4-Hydroxybenzyl alcohol

Details

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Internal ID b3095d9a-1320-4eb9-a123-4294767c653e
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl alcohols
IUPAC Name 4-(hydroxymethyl)phenol
SMILES (Canonical) C1=CC(=CC=C1CO)O
SMILES (Isomeric) C1=CC(=CC=C1CO)O
InChI InChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2
InChI Key BVJSUAQZOZWCKN-UHFFFAOYSA-N
Popularity 711 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O2
Molecular Weight 124.14 g/mol
Exact Mass 124.052429494 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.88
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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623-05-2
4-(Hydroxymethyl)phenol
p-Hydroxybenzyl alcohol
p-Methylolphenol
4-Methylolphenol
4-Hydroxybenzenemethanol
Benzenemethanol, 4-hydroxy-
4-Hydroxybenzylalcohol
p-(Hydroxymethyl)phenol
Benzyl alcohol, p-hydroxy-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Hydroxybenzyl alcohol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.9486 94.86%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8158 81.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8684 86.84%
OATP1B3 inhibitior + 0.9273 92.73%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9606 96.06%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9734 97.34%
CYP3A4 substrate - 0.7812 78.12%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.6798 67.98%
CYP3A4 inhibition - 0.8755 87.55%
CYP2C9 inhibition - 0.9496 94.96%
CYP2C19 inhibition - 0.7145 71.45%
CYP2D6 inhibition - 0.9733 97.33%
CYP1A2 inhibition - 0.6005 60.05%
CYP2C8 inhibition - 0.7324 73.24%
CYP inhibitory promiscuity - 0.7086 70.86%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6348 63.48%
Carcinogenicity (trinary) Non-required 0.6749 67.49%
Eye corrosion + 0.6755 67.55%
Eye irritation + 0.9969 99.69%
Skin irritation + 0.8260 82.60%
Skin corrosion - 0.6286 62.86%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8504 85.04%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation + 0.9214 92.14%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.6538 65.38%
Acute Oral Toxicity (c) II 0.4871 48.71%
Estrogen receptor binding - 0.7545 75.45%
Androgen receptor binding - 0.5782 57.82%
Thyroid receptor binding - 0.8426 84.26%
Glucocorticoid receptor binding - 0.8734 87.34%
Aromatase binding - 0.7525 75.25%
PPAR gamma - 0.6859 68.59%
Honey bee toxicity - 0.9467 94.67%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.6062 60.62%

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 87.94% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 87.33% 98.35%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.27% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.19% 96.09%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.43% 93.10%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.46% 91.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.87% 99.17%

Cross-Links

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PubChem 125
NPASS NPC300478
LOTUS LTS0094565
wikiData Q5526828