3-(4-Hydroxy-3,5-dimethoxyphenyl)-3-methoxypropane-1,2-diol

Details

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Internal ID 390d0fd3-048c-4649-8f5b-f25af9f3a1cf
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3-(4-hydroxy-3,5-dimethoxyphenyl)-3-methoxypropane-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O6/c1-16-9-4-7(5-10(17-2)11(9)15)12(18-3)8(14)6-13/h4-5,8,12-15H,6H2,1-3H3
InChI Key AMYOXKTVQPGCHF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O6
Molecular Weight 258.27 g/mol
Exact Mass 258.11033829 g/mol
Topological Polar Surface Area (TPSA) 88.40 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.45
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Hydroxy-3,5-dimethoxyphenyl)-3-methoxypropane-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9573 95.73%
Caco-2 + 0.6395 63.95%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8015 80.15%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8125 81.25%
OATP1B3 inhibitior + 0.9329 93.29%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9356 93.56%
P-glycoprotein inhibitior - 0.9018 90.18%
P-glycoprotein substrate - 0.7706 77.06%
CYP3A4 substrate - 0.6374 63.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6723 67.23%
CYP3A4 inhibition - 0.8276 82.76%
CYP2C9 inhibition - 0.9582 95.82%
CYP2C19 inhibition - 0.8828 88.28%
CYP2D6 inhibition - 0.9404 94.04%
CYP1A2 inhibition - 0.6906 69.06%
CYP2C8 inhibition - 0.8685 86.85%
CYP inhibitory promiscuity - 0.9149 91.49%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8308 83.08%
Carcinogenicity (trinary) Non-required 0.6965 69.65%
Eye corrosion - 0.9799 97.99%
Eye irritation - 0.8647 86.47%
Skin irritation - 0.7454 74.54%
Skin corrosion - 0.9526 95.26%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6896 68.96%
Micronuclear - 0.7086 70.86%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation + 0.6125 61.25%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7741 77.41%
Acute Oral Toxicity (c) III 0.8156 81.56%
Estrogen receptor binding - 0.5761 57.61%
Androgen receptor binding - 0.6229 62.29%
Thyroid receptor binding + 0.6788 67.88%
Glucocorticoid receptor binding - 0.5548 55.48%
Aromatase binding - 0.7718 77.18%
PPAR gamma - 0.6108 61.08%
Honey bee toxicity - 0.9548 95.48%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.6134 61.34%

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 97.00% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.57% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.68% 85.14%
CHEMBL2581 P07339 Cathepsin D 88.92% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.86% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.85% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.19% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 85.37% 90.20%
CHEMBL4208 P20618 Proteasome component C5 84.51% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.74% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.77% 89.62%

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.
Laguncularia racemosa

Cross-Links

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PubChem 162987621
LOTUS LTS0270303
wikiData Q104915022