2,3,5-Trimethoxytoluene

Details

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Internal ID 376861fa-1c0c-4fda-b3ab-732e6341f76f
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 1,2,5-trimethoxy-3-methylbenzene
SMILES (Canonical) CC1=CC(=CC(=C1OC)OC)OC
SMILES (Isomeric) CC1=CC(=CC(=C1OC)OC)OC
InChI InChI=1S/C10H14O3/c1-7-5-8(11-2)6-9(12-3)10(7)13-4/h5-6H,1-4H3
InChI Key HLFDEAPOXFIBPC-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O3
Molecular Weight 182.22 g/mol
Exact Mass 182.094294304 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1,2,5-Trimethoxy-3-methylbenzene
38790-14-6
benzene, 1,2,5-trimethoxy-3-methyl-
3,5,6-Trimethoxytoluene
SCHEMBL684136
DTXSID40192059
CHEBI:167414
HLFDEAPOXFIBPC-UHFFFAOYSA-N
InChI=1/C10H14O3/c1-7-5-8(11-2)6-9(12-3)10(7)13-4/h5-6H,1-4H

2D Structure

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2D Structure of 2,3,5-Trimethoxytoluene

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 + 0.8078 80.78%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.8420 84.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9667 96.67%
OATP1B3 inhibitior + 0.9852 98.52%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8657 86.57%
P-glycoprotein inhibitior - 0.9640 96.40%
P-glycoprotein substrate - 0.9764 97.64%
CYP3A4 substrate - 0.6776 67.76%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate + 0.3972 39.72%
CYP3A4 inhibition - 0.9251 92.51%
CYP2C9 inhibition - 0.9892 98.92%
CYP2C19 inhibition - 0.7868 78.68%
CYP2D6 inhibition - 0.9654 96.54%
CYP1A2 inhibition + 0.6001 60.01%
CYP2C8 inhibition - 0.7975 79.75%
CYP inhibitory promiscuity - 0.6083 60.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7450 74.50%
Carcinogenicity (trinary) Warning 0.4765 47.65%
Eye corrosion + 0.8222 82.22%
Eye irritation + 0.9811 98.11%
Skin irritation + 0.5900 59.00%
Skin corrosion - 0.9175 91.75%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4436 44.36%
Micronuclear - 0.6867 68.67%
Hepatotoxicity + 0.5085 50.85%
skin sensitisation - 0.6526 65.26%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.6574 65.74%
Acute Oral Toxicity (c) III 0.7868 78.68%
Estrogen receptor binding - 0.9201 92.01%
Androgen receptor binding - 0.8245 82.45%
Thyroid receptor binding - 0.7649 76.49%
Glucocorticoid receptor binding - 0.8891 88.91%
Aromatase binding - 0.8060 80.60%
PPAR gamma - 0.8912 89.12%
Honey bee toxicity - 0.9327 93.27%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.7957 79.57%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.19% 95.56%
CHEMBL4208 P20618 Proteasome component C5 87.16% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.11% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.38% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.71% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.20% 86.33%
CHEMBL2535 P11166 Glucose transporter 82.21% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 81.37% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.02% 99.17%

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.
Asarum heterotropoides
Asarum sieboldii

Cross-Links

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PubChem 170114
NPASS NPC149412