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

Details

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Internal ID d62f4c97-b64e-4852-a275-e622d3a132d1
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 1-(2-hydroxy-4-methoxy-5-methylphenyl)hexa-2,4-dien-1-one
SMILES (Canonical) CC=CC=CC(=O)C1=C(C=C(C(=C1)C)OC)O
SMILES (Isomeric) CC=CC=CC(=O)C1=C(C=C(C(=C1)C)OC)O
InChI InChI=1S/C14H16O3/c1-4-5-6-7-12(15)11-8-10(2)14(17-3)9-13(11)16/h4-9,16H,1-3H3
InChI Key RIXFUJVWYPOMHN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O3
Molecular Weight 232.27 g/mol
Exact Mass 232.109944368 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2-Hydroxy-4-methoxy-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 + 0.9974 99.74%
Caco-2 + 0.9461 94.61%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8948 89.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9284 92.84%
OATP1B3 inhibitior + 0.9854 98.54%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6791 67.91%
P-glycoprotein inhibitior - 0.8638 86.38%
P-glycoprotein substrate - 0.9419 94.19%
CYP3A4 substrate - 0.5752 57.52%
CYP2C9 substrate - 0.7931 79.31%
CYP2D6 substrate - 0.8493 84.93%
CYP3A4 inhibition - 0.7892 78.92%
CYP2C9 inhibition - 0.9884 98.84%
CYP2C19 inhibition - 0.7039 70.39%
CYP2D6 inhibition - 0.9459 94.59%
CYP1A2 inhibition - 0.5415 54.15%
CYP2C8 inhibition - 0.6792 67.92%
CYP inhibitory promiscuity - 0.6392 63.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6960 69.60%
Carcinogenicity (trinary) Non-required 0.6540 65.40%
Eye corrosion + 0.6500 65.00%
Eye irritation + 0.9404 94.04%
Skin irritation + 0.6806 68.06%
Skin corrosion - 0.9692 96.92%
Ames mutagenesis - 0.6278 62.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5436 54.36%
Micronuclear - 0.5167 51.67%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.7299 72.99%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6086 60.86%
Acute Oral Toxicity (c) III 0.8581 85.81%
Estrogen receptor binding + 0.8487 84.87%
Androgen receptor binding - 0.7727 77.27%
Thyroid receptor binding + 0.7074 70.74%
Glucocorticoid receptor binding + 0.6392 63.92%
Aromatase binding + 0.8390 83.90%
PPAR gamma + 0.5298 52.98%
Honey bee toxicity - 0.9113 91.13%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9381 93.81%

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 95.63% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.79% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.31% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.37% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.76% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.29% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.74% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.16% 97.36%
CHEMBL3194 P02766 Transthyretin 82.87% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.70% 92.94%
CHEMBL4208 P20618 Proteasome component C5 81.03% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.30% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 80.02% 94.73%

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 73023204
LOTUS LTS0184503
wikiData Q104196651