Benzyl 2-hydroxy-3,6-dimethoxybenzoate

Details

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Internal ID ae34f630-19a5-45e6-b80b-96670b2dbb9a
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > O-methoxybenzoic acids and derivatives
IUPAC Name benzyl 2-hydroxy-3,6-dimethoxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H16O5/c1-19-12-8-9-13(20-2)15(17)14(12)16(18)21-10-11-6-4-3-5-7-11/h3-9,17H,10H2,1-2H3
InChI Key ASQGNSYUWXVREW-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O5
Molecular Weight 288.29 g/mol
Exact Mass 288.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Benzyl 2-hydroxy-3,6-dimethoxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 + 0.8880 88.80%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.9210 92.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9118 91.18%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6746 67.46%
P-glycoprotein inhibitior - 0.4596 45.96%
P-glycoprotein substrate - 0.9293 92.93%
CYP3A4 substrate - 0.5067 50.67%
CYP2C9 substrate - 0.8157 81.57%
CYP2D6 substrate - 0.8398 83.98%
CYP3A4 inhibition - 0.8433 84.33%
CYP2C9 inhibition - 0.7048 70.48%
CYP2C19 inhibition - 0.6050 60.50%
CYP2D6 inhibition - 0.9035 90.35%
CYP1A2 inhibition - 0.6072 60.72%
CYP2C8 inhibition + 0.7055 70.55%
CYP inhibitory promiscuity - 0.5194 51.94%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7843 78.43%
Carcinogenicity (trinary) Non-required 0.7416 74.16%
Eye corrosion - 0.9728 97.28%
Eye irritation + 0.8144 81.44%
Skin irritation - 0.7305 73.05%
Skin corrosion - 0.9897 98.97%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4758 47.58%
Micronuclear + 0.5673 56.73%
Hepatotoxicity + 0.5850 58.50%
skin sensitisation - 0.8805 88.05%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.6948 69.48%
Acute Oral Toxicity (c) III 0.7228 72.28%
Estrogen receptor binding + 0.8329 83.29%
Androgen receptor binding + 0.7648 76.48%
Thyroid receptor binding + 0.5154 51.54%
Glucocorticoid receptor binding - 0.6424 64.24%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.5752 57.52%
Honey bee toxicity - 0.9619 96.19%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6529 65.29%
Fish aquatic toxicity + 0.9730 97.30%

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 96.17% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.38% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.85% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.59% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.91% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.75% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 84.18% 90.20%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.99% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 81.71% 94.73%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.59% 92.67%

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.
Brickellia veronicaefolia
Cassia fistula

Cross-Links

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PubChem 11077057
LOTUS LTS0049776
wikiData Q104918004