5-Bromo-2-(3,7-dimethylocta-2,6-dienyl)-4-methoxyphenol

Details

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Internal ID 91eff03c-8ea7-43fd-b846-c981bf8eab5a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 5-bromo-2-(3,7-dimethylocta-2,6-dienyl)-4-methoxyphenol
SMILES (Canonical) CC(=CCCC(=CCC1=CC(=C(C=C1O)Br)OC)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=CC(=C(C=C1O)Br)OC)C)C
InChI InChI=1S/C17H23BrO2/c1-12(2)6-5-7-13(3)8-9-14-10-17(20-4)15(18)11-16(14)19/h6,8,10-11,19H,5,7,9H2,1-4H3
InChI Key XJQXXTLWABCJIB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H23BrO2
Molecular Weight 339.30 g/mol
Exact Mass 338.08814 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.40
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Bromo-2-(3,7-dimethylocta-2,6-dienyl)-4-methoxyphenol

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 + 0.8739 87.39%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8378 83.78%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.8928 89.28%
OATP1B3 inhibitior + 0.9200 92.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.5783 57.83%
P-glycoprotein inhibitior - 0.7533 75.33%
P-glycoprotein substrate - 0.8775 87.75%
CYP3A4 substrate - 0.5407 54.07%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.3971 39.71%
CYP3A4 inhibition - 0.6154 61.54%
CYP2C9 inhibition - 0.5893 58.93%
CYP2C19 inhibition + 0.5317 53.17%
CYP2D6 inhibition - 0.8585 85.85%
CYP1A2 inhibition + 0.5560 55.60%
CYP2C8 inhibition - 0.6411 64.11%
CYP inhibitory promiscuity + 0.5936 59.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6780 67.80%
Carcinogenicity (trinary) Non-required 0.6390 63.90%
Eye corrosion - 0.9571 95.71%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7323 73.23%
Skin corrosion - 0.9130 91.30%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6867 68.67%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6628 66.28%
Acute Oral Toxicity (c) III 0.6346 63.46%
Estrogen receptor binding + 0.8478 84.78%
Androgen receptor binding - 0.6863 68.63%
Thyroid receptor binding + 0.6392 63.92%
Glucocorticoid receptor binding + 0.6027 60.27%
Aromatase binding + 0.5818 58.18%
PPAR gamma + 0.8711 87.11%
Honey bee toxicity - 0.8856 88.56%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.50% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.45% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.35% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.14% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.67% 89.62%
CHEMBL2581 P07339 Cathepsin D 90.87% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.53% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.64% 86.33%
CHEMBL2535 P11166 Glucose transporter 87.11% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.42% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.93% 94.73%
CHEMBL4208 P20618 Proteasome component C5 83.23% 90.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.74% 97.21%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.36% 92.94%

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 73817255
LOTUS LTS0021898
wikiData Q105329150