Methyl 3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)propanoate

Details

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Internal ID 4e0d27b5-7352-460c-bbb8-e747ffacb106
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name methyl 3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)propanoate
SMILES (Canonical) COC1=C(C=CC(=C1)C(CO)C(=O)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C(CO)C(=O)OC)O
InChI InChI=1S/C11H14O5/c1-15-10-5-7(3-4-9(10)13)8(6-12)11(14)16-2/h3-5,8,12-13H,6H2,1-2H3
InChI Key ZQMCMXRXLGCJJJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O5
Molecular Weight 226.23 g/mol
Exact Mass 226.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.65
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)propanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9621 96.21%
Caco-2 + 0.6083 60.83%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8727 87.27%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9381 93.81%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8729 87.29%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.8475 84.75%
CYP3A4 substrate - 0.6367 63.67%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8000 80.00%
CYP3A4 inhibition - 0.8914 89.14%
CYP2C9 inhibition - 0.8742 87.42%
CYP2C19 inhibition - 0.8771 87.71%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.8507 85.07%
CYP2C8 inhibition - 0.8783 87.83%
CYP inhibitory promiscuity - 0.7910 79.10%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7383 73.83%
Carcinogenicity (trinary) Non-required 0.7658 76.58%
Eye corrosion - 0.9262 92.62%
Eye irritation + 0.6447 64.47%
Skin irritation - 0.6170 61.70%
Skin corrosion - 0.9682 96.82%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7021 70.21%
Micronuclear - 0.6560 65.60%
Hepatotoxicity - 0.8948 89.48%
skin sensitisation - 0.5583 55.83%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7846 78.46%
Acute Oral Toxicity (c) III 0.7294 72.94%
Estrogen receptor binding - 0.6334 63.34%
Androgen receptor binding - 0.5774 57.74%
Thyroid receptor binding - 0.6309 63.09%
Glucocorticoid receptor binding - 0.6691 66.91%
Aromatase binding - 0.6316 63.16%
PPAR gamma + 0.5639 56.39%
Honey bee toxicity - 0.9279 92.79%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6249 62.49%
Fish aquatic toxicity + 0.8142 81.42%

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 97.26% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.19% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.70% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.46% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.90% 89.62%
CHEMBL2535 P11166 Glucose transporter 88.71% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.97% 95.56%
CHEMBL4208 P20618 Proteasome component C5 87.68% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.18% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 86.50% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.37% 99.15%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.65% 86.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.16% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.04% 91.19%

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.
Brucea javanica
Hibiscus taiwanensis

Cross-Links

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PubChem 162867206
LOTUS LTS0022181
wikiData Q105381544