Kanzakiflavone 1

Details

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Internal ID 11a9c3f4-bdd7-44fe-b09c-14e937130a86
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 4-O-methylated flavonoids
IUPAC Name 4,9-dihydroxy-6-(4-methoxyphenyl)-[1,3]dioxolo[4,5-g]chromen-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H12O7/c1-21-9-4-2-8(3-5-9)11-6-10(18)12-13(19)16-17(23-7-22-16)14(20)15(12)24-11/h2-6,19-20H,7H2,1H3
InChI Key ZVMXYXZXCSMOLC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H12O7
Molecular Weight 328.27 g/mol
Exact Mass 328.05830272 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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Kanzakiflavone-1
ZVMXYXZXCSMOLC-UHFFFAOYSA-N
LMPK12111452

2D Structure

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2D Structure of Kanzakiflavone 1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9551 95.51%
Caco-2 + 0.6268 62.68%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8408 84.08%
OATP2B1 inhibitior - 0.7120 71.20%
OATP1B1 inhibitior + 0.9062 90.62%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior + 0.5200 52.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6810 68.10%
P-glycoprotein inhibitior + 0.6281 62.81%
P-glycoprotein substrate - 0.9022 90.22%
CYP3A4 substrate + 0.5285 52.85%
CYP2C9 substrate - 0.8007 80.07%
CYP2D6 substrate - 0.8454 84.54%
CYP3A4 inhibition + 0.8113 81.13%
CYP2C9 inhibition + 0.9191 91.91%
CYP2C19 inhibition + 0.8482 84.82%
CYP2D6 inhibition + 0.6777 67.77%
CYP1A2 inhibition - 0.5101 51.01%
CYP2C8 inhibition + 0.4439 44.39%
CYP inhibitory promiscuity + 0.8801 88.01%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4284 42.84%
Eye corrosion - 0.9828 98.28%
Eye irritation + 0.5289 52.89%
Skin irritation - 0.7450 74.50%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis + 0.5336 53.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5442 54.42%
Micronuclear + 0.8474 84.74%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.8780 87.80%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7872 78.72%
Acute Oral Toxicity (c) III 0.6548 65.48%
Estrogen receptor binding + 0.9034 90.34%
Androgen receptor binding + 0.9125 91.25%
Thyroid receptor binding + 0.6054 60.54%
Glucocorticoid receptor binding + 0.8780 87.80%
Aromatase binding + 0.8446 84.46%
PPAR gamma + 0.9171 91.71%
Honey bee toxicity - 0.8663 86.63%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8655 86.55%

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 99.55% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.18% 94.00%
CHEMBL2581 P07339 Cathepsin D 96.25% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.73% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.88% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.55% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.43% 96.77%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.88% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.25% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.21% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.76% 86.33%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.15% 85.30%
CHEMBL4208 P20618 Proteasome component C5 86.01% 90.00%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 84.61% 89.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.89% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.34% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 81.89% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 81.08% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.02% 99.17%

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.
Iris unguicularis

Cross-Links

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PubChem 44258636
LOTUS LTS0039689
wikiData Q105384445