(S)-4-(1-Hydroxyallyl)phenyl acetate

Details

Top
Internal ID b91e47ba-b7f2-472f-98ed-df6044b73e99
Taxonomy Benzenoids > Phenol esters
IUPAC Name [4-[(1S)-1-hydroxyprop-2-enyl]phenyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O3/c1-3-11(13)9-4-6-10(7-5-9)14-8(2)12/h3-7,11,13H,1H2,2H3/t11-/m0/s1
InChI Key GKYVDAMMLMMJGZ-NSHDSACASA-N
Popularity 7 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H12O3
Molecular Weight 192.21 g/mol
Exact Mass 192.078644241 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
GKYVDAMMLMMJGZ-NSHDSACASA-N
(S)-4-(1-Hydroxyallyl)phenyl acetate
Benzenemethanol, 4-(acetyloxy)-.alpha.-ethenyl-, (.alpha.S)-

2D Structure

Top
2D Structure of (S)-4-(1-Hydroxyallyl)phenyl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.7905 79.05%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8472 84.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9443 94.43%
OATP1B3 inhibitior + 0.9761 97.61%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8535 85.35%
P-glycoprotein inhibitior - 0.9744 97.44%
P-glycoprotein substrate - 0.9690 96.90%
CYP3A4 substrate - 0.6499 64.99%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8363 83.63%
CYP3A4 inhibition - 0.7364 73.64%
CYP2C9 inhibition - 0.9353 93.53%
CYP2C19 inhibition - 0.8066 80.66%
CYP2D6 inhibition - 0.9723 97.23%
CYP1A2 inhibition - 0.7605 76.05%
CYP2C8 inhibition - 0.9467 94.67%
CYP inhibitory promiscuity - 0.9050 90.50%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.5940 59.40%
Eye corrosion + 0.6591 65.91%
Eye irritation + 0.9683 96.83%
Skin irritation + 0.6944 69.44%
Skin corrosion - 0.7764 77.64%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7426 74.26%
Micronuclear - 0.5586 55.86%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.5512 55.12%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6461 64.61%
Acute Oral Toxicity (c) III 0.8262 82.62%
Estrogen receptor binding - 0.5612 56.12%
Androgen receptor binding - 0.6653 66.53%
Thyroid receptor binding - 0.7815 78.15%
Glucocorticoid receptor binding - 0.8286 82.86%
Aromatase binding - 0.6352 63.52%
PPAR gamma - 0.6812 68.12%
Honey bee toxicity - 0.5956 59.56%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9783 97.83%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.02% 96.09%
CHEMBL4208 P20618 Proteasome component C5 93.22% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.08% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.39% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.37% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.36% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.17% 94.80%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.14% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.37% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.28% 86.33%

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.
Alpinia galanga

Cross-Links

Top
PubChem 21119823
NPASS NPC235250
LOTUS LTS0064806
wikiData Q105010563