2,4,6-Trichloroanisole

Details

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Internal ID 77e47c2b-5b93-4099-9682-6c5ef73b2427
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 1,3,5-trichloro-2-methoxybenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H5Cl3O/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H3
InChI Key WCVOGSZTONGSQY-UHFFFAOYSA-N
Popularity 322 references in papers

Physical and Chemical Properties

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Molecular Formula C7H5Cl3O
Molecular Weight 211.50 g/mol
Exact Mass 209.940598 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.66
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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87-40-1
1,3,5-Trichloro-2-methoxybenzene
Tyrene
2,4,6-Trichloro-1-methoxybenzene
TRICHLOROANISOLE
Benzene, 1,3,5-trichloro-2-methoxy-
Methyl 2,4,6-trichlorophenyl ether
Anisole, 2,4,6-trichloro-
2,4.6-Trichloroanisole
1,3,5-trichloro-2-methoxy-benzene
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-Trichloroanisole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8864 88.64%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.8519 85.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9730 97.30%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8522 85.22%
P-glycoprotein inhibitior - 0.9779 97.79%
P-glycoprotein substrate - 0.9946 99.46%
CYP3A4 substrate - 0.6419 64.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3695 36.95%
CYP3A4 inhibition - 0.9250 92.50%
CYP2C9 inhibition - 0.7240 72.40%
CYP2C19 inhibition + 0.7738 77.38%
CYP2D6 inhibition - 0.9209 92.09%
CYP1A2 inhibition + 0.8965 89.65%
CYP2C8 inhibition - 0.8415 84.15%
CYP inhibitory promiscuity + 0.5233 52.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5325 53.25%
Carcinogenicity (trinary) Warning 0.4922 49.22%
Eye corrosion + 0.9197 91.97%
Eye irritation + 0.9720 97.20%
Skin irritation + 0.6503 65.03%
Skin corrosion + 0.8178 81.78%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6292 62.92%
Micronuclear - 0.8410 84.10%
Hepatotoxicity + 0.7200 72.00%
skin sensitisation + 0.7525 75.25%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6494 64.94%
Acute Oral Toxicity (c) III 0.6590 65.90%
Estrogen receptor binding - 0.8061 80.61%
Androgen receptor binding - 0.7236 72.36%
Thyroid receptor binding + 0.5272 52.72%
Glucocorticoid receptor binding - 0.7585 75.85%
Aromatase binding - 0.7274 72.74%
PPAR gamma - 0.6237 62.37%
Honey bee toxicity - 0.9415 94.15%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.8982 89.82%
Fish aquatic toxicity + 0.9396 93.96%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.57% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.27% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.90% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.46% 94.73%
CHEMBL4208 P20618 Proteasome component C5 85.09% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.62% 94.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.23% 86.92%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.14% 94.03%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.73% 97.21%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.59% 96.00%
CHEMBL5957 P21589 5'-nucleotidase 80.20% 97.78%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.13% 100.00%

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.
Achillea ageratifolia

Cross-Links

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PubChem 6884
LOTUS LTS0009361
wikiData Q105379025