1-(2,4-Dihydroxy-5-methylphenyl)hexa-2,4-dien-1-one

Details

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Internal ID 03cc9327-cf32-48aa-a294-4613c54d271c
Taxonomy Benzenoids > Phenols > Benzenediols > Resorcinols
IUPAC Name 1-(2,4-dihydroxy-5-methylphenyl)hexa-2,4-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O3/c1-3-4-5-6-11(14)10-7-9(2)12(15)8-13(10)16/h3-8,15-16H,1-2H3
InChI Key YNRLVGAXEGGYPN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O3
Molecular Weight 218.25 g/mol
Exact Mass 218.094294304 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2,4-Dihydroxy-5-methylphenyl)hexa-2,4-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.8524 85.24%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8536 85.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9171 91.71%
OATP1B3 inhibitior + 0.9872 98.72%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9588 95.88%
BSEP inhibitior - 0.7565 75.65%
P-glycoprotein inhibitior - 0.9517 95.17%
P-glycoprotein substrate - 0.9662 96.62%
CYP3A4 substrate - 0.6577 65.77%
CYP2C9 substrate - 0.7925 79.25%
CYP2D6 substrate - 0.8666 86.66%
CYP3A4 inhibition + 0.6705 67.05%
CYP2C9 inhibition + 0.6363 63.63%
CYP2C19 inhibition + 0.6884 68.84%
CYP2D6 inhibition - 0.9100 91.00%
CYP1A2 inhibition + 0.7771 77.71%
CYP2C8 inhibition - 0.8668 86.68%
CYP inhibitory promiscuity + 0.6234 62.34%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7683 76.83%
Carcinogenicity (trinary) Non-required 0.7579 75.79%
Eye corrosion + 0.7843 78.43%
Eye irritation + 0.9376 93.76%
Skin irritation + 0.8244 82.44%
Skin corrosion + 0.5536 55.36%
Ames mutagenesis - 0.7178 71.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7032 70.32%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.9479 94.79%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7122 71.22%
Acute Oral Toxicity (c) III 0.8909 89.09%
Estrogen receptor binding + 0.8660 86.60%
Androgen receptor binding - 0.6000 60.00%
Thyroid receptor binding + 0.7004 70.04%
Glucocorticoid receptor binding + 0.8053 80.53%
Aromatase binding + 0.7366 73.66%
PPAR gamma + 0.6439 64.39%
Honey bee toxicity - 0.9569 95.69%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9567 95.67%

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 94.46% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.69% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.86% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.78% 95.50%
CHEMBL2581 P07339 Cathepsin D 82.80% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.91% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.35% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.16% 93.65%

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 131413575
LOTUS LTS0221136
wikiData Q104201883