4-Methoxy-2,3,6-trimethylphenol

Details

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Internal ID 2bf9ce94-fc7d-4ea5-b7be-9b73ceec30e1
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 4-methoxy-2,3,6-trimethylphenol
SMILES (Canonical) CC1=CC(=C(C(=C1O)C)C)OC
SMILES (Isomeric) CC1=CC(=C(C(=C1O)C)C)OC
InChI InChI=1S/C10H14O2/c1-6-5-9(12-4)7(2)8(3)10(6)11/h5,11H,1-4H3
InChI Key SJIRRMZHJWPOCJ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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53651-61-9
4-Methoxy-2,3,6-trimethyl-phenol
NSC168489
SCHEMBL24407972
DTXSID30304947
SJIRRMZHJWPOCJ-UHFFFAOYSA-N
2,3,6-trimethyl-4-methoxyphenol
MFCD24713549
4-Methoxy-2,3,6-trimethylphenol #
AKOS022519819
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methoxy-2,3,6-trimethylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.6348 63.48%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.8942 89.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.9735 97.35%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9160 91.60%
P-glycoprotein inhibitior - 0.9615 96.15%
P-glycoprotein substrate - 0.9684 96.84%
CYP3A4 substrate - 0.6611 66.11%
CYP2C9 substrate - 0.7529 75.29%
CYP2D6 substrate + 0.3984 39.84%
CYP3A4 inhibition - 0.9282 92.82%
CYP2C9 inhibition - 0.9870 98.70%
CYP2C19 inhibition - 0.8695 86.95%
CYP2D6 inhibition - 0.9381 93.81%
CYP1A2 inhibition - 0.5529 55.29%
CYP2C8 inhibition - 0.7332 73.32%
CYP inhibitory promiscuity - 0.7721 77.21%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6372 63.72%
Carcinogenicity (trinary) Non-required 0.5886 58.86%
Eye corrosion + 0.8156 81.56%
Eye irritation + 0.9687 96.87%
Skin irritation + 0.7221 72.21%
Skin corrosion - 0.7113 71.13%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7376 73.76%
Micronuclear - 0.8867 88.67%
Hepatotoxicity + 0.5940 59.40%
skin sensitisation + 0.7195 71.95%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.7831 78.31%
Acute Oral Toxicity (c) III 0.8484 84.84%
Estrogen receptor binding - 0.5629 56.29%
Androgen receptor binding - 0.5560 55.60%
Thyroid receptor binding - 0.6967 69.67%
Glucocorticoid receptor binding - 0.7067 70.67%
Aromatase binding - 0.7403 74.03%
PPAR gamma - 0.7627 76.27%
Honey bee toxicity - 0.9654 96.54%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.7335 73.35%

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 92.30% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.38% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.27% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.74% 86.33%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.86% 89.62%
CHEMBL4208 P20618 Proteasome component C5 82.00% 90.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.42% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.82% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.16% 99.15%

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.
Thymus quinquecostatus
Thymus vulgaris

Cross-Links

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PubChem 297360
NPASS NPC211493