3-(4-hydroxy-3,5-dimethoxy-phenyl)propyl Benzoate

Details

Top
Internal ID d7939c45-6e1b-4607-af4c-6fbb81218723
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 3-(4-hydroxy-3,5-dimethoxyphenyl)propyl benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H20O5/c1-21-15-11-13(12-16(22-2)17(15)19)7-6-10-23-18(20)14-8-4-3-5-9-14/h3-5,8-9,11-12,19H,6-7,10H2,1-2H3
InChI Key COFCMLKODGVUBA-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H20O5
Molecular Weight 316.30 g/mol
Exact Mass 316.13107373 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

Top
Benzenepropanol, 4-hydroxy-3,5-dimethoxy-, benzoate

2D Structure

Top
2D Structure of 3-(4-hydroxy-3,5-dimethoxy-phenyl)propyl Benzoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9796 97.96%
Caco-2 + 0.7481 74.81%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.9434 94.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8217 82.17%
OATP1B3 inhibitior + 0.9392 93.92%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7277 72.77%
P-glycoprotein inhibitior - 0.5091 50.91%
P-glycoprotein substrate - 0.6962 69.62%
CYP3A4 substrate + 0.5481 54.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7372 73.72%
CYP3A4 inhibition - 0.8491 84.91%
CYP2C9 inhibition + 0.5778 57.78%
CYP2C19 inhibition + 0.6423 64.23%
CYP2D6 inhibition - 0.9102 91.02%
CYP1A2 inhibition + 0.6723 67.23%
CYP2C8 inhibition + 0.9171 91.71%
CYP inhibitory promiscuity - 0.6592 65.92%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7943 79.43%
Carcinogenicity (trinary) Non-required 0.7359 73.59%
Eye corrosion - 0.9814 98.14%
Eye irritation + 0.7500 75.00%
Skin irritation - 0.8198 81.98%
Skin corrosion - 0.9858 98.58%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5941 59.41%
Micronuclear - 0.6575 65.75%
Hepatotoxicity - 0.5841 58.41%
skin sensitisation - 0.9195 91.95%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.8195 81.95%
Acute Oral Toxicity (c) III 0.8118 81.18%
Estrogen receptor binding + 0.8949 89.49%
Androgen receptor binding + 0.7269 72.69%
Thyroid receptor binding + 0.6406 64.06%
Glucocorticoid receptor binding + 0.7159 71.59%
Aromatase binding + 0.5459 54.59%
PPAR gamma + 0.6592 65.92%
Honey bee toxicity - 0.9610 96.10%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9071 90.71%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.10% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.73% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.17% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.92% 99.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.67% 95.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.86% 91.11%
CHEMBL2535 P11166 Glucose transporter 88.96% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 86.27% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.36% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.77% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.16% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 80.13% 94.73%

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.
Croton hutchinsonianus
Croton laevigatus

Cross-Links

Top
PubChem 11623835
LOTUS LTS0272151
wikiData Q104966829