Methyl 3-hydroxy-2-methoxy-4-propan-2-ylbenzoate

Details

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Internal ID dbba3b11-57a9-4699-b172-339154653e88
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > O-methoxybenzoic acids and derivatives
IUPAC Name methyl 3-hydroxy-2-methoxy-4-propan-2-ylbenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O4/c1-7(2)8-5-6-9(12(14)16-4)11(15-3)10(8)13/h5-7,13H,1-4H3
InChI Key NYCNVIRWOMOART-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O4
Molecular Weight 224.25 g/mol
Exact Mass 224.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 4
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 Methyl 3-hydroxy-2-methoxy-4-propan-2-ylbenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 + 0.7036 70.36%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8979 89.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9348 93.48%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9296 92.96%
P-glycoprotein inhibitior - 0.9303 93.03%
P-glycoprotein substrate - 0.9041 90.41%
CYP3A4 substrate - 0.5777 57.77%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8204 82.04%
CYP3A4 inhibition - 0.9304 93.04%
CYP2C9 inhibition - 0.9589 95.89%
CYP2C19 inhibition - 0.8953 89.53%
CYP2D6 inhibition - 0.9513 95.13%
CYP1A2 inhibition - 0.8625 86.25%
CYP2C8 inhibition - 0.8539 85.39%
CYP inhibitory promiscuity - 0.9067 90.67%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6769 67.69%
Carcinogenicity (trinary) Non-required 0.6898 68.98%
Eye corrosion - 0.6684 66.84%
Eye irritation + 0.8764 87.64%
Skin irritation - 0.6023 60.23%
Skin corrosion - 0.9723 97.23%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7082 70.82%
Micronuclear - 0.5652 56.52%
Hepatotoxicity - 0.5075 50.75%
skin sensitisation - 0.9044 90.44%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7247 72.47%
Acute Oral Toxicity (c) II 0.4842 48.42%
Estrogen receptor binding - 0.6795 67.95%
Androgen receptor binding - 0.8256 82.56%
Thyroid receptor binding - 0.5496 54.96%
Glucocorticoid receptor binding - 0.8277 82.77%
Aromatase binding - 0.6543 65.43%
PPAR gamma - 0.5606 56.06%
Honey bee toxicity - 0.9433 94.33%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9374 93.74%

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 96.56% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.02% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.58% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.73% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.64% 93.56%
CHEMBL2535 P11166 Glucose transporter 88.06% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.65% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.14% 94.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.06% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.14% 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.
Relhania acerosa

Cross-Links

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PubChem 162965169
LOTUS LTS0087201
wikiData Q105187448