Benzenemethanol, alpha-methoxy-, benzoate

Details

Top
Internal ID 23ff38c9-9b15-4cee-9e55-f51851b593c0
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name [methoxy(phenyl)methyl] benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O3/c1-17-15(13-10-6-3-7-11-13)18-14(16)12-8-4-2-5-9-12/h2-11,15H,1H3
InChI Key ASEDDVACKHIDHS-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H14O3
Molecular Weight 242.27 g/mol
Exact Mass 242.094294304 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
Benzenemethanol, .alpha.-methoxy-, benzoate
Methoxy(phenyl)methyl benzoate #
ASEDDVACKHIDHS-UHFFFAOYSA-N

2D Structure

Top
2D Structure of Benzenemethanol, alpha-methoxy-, benzoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8381 83.81%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7949 79.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9480 94.80%
OATP1B3 inhibitior + 0.9768 97.68%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5996 59.96%
P-glycoprotein inhibitior - 0.8600 86.00%
P-glycoprotein substrate - 0.9530 95.30%
CYP3A4 substrate - 0.6722 67.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8325 83.25%
CYP3A4 inhibition - 0.9667 96.67%
CYP2C9 inhibition - 0.8917 89.17%
CYP2C19 inhibition - 0.7318 73.18%
CYP2D6 inhibition - 0.9685 96.85%
CYP1A2 inhibition + 0.8175 81.75%
CYP2C8 inhibition - 0.8770 87.70%
CYP inhibitory promiscuity - 0.6034 60.34%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5013 50.13%
Carcinogenicity (trinary) Non-required 0.6238 62.38%
Eye corrosion - 0.5669 56.69%
Eye irritation + 0.7131 71.31%
Skin irritation - 0.5488 54.88%
Skin corrosion - 0.9371 93.71%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4377 43.77%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.7232 72.32%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5167 51.67%
Acute Oral Toxicity (c) IV 0.5326 53.26%
Estrogen receptor binding + 0.5481 54.81%
Androgen receptor binding - 0.6903 69.03%
Thyroid receptor binding - 0.7955 79.55%
Glucocorticoid receptor binding - 0.8736 87.36%
Aromatase binding + 0.6401 64.01%
PPAR gamma - 0.7685 76.85%
Honey bee toxicity - 0.9112 91.12%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.9665 96.65%

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
CHEMBL221 P23219 Cyclooxygenase-1 91.88% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.07% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.27% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.92% 95.56%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.48% 94.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.47% 96.09%
CHEMBL2535 P11166 Glucose transporter 86.32% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 85.35% 90.20%
CHEMBL4267 P37173 TGF-beta receptor type II 83.54% 88.18%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.29% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.12% 95.50%

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.
Uvaria chamae

Cross-Links

Top
PubChem 578269
LOTUS LTS0228609
wikiData Q104376111