4-Hydroxy-3,5-dimethoxy-cinnamyl alcohol

Details

Top
Internal ID 6ad923a9-086e-453d-bd89-3e2a2c69cc36
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenol
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C=CCO
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)C=CCO
InChI InChI=1S/C11H14O4/c1-14-9-6-8(4-3-5-12)7-10(15-2)11(9)13/h3-4,6-7,12-13H,5H2,1-2H3
InChI Key LZFOPEXOUVTGJS-UHFFFAOYSA-N
Popularity 133 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H14O4
Molecular Weight 210.23 g/mol
Exact Mass 210.08920892 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
AKOS028113328
4-hydroxy-3,5-dimethoxy-cinnamyl alcohol
4-(3-Hydroxy-1-propen-1-yl)-2,6-dimethoxyphenol

2D Structure

Top
2D Structure of 4-Hydroxy-3,5-dimethoxy-cinnamyl alcohol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9779 97.79%
Caco-2 + 0.6267 62.67%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7812 78.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7933 79.33%
OATP1B3 inhibitior + 0.9726 97.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8751 87.51%
P-glycoprotein inhibitior - 0.9529 95.29%
P-glycoprotein substrate - 0.9297 92.97%
CYP3A4 substrate - 0.6506 65.06%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.6970 69.70%
CYP3A4 inhibition - 0.6052 60.52%
CYP2C9 inhibition - 0.8320 83.20%
CYP2C19 inhibition - 0.6156 61.56%
CYP2D6 inhibition - 0.8940 89.40%
CYP1A2 inhibition + 0.5341 53.41%
CYP2C8 inhibition - 0.6983 69.83%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7918 79.18%
Carcinogenicity (trinary) Non-required 0.7441 74.41%
Eye corrosion - 0.8984 89.84%
Eye irritation + 0.9622 96.22%
Skin irritation - 0.5921 59.21%
Skin corrosion - 0.9183 91.83%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8583 85.83%
Micronuclear - 0.6819 68.19%
Hepatotoxicity - 0.6214 62.14%
skin sensitisation + 0.7338 73.38%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6873 68.73%
Acute Oral Toxicity (c) III 0.7371 73.71%
Estrogen receptor binding + 0.5324 53.24%
Androgen receptor binding - 0.6041 60.41%
Thyroid receptor binding - 0.5342 53.42%
Glucocorticoid receptor binding - 0.5286 52.86%
Aromatase binding - 0.7162 71.62%
PPAR gamma - 0.5695 56.95%
Honey bee toxicity - 0.9377 93.77%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.7968 79.68%

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 97.03% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.63% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.87% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.73% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.86% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.91% 99.17%
CHEMBL3194 P02766 Transthyretin 83.40% 90.71%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.43% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 80.97% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.04% 86.92%

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.
Fagus grandifolia
Ginkgo biloba

Cross-Links

Top
PubChem 439703
LOTUS LTS0268592
wikiData Q105159850