4-Phenyl-2-butanol

Details

Top
Internal ID d9ae131e-7282-4d9b-846f-acba7499eb78
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 4-phenylbutan-2-ol
SMILES (Canonical) CC(CCC1=CC=CC=C1)O
SMILES (Isomeric) CC(CCC1=CC=CC=C1)O
InChI InChI=1S/C10H14O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6,9,11H,7-8H2,1H3
InChI Key GDWRKZLROIFUML-UHFFFAOYSA-N
Popularity 121 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
4-Phenylbutan-2-ol
2344-70-9
1-Phenyl-3-butanol
BENZENEPROPANOL, ALPHA-METHYL-
Methylphenethylcarbinol
2-Butanol, 4-phenyl-
2-Hydroxy-4-phenylbutane
FEMA No. 2879
Benzenepropanol, .alpha.-methyl-
SZ2IE5UDQR
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 4-Phenyl-2-butanol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.9164 91.64%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5319 53.19%
OATP2B1 inhibitior - 0.8717 87.17%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8686 86.86%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.7922 79.22%
CYP3A4 substrate - 0.7206 72.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4365 43.65%
CYP3A4 inhibition - 0.9226 92.26%
CYP2C9 inhibition - 0.9402 94.02%
CYP2C19 inhibition - 0.8129 81.29%
CYP2D6 inhibition - 0.8791 87.91%
CYP1A2 inhibition + 0.6152 61.52%
CYP2C8 inhibition - 0.9812 98.12%
CYP inhibitory promiscuity - 0.8931 89.31%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6711 67.11%
Carcinogenicity (trinary) Non-required 0.6932 69.32%
Eye corrosion + 0.5867 58.67%
Eye irritation + 0.7789 77.89%
Skin irritation + 0.9156 91.56%
Skin corrosion + 0.5599 55.99%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6718 67.18%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5306 53.06%
skin sensitisation + 0.8575 85.75%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity - 0.6171 61.71%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.8213 82.13%
Acute Oral Toxicity (c) III 0.6275 62.75%
Estrogen receptor binding - 0.8731 87.31%
Androgen receptor binding - 0.7072 70.72%
Thyroid receptor binding - 0.8591 85.91%
Glucocorticoid receptor binding - 0.7627 76.27%
Aromatase binding - 0.9371 93.71%
PPAR gamma - 0.7964 79.64%
Honey bee toxicity - 0.9685 96.85%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.4229 42.29%

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 97.64% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.32% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.00% 94.62%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 88.10% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 87.42% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 85.78% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.38% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.11% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 82.89% 93.31%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.51% 95.50%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.96% 93.81%

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.
Artemisia xanthochroa

Cross-Links

Top
PubChem 61302
LOTUS LTS0222632
wikiData Q27289473