Kushenol W

Details

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Internal ID e5bf03ab-c93c-4764-a293-306eb4f1eada
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name 2-(2,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O7/c1-10(2)4-5-11-13(22)8-16(25)20-17(26)9-18(28-21(11)20)12-6-19(27-3)15(24)7-14(12)23/h4,6-8,18,22-25H,5,9H2,1-3H3
InChI Key IPQQRODECSTJDH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O7
Molecular Weight 386.40 g/mol
Exact Mass 386.13655304 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.73
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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254886-76-5
2-(2,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
5,7,2',4'-Tetrahydroxy-5'-methoxy-8-prenylflavanone
KushenolW
CHEMBL479476
CHEBI:197284
HY-N8097
LMPK12140492
AKOS040760510
CS-0139944

2D Structure

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2D Structure of Kushenol W

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9726 97.26%
Caco-2 + 0.6962 69.62%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5708 57.08%
OATP2B1 inhibitior - 0.7083 70.83%
OATP1B1 inhibitior + 0.8932 89.32%
OATP1B3 inhibitior + 0.9251 92.51%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7170 71.70%
P-glycoprotein inhibitior - 0.5640 56.40%
P-glycoprotein substrate - 0.7358 73.58%
CYP3A4 substrate + 0.5871 58.71%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7912 79.12%
CYP3A4 inhibition - 0.6646 66.46%
CYP2C9 inhibition + 0.8313 83.13%
CYP2C19 inhibition + 0.9035 90.35%
CYP2D6 inhibition + 0.6981 69.81%
CYP1A2 inhibition + 0.7999 79.99%
CYP2C8 inhibition - 0.6948 69.48%
CYP inhibitory promiscuity + 0.8964 89.64%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6912 69.12%
Eye corrosion - 0.9890 98.90%
Eye irritation + 0.5703 57.03%
Skin irritation - 0.7726 77.26%
Skin corrosion - 0.9434 94.34%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6265 62.65%
Micronuclear + 0.5259 52.59%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.8416 84.16%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.5665 56.65%
Acute Oral Toxicity (c) III 0.5393 53.93%
Estrogen receptor binding + 0.9172 91.72%
Androgen receptor binding + 0.5905 59.05%
Thyroid receptor binding + 0.5541 55.41%
Glucocorticoid receptor binding + 0.8118 81.18%
Aromatase binding - 0.6072 60.72%
PPAR gamma + 0.7802 78.02%
Honey bee toxicity - 0.7278 72.78%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9751 97.51%

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 98.81% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.10% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.75% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.95% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.24% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.67% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.19% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.27% 99.17%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.29% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.11% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.16% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.65% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.25% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 82.99% 94.73%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.57% 89.50%
CHEMBL2535 P11166 Glucose transporter 81.38% 98.75%
CHEMBL4208 P20618 Proteasome component C5 81.00% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.22% 99.23%

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 flavescens

Cross-Links

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PubChem 42608033
LOTUS LTS0170215
wikiData Q105117410