2-(2,4-Dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-2,3-dihydrochromen-4-one

Details

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Internal ID 3ca42bfe-8090-4612-8fe1-783f173c0fb1
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 2-(2,4-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O7/c1-22-14-7-13-15(16(21)17(14)23-2)11(20)6-12(24-13)9-4-3-8(18)5-10(9)19/h3-5,7,12,18-19,21H,6H2,1-2H3
InChI Key XBTHWGFPZWQGLZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O7
Molecular Weight 332.30 g/mol
Exact Mass 332.08960285 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2,4-Dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8896 88.96%
Caco-2 + 0.7119 71.19%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6677 66.77%
OATP2B1 inhibitior - 0.7203 72.03%
OATP1B1 inhibitior + 0.9289 92.89%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7510 75.10%
P-glycoprotein inhibitior - 0.8220 82.20%
P-glycoprotein substrate - 0.7605 76.05%
CYP3A4 substrate + 0.6095 60.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7429 74.29%
CYP3A4 inhibition + 0.8405 84.05%
CYP2C9 inhibition + 0.7985 79.85%
CYP2C19 inhibition + 0.8607 86.07%
CYP2D6 inhibition + 0.6848 68.48%
CYP1A2 inhibition + 0.8659 86.59%
CYP2C8 inhibition + 0.5904 59.04%
CYP inhibitory promiscuity + 0.7970 79.70%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6313 63.13%
Eye corrosion - 0.9856 98.56%
Eye irritation + 0.7549 75.49%
Skin irritation - 0.7056 70.56%
Skin corrosion - 0.9385 93.85%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7293 72.93%
Micronuclear + 0.8559 85.59%
Hepatotoxicity - 0.5197 51.97%
skin sensitisation - 0.9243 92.43%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7198 71.98%
Acute Oral Toxicity (c) III 0.5400 54.00%
Estrogen receptor binding + 0.7668 76.68%
Androgen receptor binding + 0.6077 60.77%
Thyroid receptor binding + 0.5670 56.70%
Glucocorticoid receptor binding + 0.7438 74.38%
Aromatase binding - 0.6505 65.05%
PPAR gamma + 0.7362 73.62%
Honey bee toxicity - 0.8348 83.48%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7689 76.89%

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 97.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.10% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.93% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.62% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.42% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.57% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.37% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.26% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.50% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.54% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.08% 99.23%
CHEMBL2535 P11166 Glucose transporter 88.92% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.48% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.37% 93.99%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.87% 95.89%
CHEMBL217 P14416 Dopamine D2 receptor 86.62% 95.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.13% 90.71%
CHEMBL2056 P21728 Dopamine D1 receptor 81.87% 91.00%
CHEMBL4208 P20618 Proteasome component C5 81.68% 90.00%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 81.07% 89.32%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.81% 91.07%

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.
Artemisia annua

Cross-Links

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PubChem 162898919
LOTUS LTS0108962
wikiData Q105324666