5,3'-Dihydroxy-7,2'-dimethoxyflavanone

Details

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Internal ID fd82aa71-b7fc-499d-8de3-9f9556ce218f
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O6/c1-21-9-6-12(19)16-13(20)8-14(23-15(16)7-9)10-4-3-5-11(18)17(10)22-2/h3-7,14,18-19H,8H2,1-2H3
InChI Key SFYHUOCTRYJKKC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O6
Molecular Weight 316.30 g/mol
Exact Mass 316.09468823 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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LMPK12140129

2D Structure

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2D Structure of 5,3'-Dihydroxy-7,2'-dimethoxyflavanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9464 94.64%
Caco-2 + 0.8216 82.16%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8136 81.36%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9358 93.58%
OATP1B3 inhibitior + 0.9808 98.08%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6425 64.25%
P-glycoprotein inhibitior - 0.7607 76.07%
P-glycoprotein substrate - 0.9094 90.94%
CYP3A4 substrate + 0.6232 62.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7429 74.29%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition + 0.8724 87.24%
CYP2C19 inhibition + 0.9130 91.30%
CYP2D6 inhibition + 0.5462 54.62%
CYP1A2 inhibition + 0.8681 86.81%
CYP2C8 inhibition + 0.4841 48.41%
CYP inhibitory promiscuity + 0.7191 71.91%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5893 58.93%
Eye corrosion - 0.9863 98.63%
Eye irritation + 0.6002 60.02%
Skin irritation - 0.7064 70.64%
Skin corrosion - 0.9589 95.89%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6096 60.96%
Micronuclear + 0.8559 85.59%
Hepatotoxicity + 0.5157 51.57%
skin sensitisation - 0.9398 93.98%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5583 55.83%
Acute Oral Toxicity (c) III 0.4951 49.51%
Estrogen receptor binding + 0.6446 64.46%
Androgen receptor binding - 0.4874 48.74%
Thyroid receptor binding + 0.5333 53.33%
Glucocorticoid receptor binding + 0.7149 71.49%
Aromatase binding - 0.5757 57.57%
PPAR gamma + 0.6682 66.82%
Honey bee toxicity - 0.8407 84.07%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5147 51.47%
Fish aquatic toxicity + 0.8077 80.77%

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 98.95% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.57% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.63% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.58% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.75% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.17% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.03% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.77% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.86% 99.23%
CHEMBL2535 P11166 Glucose transporter 87.73% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.25% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.73% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.06% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.37% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 84.08% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.93% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.76% 85.14%
CHEMBL4208 P20618 Proteasome component C5 83.39% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.35% 92.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.08% 97.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.70% 94.80%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.45% 92.68%
CHEMBL1929 P47989 Xanthine dehydrogenase 80.23% 96.12%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.13% 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.
Iris tenuifolia

Cross-Links

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PubChem 42607852
LOTUS LTS0037711
wikiData Q105252143