3-Undecylphenol

Details

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Internal ID 27c2ed4c-0b42-4e03-82ae-acc5d07ce5d8
Taxonomy Benzenoids > Phenols > 1-hydroxy-4-unsubstituted benzenoids
IUPAC Name 3-undecylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H28O/c1-2-3-4-5-6-7-8-9-10-12-16-13-11-14-17(18)15-16/h11,13-15,18H,2-10,12H2,1H3
InChI Key HWIKMSXIILZULT-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O
Molecular Weight 248.40 g/mol
Exact Mass 248.214015512 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 7.30
Atomic LogP (AlogP) 5.47
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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CHEMBL465077
SCHEMBL6558135
DTXSID70632312
HWIKMSXIILZULT-UHFFFAOYSA-N
20056-72-8

2D Structure

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2D Structure of 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 + 0.9964 99.64%
Caco-2 + 0.9116 91.16%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6493 64.93%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.8711 87.11%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5974 59.74%
P-glycoprotein inhibitior - 0.8745 87.45%
P-glycoprotein substrate + 0.5126 51.26%
CYP3A4 substrate - 0.5640 56.40%
CYP2C9 substrate - 0.7842 78.42%
CYP2D6 substrate + 0.4159 41.59%
CYP3A4 inhibition - 0.7264 72.64%
CYP2C9 inhibition - 0.7677 76.77%
CYP2C19 inhibition - 0.6883 68.83%
CYP2D6 inhibition - 0.8666 86.66%
CYP1A2 inhibition + 0.6612 66.12%
CYP2C8 inhibition + 0.7039 70.39%
CYP inhibitory promiscuity - 0.5778 57.78%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7411 74.11%
Carcinogenicity (trinary) Non-required 0.6368 63.68%
Eye corrosion + 0.9682 96.82%
Eye irritation + 0.9471 94.71%
Skin irritation + 0.8441 84.41%
Skin corrosion + 0.9720 97.20%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7862 78.62%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6509 65.09%
skin sensitisation + 0.9116 91.16%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5247 52.47%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6898 68.98%
Acute Oral Toxicity (c) III 0.8513 85.13%
Estrogen receptor binding + 0.8299 82.99%
Androgen receptor binding - 0.5708 57.08%
Thyroid receptor binding + 0.7829 78.29%
Glucocorticoid receptor binding - 0.6445 64.45%
Aromatase binding - 0.5873 58.73%
PPAR gamma + 0.9082 90.82%
Honey bee toxicity - 0.9927 99.27%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7823 78.23%
Fish aquatic toxicity + 0.9867 98.67%

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
CHEMBL2581 P07339 Cathepsin D 98.95% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 98.00% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.25% 96.09%
CHEMBL240 Q12809 HERG 93.23% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.94% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.35% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 92.05% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.47% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 86.68% 93.31%
CHEMBL1951 P21397 Monoamine oxidase A 84.16% 91.49%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.46% 96.25%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.04% 91.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.38% 95.56%
CHEMBL2535 P11166 Glucose transporter 80.65% 98.75%

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.
Knema hookeriana
Schistochila appendiculata

Cross-Links

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PubChem 23274807
LOTUS LTS0089380
wikiData Q82539864