Exiguaflavanone F

Details

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Internal ID b3a3bc62-8e9a-4227-b648-99f85279bb0b
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name 2-(2,5-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H30O6/c1-14(2)6-7-16(15(3)4)10-19-23(31-5)12-21(29)25-22(30)13-24(32-26(19)25)18-11-17(27)8-9-20(18)28/h6,8-9,11-12,16,24,27-29H,3,7,10,13H2,1-2,4-5H3
InChI Key ZJKKLHCVHLKAGC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30O6
Molecular Weight 438.50 g/mol
Exact Mass 438.20423867 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.61
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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LMPK12140113

2D Structure

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2D Structure of Exiguaflavanone F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9835 98.35%
Caco-2 - 0.6153 61.53%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7843 78.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8452 84.52%
OATP1B3 inhibitior + 0.8994 89.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9295 92.95%
P-glycoprotein inhibitior + 0.7468 74.68%
P-glycoprotein substrate - 0.5538 55.38%
CYP3A4 substrate + 0.6345 63.45%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.7963 79.63%
CYP3A4 inhibition - 0.6057 60.57%
CYP2C9 inhibition + 0.8362 83.62%
CYP2C19 inhibition + 0.9062 90.62%
CYP2D6 inhibition - 0.5921 59.21%
CYP1A2 inhibition + 0.7802 78.02%
CYP2C8 inhibition + 0.6171 61.71%
CYP inhibitory promiscuity + 0.9117 91.17%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6978 69.78%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.7523 75.23%
Skin irritation - 0.7818 78.18%
Skin corrosion - 0.9514 95.14%
Ames mutagenesis - 0.5537 55.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6987 69.87%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.8097 80.97%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5112 51.12%
Acute Oral Toxicity (c) III 0.5603 56.03%
Estrogen receptor binding + 0.8495 84.95%
Androgen receptor binding + 0.6698 66.98%
Thyroid receptor binding + 0.6248 62.48%
Glucocorticoid receptor binding + 0.8094 80.94%
Aromatase binding + 0.5392 53.92%
PPAR gamma + 0.7187 71.87%
Honey bee toxicity - 0.6589 65.89%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9925 99.25%

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 99.11% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.08% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.46% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.91% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.66% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.80% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.32% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.48% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.80% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.81% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.51% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.21% 91.07%
CHEMBL2535 P11166 Glucose transporter 84.46% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.45% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.97% 99.23%
CHEMBL1902 P62942 FK506-binding protein 1A 81.37% 97.05%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.36% 92.62%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.21% 89.62%
CHEMBL4208 P20618 Proteasome component C5 80.92% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.58% 97.09%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.19% 91.03%

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.
Sophora exigua

Cross-Links

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PubChem 42607845
LOTUS LTS0095194
wikiData Q105377950