3,5,6,7,2',3',4'-Heptamethoxyflavone

Details

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Internal ID 1f2d3061-3ede-468a-aef7-9b0829912754
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 3,5,6,7-tetramethoxy-2-(2,3,4-trimethoxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O9/c1-24-12-9-8-11(17(26-3)19(12)27-4)18-22(30-7)16(23)15-13(31-18)10-14(25-2)20(28-5)21(15)29-6/h8-10H,1-7H3
InChI Key GNXIYGACTWSGIG-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O9
Molecular Weight 432.40 g/mol
Exact Mass 432.14203234 g/mol
Topological Polar Surface Area (TPSA) 90.90 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.8194 81.94%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7006 70.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9346 93.46%
OATP1B3 inhibitior + 0.9919 99.19%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7901 79.01%
P-glycoprotein inhibitior + 0.9270 92.70%
P-glycoprotein substrate - 0.6376 63.76%
CYP3A4 substrate + 0.5203 52.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7654 76.54%
CYP3A4 inhibition + 0.6138 61.38%
CYP2C9 inhibition - 0.7985 79.85%
CYP2C19 inhibition + 0.7445 74.45%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition + 0.9694 96.94%
CYP2C8 inhibition + 0.5671 56.71%
CYP inhibitory promiscuity + 0.8123 81.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5636 56.36%
Eye corrosion - 0.9682 96.82%
Eye irritation - 0.7058 70.58%
Skin irritation - 0.7565 75.65%
Skin corrosion - 0.9845 98.45%
Ames mutagenesis + 0.5136 51.36%
Human Ether-a-go-go-Related Gene inhibition + 0.7010 70.10%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9439 94.39%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6131 61.31%
Acute Oral Toxicity (c) II 0.6245 62.45%
Estrogen receptor binding + 0.8766 87.66%
Androgen receptor binding + 0.7695 76.95%
Thyroid receptor binding + 0.6721 67.21%
Glucocorticoid receptor binding + 0.7570 75.70%
Aromatase binding + 0.6503 65.03%
PPAR gamma + 0.7798 77.98%
Honey bee toxicity - 0.8806 88.06%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9192 91.92%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.47% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.18% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.99% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.65% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.62% 91.11%
CHEMBL4302 P08183 P-glycoprotein 1 87.63% 92.98%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.33% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.18% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 85.28% 90.20%
CHEMBL2535 P11166 Glucose transporter 84.17% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.54% 99.17%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.24% 96.67%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 81.91% 95.72%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.15% 94.42%

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.
Apuleia leiocarpa

Cross-Links

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PubChem 14376432
LOTUS LTS0099733
wikiData Q104167329