2-Allyl-6-methylphenol

Details

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Internal ID 9dba7ac1-1154-460f-9579-b184c33d530f
Taxonomy Benzenoids > Phenols > Cresols > Ortho cresols
IUPAC Name 2-methyl-6-prop-2-enylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H12O/c1-3-5-9-7-4-6-8(2)10(9)11/h3-4,6-7,11H,1,5H2,2H3
InChI Key WREVCRYZAWNLRZ-UHFFFAOYSA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.43
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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3354-58-3
6-Allyl-o-cresol
Phenol, 2-methyl-6-(2-propenyl)-
2-ALLYL-6-METHYL-PHENOL
2-methyl-6-(prop-2-en-1-yl)phenol
2-methyl-6-allylphenol
BGU079WOI3
EINECS 222-124-6
NSC-60286
AI3-17108
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-Allyl-6-methylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8325 83.25%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7632 76.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8876 88.76%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8800 88.00%
P-glycoprotein inhibitior - 0.9853 98.53%
P-glycoprotein substrate - 0.9558 95.58%
CYP3A4 substrate - 0.6570 65.70%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate + 0.3876 38.76%
CYP3A4 inhibition - 0.8633 86.33%
CYP2C9 inhibition - 0.8275 82.75%
CYP2C19 inhibition - 0.6446 64.46%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition + 0.5104 51.04%
CYP2C8 inhibition - 0.7079 70.79%
CYP inhibitory promiscuity + 0.5360 53.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6150 61.50%
Carcinogenicity (trinary) Non-required 0.6631 66.31%
Eye corrosion + 0.9517 95.17%
Eye irritation + 0.9565 95.65%
Skin irritation + 0.6959 69.59%
Skin corrosion + 0.9484 94.84%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7564 75.64%
Micronuclear - 0.7593 75.93%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.9783 97.83%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6135 61.35%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.7505 75.05%
Acute Oral Toxicity (c) III 0.5093 50.93%
Estrogen receptor binding - 0.7897 78.97%
Androgen receptor binding - 0.7582 75.82%
Thyroid receptor binding - 0.8028 80.28%
Glucocorticoid receptor binding - 0.7985 79.85%
Aromatase binding - 0.7993 79.93%
PPAR gamma - 0.6882 68.82%
Honey bee toxicity - 0.9654 96.54%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9776 97.76%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.65% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.78% 94.73%
CHEMBL2581 P07339 Cathepsin D 90.27% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.23% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 87.39% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.79% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 76883
NPASS NPC79457