3,5-Dihydroxy-6,7-dimethoxyflavone

Details

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Internal ID 09d22d25-0c76-4357-a2b8-5ba90cdfeac3
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > Flavonols
IUPAC Name 3,5-dihydroxy-6,7-dimethoxy-2-phenylchromen-4-one
SMILES (Canonical) COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O)OC
InChI InChI=1S/C17H14O6/c1-21-11-8-10-12(14(19)17(11)22-2)13(18)15(20)16(23-10)9-6-4-3-5-7-9/h3-8,19-20H,1-2H3
InChI Key WNIPXMMUMPJVNI-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O6
Molecular Weight 314.29 g/mol
Exact Mass 314.07903816 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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dimethoxydihydroxy flavone
LMPK12112808

2D Structure

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2D Structure of 3,5-Dihydroxy-6,7-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 - 0.5890 58.90%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.8156 81.56%
OATP2B1 inhibitior - 0.5718 57.18%
OATP1B1 inhibitior + 0.9424 94.24%
OATP1B3 inhibitior + 0.9738 97.38%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5957 59.57%
P-glycoprotein inhibitior + 0.8956 89.56%
P-glycoprotein substrate - 0.7794 77.94%
CYP3A4 substrate + 0.5137 51.37%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
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 + 0.8563 85.63%
CYP inhibitory promiscuity + 0.7750 77.50%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6135 61.35%
Eye corrosion - 0.9782 97.82%
Eye irritation + 0.7313 73.13%
Skin irritation - 0.6511 65.11%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis - 0.6464 64.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5785 57.85%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.9410 94.10%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8400 84.00%
Acute Oral Toxicity (c) III 0.5602 56.02%
Estrogen receptor binding + 0.8008 80.08%
Androgen receptor binding + 0.7070 70.70%
Thyroid receptor binding + 0.6376 63.76%
Glucocorticoid receptor binding + 0.8268 82.68%
Aromatase binding + 0.7531 75.31%
PPAR gamma + 0.8156 81.56%
Honey bee toxicity - 0.8793 87.93%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5851 58.51%
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 98.54% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.38% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.66% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.78% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.32% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.55% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.52% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.79% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.76% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.10% 99.23%
CHEMBL1255126 O15151 Protein Mdm4 84.87% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.94% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 80.63% 94.73%

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.
Helichrysum stoechas subsp. stoechas
Muntingia calabura

Cross-Links

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PubChem 13291608
LOTUS LTS0048293
wikiData Q105309109