2'-Hydroxy-2,3,4,5,6'-pentamethoxy-4',5'-methylenedioxychalcone

Details

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Internal ID 048a3131-1ed3-4521-9f0c-fbc603387bc0
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxychalcones
IUPAC Name 1-(6-hydroxy-4-methoxy-1,3-benzodioxol-5-yl)-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O9/c1-24-14-8-11(17(25-2)21(28-5)18(14)26-3)6-7-12(22)16-13(23)9-15-19(20(16)27-4)30-10-29-15/h6-9,23H,10H2,1-5H3
InChI Key OBPLDMNJOKPNQM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O9
Molecular Weight 418.40 g/mol
Exact Mass 418.12638228 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2'-Hydroxy-2,3,4,5,6'-pentamethoxy-4',5'-methylenedioxychalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8973 89.73%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7160 71.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9026 90.26%
OATP1B3 inhibitior + 0.9280 92.80%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.7593 75.93%
P-glycoprotein inhibitior + 0.7152 71.52%
P-glycoprotein substrate - 0.8622 86.22%
CYP3A4 substrate + 0.5370 53.70%
CYP2C9 substrate - 0.7968 79.68%
CYP2D6 substrate - 0.8492 84.92%
CYP3A4 inhibition + 0.8626 86.26%
CYP2C9 inhibition + 0.7917 79.17%
CYP2C19 inhibition + 0.8438 84.38%
CYP2D6 inhibition + 0.6521 65.21%
CYP1A2 inhibition - 0.7785 77.85%
CYP2C8 inhibition + 0.5925 59.25%
CYP inhibitory promiscuity + 0.8390 83.90%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Danger 0.4770 47.70%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.7233 72.33%
Skin irritation - 0.7538 75.38%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.5554 55.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5703 57.03%
Micronuclear + 0.8074 80.74%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.6153 61.53%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6695 66.95%
Acute Oral Toxicity (c) II 0.4678 46.78%
Estrogen receptor binding + 0.8807 88.07%
Androgen receptor binding - 0.5158 51.58%
Thyroid receptor binding + 0.6790 67.90%
Glucocorticoid receptor binding + 0.7558 75.58%
Aromatase binding + 0.5380 53.80%
PPAR gamma + 0.7698 76.98%
Honey bee toxicity - 0.8543 85.43%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6755 67.55%
Fish aquatic toxicity + 0.9803 98.03%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.53% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.33% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.14% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.33% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.24% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.65% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.52% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.00% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.48% 92.62%
CHEMBL3194 P02766 Transthyretin 85.44% 90.71%
CHEMBL4208 P20618 Proteasome component C5 84.99% 90.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.63% 85.30%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.29% 82.67%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.79% 89.50%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.77% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 82.41% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 81.73% 91.19%
CHEMBL2535 P11166 Glucose transporter 80.15% 98.75%

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.
Scutellaria indica

Cross-Links

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PubChem 72730056
LOTUS LTS0273992
wikiData Q105189107