3-(14-Phenyltetradecyl)phenol

Details

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Internal ID f4deeb38-3c8f-4244-994f-364e477e859c
Taxonomy Benzenoids > Phenols > 1-hydroxy-4-unsubstituted benzenoids
IUPAC Name 3-(14-phenyltetradecyl)phenol
SMILES (Canonical) C1=CC=C(C=C1)CCCCCCCCCCCCCCC2=CC(=CC=C2)O
SMILES (Isomeric) C1=CC=C(C=C1)CCCCCCCCCCCCCCC2=CC(=CC=C2)O
InChI InChI=1S/C26H38O/c27-26-22-16-21-25(23-26)20-13-10-8-6-4-2-1-3-5-7-9-12-17-24-18-14-11-15-19-24/h11,14-16,18-19,21-23,27H,1-10,12-13,17,20H2
InChI Key NKIVMWHPFMFYBF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H38O
Molecular Weight 366.60 g/mol
Exact Mass 366.292265831 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 10.30
Atomic LogP (AlogP) 7.86
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(14-Phenyltetradecyl)phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 - 0.6030 60.30%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8153 81.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9142 91.42%
OATP1B3 inhibitior + 0.9191 91.91%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.4738 47.38%
P-glycoprotein inhibitior - 0.4608 46.08%
P-glycoprotein substrate - 0.7246 72.46%
CYP3A4 substrate - 0.6028 60.28%
CYP2C9 substrate - 0.8036 80.36%
CYP2D6 substrate + 0.4561 45.61%
CYP3A4 inhibition - 0.7649 76.49%
CYP2C9 inhibition + 0.5410 54.10%
CYP2C19 inhibition + 0.6362 63.62%
CYP2D6 inhibition - 0.9033 90.33%
CYP1A2 inhibition + 0.6186 61.86%
CYP2C8 inhibition + 0.7420 74.20%
CYP inhibitory promiscuity + 0.6210 62.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7011 70.11%
Carcinogenicity (trinary) Non-required 0.5660 56.60%
Eye corrosion - 0.6047 60.47%
Eye irritation + 0.6096 60.96%
Skin irritation + 0.5446 54.46%
Skin corrosion + 0.5140 51.40%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8238 82.38%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5459 54.59%
skin sensitisation + 0.6397 63.97%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6099 60.99%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7653 76.53%
Acute Oral Toxicity (c) III 0.7277 72.77%
Estrogen receptor binding + 0.8042 80.42%
Androgen receptor binding + 0.7149 71.49%
Thyroid receptor binding + 0.7338 73.38%
Glucocorticoid receptor binding - 0.6450 64.50%
Aromatase binding + 0.6253 62.53%
PPAR gamma + 0.7971 79.71%
Honey bee toxicity - 0.9573 95.73%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5550 55.50%
Fish aquatic toxicity + 0.9666 96.66%

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 96.75% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.81% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.73% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.96% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.53% 96.09%
CHEMBL5805 Q9NR97 Toll-like receptor 8 88.40% 96.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.52% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.17% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 86.59% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.38% 91.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.20% 95.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.46% 93.81%
CHEMBL3891 P07384 Calpain 1 82.57% 93.04%
CHEMBL3761 Q9HCG7 Beta-glucosidase 81.76% 99.00%
CHEMBL2535 P11166 Glucose transporter 81.01% 98.75%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 80.23% 100.00%

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.
Tapirira obtusa

Cross-Links

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PubChem 90726277
LOTUS LTS0128590
wikiData Q105180613