Dihydrostyryl-2-pyrone

Details

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Internal ID 2e83a037-ff9a-409e-8f87-51caeab891d6
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-(2-cyclohexa-2,4-dien-1-ylethenyl)pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O2/c14-13-12(7-4-10-15-13)9-8-11-5-2-1-3-6-11/h1-5,7-11H,6H2
InChI Key ZHCFKDFPHNHTDA-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O2
Molecular Weight 200.23 g/mol
Exact Mass 200.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dihydrostyryl-2-pyrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8728 87.28%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7281 72.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9195 91.95%
OATP1B3 inhibitior + 0.9725 97.25%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7721 77.21%
P-glycoprotein inhibitior - 0.9685 96.85%
P-glycoprotein substrate - 0.9260 92.60%
CYP3A4 substrate - 0.5087 50.87%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate - 0.8228 82.28%
CYP3A4 inhibition - 0.8651 86.51%
CYP2C9 inhibition + 0.5703 57.03%
CYP2C19 inhibition + 0.7140 71.40%
CYP2D6 inhibition - 0.9017 90.17%
CYP1A2 inhibition + 0.5310 53.10%
CYP2C8 inhibition - 0.8407 84.07%
CYP inhibitory promiscuity - 0.5072 50.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8213 82.13%
Carcinogenicity (trinary) Non-required 0.5212 52.12%
Eye corrosion - 0.6557 65.57%
Eye irritation + 0.5963 59.63%
Skin irritation + 0.8399 83.99%
Skin corrosion - 0.8361 83.61%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7267 72.67%
Micronuclear - 0.5060 50.60%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8415 84.15%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6964 69.64%
Acute Oral Toxicity (c) III 0.4299 42.99%
Estrogen receptor binding + 0.5999 59.99%
Androgen receptor binding - 0.6232 62.32%
Thyroid receptor binding - 0.8264 82.64%
Glucocorticoid receptor binding - 0.7138 71.38%
Aromatase binding + 0.7562 75.62%
PPAR gamma - 0.5340 53.40%
Honey bee toxicity - 0.7920 79.20%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9543 95.43%

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 97.60% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.83% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 85.97% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.77% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.09% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.38% 97.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.25% 96.00%

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.
Garcinia oblongifolia

Cross-Links

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PubChem 129650702
LOTUS LTS0060310
wikiData Q105145058