2'Hydroxy-2,3,4',6'-tetramethoxychalcone

Details

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Internal ID 13fc2d8e-52d5-4325-9e52-befd1f6f3e06
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxychalcones
IUPAC Name 3-(2,3-dimethoxyphenyl)-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one
SMILES (Canonical) COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2OC)OC)O
SMILES (Isomeric) COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2OC)OC)O
InChI InChI=1S/C19H20O6/c1-22-13-10-15(21)18(17(11-13)24-3)14(20)9-8-12-6-5-7-16(23-2)19(12)25-4/h5-11,21H,1-4H3
InChI Key LYUYMCWIWGASRX-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O6
Molecular Weight 344.40 g/mol
Exact Mass 344.12598835 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2'Hydroxy-2,3,4',6'-tetramethoxychalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.9267 92.67%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8159 81.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9399 93.99%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7706 77.06%
P-glycoprotein inhibitior + 0.7800 78.00%
P-glycoprotein substrate - 0.8660 86.60%
CYP3A4 substrate + 0.5171 51.71%
CYP2C9 substrate - 0.8053 80.53%
CYP2D6 substrate - 0.8356 83.56%
CYP3A4 inhibition + 0.5168 51.68%
CYP2C9 inhibition - 0.9746 97.46%
CYP2C19 inhibition + 0.5781 57.81%
CYP2D6 inhibition - 0.9008 90.08%
CYP1A2 inhibition + 0.7048 70.48%
CYP2C8 inhibition + 0.7305 73.05%
CYP inhibitory promiscuity + 0.6325 63.25%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7825 78.25%
Carcinogenicity (trinary) Non-required 0.6008 60.08%
Eye corrosion - 0.9615 96.15%
Eye irritation - 0.6053 60.53%
Skin irritation - 0.7313 73.13%
Skin corrosion - 0.9864 98.64%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5564 55.64%
Micronuclear + 0.5733 57.33%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8715 87.15%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.4827 48.27%
Acute Oral Toxicity (c) III 0.6006 60.06%
Estrogen receptor binding + 0.9275 92.75%
Androgen receptor binding + 0.5852 58.52%
Thyroid receptor binding + 0.7290 72.90%
Glucocorticoid receptor binding + 0.6683 66.83%
Aromatase binding + 0.6407 64.07%
PPAR gamma + 0.6664 66.64%
Honey bee toxicity - 0.9388 93.88%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 0.9852 98.52%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.32% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.91% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.52% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.74% 96.09%
CHEMBL2535 P11166 Glucose transporter 93.72% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.71% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.27% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.00% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.66% 99.15%
CHEMBL3194 P02766 Transthyretin 89.19% 90.71%
CHEMBL2581 P07339 Cathepsin D 85.59% 98.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.64% 91.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.55% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.40% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 81.04% 90.20%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.81% 91.07%
CHEMBL4208 P20618 Proteasome component C5 80.80% 90.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.37% 91.19%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.33% 100.00%

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.
Caesalpinia pulcherrima

Cross-Links

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PubChem 53405570
LOTUS LTS0141461
wikiData Q105159595