2,5-Dimethoxy-3-undecylphenol

Details

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Internal ID 1704948b-77b6-4f08-889e-b59771bd4105
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2,5-dimethoxy-3-undecylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H32O3/c1-4-5-6-7-8-9-10-11-12-13-16-14-17(21-2)15-18(20)19(16)22-3/h14-15,20H,4-13H2,1-3H3
InChI Key IXMXPKGDLIPGOO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H32O3
Molecular Weight 308.50 g/mol
Exact Mass 308.23514488 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 7.20
Atomic LogP (AlogP) 5.48
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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SCHEMBL15229247

2D Structure

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2D Structure of 2,5-Dimethoxy-3-undecylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.9105 91.05%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8433 84.33%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9061 90.61%
OATP1B3 inhibitior + 0.9346 93.46%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7418 74.18%
P-glycoprotein inhibitior - 0.5750 57.50%
P-glycoprotein substrate - 0.8368 83.68%
CYP3A4 substrate - 0.5635 56.35%
CYP2C9 substrate - 0.5890 58.90%
CYP2D6 substrate + 0.4683 46.83%
CYP3A4 inhibition - 0.7567 75.67%
CYP2C9 inhibition - 0.7900 79.00%
CYP2C19 inhibition + 0.5420 54.20%
CYP2D6 inhibition - 0.8425 84.25%
CYP1A2 inhibition + 0.5512 55.12%
CYP2C8 inhibition + 0.6740 67.40%
CYP inhibitory promiscuity - 0.6511 65.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7543 75.43%
Carcinogenicity (trinary) Non-required 0.6532 65.32%
Eye corrosion - 0.8891 88.91%
Eye irritation - 0.5248 52.48%
Skin irritation - 0.6253 62.53%
Skin corrosion - 0.7724 77.24%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8614 86.14%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation + 0.5417 54.17%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5411 54.11%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.6000 60.00%
Acute Oral Toxicity (c) III 0.7215 72.15%
Estrogen receptor binding + 0.7795 77.95%
Androgen receptor binding - 0.6116 61.16%
Thyroid receptor binding + 0.8056 80.56%
Glucocorticoid receptor binding - 0.5789 57.89%
Aromatase binding - 0.5243 52.43%
PPAR gamma + 0.8083 80.83%
Honey bee toxicity - 0.9782 97.82%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7560 75.60%
Fish aquatic toxicity + 0.9856 98.56%

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 98.21% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.79% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.03% 99.17%
CHEMBL240 Q12809 HERG 94.49% 89.76%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 94.18% 92.68%
CHEMBL2581 P07339 Cathepsin D 93.05% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.66% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.07% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.31% 96.95%
CHEMBL1907 P15144 Aminopeptidase N 84.02% 93.31%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.56% 97.29%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.35% 92.62%
CHEMBL4208 P20618 Proteasome component C5 80.88% 90.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.46% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 80.04% 94.73%

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.
Averrhoa carambola

Cross-Links

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PubChem 89782462
LOTUS LTS0140098
wikiData Q105122269