3-Buten-2-one, (Z)-

Details

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Internal ID 219d6c0d-9876-474a-a66b-25db2fe54fb4
Taxonomy Organoheterocyclic compounds > Furans > Nitrofurans
IUPAC Name (Z)-4-(5-nitrofuran-2-yl)but-3-en-2-one
SMILES (Canonical) CC(=O)C=CC1=CC=C(O1)[N+](=O)[O-]
SMILES (Isomeric) CC(=O)/C=C\C1=CC=C(O1)[N+](=O)[O-]
InChI InChI=1S/C8H7NO4/c1-6(10)2-3-7-4-5-8(13-7)9(11)12/h2-5H,1H3/b3-2-
InChI Key AYSGEAZAKMPTSE-IHWYPQMZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7NO4
Molecular Weight 181.15 g/mol
Exact Mass 181.03750770 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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NSC190646
NSC-190646

2D Structure

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2D Structure of 3-Buten-2-one, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9300 93.00%
Caco-2 + 0.6766 67.66%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5922 59.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9177 91.77%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8445 84.45%
P-glycoprotein inhibitior - 0.9820 98.20%
P-glycoprotein substrate - 0.9514 95.14%
CYP3A4 substrate - 0.5810 58.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8632 86.32%
CYP3A4 inhibition - 0.9385 93.85%
CYP2C9 inhibition - 0.8386 83.86%
CYP2C19 inhibition - 0.6789 67.89%
CYP2D6 inhibition - 0.8401 84.01%
CYP1A2 inhibition + 0.7607 76.07%
CYP2C8 inhibition - 0.9234 92.34%
CYP inhibitory promiscuity - 0.7642 76.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5316 53.16%
Carcinogenicity (trinary) Non-required 0.3726 37.26%
Eye corrosion - 0.9008 90.08%
Eye irritation + 0.9493 94.93%
Skin irritation - 0.6097 60.97%
Skin corrosion - 0.9283 92.83%
Ames mutagenesis + 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8549 85.49%
Micronuclear + 0.9900 99.00%
Hepatotoxicity + 0.8500 85.00%
skin sensitisation - 0.8115 81.15%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6061 60.61%
Acute Oral Toxicity (c) III 0.6375 63.75%
Estrogen receptor binding - 0.7872 78.72%
Androgen receptor binding - 0.7900 79.00%
Thyroid receptor binding - 0.8716 87.16%
Glucocorticoid receptor binding - 0.8672 86.72%
Aromatase binding - 0.8781 87.81%
PPAR gamma - 0.6560 65.60%
Honey bee toxicity - 0.9569 95.69%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.7668 76.68%

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
CHEMBL3401 O75469 Pregnane X receptor 91.38% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.89% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.84% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.31% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.95% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.52% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.11% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.52% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.13% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.18% 94.45%

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.
Artemisia argyi
Artemisia montana
Artemisia princeps
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 5383729
NPASS NPC309856