2,4,6-Trimethoxyphenol

Details

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Internal ID e8a0cccd-af2c-48e8-a690-b45244d2c8b7
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2,4,6-trimethoxyphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O4/c1-11-6-4-7(12-2)9(10)8(5-6)13-3/h4-5,10H,1-3H3
InChI Key HSJYYLNJWGKZMD-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O4
Molecular Weight 184.19 g/mol
Exact Mass 184.07355886 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.42
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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20491-92-3
Phenol, 2,4,6-trimethoxy-
4MJL0GD54W
EINECS 243-851-5
UNII-4MJL0GD54W
CHEMBL225314
SCHEMBL1047550
DTXSID70174469
HSJYYLNJWGKZMD-UHFFFAOYSA-N
MFCD00017159
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4,6-Trimethoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9822 98.22%
Caco-2 + 0.5215 52.15%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8262 82.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9743 97.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9332 93.32%
P-glycoprotein inhibitior - 0.9644 96.44%
P-glycoprotein substrate - 0.9614 96.14%
CYP3A4 substrate - 0.7222 72.22%
CYP2C9 substrate - 0.7845 78.45%
CYP2D6 substrate + 0.4222 42.22%
CYP3A4 inhibition - 0.8694 86.94%
CYP2C9 inhibition - 0.9924 99.24%
CYP2C19 inhibition - 0.8607 86.07%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.7735 77.35%
CYP2C8 inhibition - 0.8024 80.24%
CYP inhibitory promiscuity - 0.7873 78.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7550 75.50%
Carcinogenicity (trinary) Non-required 0.6154 61.54%
Eye corrosion + 0.5237 52.37%
Eye irritation + 0.9896 98.96%
Skin irritation + 0.5505 55.05%
Skin corrosion - 0.9130 91.30%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7817 78.17%
Micronuclear - 0.6467 64.67%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.6669 66.69%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6478 64.78%
Acute Oral Toxicity (c) III 0.6473 64.73%
Estrogen receptor binding - 0.5459 54.59%
Androgen receptor binding - 0.7327 73.27%
Thyroid receptor binding - 0.5744 57.44%
Glucocorticoid receptor binding - 0.7281 72.81%
Aromatase binding - 0.7555 75.55%
PPAR gamma - 0.7110 71.10%
Honey bee toxicity - 0.9722 97.22%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.6351 63.51%
Fish aquatic toxicity + 0.7813 78.13%

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 95.49% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.33% 96.09%
CHEMBL4208 P20618 Proteasome component C5 87.85% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.66% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.30% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.12% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.54% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.17% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.59% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.27% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.24% 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.
Croton lechleri

Cross-Links

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PubChem 88563
LOTUS LTS0112378
wikiData Q72513814