4-(3-Ethenyl-3,7-dimethylocta-1,6-dienyl)phenol

Details

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Internal ID 39e0e2fd-a1f1-4daf-b2e9-fddd80da59ba
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 4-(3-ethenyl-3,7-dimethylocta-1,6-dienyl)phenol
SMILES (Canonical) CC(=CCCC(C)(C=C)C=CC1=CC=C(C=C1)O)C
SMILES (Isomeric) CC(=CCCC(C)(C=C)C=CC1=CC=C(C=C1)O)C
InChI InChI=1S/C18H24O/c1-5-18(4,13-6-7-15(2)3)14-12-16-8-10-17(19)11-9-16/h5,7-12,14,19H,1,6,13H2,2-4H3
InChI Key LFYJSSARVMHQJB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H24O
Molecular Weight 256.40 g/mol
Exact Mass 256.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.34
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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MFCD01707441
SY068327

2D Structure

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2D Structure of 4-(3-Ethenyl-3,7-dimethylocta-1,6-dienyl)phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8976 89.76%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.4256 42.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8598 85.98%
OATP1B3 inhibitior + 0.8857 88.57%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7868 78.68%
P-glycoprotein inhibitior - 0.9206 92.06%
P-glycoprotein substrate - 0.8756 87.56%
CYP3A4 substrate - 0.5536 55.36%
CYP2C9 substrate + 0.5905 59.05%
CYP2D6 substrate - 0.7077 70.77%
CYP3A4 inhibition + 0.5132 51.32%
CYP2C9 inhibition - 0.7029 70.29%
CYP2C19 inhibition - 0.5504 55.04%
CYP2D6 inhibition - 0.8489 84.89%
CYP1A2 inhibition - 0.5296 52.96%
CYP2C8 inhibition - 0.5712 57.12%
CYP inhibitory promiscuity - 0.6012 60.12%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6739 67.39%
Carcinogenicity (trinary) Non-required 0.6675 66.75%
Eye corrosion - 0.7297 72.97%
Eye irritation + 0.5455 54.55%
Skin irritation + 0.6737 67.37%
Skin corrosion - 0.7091 70.91%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7501 75.01%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8947 89.47%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.7539 75.39%
Acute Oral Toxicity (c) III 0.8897 88.97%
Estrogen receptor binding + 0.8989 89.89%
Androgen receptor binding + 0.6997 69.97%
Thyroid receptor binding + 0.6861 68.61%
Glucocorticoid receptor binding - 0.5634 56.34%
Aromatase binding + 0.7842 78.42%
PPAR gamma + 0.7449 74.49%
Honey bee toxicity - 0.8399 83.99%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9886 98.86%

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 94.10% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 91.23% 98.35%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.08% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 88.66% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 88.13% 94.73%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 87.74% 90.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.16% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.46% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.59% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.69% 95.56%

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.
Cullen corylifolium
Spiraea formosana

Cross-Links

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PubChem 500216
LOTUS LTS0010760
wikiData Q105151218