(2r,3r)-2,3-Dihydro-3,5-dihydroxy-7,4'-dimethoxyflavone

Details

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Internal ID 420d1674-14e3-4f86-9ecd-085f48f836e0
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name (2R,3R)-3,5-dihydroxy-7-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O6/c1-21-10-5-3-9(4-6-10)17-16(20)15(19)14-12(18)7-11(22-2)8-13(14)23-17/h3-8,16-18,20H,1-2H3/t16-,17+/m0/s1
InChI Key FEKOGNMSBYBYSO-DLBZAZTESA-N
Popularity 3 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 2.50
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2r,3r)-2,3-Dihydro-3,5-dihydroxy-7,4'-dimethoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9730 97.30%
Caco-2 + 0.5506 55.06%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.8156 81.56%
OATP2B1 inhibitior - 0.7225 72.25%
OATP1B1 inhibitior + 0.9065 90.65%
OATP1B3 inhibitior + 0.9738 97.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6960 69.60%
P-glycoprotein inhibitior + 0.5916 59.16%
P-glycoprotein substrate - 0.9603 96.03%
CYP3A4 substrate + 0.5353 53.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7873 78.73%
CYP3A4 inhibition - 0.5571 55.71%
CYP2C9 inhibition + 0.7766 77.66%
CYP2C19 inhibition + 0.8962 89.62%
CYP2D6 inhibition - 0.7334 73.34%
CYP1A2 inhibition + 0.8679 86.79%
CYP2C8 inhibition - 0.7149 71.49%
CYP inhibitory promiscuity + 0.7750 77.50%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6135 61.35%
Eye corrosion - 0.9782 97.82%
Eye irritation + 0.6932 69.32%
Skin irritation - 0.6511 65.11%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6588 65.88%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.9410 94.10%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6921 69.21%
Acute Oral Toxicity (c) III 0.5602 56.02%
Estrogen receptor binding + 0.7386 73.86%
Androgen receptor binding + 0.7268 72.68%
Thyroid receptor binding + 0.6946 69.46%
Glucocorticoid receptor binding + 0.7645 76.45%
Aromatase binding + 0.6925 69.25%
PPAR gamma + 0.8043 80.43%
Honey bee toxicity - 0.9132 91.32%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8898 88.98%

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 98.37% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.56% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.89% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.79% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.00% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.91% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.87% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.53% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.81% 86.33%
CHEMBL2581 P07339 Cathepsin D 87.58% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.95% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.07% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.87% 99.17%
CHEMBL2535 P11166 Glucose transporter 84.52% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.82% 93.99%
CHEMBL4208 P20618 Proteasome component C5 83.15% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.36% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 80.51% 91.49%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 15118763
LOTUS LTS0094976
wikiData Q104994005