2-(3,7-Dimethylocta-2,6-dien-1-yl)benzene-1,4-diol

Details

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Internal ID f55241b8-f1e4-4b15-92c9-d131d218962f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylated hydroquinones
IUPAC Name 2-(3,7-dimethylocta-2,6-dienyl)benzene-1,4-diol
SMILES (Canonical) CC(=CCCC(=CCC1=C(C=CC(=C1)O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=C(C=CC(=C1)O)O)C)C
InChI InChI=1S/C16H22O2/c1-12(2)5-4-6-13(3)7-8-14-11-15(17)9-10-16(14)18/h5,7,9-11,17-18H,4,6,8H2,1-3H3
InChI Key ZSCRTFONTNMQBL-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O2
Molecular Weight 246.34 g/mol
Exact Mass 246.161979940 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.33
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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DTXSID90864274

2D Structure

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2D Structure of 2-(3,7-Dimethylocta-2,6-dien-1-yl)benzene-1,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7570 75.70%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8162 81.62%
OATP2B1 inhibitior - 0.7107 71.07%
OATP1B1 inhibitior + 0.9079 90.79%
OATP1B3 inhibitior + 0.9168 91.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5074 50.74%
P-glycoprotein inhibitior - 0.9498 94.98%
P-glycoprotein substrate - 0.9151 91.51%
CYP3A4 substrate - 0.6291 62.91%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate + 0.3876 38.76%
CYP3A4 inhibition + 0.6903 69.03%
CYP2C9 inhibition + 0.5278 52.78%
CYP2C19 inhibition + 0.6199 61.99%
CYP2D6 inhibition - 0.7539 75.39%
CYP1A2 inhibition + 0.8353 83.53%
CYP2C8 inhibition - 0.7831 78.31%
CYP inhibitory promiscuity + 0.8054 80.54%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7139 71.39%
Carcinogenicity (trinary) Non-required 0.6806 68.06%
Eye corrosion - 0.9285 92.85%
Eye irritation + 0.6681 66.81%
Skin irritation - 0.6375 63.75%
Skin corrosion - 0.7649 76.49%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4469 44.69%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.7793 77.93%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6152 61.52%
Acute Oral Toxicity (c) III 0.6035 60.35%
Estrogen receptor binding + 0.6971 69.71%
Androgen receptor binding + 0.6351 63.51%
Thyroid receptor binding + 0.5761 57.61%
Glucocorticoid receptor binding + 0.6078 60.78%
Aromatase binding - 0.5843 58.43%
PPAR gamma + 0.8556 85.56%
Honey bee toxicity - 0.9315 93.15%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6100 61.00%
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 98.46% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.89% 92.08%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 92.68% 93.10%
CHEMBL3401 O75469 Pregnane X receptor 92.44% 94.73%
CHEMBL2581 P07339 Cathepsin D 91.76% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 88.20% 83.57%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.29% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.98% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.94% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.92% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.56% 94.45%
CHEMBL4208 P20618 Proteasome component C5 84.26% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.19% 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.
Cordia elaeagnoides
Lithospermum erythrorhizon
Phacelia crenulata

Cross-Links

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PubChem 160941
LOTUS LTS0250350
wikiData Q105382440