(2-Hydroxy-6-methoxyphenyl)methyl benzoate

Details

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Internal ID f2868183-ed28-4474-8b22-3b5532f9be04
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name (2-hydroxy-6-methoxyphenyl)methyl benzoate
SMILES (Canonical) COC1=CC=CC(=C1COC(=O)C2=CC=CC=C2)O
SMILES (Isomeric) COC1=CC=CC(=C1COC(=O)C2=CC=CC=C2)O
InChI InChI=1S/C15H14O4/c1-18-14-9-5-8-13(16)12(14)10-19-15(17)11-6-3-2-4-7-11/h2-9,16H,10H2,1H3
InChI Key ZKMNHQCDNRTISA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O4
Molecular Weight 258.27 g/mol
Exact Mass 258.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 4
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 (2-Hydroxy-6-methoxyphenyl)methyl benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.7283 72.83%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.9372 93.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9305 93.05%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7176 71.76%
P-glycoprotein inhibitior - 0.8626 86.26%
P-glycoprotein substrate - 0.9043 90.43%
CYP3A4 substrate - 0.5553 55.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7812 78.12%
CYP3A4 inhibition - 0.9191 91.91%
CYP2C9 inhibition - 0.7429 74.29%
CYP2C19 inhibition - 0.6536 65.36%
CYP2D6 inhibition - 0.9672 96.72%
CYP1A2 inhibition + 0.5404 54.04%
CYP2C8 inhibition + 0.7068 70.68%
CYP inhibitory promiscuity - 0.5454 54.54%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7492 74.92%
Carcinogenicity (trinary) Non-required 0.6815 68.15%
Eye corrosion - 0.9833 98.33%
Eye irritation + 0.8859 88.59%
Skin irritation - 0.7235 72.35%
Skin corrosion - 0.9876 98.76%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6549 65.49%
Micronuclear + 0.5266 52.66%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8918 89.18%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.5966 59.66%
Acute Oral Toxicity (c) III 0.7773 77.73%
Estrogen receptor binding + 0.6714 67.14%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.6469 64.69%
Glucocorticoid receptor binding - 0.6551 65.51%
Aromatase binding + 0.6533 65.33%
PPAR gamma - 0.5758 57.58%
Honey bee toxicity - 0.9433 94.33%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity + 0.9797 97.97%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.42% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.97% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.71% 95.56%
CHEMBL2535 P11166 Glucose transporter 91.38% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 91.00% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.84% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 88.85% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.61% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.23% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.87% 96.00%

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.
Aniba ferrea
Endlicheria dysodantha
Uvaria grandiflora

Cross-Links

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PubChem 127260385
LOTUS LTS0138919
wikiData Q105378585