1-(4-(3-(Hydroxymethyl)-5-methoxyphenoxy)-2-methoxy-6-methylphenyl)-ethanone

Details

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Internal ID 54ff1079-b4a4-45ab-9672-4ce80867f75c
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 1-[4-[3-(hydroxymethyl)-5-methoxyphenoxy]-2-methoxy-6-methylphenyl]ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H20O5/c1-11-5-15(9-17(22-4)18(11)12(2)20)23-16-7-13(10-19)6-14(8-16)21-3/h5-9,19H,10H2,1-4H3
InChI Key QILDBUQXXZSWOJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H20O5
Molecular Weight 316.30 g/mol
Exact Mass 316.13107373 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.50
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(4-(3-(Hydroxymethyl)-5-methoxyphenoxy)-2-methoxy-6-methylphenyl)-ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.7535 75.35%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.9194 91.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9130 91.30%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6167 61.67%
P-glycoprotein inhibitior - 0.5685 56.85%
P-glycoprotein substrate - 0.8576 85.76%
CYP3A4 substrate - 0.5231 52.31%
CYP2C9 substrate - 0.8028 80.28%
CYP2D6 substrate - 0.8160 81.60%
CYP3A4 inhibition - 0.6416 64.16%
CYP2C9 inhibition - 0.9307 93.07%
CYP2C19 inhibition + 0.7669 76.69%
CYP2D6 inhibition - 0.9127 91.27%
CYP1A2 inhibition + 0.7751 77.51%
CYP2C8 inhibition + 0.4529 45.29%
CYP inhibitory promiscuity + 0.6055 60.55%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7066 70.66%
Carcinogenicity (trinary) Non-required 0.7525 75.25%
Eye corrosion - 0.9766 97.66%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.8242 82.42%
Skin corrosion - 0.9916 99.16%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6720 67.20%
Micronuclear - 0.5367 53.67%
Hepatotoxicity - 0.5415 54.15%
skin sensitisation - 0.8863 88.63%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.5702 57.02%
Acute Oral Toxicity (c) III 0.5780 57.80%
Estrogen receptor binding + 0.9298 92.98%
Androgen receptor binding - 0.5333 53.33%
Thyroid receptor binding + 0.6948 69.48%
Glucocorticoid receptor binding + 0.8259 82.59%
Aromatase binding + 0.8947 89.47%
PPAR gamma + 0.5992 59.92%
Honey bee toxicity - 0.8412 84.12%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9377 93.77%

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 96.32% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.99% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.56% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.36% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.16% 99.17%
CHEMBL4208 P20618 Proteasome component C5 87.00% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.98% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.87% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.83% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.52% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.50% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.48% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.18% 91.11%
CHEMBL2535 P11166 Glucose transporter 81.12% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.95% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 80.36% 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 138402981
LOTUS LTS0205639
wikiData Q105221482