4-Hydroxybenzene ethanol

Details

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Internal ID e21056fd-a610-489d-b903-d6905efa72ab
Taxonomy Benzenoids > Phenols > 1-hydroxy-4-unsubstituted benzenoids
IUPAC Name ethanol;phenol
SMILES (Canonical) CCO.C1=CC=C(C=C1)O
SMILES (Isomeric) CCO.C1=CC=C(C=C1)O
InChI InChI=1S/C6H6O.C2H6O/c7-6-4-2-1-3-5-6;1-2-3/h1-5,7H;3H,2H2,1H3
InChI Key XXWFDPVOXNJASB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O2
Molecular Weight 140.18 g/mol
Exact Mass 140.083729621 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 0.00
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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SCHEMBL247463

2D Structure

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2D Structure of 4-Hydroxybenzene ethanol

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 + 0.9538 95.38%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7872 78.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8850 88.50%
OATP1B3 inhibitior + 0.9298 92.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9385 93.85%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9693 96.93%
CYP3A4 substrate - 0.7999 79.99%
CYP2C9 substrate - 0.8204 82.04%
CYP2D6 substrate - 0.7268 72.68%
CYP3A4 inhibition - 0.8179 81.79%
CYP2C9 inhibition - 0.8804 88.04%
CYP2C19 inhibition - 0.6776 67.76%
CYP2D6 inhibition - 0.9675 96.75%
CYP1A2 inhibition + 0.6043 60.43%
CYP2C8 inhibition - 0.7501 75.01%
CYP inhibitory promiscuity - 0.6543 65.43%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6131 61.31%
Carcinogenicity (trinary) Non-required 0.6313 63.13%
Eye corrosion + 0.4805 48.05%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.6047 60.47%
Skin corrosion - 0.7907 79.07%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8723 87.23%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6051 60.51%
skin sensitisation + 0.8051 80.51%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.7235 72.35%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5062 50.62%
Acute Oral Toxicity (c) III 0.6912 69.12%
Estrogen receptor binding - 0.8832 88.32%
Androgen receptor binding - 0.7712 77.12%
Thyroid receptor binding - 0.8242 82.42%
Glucocorticoid receptor binding - 0.9009 90.09%
Aromatase binding - 0.8644 86.44%
PPAR gamma - 0.8340 83.40%
Honey bee toxicity - 0.9937 99.37%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.5000 50.00%

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 93.00% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.92% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.33% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.73% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.46% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.30% 95.56%

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.
Cistanche deserticola
Cistanche phelypaea

Cross-Links

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PubChem 17785442
NPASS NPC295589