5,7,4'-Trihydroxy-6,3'-dimethoxyflavanon

Details

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Internal ID df701077-d299-404a-9d67-7e5a76aba3a4
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 6-O-methylated flavonoids
IUPAC Name 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O7/c1-22-13-5-8(3-4-9(13)18)12-6-10(19)15-14(24-12)7-11(20)17(23-2)16(15)21/h3-5,7,12,18,20-21H,6H2,1-2H3
InChI Key UQPOQRIRWKIBNS-UHFFFAOYSA-N
Popularity 3 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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5,7,4'-Trihydroxy-6,3'-dimethoxyflavanon

2D Structure

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2D Structure of 5,7,4'-Trihydroxy-6,3'-dimethoxyflavanon

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 + 0.7202 72.02%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6677 66.77%
OATP2B1 inhibitior - 0.7225 72.25%
OATP1B1 inhibitior + 0.9295 92.95%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8274 82.74%
P-glycoprotein inhibitior - 0.8220 82.20%
P-glycoprotein substrate - 0.9374 93.74%
CYP3A4 substrate + 0.5315 53.15%
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 - 0.6072 60.72%
CYP inhibitory promiscuity + 0.7970 79.70%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6313 63.13%
Eye corrosion - 0.9856 98.56%
Eye irritation + 0.8490 84.90%
Skin irritation - 0.7056 70.56%
Skin corrosion - 0.9385 93.85%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6487 64.87%
Micronuclear + 0.8559 85.59%
Hepatotoxicity - 0.5843 58.43%
skin sensitisation - 0.9243 92.43%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6608 66.08%
Acute Oral Toxicity (c) III 0.5400 54.00%
Estrogen receptor binding + 0.7989 79.89%
Androgen receptor binding + 0.5219 52.19%
Thyroid receptor binding + 0.6528 65.28%
Glucocorticoid receptor binding + 0.7574 75.74%
Aromatase binding - 0.7003 70.03%
PPAR gamma + 0.7140 71.40%
Honey bee toxicity - 0.8651 86.51%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5800 58.00%
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 99.39% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.68% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.46% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.60% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.93% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.74% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.45% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.48% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.21% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.83% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.15% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.94% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.05% 95.89%
CHEMBL4208 P20618 Proteasome component C5 85.00% 90.00%
CHEMBL3438 Q05513 Protein kinase C zeta 84.91% 88.48%
CHEMBL2535 P11166 Glucose transporter 83.15% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.55% 99.17%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 82.28% 96.86%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.46% 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.
Artemisia xerophytica
Eriodictyon californicum
Gutierrezia sphaerocephala

Cross-Links

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PubChem 14034286
LOTUS LTS0121215
wikiData Q105277387