3-Methoxy-5-nonadecylphenol

Details

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Internal ID 7e4ce714-3ff1-434f-9439-32d6c898fd82
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3-methoxy-5-nonadecylphenol
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCC1=CC(=CC(=C1)OC)O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCC1=CC(=CC(=C1)OC)O
InChI InChI=1S/C26H46O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24-21-25(27)23-26(22-24)28-2/h21-23,27H,3-20H2,1-2H3
InChI Key HDBBJFCAMCORCA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H46O2
Molecular Weight 390.60 g/mol
Exact Mass 390.349780706 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 11.50
Atomic LogP (AlogP) 8.59
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 19

Synonyms

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126882-75-5
SCHEMBL21925060
DTXSID90567798
5-nonadecylresorcinol monomethyl ether

2D Structure

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2D Structure of 3-Methoxy-5-nonadecylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.6497 64.97%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.7409 74.09%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.8319 83.19%
OATP1B3 inhibitior + 0.9284 92.84%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6714 67.14%
P-glycoprotein inhibitior - 0.5359 53.59%
P-glycoprotein substrate - 0.6992 69.92%
CYP3A4 substrate - 0.5424 54.24%
CYP2C9 substrate - 0.5890 58.90%
CYP2D6 substrate + 0.4683 46.83%
CYP3A4 inhibition - 0.6849 68.49%
CYP2C9 inhibition - 0.8262 82.62%
CYP2C19 inhibition + 0.5296 52.96%
CYP2D6 inhibition - 0.7905 79.05%
CYP1A2 inhibition + 0.6818 68.18%
CYP2C8 inhibition + 0.6839 68.39%
CYP inhibitory promiscuity - 0.6031 60.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6732 67.32%
Carcinogenicity (trinary) Non-required 0.6897 68.97%
Eye corrosion - 0.5990 59.90%
Eye irritation + 0.5955 59.55%
Skin irritation + 0.5265 52.65%
Skin corrosion - 0.5851 58.51%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6615 66.15%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6300 63.00%
skin sensitisation + 0.6973 69.73%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.5069 50.69%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.5900 59.00%
Acute Oral Toxicity (c) III 0.8388 83.88%
Estrogen receptor binding + 0.5959 59.59%
Androgen receptor binding + 0.6483 64.83%
Thyroid receptor binding + 0.6140 61.40%
Glucocorticoid receptor binding - 0.6188 61.88%
Aromatase binding - 0.5703 57.03%
PPAR gamma + 0.7139 71.39%
Honey bee toxicity - 0.9715 97.15%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9643 96.43%

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 97.72% 92.08%
CHEMBL2581 P07339 Cathepsin D 97.00% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.85% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.41% 99.17%
CHEMBL240 Q12809 HERG 95.31% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.85% 91.11%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 93.45% 92.68%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.05% 97.29%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.38% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.48% 94.73%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.27% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.83% 96.95%
CHEMBL1907 P15144 Aminopeptidase N 84.83% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 82.46% 87.45%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.87% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.24% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.82% 91.71%

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.
Artemisia annua

Cross-Links

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PubChem 15071190
NPASS NPC21484