3,5,6,7,8-Pentamethoxyflavone

Details

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Internal ID 2aadee27-ea5e-4f5e-98e5-97dc1f7fcde6
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 3,5,6,7,8-pentamethoxy-2-phenylchromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O7/c1-22-15-12-13(21)17(23-2)14(11-9-7-6-8-10-11)27-16(12)19(25-4)20(26-5)18(15)24-3/h6-10H,1-5H3
InChI Key FDWCURHFRQXFMX-UHFFFAOYSA-N
Popularity 32 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O7
Molecular Weight 372.40 g/mol
Exact Mass 372.12090297 g/mol
Topological Polar Surface Area (TPSA) 72.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.50
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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14221-85-3
3,5,6,7,8-Pentamethoxy-2-phenyl-4H-chromen-4-one
SCHEMBL1764663
DTXSID10332889
4H-1-Benzopyran-4-one, 3,5,6,7,8-pentamethoxy-2-phenyl-
LMPK12113297
3,5,6,7,8-Pentamethoxy-2-phenyl-4H-1-benzopyran-4-one

2D Structure

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2D Structure of 3,5,6,7,8-Pentamethoxyflavone

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 + 0.8490 84.90%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7006 70.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9646 96.46%
OATP1B3 inhibitior + 0.9919 99.19%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7302 73.02%
P-glycoprotein inhibitior + 0.9313 93.13%
P-glycoprotein substrate - 0.9391 93.91%
CYP3A4 substrate - 0.6259 62.59%
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 - 0.6636 66.36%
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 + 0.6157 61.57%
Skin irritation - 0.7565 75.65%
Skin corrosion - 0.9845 98.45%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6557 65.57%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9439 94.39%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6374 63.74%
Acute Oral Toxicity (c) II 0.6245 62.45%
Estrogen receptor binding + 0.7762 77.62%
Androgen receptor binding + 0.7249 72.49%
Thyroid receptor binding + 0.6826 68.26%
Glucocorticoid receptor binding + 0.7376 73.76%
Aromatase binding + 0.5947 59.47%
PPAR gamma + 0.7604 76.04%
Honey bee toxicity - 0.8933 89.33%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6700 67.00%
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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.93% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.22% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.40% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.53% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.13% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.60% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.39% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.65% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.45% 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 nitens
Murraya paniculata

Cross-Links

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PubChem 471720
LOTUS LTS0273733
wikiData Q82097784