Anisole

Details

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Internal ID 90dedcbe-755c-4383-9cae-13137daf880a
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name anisole
SMILES (Canonical) COC1=CC=CC=C1
SMILES (Isomeric) COC1=CC=CC=C1
InChI InChI=1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3
InChI Key RDOXTESZEPMUJZ-UHFFFAOYSA-N
Popularity 7,189 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O
Molecular Weight 108.14 g/mol
Exact Mass 108.057514874 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.70
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Methoxybenzene
100-66-3
Methyl phenyl ether
Benzene, methoxy-
Anisol
Phenyl methyl ether
Phenoxymethane
Anizol
Phenol methyl ether
Ether, methyl phenyl
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Anisole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.9372 93.72%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7654 76.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9680 96.80%
OATP1B3 inhibitior + 0.9832 98.32%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9261 92.61%
P-glycoprotein inhibitior - 0.9912 99.12%
P-glycoprotein substrate - 0.9909 99.09%
CYP3A4 substrate - 0.7573 75.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4320 43.20%
CYP3A4 inhibition - 0.9712 97.12%
CYP2C9 inhibition - 0.9566 95.66%
CYP2C19 inhibition - 0.8114 81.14%
CYP2D6 inhibition - 0.9569 95.69%
CYP1A2 inhibition + 0.7172 71.72%
CYP2C8 inhibition - 0.9287 92.87%
CYP inhibitory promiscuity - 0.7740 77.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5558 55.58%
Carcinogenicity (trinary) Warning 0.5292 52.92%
Eye corrosion + 0.9709 97.09%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.7815 78.15%
Skin corrosion - 0.6003 60.03%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7218 72.18%
Micronuclear - 0.9219 92.19%
Hepatotoxicity - 0.5290 52.90%
skin sensitisation + 0.7743 77.43%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5598 55.98%
Acute Oral Toxicity (c) III 0.8222 82.22%
Estrogen receptor binding - 0.9534 95.34%
Androgen receptor binding - 0.8255 82.55%
Thyroid receptor binding - 0.8816 88.16%
Glucocorticoid receptor binding - 0.9093 90.93%
Aromatase binding - 0.9349 93.49%
PPAR gamma - 0.9204 92.04%
Honey bee toxicity - 0.9764 97.64%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.9600 96.00%
Fish aquatic toxicity - 0.4330 43.30%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3729 P22748 Carbonic anhydrase IV 14320 nM
Ki
PMID: 22687439

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.64% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 88.27% 90.17%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.91% 94.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.41% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.89% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.36% 94.62%
CHEMBL2581 P07339 Cathepsin D 81.04% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.80% 96.00%
CHEMBL4208 P20618 Proteasome component C5 80.55% 90.00%

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 abrotanoides
Cannabis sativa
Capsicum annuum
Foeniculum vulgare
Helianthus tuberosus
Manilkara zapota
Perilla frutescens
Peristeria elata
Plectranthus ovatus
Sauromatum venosum
Zizania aquatica

Cross-Links

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PubChem 7519
NPASS NPC124576
ChEMBL CHEMBL278024
LOTUS LTS0013639
wikiData Q312244