2,4,6-Trimethylanisole

Details

Top
Internal ID b7808d23-a70d-4b1e-9675-92a65aed34c6
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 2-methoxy-1,3,5-trimethylbenzene
SMILES (Canonical) CC1=CC(=C(C(=C1)C)OC)C
SMILES (Isomeric) CC1=CC(=C(C(=C1)C)OC)C
InChI InChI=1S/C10H14O/c1-7-5-8(2)10(11-4)9(3)6-7/h5-6H,1-4H3
InChI Key NNVKEOMPDSKFGZ-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
4028-66-4
2-Methoxy-1,3,5-trimethylbenzene
Benzene, 2-methoxy-1,3,5-trimethyl-
Methoxymesitylene
Anisole, 2,4,6-trimethyl-
SCHEMBL129762
DTXSID20193266
1-methoxy-2,4,6-trimethylbenzene
MFCD03092887
2-Methoxy-1,3,5-trimethylbenzene #
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2,4,6-Trimethylanisole

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8137 81.37%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Mitochondria 0.8181 81.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9681 96.81%
OATP1B3 inhibitior + 0.9796 97.96%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8345 83.45%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.9895 98.95%
CYP3A4 substrate - 0.7572 75.72%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate + 0.3972 39.72%
CYP3A4 inhibition - 0.9540 95.40%
CYP2C9 inhibition - 0.9723 97.23%
CYP2C19 inhibition - 0.8160 81.60%
CYP2D6 inhibition - 0.9371 93.71%
CYP1A2 inhibition + 0.7645 76.45%
CYP2C8 inhibition - 0.9547 95.47%
CYP inhibitory promiscuity - 0.6109 61.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6360 63.60%
Carcinogenicity (trinary) Warning 0.4978 49.78%
Eye corrosion + 0.9375 93.75%
Eye irritation + 0.9728 97.28%
Skin irritation + 0.5798 57.98%
Skin corrosion - 0.6891 68.91%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6039 60.39%
Micronuclear - 0.9441 94.41%
Hepatotoxicity + 0.6659 66.59%
skin sensitisation + 0.6637 66.37%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.7710 77.10%
Acute Oral Toxicity (c) III 0.8329 83.29%
Estrogen receptor binding - 0.9373 93.73%
Androgen receptor binding - 0.8830 88.30%
Thyroid receptor binding - 0.7711 77.11%
Glucocorticoid receptor binding - 0.8765 87.65%
Aromatase binding - 0.8055 80.55%
PPAR gamma - 0.8608 86.08%
Honey bee toxicity - 0.9484 94.84%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.8385 83.85%

Targets

Top

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 84.50% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.26% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.35% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.07% 86.33%
CHEMBL4208 P20618 Proteasome component C5 81.15% 90.00%
CHEMBL2581 P07339 Cathepsin D 80.71% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.30% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.15% 94.00%

Plants that contains it

Top
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.
Elsholtzia ciliata
Mosla chinensis

Cross-Links

Top
PubChem 77648
NPASS NPC47392