(3-Ethylphenyl)methanol

Details

Top
Internal ID aa14325d-ac58-4009-9d01-fe99f0ec1e50
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyl alcohols
IUPAC Name (3-ethylphenyl)methanol
SMILES (Canonical) CCC1=CC(=CC=C1)CO
SMILES (Isomeric) CCC1=CC(=CC=C1)CO
InChI InChI=1S/C9H12O/c1-2-8-4-3-5-9(6-8)7-10/h3-6,10H,2,7H2,1H3
InChI Key JBXKSUUBAYVELX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12O
Molecular Weight 136.19 g/mol
Exact Mass 136.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
82657-69-0
3-Ethylbenzenemethanol
53957-34-9
Benzenemethanol, 3-ethyl-
3-Ethylphenylmethanol
3-ethylbenzyl alcohol
ar-Ethylbenzenemethanol
methylbenzylal-cohol
(3-ethyl phenyl)methanol
SCHEMBL283086
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of (3-Ethylphenyl)methanol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.9358 93.58%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4634 46.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8967 89.67%
OATP1B3 inhibitior + 0.9504 95.04%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8559 85.59%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9369 93.69%
CYP3A4 substrate - 0.7496 74.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3571 35.71%
CYP3A4 inhibition - 0.9352 93.52%
CYP2C9 inhibition - 0.8699 86.99%
CYP2C19 inhibition - 0.8176 81.76%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition - 0.5528 55.28%
CYP2C8 inhibition - 0.8646 86.46%
CYP inhibitory promiscuity - 0.8299 82.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6758 67.58%
Eye corrosion + 0.8631 86.31%
Eye irritation + 0.9961 99.61%
Skin irritation + 0.6799 67.99%
Skin corrosion - 0.9589 95.89%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7609 76.09%
Micronuclear - 0.8941 89.41%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation + 0.7937 79.37%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7275 72.75%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.8064 80.64%
Acute Oral Toxicity (c) III 0.7922 79.22%
Estrogen receptor binding - 0.8937 89.37%
Androgen receptor binding - 0.7833 78.33%
Thyroid receptor binding - 0.7989 79.89%
Glucocorticoid receptor binding - 0.8077 80.77%
Aromatase binding - 0.8885 88.85%
PPAR gamma - 0.7523 75.23%
Honey bee toxicity - 0.9806 98.06%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.7454 74.54%

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 97.06% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.71% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.29% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.00% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 81.30% 95.93%

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.
Cedronella canariensis

Cross-Links

Top
PubChem 104659
LOTUS LTS0198456
wikiData Q82951654