Methyl oxo(2,4,6-trihydroxyphenyl)acetate

Details

Top
Internal ID a819f6a7-7ffa-443a-8758-6c06861292ab
Taxonomy Benzenoids > Phenols > Benzenetriols and derivatives > Phloroglucinols and derivatives > Acylphloroglucinols and derivatives
IUPAC Name methyl 2-oxo-2-(2,4,6-trihydroxyphenyl)acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H8O6/c1-15-9(14)8(13)7-5(11)2-4(10)3-6(7)12/h2-3,10-12H,1H3
InChI Key HPGNGFWXXNDGHL-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H8O6
Molecular Weight 212.16 g/mol
Exact Mass 212.03208797 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.16
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Methyl oxo(2,4,6-trihydroxyphenyl)acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8914 89.14%
Caco-2 - 0.6236 62.36%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7773 77.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9575 95.75%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9204 92.04%
P-glycoprotein inhibitior - 0.9550 95.50%
P-glycoprotein substrate - 0.9600 96.00%
CYP3A4 substrate - 0.6413 64.13%
CYP2C9 substrate - 0.8157 81.57%
CYP2D6 substrate - 0.8607 86.07%
CYP3A4 inhibition - 0.9494 94.94%
CYP2C9 inhibition - 0.7403 74.03%
CYP2C19 inhibition - 0.9146 91.46%
CYP2D6 inhibition - 0.9464 94.64%
CYP1A2 inhibition - 0.9104 91.04%
CYP2C8 inhibition - 0.8511 85.11%
CYP inhibitory promiscuity - 0.9315 93.15%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7448 74.48%
Carcinogenicity (trinary) Non-required 0.7487 74.87%
Eye corrosion - 0.7791 77.91%
Eye irritation + 0.9754 97.54%
Skin irritation + 0.6160 61.60%
Skin corrosion - 0.7810 78.10%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7589 75.89%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7764 77.64%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.6797 67.97%
Acute Oral Toxicity (c) III 0.4873 48.73%
Estrogen receptor binding + 0.7662 76.62%
Androgen receptor binding + 0.5274 52.74%
Thyroid receptor binding - 0.7323 73.23%
Glucocorticoid receptor binding + 0.5501 55.01%
Aromatase binding - 0.6450 64.50%
PPAR gamma - 0.6941 69.41%
Honey bee toxicity - 0.9396 93.96%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8957 89.57%

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 96.11% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.30% 96.09%
CHEMBL4208 P20618 Proteasome component C5 88.11% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.04% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 84.35% 94.73%
CHEMBL2581 P07339 Cathepsin D 82.06% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.75% 94.45%
CHEMBL2535 P11166 Glucose transporter 80.49% 98.75%

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.
Allium cepa

Cross-Links

Top
PubChem 129850613
LOTUS LTS0249575
wikiData Q105031695