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

Details

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Internal ID a14d0b86-221d-4753-8878-5050e107e946
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 5,6,7-trimethoxy-2-(2,3,4,5-tetramethoxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O9/c1-24-15-8-11(18(26-3)22(30-7)20(15)28-5)13-9-12(23)17-14(31-13)10-16(25-2)19(27-4)21(17)29-6/h8,10,13H,9H2,1-7H3
InChI Key IRGHIHOWMUMHJU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H26O9
Molecular Weight 434.40 g/mol
Exact Mass 434.15768240 g/mol
Topological Polar Surface Area (TPSA) 90.90 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.45
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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CHEBI:179353
LMPK12140640
5,6,7-trimethoxy-2-(2,3,4,5-tetramethoxyphenyl)-2,3-dihydrochromen-4-one

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.8872 88.72%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7174 71.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9455 94.55%
OATP1B3 inhibitior + 0.9882 98.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7810 78.10%
P-glycoprotein inhibitior + 0.7314 73.14%
P-glycoprotein substrate - 0.8978 89.78%
CYP3A4 substrate + 0.5386 53.86%
CYP2C9 substrate - 0.8256 82.56%
CYP2D6 substrate + 0.3744 37.44%
CYP3A4 inhibition + 0.5817 58.17%
CYP2C9 inhibition - 0.8168 81.68%
CYP2C19 inhibition + 0.7186 71.86%
CYP2D6 inhibition - 0.9324 93.24%
CYP1A2 inhibition + 0.9255 92.55%
CYP2C8 inhibition - 0.7023 70.23%
CYP inhibitory promiscuity + 0.7312 73.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5681 56.81%
Eye corrosion - 0.9747 97.47%
Eye irritation - 0.7037 70.37%
Skin irritation - 0.7895 78.95%
Skin corrosion - 0.9824 98.24%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4087 40.87%
Micronuclear + 0.7418 74.18%
Hepatotoxicity + 0.6032 60.32%
skin sensitisation - 0.9278 92.78%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5824 58.24%
Acute Oral Toxicity (c) II 0.5134 51.34%
Estrogen receptor binding + 0.8813 88.13%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.7146 71.46%
Glucocorticoid receptor binding + 0.8176 81.76%
Aromatase binding - 0.6706 67.06%
PPAR gamma + 0.6545 65.45%
Honey bee toxicity - 0.7731 77.31%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.8462 84.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.67% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.38% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.70% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.67% 95.56%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 88.60% 96.86%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.78% 94.45%
CHEMBL2535 P11166 Glucose transporter 85.78% 98.75%
CHEMBL2581 P07339 Cathepsin D 85.36% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.08% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.82% 94.80%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.79% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.09% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.00% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.86% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.53% 94.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.14% 95.89%

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.
Persicaria nepalensis
Scutellaria indica

Cross-Links

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PubChem 14332451
LOTUS LTS0204509
wikiData Q105118816