2-Hydroxy-3,4,6-trimethoxychalcone

Details

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Internal ID 2dc2a1c9-0183-4d04-b0cc-ac75578ec9be
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Retrochalcones
IUPAC Name 3-(2-hydroxy-3,4,6-trimethoxyphenyl)-1-phenylprop-2-en-1-one
SMILES (Canonical) COC1=CC(=C(C(=C1C=CC(=O)C2=CC=CC=C2)O)OC)OC
SMILES (Isomeric) COC1=CC(=C(C(=C1C=CC(=O)C2=CC=CC=C2)O)OC)OC
InChI InChI=1S/C18H18O5/c1-21-15-11-16(22-2)18(23-3)17(20)13(15)9-10-14(19)12-7-5-4-6-8-12/h4-11,20H,1-3H3
InChI Key MNAQIJCVPFKJAU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H18O5
Molecular Weight 314.30 g/mol
Exact Mass 314.11542367 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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2-hydroxy-3,4,6-trimethoxychalcone

2D Structure

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2D Structure of 2-Hydroxy-3,4,6-trimethoxychalcone

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 + 0.8830 88.30%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8159 81.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9118 91.18%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6435 64.35%
P-glycoprotein inhibitior + 0.7876 78.76%
P-glycoprotein substrate - 0.9236 92.36%
CYP3A4 substrate - 0.5440 54.40%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7829 78.29%
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 + 0.9020 90.20%
CYP inhibitory promiscuity + 0.6325 63.25%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7825 78.25%
Carcinogenicity (trinary) Non-required 0.6008 60.08%
Eye corrosion - 0.9615 96.15%
Eye irritation + 0.7527 75.27%
Skin irritation - 0.7313 73.13%
Skin corrosion - 0.9864 98.64%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4528 45.28%
Micronuclear + 0.5733 57.33%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8715 87.15%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.7852 78.52%
Acute Oral Toxicity (c) III 0.6006 60.06%
Estrogen receptor binding + 0.9295 92.95%
Androgen receptor binding + 0.7011 70.11%
Thyroid receptor binding + 0.6446 64.46%
Glucocorticoid receptor binding + 0.6964 69.64%
Aromatase binding + 0.5459 54.59%
PPAR gamma + 0.6002 60.02%
Honey bee toxicity - 0.9326 93.26%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
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 96.09% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.71% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.81% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.04% 96.00%
CHEMBL2535 P11166 Glucose transporter 89.94% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.74% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.84% 93.99%
CHEMBL1255126 O15151 Protein Mdm4 86.80% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.15% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.71% 96.09%
CHEMBL2581 P07339 Cathepsin D 80.58% 98.95%
CHEMBL3194 P02766 Transthyretin 80.35% 90.71%

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.
Uvaria cuneifolia
Uvaria welwitschii

Cross-Links

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PubChem 54080897
LOTUS LTS0219297
wikiData Q105168229