5-Hydroxy-7,2',3'-trimethoxyflavone

Details

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Internal ID edf3ac8f-e544-489f-ba43-070bc9647138
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 2-(2,3-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one
SMILES (Canonical) COC1=CC=CC(=C1OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O
SMILES (Isomeric) COC1=CC=CC(=C1OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O
InChI InChI=1S/C18H16O6/c1-21-10-7-12(19)17-13(20)9-15(24-16(17)8-10)11-5-4-6-14(22-2)18(11)23-3/h4-9,19H,1-3H3
InChI Key UQCFFWBHEHCUQF-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O6
Molecular Weight 328.30 g/mol
Exact Mass 328.09468823 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-7,2',3'-trimethoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.9141 91.41%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7745 77.45%
OATP2B1 inhibitior - 0.7245 72.45%
OATP1B1 inhibitior + 0.9154 91.54%
OATP1B3 inhibitior + 0.9817 98.17%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5443 54.43%
P-glycoprotein inhibitior + 0.8675 86.75%
P-glycoprotein substrate - 0.7109 71.09%
CYP3A4 substrate + 0.5729 57.29%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.5748 57.48%
CYP2C9 inhibition - 0.8861 88.61%
CYP2C19 inhibition + 0.5778 57.78%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.8530 85.30%
CYP2C8 inhibition + 0.6449 64.49%
CYP inhibitory promiscuity + 0.6103 61.03%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5716 57.16%
Eye corrosion - 0.9793 97.93%
Eye irritation + 0.7208 72.08%
Skin irritation - 0.7150 71.50%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4800 48.00%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.9504 95.04%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4546 45.46%
Acute Oral Toxicity (c) II 0.4982 49.82%
Estrogen receptor binding + 0.9248 92.48%
Androgen receptor binding + 0.8053 80.53%
Thyroid receptor binding + 0.7261 72.61%
Glucocorticoid receptor binding + 0.7486 74.86%
Aromatase binding + 0.8341 83.41%
PPAR gamma + 0.7605 76.05%
Honey bee toxicity - 0.8636 86.36%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8902 89.02%

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 97.10% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.92% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.54% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.41% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.84% 98.95%
CHEMBL2535 P11166 Glucose transporter 94.83% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.86% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.78% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.99% 89.00%
CHEMBL3194 P02766 Transthyretin 90.87% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.29% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.46% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 85.26% 93.31%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.28% 95.50%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.68% 94.03%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.27% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 80.53% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 80.19% 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.
Andrographis paniculata

Cross-Links

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PubChem 12135219
NPASS NPC132982
LOTUS LTS0094446
wikiData Q105277147