2,6-Dimethylanisole

Details

Top
Internal ID 6d68f01d-d892-4bea-b823-9ed1ea5bbca6
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 2-methoxy-1,3-dimethylbenzene
SMILES (Canonical) CC1=C(C(=CC=C1)C)OC
SMILES (Isomeric) CC1=C(C(=CC=C1)C)OC
InChI InChI=1S/C9H12O/c1-7-5-4-6-8(2)9(7)10-3/h4-6H,1-3H3
InChI Key GFNZJAUVJCGWLW-UHFFFAOYSA-N
Popularity 45 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12O
Molecular Weight 136.19 g/mol
Exact Mass 136.088815002 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
1004-66-6
2-Methoxy-1,3-dimethylbenzene
Benzene, 2-methoxy-1,3-dimethyl-
2-Methoxy-m-xylene
EINECS 213-723-3
MFCD00008380
AI3-21152
NSC62672
2,6-dimethyl anisole
2,6-Dimethylanisole, 98%
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2,6-Dimethylanisole

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.9179 91.79%
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 + 0.9797 97.97%
OATP1B3 inhibitior + 0.9796 97.96%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9120 91.20%
P-glycoprotein inhibitior - 0.9860 98.60%
P-glycoprotein substrate - 0.9843 98.43%
CYP3A4 substrate - 0.7288 72.88%
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 - 0.9039 90.39%
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 + 0.9949 99.49%
Skin irritation + 0.5798 57.98%
Skin corrosion - 0.6891 68.91%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6186 61.86%
Micronuclear - 0.9441 94.41%
Hepatotoxicity + 0.7034 70.34%
skin sensitisation + 0.6637 66.37%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.7219 72.19%
Acute Oral Toxicity (c) III 0.8329 83.29%
Estrogen receptor binding - 0.9590 95.90%
Androgen receptor binding - 0.9631 96.31%
Thyroid receptor binding - 0.8438 84.38%
Glucocorticoid receptor binding - 0.9258 92.58%
Aromatase binding - 0.8965 89.65%
PPAR gamma - 0.8890 88.90%
Honey bee toxicity - 0.9822 98.22%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7600 76.00%
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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.32% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 86.22% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.20% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.68% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.20% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.48% 96.09%
CHEMBL2535 P11166 Glucose transporter 80.18% 98.75%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

Top
PubChem 66088
NPASS NPC275669