4-(4-Hydroxy-3-methoxybenzyl)-2-butanone

Details

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Internal ID 49c31ed4-86e4-41fa-a5b7-84de97ba1c97
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 5-(4-hydroxy-3-methoxyphenyl)pentan-2-one
SMILES (Canonical) CC(=O)CCCC1=CC(=C(C=C1)O)OC
SMILES (Isomeric) CC(=O)CCCC1=CC(=C(C=C1)O)OC
InChI InChI=1S/C12H16O3/c1-9(13)4-3-5-10-6-7-11(14)12(8-10)15-2/h6-8,14H,3-5H2,1-2H3
InChI Key GSNZRKKZTDECQE-UHFFFAOYSA-N
Popularity 1 reference 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 1.20
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4-Hydroxy-3-methoxybenzyl)-2-butanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9136 91.36%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.9133 91.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9339 93.39%
OATP1B3 inhibitior + 0.9564 95.64%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8140 81.40%
P-glycoprotein inhibitior - 0.9706 97.06%
P-glycoprotein substrate - 0.7837 78.37%
CYP3A4 substrate - 0.5249 52.49%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate + 0.3653 36.53%
CYP3A4 inhibition - 0.9346 93.46%
CYP2C9 inhibition - 0.9294 92.94%
CYP2C19 inhibition - 0.7616 76.16%
CYP2D6 inhibition - 0.8640 86.40%
CYP1A2 inhibition + 0.5436 54.36%
CYP2C8 inhibition + 0.8546 85.46%
CYP inhibitory promiscuity - 0.8787 87.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7454 74.54%
Carcinogenicity (trinary) Non-required 0.6425 64.25%
Eye corrosion - 0.7150 71.50%
Eye irritation + 0.8493 84.93%
Skin irritation + 0.5923 59.23%
Skin corrosion - 0.8806 88.06%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5907 59.07%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.5693 56.93%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7490 74.90%
Acute Oral Toxicity (c) III 0.8907 89.07%
Estrogen receptor binding - 0.5857 58.57%
Androgen receptor binding - 0.7295 72.95%
Thyroid receptor binding - 0.7379 73.79%
Glucocorticoid receptor binding - 0.5292 52.92%
Aromatase binding - 0.7106 71.06%
PPAR gamma - 0.7392 73.92%
Honey bee toxicity - 0.9299 92.99%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6904 69.04%
Fish aquatic toxicity + 0.8479 84.79%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.93% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.90% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.86% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.74% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.29% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.58% 86.33%
CHEMBL2535 P11166 Glucose transporter 87.21% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 84.37% 90.20%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.76% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.34% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.95% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.57% 95.50%

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.
Caragana sinica
Scyphiphora hydrophylacea
Tanacetum cinerariifolium

Cross-Links

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PubChem 91206832
NPASS NPC173407
LOTUS LTS0073921
wikiData Q105017452