3-Hydroxybenzyl alcohol

Details

Top
Internal ID d6ccc21e-3ed3-47c7-8aff-7258457d8be1
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl alcohols
IUPAC Name 3-(hydroxymethyl)phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H8O2/c8-5-6-2-1-3-7(9)4-6/h1-4,8-9H,5H2
InChI Key OKVJCVWFVRATSG-UHFFFAOYSA-N
Popularity 141 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H8O2
Molecular Weight 124.14 g/mol
Exact Mass 124.052429494 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.88
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
620-24-6
3-(Hydroxymethyl)phenol
Benzenemethanol, 3-hydroxy-
3-Hydroxybenzenemethanol
m-Hydroxybenzyl alcohol
Benzyl alcohol, m-hydroxy-
KSD 2405
3-Hydroxybenzylalcohol
MFCD00004643
3-Hydroxymethyl-phenol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 3-Hydroxybenzyl alcohol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 + 0.8930 89.30%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8149 81.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8895 88.95%
OATP1B3 inhibitior + 0.9364 93.64%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9589 95.89%
P-glycoprotein inhibitior - 0.9887 98.87%
P-glycoprotein substrate - 0.9331 93.31%
CYP3A4 substrate - 0.7401 74.01%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.6798 67.98%
CYP3A4 inhibition - 0.8244 82.44%
CYP2C9 inhibition - 0.9108 91.08%
CYP2C19 inhibition - 0.7071 70.71%
CYP2D6 inhibition - 0.9536 95.36%
CYP1A2 inhibition - 0.5881 58.81%
CYP2C8 inhibition - 0.7865 78.65%
CYP inhibitory promiscuity - 0.6402 64.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6637 66.37%
Carcinogenicity (trinary) Non-required 0.6708 67.08%
Eye corrosion + 0.5495 54.95%
Eye irritation + 0.9947 99.47%
Skin irritation + 0.7843 78.43%
Skin corrosion - 0.5256 52.56%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8117 81.17%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation + 0.8612 86.12%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.7389 73.89%
Acute Oral Toxicity (c) III 0.4281 42.81%
Estrogen receptor binding - 0.8384 83.84%
Androgen receptor binding - 0.7493 74.93%
Thyroid receptor binding - 0.8330 83.30%
Glucocorticoid receptor binding - 0.8457 84.57%
Aromatase binding - 0.7532 75.32%
PPAR gamma - 0.6188 61.88%
Honey bee toxicity - 0.9624 96.24%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.5814 58.14%

Targets

Top

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 94.24% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.06% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.11% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.54% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.88% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.62% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.43% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.42% 91.71%

Plants that contains it

Top
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.
Festuca rubra

Cross-Links

Top
PubChem 102
LOTUS LTS0055760
wikiData Q27102196