepsin D 84.00% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.32% 85.14%

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.
Cynomorium coccineum subsp. songaricum

Cross-Links

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PubChem 534045
NPASS NPC275358
LOTUS LTS0205142
wikiData Q82103625