(2R)-2-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

Details

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Internal ID ff955c75-3a85-4d2a-804c-4059e351d208
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name (2R)-2-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)OC)C
SMILES (Isomeric) CC(=CCC1=C(C=C(C2=C1O[C@H](CC2=O)C3=C(C=C(C=C3)O)O)O)OC)C
InChI InChI=1S/C21H22O6/c1-11(2)4-6-14-18(26-3)9-16(24)20-17(25)10-19(27-21(14)20)13-7-5-12(22)8-15(13)23/h4-5,7-9,19,22-24H,6,10H2,1-3H3/t19-/m1/s1
InChI Key KRZULWISCLYGBT-LJQANCHMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O6
Molecular Weight 370.40 g/mol
Exact Mass 370.14163842 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9751 97.51%
Caco-2 + 0.8487 84.87%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7143 71.43%
OATP2B1 inhibitior - 0.7198 71.98%
OATP1B1 inhibitior + 0.8766 87.66%
OATP1B3 inhibitior + 0.9190 91.90%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7325 73.25%
P-glycoprotein inhibitior - 0.5198 51.98%
P-glycoprotein substrate - 0.5922 59.22%
CYP3A4 substrate + 0.6198 61.98%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7912 79.12%
CYP3A4 inhibition + 0.5570 55.70%
CYP2C9 inhibition + 0.8604 86.04%
CYP2C19 inhibition + 0.9053 90.53%
CYP2D6 inhibition + 0.6037 60.37%
CYP1A2 inhibition + 0.8484 84.84%
CYP2C8 inhibition + 0.4513 45.13%
CYP inhibitory promiscuity + 0.9465 94.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6637 66.37%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.5964 59.64%
Skin irritation - 0.7762 77.62%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5290 52.90%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8299 82.99%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6156 61.56%
Acute Oral Toxicity (c) III 0.5400 54.00%
Estrogen receptor binding + 0.8484 84.84%
Androgen receptor binding + 0.7305 73.05%
Thyroid receptor binding + 0.5457 54.57%
Glucocorticoid receptor binding + 0.8146 81.46%
Aromatase binding + 0.5423 54.23%
PPAR gamma + 0.8805 88.05%
Honey bee toxicity - 0.7349 73.49%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9807 98.07%

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 98.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.13% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.98% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.14% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.65% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.49% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.27% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.15% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.53% 95.89%
CHEMBL2535 P11166 Glucose transporter 88.32% 98.75%
CHEMBL240 Q12809 HERG 87.52% 89.76%
CHEMBL3401 O75469 Pregnane X receptor 87.11% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.53% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.42% 89.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.26% 96.12%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.61% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.77% 99.23%
CHEMBL4208 P20618 Proteasome component C5 81.10% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.50% 92.62%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.33% 91.07%

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 koreensis

Cross-Links

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PubChem 163011880
LOTUS LTS0241777
wikiData Q105145321