3-Heptadec-10-enyl-5-methoxyphenol

Details

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Internal ID 58f4c9d3-bc1b-49db-aa86-43471be7bc60
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3-heptadec-10-enyl-5-methoxyphenol
SMILES (Canonical) CCCCCCC=CCCCCCCCCCC1=CC(=CC(=C1)OC)O
SMILES (Isomeric) CCCCCCC=CCCCCCCCCCC1=CC(=CC(=C1)OC)O
InChI InChI=1S/C24H40O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22-19-23(25)21-24(20-22)26-2/h8-9,19-21,25H,3-7,10-18H2,1-2H3
InChI Key AAKAGTMRUVKJKR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H40O2
Molecular Weight 360.60 g/mol
Exact Mass 360.302830514 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 9.50
Atomic LogP (AlogP) 7.59
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Heptadec-10-enyl-5-methoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.6783 67.83%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6125 61.25%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.7107 71.07%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8527 85.27%
P-glycoprotein inhibitior + 0.5932 59.32%
P-glycoprotein substrate - 0.7459 74.59%
CYP3A4 substrate + 0.5065 50.65%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.3925 39.25%
CYP3A4 inhibition - 0.6086 60.86%
CYP2C9 inhibition - 0.8387 83.87%
CYP2C19 inhibition + 0.5757 57.57%
CYP2D6 inhibition - 0.7869 78.69%
CYP1A2 inhibition + 0.7271 72.71%
CYP2C8 inhibition + 0.7301 73.01%
CYP inhibitory promiscuity + 0.5871 58.71%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6875 68.75%
Carcinogenicity (trinary) Non-required 0.6895 68.95%
Eye corrosion - 0.7557 75.57%
Eye irritation + 0.6475 64.75%
Skin irritation + 0.5518 55.18%
Skin corrosion - 0.7488 74.88%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8517 85.17%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7165 71.65%
skin sensitisation + 0.7768 77.68%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5101 51.01%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7239 72.39%
Acute Oral Toxicity (c) III 0.8197 81.97%
Estrogen receptor binding + 0.7582 75.82%
Androgen receptor binding + 0.6863 68.63%
Thyroid receptor binding + 0.5797 57.97%
Glucocorticoid receptor binding - 0.5196 51.96%
Aromatase binding - 0.6266 62.66%
PPAR gamma + 0.6776 67.76%
Honey bee toxicity - 0.9574 95.74%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.8437 84.37%
Fish aquatic toxicity + 0.9851 98.51%

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 98.47% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.11% 99.17%
CHEMBL2581 P07339 Cathepsin D 97.32% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.22% 91.11%
CHEMBL240 Q12809 HERG 96.20% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.27% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.67% 97.29%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 89.25% 92.68%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.99% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 88.37% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.16% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.65% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.21% 94.45%
CHEMBL1907 P15144 Aminopeptidase N 84.83% 93.31%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.84% 91.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.87% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.24% 95.89%
CHEMBL2885 P07451 Carbonic anhydrase III 80.49% 87.45%
CHEMBL1781 P11387 DNA topoisomerase I 80.22% 97.00%

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.
Iris sibirica

Cross-Links

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PubChem 162958541
LOTUS LTS0236800
wikiData Q104907981