3-(13-Hydroxytridecyl)-5-methoxyphenol

Details

Top
Internal ID 28415537-74a9-4a77-8ce0-9d388f5b6ca2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name 3-(13-hydroxytridecyl)-5-methoxyphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H34O3/c1-23-20-16-18(15-19(22)17-20)13-11-9-7-5-3-2-4-6-8-10-12-14-21/h15-17,21-22H,2-14H2,1H3
InChI Key FFDLRYXXOUESQY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H34O3
Molecular Weight 322.50 g/mol
Exact Mass 322.25079494 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.23
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-(13-Hydroxytridecyl)-5-methoxyphenol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.6619 66.19%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.9173 91.73%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.8444 84.44%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7542 75.42%
BSEP inhibitior + 0.6014 60.14%
P-glycoprotein inhibitior - 0.6926 69.26%
P-glycoprotein substrate - 0.7984 79.84%
CYP3A4 substrate - 0.5283 52.83%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate + 0.4347 43.47%
CYP3A4 inhibition - 0.7967 79.67%
CYP2C9 inhibition - 0.9082 90.82%
CYP2C19 inhibition - 0.6015 60.15%
CYP2D6 inhibition - 0.9113 91.13%
CYP1A2 inhibition - 0.5395 53.95%
CYP2C8 inhibition + 0.5457 54.57%
CYP inhibitory promiscuity - 0.8500 85.00%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6794 67.94%
Eye corrosion - 0.9593 95.93%
Eye irritation + 0.6641 66.41%
Skin irritation - 0.7285 72.85%
Skin corrosion - 0.9639 96.39%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9225 92.25%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6527 65.27%
skin sensitisation - 0.7586 75.86%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6438 64.38%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5594 55.94%
Acute Oral Toxicity (c) III 0.7257 72.57%
Estrogen receptor binding + 0.6804 68.04%
Androgen receptor binding + 0.6483 64.83%
Thyroid receptor binding + 0.7499 74.99%
Glucocorticoid receptor binding - 0.5357 53.57%
Aromatase binding + 0.5374 53.74%
PPAR gamma + 0.8267 82.67%
Honey bee toxicity - 0.9385 93.85%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6807 68.07%
Fish aquatic toxicity - 0.6438 64.38%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.56% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.28% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.80% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.14% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.65% 86.92%
CHEMBL2885 P07451 Carbonic anhydrase III 87.13% 87.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.01% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.77% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.23% 95.89%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.53% 97.29%
CHEMBL4208 P20618 Proteasome component C5 81.88% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.31% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.23% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.18% 95.56%

Plants that contains it

Top
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.
Ononis viscosa

Cross-Links

Top
PubChem 101664466
LOTUS LTS0257276
wikiData Q104994374