2,4,5-Trimethoxyphenol

Details

Top
Internal ID e70022b4-6608-438f-9e70-2c1a07b488ac
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2,4,5-trimethoxyphenol
SMILES (Canonical) COC1=CC(=C(C=C1O)OC)OC
SMILES (Isomeric) COC1=CC(=C(C=C1O)OC)OC
InChI InChI=1S/C9H12O4/c1-11-7-5-9(13-3)8(12-2)4-6(7)10/h4-5,10H,1-3H3
InChI Key QUPHIMRKLSEULX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12O4
Molecular Weight 184.19 g/mol
Exact Mass 184.07355886 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.42
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
20491-91-2
Asarylalkohol
1,2-Benzenedicarbonyldichloride
SCHEMBL1402467
MFCD17015434
NSC818361
STL576785
NSC-818361
AS-57806
CS-0036238
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2,4,5-Trimethoxyphenol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9822 98.22%
Caco-2 + 0.7736 77.36%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.8262 82.62%
OATP2B1 inhibitior - 0.8645 86.45%
OATP1B1 inhibitior + 0.8805 88.05%
OATP1B3 inhibitior + 0.9743 97.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8782 87.82%
P-glycoprotein inhibitior - 0.9622 96.22%
P-glycoprotein substrate - 0.9722 97.22%
CYP3A4 substrate - 0.7341 73.41%
CYP2C9 substrate - 0.7845 78.45%
CYP2D6 substrate + 0.4222 42.22%
CYP3A4 inhibition - 0.8694 86.94%
CYP2C9 inhibition - 0.9924 99.24%
CYP2C19 inhibition - 0.8607 86.07%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.7735 77.35%
CYP2C8 inhibition - 0.8696 86.96%
CYP inhibitory promiscuity - 0.7873 78.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7550 75.50%
Carcinogenicity (trinary) Non-required 0.6154 61.54%
Eye corrosion + 0.5237 52.37%
Eye irritation + 0.9904 99.04%
Skin irritation + 0.5505 55.05%
Skin corrosion - 0.9130 91.30%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6319 63.19%
Micronuclear - 0.6467 64.67%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.6669 66.69%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.4550 45.50%
Acute Oral Toxicity (c) III 0.6473 64.73%
Estrogen receptor binding - 0.7406 74.06%
Androgen receptor binding - 0.9174 91.74%
Thyroid receptor binding - 0.7023 70.23%
Glucocorticoid receptor binding - 0.8015 80.15%
Aromatase binding - 0.7993 79.93%
PPAR gamma - 0.8194 81.94%
Honey bee toxicity - 0.9519 95.19%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5851 58.51%
Fish aquatic toxicity + 0.7813 78.13%

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 92.63% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.21% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.19% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.99% 86.33%
CHEMBL2535 P11166 Glucose transporter 83.57% 98.75%
CHEMBL4208 P20618 Proteasome component C5 83.39% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.26% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.51% 94.00%
CHEMBL3194 P02766 Transthyretin 81.42% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.39% 99.17%

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.
Endiandra xanthocarpa
Helichrysum harveyanum
Hemsleya graciliflora
Senna lindheimeriana

Cross-Links

Top
PubChem 12445134
NPASS NPC122513
LOTUS LTS0007425
wikiData Q105228336