p-Methoxybenzyl p-anisate

Details

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Internal ID 004028fa-fee4-46dd-b239-e12e9bdeff80
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > P-methoxybenzoic acids and derivatives
IUPAC Name (4-methoxyphenyl)methyl 4-methoxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H16O4/c1-18-14-7-3-12(4-8-14)11-20-16(17)13-5-9-15(19-2)10-6-13/h3-10H,11H2,1-2H3
InChI Key PUXJRQHDLYGOCY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O4
Molecular Weight 272.29 g/mol
Exact Mass 272.10485899 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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24318-43-2
4-methoxybenzyl 4-methoxybenzoate
(4-methoxyphenyl)methyl 4-methoxybenzoate
MH827WPN5X
NSC-78835
Benzoic acid, 4-methoxy-, (4-methoxyphenyl)methyl ester
NSC78835
EINECS 246-159-1
AI3-18958
UNII-MH827WPN5X
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of p-Methoxybenzyl p-anisate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9303 93.03%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.9199 91.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9370 93.70%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5917 59.17%
P-glycoprotein inhibitior - 0.6920 69.20%
P-glycoprotein substrate - 0.9585 95.85%
CYP3A4 substrate - 0.6145 61.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7841 78.41%
CYP3A4 inhibition - 0.7887 78.87%
CYP2C9 inhibition - 0.6845 68.45%
CYP2C19 inhibition + 0.5710 57.10%
CYP2D6 inhibition - 0.9381 93.81%
CYP1A2 inhibition + 0.8617 86.17%
CYP2C8 inhibition + 0.4703 47.03%
CYP inhibitory promiscuity + 0.7383 73.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6609 66.09%
Carcinogenicity (trinary) Non-required 0.6750 67.50%
Eye corrosion - 0.9517 95.17%
Eye irritation + 0.9429 94.29%
Skin irritation - 0.8639 86.39%
Skin corrosion - 0.9972 99.72%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4323 43.23%
Micronuclear - 0.5293 52.93%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.9384 93.84%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7533 75.33%
Acute Oral Toxicity (c) III 0.7910 79.10%
Estrogen receptor binding + 0.8086 80.86%
Androgen receptor binding + 0.8669 86.69%
Thyroid receptor binding + 0.5471 54.71%
Glucocorticoid receptor binding + 0.5761 57.61%
Aromatase binding + 0.7317 73.17%
PPAR gamma + 0.6441 64.41%
Honey bee toxicity - 0.9585 95.85%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9728 97.28%

Targets

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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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.12% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.72% 99.17%
CHEMBL4208 P20618 Proteasome component C5 93.37% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.34% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.30% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.19% 90.24%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.92% 85.31%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.31% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.96% 90.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.86% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.10% 95.56%
CHEMBL2535 P11166 Glucose transporter 82.79% 98.75%
CHEMBL3437 Q16853 Amine oxidase, copper containing 81.35% 94.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.59% 87.67%

Plants that contains it

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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.
Euryops floribundus

Cross-Links

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PubChem 90465
LOTUS LTS0029728
wikiData Q83049586