(4R)-4-ethenyl-4-hydroxy-3-oxocyclopentene-1-carbonitrile

Details

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Internal ID 36fc1a9a-c886-48f6-ad29-2e40a1fd9b2d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Acyloins
IUPAC Name (4R)-4-ethenyl-4-hydroxy-3-oxocyclopentene-1-carbonitrile
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H7NO2/c1-2-8(11)4-6(5-9)3-7(8)10/h2-3,11H,1,4H2/t8-/m0/s1
InChI Key GFDNNKCENLWCOQ-QMMMGPOBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7NO2
Molecular Weight 149.15 g/mol
Exact Mass 149.047678466 g/mol
Topological Polar Surface Area (TPSA) 61.10 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.33
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R)-4-ethenyl-4-hydroxy-3-oxocyclopentene-1-carbonitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.7527 75.27%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6348 63.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9511 95.11%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8732 87.32%
P-glycoprotein inhibitior - 0.9752 97.52%
P-glycoprotein substrate - 0.9764 97.64%
CYP3A4 substrate - 0.5517 55.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8474 84.74%
CYP3A4 inhibition - 0.7505 75.05%
CYP2C9 inhibition - 0.9080 90.80%
CYP2C19 inhibition - 0.8435 84.35%
CYP2D6 inhibition - 0.9324 93.24%
CYP1A2 inhibition - 0.8354 83.54%
CYP2C8 inhibition - 0.9547 95.47%
CYP inhibitory promiscuity - 0.8838 88.38%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6307 63.07%
Eye corrosion - 0.7406 74.06%
Eye irritation + 0.9651 96.51%
Skin irritation + 0.5400 54.00%
Skin corrosion - 0.7866 78.66%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7593 75.93%
Micronuclear - 0.5968 59.68%
Hepatotoxicity + 0.5908 59.08%
skin sensitisation + 0.7438 74.38%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.6843 68.43%
Acute Oral Toxicity (c) III 0.4476 44.76%
Estrogen receptor binding - 0.8902 89.02%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.7163 71.63%
Glucocorticoid receptor binding - 0.6030 60.30%
Aromatase binding - 0.7853 78.53%
PPAR gamma - 0.8781 87.81%
Honey bee toxicity - 0.6874 68.74%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.6945 69.45%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.33% 91.11%
CHEMBL1871 P10275 Androgen Receptor 92.23% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.27% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.21% 86.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 84.85% 96.12%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.39% 94.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 44517342
LOTUS LTS0257002
wikiData Q105007487