Methyl 3-(2,4,5-trimethoxyphenyl)propionate

Details

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Internal ID 1e8734eb-f3f6-4d63-b439-97cc7dfc0949
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name methyl 3-(2,4,5-trimethoxyphenyl)propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O5/c1-15-10-8-12(17-3)11(16-2)7-9(10)5-6-13(14)18-4/h7-8H,5-6H2,1-4H3
InChI Key SULPGCHHOCMNSJ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O5
Molecular Weight 254.28 g/mol
Exact Mass 254.11542367 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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RefChem:157416
Methyl 3-(2,4,5-trimethoxyphenyl)propanoate
2,4,5-Trimethoxyhydrocinnamic acid methyl ester
CHEMBL506090

2D Structure

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2D Structure of Methyl 3-(2,4,5-trimethoxyphenyl)propionate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.9382 93.82%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8653 86.53%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8368 83.68%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5701 57.01%
P-glycoprotein inhibitior - 0.9163 91.63%
P-glycoprotein substrate - 0.8390 83.90%
CYP3A4 substrate - 0.6198 61.98%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7516 75.16%
CYP3A4 inhibition - 0.9175 91.75%
CYP2C9 inhibition - 0.9130 91.30%
CYP2C19 inhibition - 0.5336 53.36%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.6377 63.77%
CYP2C8 inhibition - 0.7897 78.97%
CYP inhibitory promiscuity - 0.7765 77.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7043 70.43%
Carcinogenicity (trinary) Non-required 0.6673 66.73%
Eye corrosion - 0.9075 90.75%
Eye irritation + 0.6486 64.86%
Skin irritation - 0.7489 74.89%
Skin corrosion - 0.9786 97.86%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4852 48.52%
Micronuclear - 0.8241 82.41%
Hepatotoxicity - 0.6289 62.89%
skin sensitisation - 0.9008 90.08%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.5865 58.65%
Acute Oral Toxicity (c) III 0.7764 77.64%
Estrogen receptor binding + 0.5811 58.11%
Androgen receptor binding - 0.8678 86.78%
Thyroid receptor binding - 0.5346 53.46%
Glucocorticoid receptor binding + 0.6240 62.40%
Aromatase binding - 0.5345 53.45%
PPAR gamma - 0.7122 71.22%
Honey bee toxicity - 0.9254 92.54%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8870 88.70%

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 97.13% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.63% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.23% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.24% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.47% 96.00%
CHEMBL2535 P11166 Glucose transporter 86.35% 98.75%
CHEMBL4208 P20618 Proteasome component C5 84.73% 90.00%
CHEMBL2581 P07339 Cathepsin D 82.81% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.47% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.77% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.19% 96.95%

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.
Cordia alliodora

Cross-Links

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PubChem 10377602
LOTUS LTS0073622
wikiData Q105261058