4-(4-Hydroxy-3,5-dimethoxyphenyl)-5-methyloxolan-2-one

Details

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Internal ID 72d47ebc-69a9-40dd-9b77-157aba9c3be4
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 4-(4-hydroxy-3,5-dimethoxyphenyl)-5-methyloxolan-2-one
SMILES (Canonical) CC1C(CC(=O)O1)C2=CC(=C(C(=C2)OC)O)OC
SMILES (Isomeric) CC1C(CC(=O)O1)C2=CC(=C(C(=C2)OC)O)OC
InChI InChI=1S/C13H16O5/c1-7-9(6-12(14)18-7)8-4-10(16-2)13(15)11(5-8)17-3/h4-5,7,9,15H,6H2,1-3H3
InChI Key PSCJOZBUTKHXBV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O5
Molecular Weight 252.26 g/mol
Exact Mass 252.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 5
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 4-(4-Hydroxy-3,5-dimethoxyphenyl)-5-methyloxolan-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 + 0.9816 98.16%
Caco-2 + 0.7828 78.28%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7915 79.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7778 77.78%
OATP1B3 inhibitior + 0.8986 89.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8393 83.93%
P-glycoprotein inhibitior - 0.9407 94.07%
P-glycoprotein substrate - 0.8698 86.98%
CYP3A4 substrate - 0.5397 53.97%
CYP2C9 substrate - 0.5818 58.18%
CYP2D6 substrate - 0.7795 77.95%
CYP3A4 inhibition - 0.8483 84.83%
CYP2C9 inhibition - 0.8716 87.16%
CYP2C19 inhibition - 0.6324 63.24%
CYP2D6 inhibition - 0.9532 95.32%
CYP1A2 inhibition - 0.7123 71.23%
CYP2C8 inhibition - 0.7986 79.86%
CYP inhibitory promiscuity - 0.6064 60.64%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9111 91.11%
Carcinogenicity (trinary) Non-required 0.5258 52.58%
Eye corrosion - 0.9616 96.16%
Eye irritation - 0.5995 59.95%
Skin irritation - 0.7409 74.09%
Skin corrosion - 0.9712 97.12%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5813 58.13%
Micronuclear - 0.5441 54.41%
Hepatotoxicity + 0.5657 56.57%
skin sensitisation - 0.8687 86.87%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6913 69.13%
Acute Oral Toxicity (c) III 0.4590 45.90%
Estrogen receptor binding - 0.6825 68.25%
Androgen receptor binding - 0.6100 61.00%
Thyroid receptor binding + 0.5578 55.78%
Glucocorticoid receptor binding - 0.6880 68.80%
Aromatase binding - 0.8043 80.43%
PPAR gamma - 0.6485 64.85%
Honey bee toxicity - 0.8884 88.84%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8789 87.89%

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 98.42% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.35% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.58% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.45% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.35% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.29% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.23% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.42% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.73% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.83% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.56% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.56% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.14% 94.00%

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.
Descurainia sophia

Cross-Links

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PubChem 72785168
LOTUS LTS0210736
wikiData Q105214103