1-Heptadec-10-enyl-3,5-dimethoxybenzene

Details

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Internal ID 7717079e-e178-466d-8103-f7adcd42c25e
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name 1-heptadec-10-enyl-3,5-dimethoxybenzene
SMILES (Canonical) CCCCCCC=CCCCCCCCCCC1=CC(=CC(=C1)OC)OC
SMILES (Isomeric) CCCCCCC=CCCCCCCCCCC1=CC(=CC(=C1)OC)OC
InChI InChI=1S/C25H42O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-23-20-24(26-2)22-25(21-23)27-3/h9-10,20-22H,4-8,11-19H2,1-3H3
InChI Key RHNOVGQCBCXKQI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H42O2
Molecular Weight 374.60 g/mol
Exact Mass 374.318480578 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 9.90
Atomic LogP (AlogP) 7.89
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Heptadec-10-enyl-3,5-dimethoxybenzene

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 + 0.6731 67.31%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5061 50.61%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.7229 72.29%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9050 90.50%
P-glycoprotein inhibitior + 0.6673 66.73%
P-glycoprotein substrate - 0.7493 74.93%
CYP3A4 substrate - 0.5462 54.62%
CYP2C9 substrate - 0.5856 58.56%
CYP2D6 substrate + 0.3999 39.99%
CYP3A4 inhibition - 0.7606 76.06%
CYP2C9 inhibition - 0.8860 88.60%
CYP2C19 inhibition - 0.5496 54.96%
CYP2D6 inhibition - 0.8567 85.67%
CYP1A2 inhibition + 0.6812 68.12%
CYP2C8 inhibition + 0.5299 52.99%
CYP inhibitory promiscuity + 0.5681 56.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6675 66.75%
Carcinogenicity (trinary) Non-required 0.6526 65.26%
Eye corrosion - 0.7727 77.27%
Eye irritation - 0.4862 48.62%
Skin irritation - 0.5991 59.91%
Skin corrosion - 0.9288 92.88%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8486 84.86%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7342 73.42%
skin sensitisation + 0.6211 62.11%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.5188 51.88%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.7522 75.22%
Acute Oral Toxicity (c) III 0.8261 82.61%
Estrogen receptor binding + 0.7416 74.16%
Androgen receptor binding + 0.6359 63.59%
Thyroid receptor binding + 0.5838 58.38%
Glucocorticoid receptor binding - 0.4849 48.49%
Aromatase binding - 0.6128 61.28%
PPAR gamma + 0.5655 56.55%
Honey bee toxicity - 0.9569 95.69%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.9300 93.00%
Fish aquatic toxicity + 0.9882 98.82%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 99.08% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.55% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.61% 98.95%
CHEMBL240 Q12809 HERG 94.84% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.81% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 91.21% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.80% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.60% 86.33%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 85.55% 90.24%
CHEMBL3401 O75469 Pregnane X receptor 85.48% 94.73%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 85.47% 90.75%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.47% 97.29%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.68% 96.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.16% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 83.96% 87.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.65% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.57% 96.95%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 83.38% 92.68%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.47% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.06% 95.56%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.62% 86.67%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.05% 99.18%

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 85087989
LOTUS LTS0257717
wikiData Q105236528