5-(hydroxymethyl)-3-(3-methylbut-2-enyl)-3H-oxepin-2-one

Details

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Internal ID ee5c7dbb-8871-450b-854c-b6a16c0b173c
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters > Enol esters
IUPAC Name 5-(hydroxymethyl)-3-(3-methylbut-2-enyl)-3H-oxepin-2-one
SMILES (Canonical) CC(=CCC1C=C(C=COC1=O)CO)C
SMILES (Isomeric) CC(=CCC1C=C(C=COC1=O)CO)C
InChI InChI=1S/C12H16O3/c1-9(2)3-4-11-7-10(8-13)5-6-15-12(11)14/h3,5-7,11,13H,4,8H2,1-2H3
InChI Key GBGOKTDQCPDZMS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(hydroxymethyl)-3-(3-methylbut-2-enyl)-3H-oxepin-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.7811 78.11%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6662 66.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8859 88.59%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9812 98.12%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8791 87.91%
P-glycoprotein inhibitior - 0.9859 98.59%
P-glycoprotein substrate - 0.8179 81.79%
CYP3A4 substrate - 0.5234 52.34%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.8800 88.00%
CYP3A4 inhibition - 0.9639 96.39%
CYP2C9 inhibition - 0.8746 87.46%
CYP2C19 inhibition - 0.8613 86.13%
CYP2D6 inhibition - 0.9048 90.48%
CYP1A2 inhibition - 0.8185 81.85%
CYP2C8 inhibition - 0.9513 95.13%
CYP inhibitory promiscuity - 0.9370 93.70%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7044 70.44%
Carcinogenicity (trinary) Non-required 0.7311 73.11%
Eye corrosion - 0.8380 83.80%
Eye irritation + 0.9644 96.44%
Skin irritation - 0.5359 53.59%
Skin corrosion - 0.7839 78.39%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7092 70.92%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.6181 61.81%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6461 64.61%
Acute Oral Toxicity (c) III 0.6585 65.85%
Estrogen receptor binding - 0.6774 67.74%
Androgen receptor binding - 0.7364 73.64%
Thyroid receptor binding - 0.7429 74.29%
Glucocorticoid receptor binding - 0.7679 76.79%
Aromatase binding - 0.7557 75.57%
PPAR gamma - 0.7241 72.41%
Honey bee toxicity - 0.9343 93.43%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9360 93.60%

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
CHEMBL2581 P07339 Cathepsin D 92.47% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.70% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 86.35% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.29% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.80% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.49% 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 162954681
LOTUS LTS0028868
wikiData Q104167011